US20070231573A1 - Fire retardant and heat resistant yarns and fabrics treated for increased strength and liquid shedding - Google Patents

Fire retardant and heat resistant yarns and fabrics treated for increased strength and liquid shedding Download PDF

Info

Publication number
US20070231573A1
US20070231573A1 US11/691,248 US69124807A US2007231573A1 US 20070231573 A1 US20070231573 A1 US 20070231573A1 US 69124807 A US69124807 A US 69124807A US 2007231573 A1 US2007231573 A1 US 2007231573A1
Authority
US
United States
Prior art keywords
liquid
fire retardant
heat resistant
shedding
fabric
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/691,248
Inventor
Tyler M. Thatcher
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Chapman Thermal Products Inc
Original Assignee
Chapman Thermal Products Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chapman Thermal Products Inc filed Critical Chapman Thermal Products Inc
Priority to US11/691,248 priority Critical patent/US20070231573A1/en
Priority to EP07006546A priority patent/EP1847638B1/en
Assigned to CHAPMAN THERMAL PRODUCTS, INC. reassignment CHAPMAN THERMAL PRODUCTS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: THATCHER, TYLER M.
Publication of US20070231573A1 publication Critical patent/US20070231573A1/en
Priority to US12/627,911 priority patent/US20100071119A1/en
Priority to US14/067,089 priority patent/US9630031B2/en
Priority to US15/641,696 priority patent/US20180127903A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G3/00Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
    • D02G3/22Yarns or threads characterised by constructional features, e.g. blending, filament/fibre
    • D02G3/36Cored or coated yarns or threads
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G3/00Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
    • D02G3/44Yarns or threads characterised by the purpose for which they are designed
    • D02G3/443Heat-resistant, fireproof or flame-retardant yarns or threads
    • DTEXTILES; PAPER
    • D03WEAVING
    • D03DWOVEN FABRICS; METHODS OF WEAVING; LOOMS
    • D03D1/00Woven fabrics designed to make specified articles
    • D03D1/0035Protective fabrics
    • D03D1/0041Cut or abrasion resistant
    • DTEXTILES; PAPER
    • D03WEAVING
    • D03DWOVEN FABRICS; METHODS OF WEAVING; LOOMS
    • D03D15/00Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
    • D03D15/50Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads
    • D03D15/513Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads heat-resistant or fireproof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D06M15/277Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0002Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/12Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
    • D06N3/128Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with silicon polymers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/16Synthetic fibres, other than mineral fibres
    • D06M2101/18Synthetic fibres consisting of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/26Polymers or copolymers of unsaturated carboxylic acids or derivatives thereof
    • D06M2101/28Acrylonitrile; Methacrylonitrile
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/10Repellency against liquids
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/30Flame or heat resistance, fire retardancy properties
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2331/00Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
    • D10B2331/02Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyamides
    • D10B2331/021Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyamides aromatic polyamides, e.g. aramides
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2401/00Physical properties
    • D10B2401/06Load-responsive characteristics
    • D10B2401/063Load-responsive characteristics high strength
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2503/00Domestic or personal
    • D10B2503/06Bed linen
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2933Coated or with bond, impregnation or core

Definitions

  • the present invention is in the field of fire retardant and heat resistant yarns and fabrics. More particularly, the present invention is in the field of fire retardant and heat resistant yarns comprised of oxidized polyacrylonitrile fibers and encapsulated with a liquid-shedding and strengthening polymer, as well as fabrics and articles of manufacture made therewith.
  • Fire retardant clothing is widely used to protect persons who are exposed to fire, particularly suddenly occurring and fast burning conflagrations. These include persons in diverse fields, such as race car drivers, military personnel, and fire fighters, each of which may be exposed to deadly fires and extremely dangerous incendiary conditions. For such persons, the primary line of defense against severe burns and even death is the protective clothing worn over some or all of the body.
  • Fire retardance, heat resistance, strength and abrasion resistance all play an important role in the selection of materials used to make such fabrics. However, it is difficult to satisfy all of the foregoing desired properties. There is often a compromise between fire retardance and heat resistance, on the one hand, and strength and abrasion resistance, on the other.
  • M-aramid fabrics may protect the wearer from burns for several seconds, but becomes essentially worthless as a protective shield after it has begun to char, shrink and decompose. Once this occurs, large holes can open up through which flame and heat can pass, thus burning, or even charring, the naked skin of the person wearing the fabric.
