US20040043214A1 - Method of forming a 3-dimensional fiber and a web formed from such fibers - Google Patents
Method of forming a 3-dimensional fiber and a web formed from such fibers Download PDFInfo
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- US20040043214A1 US20040043214A1 US10/232,059 US23205902A US2004043214A1 US 20040043214 A1 US20040043214 A1 US 20040043214A1 US 23205902 A US23205902 A US 23205902A US 2004043214 A1 US2004043214 A1 US 2004043214A1
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- fibers
- component
- web
- coiled
- stretched
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4391—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece characterised by the shape of the fibres
- D04H1/43912—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece characterised by the shape of the fibres fibres with noncircular cross-sections
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/28—Formation of filaments, threads, or the like while mixing different spinning solutions or melts during the spinning operation; Spinnerette packs therefor
- D01D5/30—Conjugate filaments; Spinnerette packs therefor
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/06—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyolefin as constituent
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/12—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyamide as constituent
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/14—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyester as constituent
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/16—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one other macromolecular compound obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds as constituent
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- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G1/00—Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics
- D02G1/18—Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics by combining fibres, filaments, or yarns, having different shrinkage characteristics
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4282—Addition polymers
- D04H1/4291—Olefin series
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
- D04H1/43825—Composite fibres
- D04H1/43828—Composite fibres sheath-core
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
- D04H1/43825—Composite fibres
- D04H1/43832—Composite fibres side-by-side
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
- D04H1/43835—Mixed fibres, e.g. at least two chemically different fibres or fibre blends
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
- D04H1/43838—Ultrafine fibres, e.g. microfibres
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4391—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece characterised by the shape of the fibres
- D04H1/43918—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece characterised by the shape of the fibres nonlinear fibres, e.g. crimped or coiled fibres
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2922—Nonlinear [e.g., crimped, coiled, etc.]
- Y10T428/2924—Composite
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2929—Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2929—Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
- Y10T428/2931—Fibers or filaments nonconcentric [e.g., side-by-side or eccentric, etc.]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
- Y10T442/638—Side-by-side multicomponent strand or fiber material
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
- Y10T442/641—Sheath-core multicomponent strand or fiber material
Definitions
- nonwoven webs There are numerous methods known to those skilled in the art for spinning fibers that can be later formed into a nonwoven web. Many such nonwoven webs are useful in disposable absorbent articles for absorbing body fluids and/or excrement, such as urine, fecal matter, menses, blood, perspiration, etc. Three dimensional fibers are also useful for machine direction and cross direction stretchable spunbond materials that can be made into bodyside covers, facings and liners. Manufacturers of such articles are always looking for new materials and ways to construct or use such new materials in their articles to make them more functional for the application they are designed to accomplish.
- a web of 3-dimensional, bicomponent fibers wherein the fibers are formed from at least one elastomeric material that can extend in at least one direction can be very beneficial.
- an infant diaper containing an absorbent layer formed from cellulose pulp fibers interspersed into a web of 3-dimensional nonwoven fibers will allow the absorbent layer to retain a larger quantity of body fluid if the 3-dimensional fibers can expand.
- Such an absorbent layer can provide better leakage protection for the wearer and may not have to be changed as often.
- a spunbond nonwoven facing or liner formed from a plurality of 3-dimensional fibers can provide improved stretch and controllable retraction. Such facings or liners can provide improved fit and better comfort for the wearer of absorbent articles.
- a web formed from such 3-dimensional fibers can provide one or more of the following attributes: improved fit, improved loft, better comfort, greater void volume, softer feel, improved resiliency, better stretch, controlled retraction and improved absorbency.
- this invention relates to a method of forming 3-dimensional fibers along with a web formed from such fibers.
- the method includes the steps of co-extruding a first component and a second component.
- the first component has a recovery percentage R 1 and the second component has a recovery percentage R 2 , wherein R 1 is higher than R 2
- the first and second components are directed through a spin pack to form a plurality of continuous molten fibers.
- the plurality of molten fibers is then routed through a quenching chamber to form a plurality of continuous cooled fibers.
- the plurality of cooled fibers is then routed through a drawing unit to form a plurality of continuous, solid linear fibers.
- the plurality of the solid fibers is then accumulated on a spool that can be at a later time unwound and stretched by at least about 50 percent.
- the plurality of stretched fibers are then cut and allowed to relax such that a plurality of 3-dimensional, coiled fibers is formed.
- FIG. 1 is a schematic showing the equipment needed to extrude, spin, quench and draw continuous solid fibers and accumulate them on a spool.
- FIG. 2 is a cross-section of a bicomponent fiber.
- FIG. 3 is a schematic showing unwinding a plurality of solid linear fibers, stretching the fibers, cutting the fibers and then allowing the fibers to relax to form a plurality of 3-dimensional, staple fibers.
- FIG. 4 is a side view of a helical fiber formed when the stretched fiber is cut into a staple fiber and the fiber is allowed to relax.
- FIG. 1 a schematic of the equipment needed to extrude, spin, quench and draw a plurality of continuous solid fibers and accumulate them on a plurality of spools is depicted.
- the method includes the steps of co-extruding a first component 10 and a second component 12 .
- the first and second components, 10 and 12 respectively, can be in the form of solid resin pellets or small particles.
- the first component 10 is positioned in a hopper 14 from which it can be metered and routed through a conduit 16 to a first extruder 18 .
- the second component 12 is positioned in a hopper 20 from which it can be metered and routed through a conduit 22 to a second extruder 24 .
- the first component 10 is a material that can be spun or otherwise formed into a continuous fiber. When the first component 10 is formed into a fiber, the fiber must be capable of being stretched and has a high recovery percentage R 1 .
- the “recovery percentage R 1 ” is defined as the percent the first component 10 can recover after it has been stretched at least about 50% of its initial length and upon removal of the force applied to stretch it.
- the first component 10 is an elastomeric material.
- Suitable elastomeric materials that can be used for the first component 10 include a melt extrudable thermoplastic elastomer such as a polyurethane elastomer, a copolyether ester, a polyether block polyamide copolymer, an ethylene vinyl acetate (EVA) elastomer, a styrenic block copolymer, an ether amide block copolymer, an olefinic elastomer, as well as other elastomers known to those skilled in the polymer art.
- a melt extrudable thermoplastic elastomer such as a polyurethane elastomer, a copolyether ester, a polyether block polyamide copolymer, an ethylene vinyl acetate (EVA) elastomer, a styrenic block copolymer, an ether amide block copolymer, an olefinic elastomer, as well as other elastomers
- MORTHANE® is a registered trademark of Huntsman Polyurethanes having an office in Chicago, Ill. 60606.
- ESTANE® is a registered trademark of Noveon, Inc. having an office in Cleveland, Ohio 44141.
- PEARLTHANE® a registered trademark of Merquinsa having an office in Boxford, Mass. 01921.
- Three additional elastomeric materials include a polyether block polyamide copolymer which is commercially available in various grades under the trade designation PEBAX®.
- PEBAX® is a registered trademark of Atofina Chemicals, Inc. having an office in Birdsboro, Pa. 19508.
- a second elastomeric material is a copolyether-ester sold under the trade designation ARNITEL®.
- ARNITEL® is a registered trademark of DSM having an office at Het Overloon 1, NL-6411 TE Heerlen, Netherlands.
- the third elastomeric material is a copolyether-ester sold under the trade designation HYTREL®.
- HYTREL® is a registered trademark of E. I. DuPont de Nemours having an office in Wilmington, Del. 19898.
- the first component 10 can also be formed from a styrenic block copolymer such as KRATON®.
- KRATON® is a registered trademark of Kraton Polymers having an office in Houston, Tex.
- the first component 10 can further be formed from a biodegradable elastomeric material such as polyester aliphatic polyurethanes or polyhydroxyalkanoates.
- the first component 10 can be formed from an olefinic elastomeric material, such as elastomers and plastomers.
- a plastomer is an ethylene-based resin or polymer sold under the trade designation AFFINITY®.
- AFFINITY® is a registered trademark of Dow Chemical Company having an office in Freeport, Tex.
- AFFINITY® resin is an elastomeric copolymer of ethylene and octene produced using Dow Chemical Company's INSITETM constrained geometry catalyst technology.
- EXACT® Another plastomer is sold under the trade designation EXACT® which includes single site catalyzed derived copolymers and terpolymers.
- EXACT® is a registered trademark of Exxon Mobil Corporation having an office at 5959 Las Colinas Boulevard, Irving, Tex. 75039-2298.
- Other suitable olefinic elastomers that can be used to form the first component 10 include polypropylene-derived elastomers.
- the first component 10 can further be formed from a non-elastomeric thermoplastic material which has a sufficient recovery percentage R 1 after it has been stretched at a specified temperature.
- Non-elastomeric materials useful in forming the first component 10 are extrudable thermoplastic polymers such as polyamides, nylons, polyesters, polyolefins or blends of polyolefins.
- non-elastomeric, biodegradable polylactic acid can provide a sufficient recovery percentage R 1 when stretched above its glass transition temperature of about 62° C.
- the second component 12 is a material that can be spun or otherwise formed into a continuous fiber.
- the linear fiber When the second component 12 is formed into a linear fiber, the linear fiber must be capable of being stretched and has a recovery percentage R 2 , wherein R 1 is higher than R 2
- the “recovery percentage R 2 ” is defined as the percent the component can recover after it has been stretched at least 50% of its initial length and upon removal of the force applied to stretch it.
- the first and second components, 10 and 12 respectively are formed into a linear fiber, the fiber must be capable of retracting or contracting from a stretched condition in order for the linear fiber to be useful in an absorbent article.
- the term “retracting” means the same thing as “contracting”.
- the ratio of R 1 /R 2 ranges from at least about 2 to about 100. Most desirably, the ratio of R 1 /R 2 ranges from at least about 2 to about 50.
- the reason for making R 1 greater than R 2 in a linear fiber is that upon retraction or contraction of the first and second components, 10 and 12 respectively, the 3-dimensional fiber will exhibit a very desirable, predetermined structural configuration. This structural configuration of the 3-dimensional fiber will display exceptional elongation properties in at least one direction.
- the linear fiber further obtains some of its unique properties when the first component 10 makes up a volume percent of from about 30% to about 95% of the linear fiber and the second component 12 makes up a volume percent of from about 5% to about 70% of the linear fiber.
- the first component 10 makes up a volume percent from about 40% to about 80% of the linear fiber and the second component 12 makes up a volume percent of from about 20% to about 60% of the linear fiber.
- the volume of a solid linear fiber is calculated using the following formula:
- V is the volume of the solid linear fiber
- ⁇ is a transcendental number, approximately 3.14159, representing the ratio of the circumference to the diameter of a circle and appearing as a constant in a wide range of mathematical problems;
- d is the diameter of the linear fiber
- L 1 is the initial length of the linear fiber.
- volume percents for the first component 10 and for the second component 12 allow the linear fiber to be stretched at least 50% to form a stretched linear fiber.
- the volume percent of each of the first and second components, 10 and 12 respectively also plays a vital role in the retraction or contraction of the stretched fiber to a retracted length.
- volume percent of each of the first and second components, 10 and 12 respectively one can manufacture a linear fiber that can be stretched and then retracted to a predetermined configuration and with certain desirable characteristics.
- the contact with a body fluid will cause the absorbent article to swell which will allow the fibers to elongate in at least one direction before the fiber becomes linear.
- the fibers elongate they can extend and allow the absorbent structure to receive and store additional body fluids.
- the first and second components, 10 and 12 respectively are chemically, mechanically and/or physically adhered or joined to one another to prevent the fiber from splitting when the fiber is stretched and then allowed to relax.
- the relaxed fiber will retract in length.
- the first component 10 will be strongly adhered to the second component 12 .
- the mechanical adhesion between the first and second components, 10 and 12 respectively will compliment any chemical and/or physical adhesion that is present and aid in preventing splitting or separation of the first component 10 from the second component 12 .
- This splitting or separation occurs because one component is capable of retracting to a greater extent than the other component. If a strong mutual adhesion is not present, especially during retraction, the two components can split apart and this is not desirable.
- a strong chemical and/or physical adhesion will prevent the first component 10 from splitting or separating from the second component 12 .
- the second component 12 can be formed from polyolefins, such as polyethylene or polypropylene, a polyester or a polyether.
- the second component 12 can also be a polyolefin resin, such as a fiber grade polyethylene resin sold under the trade designation ASPUN® 6811A.
- ASPUN® is a registered trademark of Dow Chemical Company having an office in Midland, Mich. 48674.
- the second component 12 can also be a polyolefin resin, such as a homopolymer polypropylene such as Himont PF 304, and PF 308, available from Basell North America, Inc. having an office at Three Little Falls Centre, 2801 ° C. enterville Road, Wilmington, Del. 19808.
- polystyrene resin from which the second component 12 can be formed is polypropylene PP 3445 available from Exxon Mobil Corporation having an office at 5959 Las Colinas Boulevard, Irving, Tex. 75039-2298.
- suitable polyolefinic materials that can be used for the second component 12 include random copolymers, such as a random copolymer containing propylene and ethylene.
- One such random copolymer is sold under the trade designation Exxon 9355, available from Exxon Mobil Corporation having an office at 5959 Las Colinas Boulevard, Irving, Tex. 75039-2298.
- the second component 12 can also be formed from a melt extrudable thermoplastic material that provides sufficient permanent deformation upon stretching. Such materials include, but are not limited to, aliphatic and aromatic polyesters, copolyesters, polyethers, polyolefins such as polypropylene or polyethylene, blends or copolymers thereof, polyamides and nylons.
- the second component 12 can further be formed from biodegradable resins, such as aliphatic polyesters.
- One such aliphatic polyester is polylactic acid (PLA).
- Other biodegradable resins include polycaprolactone, polybutylene succinate adipate and polybutylene succinate.
- Polybutylene succinate adipate and polybutylene succinate resins are sold under the trade designation BIONOLLE® which is a registered trademark of Showa High Polymers having a sales office in New York, N. Y. 1017.
- Additional biodegradable resins include copolyester resin sold under the trade designation EASTAR BIO®.
- EASTAR BIO® is a registered trademark of Eastman Chemical Company having an office in Kingsport, Tenn. 37662.
- Still other biodegradable resins that can be used for the second component 12 include polyhydroxyalkanoates (PHA) of varying composition and structure, and copolymers, blends and mixtures of the foregoing polymers.
- PHA polyhydroxyalkanoates
- suitable biodegradable polymer resins include BIONOLLE® 1003, 1020, 3020 and 3001 resins commercially available from Itochu International.
- BIONOLLE® is a registered trademark of Showa High Polymers having an office in New York, N. Y. 10017.
- the second component 12 can also be formed from a water-soluble and swellable resin.
- water-soluble and swellable resins include polyethylene oxide (PEO) and polyvinyl alcohol (PVOH). Grafted polyethylene oxide (gPEO) or chemically modified PEO can also be used.
- the water-soluble polymer can be blended with a biodegradable polymer to provide for better processing, performance, and interactions with liquids.
- the PEO resin can be chemically modified by reactive extrusion, grafting, block polymerization or branching to improve its processability.
