US20010050031A1 - Compositions for three-dimensional printing of solid objects - Google Patents

Compositions for three-dimensional printing of solid objects Download PDF

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Publication number
US20010050031A1
US20010050031A1 US09/835,292 US83529201A US2001050031A1 US 20010050031 A1 US20010050031 A1 US 20010050031A1 US 83529201 A US83529201 A US 83529201A US 2001050031 A1 US2001050031 A1 US 2001050031A1
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United States
Prior art keywords
composition
filler
adhesive
particulate material
sodium
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Abandoned
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US09/835,292
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James Bredt
Sarah Clark
Evert Uy
Matthew DiCologero
Timothy Anderson
Michael Tarkanian
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Z Corp
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Z Corp
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Priority to US09/835,292 priority Critical patent/US20010050031A1/en
Assigned to Z CORPORATION reassignment Z CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: UY, EVERT F., BREDT, JAMES F., CLARK, SARAH L., DICOLOGERO, MATTHEW, TARKANIAN, MICHAEL J., ANDERSON, TIMOTHY
Publication of US20010050031A1 publication Critical patent/US20010050031A1/en
Priority to US11/068,487 priority patent/US7550518B2/en
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00Inks
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C41/00Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
    • B29C41/003Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor characterised by the choice of material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C64/00Additive manufacturing, i.e. manufacturing of three-dimensional [3D] objects by additive deposition, additive agglomeration or additive layering, e.g. by 3D printing, stereolithography or selective laser sintering
    • B29C64/10Processes of additive manufacturing
    • B29C64/165Processes of additive manufacturing using a combination of solid and fluid materials, e.g. a powder selectively bound by a liquid binder, catalyst, inhibitor or energy absorber
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C67/00Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00
    • B29C67/24Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00 characterised by the choice of material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y10/00Processes of additive manufacturing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y70/00Materials specially adapted for additive manufacturing
    • B33Y70/10Composites of different types of material, e.g. mixtures of ceramics and polymers or mixtures of metals and biomaterials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C64/00Additive manufacturing, i.e. manufacturing of three-dimensional [3D] objects by additive deposition, additive agglomeration or additive layering, e.g. by 3D printing, stereolithography or selective laser sintering
    • B29C64/10Processes of additive manufacturing
    • B29C64/106Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material
    • B29C64/112Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material using individual droplets, e.g. from jetting heads
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2033/00Use of polymers of unsaturated acids or derivatives thereof as moulding material
    • B29K2033/04Polymers of esters
    • B29K2033/08Polymers of acrylic acid esters, e.g. PMA, i.e. polymethylacrylate
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/0097Glues or adhesives, e.g. hot melts or thermofusible adhesives
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y80/00Products made by additive manufacturing