  • Fabrics based on p-aramid are also strong and resist abrasion at room temperature but also char and shrink when exposed to flame or high temperature.
  • Flammable fabrics such as cotton, polyester, rayon, and nylon have been treated with a fire retardant finish to enhance fire retardance. While this may temporarily increase the flame retardant properties of such fabrics, typical fire retardant finishes are not permanent. Exposure of the treated fabric to UV radiation (e.g., sun light) as well as routine laundering of the fabric can greatly reduce the fire retardant properties of the fabric. The user may then have a false sense of security, thus unknowingly exposing himself to increased risk of burns. There may be no objective way to determine, short of being caught in a fiery conflagration, whether a treated garment still possesses sufficient fire retardance to offset the risks to which the wearer may be exposed.
  • UV radiation e.g., sun light
  • 4,865,906 to Smith, Jr. includes about 25-85% oxidized polyacrylonitrile fibers combined with at least two types of strengthening fibers.
  • the foregoing patents are incorporated herein by reference.
  • Some applications may require a level of tensile strength, abrasion resistance, and durability not provided by conventional fire retardant fabrics.
  • One way to improve such features is to incorporate a metallic filament, such as is disclosed in U.S. Pat. No. 6,800,367 to Hanyon et al., the disclosure of which is incorporated by reference. Including a metal filament also increases the cut resistance of the fabric. Nevertheless, adding a metallic filament may increase the ability of a fabric to transfer heat, and it does not appreciably increase the ability of the fabric to shed flammable liquids.
  • the present invention encompasses novel yarns and fabrics that include a high concentration of oxidized polyacrylonitrile (O-Pan) fibers, which maintain a high level of fire retardance and heat resistance, while also possessing improved tensile strength, abrasion resistance, durability, and the ability to shed liquids and gels.
  • the inventive yarns include O-Pan fibers, typically combined with one or more strengthening fibers, and are encapsulated by a liquid-resistant and strengthening coating, such as a silicone polymer. Encapsulating the fire retardant and heat resistant yarn with a silicone polymer increases the tensile strength, abrasion resistance, durability, and liquid and gel shedding capability of the yarn, as well as fabrics and articles made from such yarn.
  • the present invention combines the tremendous fire retardant and heat resistant characteristics of yarns made from O-Pan fibers with the strengthening and liquid and gel shedding properties imparted by a liquid resistant polymer coating.
  • Simply encapsulating the yarn of a conventional flammable fabric with a silicone polymer coating cannot yield a fabric having a flame retardance and heat resistance that is even remotely similar to the level provided by O-Pan based fabrics.
  • encapsulating aramid-based materials with a liquid-resistant and strengthening silicone polymer coating does not alter the inherent tendency of fabrics formed from such materials to char, shrink, and form holes when exposed to direct flame and/or heated to above 600° F.
  • encapsulating the yarn comprising O-Pan based fabrics with a strengthening polymer provides a much greater incremental benefit with regard to tensile strength, abrasion resistance, and durability compared to conventional fabrics which are stronger to begin with. Encapsulation of the O-Pan based yarn with a liquid-shedding polymer also greatly increases the ability of the O-Pan based fabric to shed liquids and gels, including flammable liquids and gels.
  • encapsulating the yarn of O-Pan based fabrics with a liquid-resistant and strengthening polymer reduces the tendency of such fabrics to form holes or tears while protecting the wearer from flame and heat, and it helps such fabrics to shed liquids and gels, including flammable liquids and gels that can engulf the wearer in flames if absorbed into the fabric.
  • Encapsulation of the O-Pan based yarn with a liquid-resistant and strengthening polymer coating greatly increases the range of situations where O-Pan based fabrics can provide superior protection from heat and flame as intended, even though the liquid-shedding and strengthening polymer may not itself provide any significant incremental heat or flame resistance beyond that which is already provided by the O-Pan based fabric.
  • the high level of heat and flame resistance is provided mainly or exclusively by the O-Pan based fabric.
  • the encapsulation of the O-Pan yarn comprising the fabric with a liquid-resistant and strengthening polymer coating mainly provides the auxiliary benefits of increased tensile strength, abrasion resistance, durability, and liquid and gel shedding capability (e.g., flammable liquids and gels). Nevertheless, the overall protection to the wearer against flame and heat is greatly enhanced by the auxiliary benefits imparted by encapsulating the yarn with a liquid-resistant and strengthening polymer coating, demonstrating the synergistic effect of combining O-Pan based fabrics with polymer encapsulation of the yarn comprising the fabric.