- the PEO resin can be modified by reactive extrusion or grafting as described in U. S. Pat. No. 6,172,177 issued to Wang et al. on Jan. 9, 2001.
- the second component 12 has a lower recovery percentage R 2 than the first component 10 .
- the second component 12 can be formed from a material that exhibits a low elastic recovery. Materials from which the second component 12 can be formed include, but are not limited to polyolefin resins, polypropylene, polyethylene, polyethylene oxide (PEO), polyvinyl alcohol (PVOH), polyester and polyether.
- the second component 12 can be treated or modified with hydrophilic or hydrophobic surfactants. Treatment of the second component 12 with a hydrophilic surfactant will form a wettable surface for increasing interaction with a body fluid or liquid.
- the surface of the second component 12 when the surface of the second component 12 is treated to be hydrophilic, it will become more wettable when contacted by a body fluid, especially urine. Treatment of the second component 12 with a hydrophobic surfactant will cause it to repel a body fluid or liquid. Similar treatment of the first component 10 can also be done to control its hydrophilic or hydrophobic characteristics.
- the first and second components, 10 and 12 respectively, are separately co-extruded in the two extruders 18 and 24 .
- the extruders 18 and 24 function in a manner well known to those skilled in the art.
- the solid resin pellets or small particles are heated up above their melting temperature and advanced along a path by a rotating auger.
- the first component 10 is routed through a conduit 26 while the second component 12 is simultaneously routed through a conduit 28 and both flow streams are directed into a spin pack 30 .
- a melt pump, not shown, can be positioned across one or both of the conduits 26 and 28 to regulate volumetric distribution, if needed.
- the spin pack 30 is a device for making synthetic fibers.
- the spin pack 30 includes a bottom plate having a plurality of holes or openings through which the extruded material flows.
- the number of openings per square inch in the spin pack 30 can range from about 5 to about 500 openings per square inch. Desirably, the number of openings per square inch in the spin pack 30 is from about 25 to about 250. More desirably, the number of openings per square inch in the spin pack 30 is from about 125 to about 225.
- the size of each of the openings in the spin pack 30 can vary. A typical size opening can range from about 0.1 millimeter (mm) to about 2.0 mm in diameter. Desirably, the size of each of the openings in the spin pack 30 can range from about 0.3 mm to about 1.0 mm in diameter.
- the openings in the spin pack 30 do not have to be round or circular in cross-section but can have a bilobal, trilobal, square, triangular, rectangular, oval or any other geometrical cross-sectional configuration that is desired.
- the first and second components, 10 and 12 respectively, are directed into the spin pack 30 and are routed through the openings formed in the bottom plate in such a fashion that the first component 10 will form a core 32 while the second component 12 will form a sheath 34 which surrounds the outside circumference of the core 32 .
- the first component 10 could form the sheath while the second component 12 could form the core, if desired.
- This core/sheath arrangement produces one configuration of a linear, bicomponent fiber 36 .
- Bicomponent fibers having other cross-sectional configurations can also be produced using the spin pack 30 .
- the bicomponent fiber can have a side by side configuration or a core/sheath design where the core is offset coaxially from the sheath.
- One bicomponent fiber 36 will be formed for each opening formed in the plate within the spin pack 30 . This enables a plurality of continuous molten fibers 36 , each having a predetermined diameter, to simultaneously exit the spin pack 30 at a first speed. Each linear, bicomponent fiber 36 will be spaced apart and be separated from the adjacent fibers 36 . The diameter of each bicomponent fiber 36 will be dictated by the size of the openings formed in the bottom plate of the spin pack 30 . For example, as stated above, if the diameter of the holes or openings in the bottom plate range from about 0.1 mm to about 2.0 mm, then each of the molten fibers 36 can have a diameter which ranges from about 0.1 mm to about 2.0 mm. There is a tendency for the molten fibers 36 to sometimes swell in cross-sectional area once they exit the opening formed in the plate but this expansion is relatively small.
- the plurality of continuous molten fibers 36 are routed through a quench chamber 38 to form a plurality of cooled linear, bicomponent fibers 40 .
- the molten fibers 36 are directed downward from the spin pack 30 into the quench chamber 38 .
- the reason for directing the molten fibers 36 downward is that gravity can be used to assist in moving the molten fibers 36 .
- the vertical downward movement can aid in keeping the fibers 36 separated from one another.
- the continuous molten fibers 36 are contacted by one or more streams of air.
- the temperature of the continuous molten fibers 36 exiting the spin pack 30 and entering the quench chamber 38 will be in the range of from about 150° C. to about 250° C.
- the actual temperature of the molten fibers 36 will depend upon the material from which they are constructed, the melting temperature of such material, the amount of heat applied during the extrusion process, as well as other factors.
- the continuous molten fibers 36 are contacted and surrounded by lower temperature air. The temperature of the air can range from about 0° C. to about 120° C.
- the air is cooled or chilled so as to quickly cool the molten fibers 36 .
- the air is cooled or chilled to a temperature of from about 0° C. to about 400° C. More desirably, the air is cooled or chilled to a temperature of from about 15° C. to about 300° C.
- the lower temperature air can be directed toward the molten fibers 36 at various angles but a horizontal or downward angle seems to work best.
- the velocity of the incoming air can be maintained or adjusted so as to efficiently cool the molten fibers 36 .
- the cooled or chilled air will cause the continuous molten fibers 36 to crystallize, assume a crystalline structure or phase separate and form a plurality of continuous cooled fibers 40 .
- the cooled fibers 40 are still linear in configuration at this time.
- the temperature of the cooled fibers 40 can range from about 15° C. to about 100° C. Desirably, the temperature of the cooled fibers 40 will range from about 20° C. to about 80° C. Most desirably, the temperature of the cooled fibers 40 will range from about 25° C. to about 60° C.
- the cooled fibers 40 will be at a temperature below the melting temperature of the first and second components, 10 and 12 respectively, from which the fibers 40 were formed.
- the cooled fibers 40 may have a soft plastic consistency at this stage.
- the plurality of continuous cooled fibers 40 are then routed to a draw unit 42 .
- the draw unit 42 can be vertically located below the quenching chamber 38 so as to take advantage of gravity.
- the draw unit 42 can be a rotating roll around which all of the cooled fibers 40 are funneled down into a rope or tow and are drawn by being wrapped at least once around the outer periphery of the rotating roll.
- the plurality of cooled fibers 40 can be wrapped one or more times around the outer periphery of the rotating roll. Desirably, the plurality of cooled fibers 40 can be wrapped 11 ⁇ 2 times around the outer periphery of the rotating roll wherein the fibers 40 accumulate into a rope or tow of solid fibers 44 .
- Mechanical drawing involves subjecting the cooled fibers 40 to a mechanical force that will pull or draw the molten material exiting the spin pack 30 .
- the cooled fibers 40 are drawn down mainly from the molten state and not from the cooled state.
- the downward force in the draw unit 42 will cause the molten material to be lengthened and elongated into solid fibers 44 .
- Lengthening of the molten material will usually shape, narrow, distort, or otherwise change the cross-sectional area of the solid fibers 44 . For example, if the molten material has a round or circular cross-sectional area upon exiting the spin pack 30 , the outside diameter of the solid fibers 44 will be reduced.
- the amount that the diameter of the solid linear fibers 44 are reduced will depend upon several factors, including the amount the molten material is drawn, the distance over which the fibers are drawn, the mechanical force used to draw the fibers, the spin line tension, etc. Desirably, the diameter of the solid linear fibers 44 will range from about 5 microns to about 10 microns. More desirably, the diameter of the solid linear fibers 44 will l range from about 10 microns to about 50 microns. Most desirably, the diameter of the solid linear fibers 44 will range from about 10 microns to about 30 microns.
- the draw unit 42 will pull the cooled fibers 40 at a second speed that is faster than the first speed displayed by the continuous molten fibers 36 exiting the spin pack 30 .
- This change in speed between the continuous molten fibers 36 and the continuous cooled fibers 40 enables the molten material to be lengthened and also to be reduced in cross-sectional area.
- the cooled fibers 40 Upon exiting the draw unit 42 , the cooled fibers 40 will be solid fibers 44 .
- the plurality of solid fibers 44 exiting the draw unit 42 are then routed in mass around a guide roll 45 to a spool 46 .
- the advancing fibers 44 are circumferentially wound onto the periphery of the spool 46 in the form of a rope.
- the spool 46 can be mounted in a support 48 and can be made to rotate as the advancing fiber 44 is directed onto the spool 46 .
- the spool 46 can be sized and shaped to accumulate a predetermined amount of solid fibers 44 .
- the solid linear fibers 44 will l be accumulated on the spool 46 until the spool 46 is filled. At this time the plurality of solid fibers 44 are cut or severed in mass by a cutter 50 .
- the advancing solid fibers 44 can then be directed onto another empty spool 46 that can be held in the support 48 .
- the process of removing a filled spool 46 and replacing it with an empty spool 46 , onto which the advancing fibers 44 can be accumulated, is well known to those skilled in the art. This process can be automated so that the advancing linear fibers 44 can be instantaneously and sequentially directed to the next available empty spool 46 .
- Each of the filled spools 46 can be stacked and stored for use at a later time at the same facility or they can be transported to another location.
- One feature of this invention is that the solid linear fibers 44 do not have to be processed into crimped staple fibers nor formed into a web in one continuous process. Instead, the method allows for an interruption, such that the solid linear fibers 44 can be further processed at a later time and at a remote location, if desired. Alternatively, a continuous method could be employed wherein the spools 46 would not need to be present.
- FIG. 3 a schematic is depicted showing the unwinding of a plurality of linear fibers, stretching the fibers, cutting the fibers and then allowing the fibers to relax to form a plurality of 3-dimensional, staple fibers.
- the method allows for the plurality of linear fibers 44 that were circumferentially wound onto the outer periphery of the spool 46 to be unwound and directed to a heater 52 .
- the heater 52 is optional, but when present, will heat the plurality of linear fibers 44 to an elevated temperature. The exact temperature will depend upon the composition of the first and second components, 10 and 12 respectively, the diameter of the fibers 44 , the amount the fibers 44 are to be stretched, the speed of the fibers 44 , etc.
- a surface treatment to the plurality of linear fibers 44 , if desired.
- the application of a surface treatment either by spraying a chemical composition onto the fibers 44 or emersion of the fibers 44 in a liquid bath is well known to those skilled in the art.
- Various types of surface treatments can be applied to the fibers 44 .
- the plurality of solid linear fibers 44 are then routed to a stretching unit 54 where the plurality of linear fibers 44 is stretched by at least about 50%.
- stretched it is meant that the continuous solid, linear fibers 44 are lengthened or elongated while in a solid state. The stretching is caused by axial tension exerted on the plurality of linear fibers 44 . As the linear fibers 44 are stretched, the cross-sectional area of the linear fibers 44 will l be reduced.
- the amount of stretch imparted into the solid fibers 44 can range from about 75% to about 1,000%. More desirably, the amount of stretch imparted into the solid fibers, 44 can range from about 100% to about 500%. Most desirably, amount of stretch imparted into the solid fibers 44 can range from about 150% to about 300%.
- the stretching unit 54 is shown as including two pairs of spaced apart rolls. It should be noted that other forms of mechanical stretching apparatus can be utilized.
- the first pair of rolls includes a first roll 56 and a second roll 58 .
- the first and second rolls, 56 and 58 respectively, can be arranged in close contact with one another so as to form a nip 60 therebetween.
- the plurality of linear fibers 44 unwound from the spool 46 , is routed around a portion of the periphery of the first roll 56 , through the nip 60 and around a portion of the periphery of the second roll 58 .
- the nip 60 can be adjusted such that little or no pressure is exerted on the fibers 44 .
- At least one of the first and second rolls, 56 and 58 respectively, is a driven roll which is set to rotate at a first predetermined surface speed.
- This surface speed caused the plurality of linear fibers 44 to be advanced at this speed.
- the surface speed can vary depending upon one's unique requirements. However, a surface speed of between about 10 meters per minute (m/min) to about 1,000 m/min will be sufficient for most applications. Desirably, the surface speed will be equal to or less than about 500 m/min. A faster surface speed is usually more desirable than a slower surface speed in order to reduce the cost of manufacture. However, at very high speeds, the fibers can lose their stretchability and become brittle. This can cause the fibers to break before they reach the desired percent of elongation.
- the second pair of rolls includes a first roll 62 and a second roll 64 .
- the first and second rolls, 62 and 64 respectively, can be arranged in close contact with one another so as to form a nip 66 therebetween.
- the plurality of linear fibers 44 exiting the first pair of rolls is routed around a portion of the periphery of the first roll 62 , through the nip 66 and around a portion of the periphery of the second roll 64 .
- the nip 66 can be adjusted such that little or no pressure is exerted on the fibers 44 .
- At least one of the first and second rolls, 62 and 64 respectively, is a driven roll which is set to rotate at a second predetermined surface speed.
- the second predetermined speed is faster than the first predetermined speed. This difference in speed caused the plurality of fibers 44 to be stretched lengthwise between the two pair of rolls to form a plurality of stretched linear fibers 68 .
- a heater 70 positioned between the two pair of rolls, 56 and 58 and 60 and 62 respectively, is a heater 70 .
- the heater 70 is capable of heating the plurality of linear fibers 44 to an elevated temperature. The exact temperature will depend upon the composition of the first and second components, 10 and 12 respectively, the diameter of the fibers 44 , the amount the fibers 44 are to be stretched, the speed of the fibers 44 , etc.
- the stretching of the plurality of fibers 44 within the stretching unit 54 will cause the cross-sectional area of each of the linear fibers 44 to be reduced by about 5% to about 90% of the cross-sectional area of the linear fibers 44 unwound from the spool 46 .
- the cross-sectional area of each of the linear fibers 44 is reduced by about 10% to about 60% of the cross-sectional area of the linear fibers 44 unwound from the spool 46 . More desirably, the cross-sectional area of each of the linear fibers 44 is reduced by about 20% to about 50% of the cross-sectional area of the linear fibers 44 unwound from the spool 46 .
- the stretched, continuous linear fibers 68 will be relatively small in diameter or cross-sectional area. Desirably, the diameter of the stretched linear fibers 68 will range from about 5 microns to about 50 microns. More desirably, the diameter of the stretched fibers 68 will range from about 5 microns to about 30 microns. Most desirably, the diameter of the stretched linear fibers 68 will range from about 10 microns to about 20 microns.
- stretched linear fibers 68 leaving the second pair of rolls 62 and 64 can be heat set, if desired, before being cut into staple fibers.
- the plurality of stretched linear fibers 68 are cut or severed by a rotary cutter 72 having at least one knife 74 secured thereto.
- the rotary cutter 72 cooperates with an anvil roll 76 and the cutter 72 and the anvil roll 76 are arranged so that the stretched linear fiber 68 passes therebetween.
- the rotary cutter 72 and the anvil roll 76 keep the stretched linear fiber 68 in tension until it has been cut by the knife 74 .
- other types of cutting mechanism can be utilized that are well known to those skilled in the cutting art. It is also possible to position a cutter downstream of a pair of cooperating rolls that maintain the stretched linear fiber 68 in tension.
- the rotary cutter 72 will cut the plurality of stretched fibers 68 into a plurality of staple fibers 78 , each having a predetermined length.