Definitions

  • Rapid prototyping involves the production of prototype articles and small quantities of functional parts, as well as structural ceramics and ceramic shell molds for metal casting, directly from computer-generated design data.
  • methods to form a three-dimensional article including a selective laser-sintering process as described in U.S. Pat. No. 4,863,568, which is incorporated herein by reference.
  • Three-dimensional printing is a process invented by Sachs et al. at Massachusetts Institute of Technology in the early 1980's.
  • an ink-jet printhead is used to deposit a liquid ink or binder onto a print plane composed of a powdered receiving medium.
  • the combination of liquid binder and solid powder solidifies to form a finished article.
  • the three-dimensional ink-jet printing technique (hereafter “liquid-binder method”) involves applying a layer of a powdered material to a surface using a counter roller. After the powdered material is applied to the surface, the ink-jet printhead delivers a liquid binder to the layer of powder. The binder infiltrates into gaps in the powder material, hardening to bond the powder material into a solidified layer. The hardened binder also bonds each layer to the previous layer.
  • the binder can be suspended in a carrier that evaporates, leaving the hardened binder behind.
  • the powdered material can be ceramic, metal, plastic or a composite material, and can also include fiber.
  • the liquid-binder material can be organic or inorganic. Typical organic binder materials used are polymeric resins, or ceramic precursors such as polycarbosilazane. Inorganic binders are used where the binder is incorporated into the final articles; silica is typically used in such an application.
  • ink-jet printing there are a number of different types of printheads distinguished by the mechanism by which ink is ejected onto the printing plane.
  • the two broadest classes of printheads are called, “continuous-jet” and “drop-on-demand.”
  • a continuous-jet printhead a liquid ink or binder is projected continuously through a nozzle.
  • the jet is deflected alternatively onto the print plane or in to a collector that masks the printing plane.
  • drop-on-demand printhead ink or binder is ejected when it is needed by sending an impulse, most usually electrical, that causes an actuator in the printhead to eject a droplet of ink or binder onto the print plane.
  • liquid-binder printing techniques with a thermal (bubble) printhead can present reliability problem associated with the spray nozzle becoming clogged with the binder material. Clogging can occur when binders having high levels of solids are used. The problem with clogging requires frequent interruptions of the build in order to clean the spray nozzle; this problem also increases the time and labor required to build parts and to maintain the equipment. Therefore, although the liquid-binder printing technique represents an advance in speed and cost over the selective laser-sintering process, it suffers from reliability problems that slow down the build rate, increasing labor and equipment maintenance costs. This problem interferes with the potential speed advantage of increased printing capability presented by the plurality of spray nozzles.
  • the materials for fabricating three-dimensional objects lead to a materials system and method that produce both appearance models and small numbers of functional parts in an office environment.
  • the materials system can include at least one solid filler and a liquid binder composition.
  • Particular binder compositions can be effectively deposited using an electromechanical printhead having suitable components.
  • the fabrication methods can be quick, reliable, safe, and inexpensive.
  • An article can be made of a mixture of particles including adhesive and at least one filler.
  • the adhesive may be activated by a fluid including a solvent.
  • the binder can also include various processing aids or additions that modify the working properties of the fluid and adhesive or that enhance the mechanical properties of the finished article.
  • the mixture of particles can also optionally include particles of fiber and various processing aids.
  • the activated adhesive causes the filler particles to adhere together, and to adhere to previously formed adjacent layers.
  • Adhesive can be supplied to the article by coating it on the fiber and/or filler, by directly mixing it with the fiber and filler before delivering the fluid and/or by dissolving or mixing the adhesive in the fluid before the fluid is delivered to the mixture of particles.
  • a particular method for producing such articles can include applying a layer of the above-mentioned mixture onto a flat surface that can be indexed downward.
  • Cross-sectional portions of an article can be defined by delivering an activating fluid, the adhesive, to the layer of the mixture of particles in a predetermined two-dimensional pattern.
  • the fluid activates the adhesive, and the activated adhesive causes the particles to adhere together in an essentially solid layer.
  • the movable surface can be indexed downward by an amount corresponding to the desired layer thickness.
  • Successive layers of the mixture of particles are applied to previous layers in the same manner.
  • Application of the fluid using an electromechanical ink-jet print head follows the application of each successive layer of the mixture of particulate material.
  • Depositing a layer of the mixture of particulate material and delivering the fluid to the layer can be repeated until the required number of cross-sectional portions have been built, completing formation of the article.
  • After formation of the article has been completed it typically remains immersed in a bed of unbound particulate material, where it can remain until the article is completely dry.
  • Delicate features of the article remain supported by the unbound particulate material while drying.
  • the finished article can then be removed from the bed of unbound particulate material and any excess unbound particulate material clinging to the finished article can be removed by a suitable cleaning process.
  • excess powder can be removed by vacuuming it off the article, by blowing it off the article, and by brushing to remove any powder left in crevices.
  • the finished article can be placed in an oven for more rapid drying.
  • optional post-processing actions can include heat-treating, resin or wax infiltration, painting and sanding.
  • Heat treating and infiltration can increase the strength and durability of the finished article. Infiltration can reduce porosity, making the article water resistant and more readily sanded.
  • Painting the article can provide a more aesthetically pleasing appearance, and may also contribute to the strength and water resistance of the final articles.
  • Sanding improves the surface smoothness, reducing any surface irregularities caused, for example, by fiber penetrating through the surface. Parts can be glued or fastened, or used as patterns for subsequent molding operations.
  • electromechanical ink-jet printheads to deliver the fluid compositions allows for the incorporation of thermally-sensitive adhesives in the fluid due to the fact that electromechanical ink-jet printheads typically operate at ambient-temperature. Further, fluids with a large amount of dissolved or suspended solids subject to degradation with temperature excursions can likewise be better accommodated by an electromechanical printhead relative to a thermal printhead.
  • the use of fluids with higher solids content with an electromechanical printhead further allows for the formation of materials that will shrink less (due to fewer escaping components) and that have higher strength and greater dimensional stability than materials formed with more dilute binders. Further still, the incorporation of adhesives in the activating fluid and the delivery of that fluid to the particulate bed allows for an increased amount of adhesive to be incorporated into the final part.
  • the composition selectively adhere particulate material to form a solid object in a three-dimensional printer.
  • the composition comprises a nonaqueous organic monomeric compound. That compound can include at least one of an alcohol, an ester, an ether, a silane, a vinyl monomer, an acrylic monomer, or a methacrylate monomer.
  • the composition can include a solvent and a solute, and in one embodiment, the compound is the solvent.
  • the solvent can include an alcohol such as methyl alcohol, ethyl alcohol, isopropanol, or t-butanol.
  • the solvent includes an ester that includes at least one of ethyl acetate, dimethyl succinate, diethyl succinate, dimethyl adipate, or ethylene glycol diacetate.
  • the compound is a solvent for a resin in the particulate material.
  • the resin can include at least one of shellac, polyvinyl pyrrolidone, polyvinyl acetate, polyvinyl alcohol, polystyrene, styrene-butadiene copolymer, or acrylonitrile-butadiene-styrene copolymer.
  • organic acids and sugars such as sucrose, dextrose, malic acid, and sodium citrate, and other compounds such as urea and hydrolized amino acids can be used as solutes in water solution. These compounds bind the particulate material together by drying in the powder, and not have any appreciable solvent character on their own.
  • the monomeric compound can include a mixed monomer vinyl-silane and can include vinyltriisopropoxysilane.
  • the acrylic monomer can include at least one of tri(propylene glycol) diacrylate, ethylene glycol phenyl ether acrylate, or 1,6 hexanediol diacrylate.
  • the methacrylic monomer can include at least one of 1,3 butylene glycol dimethacrylate, neopentyl glycol dimethacrylate, butyl methacrylate, 1,6 hexanediol dimethacrylate, or di(propylene glycol) allyl ether methacrylate.
  • the compound can be curable, in combination with a photoinitiator in a solid, by ultraviolet radiation having a wavelength between about 320-500 nm and an energy density of about 1 joule/cm 2 .
  • the particulate material can include a filler that includes an inorganic compound.
  • the filler includes at least one of clay, aluminum oxide, silicon dioxide, aluminum silicate, potassium aluminum silicate, calcium silicate, calcium hydroxide, calcium aluminate, calcium carbonate, sodium silicate, zinc oxide, titanium dioxide, or magnetite.
  • a printing aid can be dispersed throughout the filler.
  • the printing aid can include at least one of sorbitan trioleate, sorbitan mono-oleate, sorbitan monolaurate, polyoxyethylene sorbitan mono-oleate, polyethylene glycol, soybean oil, mineral oil, propylene glycol, fluroaklkyl polyoxyethylene polymers, glycerol triacetate, polypropylene glycol, ethylene glycol octanoate, ethylene glycol decanoate, ethoxylated derivatives of 2,4,7,9-Tetramethyl-5-decyne-4,7-diol, oleyl alcohol, or oleic acid.
  • a binder composition is also provided, which can include an adhesive in combination with a fluid, for selectively adhering particulate material to form a solid object in a three-dimensional printer.
  • the adhesive can include a nonaqueous organic monomeric compound.
  • an adhesive for selectively adhering particulate material to form a solid object in a three-dimensional printer includes an anionically ionizable polymer consisting of compounds selected from the group including polymethacrylic acid, polymethacrylic acid sodium salt, and sodium polystyrene sulfonate.
  • the adhesive includes a cationic polymer such as polyethyleneimine and polydiallyldimethylammonium chloride.
  • the adhesive includes a nonionic polymer.
  • the polymer can include at least one of polyvinyl pyrrolidone, polyvinyl pyrrolidone copolymer with polyvinyl acetate, polyvinyl alcohol, polyvinyl methyl ether, polyacrylamide, or poly-2-ethyl-2-oxazoline.
  • the adhesive includes a polymer selected from the group consisting of polymethacrylic acid, polymethacrylic acid sodium salt, sodium polystyrene sulfonate, and polyethyleneimine.
  • the adhesive includes a waterborne colloid such as polymethyl methacrylate, polystyrene, natural rubber, polyurethane, polyvinyl acetate, and alkyd resins.
  • the adhesive includes an inorganic solute selected from the group consisting of sodium polyphosphate, sodium tetraborate, sodium chloride, ammonium nitrate, potassium sulfate, ammonium chloride, and calcium formate.
  • FIG. 1 schematically illustrates a first layer of a mixture of particulate material deposited onto a downwardly movable surface on which an article is to be built, before any fluid has been delivered;
  • FIG. 2 schematically illustrates an electromechanical ink-jet nozzle delivering an activating fluid to a portion of the layer of particulate material of FIG. 1 in a predetermined pattern
  • FIG. 3 schematically illustrates a view of a final article made from a series of steps illustrated in FIG. 2 enclosed in the container while it is still immersed in the loose unactivated particles;
  • FIG. 4 schematically illustrates a view of the final article from FIG. 3.
  • a materials system for three-dimensional printing comprises a mixture of particles including a filler and possibly an adhesive.
  • the materials system can also include a fibrous component, a printing aid for reducing edge curl due to uneven curing of the adhesive and resultant distortion of a part that is three-dimensionally printed, and an activating fluid comprising additional adhesive and a solvent that activates the adhesive.
  • the activating fluid can also include such processing aids as a humectant, a flowrate enhancer, and a dye. The fluid activates the adhesive in the particulate mixture, adhesively bonding the material together to form an essentially solid article.
  • FIG. 1 schematically illustrates a first layer of a mixture of particulate material deposited onto a downwardly movable surface on which an article is to be built, before any fluid has been delivered.
  • a layer or film of particulate material 20 is applied on a downwardly movable surface 22 of a container 24 .
  • the layer or film of particulate material can be formed in any manner; in one embodiment, the particulate material is applied using a counter roller.
  • the particulate material applied to the surface includes a filler and, possibly, adhesive.
  • adhesive is meant to define a component that forms the primary adhesive bonds in the mixture of material between portions of the mixture that were separate prior to delivery of the activating fluid.
  • the adhesive can be included both in the particle mixture and in the activating fluid.
  • a “filler” is meant to define a component that is solid prior to application of the activating fluid, which is substantially less soluble in the fluid than the adhesive, and which gives structure to the final article.
  • the particulate mixture includes a reinforcing fiber, or a reinforcing fibrous component, added to provide structural reinforcement to the final article.
  • the particulate material may include a plurality of particles of mean diameter of about 10-300 microns.
  • fiber or “fibrous component” is meant to define a component that is solid prior to application of the activating fluid, which can be but is not necessarily insoluble in the fluid, that is added to increase the final article strength.
  • the reinforcing fiber length is restricted to a length approximately equal to the thickness of the layer of particulate mixture.
  • the reinforcing fiber is typically about 60 to about 200 microns in length, and is included in an amount not greater than 20 percent, by weight, of the total mixture.
  • a stabilizing fiber can be added to the filler to provide dimensional stability to the final article, as well as to slightly increase the article strength.
  • Spreading the particulate mixture with the counter roller becomes increasingly difficult as friction caused by an excess of stabilizing fiber in the mixture increases, reducing the packing density. Restricting both the amount and length of the stabilizing fiber increases the packing density of the mixture resulting in finished parts of greater strength.
  • the stabilizing fiber may be restricted to a length of less than half of the reinforcing fiber, in an amount not greater than 30 percent, by weight, of the total mixture. Optimal values can be determined with routine experimentation using, for example, a counter roller.
  • a printing aid in the form of an emulsifier such as sorbitan trioleate (commercially available as SPAN 85 from Sigma Chemical Co., St. Louis, Mo. USA), can be added to the particulate mixture to prevent distortions in printing.
  • the printing aid prevents fine particles of the mixture from becoming airborne while the fluid is dispensed from the print head which would distort the printed article.
  • Lecithin which also serves as a printing aid can be used as well.
  • composition of the particulate mixture and fluid (binder) of a particular embodiment using a polymer solution as the adhesive is provided in Table 1, below.
  • composition of the particulate mixture and fluid (binder) of a particular embodiment using a colloidal suspension as the adhesive is provided in Table 2, below.
  • FIG. 2 schematically illustrates an electromechanical ink-jet nozzle delivering an activating fluid to a portion of the layer of particulate material of FIG. 1 in a predetermined pattern.
  • the fluid 26 is delivered to the layer or film of particulate material in any predetermined two-dimensional pattern (circular, in the figures, for purposes of illustration only), using any convenient mechanism, such as a drop-on-demand (hereinafter “DOD”) electromechanical printhead driven by customized software which receives data from a computer-assisted-design (hereinafter “CAD”) system as described in greater detail in U.S. application Ser. No. 09/416,707, which is incorporated herein by reference in its entirety.
  • DOD drop-on-demand
  • CAD computer-assisted-design
  • piezoelectric printheads examples include the Tektronix PHASOR 340 printhead by Xerox (Stanford, Conn. USA), the PJN 320 printhead from PicoJet, Inc. (Hillsboro, Oreg. USA), and the EPSON 900 printhead from Epson America, Inc. (Portland, Oreg. USA).
  • a suitable solenoid valve printhead is the 1200 Hz INKA printhead from The Lee Co. (Westbrook, Conn. USA).
  • the first portion 30 of the particulate mixture is activated by the fluid, causing the activated adhesive to adhere the particles together to form an essentially-solid circular layer that becomes a cross-sectional portion of the final article.
  • activates is meant to define a change in state from essentially inert to adhesive.
  • a typical droplet of activating fluid has a volume of about 50 pL, and spreads to about 100 microns once it comes into contact with the particulate mixture. As the solvent dissolves the adhesive, the fluid viscosity increases dramatically, arresting further migration of the fluid from the initial point of impact.
  • An adhesive can be dissolved, suspended, or otherwise included in the activating fluid before delivery, in addition to being in the powder mixture.
  • the adhesive that is pre-mixed with the activating fluid will already be activated when delivered to the powder mixture and will adhere filler and other particles to form a solid, agglomerated structure, as described above.
  • the fluid within a few minutes after the activating fluid is delivered to the particulate mixture, the fluid (with adhesive dissolved or suspended therein) infiltrates the less-soluble and slightly-porous particles, forming adhesive bonds between the filler and the fiber.
  • the activating fluid is capable of bonding the particulate mixture in an agglomerated mass that is several times the mass of a droplet of the fluid. As volatile components of the fluid evaporate, the adhesive bonds harden, joining the filler and, optionally, fiber particulates into a rigid structure, which becomes a cross-sectional portion of the finished article.
  • any portion of the particulate mixture 32 that was not exposed to the fluid remains loose and free-flowing on the movable surface.
  • the unbound particulate mixture can be left in place until formation of the final article is complete. Leaving the unbound, loose-particulate mixture in place ensures that the article is supported during processing, allowing features such as overhangs, undercuts, and cavities (not illustrated, but conventional) to be defined without using support structures.
  • the movable surface is indexed downward.
  • a second film or layer of the particulate mixture is then applied over the first, covering both the rigid first cross-sectional portion, and any loose particulate mixture by which it is surrounded.
  • a second application of fluid follows in the manner described above, forming adhesive bonds between a portion of the previous cross-sectional portion, the filler, and, optionally, fiber of the second layer, and hardening to form a second rigid cross-sectional portion added to the first rigid cross-sectional portion of the final article.
  • the movable surface is again indexed downward.
  • FIG. 3 schematically illustrates a view of a final article made from a series of steps illustrated in FIG. 2 enclosed in the container while it is still immersed in the loose unactivated particles.
  • the final article can be completely immersed in a bed 36 of unactivated particulate material.
  • those skilled in this art would know how to build an article in layers upward from an immovable platform, by successively depositing, smoothing and printing a series of such layers.
  • FIG. 4 schematically illustrates a view of the final article from FIG. 3.
  • the unactivated particulate material can be removed by blown air or a vacuum.
  • post-processing treatment may be performed, including cleaning, infiltration with stabilizing materials, painting, etc.
  • the method of the present invention is capable of producing features on the order of about 250 ⁇ m.
  • the accuracy achieved by the method of the present invention is in the range of about +/ ⁇ 250 ⁇ m.
  • Shrinkage of the final article is about 1%, which can easily be factored into the build to increase accuracy.
  • the adhesive is a compound selected for the characteristics of high solubility in the activating fluid, low solution viscosity, low hygroscopicity, and high bonding strength.
  • the adhesive should be highly soluble in the solvent in order to ensure that it is incorporated rapidly and completely into the activating fluid. Low solution viscosity can be used to ensure that activating fluid having adhesive dissolved therein will migrate quickly to sites in the powder bed to adhesively bond together the reinforcing materials. If the adhesive is naturally a solid, the adhesive can be milled as finely as possible prior to mixing with the filler and/or activating fluid and/or prior to coating the filler particles.
  • the fine particle size enhances the available surface area, enhancing dissolution in the solvent, without being so fine as to cause “caking”, an undesirable article characteristic.
  • Typical adhesive particle grain sizes are about 5-50 ⁇ m.
  • Low hygroscopicity of an adhesive used in the particulate mixture avoids absorption of excessive moisture from the air, which causes “caking”, in which unactivated powder spuriously adheres to the outside surface of the part, resulting in poor surface definition.
  • the filler of the present invention is a compound selected for the characteristics of insolubility in the activating fluid, or extremely low solubility in the activating fluid, rapid wetting, low hygroscopicity, and high bonding strength.
  • the filler provides mechanical structure to the hardened composition. Sparingly soluble filler material is used in particular, although insoluble filler material can also be used.
  • the filler particles become adhesively bonded together when the adhesive dries/hardens after the activating fluid has been applied.
  • the filler can include a distribution of particle grain sizes, ranging from the practical maximum of about 200 ⁇ m downward, to the practical minimum of about 5 ⁇ m. Large grain sizes appear to improve the final article quality by forming large pores in the powder through which the fluid can migrate rapidly, permitting production of a more homogeneous material. Smaller grain sizes serve to reinforce article strength.
  • Compounds suitable for use as the filler of the present invention can be selected from the same general groups from which the adhesive is selected, provided that the solubility, hygroscopicity, bonding strength and solution viscosity criteria described above are met.
  • fillers which can be used alone or in combination, include starches such as maltodextrin, clay, cellulose fiber, glass, limestone, gypsum, aluminum oxide, aluminum silicate, potassium aluminum silicate, calcium silicate, calcium hydroxide, calcium aluminate, and sodium silicate; metals; metal oxides such as zinc oxide, titanium dioxide, and magnetite (Fe 3 O 4 ); carbides such as silicon carbide; and borides such as titanium diboride.
  • the filler is limestone, which can be used alone or in combination with other inorganic fillers.
  • the filler can be a combination of plaster (0-20%), limestone (calcium carbonate) (40-95%) and glass beads (0-80%).
  • the filler materials are selected on the basis of their ability to bond with the adhesive components, combined with the spreading characteristics of the dry powder. The selection of the solvent also typically determines which filler can be used.
  • the reinforcing fiber can be insoluble or can dissolve substantially slower in the fluid than the adhesive dissolves.
  • the reinforcing fiber is a stiff material chosen to increase the mechanical reinforcement and dimensional control of the final article without making the powder too difficult to spread. In order to promote wetting of the reinforcing fibers, the chosen fibers have a high affinity for the solvent.
  • a particular embodiment includes a fiber length approximately equal to the layer thickness, which provides the greatest degree of mechanical reinforcement. Using longer fibers adversely affects the surface finish, and using too much fiber of any length can make spreading of the powder increasingly difficult.
  • Fibrous material suitable for reinforcing the present invention includes, but is not limited to polymeric fiber, ceramic fiber, graphite fiber and fiberglass.
  • the polymeric fiber may be cellulose and cellulose derivatives or substituted or unsubstituted, straight or branched, alkyl or alkene, including monomers up to eight carbon atoms in length.
  • Specific useable fibrous materials include, but are not limited to cellulose fiber, silicon carbide fiber, graphite fiber, aluminosilicate fiber, polypropylene fiber, fiberglass, nylon, and rayon.
  • both the reinforcing fiber and the stabilizing fiber are can be cellulose.
  • Some of the useful properties of cellulose making it particularly suitable for use in connection with the invention are low toxicity, biodegradability, low cost and availability in a wide variety of lengths.
  • the final strength of the finished article depends largely on the quality of the adhesive contacts between the particles of the mixture, and the size of the empty pores that persist in the material after the adhesive has hardened; both of these factors vary with the grain size of the particulate material.
  • the mean size of the grains of particulate material should not be larger than the layer thickness. A distribution of grain sizes increases the packing density of the particulate material, which in turn increases both article strength and dimensional control.
  • sorbitan trioleate (SPAN 85) is used as a printing aid in the exemplary particulate mixture.
  • Sorbitan trioleate is a liquid which is only slightly soluble in water. By adding a small amount to the powder, the sorbitan trioleate provides a light adhesion between powder grains before printing, thereby reducing dust formation. After printing, the sorbitan trioleate continues to adhere insoluble grains together for a short time until it dissolves. This effect tends to reduce distortion in printed layers in the brief time that is required for the adhesive to dissolve and redistribute in the powder. Hydrophillic grades of lecithin are particularly suitable. A wide variety of other liquid compounds work for the same purpose.
  • Polypropylene glycol (PPG), especially with a molecular weight of about 400, and citronellol are two examples.
  • Other suitable printing aides include ethylene glycol octanoate, ethylene glycol decanoate, and ethoxylated derivatives of 2,4,7,9-Tetramethyl-5-decyne-4,7-diol. Sorbitan trioleate can be used in combination with lethicin, which also functions as a printing aid.
  • liquid compounds that can be used as printing aids include sorbitan mono-oleate, sorbitan monolaurate, polyoxyethylene sorbitan mono-oleate, polyethylene glycol, soybean oil, mineral oil, propylene glycol, fluroalkyl polyoxyethylene polymers, glycerol triacetate, oleyl alcohol, and oleic acid.
  • the fluid of the present invention is selected to comport with the degree of solubility required for the various particulate components of the mixture, as described above.
  • the fluid includes a solvent in which the adhesive is active, particularly soluble, and can include processing aids such as a humectant, a flowrate enhancer, and a dye.
  • An ideal solvent is one in which the adhesive component of the powder is highly soluble, and in which both the filler and fiber are substantially less soluble.
  • the solvent can be aqueous or non-aqueous, although aqueous solvents offer some advantages.
  • Suitable solvents can be selected from the following non-limiting list: water, methyl alcohol, ethyl alcohol, isopropanol, t-butanol, ethyl acetate, dimethyl succinate, diethyl succinate, dimethyl adipate, and ethylene glycol diacetate.
  • the activating fluid which can have adhesive pre-mixed, is also referred to as the “binder.”
  • the function of the binder is to infiltrate the insoluble or semi-soluble particle mixture and to bond the grains together.
  • the activating fluid, with adhesive included can belong to any one of the following classes: (1) polymer solutions, (2) colloidal suspensions, (3) inorganic (salt) solutions, (4) organic monomeric solutions, (5) non aqueous liquids. Classes 1-4 can be aqueous.
  • the following description of particular fluids and adhesives are not meant to be limiting, other suitable compounds may be used in place of or in combination with the listed compounds.
  • a water-soluble polymer can be dissolved in the binder to form a relatively low viscosity solution.
  • a water-soluble polymer can be dissolved in the binder to form a relatively low viscosity solution.
  • suitable polymers include anionically ionizable polymers, cationic polymers and nonionic polymers.
  • the anionically ionizable polymers include polymethacrylic acid, polymethacrylic acid sodium salt, and sodium polystyrene sulfonate.
  • the cationic polymers include polyethyleneimine and polydiallyldimethyl ammonium chloride.
  • polyethyleneimine comes in two forms, linear and branched, both of which are useful.
  • the nonionic soluble polymers that are particularly useful as binders are polyvinyl pyrrolidone, polyvinyl pyrrolidone copolymer with polyvinyl acetate, polyvinyl alcohol, polyvinyl methyl ether, polyacrylamide, and poly-2-ethyl-2-oxazoline.
  • a low molecular weight polymer such as sodium polystyrene sulfonate is dissolved in water to form a solution containing approximately 20% solids by weight.
  • a cosolvent such as isopropyl alcohol, at approximately 1% to 5% by weight, can modify the viscosity of the solution by controlling the conformation of the polymer chains in solution.
  • a humectant such as glycerol used at approximately 5% to 10% will reduce the tendency of the binder to dry in the printhead.
  • Other solution parameters such as pH and salt concentration may be used to modify flow properties. Added salts tend to lower the viscosity of binders that include a polyelectrolyte, such as sodium chloride, sodium phosphate, sodium sulfate, and potassium sulfate.
  • colloidal suspensions of materials can be used as binders in three-dimensional printing.
  • Organic latexes such as polymethyl methacrylate, polystyrene, styrenated polyacrylic acid, natural rubber, polyurethane latex, polyvinyl acetate latex, and alkyd resin latex are materials that can be applied to the process.
  • inorganic suspensions such as colloidal alumina, clay, and colloidal graphite could all be used to for solid articles containing substantial amounts of these technologically important materials.
  • the advantage of using a colloid over a solution is that a very large content of solid materials can be suspended without greatly increasing the viscosity of the fluid.
  • the first two classes do not necessarily exclude one another. Very often, a soluble polyelectrolyte will be used to stabilize a suspension of solid particles. The polyelectrolyte will contribute to the structure of the finished article in addition to the dispersed particles.
  • a typical embodiment of a colloid-based binder comprises a polyvinyl acetate including approximately 30% solids. Additional additives such as triethanolamine at 2% to 5% by weight are used to control the pH of the suspension. Additionally, a humectant such as glycerol at 5% to 10% is used to reduce the tendency of the latex to dry in the printhead during idle periods.
  • inorganic solutes can be dissolved in an aqueous solvent and printed as a binder.
  • Glass-forming solutes such as sodium silicate, sodium polyphosphate and sodium tetraborate can be used to deposit a ceramic binder in a finished article. This ceramic binder could be fused in a subsequent heat treatment into a glass-bonded ceramic.
  • Other inorganic solutes that could be printed include sodium chloride, ammonium nitrate, and potassium sulfate, ammonium chloride, and calcium formate.
  • Inorganic solutes participate in acid-base reactions.
  • sodium hydrogen phosphate solution could be printed onto powdered calcium carbonate.
  • the acid binder etches the alkaline powder and forms calcium phosphate that recrystallizes and cements together the grains of powder.
  • sodium silicate which can be printed in a binder solution and can react with, for example, gypsum plaster to form calcium silicate.
  • a solution of monomeric organic compounds can be printed through an electromechanical drop-on-demand printhead for three-dimensionally printed articles.
  • monomeric organic compounds generally fall into several broad classes: alcohols, esters, ethers, silanes, vinyl monomers, acrylic monomers, and methacrylate monomers.
  • Alcohols and esters that have been found to function well as the solvent phase, in addition to functioning as a solute in another solvent are: methyl alcohol, ethyl alcohol, isopropanol, t-butanol, ethyl acetate, dimethyl succinate, diethyl succinate, dimethyl adipate, and ethylene glycol diacetate. These materials act as solvents for resins in the powder bed.
  • Resins that have been found to work in a 3-D printer are: shellac, polyvinyl pyrrolidone, polyvinyl acetate, polyvinyl alcohol, polystyrene, styrene-butadiene copolymer, and acrylonitrile-butadiene-styrene copolymer. These resins can be used in combination with any filler, or they can be used by themselves. A particularly suitable combination is 100% dimethyl succinate binder printed over a powder of 100% acrylonitrile-butadiene-styrene copolymer.
  • the other monomers contain active sites for polymerization, and possess mixed characteristics.
  • the classes of polymerizable monomers are the vinyl monomers, acrylic monomers, and methacrylate monomers.
  • a exemplary mixed vinyl-silane monomer is vinyltriisopropoxysilane.
  • Acrylic monomers include tri(propylene glycol) diacrylate, ethylene glycol phenyl ether acrylate, and 1,6 hexanediol diacrylate.
  • Methacrylates include 1,3 butylene glycol dimethacrylate, neopentyl glycol dimethacrylate, butyl methacrylate, 1,6 hexanediol dimethacrylate, and di(propylene glycol) allyl ether methacrylate.
  • organic acids and sugars sucrose, dextrose, malic acid, and sodium citrate, and other compounds such as urea and the hydrolyzed amino acids that can be used as solutes in water solution. These compounds would bind by drying in the powder, and not have any appreciable solvent character on their own.
  • reactive monomers such as melamine-formaldehyde, can be printed in a liquid solution and later polymerized by heat, by an initiator, or by actinic radiation such as ultra-violet radiation.
  • the fifth class includes members that can be used with electromechanical printheads that are designed for printing molten wax, such as the Tektronix Phasor 340 printhead (which includes a temperature control).
  • a room temperature solid such as wax can be used by itself or to replace water as a medium to convey the primary adhesives discussed in categories 1-4.
  • the wax itself would serve as an adhesive to cement together powder particles.
  • Binders formulated from these materials would be appropriate for electromechanical printheads that work at elevated temperatures. At these operating temperatures, the binder would become fluid and could then be used in the three-dimensional printing process.
  • Typical wax-based binder formulations would include waxes with a low melt viscosity (less than 100 centipoise) such as different grades of natural mineral, or refined waxes. Examples include but are not limited to carnauba wax beeswax, ceresine, ozokerite, montan, orlcury wax, paraffin, and microcrystalline wax.
  • the waxes can be chemically modified to include reactive groups such as alcohols, organic acids, alcohol oxazolates, and urethane derivatives.
  • binder material properties such as melting point, melt viscosity, toughness and hardening rate, as well as to increase compatibility with added components, the waxes can be blended or compounded with resins, oils, and other polymers.
  • Resins include polyethylene, polypropylene, polybutadiene, polyethylene oxide, polyethylene glycol, polymethyl methacrylate, poly-2-ethyl-oxazoline, polyvinylpyrrollidone, polyacrylamide, and polyvinyl alcohol.
  • Adhesives in members of the first class (polymer solutions) and the second class (inorganic solutions) will often adsorb water if left exposed to ambient atmosphere. However, these adhesives will generally perform with greater reliability and efficacy if maintained in either a completely dry or wet state. By incorporating the adhesives in the liquid binder, they can thereby be maintained in a wet state and therefore exhibit the desired reliability and efficacy.
  • a humectant can be included in the inventive mixture to retard evaporation of the solvent from the printed material, and to prevent drying/clogging of the printhead delivery system.
  • Glycerol is a particularly suitable humectant when the solvent is aqueous.
  • Other polyhydric alcohols including but not limited to ethylene glycol, diethylene glycol, and propylene glycol, are also known in the art to retard evaporation.
  • Additional humectants include thiodiethanol, n-methyl pyrrolidinone, and dimethyl hydantoin.
  • a flowrate enhancer can be included that has some humectant properties, but serves mainly to alter the hydrodynamic properties or wetting characteristics of the fluid to maximize the volume of fluid delivered by the printhead.
  • Flowrate enhancement is thought to be a viscoelastic phenomena increasing the flow rate of the fluid, allowing thicker layers to be printed, thus allowing the final article to be built more quickly.
  • Specific compounds that increase the flowrate of the fluid, either by reducing friction between the fluid and the walls of the jet, or by reducing the viscosity of the fluid include ethylene glycol diacetate and potassium aluminum sulfate.
  • Suitable compounds for use as the flowrate enhancer can be selected from the following non-limiting list: tetraethylene glycol dimethylether, isopropyl alcohol, ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, dodecyl dimethylammoniopropane sulfonate, glycerol triacetate, ethyl acetoacetate, and water-soluble polymers including polyvinyl pyrrolidone with a molecular weight of about 30,000 units, polyethylene glycol, polyacrylic acid, and sodium polyacrylate.
  • the ionic polymers such as sodium polyacrylate
  • Salts that can be used to enhance flowrate include potassium sulfate, potassium aluminum sulfate, sodium hydrogen phosphate and sodium polyphosphate.
  • the fluid of the present invention can include a dye to provide a visual aid to the operator while building the article.
  • the dye provides contrast between activated and unactivated powder which allows the operator to monitor the printed layers while building the article.
  • the dye can be selected from the group including, but not limited to, naphthol blue-black and direct red. Other dyes that are compatible with the fluid can likewise be used.
  • Cosolvents can be added to an aqueous solution to alter the viscosity of a solution by altering the solvency of the liquid for the solute.
  • Long-chain molecules in solution conform themselves either into extended chains or into coiled structures. If the solvent has a high affinity for the solute, long molecules will spread out causing the viscosity of the solution to be high.
  • the polymer can be come less strongly attracted to other dissolved polymer molecules, and begin to coil into compact balls. This tends to reduce the viscosity of a polymer solution and allows more polymer to be dissolved.
  • Cosolvents include isopropanol, ethyl alcohol, ethylene glycol monobutyl ether, butyrolactone and acetone.
  • Additives that control the pH of the binder can impart increased stability to the adhesive solutions and suspensions.
  • Such materials include, but are not limited to, potassium hydroxide, ammonia, ammonium chloride, triethanolamine, sodium acetate, sodium gluconate, potassium sulfate, potassium hydrogen sulfate, sodium aluminum sulfate, and sodium tetraborate.
  • Wetting agents are substances that control the surface tension of a liquid. These can be used to modify the spreading of the liquid adhesive on the surfaces of the printhead mechanism. These include, but are not limited to, sodium dodecyl sulfate, sodium di-octyl sulfosuccinate, ethyl butyrate, diethylene glycol monobutyl ether, polyethylene glycol alkyl ether, and sodium p-toluene sulfonate.
  • Lubricants can be used to increase the rate at which liquid binder passes through the nozzles of a printhead.
  • substances such as glycerol triacetate, polyethylene oxide, polypropylene glycol, ethyl acetoacetate, diethyl succinate, and sodium polyacrylate can be used.
  • Stabilizers include emulsifiers such as sorbitan trioleate, polyoxyethylene mono-dodecyl ether, polyoxyethylene sorbitan mono-oleate, and protective colloids such as polyoxyethylene-co-polyoxypropylene, polyvinyl pyrrolidone, polyacrylic acid, gelatin, and acacia gum.
  • emulsifiers such as sorbitan trioleate, polyoxyethylene mono-dodecyl ether, polyoxyethylene sorbitan mono-oleate
  • protective colloids such as polyoxyethylene-co-polyoxypropylene, polyvinyl pyrrolidone, polyacrylic acid, gelatin, and acacia gum.
  • the equipment used in the method of the present invention is reliable, inexpensive, and easy to maintain, making it ideal for use in an office environment.
  • the materials used in the present invention are capable of achieving much better performance in 3D Printing than those presently used in the liquid binder method.
  • less equipment maintenance is required, and the reliability of the equipment is increased. Therefore, methods of the present invention can involve shorter build times and less labor than prior art methods.

Abstract

A three-dimensional printing materials system and method can produce both appearance models and small numbers of functional parts in an office environment. The method can include building cross-sectional portions of a three-dimensional article, and assembling the individual cross-sectional areas in a layer-wise fashion to form a final article. The individual cross-sectional areas can be built by using an ink-jet printhead to deliver an aqueous solvent or binder to an adhesive particulate mixture, causing the particles of the mixture to adhere together, and to previous cross-sectional areas. The binder can include at least one of nonaqueous organic monomeric compound, anionically ionizable polymer, cationic polymer, polymer, waterborne colloid, or inorganic solute.