  • Additional strength and abrasion resistance can be provided by blending one or more types of strengthening fibers with the O-Pan fibers used to make the yarn.
  • Strengthening fibers do not possess the level of fire retardance and heat resistance as 0-Pan fibers but can be used to strengthened the yarn while maintaining an adequate level of fire retardance and heat resistance in the yarn.
  • Exemplary “strengthening fibers” include, but are not limited to, polybenzimidazole (PBI), polybenzoxazole (PBO), polyphenylene-2,6-benzobisoxazole (PBO), modacrilic, p-aramid, m-aramid, polyvinyl halides, wool, fire resistant polyesters, fire resistant nylons, fire resistant rayons, cotton, and melamine.
  • the oxidized polyacrylonitrile fibers and the strengthening fibers are each first preferably carded into respective strands or carded together to form a blended strand. Multiple strands may then be intertwined together to form a yarn.
  • the yarn may include strengthening filaments made from the same materials as the foregoing strengthening fibers. Even ceramic or metal filaments may be included, though they may be unnecessary in view of the greatly increased tensile strength, abrasion resistance and durability imparted by encapsulating the yarn with the liquid-shedding polymer.
  • Exemplary liquid-resistant and strengthening polymer coatings include a wide variety of curable silicone-based polymers and polysiloxanes. Such polymers are typically encapsulated over the individual yarn strands of a tensioned fabric that is drawn through a bath of shear thinned polymer resin. Thereafter, the polymer resin is cured to form the final encapsulated yarn. The process advantageously only encapsulates the yarn strands but leaves spaces between the yarn strands that are woven or knitted together so as to permit the treated fabric to breathe. In this way, the treated fabric still feels and behaves more like an ordinary fabric rather than a laminate sheet or plugged fabric.
  • the yarn is typically encapsulated with the liquid-resistant and strengthening coating after being woven or knitted into a fabric. Nevertheless, it is within the scope of the invention to encapsulate the yarn before forming it into a fabric.
  • Individual yarn strands can be encapsulated by drawing them through a bath of shear thinned polymer composition and then curing the polymer. The treated yarn strands may then be knitted, woven or otherwise joined together to form a desired fabric.
  • Examples of articles of manufacture made using the liquid-resistant polymer treated O-Pan yarns and fabrics include clothing, jump suits, gloves, socks, welding bibs, fire blankets, padding, protective head gear, linings, undergarments, bedding, drapes, and the like.
  • the yarn or fabric may be pre-treated with a fluorochemical prior to encapsulation with the shear thinned polymer coating.
  • Pre-treatment with a fluorochemical may assist in helping the polymer encapsulated yarn or fabric repel or shed liquids and gels, such as water and hydrocarbons.
  • the fluorochemical may advantageously be applied as a suspension or solution in combination with a solvent that is driven off by evaporation. Thereafter, the silicone polymer is applied to the yarn or fabric in order to encapsulate the yarn strands.
  • the fluorochemical is at least partially impregnated into the yarn.
  • the present invention encompasses fire retardant and heat resistant yarns and fabrics in which the yarn is encapsulated by a liquid-resistant and strengthening coating to yield fabrics and articles that provide better tensile strength, abrasion resistance, durability, and the ability to shed liquids and gels compared to fabrics in the absence of such yarn encapsulation. Encapsulating the individual yarn strands, rather than coating and plugging the whole fabric, not only seals the individual yarn strands in superior fashion, it also maintains breathability of the fabric.
  • a synergistic combination is obtained (i.e., the high level of fire retardance and heat resistance of the fabric, coupled with enhanced tensile strength, abrasion resistance, durability, and liquid-shedding capabilities of the encapsulation, synergistically contribute to the ability of the fabric to protect a wearer from fire and heat).
  • the failure to provide all of these features in a single fabric can greatly undermine the otherwise excellent protection from fire, i.e., the fabric will typically only protect the wearer to the extent the fabric is able to maintain its structural integrity when protection is needed most.
  • encapsulating the yarn comprising O-Pan based fabrics provides a much greater incremental benefit with regard to tensile strength, abrasion resistance, and durability compared to conventional fabrics which are stronger to begin with. Encapsulation of the O-Pan based yarn also greatly increases the ability of the O-Pan based fabric to shed liquids and gels, including flammable liquids and gels.