- the plurality of stretched fibers 68 can be cut to a staple length of from about 5 millimeters to about 500 millimeters. Desirably, the plurality of stretched fibers 68 can be cut to a staple length of from about 10 millimeters to about 50 millimeters. More desirably, the plurality of stretched fibers 68 can be cut to a staple length of from about 12 millimeters to about 25 millimeters.
- the plurality of cut staple fibers 78 will instanteously start to relax.
- the coiled fibers 80 have a shorter length than the cut stretched fiber 78 .
- the coiled fibers 80 have a length ranging from about 3 millimeters (mm) to about 50 mm. Desirably, the coiled fibers 80 have a length ranging from about 5 mm to about 25 mm. Most desirably, the coiled fibers 80 have a length ranging from about 5 mm to about 15 mm.
- 3-dimensional fiber is meant a fiber having an x, y and z component that is formed by virtue of coils and/or curves regularly or irregularly spaced and whose extremities in the x, y and z planes form a locus of points which define a volume greater than a linear fiber.
- the 3-dimensional, coiled fibers 80 have a generally helical configuration. The helical configuration can extend along the entire length L of each of the 3-dimensional fibers 80 or it can occur over a portion of the length of the 3-dimensional fibers 80 .
- the coiled configuration extends over at least half of the length of each of the 3-dimensional fibers 80 . More desirably, the coiled configuration extends from about 50% to about 90% of the length of each of the 3-dimensional fibers 80 . Most desirably, the coiled configuration extends from about 90% to about 100% of the length of each of the 3-dimensional fibers 80 . It should be noted that the coils can be formed in the clockwise or counterclockwise directions along at least a potion of the length of the 3-dimensional, staple fibers 80 . It should also be noted that the configuration of each coil can vary along the length of each of the 3-dimensional, staple fibers 80 .
- Each of the 3-dimensional, staple fibers 80 have coils that circumscribes 360 degrees.
- the helical coils can be continuous or non-continuous over either a portion of or over the entire length of the 3-dimensional, staple fiber 80 .
- the 3-dimensional, staple fibers 80 exhibit a continuous helical coil.
- the 3-dimensional, staple fiber 80 differs from a 2-dimensional fiber in that a 2-dimensional fiber has only two components, for example, an “x” and a “y” component; an “x” and a “z” component, or a “y” and a “z” component.
- the 3-dimensional, staple fiber 80 has three components, an “x” component, a “y” component and a “z” component.
- a crimped fiber is typically a fiber that has been pressed or pinched into small, regular folds or ridges.
- a crimped fiber usually has a bend along its length.
- the 3-dimensional, staple fiber 80 has a non-linear configuration when it forms a helical coil.
- the 3-dimensional, staple fiber 80 also has an amplitude “A” that is measured perpendicular to a portion of its length L
- the amplitude “A” of the 3-dimensional, staple fiber 80 can range from about 10 microns to about 5,000 microns. Desirably, the amplitude “A” of the 3-dimensional, staple fiber 80 ranges from about 30 microns to about 1,000 microns. Most desirably, the amplitude “A” of the 3-dimensional, staple fiber 80 ranges from about 50 microns to about 500 microns.
- the 3-dimensional, staple fiber 80 further has a frequency “F” measured at two locations separated by 360 degrees between adjacent helical coils.
- the frequency “F” is used to denote the number of coils or curls formed in each inch of the coiled fiber length.
- the frequency “F” can range from about 10 to about 1,000 coils per inch. Desirably, the frequency “F” can range from about 50 to about 500 coils per inch.
- the amplitude “A” and/or the frequency “F” can vary or remain constant along at least a portion of the length L, or over the entire length, of the 3-dimensional, staple fiber 80 . Desirably, the amplitude “A” and the frequency “F” will remain constant over a majority of the length L.
- the amplitude “A” of the 3-dimensional, staple fiber 80 and the frequency “F” of the helical coils forming the 3-dimensional, staple fiber 80 affect the overall reduction in the length of the 3-dimensional, staple fiber 80 from it's stretched condition.
- the first and second components, 10 and 12 respectively, are adhered together in the spin pack 30 to form a plurality of continuous bicomponent fibers.
- the adhesion of the first component 10 to the second component 12 can be chemical, mechanical and/or physical. This ability of the first and second components, 10 and 12 respectively, to adhere to one another will prevent splitting of the components 10 and 12 at a later time when one component retracts more than the other component.
- the first component 10 in the solid linear fiber 44 has an elongation of at least about 50% deformation.
- the first component 10 is able to recover at least about 20% of the stretch deformation imparted thereto, based on its length after deformation. Desirably, the first component 10 in the solid linear fiber 44 is able to recover at least about 50% of its stretch deformation.
- the recovery or relaxation power may not be sufficient to activate helical coiling of the 3-dimensional, staple fiber 80 .
- Repetitive helical coils in the retracted 3-dimensional, staple fiber 80 are most desirable.
- a higher elongation than at least about 50% for the first component 10 is desirable. For example, an elongation of at least about 100% is good, an elongation exceeding 300% is better, and an elongation exceeding 400% is even better.
- the second component 12 in the solid linear fiber 44 has a total deformation which includes a permanent unrecoverable deformation value and a recoverable deformation value.
- the permanent unrecoverable deformation value in a solid state as a result of stretching, plastic yielding and/or drawing, is at least about 40%.
- the recoverable deformation value is at least about 0.1%.
- a higher deformation than at least about 50% for the second component 12 is desirable.
- a deformation of at least about 100% is good and a deformation exceeding about 300% is even better.
- the plastic yielding and drawing results in thinning of the second component 12 . Stretching in a solid state means that the second component 12 is stretched below its melting temperature.
- the second component 12 will fail and break during the stretching process. Also, at low deformation, the second component 12 does not provide a sufficient level of permanent plastic yielding and thinning which is desired for the formation of the repetitive helical coils in the 3-dimensional, staple fibers 80 . Stretching should not occur at very low temperatures because the fibers may be brittle and could break. Likewise, the fibers should not be stretched very quickly because this might cause the fibers to break before reaching the desired percent of elongation.
- the percent elongation of the length of the 3-dimensional, coiled fiber 80 defined as the percent change in length by which the 3-dimensional, coiled fiber 80 can be stretched before becoming straight or linear.
- the percent elongation can be expressed by the following formula:
- % E is the percent elongation of the 3-dimensional, staple fiber 80 ;
- L is the retracted length of the 3-dimensional, staple fiber 80 ;
- L 1 is the final length of the 3-dimensional, staple fiber 80 once it is stretched into a straight or uncoiled configuration.
- the retracted 3-dimensional, staple fiber 80 has the ability to be subsequently elongated to at least 100% of its retracted length. Most desirably, the retracted 3-dimensional, staple fiber 80 can be subsequently elongated from about 150% to about 900% of its retracted length. Even more desirably, the retracted 3-dimensional, staple fiber 80 can be subsequently elongated from about 250% to about 500% of its retracted length. Still more desirably, the retracted 3-dimensional, staple fiber 80 can be subsequently elongated from about 300% to about 400% of its retracted length.
- the 3-dimensional, staple fiber 80 exhibits exceptional elongation properties in at least one direction before the fiber becomes linear. Elongation is defined as the percent length by which the 3-dimensional, staple fiber 80 can be stretched before it becomes straight or linear.
- the direction of the elongation property of the 3-dimensional, staple fiber 80 normally in the same direction as the linear fiber 44 was stretched. In other words, the direction that the retracted 3-dimensional, staple fiber 80 able to subsequently elongate will be opposite to the direction of its retraction. It is possible for the retracted 3-dimensional, staple fiber 80 to have elongation properties in two or more directions. For example, the retracted 3-dimensional, staple fiber 80 can subsequently be elongated in both the x and y directions.
- the 3-dimensional, staple fiber 80 able to acquire its helical profile by the difference in recovery percentage R 1 of the first component 10 compared to the recovery percentage R 2 of the second component 12 .
- the first component 10 since the first component 10 has a higher recovery percentage R 1 than the recovery percentage R 2 of the second component 12 , the first component 10 will want to retract to a greater degree than the second component 12 .
- both the first and second components, 10 and 12 respectively will retract or contract the same amount since they are physically, chemically or mechanically adhered or joined to one another.
- the amount of coiling obtained, as well as the shape and location of the coiling, can be controlled by the selection of materials that are used to construct the linear fiber 44 . These three variables: the amount of coiling, the shape, and the location of the coiling, can also be controlled by the volume of each component, as well as the amount the linear fiber 44 is stretched.
- the time and temperature conditions under which the solid fibers 44 are stretched and allowed to retract can also affect the finish profile of the retracted 3-dimensional, staple fiber 80 .
- the first component 10 has a higher recovery percentage R 1 than the recovery percentage R 2 of the second component 12 and therefore the material from which the first component 10 is formed tends to be more tacky and elastic. For this reason, the material with the higher recovery percentage R 1 is used to form the inner core while the material having a lower recovery percentage R 2 tends to be used to form the outer sheath.
- the first and second components, 10 and 12 respectively, try to retract from the stretched condition; the outer sheath will retract or contract less. This means that the first component 10 will not be able to retract fully to an amount that it could if it was by itself. This pent up force creates the twist or helical coil effect in the retracted 3-dimensional, staple fiber 80 .
- Table 1 shows the recovery percent of individual materials that have been stretched to varying percentages.
- the material forming each sample was cut out from a thin sheet of a particular thickness in the shape of a dogbone or dumbbell.
- the dogbone shaped sample had an initial length of 63 millimeters (mm) measured from a first enlarged end to a second enlarged end. In between the two oppositely aligned, enlarged ends was a narrow section having a length of 18 mm and a width of 3 mm.
- the material was then placed in a tensile tester and stretched at a rate of 5 inches per minute, in the machine direction of the material. This stretching caused the narrow section of the sample to elongate.
- the dogbone shaped sample had a narrow section I 1 located between its first and second enlarged ends.
- Each of the enlarged ends of the dog bone sample was secured in a tensile tester and a force was applied causing the material to be stretched, in the machine direction of the material, a predetermined amount at a specific temperature.
- the narrow section is stretched to a length I 2 .
- the length I 2 is greater than the initial length I 1 .
- the force exerted on the sample was then removed and the sample was allowed to retract such that the narrow section is shortened to a length I 3 .
- the retracted length I 3 is smaller than the stretched length I 2 but is greater than the initial length I 1 .
- the recovery percent (R %) of the different materials that can be used in forming the fiber can be calculated using the following formula:
- I 2 is the stretched length of the narrow section of the sample
- I 3 is the retracted length of the narrow section of the sample.
- the coiled fibers 80 can be mixed with other kinds of fibers, such as cellulose fibers, wood pulp fibers, other synthetic fibers, etc. and/or a superabsorbent to form a web.
- the web can be an airlaid web, an air formed web, a coform web, a wet laid wet, etc.
- the web can be used in various kinds of products. The web is especially useful when used in a disposable absorbent article, such as an infant diaper, a training pant, an incontinent garment including a pad, brief, pant and refastenable pant, a sanitary napkin or tampon, a wet wipe product, etc.
- the method of admixing such fibers and/or superabsorbent particles is known to those skilled in the art.
- the percentage of each kind of fiber used to form the web can vary to meet one's particular needs.
- superabsorbent material preferably in the form of particles, can be mixed with one or more kinds of fibers to form an absorbent web.
- the web can also be stabilized and/or bonded using various methods known to those skilled in the art.
- a recognized limitation of stabilized and bonded absorbent webs is that the superabsorbent material present in the web is constrained from swelling to its full capacity.
- the use of the 3-dimensional fibers of this invention will allow an absorbent web structure containing superabsorbent material to expand and accommodate the entire extent the superabsorbent material can swell.
- the coiled fibers 80 can be laminated to a stretchable material, an elastic film or elastic fibers to form a thin, absorbent or non-absorbent material.
- This laminate material can be used as the bodyside cover or facing layer on a disposable absorbent article such as a diaper, training pant, incontinence garment, sanitary napkin, etc.
- This laminate material can also be used in health care products such as wound dressings, surgical gowns, gloves, etc.
Abstract
Description
- There are numerous methods known to those skilled in the art for spinning fibers that can be later formed into a nonwoven web. Many such nonwoven webs are useful in disposable absorbent articles for absorbing body fluids and/or excrement, such as urine, fecal matter, menses, blood, perspiration, etc. Three dimensional fibers are also useful for machine direction and cross direction stretchable spunbond materials that can be made into bodyside covers, facings and liners. Manufacturers of such articles are always looking for new materials and ways to construct or use such new materials in their articles to make them more functional for the application they are designed to accomplish. The creation of a web of 3-dimensional, bicomponent fibers wherein the fibers are formed from at least one elastomeric material that can extend in at least one direction can be very beneficial. For example, an infant diaper containing an absorbent layer formed from cellulose pulp fibers interspersed into a web of 3-dimensional nonwoven fibers will allow the absorbent layer to retain a larger quantity of body fluid if the 3-dimensional fibers can expand. Such an absorbent layer can provide better leakage protection for the wearer and may not have to be changed as often. In another example, a spunbond nonwoven facing or liner formed from a plurality of 3-dimensional fibers can provide improved stretch and controllable retraction. Such facings or liners can provide improved fit and better comfort for the wearer of absorbent articles.
- A web formed from such 3-dimensional fibers can provide one or more of the following attributes: improved fit, improved loft, better comfort, greater void volume, softer feel, improved resiliency, better stretch, controlled retraction and improved absorbency.
- The exact method utilized in forming a nonwoven web can create unique properties and characteristics in the web which can not be duplicated in another manner. Now, a new method of forming a 3-dimensional fiber has been invented which allows the fibers to be later formed into a web that can exhibit very desirable properties which are useful when the web is incorporated into a disposable absorbent article.
- Briefly, this invention relates to a method of forming 3-dimensional fibers along with a web formed from such fibers. The method includes the steps of co-extruding a first component and a second component. The first component has a recovery percentage R1 and the second component has a recovery percentage R2, wherein R1 is higher than R2 The first and second components are directed through a spin pack to form a plurality of continuous molten fibers. The plurality of molten fibers is then routed through a quenching chamber to form a plurality of continuous cooled fibers. The plurality of cooled fibers is then routed through a drawing unit to form a plurality of continuous, solid linear fibers. The plurality of the solid fibers is then accumulated on a spool that can be at a later time unwound and stretched by at least about 50 percent. The plurality of stretched fibers are then cut and allowed to relax such that a plurality of 3-dimensional, coiled fibers is formed.
- FIG. 1 is a schematic showing the equipment needed to extrude, spin, quench and draw continuous solid fibers and accumulate them on a spool.
- FIG. 2 is a cross-section of a bicomponent fiber.
- FIG. 3 is a schematic showing unwinding a plurality of solid linear fibers, stretching the fibers, cutting the fibers and then allowing the fibers to relax to form a plurality of 3-dimensional, staple fibers.
- FIG. 4 is a side view of a helical fiber formed when the stretched fiber is cut into a staple fiber and the fiber is allowed to relax.