Description

    RELATED APPLICATIONS
  • This application claims the benefit of U.S. Provisional Application Nos. 60/197,118 and 60/197,526, both filed Apr. 14, 2000. This application is related to U.S. application Ser. No. 09/234,349, filed Jan. 20, 1999, which is a divisional application of U.S. Pat. No. 5,902,441, issued May 11, 1999, and to U.S. application Ser. No. 09/416,787, which is a continuation-in-part of U.S. Pat. No. 6,007,318. The teachings of each of these references are incorporated herein by reference in their entirety.[0001]
  • BACKGROUND
  • Rapid prototyping involves the production of prototype articles and small quantities of functional parts, as well as structural ceramics and ceramic shell molds for metal casting, directly from computer-generated design data. There are a variety of methods to form a three-dimensional article including a selective laser-sintering process as described in U.S. Pat. No. 4,863,568, which is incorporated herein by reference. [0002]
  • Three-dimensional printing is a process invented by Sachs et al. at Massachusetts Institute of Technology in the early 1980's. In accordance with the process, an ink-jet printhead is used to deposit a liquid ink or binder onto a print plane composed of a powdered receiving medium. The combination of liquid binder and solid powder solidifies to form a finished article. [0003]
  • U.S. Pat. No. 5,204,055, incorporated herein by reference, describes an early three-dimensional printing technique that involves the use of an ink-jet printing head to deliver a liquid or colloidal binder material to layers of powdered material. The three-dimensional ink-jet printing technique (hereafter “liquid-binder method”) involves applying a layer of a powdered material to a surface using a counter roller. After the powdered material is applied to the surface, the ink-jet printhead delivers a liquid binder to the layer of powder. The binder infiltrates into gaps in the powder material, hardening to bond the powder material into a solidified layer. The hardened binder also bonds each layer to the previous layer. After the first cross-sectional portion is formed, the previous steps are repeated, building successive cross-sectional portions until the final article is formed. Optionally, the binder can be suspended in a carrier that evaporates, leaving the hardened binder behind. The powdered material can be ceramic, metal, plastic or a composite material, and can also include fiber. The liquid-binder material can be organic or inorganic. Typical organic binder materials used are polymeric resins, or ceramic precursors such as polycarbosilazane. Inorganic binders are used where the binder is incorporated into the final articles; silica is typically used in such an application. [0004]
  • In the technology of ink-jet printing, there are a number of different types of printheads distinguished by the mechanism by which ink is ejected onto the printing plane. The two broadest classes of printheads are called, “continuous-jet” and “drop-on-demand.” In a continuous-jet printhead, a liquid ink or binder is projected continuously through a nozzle. To print segmented lines, the jet is deflected alternatively onto the print plane or in to a collector that masks the printing plane. In a drop-on-demand printhead, ink or binder is ejected when it is needed by sending an impulse, most usually electrical, that causes an actuator in the printhead to eject a droplet of ink or binder onto the print plane. [0005]
  • SUMMARY
  • The use of liquid-binder printing techniques with a thermal (bubble) printhead can present reliability problem associated with the spray nozzle becoming clogged with the binder material. Clogging can occur when binders having high levels of solids are used. The problem with clogging requires frequent interruptions of the build in order to clean the spray nozzle; this problem also increases the time and labor required to build parts and to maintain the equipment. Therefore, although the liquid-binder printing technique represents an advance in speed and cost over the selective laser-sintering process, it suffers from reliability problems that slow down the build rate, increasing labor and equipment maintenance costs. This problem interferes with the potential speed advantage of increased printing capability presented by the plurality of spray nozzles. [0006]
  • The materials for fabricating three-dimensional objects lead to a materials system and method that produce both appearance models and small numbers of functional parts in an office environment. The materials system can include at least one solid filler and a liquid binder composition. Particular binder compositions can be effectively deposited using an electromechanical printhead having suitable components. The fabrication methods can be quick, reliable, safe, and inexpensive. [0007]
  • An article can be made of a mixture of particles including adhesive and at least one filler. The adhesive may be activated by a fluid including a solvent. Optionally, the binder can also include various processing aids or additions that modify the working properties of the fluid and adhesive or that enhance the mechanical properties of the finished article. The mixture of particles can also optionally include particles of fiber and various processing aids. The activated adhesive causes the filler particles to adhere together, and to adhere to previously formed adjacent layers. Adhesive can be supplied to the article by coating it on the fiber and/or filler, by directly mixing it with the fiber and filler before delivering the fluid and/or by dissolving or mixing the adhesive in the fluid before the fluid is delivered to the mixture of particles. [0008]
  • A particular method for producing such articles can include applying a layer of the above-mentioned mixture onto a flat surface that can be indexed downward. Cross-sectional portions of an article can be defined by delivering an activating fluid, the adhesive, to the layer of the mixture of particles in a predetermined two-dimensional pattern. The fluid activates the adhesive, and the activated adhesive causes the particles to adhere together in an essentially solid layer. After the first cross-sectional portion of the article is formed, the movable surface can be indexed downward by an amount corresponding to the desired layer thickness. Successive layers of the mixture of particles are applied to previous layers in the same manner. Application of the fluid using an electromechanical ink-jet print head follows the application of each successive layer of the mixture of particulate material. [0009]
  • Depositing a layer of the mixture of particulate material and delivering the fluid to the layer can be repeated until the required number of cross-sectional portions have been built, completing formation of the article. After formation of the article has been completed, it typically remains immersed in a bed of unbound particulate material, where it can remain until the article is completely dry. Delicate features of the article remain supported by the unbound particulate material while drying. The finished article can then be removed from the bed of unbound particulate material and any excess unbound particulate material clinging to the finished article can be removed by a suitable cleaning process. For example, excess powder can be removed by vacuuming it off the article, by blowing it off the article, and by brushing to remove any powder left in crevices. In addition, the finished article can be placed in an oven for more rapid drying. [0010]
  • After cleaning, optional post-processing actions can include heat-treating, resin or wax infiltration, painting and sanding. Heat treating and infiltration can increase the strength and durability of the finished article. Infiltration can reduce porosity, making the article water resistant and more readily sanded. Painting the article can provide a more aesthetically pleasing appearance, and may also contribute to the strength and water resistance of the final articles. Sanding improves the surface smoothness, reducing any surface irregularities caused, for example, by fiber penetrating through the surface. Parts can be glued or fastened, or used as patterns for subsequent molding operations. [0011]
  • Various materials systems and methods offer the advantages of being able to fabricate relatively complex shapes reliably, quickly, safely and inexpensively compared to the selective laser-sintering and liquid-binder methods. Because various materials used in the present system present little or no problems with clogging, higher reliability can be offered relative to prior art methods, particularly prior art methods in which high levels of suspended solids are contained in the binder. The higher reliability results in reduced build times compared with prior art methods. Further, embodiments can be made and practiced more economically than prior art methods because inexpensive equipment and materials can be used, and the high reliability associated with materials and methods reduces cost even further. In addition, because non-toxic materials can be used, these methods can be carried out safely in a typical office environment. [0012]
  • Additionally, the use of electromechanical ink-jet printheads to deliver the fluid compositions allows for the incorporation of thermally-sensitive adhesives in the fluid due to the fact that electromechanical ink-jet printheads typically operate at ambient-temperature. Further, fluids with a large amount of dissolved or suspended solids subject to degradation with temperature excursions can likewise be better accommodated by an electromechanical printhead relative to a thermal printhead. The use of fluids with higher solids content with an electromechanical printhead further allows for the formation of materials that will shrink less (due to fewer escaping components) and that have higher strength and greater dimensional stability than materials formed with more dilute binders. Further still, the incorporation of adhesives in the activating fluid and the delivery of that fluid to the particulate bed allows for an increased amount of adhesive to be incorporated into the final part. [0013]
  • The composition selectively adhere particulate material to form a solid object in a three-dimensional printer. In one embodiment, the composition comprises a nonaqueous organic monomeric compound. That compound can include at least one of an alcohol, an ester, an ether, a silane, a vinyl monomer, an acrylic monomer, or a methacrylate monomer. [0014]
  • The composition can include a solvent and a solute, and in one embodiment, the compound is the solvent. The solvent can include an alcohol such as methyl alcohol, ethyl alcohol, isopropanol, or t-butanol. In alternative embodiments, the solvent includes an ester that includes at least one of ethyl acetate, dimethyl succinate, diethyl succinate, dimethyl adipate, or ethylene glycol diacetate. [0015]
  • In alternative embodiments, the compound is a solvent for a resin in the particulate material. The resin can include at least one of shellac, polyvinyl pyrrolidone, polyvinyl acetate, polyvinyl alcohol, polystyrene, styrene-butadiene copolymer, or acrylonitrile-butadiene-styrene copolymer. [0016]
  • Additionally, organic acids and sugars such as sucrose, dextrose, malic acid, and sodium citrate, and other compounds such as urea and hydrolized amino acids can be used as solutes in water solution. These compounds bind the particulate material together by drying in the powder, and not have any appreciable solvent character on their own. [0017]
  • The monomeric compound can include a mixed monomer vinyl-silane and can include vinyltriisopropoxysilane. [0018]
  • The acrylic monomer can include at least one of tri(propylene glycol) diacrylate, ethylene glycol phenyl ether acrylate, or 1,6 hexanediol diacrylate. The methacrylic monomer can include at least one of 1,3 butylene glycol dimethacrylate, neopentyl glycol dimethacrylate, butyl methacrylate, 1,6 hexanediol dimethacrylate, or di(propylene glycol) allyl ether methacrylate. [0019]
  • The compound can be curable, in combination with a photoinitiator in a solid, by ultraviolet radiation having a wavelength between about 320-500 nm and an energy density of about 1 joule/cm[0020] 2.
  • The particulate material can include a filler that includes an inorganic compound. In one embodiment, the filler includes at least one of clay, aluminum oxide, silicon dioxide, aluminum silicate, potassium aluminum silicate, calcium silicate, calcium hydroxide, calcium aluminate, calcium carbonate, sodium silicate, zinc oxide, titanium dioxide, or magnetite. A printing aid can be dispersed throughout the filler. The printing aid can include at least one of sorbitan trioleate, sorbitan mono-oleate, sorbitan monolaurate, polyoxyethylene sorbitan mono-oleate, polyethylene glycol, soybean oil, mineral oil, propylene glycol, fluroaklkyl polyoxyethylene polymers, glycerol triacetate, polypropylene glycol, ethylene glycol octanoate, ethylene glycol decanoate, ethoxylated derivatives of 2,4,7,9-Tetramethyl-5-decyne-4,7-diol, oleyl alcohol, or oleic acid. [0021]
  • A binder composition is also provided, which can include an adhesive in combination with a fluid, for selectively adhering particulate material to form a solid object in a three-dimensional printer. In one embodiment, the adhesive can include a nonaqueous organic monomeric compound. [0022]
  • In alternative embodiments, an adhesive for selectively adhering particulate material to form a solid object in a three-dimensional printer includes an anionically ionizable polymer consisting of compounds selected from the group including polymethacrylic acid, polymethacrylic acid sodium salt, and sodium polystyrene sulfonate. [0023]
  • In other embodiments, the adhesive includes a cationic polymer such as polyethyleneimine and polydiallyldimethylammonium chloride. In other embodiments, the adhesive includes a nonionic polymer. The polymer can include at least one of polyvinyl pyrrolidone, polyvinyl pyrrolidone copolymer with polyvinyl acetate, polyvinyl alcohol, polyvinyl methyl ether, polyacrylamide, or poly-2-ethyl-2-oxazoline. In yet other embodiments, the adhesive includes a polymer selected from the group consisting of polymethacrylic acid, polymethacrylic acid sodium salt, sodium polystyrene sulfonate, and polyethyleneimine. [0024]
  • In further embodiments, the adhesive includes a waterborne colloid such as polymethyl methacrylate, polystyrene, natural rubber, polyurethane, polyvinyl acetate, and alkyd resins. In yet other embodiments, the adhesive includes an inorganic solute selected from the group consisting of sodium polyphosphate, sodium tetraborate, sodium chloride, ammonium nitrate, potassium sulfate, ammonium chloride, and calcium formate.[0025]
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 schematically illustrates a first layer of a mixture of particulate material deposited onto a downwardly movable surface on which an article is to be built, before any fluid has been delivered; [0026]
  • FIG. 2 schematically illustrates an electromechanical ink-jet nozzle delivering an activating fluid to a portion of the layer of particulate material of FIG. 1 in a predetermined pattern; [0027]
  • FIG. 3 schematically illustrates a view of a final article made from a series of steps illustrated in FIG. 2 enclosed in the container while it is still immersed in the loose unactivated particles; [0028]
  • FIG. 4 schematically illustrates a view of the final article from FIG. 3.[0029]
  • The foregoing and other objects, features and advantages will be apparent from the following more particular description of embodiments, as illustrated in the accompanying drawings in which like reference characters refer to the same parts throughout the different views. The drawings are not necessarily to scale, emphasis instead being placed upon illustrating the principles of the invention. [0030]
  • DETAILED DESCRIPTION
  • A materials system for three-dimensional printing comprises a mixture of particles including a filler and possibly an adhesive. The materials system can also include a fibrous component, a printing aid for reducing edge curl due to uneven curing of the adhesive and resultant distortion of a part that is three-dimensionally printed, and an activating fluid comprising additional adhesive and a solvent that activates the adhesive. The activating fluid can also include such processing aids as a humectant, a flowrate enhancer, and a dye. The fluid activates the adhesive in the particulate mixture, adhesively bonding the material together to form an essentially solid article. [0031]
  • FIG. 1 schematically illustrates a first layer of a mixture of particulate material deposited onto a downwardly movable surface on which an article is to be built, before any fluid has been delivered. According to the method, a layer or film of [0032] particulate material 20 is applied on a downwardly movable surface 22 of a container 24. The layer or film of particulate material can be formed in any manner; in one embodiment, the particulate material is applied using a counter roller. The particulate material applied to the surface includes a filler and, possibly, adhesive.
  • As used herein, “adhesive” is meant to define a component that forms the primary adhesive bonds in the mixture of material between portions of the mixture that were separate prior to delivery of the activating fluid. The adhesive can be included both in the particle mixture and in the activating fluid. As used herein, a “filler” is meant to define a component that is solid prior to application of the activating fluid, which is substantially less soluble in the fluid than the adhesive, and which gives structure to the final article. [0033]
  • According to a particular embodiment, the particulate mixture includes a reinforcing fiber, or a reinforcing fibrous component, added to provide structural reinforcement to the final article. The particulate material may include a plurality of particles of mean diameter of about 10-300 microns. As used herein, “fiber” or “fibrous component” is meant to define a component that is solid prior to application of the activating fluid, which can be but is not necessarily insoluble in the fluid, that is added to increase the final article strength. The reinforcing fiber length is restricted to a length approximately equal to the thickness of the layer of particulate mixture. The reinforcing fiber is typically about 60 to about 200 microns in length, and is included in an amount not greater than 20 percent, by weight, of the total mixture. [0034]
  • Additionally, a stabilizing fiber can be added to the filler to provide dimensional stability to the final article, as well as to slightly increase the article strength. Spreading the particulate mixture with the counter roller becomes increasingly difficult as friction caused by an excess of stabilizing fiber in the mixture increases, reducing the packing density. Restricting both the amount and length of the stabilizing fiber increases the packing density of the mixture resulting in finished parts of greater strength. The stabilizing fiber may be restricted to a length of less than half of the reinforcing fiber, in an amount not greater than 30 percent, by weight, of the total mixture. Optimal values can be determined with routine experimentation using, for example, a counter roller. [0035]
  • According to another particular embodiment, a printing aid in the form of an emulsifier, such as sorbitan trioleate (commercially available as SPAN 85 from Sigma Chemical Co., St. Louis, Mo. USA), can be added to the particulate mixture to prevent distortions in printing. The printing aid prevents fine particles of the mixture from becoming airborne while the fluid is dispensed from the print head which would distort the printed article. Lecithin, which also serves as a printing aid can be used as well. [0036]
  • The composition of the particulate mixture and fluid (binder) of a particular embodiment using a polymer solution as the adhesive is provided in Table 1, below. The composition of the particulate mixture and fluid (binder) of a particular embodiment using a colloidal suspension as the adhesive is provided in Table 2, below. [0037]
    TABLE 1
    Example Example Particle
    Particular Composition Composition Size
    Ingredient Compound Range (W/W) (W/W) Range (μm)
    Particulate Mixture
    Adhesive sucrose 10-50% 30% 10
    Reinforcing cellulose  0-20% 10% 100
    Fiber
    Filler maltodextrin  0-80% 50% <300
    (dextrose
    equivalent =
    5)
    Stabilizing cellulose  0-30% 10% 60
    Fiber
    Printing lecithin 0-3%  0.27% N/A
    Aids sorbitan 0-3%  0.03% N/A
    trioleate
    Fluid
    Solvent water 20-88% 68% N/A
    Solvent isopropyl 0-5%  1% N/A
    alcohol
    water-sol. sulfonated 10-50% 25% N/A
    adhesive polystyrene
    Humectant glycerol  0-15%  5% N/A
    Flowrate diethylene  0-10%  1% N/A
    Enhancer glycol mono-
    butyl ether
    Dye naphthol   0-0.1%  0.1% N/A
    blue-black
  • [0038]
    TABLE 2
    Example Example Particle
    Particular Composition Composition Size
    Ingredient Compound Range (W/W) (W/W) Range (μm)
    Particulate Mixture
    Adhesive sucrose 10-50% 30% 10
    Reinforcing cellulose  0-20% 10% 100
    Fiber
    Filler maltodextrin  0-80% 50% <300
    (dextrose
    equivalent =
    5)
    Stabilizing cellulose  0-30% 10% 60
    Fiber
    Printing lecithin 0-3%  0.27% N/A
    Aids sorbitan 0-3%  0.03% N/A
    trioleate
    Fluid
    Suspending water 20-88% 72% N/A
    Fluid
    Solvent isopropyl 0-5%  1% N/A
    alcohol
    Colloid polyvinyl 10-50% 20% 50-500 nm
    Adhesive acetate
    Inorganic acetic acid 0-2%  1% N/A
    Buffer
    Humectant glycerol  0-15%  5% N/A
    Flowrate diethylene  0-10%  1% N/A
    Enhancer glycol mono-
    butyl ether
    Dye naphthol   0-0.1%  0.1% N/A
    blue-black
  • FIG. 2 schematically illustrates an electromechanical ink-jet nozzle delivering an activating fluid to a portion of the layer of particulate material of FIG. 1 in a predetermined pattern. The fluid [0039] 26 is delivered to the layer or film of particulate material in any predetermined two-dimensional pattern (circular, in the figures, for purposes of illustration only), using any convenient mechanism, such as a drop-on-demand (hereinafter “DOD”) electromechanical printhead driven by customized software which receives data from a computer-assisted-design (hereinafter “CAD”) system as described in greater detail in U.S. application Ser. No. 09/416,707, which is incorporated herein by reference in its entirety. Examples of suitable piezoelectric printheads include the Tektronix PHASOR 340 printhead by Xerox (Stanford, Conn. USA), the PJN 320 printhead from PicoJet, Inc. (Hillsboro, Oreg. USA), and the EPSON 900 printhead from Epson America, Inc. (Portland, Oreg. USA). A suitable solenoid valve printhead is the 1200 Hz INKA printhead from The Lee Co. (Westbrook, Conn. USA).
  • In one embodiment, where adhesive is mixed with the other particles, the [0040] first portion 30 of the particulate mixture is activated by the fluid, causing the activated adhesive to adhere the particles together to form an essentially-solid circular layer that becomes a cross-sectional portion of the final article. As used herein, “activates” is meant to define a change in state from essentially inert to adhesive. When the fluid initially comes into contact with the particulate mixture, it immediately flows outward (on the microscopic scale) from the point of impact by capillary action, dissolving the adhesive in the particulate mixture within the first few seconds. A typical droplet of activating fluid has a volume of about 50 pL, and spreads to about 100 microns once it comes into contact with the particulate mixture. As the solvent dissolves the adhesive, the fluid viscosity increases dramatically, arresting further migration of the fluid from the initial point of impact.
  • An adhesive can be dissolved, suspended, or otherwise included in the activating fluid before delivery, in addition to being in the powder mixture. The adhesive that is pre-mixed with the activating fluid will already be activated when delivered to the powder mixture and will adhere filler and other particles to form a solid, agglomerated structure, as described above. [0041]
  • Within a few minutes after the activating fluid is delivered to the particulate mixture, the fluid (with adhesive dissolved or suspended therein) infiltrates the less-soluble and slightly-porous particles, forming adhesive bonds between the filler and the fiber. The activating fluid is capable of bonding the particulate mixture in an agglomerated mass that is several times the mass of a droplet of the fluid. As volatile components of the fluid evaporate, the adhesive bonds harden, joining the filler and, optionally, fiber particulates into a rigid structure, which becomes a cross-sectional portion of the finished article. [0042]
  • Any portion of the [0043] particulate mixture 32 that was not exposed to the fluid remains loose and free-flowing on the movable surface. The unbound particulate mixture can be left in place until formation of the final article is complete. Leaving the unbound, loose-particulate mixture in place ensures that the article is supported during processing, allowing features such as overhangs, undercuts, and cavities (not illustrated, but conventional) to be defined without using support structures. After formation of the first cross-sectional portion of the final article, the movable surface is indexed downward.