- Referring to FIG. 1, a schematic of the equipment needed to extrude, spin, quench and draw a plurality of continuous solid fibers and accumulate them on a plurality of spools is depicted. The method includes the steps of co-extruding a
first component 10 and asecond component 12. The first and second components, 10 and 12 respectively, can be in the form of solid resin pellets or small particles. Thefirst component 10 is positioned in ahopper 14 from which it can be metered and routed through aconduit 16 to afirst extruder 18. Likewise, thesecond component 12 is positioned in ahopper 20 from which it can be metered and routed through aconduit 22 to asecond extruder 24. - The
first component 10 is a material that can be spun or otherwise formed into a continuous fiber. When thefirst component 10 is formed into a fiber, the fiber must be capable of being stretched and has a high recovery percentage R1. The “recovery percentage R1” is defined as the percent thefirst component 10 can recover after it has been stretched at least about 50% of its initial length and upon removal of the force applied to stretch it. Desirably, thefirst component 10 is an elastomeric material. Suitable elastomeric materials that can be used for thefirst component 10 include a melt extrudable thermoplastic elastomer such as a polyurethane elastomer, a copolyether ester, a polyether block polyamide copolymer, an ethylene vinyl acetate (EVA) elastomer, a styrenic block copolymer, an ether amide block copolymer, an olefinic elastomer, as well as other elastomers known to those skilled in the polymer art. Useful elastomeric resins include polyester polyurethane and polyether polyurethane. Examples of two commercially available elastomeric resins are sold under the trade designations PN 3429-219 and PS 370-200 MORTHANE® polyurethanes. MORTHANE® is a registered trademark of Huntsman Polyurethanes having an office in Chicago, Ill. 60606. Another suitable elastomeric material is ESTANE®, a registered trademark of Noveon, Inc. having an office in Cleveland, Ohio 44141. Still another suitable elastomeric material is PEARLTHANE®, a registered trademark of Merquinsa having an office in Boxford, Mass. 01921. - Three additional elastomeric materials include a polyether block polyamide copolymer which is commercially available in various grades under the trade designation PEBAX®. PEBAX® is a registered trademark of Atofina Chemicals, Inc. having an office in Birdsboro, Pa. 19508. A second elastomeric material is a copolyether-ester sold under the trade designation ARNITEL®. ARNITEL® is a registered trademark of DSM having an office at Het Overloon 1, NL-6411 TE Heerlen, Netherlands. The third elastomeric material is a copolyether-ester sold under the trade designation HYTREL®. HYTREL® is a registered trademark of E. I. DuPont de Nemours having an office in Wilmington, Del. 19898.
- The
first component 10 can also be formed from a styrenic block copolymer such as KRATON®. KRATON® is a registered trademark of Kraton Polymers having an office in Houston, Tex. - The
first component 10 can further be formed from a biodegradable elastomeric material such as polyester aliphatic polyurethanes or polyhydroxyalkanoates. Thefirst component 10 can be formed from an olefinic elastomeric material, such as elastomers and plastomers. One such plastomer is an ethylene-based resin or polymer sold under the trade designation AFFINITY®. AFFINITY® is a registered trademark of Dow Chemical Company having an office in Freeport, Tex. AFFINITY® resin is an elastomeric copolymer of ethylene and octene produced using Dow Chemical Company's INSITE™ constrained geometry catalyst technology. Another plastomer is sold under the trade designation EXACT® which includes single site catalyzed derived copolymers and terpolymers. EXACT® is a registered trademark of Exxon Mobil Corporation having an office at 5959 Las Colinas Boulevard, Irving, Tex. 75039-2298. Other suitable olefinic elastomers that can be used to form thefirst component 10 include polypropylene-derived elastomers. - The
first component 10 can further be formed from a non-elastomeric thermoplastic material which has a sufficient recovery percentage R1 after it has been stretched at a specified temperature. Non-elastomeric materials useful in forming thefirst component 10 are extrudable thermoplastic polymers such as polyamides, nylons, polyesters, polyolefins or blends of polyolefins. For example, non-elastomeric, biodegradable polylactic acid can provide a sufficient recovery percentage R1 when stretched above its glass transition temperature of about 62° C. - The
second component 12, like thefirst component 10, is a material that can be spun or otherwise formed into a continuous fiber. When thesecond component 12 is formed into a linear fiber, the linear fiber must be capable of being stretched and has a recovery percentage R2, wherein R1 is higher than R2 The “recovery percentage R2” is defined as the percent the component can recover after it has been stretched at least 50% of its initial length and upon removal of the force applied to stretch it. When the first and second components, 10 and 12 respectively, are formed into a linear fiber, the fiber must be capable of retracting or contracting from a stretched condition in order for the linear fiber to be useful in an absorbent article. As referred to herein, the term “retracting” means the same thing as “contracting”. Desirably, the ratio of R1/R2 ranges from at least about 2 to about 100. Most desirably, the ratio of R1/R2 ranges from at least about 2 to about 50. The reason for making R1 greater than R2 in a linear fiber is that upon retraction or contraction of the first and second components, 10 and 12 respectively, the 3-dimensional fiber will exhibit a very desirable, predetermined structural configuration. This structural configuration of the 3-dimensional fiber will display exceptional elongation properties in at least one direction. - The linear fiber further obtains some of its unique properties when the
first component 10 makes up a volume percent of from about 30% to about 95% of the linear fiber and thesecond component 12 makes up a volume percent of from about 5% to about 70% of the linear fiber. Desirably, thefirst component 10 makes up a volume percent from about 40% to about 80% of the linear fiber and thesecond component 12 makes up a volume percent of from about 20% to about 60% of the linear fiber. The volume of a solid linear fiber is calculated using the following formula: - V=π(d 2/4)L 1
- where: V is the volume of the solid linear fiber;
- π is a transcendental number, approximately 3.14159, representing the ratio of the circumference to the diameter of a circle and appearing as a constant in a wide range of mathematical problems;
- d is the diameter of the linear fiber; and
- L1 is the initial length of the linear fiber.
- The above described ranges of volume percents for the
first component 10 and for thesecond component 12 allow the linear fiber to be stretched at least 50% to form a stretched linear fiber. The volume percent of each of the first and second components, 10 and 12 respectively, also plays a vital role in the retraction or contraction of the stretched fiber to a retracted length. By varying the volume percent of each of the first and second components, 10 and 12 respectively, one can manufacture a linear fiber that can be stretched and then retracted to a predetermined configuration and with certain desirable characteristics. At a later time, after such fibers are formed into a disposable absorbent article, the contact with a body fluid will cause the absorbent article to swell which will allow the fibers to elongate in at least one direction before the fiber becomes linear. As the fibers elongate, they can extend and allow the absorbent structure to receive and store additional body fluids. - The first and second components,10 and 12 respectively, are chemically, mechanically and/or physically adhered or joined to one another to prevent the fiber from splitting when the fiber is stretched and then allowed to relax. The relaxed fiber will retract in length. Desirably, the
first component 10 will be strongly adhered to thesecond component 12. In the core/sheath arrangement, the mechanical adhesion between the first and second components, 10 and 12 respectively, will compliment any chemical and/or physical adhesion that is present and aid in preventing splitting or separation of thefirst component 10 from thesecond component 12. This splitting or separation occurs because one component is capable of retracting to a greater extent than the other component. If a strong mutual adhesion is not present, especially during retraction, the two components can split apart and this is not desirable. In a fiber formed of two components arranged in a side by side or wedge shape configuration, a strong chemical and/or physical adhesion will prevent thefirst component 10 from splitting or separating from thesecond component 12. - The
second component 12 can be formed from polyolefins, such as polyethylene or polypropylene, a polyester or a polyether. Thesecond component 12 can also be a polyolefin resin, such as a fiber grade polyethylene resin sold under the trade designation ASPUN® 6811A. ASPUN® is a registered trademark of Dow Chemical Company having an office in Midland, Mich. 48674. Thesecond component 12 can also be a polyolefin resin, such as a homopolymer polypropylene such as Himont PF 304, and PF 308, available from Basell North America, Inc. having an office at Three Little Falls Centre, 2801 ° C. enterville Road, Wilmington, Del. 19808. Another example of a polyolefin resin from which thesecond component 12 can be formed is polypropylene PP 3445 available from Exxon Mobil Corporation having an office at 5959 Las Colinas Boulevard, Irving, Tex. 75039-2298. Still other suitable polyolefinic materials that can be used for thesecond component 12 include random copolymers, such as a random copolymer containing propylene and ethylene. One such random copolymer is sold under the trade designation Exxon 9355, available from Exxon Mobil Corporation having an office at 5959 Las Colinas Boulevard, Irving, Tex. 75039-2298. - The
second component 12 can also be formed from a melt extrudable thermoplastic material that provides sufficient permanent deformation upon stretching. Such materials include, but are not limited to, aliphatic and aromatic polyesters, copolyesters, polyethers, polyolefins such as polypropylene or polyethylene, blends or copolymers thereof, polyamides and nylons. Thesecond component 12 can further be formed from biodegradable resins, such as aliphatic polyesters. One such aliphatic polyester is polylactic acid (PLA). Other biodegradable resins include polycaprolactone, polybutylene succinate adipate and polybutylene succinate. Polybutylene succinate adipate and polybutylene succinate resins are sold under the trade designation BIONOLLE® which is a registered trademark of Showa High Polymers having a sales office in New York, N. Y. 1017. Additional biodegradable resins include copolyester resin sold under the trade designation EASTAR BIO®. EASTAR BIO® is a registered trademark of Eastman Chemical Company having an office in Kingsport, Tenn. 37662. Still other biodegradable resins that can be used for thesecond component 12 include polyhydroxyalkanoates (PHA) of varying composition and structure, and copolymers, blends and mixtures of the foregoing polymers. Specific examples of suitable biodegradable polymer resins include BIONOLLE® 1003, 1020, 3020 and 3001 resins commercially available from Itochu International. BIONOLLE® is a registered trademark of Showa High Polymers having an office in New York, N. Y. 10017. - The
second component 12 can also be formed from a water-soluble and swellable resin. Examples of such water-soluble and swellable resins include polyethylene oxide (PEO) and polyvinyl alcohol (PVOH). Grafted polyethylene oxide (gPEO) or chemically modified PEO can also be used. The water-soluble polymer can be blended with a biodegradable polymer to provide for better processing, performance, and interactions with liquids. - It should be noted that the PEO resin can be chemically modified by reactive extrusion, grafting, block polymerization or branching to improve its processability. The PEO resin can be modified by reactive extrusion or grafting as described in U. S. Pat. No. 6,172,177 issued to Wang et al. on Jan. 9, 2001.
- Lastly, the
second component 12 has a lower recovery percentage R2 than thefirst component 10. Thesecond component 12 can be formed from a material that exhibits a low elastic recovery. Materials from which thesecond component 12 can be formed include, but are not limited to polyolefin resins, polypropylene, polyethylene, polyethylene oxide (PEO), polyvinyl alcohol (PVOH), polyester and polyether. Thesecond component 12 can be treated or modified with hydrophilic or hydrophobic surfactants. Treatment of thesecond component 12 with a hydrophilic surfactant will form a wettable surface for increasing interaction with a body fluid or liquid. For example, when the surface of thesecond component 12 is treated to be hydrophilic, it will become more wettable when contacted by a body fluid, especially urine. Treatment of thesecond component 12 with a hydrophobic surfactant will cause it to repel a body fluid or liquid. Similar treatment of thefirst component 10 can also be done to control its hydrophilic or hydrophobic characteristics. - Referring again to FIG. 1, the first and second components,10 and 12 respectively, are separately co-extruded in the two
extruders extruders first component 10 is routed through aconduit 26 while thesecond component 12 is simultaneously routed through aconduit 28 and both flow streams are directed into a spin pack 30. A melt pump, not shown, can be positioned across one or both of theconduits - It should be noted that the openings in the spin pack30 do not have to be round or circular in cross-section but can have a bilobal, trilobal, square, triangular, rectangular, oval or any other geometrical cross-sectional configuration that is desired.
- Referring to FIGS. 1 and 2, the first and second components,10 and 12 respectively, are directed into the spin pack 30 and are routed through the openings formed in the bottom plate in such a fashion that the
first component 10 will form acore 32 while thesecond component 12 will form asheath 34 which surrounds the outside circumference of thecore 32. It should be noted that thefirst component 10 could form the sheath while thesecond component 12 could form the core, if desired. This core/sheath arrangement produces one configuration of a linear,bicomponent fiber 36. Bicomponent fibers having other cross-sectional configurations can also be produced using the spin pack 30. For example, the bicomponent fiber can have a side by side configuration or a core/sheath design where the core is offset coaxially from the sheath. - One
bicomponent fiber 36 will be formed for each opening formed in the plate within the spin pack 30. This enables a plurality of continuousmolten fibers 36, each having a predetermined diameter, to simultaneously exit the spin pack 30 at a first speed. Each linear,bicomponent fiber 36 will be spaced apart and be separated from theadjacent fibers 36. The diameter of eachbicomponent fiber 36 will be dictated by the size of the openings formed in the bottom plate of the spin pack 30. For example, as stated above, if the diameter of the holes or openings in the bottom plate range from about 0.1 mm to about 2.0 mm, then each of themolten fibers 36 can have a diameter which ranges from about 0.1 mm to about 2.0 mm. There is a tendency for themolten fibers 36 to sometimes swell in cross-sectional area once they exit the opening formed in the plate but this expansion is relatively small. - The plurality of continuous
molten fibers 36 are routed through a quenchchamber 38 to form a plurality of cooled linear,bicomponent fibers 40. Desirably, themolten fibers 36 are directed downward from the spin pack 30 into the quenchchamber 38. The reason for directing themolten fibers 36 downward is that gravity can be used to assist in moving themolten fibers 36. In addition, the vertical downward movement can aid in keeping thefibers 36 separated from one another. - In the quench
chamber 38, the continuousmolten fibers 36 are contacted by one or more streams of air. Normally, the temperature of the continuousmolten fibers 36 exiting the spin pack 30 and entering the quenchchamber 38 will be in the range of from about 150° C. to about 250° C. The actual temperature of themolten fibers 36 will depend upon the material from which they are constructed, the melting temperature of such material, the amount of heat applied during the extrusion process, as well as other factors. Within the quenchchamber 38, the continuousmolten fibers 36 are contacted and surrounded by lower temperature air. The temperature of the air can range from about 0° C. to about 120° C. Desirably, the air is cooled or chilled so as to quickly cool themolten fibers 36. However, for certain materials used to form thebicomponent fibers 36; it is advantageous to use ambient air or even heated air. However, for most elastomeric materials, the air is cooled or chilled to a temperature of from about 0° C. to about 400° C. More desirably, the air is cooled or chilled to a temperature of from about 15° C. to about 300° C. The lower temperature air can be directed toward themolten fibers 36 at various angles but a horizontal or downward angle seems to work best. The velocity of the incoming air can be maintained or adjusted so as to efficiently cool themolten fibers 36. - The cooled or chilled air will cause the continuous
molten fibers 36 to crystallize, assume a crystalline structure or phase separate and form a plurality of continuous cooledfibers 40. The cooledfibers 40 are still linear in configuration at this time. Upon exiting the quenchchamber 38, the temperature of the cooledfibers 40 can range from about 15° C. to about 100° C. Desirably, the temperature of the cooledfibers 40 will range from about 20° C. to about 80° C. Most desirably, the temperature of the cooledfibers 40 will range from about 25° C. to about 60° C. The cooledfibers 40 will be at a temperature below the melting temperature of the first and second components, 10 and 12 respectively, from which thefibers 40 were formed. The cooledfibers 40 may have a soft plastic consistency at this stage. - The plurality of continuous cooled
fibers 40 are then routed to adraw unit 42. Thedraw unit 42 can be vertically located below the quenchingchamber 38 so as to take advantage of gravity. Thedraw unit 42 can be a rotating roll around which all of the cooledfibers 40 are funneled down into a rope or tow and are drawn by being wrapped at least once around the outer periphery of the rotating roll. The plurality of cooledfibers 40 can be wrapped one or more times around the outer periphery of the rotating roll. Desirably, the plurality of cooledfibers 40 can be wrapped 1½ times around the outer periphery of the rotating roll wherein thefibers 40 accumulate into a rope or tow ofsolid fibers 44. Mechanical drawing involves subjecting the cooledfibers 40 to a mechanical force that will pull or draw the molten material exiting the spin pack 30. - The cooled
fibers 40 are drawn down mainly from the molten state and not from the cooled state. The downward force in thedraw unit 42 will cause the molten material to be lengthened and elongated intosolid fibers 44. Lengthening of the molten material will usually shape, narrow, distort, or otherwise change the cross-sectional area of thesolid fibers 44. For example, if the molten material has a round or circular cross-sectional area upon exiting the spin pack 30, the outside diameter of thesolid fibers 44 will be reduced. The amount that the diameter of the solidlinear fibers 44 are reduced will depend upon several factors, including the amount the molten material is drawn, the distance over which the fibers are drawn, the mechanical force used to draw the fibers, the spin line tension, etc. Desirably, the diameter of the solidlinear fibers 44 will range from about 5 microns to about 10 microns. More desirably, the diameter of the solidlinear fibers 44 will l range from about 10 microns to about 50 microns. Most desirably, the diameter of the solidlinear fibers 44 will range from about 10 microns to about 30 microns. - The
draw unit 42 will pull the cooledfibers 40 at a second speed that is faster than the first speed displayed by the continuousmolten fibers 36 exiting the spin pack 30. This change in speed between the continuousmolten fibers 36 and the continuous cooledfibers 40 enables the molten material to be lengthened and also to be reduced in cross-sectional area. Upon exiting thedraw unit 42, the cooledfibers 40 will besolid fibers 44. - The plurality of
solid fibers 44 exiting thedraw unit 42 are then routed in mass around aguide roll 45 to aspool 46. The advancingfibers 44 are circumferentially wound onto the periphery of thespool 46 in the form of a rope. Thespool 46 can be mounted in asupport 48 and can be made to rotate as the advancingfiber 44 is directed onto thespool 46. Thespool 46 can be sized and shaped to accumulate a predetermined amount ofsolid fibers 44. The solidlinear fibers 44 will l be accumulated on thespool 46 until thespool 46 is filled. At this time the plurality ofsolid fibers 44 are cut or severed in mass by acutter 50. The advancingsolid fibers 44 can then be directed onto anotherempty spool 46 that can be held in thesupport 48. The process of removing a filledspool 46 and replacing it with anempty spool 46, onto which the advancingfibers 44 can be accumulated, is well known to those skilled in the art. This process can be automated so that the advancinglinear fibers 44 can be instantaneously and sequentially directed to the next availableempty spool 46. - Each of the filled spools46 can be stacked and stored for use at a later time at the same facility or they can be transported to another location. One feature of this invention is that the solid
linear fibers 44 do not have to be processed into crimped staple fibers nor formed into a web in one continuous process. Instead, the method allows for an interruption, such that the solidlinear fibers 44 can be further processed at a later time and at a remote location, if desired. Alternatively, a continuous method could be employed wherein thespools 46 would not need to be present. - Referring to FIG. 3, a schematic is depicted showing the unwinding of a plurality of linear fibers, stretching the fibers, cutting the fibers and then allowing the fibers to relax to form a plurality of 3-dimensional, staple fibers. The method allows for the plurality of
linear fibers 44 that were circumferentially wound onto the outer periphery of thespool 46 to be unwound and directed to aheater 52. Theheater 52 is optional, but when present, will heat the plurality oflinear fibers 44 to an elevated temperature. The exact temperature will depend upon the composition of the first and second components, 10 and 12 respectively, the diameter of thefibers 44, the amount thefibers 44 are to be stretched, the speed of thefibers 44, etc. It is also possible at this time to apply a surface treatment to the plurality oflinear fibers 44, if desired. The application of a surface treatment either by spraying a chemical composition onto thefibers 44 or emersion of thefibers 44 in a liquid bath is well known to those skilled in the art. Various types of surface treatments can be applied to thefibers 44. - The plurality of solid
linear fibers 44 are then routed to a stretchingunit 54 where the plurality oflinear fibers 44 is stretched by at least about 50%. By “stretched” it is meant that the continuous solid,linear fibers 44 are lengthened or elongated while in a solid state. The stretching is caused by axial tension exerted on the plurality oflinear fibers 44. As thelinear fibers 44 are stretched, the cross-sectional area of thelinear fibers 44 will l be reduced. Desirably, the amount of stretch imparted into thesolid fibers 44 can range from about 75% to about 1,000%. More desirably, the amount of stretch imparted into the solid fibers, 44 can range from about 100% to about 500%. Most desirably, amount of stretch imparted into thesolid fibers 44 can range from about 150% to about 300%. - The stretching
unit 54 is shown as including two pairs of spaced apart rolls. It should be noted that other forms of mechanical stretching apparatus can be utilized. The first pair of rolls includes afirst roll 56 and asecond roll 58. The first and second rolls, 56 and 58 respectively, can be arranged in close contact with one another so as to form a nip 60 therebetween. The plurality oflinear fibers 44, unwound from thespool 46, is routed around a portion of the periphery of thefirst roll 56, through thenip 60 and around a portion of the periphery of thesecond roll 58. The nip 60 can be adjusted such that little or no pressure is exerted on thefibers 44. At least one of the first and second rolls, 56 and 58 respectively, is a driven roll which is set to rotate at a first predetermined surface speed. This surface speed caused the plurality oflinear fibers 44 to be advanced at this speed. The surface speed can vary depending upon one's unique requirements. However, a surface speed of between about 10 meters per minute (m/min) to about 1,000 m/min will be sufficient for most applications. Desirably, the surface speed will be equal to or less than about 500 m/min. A faster surface speed is usually more desirable than a slower surface speed in order to reduce the cost of manufacture. However, at very high speeds, the fibers can lose their stretchability and become brittle. This can cause the fibers to break before they reach the desired percent of elongation. - Spaced downstream a desired distance from the first pair of rolls is the second pair of rolls. The second pair of rolls includes a
first roll 62 and asecond roll 64. The first and second rolls, 62 and 64 respectively, can be arranged in close contact with one another so as to form a nip 66 therebetween. The plurality oflinear fibers 44 exiting the first pair of rolls is routed around a portion of the periphery of thefirst roll 62, through thenip 66 and around a portion of the periphery of thesecond roll 64. The nip 66 can be adjusted such that little or no pressure is exerted on thefibers 44. At least one of the first and second rolls, 62 and 64 respectively, is a driven roll which is set to rotate at a second predetermined surface speed. The second predetermined speed is faster than the first predetermined speed. This difference in speed caused the plurality offibers 44 to be stretched lengthwise between the two pair of rolls to form a plurality of stretchedlinear fibers 68. - It should be noted that multiple rolls or pairs of rolls that rotate at different, and preferably increasing surface speeds, can also be utilized.
- Optionally, positioned between the two pair of rolls,56 and 58 and 60 and 62 respectively, is a
heater 70. Theheater 70 is capable of heating the plurality oflinear fibers 44 to an elevated temperature. The exact temperature will depend upon the composition of the first and second components, 10 and 12 respectively, the diameter of thefibers 44, the amount thefibers 44 are to be stretched, the speed of thefibers 44, etc. - The stretching of the plurality of
fibers 44 within the stretchingunit 54 will cause the cross-sectional area of each of thelinear fibers 44 to be reduced by about 5% to about 90% of the cross-sectional area of thelinear fibers 44 unwound from thespool 46. Desirably, the cross-sectional area of each of thelinear fibers 44 is reduced by about 10% to about 60% of the cross-sectional area of thelinear fibers 44 unwound from thespool 46. More desirably, the cross-sectional area of each of thelinear fibers 44 is reduced by about 20% to about 50% of the cross-sectional area of thelinear fibers 44 unwound from thespool 46. - The stretched, continuous
linear fibers 68 will be relatively small in diameter or cross-sectional area. Desirably, the diameter of the stretchedlinear fibers 68 will range from about 5 microns to about 50 microns. More desirably, the diameter of the stretchedfibers 68 will range from about 5 microns to about 30 microns. Most desirably, the diameter of the stretchedlinear fibers 68 will range from about 10 microns to about 20 microns. - It should be noted that the stretched
linear fibers 68 leaving the second pair ofrolls - Still referring to FIG. 3, upon exiting the stretching
unit 54, the plurality of stretchedlinear fibers 68 are cut or severed by arotary cutter 72 having at least oneknife 74 secured thereto. Therotary cutter 72 cooperates with ananvil roll 76 and thecutter 72 and theanvil roll 76 are arranged so that the stretchedlinear fiber 68 passes therebetween. Therotary cutter 72 and theanvil roll 76 keep the stretchedlinear fiber 68 in tension until it has been cut by theknife 74. It should be noted that other types of cutting mechanism can be utilized that are well known to those skilled in the cutting art. It is also possible to position a cutter downstream of a pair of cooperating rolls that maintain the stretchedlinear fiber 68 in tension. Therotary cutter 72 will cut the plurality of stretchedfibers 68 into a plurality ofstaple fibers 78, each having a predetermined length. The plurality of stretchedfibers 68 can be cut to a staple length of from about 5 millimeters to about 500 millimeters. Desirably, the plurality of stretchedfibers 68 can be cut to a staple length of from about 10 millimeters to about 50 millimeters. More desirably, the plurality of stretchedfibers 68 can be cut to a staple length of from about 12 millimeters to about 25 millimeters. The plurality ofcut staple fibers 78 will instanteously start to relax. This relaxation allows thestaple fibers 78 to retract or contract into a plurality of 3-dimensional, coiledfibers 80. Thecoiled fibers 80 have a shorter length than the cut stretchedfiber 78. Thecoiled fibers 80 have a length ranging from about 3 millimeters (mm) to about 50 mm. Desirably, thecoiled fibers 80 have a length ranging from about 5 mm to about 25 mm. Most desirably, thecoiled fibers 80 have a length ranging from about 5 mm to about 15 mm. Thesecoiled fibers 80 can be collected in a hopper orcontainer 82. - Referring to FIG. 4, a portion of a 3-dimensional,