  • Using, for example, a counter-rolling mechanism, a second film or layer of the particulate mixture is then applied over the first, covering both the rigid first cross-sectional portion, and any loose particulate mixture by which it is surrounded. A second application of fluid follows in the manner described above, forming adhesive bonds between a portion of the previous cross-sectional portion, the filler, and, optionally, fiber of the second layer, and hardening to form a second rigid cross-sectional portion added to the first rigid cross-sectional portion of the final article. The movable surface is again indexed downward. [0044]
  • The previous steps of applying a layer of particulate mixture, applying the fluid, and indexing the movable surface downward are repeated until the final article is completed. [0045]
  • FIG. 3 schematically illustrates a view of a final article made from a series of steps illustrated in FIG. 2 enclosed in the container while it is still immersed in the loose unactivated particles. The final article can be completely immersed in a [0046] bed 36 of unactivated particulate material. Alternatively, those skilled in this art would know how to build an article in layers upward from an immovable platform, by successively depositing, smoothing and printing a series of such layers.
  • FIG. 4 schematically illustrates a view of the final article from FIG. 3. The unactivated particulate material can be removed by blown air or a vacuum. After removal of the unactivated particulate material from the [0047] final article 38, post-processing treatment may be performed, including cleaning, infiltration with stabilizing materials, painting, etc.
  • The method of the present invention is capable of producing features on the order of about 250 μm. The accuracy achieved by the method of the present invention is in the range of about +/−250 μm. Shrinkage of the final article is about 1%, which can easily be factored into the build to increase accuracy. [0048]
  • Adhesive
  • The adhesive is a compound selected for the characteristics of high solubility in the activating fluid, low solution viscosity, low hygroscopicity, and high bonding strength. The adhesive should be highly soluble in the solvent in order to ensure that it is incorporated rapidly and completely into the activating fluid. Low solution viscosity can be used to ensure that activating fluid having adhesive dissolved therein will migrate quickly to sites in the powder bed to adhesively bond together the reinforcing materials. If the adhesive is naturally a solid, the adhesive can be milled as finely as possible prior to mixing with the filler and/or activating fluid and/or prior to coating the filler particles. The fine particle size enhances the available surface area, enhancing dissolution in the solvent, without being so fine as to cause “caking”, an undesirable article characteristic. Typical adhesive particle grain sizes are about 5-50 μm. Low hygroscopicity of an adhesive used in the particulate mixture avoids absorption of excessive moisture from the air, which causes “caking”, in which unactivated powder spuriously adheres to the outside surface of the part, resulting in poor surface definition. [0049]
  • Various types of adhesives that can be used with this invention are further and more specifically described under the section entitled, “Activating Fluid,” below. [0050]
  • Filler
  • The filler of the present invention is a compound selected for the characteristics of insolubility in the activating fluid, or extremely low solubility in the activating fluid, rapid wetting, low hygroscopicity, and high bonding strength. The filler provides mechanical structure to the hardened composition. Sparingly soluble filler material is used in particular, although insoluble filler material can also be used. The filler particles become adhesively bonded together when the adhesive dries/hardens after the activating fluid has been applied. The filler can include a distribution of particle grain sizes, ranging from the practical maximum of about 200 μm downward, to the practical minimum of about 5 μm. Large grain sizes appear to improve the final article quality by forming large pores in the powder through which the fluid can migrate rapidly, permitting production of a more homogeneous material. Smaller grain sizes serve to reinforce article strength. [0051]
  • Compounds suitable for use as the filler of the present invention can be selected from the same general groups from which the adhesive is selected, provided that the solubility, hygroscopicity, bonding strength and solution viscosity criteria described above are met. Examples of such fillers, which can be used alone or in combination, include starches such as maltodextrin, clay, cellulose fiber, glass, limestone, gypsum, aluminum oxide, aluminum silicate, potassium aluminum silicate, calcium silicate, calcium hydroxide, calcium aluminate, and sodium silicate; metals; metal oxides such as zinc oxide, titanium dioxide, and magnetite (Fe[0052] 3O4); carbides such as silicon carbide; and borides such as titanium diboride. In other embodiments, the filler is limestone, which can be used alone or in combination with other inorganic fillers. For example, the filler can be a combination of plaster (0-20%), limestone (calcium carbonate) (40-95%) and glass beads (0-80%). Generally the filler materials are selected on the basis of their ability to bond with the adhesive components, combined with the spreading characteristics of the dry powder. The selection of the solvent also typically determines which filler can be used.
  • Reinforcing Fiber
  • The reinforcing fiber can be insoluble or can dissolve substantially slower in the fluid than the adhesive dissolves. The reinforcing fiber is a stiff material chosen to increase the mechanical reinforcement and dimensional control of the final article without making the powder too difficult to spread. In order to promote wetting of the reinforcing fibers, the chosen fibers have a high affinity for the solvent. A particular embodiment includes a fiber length approximately equal to the layer thickness, which provides the greatest degree of mechanical reinforcement. Using longer fibers adversely affects the surface finish, and using too much fiber of any length can make spreading of the powder increasingly difficult. Fibrous material suitable for reinforcing the present invention includes, but is not limited to polymeric fiber, ceramic fiber, graphite fiber and fiberglass. The polymeric fiber may be cellulose and cellulose derivatives or substituted or unsubstituted, straight or branched, alkyl or alkene, including monomers up to eight carbon atoms in length. Specific useable fibrous materials include, but are not limited to cellulose fiber, silicon carbide fiber, graphite fiber, aluminosilicate fiber, polypropylene fiber, fiberglass, nylon, and rayon. [0053]
  • As indicated in Table 1, both the reinforcing fiber and the stabilizing fiber are can be cellulose. Some of the useful properties of cellulose making it particularly suitable for use in connection with the invention are low toxicity, biodegradability, low cost and availability in a wide variety of lengths. [0054]
  • Further considerations when selecting the adhesive, filler and fiber depend on the desired properties of the final article. The final strength of the finished article depends largely on the quality of the adhesive contacts between the particles of the mixture, and the size of the empty pores that persist in the material after the adhesive has hardened; both of these factors vary with the grain size of the particulate material. In general, the mean size of the grains of particulate material should not be larger than the layer thickness. A distribution of grain sizes increases the packing density of the particulate material, which in turn increases both article strength and dimensional control. [0055]
  • Printing Aid
  • As indicated in Table 1, sorbitan trioleate (SPAN 85) is used as a printing aid in the exemplary particulate mixture. Sorbitan trioleate is a liquid which is only slightly soluble in water. By adding a small amount to the powder, the sorbitan trioleate provides a light adhesion between powder grains before printing, thereby reducing dust formation. After printing, the sorbitan trioleate continues to adhere insoluble grains together for a short time until it dissolves. This effect tends to reduce distortion in printed layers in the brief time that is required for the adhesive to dissolve and redistribute in the powder. Hydrophillic grades of lecithin are particularly suitable. A wide variety of other liquid compounds work for the same purpose. Polypropylene glycol (PPG), especially with a molecular weight of about 400, and citronellol are two examples. Other suitable printing aides include ethylene glycol octanoate, ethylene glycol decanoate, and ethoxylated derivatives of 2,4,7,9-Tetramethyl-5-decyne-4,7-diol. Sorbitan trioleate can be used in combination with lethicin, which also functions as a printing aid. Other liquid compounds that can be used as printing aids include sorbitan mono-oleate, sorbitan monolaurate, polyoxyethylene sorbitan mono-oleate, polyethylene glycol, soybean oil, mineral oil, propylene glycol, fluroalkyl polyoxyethylene polymers, glycerol triacetate, oleyl alcohol, and oleic acid. [0056]
  • Activating Fluid
  • The fluid of the present invention is selected to comport with the degree of solubility required for the various particulate components of the mixture, as described above. The fluid includes a solvent in which the adhesive is active, particularly soluble, and can include processing aids such as a humectant, a flowrate enhancer, and a dye. An ideal solvent is one in which the adhesive component of the powder is highly soluble, and in which both the filler and fiber are substantially less soluble. The solvent can be aqueous or non-aqueous, although aqueous solvents offer some advantages. Suitable solvents can be selected from the following non-limiting list: water, methyl alcohol, ethyl alcohol, isopropanol, t-butanol, ethyl acetate, dimethyl succinate, diethyl succinate, dimethyl adipate, and ethylene glycol diacetate. [0057]
  • The activating fluid, which can have adhesive pre-mixed, is also referred to as the “binder.” The function of the binder is to infiltrate the insoluble or semi-soluble particle mixture and to bond the grains together. The activating fluid, with adhesive included, can belong to any one of the following classes: (1) polymer solutions, (2) colloidal suspensions, (3) inorganic (salt) solutions, (4) organic monomeric solutions, (5) non aqueous liquids. Classes 1-4 can be aqueous. The following description of particular fluids and adhesives are not meant to be limiting, other suitable compounds may be used in place of or in combination with the listed compounds. [0058]
  • There also exists a collection of water-based compounds that have been found to work particularly well in electromechanical printheads. In the first category, a water-soluble polymer can be dissolved in the binder to form a relatively low viscosity solution. Of these, there are a few particularly suitable polymers. These are anionically ionizable polymers, cationic polymers and nonionic polymers. The anionically ionizable polymers include polymethacrylic acid, polymethacrylic acid sodium salt, and sodium polystyrene sulfonate. The cationic polymers include polyethyleneimine and polydiallyldimethyl ammonium chloride. As a class, polyethyleneimine comes in two forms, linear and branched, both of which are useful. The nonionic soluble polymers that are particularly useful as binders are polyvinyl pyrrolidone, polyvinyl pyrrolidone copolymer with polyvinyl acetate, polyvinyl alcohol, polyvinyl methyl ether, polyacrylamide, and poly-2-ethyl-2-oxazoline. [0059]
  • In a typical embodiment, a low molecular weight polymer such as sodium polystyrene sulfonate is dissolved in water to form a solution containing approximately 20% solids by weight. A cosolvent such as isopropyl alcohol, at approximately 1% to 5% by weight, can modify the viscosity of the solution by controlling the conformation of the polymer chains in solution. A humectant such as glycerol used at approximately 5% to 10% will reduce the tendency of the binder to dry in the printhead. Other solution parameters such as pH and salt concentration may be used to modify flow properties. Added salts tend to lower the viscosity of binders that include a polyelectrolyte, such as sodium chloride, sodium phosphate, sodium sulfate, and potassium sulfate. [0060]
  • In the second category, colloidal suspensions of materials can be used as binders in three-dimensional printing. Organic latexes such as polymethyl methacrylate, polystyrene, styrenated polyacrylic acid, natural rubber, polyurethane latex, polyvinyl acetate latex, and alkyd resin latex are materials that can be applied to the process. Additionally, inorganic suspensions such as colloidal alumina, clay, and colloidal graphite could all be used to for solid articles containing substantial amounts of these technologically important materials. The advantage of using a colloid over a solution is that a very large content of solid materials can be suspended without greatly increasing the viscosity of the fluid. [0061]
  • The first two classes do not necessarily exclude one another. Very often, a soluble polyelectrolyte will be used to stabilize a suspension of solid particles. The polyelectrolyte will contribute to the structure of the finished article in addition to the dispersed particles. [0062]
  • A typical embodiment of a colloid-based binder comprises a polyvinyl acetate including approximately 30% solids. Additional additives such as triethanolamine at 2% to 5% by weight are used to control the pH of the suspension. Additionally, a humectant such as glycerol at 5% to 10% is used to reduce the tendency of the latex to dry in the printhead during idle periods. [0063]
  • In the third category, inorganic solutes can be dissolved in an aqueous solvent and printed as a binder. Glass-forming solutes such as sodium silicate, sodium polyphosphate and sodium tetraborate can be used to deposit a ceramic binder in a finished article. This ceramic binder could be fused in a subsequent heat treatment into a glass-bonded ceramic. Other inorganic solutes that could be printed include sodium chloride, ammonium nitrate, and potassium sulfate, ammonium chloride, and calcium formate. [0064]
  • Inorganic solutes participate in acid-base reactions. For example, sodium hydrogen phosphate solution could be printed onto powdered calcium carbonate. The acid binder etches the alkaline powder and forms calcium phosphate that recrystallizes and cements together the grains of powder. Another example is sodium silicate, which can be printed in a binder solution and can react with, for example, gypsum plaster to form calcium silicate. [0065]
  • In the fourth category, a solution of monomeric organic compounds can be printed through an electromechanical drop-on-demand printhead for three-dimensionally printed articles. These monomeric organic compounds generally fall into several broad classes: alcohols, esters, ethers, silanes, vinyl monomers, acrylic monomers, and methacrylate monomers. [0066]
  • Alcohols and esters that have been found to function well as the solvent phase, in addition to functioning as a solute in another solvent (usually water) are: methyl alcohol, ethyl alcohol, isopropanol, t-butanol, ethyl acetate, dimethyl succinate, diethyl succinate, dimethyl adipate, and ethylene glycol diacetate. These materials act as solvents for resins in the powder bed. [0067]
  • Resins that have been found to work in a 3-D printer are: shellac, polyvinyl pyrrolidone, polyvinyl acetate, polyvinyl alcohol, polystyrene, styrene-butadiene copolymer, and acrylonitrile-butadiene-styrene copolymer. These resins can be used in combination with any filler, or they can be used by themselves. A particularly suitable combination is 100% dimethyl succinate binder printed over a powder of 100% acrylonitrile-butadiene-styrene copolymer. [0068]
  • The other monomers contain active sites for polymerization, and possess mixed characteristics. The classes of polymerizable monomers are the vinyl monomers, acrylic monomers, and methacrylate monomers. A exemplary mixed vinyl-silane monomer is vinyltriisopropoxysilane. Acrylic monomers include tri(propylene glycol) diacrylate, ethylene glycol phenyl ether acrylate, and 1,6 hexanediol diacrylate. Methacrylates include 1,3 butylene glycol dimethacrylate, neopentyl glycol dimethacrylate, butyl methacrylate, 1,6 hexanediol dimethacrylate, and di(propylene glycol) allyl ether methacrylate. [0069]
  • In addition, there are some proprietary monomers of unknown character that have been found to print well. These are manufactured by Sartomer Co. of Exton, Pa., with designations SR 521, SR 516, and CN 131. These materials are reactive, and when mixed with a photoinitiator, they can be solidified by applying ultraviolet radiation. A particularly suitable binder formula for this polymerizable class is 99% neopentyl glycol dimethacrylate mixed with 1% of Sartomer product # KT046 as a photoinitiator. Any of the above-listed monomers can be made to work, but this formula yields a suitable flow through the printhead and suitable reactivity. The radiation necessary to cure these materials is ultraviolet light with a wavelength of 363-378 nm and an energy density of 1 joule/cm[0070] 2. A particularly suitable powder formula for this mixture is given in Table 1, above.
  • Additionally, there are organic acids and sugars: sucrose, dextrose, malic acid, and sodium citrate, and other compounds such as urea and the hydrolyzed amino acids that can be used as solutes in water solution. These compounds would bind by drying in the powder, and not have any appreciable solvent character on their own. In addition, reactive monomers, such as melamine-formaldehyde, can be printed in a liquid solution and later polymerized by heat, by an initiator, or by actinic radiation such as ultra-violet radiation. [0071]
  • The fifth class includes members that can be used with electromechanical printheads that are designed for printing molten wax, such as the Tektronix Phasor 340 printhead (which includes a temperature control). In this category, a room temperature solid such as wax can be used by itself or to replace water as a medium to convey the primary adhesives discussed in categories 1-4. The wax itself would serve as an adhesive to cement together powder particles. Binders formulated from these materials would be appropriate for electromechanical printheads that work at elevated temperatures. At these operating temperatures, the binder would become fluid and could then be used in the three-dimensional printing process. [0072]
  • Typical wax-based binder formulations would include waxes with a low melt viscosity (less than 100 centipoise) such as different grades of natural mineral, or refined waxes. Examples include but are not limited to carnauba wax beeswax, ceresine, ozokerite, montan, orlcury wax, paraffin, and microcrystalline wax. The waxes can be chemically modified to include reactive groups such as alcohols, organic acids, alcohol oxazolates, and urethane derivatives. To modify binder material properties such as melting point, melt viscosity, toughness and hardening rate, as well as to increase compatibility with added components, the waxes can be blended or compounded with resins, oils, and other polymers. Additional components include rosin, fatty acids, fatty acid salts, mono and diglycerides, mineral oils, and turpentines. Resins include polyethylene, polypropylene, polybutadiene, polyethylene oxide, polyethylene glycol, polymethyl methacrylate, poly-2-ethyl-oxazoline, polyvinylpyrrollidone, polyacrylamide, and polyvinyl alcohol. [0073]
  • Adhesives in members of the first class (polymer solutions) and the second class (inorganic solutions) will often adsorb water if left exposed to ambient atmosphere. However, these adhesives will generally perform with greater reliability and efficacy if maintained in either a completely dry or wet state. By incorporating the adhesives in the liquid binder, they can thereby be maintained in a wet state and therefore exhibit the desired reliability and efficacy. [0074]
  • Humectant
  • A humectant can be included in the inventive mixture to retard evaporation of the solvent from the printed material, and to prevent drying/clogging of the printhead delivery system. Glycerol is a particularly suitable humectant when the solvent is aqueous. Other polyhydric alcohols, including but not limited to ethylene glycol, diethylene glycol, and propylene glycol, are also known in the art to retard evaporation. Additional humectants include thiodiethanol, n-methyl pyrrolidinone, and dimethyl hydantoin. [0075]
  • Flowrate Enhancer
  • A flowrate enhancer can be included that has some humectant properties, but serves mainly to alter the hydrodynamic properties or wetting characteristics of the fluid to maximize the volume of fluid delivered by the printhead. Flowrate enhancement is thought to be a viscoelastic phenomena increasing the flow rate of the fluid, allowing thicker layers to be printed, thus allowing the final article to be built more quickly. Specific compounds that increase the flowrate of the fluid, either by reducing friction between the fluid and the walls of the jet, or by reducing the viscosity of the fluid, include ethylene glycol diacetate and potassium aluminum sulfate. Other suitable compounds for use as the flowrate enhancer can be selected from the following non-limiting list: tetraethylene glycol dimethylether, isopropyl alcohol, ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, dodecyl dimethylammoniopropane sulfonate, glycerol triacetate, ethyl acetoacetate, and water-soluble polymers including polyvinyl pyrrolidone with a molecular weight of about 30,000 units, polyethylene glycol, polyacrylic acid, and sodium polyacrylate. For the ionic polymers, such as sodium polyacrylate, the increase in flow rate varies with pH. Salts that can be used to enhance flowrate include potassium sulfate, potassium aluminum sulfate, sodium hydrogen phosphate and sodium polyphosphate. [0076]
  • Dye
  • The fluid of the present invention can include a dye to provide a visual aid to the operator while building the article. The dye provides contrast between activated and unactivated powder which allows the operator to monitor the printed layers while building the article. The dye can be selected from the group including, but not limited to, naphthol blue-black and direct red. Other dyes that are compatible with the fluid can likewise be used. [0077]
  • Additional Ingredients in the Activating Fluid
  • Cosolvents can be added to an aqueous solution to alter the viscosity of a solution by altering the solvency of the liquid for the solute. Long-chain molecules in solution conform themselves either into extended chains or into coiled structures. If the solvent has a high affinity for the solute, long molecules will spread out causing the viscosity of the solution to be high. By adding a cosolvent to the solution, the polymer can be come less strongly attracted to other dissolved polymer molecules, and begin to coil into compact balls. This tends to reduce the viscosity of a polymer solution and allows more polymer to be dissolved. Cosolvents include isopropanol, ethyl alcohol, ethylene glycol monobutyl ether, butyrolactone and acetone. [0078]
  • Additives that control the pH of the binder, generally called buffers, can impart increased stability to the adhesive solutions and suspensions. Such materials include, but are not limited to, potassium hydroxide, ammonia, ammonium chloride, triethanolamine, sodium acetate, sodium gluconate, potassium sulfate, potassium hydrogen sulfate, sodium aluminum sulfate, and sodium tetraborate. [0079]
  • Wetting agents are substances that control the surface tension of a liquid. These can be used to modify the spreading of the liquid adhesive on the surfaces of the printhead mechanism. These include, but are not limited to, sodium dodecyl sulfate, sodium di-octyl sulfosuccinate, ethyl butyrate, diethylene glycol monobutyl ether, polyethylene glycol alkyl ether, and sodium p-toluene sulfonate. [0080]
  • Lubricants can be used to increase the rate at which liquid binder passes through the nozzles of a printhead. Depending on the materials of construction, substances such as glycerol triacetate, polyethylene oxide, polypropylene glycol, ethyl acetoacetate, diethyl succinate, and sodium polyacrylate can be used. [0081]
  • Additional substances can be used to promote the stability of suspensions. Stabilizers include emulsifiers such as sorbitan trioleate, polyoxyethylene mono-dodecyl ether, polyoxyethylene sorbitan mono-oleate, and protective colloids such as polyoxyethylene-co-polyoxypropylene, polyvinyl pyrrolidone, polyacrylic acid, gelatin, and acacia gum. [0082]
  • The equipment used in the method of the present invention is reliable, inexpensive, and easy to maintain, making it ideal for use in an office environment. The materials used in the present invention are capable of achieving much better performance in 3D Printing than those presently used in the liquid binder method. Thus, less equipment maintenance is required, and the reliability of the equipment is increased. Therefore, methods of the present invention can involve shorter build times and less labor than prior art methods. [0083]
  • Those skilled in the art will readily appreciate that all parameters listed herein are meant to be exemplary and actual parameters depend upon the specific application for which the methods and materials of the present invention are used. It is, therefore, to be understood that the foregoing embodiments are presented by way of example only and that, within the scope of the appended claims and equivalents thereto, the invention can be practiced otherwise than as specifically described. [0084]