staple fiber 80 depicted in the shape of a helix or helical coil that has a longitudinal central axis x-x. By “3-dimensional fiber” is meant a fiber having an x, y and z component that is formed by virtue of coils and/or curves regularly or irregularly spaced and whose extremities in the x, y and z planes form a locus of points which define a volume greater than a linear fiber. The 3-dimensional, coiledfibers 80 have a generally helical configuration. The helical configuration can extend along the entire length L of each of the 3-dimensional fibers 80 or it can occur over a portion of the length of the 3-dimensional fibers 80. Desirably, the coiled configuration extends over at least half of the length of each of the 3-dimensional fibers 80. More desirably, the coiled configuration extends from about 50% to about 90% of the length of each of the 3-dimensional fibers 80. Most desirably, the coiled configuration extends from about 90% to about 100% of the length of each of the 3-dimensional fibers 80. It should be noted that the coils can be formed in the clockwise or counterclockwise directions along at least a potion of the length of the 3-dimensional,staple fibers 80. It should also be noted that the configuration of each coil can vary along the length of each of the 3-dimensional,staple fibers 80. - Each of the 3-dimensional,
staple fibers 80 have coils that circumscribes 360 degrees. The helical coils can be continuous or non-continuous over either a portion of or over the entire length of the 3-dimensional,staple fiber 80. Most desirably, the 3-dimensional,staple fibers 80 exhibit a continuous helical coil. The 3-dimensional,staple fiber 80 differs from a 2-dimensional fiber in that a 2-dimensional fiber has only two components, for example, an “x” and a “y” component; an “x” and a “z” component, or a “y” and a “z” component. The 3-dimensional,staple fiber 80 has three components, an “x” component, a “y” component and a “z” component. Many crimp fibers are 2-dimensional fibers that are flat and extend in only two directions. A crimped fiber is typically a fiber that has been pressed or pinched into small, regular folds or ridges. A crimped fiber usually has a bend along its length. - The 3-dimensional,
staple fiber 80 has a non-linear configuration when it forms a helical coil. The 3-dimensional,staple fiber 80 also has an amplitude “A” that is measured perpendicular to a portion of its length L The amplitude “A” of the 3-dimensional,staple fiber 80 can range from about 10 microns to about 5,000 microns. Desirably, the amplitude “A” of the 3-dimensional,staple fiber 80 ranges from about 30 microns to about 1,000 microns. Most desirably, the amplitude “A” of the 3-dimensional,staple fiber 80 ranges from about 50 microns to about 500 microns. The 3-dimensional,staple fiber 80 further has a frequency “F” measured at two locations separated by 360 degrees between adjacent helical coils. The frequency “F” is used to denote the number of coils or curls formed in each inch of the coiled fiber length. The frequency “F” can range from about 10 to about 1,000 coils per inch. Desirably, the frequency “F” can range from about 50 to about 500 coils per inch. It should be noted that the amplitude “A” and/or the frequency “F” can vary or remain constant along at least a portion of the length L, or over the entire length, of the 3-dimensional,staple fiber 80. Desirably, the amplitude “A” and the frequency “F” will remain constant over a majority of the length L. The amplitude “A” of the 3-dimensional,staple fiber 80 and the frequency “F” of the helical coils forming the 3-dimensional,staple fiber 80 affect the overall reduction in the length of the 3-dimensional,staple fiber 80 from it's stretched condition. - It should be noted that the deformation properties of the first and second components,10 and 12 respectively, will affect the configuration and size of the helical coils developed as the stretched
fibers 78 retracts into the 3-dimensional, coiledfibers 80. - The first and second components,10 and 12 respectively, are adhered together in the spin pack 30 to form a plurality of continuous bicomponent fibers. The adhesion of the
first component 10 to thesecond component 12 can be chemical, mechanical and/or physical. This ability of the first and second components, 10 and 12 respectively, to adhere to one another will prevent splitting of thecomponents first component 10 in the solidlinear fiber 44 has an elongation of at least about 50% deformation. Thefirst component 10 is able to recover at least about 20% of the stretch deformation imparted thereto, based on its length after deformation. Desirably, thefirst component 10 in the solidlinear fiber 44 is able to recover at least about 50% of its stretch deformation. If thefirst component 10 has an elongation below at least about 50%, the recovery or relaxation power may not be sufficient to activate helical coiling of the 3-dimensional,staple fiber 80. Repetitive helical coils in the retracted 3-dimensional,staple fiber 80 are most desirable. A higher elongation than at least about 50% for thefirst component 10 is desirable. For example, an elongation of at least about 100% is good, an elongation exceeding 300% is better, and an elongation exceeding 400% is even better. - The
second component 12 in the solidlinear fiber 44 has a total deformation which includes a permanent unrecoverable deformation value and a recoverable deformation value. The permanent unrecoverable deformation value in a solid state, as a result of stretching, plastic yielding and/or drawing, is at least about 40%. The recoverable deformation value is at least about 0.1%. A higher deformation than at least about 50% for thesecond component 12 is desirable. A deformation of at least about 100% is good and a deformation exceeding about 300% is even better. The plastic yielding and drawing results in thinning of thesecond component 12. Stretching in a solid state means that thesecond component 12 is stretched below its melting temperature. If the total deformation of thesecond component 12 is below at least about 50%, thesecond component 12 will fail and break during the stretching process. Also, at low deformation, thesecond component 12 does not provide a sufficient level of permanent plastic yielding and thinning which is desired for the formation of the repetitive helical coils in the 3-dimensional,staple fibers 80. Stretching should not occur at very low temperatures because the fibers may be brittle and could break. Likewise, the fibers should not be stretched very quickly because this might cause the fibers to break before reaching the desired percent of elongation. - The percent elongation of the length of the 3-dimensional, coiled
fiber 80 defined as the percent change in length by which the 3-dimensional, coiledfiber 80 can be stretched before becoming straight or linear. The percent elongation can be expressed by the following formula: - %E=100×(L 1 −L)/L
- where: % E is the percent elongation of the 3-dimensional,
staple fiber 80; - L is the retracted length of the 3-dimensional,
staple fiber 80; and - L1 is the final length of the 3-dimensional,
staple fiber 80 once it is stretched into a straight or uncoiled configuration. - The retracted 3-dimensional,
staple fiber 80 has the ability to be subsequently elongated to at least 100% of its retracted length. Most desirably, the retracted 3-dimensional,staple fiber 80 can be subsequently elongated from about 150% to about 900% of its retracted length. Even more desirably, the retracted 3-dimensional,staple fiber 80 can be subsequently elongated from about 250% to about 500% of its retracted length. Still more desirably, the retracted 3-dimensional,staple fiber 80 can be subsequently elongated from about 300% to about 400% of its retracted length. - The 3-dimensional,
staple fiber 80 exhibits exceptional elongation properties in at least one direction before the fiber becomes linear. Elongation is defined as the percent length by which the 3-dimensional,staple fiber 80 can be stretched before it becomes straight or linear. The direction of the elongation property of the 3-dimensional,staple fiber 80 normally in the same direction as thelinear fiber 44 was stretched. In other words, the direction that the retracted 3-dimensional,staple fiber 80 able to subsequently elongate will be opposite to the direction of its retraction. It is possible for the retracted 3-dimensional,staple fiber 80 to have elongation properties in two or more directions. For example, the retracted 3-dimensional,staple fiber 80 can subsequently be elongated in both the x and y directions. - The 3-dimensional,
staple fiber 80 obtained once the stretchedfiber 78 is allowed to relax or retract. The 3-dimensional,staple fiber 80 able to acquire its helical profile by the difference in recovery percentage R1 of thefirst component 10 compared to the recovery percentage R2 of thesecond component 12. For example, since thefirst component 10 has a higher recovery percentage R1 than the recovery percentage R2 of thesecond component 12, thefirst component 10 will want to retract to a greater degree than thesecond component 12. However, both the first and second components, 10 and 12 respectively, will retract or contract the same amount since they are physically, chemically or mechanically adhered or joined to one another. The combination of the volume percent and the recovery percent of the first and second components, 10 and 12 respectively, creates the unique 3-dimensional configuration of thefiber 80. The retraction or recovery of the first and second components, 10 and 12 respectively, establishes the twist or coiling effect in the retracted 3-dimensional,staple fiber 80. The amount of coiling obtained, as well as the shape and location of the coiling, can be controlled by the selection of materials that are used to construct thelinear fiber 44. These three variables: the amount of coiling, the shape, and the location of the coiling, can also be controlled by the volume of each component, as well as the amount thelinear fiber 44 is stretched. The time and temperature conditions under which thesolid fibers 44 are stretched and allowed to retract can also affect the finish profile of the retracted 3-dimensional,staple fiber 80. - The
first component 10 has a higher recovery percentage R1 than the recovery percentage R2 of thesecond component 12 and therefore the material from which thefirst component 10 is formed tends to be more tacky and elastic. For this reason, the material with the higher recovery percentage R1 is used to form the inner core while the material having a lower recovery percentage R2 tends to be used to form the outer sheath. As the first and second components, 10 and 12 respectively, try to retract from the stretched condition; the outer sheath will retract or contract less. This means that thefirst component 10 will not be able to retract fully to an amount that it could if it was by itself. This pent up force creates the twist or helical coil effect in the retracted 3-dimensional,staple fiber 80. By varying the materials used to form thelinear fiber 44 and by controlling the conditions to which thelinear fiber 44 is stretched and then retracted, one can manufacture uniquely configured 3-dimensional,staple fibers 80 that will subsequently elongate in a predetermined way. This characteristic has been identified as being extremely useful in constructing disposable absorbent articles. This characteristic may also exhibit beneficial features in other articles as well. - The following Table 1 shows the recovery percent of individual materials that have been stretched to varying percentages. The material forming each sample was cut out from a thin sheet of a particular thickness in the shape of a dogbone or dumbbell. The dogbone shaped sample had an initial length of 63 millimeters (mm) measured from a first enlarged end to a second enlarged end. In between the two oppositely aligned, enlarged ends was a narrow section having a length of 18 mm and a width of 3 mm. The material was then placed in a tensile tester and stretched at a rate of 5 inches per minute, in the machine direction of the material. This stretching caused the narrow section of the sample to elongate. The force used to stretch the sample was then removed and the sample was allowed to retract or recover. The retracted length of the narrow section, known as the finished recovery length, was measured and recorded as a percentage of the stretched length. One can extrapolate from this information that when such a material is combined with another material to form a
linear fiber 44, those similar ranges of recovery or contraction can be experienced.TABLE 1 50% 100% 200% 700% Thickness Stretch stretched stretched stretched stretched Material in mils Temp. C.° & recovered & recovered & recovered & recovered Polyurethane 5 25 24.5% 39.1% 54.4% — Polypropylene 3 25 5.4% 5.5% 5.1% — Polypropylene 3 75 — 8.7% 7.3% 6.4% - In Table 1, the dogbone shaped sample had a narrow section I1 located between its first and second enlarged ends. Each of the enlarged ends of the dog bone sample was secured in a tensile tester and a force was applied causing the material to be stretched, in the machine direction of the material, a predetermined amount at a specific temperature. By stretching the sample, the narrow section is stretched to a length I2. The length I2 is greater than the initial length I1. The force exerted on the sample was then removed and the sample was allowed to retract such that the narrow section is shortened to a length I3. The retracted length I3 is smaller than the stretched length I2 but is greater than the initial length I1. The recovery percent (R %) of the different materials that can be used in forming the fiber can be calculated using the following formula:
- Recovery %=[(I 2 −I 3)/I 2]×100
- where: I2 is the stretched length of the narrow section of the sample; and
- I3 is the retracted length of the narrow section of the sample.
- It should be noted that the
coiled fibers 80 can be mixed with other kinds of fibers, such as cellulose fibers, wood pulp fibers, other synthetic fibers, etc. and/or a superabsorbent to form a web. The web can be an airlaid web, an air formed web, a coform web, a wet laid wet, etc. The web can be used in various kinds of products. The web is especially useful when used in a disposable absorbent article, such as an infant diaper, a training pant, an incontinent garment including a pad, brief, pant and refastenable pant, a sanitary napkin or tampon, a wet wipe product, etc. The method of admixing such fibers and/or superabsorbent particles is known to those skilled in the art. The percentage of each kind of fiber used to form the web can vary to meet one's particular needs. It should be noted that superabsorbent material, preferably in the form of particles, can be mixed with one or more kinds of fibers to form an absorbent web. The web can also be stabilized and/or bonded using various methods known to those skilled in the art. - A recognized limitation of stabilized and bonded absorbent webs is that the superabsorbent material present in the web is constrained from swelling to its full capacity. The use of the 3-dimensional fibers of this invention will allow an absorbent web structure containing superabsorbent material to expand and accommodate the entire extent the superabsorbent material can swell.
- It should also be noted that the
coiled fibers 80 can be laminated to a stretchable material, an elastic film or elastic fibers to form a thin, absorbent or non-absorbent material. This laminate material can be used as the bodyside cover or facing layer on a disposable absorbent article such as a diaper, training pant, incontinence garment, sanitary napkin, etc. This laminate material can also be used in health care products such as wound dressings, surgical gowns, gloves, etc. - While the invention has been described in conjunction with several specific embodiments, it is to be understood that many alternatives, modifications and variations will be apparent to those skilled in the art in light of the aforegoing description. Accordingly, this invention is intended to embrace all such alternatives, modifications and variations that fall within the spirit and scope of the appended claims.
Claims (30)
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
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US10/232,059 US20040043214A1 (en) | 2002-08-30 | 2002-08-30 | Method of forming a 3-dimensional fiber and a web formed from such fibers |
EP20030791601 EP1532298A1 (en) | 2002-08-30 | 2003-07-24 | Method of forming a 3-dimensional fiber and a web formed from such fibers |
MXPA05001641A MXPA05001641A (en) | 2002-08-30 | 2003-07-24 | Method of forming a 3-dimensional fiber and a web formed from such fibers. |
BR0313446A BR0313446A (en) | 2002-08-30 | 2003-07-24 | Methods of forming a three-dimensional fiber and mat formed from these fibers |
JP2004532820A JP2005537403A (en) | 2002-08-30 | 2003-07-24 | Three-dimensional fiber and method for producing a web formed from such fiber |
KR1020057002206A KR20060006759A (en) | 2002-08-30 | 2003-07-24 | Method of forming a 3-dimensional fiber and a web formed from such fibers |
AU2003256753A AU2003256753A1 (en) | 2002-08-30 | 2003-07-24 | Method of forming a 3-dimensional fiber and a web formed from such fibers |
PCT/US2003/023147 WO2004020709A1 (en) | 2002-08-30 | 2003-07-24 | Method of forming a 3-dimensional fiber and a web formed from such fibers |
ARP030103046 AR041041A1 (en) | 2002-08-30 | 2003-08-22 | A METHOD FOR FORMING THREE-DIMENSIONAL FIBERS AND THE FABRIC FORMED BY SUCH FIBERS |
Applications Claiming Priority (1)
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US10/232,059 US20040043214A1 (en) | 2002-08-30 | 2002-08-30 | Method of forming a 3-dimensional fiber and a web formed from such fibers |
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US20040043214A1 true US20040043214A1 (en) | 2004-03-04 |
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US10/232,059 Abandoned US20040043214A1 (en) | 2002-08-30 | 2002-08-30 | Method of forming a 3-dimensional fiber and a web formed from such fibers |
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US (1) | US20040043214A1 (en) |
EP (1) | EP1532298A1 (en) |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008079059A1 (en) * | 2006-12-22 | 2008-07-03 | Sca Hygiene Products Ab | Bicomponent superabsorbent fibre |
EP2074975A2 (en) | 2003-12-30 | 2009-07-01 | Kimberly-Clark Worldwide, Inc. | Customizable absorbent article with extensible layers |
US7694379B2 (en) | 2005-09-30 | 2010-04-13 | First Quality Retail Services, Llc | Absorbent cleaning pad and method of making same |
US7962993B2 (en) | 2005-09-30 | 2011-06-21 | First Quality Retail Services, Llc | Surface cleaning pad having zoned absorbency and method of making same |
US20120097035A1 (en) * | 2010-10-25 | 2012-04-26 | Chapman Rick L | Filtration materials using fiber blends that contain strategically shaped fibers and/or charge control agents |
US20140342629A1 (en) * | 2012-01-31 | 2014-11-20 | Kuraray Co., Ltd. | Composite fiber, method for producing polyurethane elastomer fabric, and polyurethane elastomer fabric |
Citations (94)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US518885A (en) * | 1894-04-24 | hollerith | ||
US3233029A (en) * | 1961-06-09 | 1966-02-01 | Phillips Petroleum Co | Method of cold-stretching orientable sheet material |
US3383449A (en) * | 1964-10-01 | 1968-05-14 | Muller Paul Adolf | Method for producing an endless filter string |
US3502763A (en) * | 1962-02-03 | 1970-03-24 | Freudenberg Carl Kg | Process of producing non-woven fabric fleece |
US3502538A (en) * | 1964-08-17 | 1970-03-24 | Du Pont | Bonded nonwoven sheets with a defined distribution of bond strengths |
US3802817A (en) * | 1969-10-01 | 1974-04-09 | Asahi Chemical Ind | Apparatus for producing non-woven fleeces |
US3870593A (en) * | 1972-06-06 | 1975-03-11 | Minnesota Mining & Mfg | Stretch-oriented porous films and preparation and use thereof |
US3880966A (en) * | 1971-09-23 | 1975-04-29 | Celanese Corp | Corona treated microporous film |
US4136218A (en) * | 1974-08-31 | 1979-01-23 | Hoechst Aktiengesellschaft | Process for the improvement of the water-absorbing capacity and the absorptivity of textile materials |
US4138459A (en) * | 1975-09-08 | 1979-02-06 | Celanese Corporation | Process for preparing a microporous polymer film |
US4144008A (en) * | 1975-03-31 | 1979-03-13 | Biax-Fiberfilm Corporation | Apparatus for stretching a tubularly-formed sheet of thermoplastic material |
US4153664A (en) * | 1976-07-30 | 1979-05-08 | Sabee Reinhardt N | Process for pattern drawing of webs |
US4153751A (en) * | 1975-03-31 | 1979-05-08 | Biax-Fiberfilm Corporation | Process for stretching an impregnated film of material and the microporous product produced thereby |
US4243802A (en) * | 1979-06-06 | 1981-01-06 | Hercules Incorporated | Surfactant-soluble cellulose derivatives |
US4251585A (en) * | 1978-05-01 | 1981-02-17 | Biax Fiberfilm Corporation | Product and process for stretching a tubularly formed sheet of orientable thermoplastic material |
US4368565A (en) * | 1978-03-28 | 1983-01-18 | Biax-Fiberfilm Corporation | Grooved roller assembly for laterally stretching film |
US4374175A (en) * | 1979-01-16 | 1983-02-15 | Japan Exlan Co., Ltd. | Novel water-swellable fibers and process for producing the same |
US4374888A (en) * | 1981-09-25 | 1983-02-22 | Kimberly-Clark Corporation | Nonwoven laminate for recreation fabric |
US4384023A (en) * | 1981-01-16 | 1983-05-17 | Mitsubishi Rayon Company, Limited | Porous polyethylene film |
US4424257A (en) * | 1981-11-12 | 1984-01-03 | Monsanto Company | Self-crimping multi-component polyamide filament wherein the components contain differing amounts of polyolefin |
US4438167A (en) * | 1979-10-15 | 1984-03-20 | Biax Fiberfilm Corporation | Novel porous fabric |
US4443513A (en) * | 1982-02-24 | 1984-04-17 | Kimberly-Clark Corporation | Soft thermoplastic fiber webs and method of making |
US4517714A (en) * | 1982-07-23 | 1985-05-21 | The Procter & Gamble Company | Nonwoven fabric barrier layer |
US4563229A (en) * | 1983-11-21 | 1986-01-07 | Prouvost S.A. | Method and means for the continuous manufacture of a flexible multi-layer compound structure of controlled perviousness |
US4590124A (en) * | 1984-05-10 | 1986-05-20 | W. R. Grace & Co., Cryovac Div. | Storm window film |
US4663220A (en) * | 1985-07-30 | 1987-05-05 | Kimberly-Clark Corporation | Polyolefin-containing extrudable compositions and methods for their formation into elastomeric products including microfibers |
US4720415A (en) * | 1985-07-30 | 1988-01-19 | Kimberly-Clark Corporation | Composite elastomeric material and process for making the same |
US4795668A (en) * | 1983-10-11 | 1989-01-03 | Minnesota Mining And Manufacturing Company | Bicomponent fibers and webs made therefrom |
US4806300A (en) * | 1985-12-09 | 1989-02-21 | Richard R. Walton | Method for softening a nonwoven web |
US4818464A (en) * | 1984-08-30 | 1989-04-04 | Kimberly-Clark Corporation | Extrusion process using a central air jet |
US4820590A (en) * | 1985-05-08 | 1989-04-11 | Exxon Chemical Patents Inc. | Oriented elastomeric film and method of manufacture |
US4833172A (en) * | 1987-04-24 | 1989-05-23 | Ppg Industries, Inc. | Stretched microporous material |
US4981747A (en) * | 1988-09-23 | 1991-01-01 | Kimberly-Clark Corporation | Composite elastic material including a reversibly necked material |
US4992124A (en) * | 1989-01-27 | 1991-02-12 | Nippon Petrochemicals Co., Ltd. | Method of making cross-laminated stretched non-woven fabric |
US4994335A (en) * | 1988-09-10 | 1991-02-19 | Ube Industries, Ltd. | Microporous film, battery separator employing the same, and method of producing them |
US5108820A (en) * | 1989-04-25 | 1992-04-28 | Mitsui Petrochemical Industries, Ltd. | Soft nonwoven fabric of filaments |
US5108827A (en) * | 1989-04-28 | 1992-04-28 | Fiberweb North America, Inc. | Strong nonwoven fabrics from engineered multiconstituent fibers |
US5116662A (en) * | 1989-12-15 | 1992-05-26 | Kimberly-Clark Corporation | Multi-direction stretch composite elastic material |
US5178931A (en) * | 1990-11-26 | 1993-01-12 | Kimberly-Clark Corporation | Three-layer nonwoven laminiferous structure |
US5204429A (en) * | 1987-08-07 | 1993-04-20 | Hoechst Aktiengesellschaft | Process for the preparation of an olefin polymer |
US5277976A (en) * | 1991-10-07 | 1994-01-11 | Minnesota Mining And Manufacturing Company | Oriented profile fibers |
US5288791A (en) * | 1990-01-10 | 1994-02-22 | Kimberly-Clark Corporation | Low stress relaxation elastomeric fibers |
US5296184A (en) * | 1990-02-12 | 1994-03-22 | Clopay Plastic Products Company, Inc. | Method of making an ultra soft cloth-like embossed plastic film having post-embossed stretched areas |
US5304599A (en) * | 1990-04-23 | 1994-04-19 | Shell Oil Company | Low stress relaxation extrudable elastomeric composition |
US5380313A (en) * | 1987-06-19 | 1995-01-10 | The Proctor & Gamble Company | Loop fastening material for fastening device and method of making same |
US5380578A (en) * | 1988-06-30 | 1995-01-10 | Arlington Fabrics Corporation | Elastic fabric having a grooved outer surface and garments made therefrom |
US5382400A (en) * | 1992-08-21 | 1995-01-17 | Kimberly-Clark Corporation | Nonwoven multicomponent polymeric fabric and method for making same |
US5395810A (en) * | 1991-09-30 | 1995-03-07 | Fina Technology, Inc. | Method of making a homogeneous-heterogenous catalyst system for olefin polymerization |
US5405887A (en) * | 1991-04-26 | 1995-04-11 | Mitsui Toatsu Chemicals, Inc. | Porous film |
US5411636A (en) * | 1993-05-21 | 1995-05-02 | Kimberly-Clark | Method for increasing the internal bulk of wet-pressed tissue |
US5498468A (en) * | 1994-09-23 | 1996-03-12 | Kimberly-Clark Corporation | Fabrics composed of ribbon-like fibrous material and method to make the same |
US5501679A (en) * | 1989-11-17 | 1996-03-26 | Minnesota Mining And Manufacturing Company | Elastomeric laminates with microtextured skin layers |
USRE35206E (en) * | 1992-03-26 | 1996-04-16 | The University Of Tennessee Research Corporation | Post-treatment of nonwoven webs |
US5514634A (en) * | 1991-11-06 | 1996-05-07 | Mobil Oil Corporation | High activity polyethylene catalysts |
US5514470A (en) * | 1988-09-23 | 1996-05-07 | Kimberly-Clark Corporation | Composite elastic necked-bonded material |
US5518801A (en) * | 1993-08-03 | 1996-05-21 | The Procter & Gamble Company | Web materials exhibiting elastic-like behavior |
US5599420A (en) * | 1993-04-06 | 1997-02-04 | Kimberly-Clark Corporation | Patterned embossed nonwoven fabric, cloth-like liquid barrier material and method for making same |
US5604036A (en) * | 1994-03-14 | 1997-02-18 | E. I. Du Pont De Nemours And Company | Hollow nylon filaments |
US5614281A (en) * | 1995-11-29 | 1997-03-25 | Kimberly-Clark Corporation | Creped nonwoven laminate loop fastening material for mechanical fastening systems |
US5624427A (en) * | 1995-01-18 | 1997-04-29 | The Procter & Gamble Company | Female component for refastenable fastening device |
US5628097A (en) * | 1995-09-29 | 1997-05-13 | The Procter & Gamble Company | Method for selectively aperturing a nonwoven web |
US5707468A (en) * | 1994-12-22 | 1998-01-13 | Kimberly-Clark Worldwide, Inc. | Compaction-free method of increasing the integrity of a nonwoven web |
US5723546A (en) * | 1997-03-24 | 1998-03-03 | Rexene Corporation | Low- and high-molecular weight amorphous polyalphaolefin polymer blends having high melt viscosity, and products thereof |
US5733628A (en) * | 1996-10-10 | 1998-03-31 | Tredegar Industries, Inc. | Breathable elastic polymeric film laminates |
US5735840A (en) * | 1996-09-20 | 1998-04-07 | The Procter & Gamble Company | Disposable diaper with integral backsheet landing zone |
US5743999A (en) * | 1993-04-12 | 1998-04-28 | Kimberly-Clark Worldwide, Inc. | Method for making soft tissue |
US5747405A (en) * | 1992-09-04 | 1998-05-05 | Bp Chemicals Limited | Catalyst compositions and process for preparing polyolefins |
US5756580A (en) * | 1994-11-21 | 1998-05-26 | Asahi Kasei Kogyo Kabushiki Kaisha | Polymeric composite material |
US5883028A (en) * | 1997-05-30 | 1999-03-16 | Kimberly-Clark Worldwide, Inc. | Breathable elastic film/nonwoven laminate |
US5885908A (en) * | 1996-10-04 | 1999-03-23 | Minnesota Mining And Manufacturing Co. | Anisotropic elastic films |
US5888607A (en) * | 1997-07-03 | 1999-03-30 | Minnesota Mining And Manufacturing Co. | Soft loop laminate and method of making |
US5900306A (en) * | 1995-05-02 | 1999-05-04 | Kimberly-Clark Worldwide, Inc. | Nonwoven-film laminates |
US6015764A (en) * | 1996-12-27 | 2000-01-18 | Kimberly-Clark Worldwide, Inc. | Microporous elastomeric film/nonwoven breathable laminate and method for making the same |
US6017832A (en) * | 1996-09-04 | 2000-01-25 | Kimberly-Clark Worldwide, Inc. | Method and composition for treating substrates for wettability |
US6028016A (en) * | 1996-09-04 | 2000-02-22 | Kimberly-Clark Worldwide, Inc. | Nonwoven Fabric Substrates Having a Durable Treatment |
US6037417A (en) * | 1998-08-18 | 2000-03-14 | Montell Technology Company Bv | Polypropylene composition useful for making solid state oriented film |
US6045900A (en) * | 1997-09-15 | 2000-04-04 | Kimberly-Clark Worldwide, Inc. | Breathable filled film laminate |
US6054002A (en) * | 1996-06-27 | 2000-04-25 | Kimberly-Clark Worldwide, Inc. | Method of making a seamless tubular band |
US6169045B1 (en) * | 1993-11-16 | 2001-01-02 | Kimberly-Clark Worldwide, Inc. | Nonwoven filter media |
US6172177B1 (en) * | 1997-12-31 | 2001-01-09 | Kimberly-Clark Worldwide, Inc. | Grafted poly(ethylene oxide) compositions |
US6174602B1 (en) * | 1996-05-14 | 2001-01-16 | Shimadzu Corporation | Spontaneously degradable fibers and goods made thereof |
US6179939B1 (en) * | 1997-05-12 | 2001-01-30 | Kimberly-Clark Worldwide, Inc. | Methods of making stretched filled microporous films |
US6194532B1 (en) * | 1991-10-15 | 2001-02-27 | The Dow Chemical Company | Elastic fibers |
US6203654B1 (en) * | 1998-02-20 | 2001-03-20 | The Procter & Gamble Company | Method of making a slitted or particulate absorbent material |
US6204208B1 (en) * | 1996-09-04 | 2001-03-20 | Kimberly-Clark Worldwide, Inc. | Method and composition for treating substrates for wettability and skin wellness |
US6214274B1 (en) * | 1999-05-14 | 2001-04-10 | Kimberly-Clark Worldwide, Inc. | Process for compressing a web which contains superabsorbent material |
US6225243B1 (en) * | 1998-08-03 | 2001-05-01 | Bba Nonwovens Simpsonville, Inc. | Elastic nonwoven fabric prepared from bi-component filaments |
US6355200B1 (en) * | 1996-05-28 | 2002-03-12 | The Procter & Gamble Company | Method for making fluid distribution materials |
US6518208B2 (en) * | 1995-06-06 | 2003-02-11 | Chisso Corporation | Continuous fiber nonwoven and the method for producing it |
US20030045844A1 (en) * | 2000-04-14 | 2003-03-06 | Taylor Jack Draper | Dimensionally stable, breathable, stretch-thinned, elastic films |
US6541403B2 (en) * | 1999-11-29 | 2003-04-01 | Aplix | Elastic core fibre and an elastic nonwoven |
US20030071391A1 (en) * | 1996-07-31 | 2003-04-17 | Kevin A. Brady | Process of adjusting wvtr of polyolefin film |
US6559195B1 (en) * | 1999-08-31 | 2003-05-06 | Nitto Denko Corporation | Microporous film |
US6706228B2 (en) * | 1998-10-16 | 2004-03-16 | Exxonmobil Chemical Company | Process for producing polyolefin microporous breathable film |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3569972B2 (en) * | 1994-08-11 | 2004-09-29 | チッソ株式会社 | Heat-fusible composite fiber and heat-fusible nonwoven fabric |