Claims (40)

What is claimed is:
1. A chemical composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the component comprising a nonaqueous organic monomeric compound.
2. The compositing of
claim 1
, wherein the compound includes at least one of an alcohol, an ester, an ether, a silane, a vinyl monomer, an acrylic monomer, or a methacrylate monomer.
3. The composition of
claim 1
, comprising a solvent and a solute, and wherein the compound is the solvent.
4. The composition of
claim 3
, wherein the solvent includes an alcohol.
5. The composition of
claim 4
, wherein the alcohol is methyl alcohol, ethyl alcohol, isopropanol, or t-butanol.
6. The composition of
claim 3
, wherein the solvent includes an ester.
7. The composition of
claim 6
, wherein the ester includes at least one of ethyl acetate, dimethyl succinate, diethyl succinate, dimethyl adipate, or ethylene glycol diacetate.
8. The composition of
claim 2
, wherein the compound includes a mixed vinyl-silane monomer.
9. The composition of
claim 8
, wherein the mixed monomer includes vinyltriisopropoxysilane.
10. The composition of
claim 2
, wherein the acrylic monomer includes at least one of tri(propylene glycol) diacrylate, ethylene glycol phenyl ether acrylate, or 1,6 hexanediol diacrylate.
11. The composition of
claim 2
, wherein the methacrylic monomer includes at least one of 1,3 butylene glycol dimethacrylate, neopentyl glycol dimethacrylate, butyl methacrylate, 1,6 hexanediol dimethacrylate, or di(propylene glycol) allyl ether methacrylate.
12. The composition of
claim 1
, wherein the compound is curable in combination with a photoinitiator to form a solid, by ultraviolet radiation having a wavelength between about 320-500 nm and an energy density of about 1 joule/cm2.
13. The composition of
claim 1
, wherein the compound is a solvent for a resin in the particulate material.
14. The composition of
claim 13
, wherein the resin includes at least one of shellac, polyvinyl pyrrolidone, polyvinyl acetate, polyvinyl alcohol, polystyrene, styrene-butadiene copolymer, or acrylonitrile-butadiene-styrene copolymer.
15. The composition of
claim 1
, wherein the particulate material includes a filler that includes an inorganic compound.
16. The composition of
claim 15
, wherein the filler includes at least one of clay, aluminum oxide, silicon dioxide, aluminum silicate, potassium aluminum silicate, calcium silicate, calcium hydroxide, calcium aluminate, calcium carbonate, sodium silicate, zinc oxide, titanium dioxide, or magnetite.
17. The composition of
claim 15
, further comprising a printing aid dispersed throughout the filler.
18. The composition of
claim 17
, wherein the printing aid includes at least one of sorbitan trioleate, sorbitan mono-oleate, sorbitan monolaurate, polyoxyethylene sorbitan mono-oleate, polyethylene glycol, soybean oil, mineral oil, propylene glycol, fluroaklkyl polyoxyethylene polymers, glycerol triacetate, polypropylene glycol, ethylene glycol octanoate, ethylene glycol decanoate, ethoxylated derivatives of 2,4,7,9-Tetramethyl-5-decyne-4,7-diol, oleyl alcohol, or oleic acid.
19. A binder composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the binder composition including an adhesive in combination with a fluid, the adhesive comprising a nonaqueous organic monomeric compound.
20. A chemical composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the composition comprising an anionically ionizable polymer consisting of compounds selected from the group including polymethacrylic acid, polymethacrylic acid sodium salt, and sodium polystyrene sulfonate.
21. A chemical composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the composition including an adhesive in combination with a fluid, the adhesive comprising an anionically ionizable polymer consisting of compounds selected from the group including polymethacrylic acid, polymethacrylic acid sodium salt, and sodium polystyrene sulfonate.
22. A chemical composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the composition comprising a cationic polymer.
23. The composition of
claim 22
, wherein the polymer includes polyethyleneimine and polydiallyldimethylammonium chloride.
24. A binder composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the binder composition including an adhesive in combination with a fluid, the adhesive comprising a cationic polymer.
25. A chemical composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the composition comprising a nonionic polymer.
26. The composition of
claim 25
, wherein the polymer includes at least one of polyvinyl pyrrolidone, polyvinyl pyrrolidone copolymer with polyvinyl acetate, polyvinyl alcohol, polyvinyl methyl ether, polyacrylamide, or poly-2-ethyl-2-oxazoline.
27. A binder composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the binder including an adhesive in combination with a fluid, the adhesive comprising a nonionic polymer.
28. A chemical composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the adhesive comprising a polymer selected from the group consisting of polymethacrylic acid, polymethacrylic acid sodium salt, sodium polystyrene sulfonate, and polyethyleneimine.
29. A binder composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the binder including an adhesive in combination with a fluid, the adhesive comprising a polymer selected from the group consisting of polymethacrylic acid, polymethacrylic acid sodium salt, sodium polystyrene sulfonate, and polyethyleneimine.
30. A chemical composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the adhesive comprising a waterborne colloid selected from the group consisting of polymethyl methacrylate, polystyrene, natural rubber, polyurethane, polyvinyl acetate, and alkyd resins.
31. A binder composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the binder including an adhesive in combination with a fluid, the adhesive comprising a polymer selected from the group consisting of polymethyl methacrylate, polystyrene, natural rubber, polyurethane, polyvinyl acetate, and alkyd resins.
32. A chemical composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the adhesive comprising an inorganic solute selected from the group consisting of sodium polyphosphate, sodium hydrogen phosphate, sodium hydrogen pyrophosphate, sodium tetraborate, ammonium hydrogen phosphate, sodium chloride, ammonium nitrate, potassium sulfate, ammonium chloride, and calcium formate.
33. A binder composition for selectively adhering particulate material to form a solid object in a three-dimensional printer, the binder including an adhesive in combination with a fluid, the adhesive comprising an inorganic solute selected from the group consisting of sodium polyphosphate, sodium tetraborate, sodium chloride, ammonium nitrate, potassium sulfate, ammonium chloride, and calcium formate.
34. A method of forming a three-dimensional object, comprising:
forming a layer of filler that includes a particulate material; and
applying a chemical composition to the layer of filler at particular locations to bind the filler at particular locations, the composition including a nonaqueous organic monomeric compound.
35. A method of forming a three-dimensional object, comprising:
forming a layer of filler that includes a particulate material; and
applying a chemical composition to the layer of filler at particular locations to bind the filler at particular locations, the composition comprising an anionically ionizable polymer consisting of compounds selected from the group including polymethacrylic acid, polymethacrylic acid sodium salt, and sodium polystyrene sulfonate.
36. A method of forming a three-dimensional object, comprising:
forming a layer of filler that includes a particulate material; and
applying a chemical composition to the layer of filler at particular locations to bind the filler at particular locations, the composition comprising a cationic polymer.
37. A method of forming a three-dimensional object, comprising:
forming a layer of filler that includes a particulate material; and
applying a chemical composition to the layer of filler at particular locations to bind the filler at particular locations, the composition comprising a nonionic polymer.
38. A method of forming a three-dimensional object, comprising:
forming a layer of filler that includes a particulate material; and
applying a chemical composition to the layer of filler at particular locations to bind the filler at particular locations, the composition comprising a polymer selected from the group consisting of polymethacrylic acid, polymethacrylic acid sodium salt, sodium polystyrene sulfonate, and polyethyleneimine.
39. A method of forming a three-dimensional object, comprising:
forming a layer of filler that includes a particulate material; and
applying a chemical composition to the layer of filler at particular locations to bind the filler at particular locations, the composition comprising a waterborne colloid selected from the group consisting of polymethyl methacrylate, polystyrene, natural rubber, polyurethane, polyvinyl acetate, and alkyd resins.
40. A method of forming a three-dimensional object, comprising:
forming a layer of filler that includes a particulate material; and
applying a chemical composition to the layer of filler at particular locations to bind the filler at particular locations, the composition comprising an inorganic solute selected from the group consisting of sodium polyphosphate, sodium tetraborate, sodium chloride, ammonium nitrate, potassium sulfate, ammonium chloride, and calcium formate.
US09/835,292 2000-04-14 2001-04-13 Compositions for three-dimensional printing of solid objects Abandoned US20010050031A1 (en)

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Cited By (114)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040025905A1 (en) * 2000-10-04 2004-02-12 Ingo Ederer Method for unpacking shaped bodies embedded inside unbound particle material
US6742456B1 (en) * 2002-11-14 2004-06-01 Hewlett-Packard Development Company, L.P. Rapid prototyping material systems
US20040145088A1 (en) * 2001-05-24 2004-07-29 Patel Ranjana C Three-dimensional structured printing
EP1491516A2 (en) * 2003-06-24 2004-12-29 Hewlett-Packard Development Company, L.P. Calcium aluminate cement compositions for solid freeform fabrication
US20050059757A1 (en) * 2003-08-29 2005-03-17 Z Corporation Absorbent fillers for three-dimensional printing
US20050061241A1 (en) * 2003-07-14 2005-03-24 Therics, Inc. Three-dimensional printing apparatus and methods of manufacture including sterilization or disinfection, for example, using ultraviolet light
US20050079086A1 (en) * 2003-10-14 2005-04-14 Isaac Farr System and method for fabricating a three-dimensional metal object using solid free-form fabrication
US20050089636A1 (en) * 2003-10-28 2005-04-28 Christopher Oriakhi Resin-modified inorganic phosphate cement for solid freeform fabrication
EP1541321A2 (en) * 2003-10-28 2005-06-15 Hewlett-Packard Development Company, L.P. System and method for fabricating three-dimensional objects using solid free-form fabrication
WO2005070654A1 (en) * 2004-01-23 2005-08-04 Eos Gmbh Electro Optical Systems Layer-structuring method for the production of a three-dimensional object, and material systems suitable therefor
US20060108090A1 (en) * 2000-09-26 2006-05-25 Ingo Ederer Device for pattern building in layers
US20060289014A1 (en) * 2002-09-06 2006-12-28 Apneon, Inc. Devices, systems, and methods using magnetic force systems in or on tissue in an airway
US20070125539A1 (en) * 2005-12-01 2007-06-07 Halliburton Energy Services Methods of Cementing Subterranean Formations Using Cement Compositions Comprising Maltodextrin
US20070129260A1 (en) * 2005-12-01 2007-06-07 Caveny William J Additives comprising chlorinated carbohydrates
US20070125278A1 (en) * 2005-12-01 2007-06-07 Halliburton Energy Services Cement compositions comprising maltodextrin
US20070129261A1 (en) * 2005-12-01 2007-06-07 Halliburton Energy Services Additives Comprising Maltodextrin
US20070125538A1 (en) * 2005-12-01 2007-06-07 Caveny William J Methods of treating subterranean formations using treatment fluids comprising chlorinated carbohydrates
US20070125277A1 (en) * 2005-12-01 2007-06-07 Caveny William J Treatment fluids comprising chlorinated carbohydrates
US20070183918A1 (en) * 2004-03-16 2007-08-09 Degussa Ag Method and device for producing three-dimensional objects using laser technology and for applying an absorber using an ink jet method
US20070238056A1 (en) * 2004-04-27 2007-10-11 Degussa Ag Method and Device for Production of Three-Dimensional Objects by Means of Electromagnetic Radiation of Electromagnetic Radiation and Application of an Absorber by Means of an Ink-Jet Method
US20070246683A1 (en) * 2006-04-24 2007-10-25 David Paul Miller Reduced dusting gypsum composites and method of making them
US20070267766A1 (en) * 2004-03-21 2007-11-22 Toyota Motorsport Gmbh Powder for Rapid Prototyping and Associated Production Method
WO2007138619A1 (en) * 2006-05-26 2007-12-06 Matteo Mantovani Method for rapid production of objects anyhow shaped
US20080152910A1 (en) * 2004-03-21 2008-06-26 Eos Gmbh Electro Optical Systems N/a
US20080157436A1 (en) * 2001-02-15 2008-07-03 Huntsman Advanced Materials Americas Inc. Three-dimensional structered printing
US20080233302A1 (en) * 2004-05-24 2008-09-25 Technische Universität Berlin Method and Device for Production of a Three-Dimensional Article
US20080260945A1 (en) * 2004-02-19 2008-10-23 Ingo Ederer Method and Device for Applying Fluids
WO2009037550A2 (en) * 2007-09-17 2009-03-26 Enrico Dini Improved method for automatically producing a conglomerate structure and apparatus therefor
US20090298033A1 (en) * 2006-04-21 2009-12-03 Next21 K.K. Figure-forming composition, process for production of figures in three dimensions by using the composition and process for production of three-dimensional structures
US7665636B2 (en) 2002-05-20 2010-02-23 Ingo Ederer Device for feeding fluids
US20100068330A1 (en) * 2006-11-09 2010-03-18 Valspar Sourcing, Inc. Powder Compositions and Methods of Manufacturing Articles Therefrom
US7686995B2 (en) 1996-12-20 2010-03-30 Z Corporation Three-dimensional printer
US7736578B2 (en) 2006-06-30 2010-06-15 Ingo Ederer Method for the construction of a laminated compound
US20100155069A1 (en) * 2008-12-19 2010-06-24 Halliburton Energy Services, Inc. Cement Compositions Comprising Stevia Retarders
US20100160547A1 (en) * 2006-11-09 2010-06-24 Valspar Sourcing, Inc. Polyester powder compositions, methods and articles
US7795349B2 (en) 1999-11-05 2010-09-14 Z Corporation Material systems and methods of three-dimensional printing
US7807077B2 (en) 2003-06-16 2010-10-05 Voxeljet Technology Gmbh Methods and systems for the manufacture of layered three-dimensional forms
US20100279007A1 (en) * 2007-08-14 2010-11-04 The Penn State Research Foundation 3-D Printing of near net shape products
US7828022B2 (en) 2006-05-26 2010-11-09 Z Corporation Apparatus and methods for handling materials in a 3-D printer
US7879393B2 (en) 2001-04-10 2011-02-01 Ingo Ederer Method and device for applying fluids
US7905951B2 (en) 2006-12-08 2011-03-15 Z Corporation Three dimensional printing material system and method using peroxide cure
US7955537B2 (en) 2002-06-05 2011-06-07 Ingo Ederer Method for constructing patterns in a layered manner
US7968626B2 (en) 2007-02-22 2011-06-28 Z Corporation Three dimensional printing material system and method using plasticizer-assisted sintering
US8167999B2 (en) 2007-01-10 2012-05-01 3D Systems, Inc. Three-dimensional printing material system with improved color, article performance, and ease of use
US8349233B2 (en) 2007-10-11 2013-01-08 Voxeljet Gmbh Material system and method for changing properties of a plastic component
US8715832B2 (en) 2008-11-20 2014-05-06 Voxeljet Ag Method for the layered construction of plastic models
US8727672B2 (en) 2007-10-21 2014-05-20 Voxeljet Ag Method and device for conveying particulate material during the layer-wise production of patterns
CN103819164A (en) * 2014-02-28 2014-05-28 广州丽格打印耗材有限公司 Powder for 3D printers and preparation method thereof
US8741194B1 (en) 2000-09-25 2014-06-03 Voxeljet Ag Method for producing a part using a depostion technique
US8911226B2 (en) 2010-04-14 2014-12-16 Voxeljet Ag Device for producing three-dimensional models
US8956144B2 (en) 2010-02-04 2015-02-17 Voxeijet AG Device for producing three-demensional models
US8992205B2 (en) 2007-10-23 2015-03-31 Voxeijet AG Device for the layer-wise production of patterns
US20150232648A1 (en) * 2014-02-20 2015-08-20 Microjet Technology Co., Ltd. Three-dimensional prototyping composition
US9174391B2 (en) 2010-03-31 2015-11-03 Voxeljet Ag Device for producing three-dimensional models
US20150360288A1 (en) * 2014-06-13 2015-12-17 Zin Technologies, Inc. Optimized additive manufacturing process
US20150366327A1 (en) * 2014-06-20 2015-12-24 Richard Joseph LaHood, SR. Cosmetics Applicator System and Method
US9242413B2 (en) 2011-01-05 2016-01-26 Voxeljet Ag Device and method for constructing a laminar body comprising at least one position adjustable body defining the working area
CN105283281A (en) * 2013-02-28 2016-01-27 沃克斯艾捷特股份有限公司 Process for producing a moulding using a water-soluble casting mould and material system for the production thereof
US9333709B2 (en) 2010-03-31 2016-05-10 Voxeljet Ag Device and method for producing three-dimensional models
US20160325495A1 (en) * 2013-12-23 2016-11-10 The Exone Company Methods and Systems for Three-Dimensional Printing Utilizing a Jetted-Particle Binder Fluid
US9505176B2 (en) 2007-07-18 2016-11-29 Voxeljet Ag Method for producing three-dimensional components
EP2209572B1 (en) 2007-10-30 2016-12-14 ASK Chemicals GmbH Mould material mixture having improved flowability
EP3030367A4 (en) * 2013-08-06 2017-03-22 Wisys Technology Foundation, Inc. 3-d printed casting shell and method of manufacture
WO2017062031A1 (en) * 2015-10-09 2017-04-13 Hewlett-Packard Development Company, L.P. Particulate mixtures
US9643360B2 (en) 2006-08-20 2017-05-09 Voxeljet Ag Self-hardening material and process for layerwise formation of models
WO2017086995A1 (en) * 2015-11-20 2017-05-26 Hewlett-Packard Development Company, L.P. Three-dimensional (3d) printing
US20170246686A1 (en) * 2014-09-26 2017-08-31 Hewlett-Packard Development Company, L.P. Pastes for printing three-dimensional objects in additive manufacturing processes
US9770867B2 (en) 2010-12-29 2017-09-26 Voxeljet Ag Method and material system for building models in layers
US9833788B2 (en) 2004-03-21 2017-12-05 Eos Gmbh Electro Optical Systems Powder for layerwise manufacturing of objects
US9878494B2 (en) 2011-08-31 2018-01-30 Voxeljet Ag Device for constructing models in layers
US9914169B2 (en) 2010-04-17 2018-03-13 Voxeljet Ag Method and device for producing three-dimensional models
US9943981B2 (en) 2013-12-11 2018-04-17 Voxeljet Ag 3D infiltration method
EP2849931B1 (en) * 2012-05-18 2018-04-25 3D Systems, Inc. Use of an adhesive for 3d printing
US9987682B2 (en) 2016-08-03 2018-06-05 3Deo, Inc. Devices and methods for three-dimensional printing
US10052682B2 (en) 2012-10-12 2018-08-21 Voxeljet Ag 3D multi-stage method
US10059062B2 (en) 2012-05-25 2018-08-28 Voxeljet Ag Device for producing three-dimensional models with special building platforms and drive systems
US10059058B2 (en) 2012-06-22 2018-08-28 Voxeljet Ag Device for building a multilayer structure with storage container or filling container movable along the dispensing container
WO2018186845A1 (en) * 2017-04-05 2018-10-11 Hewlett-Packard Development Company, L.P. Reducing stresses in metal layers
EP3431141A1 (en) * 2013-03-15 2019-01-23 Aprecia Pharmaceuticals LLC Three-dimensional printing method
US10213831B2 (en) 2012-11-25 2019-02-26 Voxeljet Ag Construction of a 3D printing device for producing components
US10220567B2 (en) 2012-03-06 2019-03-05 Voxeljet Ag Method and device for producing three-dimensional models
US10220568B2 (en) 2013-12-02 2019-03-05 Voxeljet Ag Interchangeable container with moveable side walls
US10226919B2 (en) 2007-07-18 2019-03-12 Voxeljet Ag Articles and structures prepared by three-dimensional printing method
US10428248B1 (en) * 2015-10-12 2019-10-01 Wolf & Associates, Inc. Compositions, materials, and methods for enhancing 3D printer platform adhesion and/or reducing warpage in printed parts
US10442170B2 (en) 2013-12-20 2019-10-15 Voxeljet Ag Device, special paper, and method for producing shaped articles
US10556380B2 (en) 2015-01-30 2020-02-11 Renaissance Of Technology Corporation Three-dimensional molding producing method, three-dimensional molding producing apparatus, three-dimensional molding, and molding material
CN111050953A (en) * 2017-07-06 2020-04-21 惠普发展公司,有限责任合伙企业 Three-dimensional (3D) printing
US10682809B2 (en) 2014-12-22 2020-06-16 Voxeljet Ag Method and device for producing 3D moulded parts by means of a layer construction technique
US10683381B2 (en) 2014-12-23 2020-06-16 Bridgestone Americas Tire Operations, Llc Actinic radiation curable polymeric mixtures, cured polymeric mixtures and related processes
US10753211B2 (en) 2016-12-12 2020-08-25 General Electric Company Heterogeneous composition, article comprising heterogeneous composition, and method for forming article
US10786945B2 (en) 2013-10-30 2020-09-29 Voxeljet Ag Method and device for producing three-dimensional models using a binding agent system
US10843404B2 (en) 2015-05-20 2020-11-24 Voxeljet Ag Phenolic resin method
US10882110B2 (en) 2015-09-09 2021-01-05 Voxeljet Ag Method and device for applying fluids
US10913207B2 (en) 2014-05-26 2021-02-09 Voxeljet Ag 3D reverse printing method and device
US10946556B2 (en) 2014-08-02 2021-03-16 Voxeljet Ag Method and casting mold, in particular for use in cold casting methods
US11008437B2 (en) 2015-11-13 2021-05-18 Ricoh Company, Ltd. Material set for forming three-dimensional object, three-dimensional object producing method, and three-dimensional object producing apparatus
US11077611B2 (en) 2015-03-17 2021-08-03 Voxeljet Ag Method and device for producing 3D shaped articles with a double recoater
US11097531B2 (en) 2015-12-17 2021-08-24 Bridgestone Americas Tire Operations, Llc Additive manufacturing cartridges and processes for producing cured polymeric products by additive manufacturing
US11097471B2 (en) 2014-03-31 2021-08-24 Voxeljet Ag Method and device for 3D printing using temperature-controlled processing
US11097469B2 (en) 2012-10-15 2021-08-24 Voxeljet Ag Method and device for producing three-dimensional models with a temperature-controllable print head
US11235518B2 (en) 2015-12-01 2022-02-01 Voxeljet Ag Method and device for producing three-dimensional components with the aid of an overfeed sensor
US11273605B2 (en) 2016-11-15 2022-03-15 Voxeljet Ag Integrated print head maintenance station for powder bed-based 3D printing
US11279087B2 (en) 2017-07-21 2022-03-22 Voxeljet Ag Process and apparatus for producing 3D moldings comprising a spectrum converter
US11389867B2 (en) 2017-02-24 2022-07-19 Hewlett-Packard Development Company, L.P. Three-dimensional (3D) printing
US11407180B2 (en) 2018-05-04 2022-08-09 Desktop Metal, Inc. Support edifice for three-dimensional printing
US11453161B2 (en) 2016-10-27 2022-09-27 Bridgestone Americas Tire Operations, Llc Processes for producing cured polymeric products by additive manufacturing
US11504879B2 (en) 2020-04-17 2022-11-22 Beehive Industries, LLC Powder spreading apparatus and system
WO2023002127A1 (en) * 2021-07-22 2023-01-26 Universite De Bretagne Sud Material based on natural colloids and wax of natural origin with liquid-solid phase change
US11577316B2 (en) * 2017-02-24 2023-02-14 Hewlett-Packard Development Company, L.P. Three-dimensional printing
US11633908B2 (en) * 2018-03-02 2023-04-25 Formlabs, Inc. Latent cure resins and related methods
US11720946B1 (en) * 2010-07-16 2023-08-08 George Gabriel Arenas Method of customizing a product with a digitally printed attaching member
US11820076B2 (en) 2019-11-01 2023-11-21 Voxeljet Ag 3D printing process and molding produced by this process using lignosulfate
US11826958B2 (en) 2019-02-05 2023-11-28 Voxeljet Ag Exchangeable process unit
US11890810B2 (en) 2015-09-16 2024-02-06 Voxeljet Ag Device and method for producing three-dimensional shaped parts