JP3389968B2 (en) * | 1997-11-26 | 2003-03-24 | 東洋紡績株式会社 | Polyester staple fiber for wet-type nonwoven fabric having latent crimp development and method for producing the same |
TW479087B (en) * | 1998-11-13 | 2002-03-11 | Kimberly Clark Co | Pulp-modified bicomponent continuous filament nonwoven webs and articles |
-
2002
- 2002-08-30 US US10/232,059 patent/US20040043214A1/en not_active Abandoned
-
2003
- 2003-07-24 AU AU2003256753A patent/AU2003256753A1/en not_active Abandoned
- 2003-07-24 WO PCT/US2003/023147 patent/WO2004020709A1/en not_active Application Discontinuation
- 2003-07-24 JP JP2004532820A patent/JP2005537403A/en active Pending
- 2003-07-24 MX MXPA05001641A patent/MXPA05001641A/en unknown
- 2003-07-24 EP EP20030791601 patent/EP1532298A1/en not_active Withdrawn
- 2003-07-24 KR KR1020057002206A patent/KR20060006759A/en not_active Application Discontinuation
- 2003-07-24 BR BR0313446A patent/BR0313446A/en not_active IP Right Cessation
- 2003-08-22 AR ARP030103046 patent/AR041041A1/en unknown
Patent Citations (99)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US518885A (en) * | 1894-04-24 | hollerith | ||
US3233029A (en) * | 1961-06-09 | 1966-02-01 | Phillips Petroleum Co | Method of cold-stretching orientable sheet material |
US3502763A (en) * | 1962-02-03 | 1970-03-24 | Freudenberg Carl Kg | Process of producing non-woven fabric fleece |
US3502538A (en) * | 1964-08-17 | 1970-03-24 | Du Pont | Bonded nonwoven sheets with a defined distribution of bond strengths |
US3383449A (en) * | 1964-10-01 | 1968-05-14 | Muller Paul Adolf | Method for producing an endless filter string |
US3802817A (en) * | 1969-10-01 | 1974-04-09 | Asahi Chemical Ind | Apparatus for producing non-woven fleeces |
US3880966A (en) * | 1971-09-23 | 1975-04-29 | Celanese Corp | Corona treated microporous film |
US3870593A (en) * | 1972-06-06 | 1975-03-11 | Minnesota Mining & Mfg | Stretch-oriented porous films and preparation and use thereof |
US4136218A (en) * | 1974-08-31 | 1979-01-23 | Hoechst Aktiengesellschaft | Process for the improvement of the water-absorbing capacity and the absorptivity of textile materials |
US4153751A (en) * | 1975-03-31 | 1979-05-08 | Biax-Fiberfilm Corporation | Process for stretching an impregnated film of material and the microporous product produced thereby |
US4144008A (en) * | 1975-03-31 | 1979-03-13 | Biax-Fiberfilm Corporation | Apparatus for stretching a tubularly-formed sheet of thermoplastic material |
US4138459A (en) * | 1975-09-08 | 1979-02-06 | Celanese Corporation | Process for preparing a microporous polymer film |
US4153664A (en) * | 1976-07-30 | 1979-05-08 | Sabee Reinhardt N | Process for pattern drawing of webs |
US4368565A (en) * | 1978-03-28 | 1983-01-18 | Biax-Fiberfilm Corporation | Grooved roller assembly for laterally stretching film |
US4251585A (en) * | 1978-05-01 | 1981-02-17 | Biax Fiberfilm Corporation | Product and process for stretching a tubularly formed sheet of orientable thermoplastic material |
US4374175A (en) * | 1979-01-16 | 1983-02-15 | Japan Exlan Co., Ltd. | Novel water-swellable fibers and process for producing the same |
US4243802A (en) * | 1979-06-06 | 1981-01-06 | Hercules Incorporated | Surfactant-soluble cellulose derivatives |
US4438167A (en) * | 1979-10-15 | 1984-03-20 | Biax Fiberfilm Corporation | Novel porous fabric |
US4384023A (en) * | 1981-01-16 | 1983-05-17 | Mitsubishi Rayon Company, Limited | Porous polyethylene film |
US4374888A (en) * | 1981-09-25 | 1983-02-22 | Kimberly-Clark Corporation | Nonwoven laminate for recreation fabric |
US4424257A (en) * | 1981-11-12 | 1984-01-03 | Monsanto Company | Self-crimping multi-component polyamide filament wherein the components contain differing amounts of polyolefin |
US4443513A (en) * | 1982-02-24 | 1984-04-17 | Kimberly-Clark Corporation | Soft thermoplastic fiber webs and method of making |
US4517714A (en) * | 1982-07-23 | 1985-05-21 | The Procter & Gamble Company | Nonwoven fabric barrier layer |
US4795668A (en) * | 1983-10-11 | 1989-01-03 | Minnesota Mining And Manufacturing Company | Bicomponent fibers and webs made therefrom |
US4563229A (en) * | 1983-11-21 | 1986-01-07 | Prouvost S.A. | Method and means for the continuous manufacture of a flexible multi-layer compound structure of controlled perviousness |
US4590124A (en) * | 1984-05-10 | 1986-05-20 | W. R. Grace & Co., Cryovac Div. | Storm window film |
US4818464A (en) * | 1984-08-30 | 1989-04-04 | Kimberly-Clark Corporation | Extrusion process using a central air jet |
US4820590A (en) * | 1985-05-08 | 1989-04-11 | Exxon Chemical Patents Inc. | Oriented elastomeric film and method of manufacture |
US4720415A (en) * | 1985-07-30 | 1988-01-19 | Kimberly-Clark Corporation | Composite elastomeric material and process for making the same |
US4663220A (en) * | 1985-07-30 | 1987-05-05 | Kimberly-Clark Corporation | Polyolefin-containing extrudable compositions and methods for their formation into elastomeric products including microfibers |
US4806300A (en) * | 1985-12-09 | 1989-02-21 | Richard R. Walton | Method for softening a nonwoven web |
US4833172A (en) * | 1987-04-24 | 1989-05-23 | Ppg Industries, Inc. | Stretched microporous material |
US5380313A (en) * | 1987-06-19 | 1995-01-10 | The Proctor & Gamble Company | Loop fastening material for fastening device and method of making same |
US5204429A (en) * | 1987-08-07 | 1993-04-20 | Hoechst Aktiengesellschaft | Process for the preparation of an olefin polymer |
US5380578A (en) * | 1988-06-30 | 1995-01-10 | Arlington Fabrics Corporation | Elastic fabric having a grooved outer surface and garments made therefrom |
US4994335A (en) * | 1988-09-10 | 1991-02-19 | Ube Industries, Ltd. | Microporous film, battery separator employing the same, and method of producing them |
US4981747A (en) * | 1988-09-23 | 1991-01-01 | Kimberly-Clark Corporation | Composite elastic material including a reversibly necked material |
US5514470A (en) * | 1988-09-23 | 1996-05-07 | Kimberly-Clark Corporation | Composite elastic necked-bonded material |
US4992124A (en) * | 1989-01-27 | 1991-02-12 | Nippon Petrochemicals Co., Ltd. | Method of making cross-laminated stretched non-woven fabric |
US5108820A (en) * | 1989-04-25 | 1992-04-28 | Mitsui Petrochemical Industries, Ltd. | Soft nonwoven fabric of filaments |
US5108827A (en) * | 1989-04-28 | 1992-04-28 | Fiberweb North America, Inc. | Strong nonwoven fabrics from engineered multiconstituent fibers |
US5294482A (en) * | 1989-04-28 | 1994-03-15 | Fiberweb North America, Inc. | Strong nonwoven fabric laminates from engineered multiconstituent fibers |
US5501679A (en) * | 1989-11-17 | 1996-03-26 | Minnesota Mining And Manufacturing Company | Elastomeric laminates with microtextured skin layers |
US5116662A (en) * | 1989-12-15 | 1992-05-26 | Kimberly-Clark Corporation | Multi-direction stretch composite elastic material |
US5288791A (en) * | 1990-01-10 | 1994-02-22 | Kimberly-Clark Corporation | Low stress relaxation elastomeric fibers |
US5296184A (en) * | 1990-02-12 | 1994-03-22 | Clopay Plastic Products Company, Inc. | Method of making an ultra soft cloth-like embossed plastic film having post-embossed stretched areas |
US5304599A (en) * | 1990-04-23 | 1994-04-19 | Shell Oil Company | Low stress relaxation extrudable elastomeric composition |
US5178931A (en) * | 1990-11-26 | 1993-01-12 | Kimberly-Clark Corporation | Three-layer nonwoven laminiferous structure |
US5405887A (en) * | 1991-04-26 | 1995-04-11 | Mitsui Toatsu Chemicals, Inc. | Porous film |
US5395810A (en) * | 1991-09-30 | 1995-03-07 | Fina Technology, Inc. | Method of making a homogeneous-heterogenous catalyst system for olefin polymerization |
US5277976A (en) * | 1991-10-07 | 1994-01-11 | Minnesota Mining And Manufacturing Company | Oriented profile fibers |
US6194532B1 (en) * | 1991-10-15 | 2001-02-27 | The Dow Chemical Company | Elastic fibers |
US5514634A (en) * | 1991-11-06 | 1996-05-07 | Mobil Oil Corporation | High activity polyethylene catalysts |
USRE35206E (en) * | 1992-03-26 | 1996-04-16 | The University Of Tennessee Research Corporation | Post-treatment of nonwoven webs |
US5418045A (en) * | 1992-08-21 | 1995-05-23 | Kimberly-Clark Corporation | Nonwoven multicomponent polymeric fabric |
US5382400A (en) * | 1992-08-21 | 1995-01-17 | Kimberly-Clark Corporation | Nonwoven multicomponent polymeric fabric and method for making same |
US5747405A (en) * | 1992-09-04 | 1998-05-05 | Bp Chemicals Limited | Catalyst compositions and process for preparing polyolefins |
US5599420A (en) * | 1993-04-06 | 1997-02-04 | Kimberly-Clark Corporation | Patterned embossed nonwoven fabric, cloth-like liquid barrier material and method for making same |
US5743999A (en) * | 1993-04-12 | 1998-04-28 | Kimberly-Clark Worldwide, Inc. | Method for making soft tissue |
US5492598A (en) * | 1993-05-21 | 1996-02-20 | Kimberly-Clark Corporation | Method for increasing the internal bulk of throughdried tissue |
US5411636A (en) * | 1993-05-21 | 1995-05-02 | Kimberly-Clark | Method for increasing the internal bulk of wet-pressed tissue |
US5518801A (en) * | 1993-08-03 | 1996-05-21 | The Procter & Gamble Company | Web materials exhibiting elastic-like behavior |
US5723087A (en) * | 1993-08-03 | 1998-03-03 | The Procter & Gamble Company | Web materials exhibiting elastic-like behavior |
US6169045B1 (en) * | 1993-11-16 | 2001-01-02 | Kimberly-Clark Worldwide, Inc. | Nonwoven filter media |
US5604036A (en) * | 1994-03-14 | 1997-02-18 | E. I. Du Pont De Nemours And Company | Hollow nylon filaments |
US5498468A (en) * | 1994-09-23 | 1996-03-12 | Kimberly-Clark Corporation | Fabrics composed of ribbon-like fibrous material and method to make the same |
US5756580A (en) * | 1994-11-21 | 1998-05-26 | Asahi Kasei Kogyo Kabushiki Kaisha | Polymeric composite material |
US5707468A (en) * | 1994-12-22 | 1998-01-13 | Kimberly-Clark Worldwide, Inc. | Compaction-free method of increasing the integrity of a nonwoven web |
US5624427A (en) * | 1995-01-18 | 1997-04-29 | The Procter & Gamble Company | Female component for refastenable fastening device |
US6190758B1 (en) * | 1995-05-02 | 2001-02-20 | Kimberly-Clark Worldwide, Inc. | Nonwoven-film laminates |
US5900306A (en) * | 1995-05-02 | 1999-05-04 | Kimberly-Clark Worldwide, Inc. | Nonwoven-film laminates |
US6518208B2 (en) * | 1995-06-06 | 2003-02-11 | Chisso Corporation | Continuous fiber nonwoven and the method for producing it |
US5628097A (en) * | 1995-09-29 | 1997-05-13 | The Procter & Gamble Company | Method for selectively aperturing a nonwoven web |
US5614281A (en) * | 1995-11-29 | 1997-03-25 | Kimberly-Clark Corporation | Creped nonwoven laminate loop fastening material for mechanical fastening systems |
US6174602B1 (en) * | 1996-05-14 | 2001-01-16 | Shimadzu Corporation | Spontaneously degradable fibers and goods made thereof |
US6355200B1 (en) * | 1996-05-28 | 2002-03-12 | The Procter & Gamble Company | Method for making fluid distribution materials |
US6054002A (en) * | 1996-06-27 | 2000-04-25 | Kimberly-Clark Worldwide, Inc. | Method of making a seamless tubular band |
US20030071391A1 (en) * | 1996-07-31 | 2003-04-17 | Kevin A. Brady | Process of adjusting wvtr of polyolefin film |
US6017832A (en) * | 1996-09-04 | 2000-01-25 | Kimberly-Clark Worldwide, Inc. | Method and composition for treating substrates for wettability |
US6028016A (en) * | 1996-09-04 | 2000-02-22 | Kimberly-Clark Worldwide, Inc. | Nonwoven Fabric Substrates Having a Durable Treatment |
US6204208B1 (en) * | 1996-09-04 | 2001-03-20 | Kimberly-Clark Worldwide, Inc. | Method and composition for treating substrates for wettability and skin wellness |
US5735840A (en) * | 1996-09-20 | 1998-04-07 | The Procter & Gamble Company | Disposable diaper with integral backsheet landing zone |
US5885908A (en) * | 1996-10-04 | 1999-03-23 | Minnesota Mining And Manufacturing Co. | Anisotropic elastic films |
US5733628A (en) * | 1996-10-10 | 1998-03-31 | Tredegar Industries, Inc. | Breathable elastic polymeric film laminates |
US6015764A (en) * | 1996-12-27 | 2000-01-18 | Kimberly-Clark Worldwide, Inc. | Microporous elastomeric film/nonwoven breathable laminate and method for making the same |
US5723546A (en) * | 1997-03-24 | 1998-03-03 | Rexene Corporation | Low- and high-molecular weight amorphous polyalphaolefin polymer blends having high melt viscosity, and products thereof |
US6179939B1 (en) * | 1997-05-12 | 2001-01-30 | Kimberly-Clark Worldwide, Inc. | Methods of making stretched filled microporous films |
US5883028A (en) * | 1997-05-30 | 1999-03-16 | Kimberly-Clark Worldwide, Inc. | Breathable elastic film/nonwoven laminate |
US5888607A (en) * | 1997-07-03 | 1999-03-30 | Minnesota Mining And Manufacturing Co. | Soft loop laminate and method of making |
US6045900A (en) * | 1997-09-15 | 2000-04-04 | Kimberly-Clark Worldwide, Inc. | Breathable filled film laminate |
US6172177B1 (en) * | 1997-12-31 | 2001-01-09 | Kimberly-Clark Worldwide, Inc. | Grafted poly(ethylene oxide) compositions |
US6203654B1 (en) * | 1998-02-20 | 2001-03-20 | The Procter & Gamble Company | Method of making a slitted or particulate absorbent material |
US6225243B1 (en) * | 1998-08-03 | 2001-05-01 | Bba Nonwovens Simpsonville, Inc. | Elastic nonwoven fabric prepared from bi-component filaments |
US6037417A (en) * | 1998-08-18 | 2000-03-14 | Montell Technology Company Bv | Polypropylene composition useful for making solid state oriented film |
US6706228B2 (en) * | 1998-10-16 | 2004-03-16 | Exxonmobil Chemical Company | Process for producing polyolefin microporous breathable film |
US6214274B1 (en) * | 1999-05-14 | 2001-04-10 | Kimberly-Clark Worldwide, Inc. | Process for compressing a web which contains superabsorbent material |
US6559195B1 (en) * | 1999-08-31 | 2003-05-06 | Nitto Denko Corporation | Microporous film |
US6541403B2 (en) * | 1999-11-29 | 2003-04-01 | Aplix | Elastic core fibre and an elastic nonwoven |
US20030045844A1 (en) * | 2000-04-14 | 2003-03-06 | Taylor Jack Draper | Dimensionally stable, breathable, stretch-thinned, elastic films |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2074975A2 (en) | 2003-12-30 | 2009-07-01 | Kimberly-Clark Worldwide, Inc. | Customizable absorbent article with extensible layers |
US7694379B2 (en) | 2005-09-30 | 2010-04-13 | First Quality Retail Services, Llc | Absorbent cleaning pad and method of making same |
US7962993B2 (en) | 2005-09-30 | 2011-06-21 | First Quality Retail Services, Llc | Surface cleaning pad having zoned absorbency and method of making same |
US8026408B2 (en) | 2005-09-30 | 2011-09-27 | First Quality Retail Services, Llc | Surface cleaning pad having zoned absorbency and method of making same |
WO2008079059A1 (en) * | 2006-12-22 | 2008-07-03 | Sca Hygiene Products Ab | Bicomponent superabsorbent fibre |
US20100003517A1 (en) * | 2006-12-22 | 2010-01-07 | Sca Hygiene Products Ab | Bicomponent superabsorbent fibre |
US8043700B2 (en) | 2006-12-22 | 2011-10-25 | Sca Hygiene Products Ab | Bicomponent superabsorbent fibre |
US20120097035A1 (en) * | 2010-10-25 | 2012-04-26 | Chapman Rick L | Filtration materials using fiber blends that contain strategically shaped fibers and/or charge control agents |
US9074301B2 (en) * | 2010-10-25 | 2015-07-07 | Rick L. Chapman | Filtration materials using fiber blends that contain strategically shaped fibers and/or charge control agents |
US10571137B2 (en) | 2010-10-25 | 2020-02-25 | Delstar Technologies, Inc. | Filtration materials using fiber blends that contain strategically shaped fibers and/or charge control agents |
US20140342629A1 (en) * | 2012-01-31 | 2014-11-20 | Kuraray Co., Ltd. | Composite fiber, method for producing polyurethane elastomer fabric, and polyurethane elastomer fabric |
Also Published As
Publication number | Publication date |
---|---|
MXPA05001641A (en) | 2005-04-25 |
WO2004020709A1 (en) | 2004-03-11 |
EP1532298A1 (en) | 2005-05-25 |
KR20060006759A (en) | 2006-01-19 |
BR0313446A (en) | 2005-07-12 |
AU2003256753A1 (en) | 2004-03-19 |
JP2005537403A (en) | 2005-12-08 |
AR041041A1 (en) | 2005-04-27 |
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