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050087902A1 (en) * 2003-10-28 2005-04-28 Isaac Farr Alginate-based materials, methods of application thereof, and systems for using the alginate-based materials
CN101528158B (en) * 2006-08-21 2011-10-05 21世纪国际新技术株式会社 Bone model, bone filler and process for producing bone filler
US20110129640A1 (en) * 2009-11-30 2011-06-02 George Halsey Beall Method and binder for porous articles
GB201009512D0 (en) 2010-06-07 2010-07-21 Univ The West Of England Product and process
US8888480B2 (en) 2012-09-05 2014-11-18 Aprecia Pharmaceuticals Company Three-dimensional printing system and equipment assembly
EP2892708B1 (en) 2012-09-05 2018-10-10 Aprecia Pharmaceuticals LLC Three-dimensional printing system and equipment assembly
KR20150081446A (en) * 2012-11-05 2015-07-14 스트라타시스 엘티디. System and method for direct inkjet printing of 3d objects
WO2014077848A1 (en) 2012-11-19 2014-05-22 Hewlett-Packard Development Company, L.P. Compositions for three-dimensional (3d) printing
US9050820B2 (en) 2012-12-29 2015-06-09 Atasheh Soleimani-Gorgani Three-dimensional ink-jet printing by home and office ink-jet printer
US8916334B2 (en) 2013-01-28 2014-12-23 Hewlett-Packard Development Company, L.P. Micro-composite material for three-dimensional printing
US9339489B2 (en) 2013-03-15 2016-05-17 Aprecia Pharmaceuticals Company Rapid disperse dosage form containing levetiracetam
EP3415254A1 (en) * 2013-06-10 2018-12-19 Renishaw PLC Selective laser solidification apparatus and method
JP6376831B2 (en) * 2013-06-20 2018-08-22 キヤノン株式会社 Manufacturing method of structure
EP3838593A1 (en) 2013-07-11 2021-06-23 Tundra Composites, LLC Surface modified particulate and sintered or injection molded products
US9604412B2 (en) 2013-07-12 2017-03-28 Xerox Corporation Digital manufacturing system for printing three-dimensional objects on a rotating surface
US9701064B2 (en) 2013-07-15 2017-07-11 Xerox Corporation Digital manufacturing system for printing three-dimensional objects on a rotating core
US10471497B2 (en) 2013-08-16 2019-11-12 The Exone Company Three-dimensional printed metal-casting molds and methods for making the same
US11028299B2 (en) 2013-11-19 2021-06-08 Mitsubishi Polyester Film, Inc Anti-powdering and anti-static polymer film for digital printing
US9545302B2 (en) 2013-11-20 2017-01-17 Dermagenesis Llc Skin printing and auto-grafting
WO2015167530A2 (en) 2014-04-30 2015-11-05 Hewlett-Packard Development Company, L.P. Three-dimensional (3d) printing method
CN106687281B (en) * 2014-09-02 2019-12-20 惠普发展公司有限责任合伙企业 Additive manufacturing for overhanging portion
GB201505458D0 (en) 2015-03-30 2015-05-13 Renishaw Plc Additive manufacturing apparatus and methods
RU2597675C1 (en) * 2015-04-20 2016-09-20 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Башкирский государственный университет" Electric conductive polymer composition for 3d printing
KR101647598B1 (en) * 2015-04-24 2016-08-11 한양대학교 에리카산학협력단 Fabrication of piezodriven micro-positioning 3-dof stage with flexure hinges using multi-material 3-d printer
WO2016175832A1 (en) 2015-04-30 2016-11-03 Hewlett-Packard Development Company, L.P. Three-dimensional (3d) printing
US10029299B2 (en) * 2015-07-09 2018-07-24 General Electric Company Three-dimensional manufacturing methods and systems for turbine components
RU2018109736A (en) 2015-08-21 2019-09-23 АПРЕЦИЯ ФАРМАСЬЮТИКАЛЗ ЭлЭлСи SYSTEM AND HARDWARE UNIT OF 3D PRINTING
WO2017131709A1 (en) * 2016-01-28 2017-08-03 Hewlett-Packard Development Company, L.P. Three-dimensional (3d) printing with a detailing agent fluid and a liquid functional material
CN107603201B (en) * 2017-09-07 2021-02-26 金华造物新材料有限公司 3D printing photosensitive resin for precision casting of ornaments and dentistry
US11351724B2 (en) 2017-10-03 2022-06-07 General Electric Company Selective sintering additive manufacturing method
US11420384B2 (en) 2017-10-03 2022-08-23 General Electric Company Selective curing additive manufacturing method
US11254052B2 (en) 2017-11-02 2022-02-22 General Electric Company Vatless additive manufacturing apparatus and method
US11590691B2 (en) 2017-11-02 2023-02-28 General Electric Company Plate-based additive manufacturing apparatus and method
US10821669B2 (en) 2018-01-26 2020-11-03 General Electric Company Method for producing a component layer-by-layer
US10821668B2 (en) 2018-01-26 2020-11-03 General Electric Company Method for producing a component layer-by- layer
US11794412B2 (en) 2019-02-20 2023-10-24 General Electric Company Method and apparatus for layer thickness control in additive manufacturing
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US11179891B2 (en) 2019-03-15 2021-11-23 General Electric Company Method and apparatus for additive manufacturing with shared components
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US11951679B2 (en) 2021-06-16 2024-04-09 General Electric Company Additive manufacturing system
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Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4369025A (en) * 1978-02-13 1983-01-18 Epsi Brevets Et Participations S.A. Apparatus for manufacturing elements by means of a hardenable binding agent to which a liquid is added
US4863538A (en) * 1986-10-17 1989-09-05 Board Of Regents, The University Of Texas System Method and apparatus for producing parts by selective sintering
US4942003A (en) * 1984-10-27 1990-07-17 "Wurtex" Maschinenbau Hofmann GmbH & Co. Method for continuously producing molded members from a mixture of gypsum and fibrous material
US5155324A (en) * 1986-10-17 1992-10-13 Deckard Carl R Method for selective laser sintering with layerwise cross-scanning
US5204055A (en) * 1989-12-08 1993-04-20 Massachusetts Institute Of Technology Three-dimensional printing techniques
US5342566A (en) * 1990-08-23 1994-08-30 Carl Schenck Ag Method of manufacturing fiber gypsum board
US5382308A (en) * 1986-10-17 1995-01-17 Board Of Regents, The University Of Texas System Multiple material systems for selective beam sintering
US5902441A (en) * 1996-09-04 1999-05-11 Z Corporation Method of three dimensional printing
US5943235A (en) * 1995-09-27 1999-08-24 3D Systems, Inc. Rapid prototyping system and method with support region data processing

Family Cites Families (159)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US597043A (en) * 1898-01-11 Ratchet-wrench
EP0833267B1 (en) * 1996-09-30 2004-02-25 STMicroelectronics S.r.l. Charge injection circuit for an insulated gate MOS transistor and computing devices using the same
US2522548A (en) 1946-10-03 1950-09-19 Thoger G Jungersen Method of making a phosphate gel and mold with phosphate gel binder
US2662024A (en) 1951-03-01 1953-12-08 Kaiser Gypsum Company Inc Cementitious compositions
US3303147A (en) 1963-01-15 1967-02-07 Nat Gypsum Co Dry powder for wallboard joint treatment
US3297601A (en) 1963-08-13 1967-01-10 United States Gypsum Co Substantially dry joint compound comprising calcium sulfate, polyvinyl acetate and starch
US3309328A (en) 1964-06-03 1967-03-14 Allied Chem High strength adhesive for building materials
CH423346A (en) 1964-08-27 1966-10-31 Jacques Dr Jenny Process for the production of a hoof covering, and the covering produced according to this
US4041476A (en) 1971-07-23 1977-08-09 Wyn Kelly Swainson Method, medium and apparatus for producing three-dimensional figure product
US3525632A (en) 1967-11-08 1970-08-25 Resco Products Inc Method for forming a concrete cement composition
US3821006A (en) 1971-04-16 1974-06-28 Dentsply Int Inc Patching method
CH1917171A4 (en) 1971-12-30 1975-04-30
US3852083A (en) 1972-03-30 1974-12-03 J Yang Manufacture of plaster of paris products containing latex
US3930872A (en) 1973-04-17 1976-01-06 Ashland Oil, Inc. Binder compositions
US3835074A (en) 1973-04-26 1974-09-10 Hercules Inc Joint cement compositions
US3870538A (en) 1973-05-07 1975-03-11 Nat Gypsum Co Gypsum set accelerator
US3926870A (en) 1973-10-15 1975-12-16 Warner Lambert Co Denture adhesive preparation containing an anionic protein material
US3932923A (en) 1974-10-21 1976-01-20 Dynell Electronics Corporation Method of generating and constructing three-dimensional bodies
US4078229A (en) 1975-01-27 1978-03-07 Swanson Wyn K Three dimensional systems
GB1498057A (en) 1975-04-17 1978-01-18 Ass Portland Cement Hydraulic cements
US4288861A (en) 1977-12-01 1981-09-08 Formigraphic Engine Corporation Three-dimensional systems
US4247508B1 (en) 1979-12-03 1996-10-01 Dtm Corp Molding process
US4310996A (en) 1980-04-23 1982-01-19 General Electric Co. Cement reinforced gypsum foam with mineral wool
US4327156A (en) 1980-05-12 1982-04-27 Minnesota Mining And Manufacturing Company Infiltrated powdered metal composite article
DE3041794A1 (en) 1980-11-06 1982-05-13 Dynamit Nobel Ag, 5210 Troisdorf METHOD FOR PRODUCING DESSINED MOLDED BODIES FROM A CURABLE DIMENSION BASED ON DUROPLASTIC PLASTICS
EP0077618B1 (en) 1981-10-15 1986-12-17 Ciba Specialty Chemicals Water Treatments Limited Adhesives for prepasted wallcoverings
EP0091262B1 (en) 1982-04-07 1986-03-05 Adnovum Ag Heat-activatable multi-component sheet material and process for making same
US4444594A (en) 1982-12-09 1984-04-24 Armstrong World Industries, Inc. Acid cured inorganic binder compositions which are compatible with mineral wool
US4613627A (en) 1982-12-13 1986-09-23 Usg Acoustical Products Company Process for the manufacture of shaped fibrous products and the resultant product
US4618390A (en) 1983-06-13 1986-10-21 Ashland Oil, Inc. Method for preparing laminated articles
US4755227A (en) 1983-08-11 1988-07-05 Stauffer Chemical Company Production of solid phosphorus pentioxide containing materials for fast-setting cements
US4665492A (en) 1984-07-02 1987-05-12 Masters William E Computer automated manufacturing process and system
US4575330A (en) 1984-08-08 1986-03-11 Uvp, Inc. Apparatus for production of three-dimensional objects by stereolithography
US4929402A (en) 1984-08-08 1990-05-29 3D Systems, Inc. Method for production of three-dimensional objects by stereolithography
US4665892A (en) * 1985-06-24 1987-05-19 The Stanley Works Oven door hinge assembly
DE3750709T2 (en) 1986-06-03 1995-03-16 Cubital Ltd Device for developing three-dimensional models.
US4752352A (en) 1986-06-06 1988-06-21 Michael Feygin Apparatus and method for forming an integral object from laminations
US5147587A (en) 1986-10-17 1992-09-15 Board Of Regents, The University Of Texas System Method of producing parts and molds using composite ceramic powders
US5017753A (en) 1986-10-17 1991-05-21 Board Of Regents, The University Of Texas System Method and apparatus for producing parts by selective sintering
US4944817A (en) 1986-10-17 1990-07-31 Board Of Regents, The University Of Texas System Multiple material systems for selective beam sintering
DE3750931T3 (en) * 1986-10-17 1999-12-02 Univ Texas METHOD AND DEVICE FOR PRODUCING MOLDED BODIES BY PARTIAL INTERSTERING.
US5076869A (en) 1986-10-17 1991-12-31 Board Of Regents, The University Of Texas System Multiple material systems for selective beam sintering
US4758278A (en) 1986-11-28 1988-07-19 E. I. Du Pont De Nemours And Company Magnesium oxide powder for workable, rapid-setting phosphate-containing cement compositions
US4752498A (en) 1987-03-02 1988-06-21 Fudim Efrem V Method and apparatus for production of three-dimensional objects by photosolidification
US4801477A (en) 1987-09-29 1989-01-31 Fudim Efrem V Method and apparatus for production of three-dimensional objects by photosolidification
US5015312A (en) 1987-09-29 1991-05-14 Kinzie Norman F Method and apparatus for constructing a three-dimensional surface of predetermined shape and color
IL84752A (en) 1987-12-08 1991-11-21 Elscint Ltd Anatomical models and methods for manufacturing such models
IL109511A (en) 1987-12-23 1996-10-16 Cubital Ltd Three-dimensional modelling apparatus
US4942001A (en) 1988-03-02 1990-07-17 Inc. DeSoto Method of forming a three-dimensional object by stereolithography and composition therefore
US4996282A (en) 1988-03-24 1991-02-26 Desoto, Inc. Cationically curable polyurethane compositions having vinyl ether functionality
US4945032A (en) 1988-03-31 1990-07-31 Desoto, Inc. Stereolithography using repeated exposures to increase strength and reduce distortion
EP0366748A4 (en) 1988-04-11 1991-09-25 Australasian Lasers Pty. Ltd. Laser based plastic model making workstation
US4999143A (en) 1988-04-18 1991-03-12 3D Systems, Inc. Methods and apparatus for production of three-dimensional objects by stereolithography
US5130064A (en) 1988-04-18 1992-07-14 3D Systems, Inc. Method of making a three dimensional object by stereolithography
US5076974A (en) 1988-04-18 1991-12-31 3 D Systems, Inc. Methods of curing partially polymerized parts
US5772947A (en) * 1988-04-18 1998-06-30 3D Systems Inc Stereolithographic curl reduction
US4996010A (en) 1988-04-18 1991-02-26 3D Systems, Inc. Methods and apparatus for production of three-dimensional objects by stereolithography
US5059359A (en) 1988-04-18 1991-10-22 3 D Systems, Inc. Methods and apparatus for production of three-dimensional objects by stereolithography
US5015424A (en) 1988-04-18 1991-05-14 3D Systems, Inc. Methods and apparatus for production of three-dimensional objects by stereolithography
US5104592A (en) 1988-04-18 1992-04-14 3D Systems, Inc. Method of and apparatus for production of three-dimensional objects by stereolithography with reduced curl
US5137662A (en) 1988-11-08 1992-08-11 3-D Systems, Inc. Method and apparatus for production of three-dimensional objects by stereolithography
US5141680A (en) 1988-04-18 1992-08-25 3D Systems, Inc. Thermal stereolighography
US5184307A (en) * 1988-04-18 1993-02-02 3D Systems, Inc. Method and apparatus for production of high resolution three-dimensional objects by stereolithography
US4844144A (en) 1988-08-08 1989-07-04 Desoto, Inc. Investment casting utilizing patterns produced by stereolithography
US4943928A (en) 1988-09-19 1990-07-24 Campbell Albert E Elongated carrier with a plurality of spot-sources of heat for use with stereolithographic system
US5637175A (en) * 1988-10-05 1997-06-10 Helisys Corporation Apparatus for forming an integral object from laminations
IL88359A (en) 1988-11-10 1993-06-10 Cubital Ltd Method and apparatus for volumetric digitization of 3-dimensional objects
US5135379A (en) 1988-11-29 1992-08-04 Fudim Efrem V Apparatus for production of three-dimensional objects by photosolidification
GB8827952D0 (en) 1988-11-30 1989-01-05 Screen Form Inc Display device
IL88626A0 (en) 1988-12-07 1989-07-31 N C T Limited Method and apparatus for making three-dimensional objects
US5089184A (en) 1989-01-18 1992-02-18 Mitsui Engineering And Shipbuilding Co., Ltd. Optical molding method
US5038014A (en) 1989-02-08 1991-08-06 General Electric Company Fabrication of components by layered deposition
JP2715527B2 (en) 1989-03-14 1998-02-18 ソニー株式会社 3D shape forming method
US4942060A (en) 1989-04-21 1990-07-17 E. I. Du Pont De Nemours And Company Solid imaging method utilizing photohardenable compositions of self limiting thickness by phase separation
US5128235A (en) 1989-04-21 1992-07-07 E. I. Du Pont De Nemours And Company Method of forming a three-dimensional object comprising additives imparting reduction of shrinkage to photohardenable compositions
US5051334A (en) 1989-04-21 1991-09-24 E. I. Du Pont De Nemours And Company Solid imaging method using photohardenable compositions containing hollow spheres
US5011635A (en) 1989-05-18 1991-04-30 Desoto, Inc. Stereolithographic method and apparatus in which a membrane separates phases
GB2233928B (en) 1989-05-23 1992-12-23 Brother Ind Ltd Apparatus and method for forming three-dimensional article
US5143663A (en) 1989-06-12 1992-09-01 3D Systems, Inc. Stereolithography method and apparatus
US5134569A (en) 1989-06-26 1992-07-28 Masters William E System and method for computer automated manufacturing using fluent material
JPH0336019A (en) 1989-07-03 1991-02-15 Brother Ind Ltd Three-dimensional molding method and device thereof
JPH0624773B2 (en) 1989-07-07 1994-04-06 三井造船株式会社 Optical modeling method
US5096491A (en) 1989-07-19 1992-03-17 Honshu Paper Co., Ltd. Aqueous starch slurry adhesive
US5053090A (en) 1989-09-05 1991-10-01 Board Of Regents, The University Of Texas System Selective laser sintering with assisted powder handling
US5632848A (en) * 1989-10-12 1997-05-27 Georgia-Pacific Corporation Continuous processing equipment for making fiberboard
US5088047A (en) 1989-10-16 1992-02-11 Bynum David K Automated manufacturing system using thin sections
US5133987A (en) 1989-10-27 1992-07-28 3D Systems, Inc. Stereolithographic apparatus and method
US5121329A (en) 1989-10-30 1992-06-09 Stratasys, Inc. Apparatus and method for creating three-dimensional objects
US5017317A (en) 1989-12-04 1991-05-21 Board Of Regents, The Uni. Of Texas System Gas phase selective beam deposition
US5135695A (en) 1989-12-04 1992-08-04 Board Of Regents The University Of Texas System Positioning, focusing and monitoring of gas phase selective beam deposition
US5009585A (en) 1989-12-18 1991-04-23 Mitsui Engineering & Shipbuilding Co., Ltd. Optical molding apparatus and movable base device therefor
US5143817A (en) 1989-12-22 1992-09-01 E. I. Du Pont De Nemours And Company Solid imaging system
US5139711A (en) 1989-12-25 1992-08-18 Matsushita Electric Works, Ltd. Process of and apparatus for making three dimensional objects
US5071337A (en) 1990-02-15 1991-12-10 Quadrax Corporation Apparatus for forming a solid three-dimensional article from a liquid medium
US5338611A (en) * 1990-02-20 1994-08-16 Aluminum Company Of America Method of welding thermoplastic substrates with microwave frequencies
US5094935A (en) 1990-06-26 1992-03-10 E. I. Dupont De Nemours And Company Method and apparatus for fabricating three dimensional objects from photoformed precursor sheets
US5096530A (en) 1990-06-28 1992-03-17 3D Systems, Inc. Resin film recoating method and apparatus
US5127037A (en) 1990-08-15 1992-06-30 Bynum David K Apparatus for forming a three-dimensional reproduction of an object from laminations
US5122441A (en) 1990-10-29 1992-06-16 E. I. Du Pont De Nemours And Company Method for fabricating an integral three-dimensional object from layers of a photoformable composition
US5328539A (en) * 1990-11-28 1994-07-12 H. B. Fuller Licensing & Financing Inc. Radio frequency heating of thermoplastic receptor compositions
US5182134A (en) * 1990-11-28 1993-01-26 H. B. Fuller Licensing & Financing Inc. Radio frequency cure of thermoset-receptor compositions
US5286573A (en) * 1990-12-03 1994-02-15 Fritz Prinz Method and support structures for creation of objects by layer deposition
US5176188A (en) * 1991-02-14 1993-01-05 E. I. Du Pont De Nemours And Company Investment casting method and pattern material comprising thermally-collapsible expanded microspheres
US5154762A (en) 1991-05-31 1992-10-13 Minnesota Mining And Manufacturing Company Universal water-based medical and dental cement
US5314003A (en) * 1991-12-24 1994-05-24 Microelectronics And Computer Technology Corporation Three-dimensional metal fabrication using a laser
US5342919A (en) * 1992-11-23 1994-08-30 Dtm Corporation Sinterable semi-crystalline powder and near-fully dense article formed therewith
US5527877A (en) * 1992-11-23 1996-06-18 Dtm Corporation Sinterable semi-crystalline powder and near-fully dense article formed therewith
US5648450A (en) * 1992-11-23 1997-07-15 Dtm Corporation Sinterable semi-crystalline powder and near-fully dense article formed therein
US5490882A (en) * 1992-11-30 1996-02-13 Massachusetts Institute Of Technology Process for removing loose powder particles from interior passages of a body
US5430666A (en) * 1992-12-18 1995-07-04 Dtm Corporation Automated method and apparatus for calibration of laser scanning in a selective laser sintering apparatus
DE4302418A1 (en) * 1993-01-28 1994-08-11 Eos Electro Optical Syst Method and device for producing a three-dimensional object
ES2150977T3 (en) * 1993-08-09 2000-12-16 Vantico Ag NEW (MET) ACRYLATES CONTAINING URETANIAN GROUPS.
AU684546B2 (en) * 1993-09-10 1997-12-18 University Of Queensland, The Stereolithographic anatomical modelling process
US5490962A (en) * 1993-10-18 1996-02-13 Massachusetts Institute Of Technology Preparation of medical devices by solid free-form fabrication methods
US5518680A (en) * 1993-10-18 1996-05-21 Massachusetts Institute Of Technology Tissue regeneration matrices by solid free form fabrication techniques
FR2714668B1 (en) * 1993-12-31 1996-01-26 Rhone Poulenc Chimie Preparation of phosphomagnesium cements.
US5433280A (en) * 1994-03-16 1995-07-18 Baker Hughes Incorporated Fabrication method for rotary bits and bit components and bits and components produced thereby
US5429788A (en) * 1994-03-28 1995-07-04 Kimberly-Clark Corporation Apparatus and method for depositing particulate material in a composite substrate
EP0758952B1 (en) * 1994-05-13 1998-04-08 EOS GmbH ELECTRO OPTICAL SYSTEMS Process and device for manufacturing three-dimensional objects
US5639402A (en) * 1994-08-08 1997-06-17 Barlow; Joel W. Method for fabricating artificial bone implant green parts
EP0807014B1 (en) * 1995-02-01 2002-05-02 3D Systems, Inc. Rapid recoating of three-dimensional objects formed on a cross-sectional basis
US5593431A (en) * 1995-03-30 1997-01-14 Medtronic, Inc. Medical service employing multiple DC accelerometers for patient activity and posture sensing and method
DE19511772C2 (en) * 1995-03-30 1997-09-04 Eos Electro Optical Syst Device and method for producing a three-dimensional object
US5733497A (en) * 1995-03-31 1998-03-31 Dtm Corporation Selective laser sintering with composite plastic material
DE19514740C1 (en) * 1995-04-21 1996-04-11 Eos Electro Optical Syst Appts. for producing three-dimensional objects by laser sintering
US5622577A (en) * 1995-08-28 1997-04-22 Delco Electronics Corp. Rapid prototyping process and cooling chamber therefor
US5653925A (en) * 1995-09-26 1997-08-05 Stratasys, Inc. Method for controlled porosity three-dimensional modeling
US5749041A (en) * 1995-10-13 1998-05-05 Dtm Corporation Method of forming three-dimensional articles using thermosetting materials
US5640667A (en) * 1995-11-27 1997-06-17 Board Of Regents, The University Of Texas System Laser-directed fabrication of full-density metal articles using hot isostatic processing
US5660621A (en) * 1995-12-29 1997-08-26 Massachusetts Institute Of Technology Binder composition for use in three dimensional printing
US7332537B2 (en) * 1996-09-04 2008-02-19 Z Corporation Three dimensional printing material system and method
US6007318A (en) * 1996-12-20 1999-12-28 Z Corporation Method and apparatus for prototyping a three-dimensional object
US7037382B2 (en) * 1996-12-20 2006-05-02 Z Corporation Three-dimensional printer
US6989115B2 (en) * 1996-12-20 2006-01-24 Z Corporation Method and apparatus for prototyping a three-dimensional object
US5940674A (en) * 1997-04-09 1999-08-17 Massachusetts Institute Of Technology Three-dimensional product manufacture using masks
DE19715582B4 (en) * 1997-04-15 2009-02-12 Ederer, Ingo, Dr. Method and system for generating three-dimensional bodies from computer data
SE509088C2 (en) * 1997-04-30 1998-12-07 Ralf Larsson Methods and apparatus for the production of volume bodies
NL1006059C2 (en) * 1997-05-14 1998-11-17 Geest Adrianus F Van Der Method and device for manufacturing a shaped body.
US6348679B1 (en) * 1998-03-17 2002-02-19 Ameritherm, Inc. RF active compositions for use in adhesion, bonding and coating
US6821462B2 (en) * 1998-07-10 2004-11-23 Jeneric/Pentron, Inc. Mass production of shells and models for dental restorations produced by solid free-form fabrication methods
US6363606B1 (en) * 1998-10-16 2002-04-02 Agere Systems Guardian Corp. Process for forming integrated structures using three dimensional printing techniques
US6433038B1 (en) * 1999-03-16 2002-08-13 Seiko Epson Corporation Photocurable ink composition for ink jet recording and ink jet recording method using the same
JP2001150556A (en) * 1999-09-14 2001-06-05 Minolta Co Ltd Three-dimensional shaping device and three-dimensional shaping method
ES2230086T3 (en) * 2000-03-24 2005-05-01 Voxeljet Technology Gmbh METHOD AND APPLIANCE FOR MANUFACTURING A STRUCTURAL PART BY MULTI-LAYER DEPOSITION TECHNIQUE AND MALE MOLDING MANUFACTURED WITH THE METHOD.
US6397922B1 (en) * 2000-05-24 2002-06-04 Massachusetts Institute Of Technology Molds for casting with customized internal structure to collapse upon cooling and to facilitate control of heat transfer
EP1301177A2 (en) * 2000-07-10 2003-04-16 Therics, Inc. Method and materials for controlling migration of binder liquid in a powder
US6780368B2 (en) * 2001-04-10 2004-08-24 Nanotek Instruments, Inc. Layer manufacturing of a multi-material or multi-color 3-D object using electrostatic imaging and lamination
US7011783B2 (en) * 2001-10-24 2006-03-14 3D Systems, Inc. Cooling techniques in solid freeform fabrication
US6713125B1 (en) * 2002-03-13 2004-03-30 3D Systems, Inc. Infiltration of three-dimensional objects formed by solid freeform fabrication
US20040038009A1 (en) * 2002-08-21 2004-02-26 Leyden Richard Noel Water-based material systems and methods for 3D printing
US7087109B2 (en) * 2002-09-25 2006-08-08 Z Corporation Three dimensional printing material system and method
US6742456B1 (en) * 2002-11-14 2004-06-01 Hewlett-Packard Development Company, L.P. Rapid prototyping material systems
US6930144B2 (en) * 2003-06-24 2005-08-16 Hewlett-Packard Development Company, L.P. Cement system including a binder for use in freeform fabrication
WO2005021248A1 (en) * 2003-08-27 2005-03-10 Fuji Photo Film Co., Ltd. Method of producing three-dimensional model
US20050059757A1 (en) * 2003-08-29 2005-03-17 Z Corporation Absorbent fillers for three-dimensional printing
US20070029698A1 (en) * 2003-09-11 2007-02-08 Rynerson Michael L Layered manufactured articles having small-diameter fluid conduction vents and method of making same
US7381360B2 (en) * 2003-11-03 2008-06-03 Hewlett-Packard Development Company, L.P. Solid free-form fabrication of three-dimensional objects
US7608672B2 (en) * 2004-02-12 2009-10-27 Illinois Tool Works Inc. Infiltrant system for rapid prototyping process
US7389154B2 (en) * 2004-09-29 2008-06-17 Hewlett-Packard Development Company, L.P. Fabricating a three-dimensional object

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4369025A (en) * 1978-02-13 1983-01-18 Epsi Brevets Et Participations S.A. Apparatus for manufacturing elements by means of a hardenable binding agent to which a liquid is added
US4942003A (en) * 1984-10-27 1990-07-17 "Wurtex" Maschinenbau Hofmann GmbH & Co. Method for continuously producing molded members from a mixture of gypsum and fibrous material
US4863538A (en) * 1986-10-17 1989-09-05 Board Of Regents, The University Of Texas System Method and apparatus for producing parts by selective sintering
US5155324A (en) * 1986-10-17 1992-10-13 Deckard Carl R Method for selective laser sintering with layerwise cross-scanning
US5382308A (en) * 1986-10-17 1995-01-17 Board Of Regents, The University Of Texas System Multiple material systems for selective beam sintering
US5204055A (en) * 1989-12-08 1993-04-20 Massachusetts Institute Of Technology Three-dimensional printing techniques
US5342566A (en) * 1990-08-23 1994-08-30 Carl Schenck Ag Method of manufacturing fiber gypsum board
US5943235A (en) * 1995-09-27 1999-08-24 3D Systems, Inc. Rapid prototyping system and method with support region data processing
US5902441A (en) * 1996-09-04 1999-05-11 Z Corporation Method of three dimensional printing

Cited By (204)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8017055B2 (en) 1996-12-20 2011-09-13 Z Corporation Three-dimensional printer
US7686995B2 (en) 1996-12-20 2010-03-30 Z Corporation Three-dimensional printer
US7795349B2 (en) 1999-11-05 2010-09-14 Z Corporation Material systems and methods of three-dimensional printing
US8741194B1 (en) 2000-09-25 2014-06-03 Voxeljet Ag Method for producing a part using a depostion technique
US10213938B2 (en) 2000-09-25 2019-02-26 Voxeljet Ag Method for producing a part using a deposition technique
US9403324B2 (en) 2000-09-25 2016-08-02 Voxeljet Ag Method for producing a part using a deposition technique
US7137431B2 (en) 2000-09-26 2006-11-21 Ingo Ederer Device for pattern building in layers
US20060108090A1 (en) * 2000-09-26 2006-05-25 Ingo Ederer Device for pattern building in layers
US20040025905A1 (en) * 2000-10-04 2004-02-12 Ingo Ederer Method for unpacking shaped bodies embedded inside unbound particle material
US7455804B2 (en) 2001-02-15 2008-11-25 Huntsman Advanced Materials Americas Inc. Three-dimensional structured printing
US20080157436A1 (en) * 2001-02-15 2008-07-03 Huntsman Advanced Materials Americas Inc. Three-dimensional structered printing
US7767132B2 (en) 2001-02-15 2010-08-03 Huntsman Advanced Materials Americas, Inc. Three-dimensional structured printing
US7879393B2 (en) 2001-04-10 2011-02-01 Ingo Ederer Method and device for applying fluids
US20040145088A1 (en) * 2001-05-24 2004-07-29 Patel Ranjana C Three-dimensional structured printing
US7578958B2 (en) * 2001-05-24 2009-08-25 Huntsman Advanced Materials Americas Inc. Three-dimensional structured printing
US7665636B2 (en) 2002-05-20 2010-02-23 Ingo Ederer Device for feeding fluids
US7955537B2 (en) 2002-06-05 2011-06-07 Ingo Ederer Method for constructing patterns in a layered manner
US20060289014A1 (en) * 2002-09-06 2006-12-28 Apneon, Inc. Devices, systems, and methods using magnetic force systems in or on tissue in an airway
US6742456B1 (en) * 2002-11-14 2004-06-01 Hewlett-Packard Development Company, L.P. Rapid prototyping material systems
US8506870B2 (en) 2003-06-16 2013-08-13 Voxeljet Technology Gmbh Methods of manufacturing layered three-dimensional forms
US7807077B2 (en) 2003-06-16 2010-10-05 Voxeljet Technology Gmbh Methods and systems for the manufacture of layered three-dimensional forms
US7258736B2 (en) * 2003-06-24 2007-08-21 Hewlett-Packard Development Company, L.P. Calcium aluminate cement compositions for solid freeform fabrication
US20040261664A1 (en) * 2003-06-24 2004-12-30 Oriakhi Christ Pher Calcium aluminate cement compositions for solid freeform fabrication
EP1491516A3 (en) * 2003-06-24 2008-02-20 Hewlett-Packard Development Company, L.P. Calcium aluminate cement compositions for solid freeform fabrication
EP1491516A2 (en) * 2003-06-24 2004-12-29 Hewlett-Packard Development Company, L.P. Calcium aluminate cement compositions for solid freeform fabrication
US20050061241A1 (en) * 2003-07-14 2005-03-24 Therics, Inc. Three-dimensional printing apparatus and methods of manufacture including sterilization or disinfection, for example, using ultraviolet light
US7445441B2 (en) * 2003-07-14 2008-11-04 Therics, Llc Three-dimensional printing apparatus and methods of manufacture including sterilization or disinfection, for example, using ultraviolet light
US20050059757A1 (en) * 2003-08-29 2005-03-17 Z Corporation Absorbent fillers for three-dimensional printing
US20050079086A1 (en) * 2003-10-14 2005-04-14 Isaac Farr System and method for fabricating a three-dimensional metal object using solid free-form fabrication
US7220380B2 (en) * 2003-10-14 2007-05-22 Hewlett-Packard Development Company, L.P. System and method for fabricating a three-dimensional metal object using solid free-form fabrication
EP1541321A2 (en) * 2003-10-28 2005-06-15 Hewlett-Packard Development Company, L.P. System and method for fabricating three-dimensional objects using solid free-form fabrication
US7455805B2 (en) * 2003-10-28 2008-11-25 Hewlett-Packard Development Company, L.P. Resin-modified inorganic phosphate cement for solid freeform fabrication
EP1541321A3 (en) * 2003-10-28 2009-05-20 Hewlett-Packard Development Company, L.P. System and method for fabricating three-dimensional objects using solid free-form fabrication
US20050089636A1 (en) * 2003-10-28 2005-04-28 Christopher Oriakhi Resin-modified inorganic phosphate cement for solid freeform fabrication
US20070267784A1 (en) * 2004-01-23 2007-11-22 Ralph Greiner Method for the Manufacturing of a Three-Dimensional Object in a Layer-Wise Fashion and Material Systems Suitable Therefor
WO2005070654A1 (en) * 2004-01-23 2005-08-04 Eos Gmbh Electro Optical Systems Layer-structuring method for the production of a three-dimensional object, and material systems suitable therefor
US20080260945A1 (en) * 2004-02-19 2008-10-23 Ingo Ederer Method and Device for Applying Fluids
US8096262B2 (en) 2004-02-19 2012-01-17 Ingo Ederer Method and device for applying fluids
US9463488B2 (en) 2004-02-19 2016-10-11 Voxeljet Ag Method for applying particle material including a metering system and leveling element
US9114567B2 (en) * 2004-03-16 2015-08-25 Evonik Degussa Gmbh Method and device for producing three-dimensional objects using laser technology and for applying an absorber using an ink jet method
US10118222B2 (en) 2004-03-16 2018-11-06 Evonik Degussa Gmbh Method and device for producing three-dimensional objects using laser technology and for applying an absorber using an inkjet method
US20070183918A1 (en) * 2004-03-16 2007-08-09 Degussa Ag Method and device for producing three-dimensional objects using laser technology and for applying an absorber using an ink jet method
US20080152910A1 (en) * 2004-03-21 2008-06-26 Eos Gmbh Electro Optical Systems N/a
US20070267766A1 (en) * 2004-03-21 2007-11-22 Toyota Motorsport Gmbh Powder for Rapid Prototyping and Associated Production Method
US8313087B2 (en) 2004-03-21 2012-11-20 Eos Gmbh Electro Optical Systems Powder for rapid prototyping and associated production method
US9833788B2 (en) 2004-03-21 2017-12-05 Eos Gmbh Electro Optical Systems Powder for layerwise manufacturing of objects
EP1660566B2 (en) 2004-03-21 2017-06-21 EOS GmbH Electro Optical Systems Powder for rapid prototyping and associated production method
US8710144B2 (en) * 2004-03-21 2014-04-29 Eos Gmbh Electro Optical Systems Powder for layerwise manufacturing of objects
US20070238056A1 (en) * 2004-04-27 2007-10-11 Degussa Ag Method and Device for Production of Three-Dimensional Objects by Means of Electromagnetic Radiation of Electromagnetic Radiation and Application of an Absorber by Means of an Ink-Jet Method
US9643359B2 (en) * 2004-04-27 2017-05-09 Evonik Degussa Gmbh Method and device for production of three-dimensional objects by means of electromagnetic radiation and application of an absorber by means of an ink-jet method
US7767130B2 (en) 2004-05-24 2010-08-03 Voxeljet Technology Gmbh Method and device for production of a three-dimensional article
US20080233302A1 (en) * 2004-05-24 2008-09-25 Technische Universität Berlin Method and Device for Production of a Three-Dimensional Article
US20070129261A1 (en) * 2005-12-01 2007-06-07 Halliburton Energy Services Additives Comprising Maltodextrin
US7547664B2 (en) 2005-12-01 2009-06-16 Halliburton Energy Services, Inc. Additives comprising chlorinated carbohydrates
US20070125538A1 (en) * 2005-12-01 2007-06-07 Caveny William J Methods of treating subterranean formations using treatment fluids comprising chlorinated carbohydrates
US7422062B2 (en) 2005-12-01 2008-09-09 Halliburton Energy Services, Inc. Methods of treating subterranean formations using treatment fluids comprising chlorinated carbohydrates
US20070125539A1 (en) * 2005-12-01 2007-06-07 Halliburton Energy Services Methods of Cementing Subterranean Formations Using Cement Compositions Comprising Maltodextrin
US7395861B2 (en) * 2005-12-01 2008-07-08 Halliburton Energy Services, Inc. Methods of cementing subterranean formations using cement compositions comprising maltodextrin
US20070129260A1 (en) * 2005-12-01 2007-06-07 Caveny William J Additives comprising chlorinated carbohydrates
US20070125278A1 (en) * 2005-12-01 2007-06-07 Halliburton Energy Services Cement compositions comprising maltodextrin
US7303625B2 (en) 2005-12-01 2007-12-04 Halliburton Energy Services, Inc. Treatment fluids comprising chlorinated carbohydrates
US20070125277A1 (en) * 2005-12-01 2007-06-07 Caveny William J Treatment fluids comprising chlorinated carbohydrates
US7435293B2 (en) * 2005-12-01 2008-10-14 Halliburton Energy Services, Inc. Cement compositions comprising maltodextrin
US8105517B2 (en) 2006-04-21 2012-01-31 Next21 K.K. Figure-forming composition, method for forming three-dimensional figures and three-dimensional structures by using the same
US20090298033A1 (en) * 2006-04-21 2009-12-03 Next21 K.K. Figure-forming composition, process for production of figures in three dimensions by using the composition and process for production of three-dimensional structures
US20070246683A1 (en) * 2006-04-24 2007-10-25 David Paul Miller Reduced dusting gypsum composites and method of making them
US7828022B2 (en) 2006-05-26 2010-11-09 Z Corporation Apparatus and methods for handling materials in a 3-D printer
US7979152B2 (en) 2006-05-26 2011-07-12 Z Corporation Apparatus and methods for handling materials in a 3-D printer
US8185229B2 (en) 2006-05-26 2012-05-22 3D Systems, Inc. Apparatus and methods for handling materials in a 3-D printer
WO2007138619A1 (en) * 2006-05-26 2007-12-06 Matteo Mantovani Method for rapid production of objects anyhow shaped
US7971991B2 (en) 2006-05-26 2011-07-05 Z Corporation Apparatus and methods for handling materials in a 3-D printer
US20100243123A1 (en) * 2006-06-30 2010-09-30 Voxeljet Technology Gmbh Method for the construction of a laminated compound
US7736578B2 (en) 2006-06-30 2010-06-15 Ingo Ederer Method for the construction of a laminated compound
US7927539B2 (en) 2006-06-30 2011-04-19 Ingo Ederer Method for the construction of a laminated compound
US9676143B2 (en) 2006-08-10 2017-06-13 Voxeljet Ag Self-hardening material and process for layerwise formation of models
US9643360B2 (en) 2006-08-20 2017-05-09 Voxeljet Ag Self-hardening material and process for layerwise formation of models
US10870232B2 (en) 2006-11-09 2020-12-22 3D Systems, Inc. Polyester powder compositions, methods and articles
US8247492B2 (en) 2006-11-09 2012-08-21 Valspar Sourcing, Inc. Polyester powder compositions, methods and articles
US9233505B2 (en) 2006-11-09 2016-01-12 3D Systems, Inc. Powder compositions and methods of manufacturing articles therefrom
US8592519B2 (en) 2006-11-09 2013-11-26 Valspar Sourcing, Inc. Polyeste powder compositions, methods and articles
US20100160547A1 (en) * 2006-11-09 2010-06-24 Valspar Sourcing, Inc. Polyester powder compositions, methods and articles
US10150256B2 (en) 2006-11-09 2018-12-11 3D Systems, Inc. Polyester powder compositions, methods and articles
US20100068330A1 (en) * 2006-11-09 2010-03-18 Valspar Sourcing, Inc. Powder Compositions and Methods of Manufacturing Articles Therefrom
US9561625B2 (en) 2006-11-09 2017-02-07 3D Systems, Inc. Polyester powder compositions, methods and articles
US8157908B2 (en) 2006-12-08 2012-04-17 3D Systems, Inc. Three dimensional printing material system and method using peroxide cure
US7905951B2 (en) 2006-12-08 2011-03-15 Z Corporation Three dimensional printing material system and method using peroxide cure
US8167999B2 (en) 2007-01-10 2012-05-01 3D Systems, Inc. Three-dimensional printing material system with improved color, article performance, and ease of use
US7968626B2 (en) 2007-02-22 2011-06-28 Z Corporation Three dimensional printing material system and method using plasticizer-assisted sintering
US8506862B2 (en) 2007-02-22 2013-08-13 3D Systems, Inc. Three dimensional printing material system and method using plasticizer-assisted sintering
US10226919B2 (en) 2007-07-18 2019-03-12 Voxeljet Ag Articles and structures prepared by three-dimensional printing method
US10960655B2 (en) 2007-07-18 2021-03-30 Voxeljet Ag Articles and structures prepared by three-dimensional printing method
US9505176B2 (en) 2007-07-18 2016-11-29 Voxeljet Ag Method for producing three-dimensional components
US20100279007A1 (en) * 2007-08-14 2010-11-04 The Penn State Research Foundation 3-D Printing of near net shape products
WO2009037550A3 (en) * 2007-09-17 2009-07-23 Enrico Dini Improved method for automatically producing a conglomerate structure and apparatus therefor
US20100207288A1 (en) * 2007-09-17 2010-08-19 Enrico Dini Method for automatically producing a conglomerate structure and apparatus therefor
US8337736B2 (en) 2007-09-17 2012-12-25 Enrico Dini Method for automatically producing a conglomerate structure and apparatus therefor
WO2009037550A2 (en) * 2007-09-17 2009-03-26 Enrico Dini Improved method for automatically producing a conglomerate structure and apparatus therefor
US8349233B2 (en) 2007-10-11 2013-01-08 Voxeljet Gmbh Material system and method for changing properties of a plastic component
US9469074B2 (en) 2007-10-21 2016-10-18 Voxeljet Ag Method and device for conveying particulate material during the layer-wise production of patterns
US10099426B2 (en) 2007-10-21 2018-10-16 Voxeljet Ag Method and device for layer-wise production of patterns
US8727672B2 (en) 2007-10-21 2014-05-20 Voxeljet Ag Method and device for conveying particulate material during the layer-wise production of patterns
US9757831B2 (en) 2007-10-23 2017-09-12 Voxeljet Ag Methods for assembling a device for the layer-wise production of patterns
US8992205B2 (en) 2007-10-23 2015-03-31 Voxeijet AG Device for the layer-wise production of patterns
US10799989B2 (en) 2007-10-23 2020-10-13 Voxeljet Ag Pre-assembled module for a device for the layer-wise production of patterns
EP2209572B1 (en) 2007-10-30 2016-12-14 ASK Chemicals GmbH Mould material mixture having improved flowability
US10232430B2 (en) 2007-10-30 2019-03-19 Ask Chemicals Gmbh Mould material mixture having improved flowability
US8715832B2 (en) 2008-11-20 2014-05-06 Voxeljet Ag Method for the layered construction of plastic models
US7836954B2 (en) 2008-12-19 2010-11-23 Halliburton Energy Services. Inc. Cement compositions comprising stevia retarders
US20100155069A1 (en) * 2008-12-19 2010-06-24 Halliburton Energy Services, Inc. Cement Compositions Comprising Stevia Retarders
US8956144B2 (en) 2010-02-04 2015-02-17 Voxeijet AG Device for producing three-demensional models
US9925721B2 (en) 2010-02-04 2018-03-27 Voxeljet Ag Device for producing three-dimensional models
US9333709B2 (en) 2010-03-31 2016-05-10 Voxeljet Ag Device and method for producing three-dimensional models
US9656423B2 (en) 2010-03-31 2017-05-23 Voxeljet Ag Device and method for producing three-dimensional models
US9993975B2 (en) 2010-03-31 2018-06-12 Voxeljet Ag Device for producing three-dimensional models
US9815243B2 (en) 2010-03-31 2017-11-14 Voxeljet Ag Device for producing three-dimensional models
US9174391B2 (en) 2010-03-31 2015-11-03 Voxeljet Ag Device for producing three-dimensional models
US9962885B2 (en) 2010-04-14 2018-05-08 Voxeljet Ag Device for producing three-dimensional models
US8911226B2 (en) 2010-04-14 2014-12-16 Voxeljet Ag Device for producing three-dimensional models
US10179365B2 (en) 2010-04-17 2019-01-15 Voxeljet Ag Method and device for producing three-dimensional models
US10639715B2 (en) 2010-04-17 2020-05-05 Voxeljet Ag Method and device for producing three-dimensional models
US9914169B2 (en) 2010-04-17 2018-03-13 Voxeljet Ag Method and device for producing three-dimensional models
US11720946B1 (en) * 2010-07-16 2023-08-08 George Gabriel Arenas Method of customizing a product with a digitally printed attaching member
US9770867B2 (en) 2010-12-29 2017-09-26 Voxeljet Ag Method and material system for building models in layers
US9649812B2 (en) 2011-01-05 2017-05-16 Voxeljet Ag Device and method for constructing a laminar body comprising at least one position-adjustable body defining the working area
US10946636B2 (en) 2011-01-05 2021-03-16 Voxeljet Ag Device and method for constructing a layer body
US9242413B2 (en) 2011-01-05 2016-01-26 Voxeljet Ag Device and method for constructing a laminar body comprising at least one position adjustable body defining the working area
US11407216B2 (en) 2011-01-05 2022-08-09 Voxeljet Ag Device and method for constructing a layer body
US10513105B2 (en) 2011-01-05 2019-12-24 Voxeljet Ag Device and method for constructing a layer body
US9878494B2 (en) 2011-08-31 2018-01-30 Voxeljet Ag Device for constructing models in layers
US10913204B2 (en) 2011-08-31 2021-02-09 Voxeljet Ag Device for constructing models in layers and methods thereof
US10589460B2 (en) 2012-03-06 2020-03-17 Voxeljet Ag Method and device for producing three-dimensional models
US10220567B2 (en) 2012-03-06 2019-03-05 Voxeljet Ag Method and device for producing three-dimensional models
EP2849931B1 (en) * 2012-05-18 2018-04-25 3D Systems, Inc. Use of an adhesive for 3d printing
US10059062B2 (en) 2012-05-25 2018-08-28 Voxeljet Ag Device for producing three-dimensional models with special building platforms and drive systems
US11225029B2 (en) 2012-05-25 2022-01-18 Voxeljet Ag Device for producing three-dimensional models and methods thereof
US10059058B2 (en) 2012-06-22 2018-08-28 Voxeljet Ag Device for building a multilayer structure with storage container or filling container movable along the dispensing container
US10052682B2 (en) 2012-10-12 2018-08-21 Voxeljet Ag 3D multi-stage method
US11097469B2 (en) 2012-10-15 2021-08-24 Voxeljet Ag Method and device for producing three-dimensional models with a temperature-controllable print head
US11130290B2 (en) 2012-11-25 2021-09-28 Voxeljet Ag Construction of a 3D printing device for producing components
US10213831B2 (en) 2012-11-25 2019-02-26 Voxeljet Ag Construction of a 3D printing device for producing components
US10343301B2 (en) 2013-02-28 2019-07-09 Voxeljet Ag Process for producing a moulding using a water-soluble casting mould and material system for the production thereof
US11072090B2 (en) 2013-02-28 2021-07-27 Voxeljet Ag Material system for producing a molded part using a water-soluble casting mold
CN105283281A (en) * 2013-02-28 2016-01-27 沃克斯艾捷特股份有限公司 Process for producing a moulding using a water-soluble casting mould and material system for the production thereof
EP3431141A1 (en) * 2013-03-15 2019-01-23 Aprecia Pharmaceuticals LLC Three-dimensional printing method
EP3030367A4 (en) * 2013-08-06 2017-03-22 Wisys Technology Foundation, Inc. 3-d printed casting shell and method of manufacture
US11541596B2 (en) 2013-10-30 2023-01-03 Voxeljet Ag Method and device for producing three-dimensional models using a binding agent system
US10786945B2 (en) 2013-10-30 2020-09-29 Voxeljet Ag Method and device for producing three-dimensional models using a binding agent system
US10220568B2 (en) 2013-12-02 2019-03-05 Voxeljet Ag Interchangeable container with moveable side walls
US11292188B2 (en) 2013-12-02 2022-04-05 Voxeljet Ag Interchangeable container with moveable side walls
US11850796B2 (en) 2013-12-02 2023-12-26 Voxeljet Ag Interchangeable container with moveable side walls
US9943981B2 (en) 2013-12-11 2018-04-17 Voxeljet Ag 3D infiltration method
US10442170B2 (en) 2013-12-20 2019-10-15 Voxeljet Ag Device, special paper, and method for producing shaped articles
US10889055B2 (en) 2013-12-20 2021-01-12 Voxeljet Ag Device, special paper, and method for producing shaped articles
US20160325495A1 (en) * 2013-12-23 2016-11-10 The Exone Company Methods and Systems for Three-Dimensional Printing Utilizing a Jetted-Particle Binder Fluid
US20150232648A1 (en) * 2014-02-20 2015-08-20 Microjet Technology Co., Ltd. Three-dimensional prototyping composition
CN103819164A (en) * 2014-02-28 2014-05-28 广州丽格打印耗材有限公司 Powder for 3D printers and preparation method thereof
US11097471B2 (en) 2014-03-31 2021-08-24 Voxeljet Ag Method and device for 3D printing using temperature-controlled processing
US10913207B2 (en) 2014-05-26 2021-02-09 Voxeljet Ag 3D reverse printing method and device
US20150360288A1 (en) * 2014-06-13 2015-12-17 Zin Technologies, Inc. Optimized additive manufacturing process
US9643251B2 (en) * 2014-06-13 2017-05-09 Zin Technologies, Inc. Optimized additive manufacturing process
US9867449B2 (en) * 2014-06-20 2018-01-16 Richard Joseph LaHood, SR. System and method of manufacturing a three-dimensional cosmetic product
US20150366327A1 (en) * 2014-06-20 2015-12-24 Richard Joseph LaHood, SR. Cosmetics Applicator System and Method
US10946556B2 (en) 2014-08-02 2021-03-16 Voxeljet Ag Method and casting mold, in particular for use in cold casting methods
US20170246686A1 (en) * 2014-09-26 2017-08-31 Hewlett-Packard Development Company, L.P. Pastes for printing three-dimensional objects in additive manufacturing processes
US10682809B2 (en) 2014-12-22 2020-06-16 Voxeljet Ag Method and device for producing 3D moulded parts by means of a layer construction technique
US10683381B2 (en) 2014-12-23 2020-06-16 Bridgestone Americas Tire Operations, Llc Actinic radiation curable polymeric mixtures, cured polymeric mixtures and related processes
US11261279B2 (en) 2014-12-23 2022-03-01 Bridgestone Americas Tire Operations, Llc Actinic radiation curable polymeric mixtures, cured polymeric mixtures and related processes
US11926688B2 (en) 2014-12-23 2024-03-12 Bridgestone Americas Tire Operations, Llc Actinic radiation curable polymeric mixtures, cured polymeric mixtures and related processes
US10556380B2 (en) 2015-01-30 2020-02-11 Renaissance Of Technology Corporation Three-dimensional molding producing method, three-dimensional molding producing apparatus, three-dimensional molding, and molding material
US11077611B2 (en) 2015-03-17 2021-08-03 Voxeljet Ag Method and device for producing 3D shaped articles with a double recoater
US10843404B2 (en) 2015-05-20 2020-11-24 Voxeljet Ag Phenolic resin method
US10882110B2 (en) 2015-09-09 2021-01-05 Voxeljet Ag Method and device for applying fluids
US11890810B2 (en) 2015-09-16 2024-02-06 Voxeljet Ag Device and method for producing three-dimensional shaped parts
WO2017062031A1 (en) * 2015-10-09 2017-04-13 Hewlett-Packard Development Company, L.P. Particulate mixtures
CN108473714A (en) * 2015-10-09 2018-08-31 惠普发展公司,有限责任合伙企业 Particle mixture
US10428248B1 (en) * 2015-10-12 2019-10-01 Wolf & Associates, Inc. Compositions, materials, and methods for enhancing 3D printer platform adhesion and/or reducing warpage in printed parts
US11008437B2 (en) 2015-11-13 2021-05-18 Ricoh Company, Ltd. Material set for forming three-dimensional object, three-dimensional object producing method, and three-dimensional object producing apparatus
WO2017086995A1 (en) * 2015-11-20 2017-05-26 Hewlett-Packard Development Company, L.P. Three-dimensional (3d) printing
US10759085B2 (en) 2015-11-20 2020-09-01 Hewlett-Packard Development Company, L.P. Three-dimensional (3D) printing
US11235518B2 (en) 2015-12-01 2022-02-01 Voxeljet Ag Method and device for producing three-dimensional components with the aid of an overfeed sensor
US11097531B2 (en) 2015-12-17 2021-08-24 Bridgestone Americas Tire Operations, Llc Additive manufacturing cartridges and processes for producing cured polymeric products by additive manufacturing
US10737323B2 (en) 2016-08-03 2020-08-11 3Deo, Inc. Devices and methods for three-dimensional printing
US9987682B2 (en) 2016-08-03 2018-06-05 3Deo, Inc. Devices and methods for three-dimensional printing
US10792731B2 (en) 2016-08-03 2020-10-06 3Deo, Inc. Devices and methods for three-dimensional printing
US11453161B2 (en) 2016-10-27 2022-09-27 Bridgestone Americas Tire Operations, Llc Processes for producing cured polymeric products by additive manufacturing
US11273605B2 (en) 2016-11-15 2022-03-15 Voxeljet Ag Integrated print head maintenance station for powder bed-based 3D printing
US11760023B2 (en) 2016-11-15 2023-09-19 Voxeljet Ag Print head parking or maintenance unit for powder bed-based 3D printing, 3D printing systems and methods thereof
US10753211B2 (en) 2016-12-12 2020-08-25 General Electric Company Heterogeneous composition, article comprising heterogeneous composition, and method for forming article
US11583920B2 (en) 2017-02-24 2023-02-21 Hewlett-Packard Development Company, L.P. Three-dimensional printing
US11389867B2 (en) 2017-02-24 2022-07-19 Hewlett-Packard Development Company, L.P. Three-dimensional (3D) printing
US11511338B2 (en) 2017-02-24 2022-11-29 Hewlett-Packard Development Company, L.P. Three-dimensional printing
US11577316B2 (en) * 2017-02-24 2023-02-14 Hewlett-Packard Development Company, L.P. Three-dimensional printing
US11766826B2 (en) 2017-04-05 2023-09-26 Hewlett-Packard Development Company, L.P. Reducing stresses in metal layers
WO2018186845A1 (en) * 2017-04-05 2018-10-11 Hewlett-Packard Development Company, L.P. Reducing stresses in metal layers
CN111050953A (en) * 2017-07-06 2020-04-21 惠普发展公司,有限责任合伙企业 Three-dimensional (3D) printing
US11872747B2 (en) * 2017-07-06 2024-01-16 Hewlett-Packard Development Company, L.P. Three-dimensional (3D) printing
US11731361B2 (en) 2017-07-21 2023-08-22 Voxeljet Ag Process and apparatus for producing 3D moldings comprising a spectrum converter
US11279087B2 (en) 2017-07-21 2022-03-22 Voxeljet Ag Process and apparatus for producing 3D moldings comprising a spectrum converter
US11633908B2 (en) * 2018-03-02 2023-04-25 Formlabs, Inc. Latent cure resins and related methods
US11407180B2 (en) 2018-05-04 2022-08-09 Desktop Metal, Inc. Support edifice for three-dimensional printing
US11826958B2 (en) 2019-02-05 2023-11-28 Voxeljet Ag Exchangeable process unit
US11820076B2 (en) 2019-11-01 2023-11-21 Voxeljet Ag 3D printing process and molding produced by this process using lignosulfate
US11504879B2 (en) 2020-04-17 2022-11-22 Beehive Industries, LLC Powder spreading apparatus and system
WO2023002127A1 (en) * 2021-07-22 2023-01-26 Universite De Bretagne Sud Material based on natural colloids and wax of natural origin with liquid-solid phase change

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