  • LOI Limiting Oxygen Index
  • continuous operating temperature measures the maximum temperature, or temperature range, at which a particular fabric will maintain its strength and integrity over time when exposed to constant heat of a given temperature or range. For instance, a fabric that has a continuous operating temperature of 400° F. can be exposed to temperatures of up to 400° F. for prolonged periods of time without significant degradation of fiber strength, fabric integrity, and protection of the user. In some cases, a fabric having a continuous operating temperature of 400° F. may be exposed to brief periods of heat at higher temperatures without significant degradation.
  • the presently accepted standard for continuous operating temperature in the auto racing industry rates fabrics as being “flame retardant” if they have a continuous operating temperature of between 375° F. to 600° F.
  • fire retardant refers to a fabric, felt, yarn or strand that is self extinguishing.
  • nonflammable refers to a fabric, felt, yarn or strand that will not burn.
  • Thermal Protective Performance (or “TPP”) relates to a fabric's ability to provide continuous and reliable protection to a person's skin beneath a fabric when the fabric is exposed to a direct flame or radiant heat.
  • TPP Thermal Protective Performance
  • SFI rating which is an approximation of the time it takes before a standard quantity of heat causes a second degree burn to occur.
  • SFI Rating is a measurement of the length of time it takes for someone wearing a specific fabric to suffer a second degree burn when the fabric is exposed to a standard temperature.
  • the SFI Rating is printed on a driver's suit.
  • the SFI Rating is not only dependent on the number of fabric layers in the garment, but also on the LOI, continuous operating temperature and TPP of the fabric or fabrics from which a garment is manufactured.
  • the standard SFI Ratings are as follows:
  • a secondary test for flame retardance is the after-flame test, which measures the length of time it takes for a flame retardant fabric to self extinguish after a direct flame that envelopes the fabric is removed.
  • the term “after-flame time” is the measurement of the time it takes for a fabric to self extinguish. According to SFI standards, a fabric must self extinguish in 2.0 seconds or less in order to pass and be certifiably “flame retardant”.
  • tensile strength refers to the maximum amount of stress that can be applied to a material before rupture or failure.
  • the “tear strength” is the amount of force required to tear a fabric.
  • the tensile strength of a fabric relates to how easily the fabric will tear or rip.
  • the tensile strength may also relate to the ability of the fabric to avoid becoming permanently stretched or deformed.
  • the tensile and tear strengths of a fabric should be high enough so as to prevent ripping, tearing, or permanent deformation of the garment in a manner that would significantly compromise the intended level of thermal protection of the garment.
  • abrasion resistance refers to the tendency of a fabric to resist fraying and thinning during normal wear. Although related to tensile strength, abrasion resistance also relates to other measurements of yarn strength, such as shear strength and modulus of elasticity, as well as the tightness and type of the weave or knit.
  • fiber refers to any slender, elongated structure that can be carded or otherwise formed into a thread. Fibers typically have a length of about 2 mm to about 25 mm and an aspect ratio of at least about 100:1. Examples include “staple fibers”, a term that is well-known in the textile art. The term “fiber” differs from the term “filament”, which is defined separately below and which comprises a different component of the inventive yarns.
  • read shall refer to continuous or discontinuous elongated strands formed by carding or otherwise joining together one or more different kinds of fibers.
  • filament shall refer to a thread of indefinite length, whether comprising multiple fibers or a monofilament.
  • bin shall refer to a continuous strand comprises of a multiplicity of fibers, filaments, or the like in bundled form, such as may be suitable for knitting, weaving or otherwise used to form a fabric.
  • fabric shall refer to an article of manufacture formed by knitting, weaving or otherwise joining a plurality of yarn strands together to form a multi-dimensional structure used to manufacture a wide variety of useful articles.
  • encapsulate and outer shell shall refer to the positioning or placement of a liquid-shedding polymer material around an inner core comprising a yarn strand, before or after the yarn is formed into a fabric.
  • the terms “encapsulate” and “outer shell” refer to the fact that at least some of the liquid-shedding polymer material is located on an outer perimeter of the yarn strand(s). They do not mean that some of the liquid-shedding polymer material that “encapsulates” the inner yarn core cannot also be located in interstitial spaces or pores within the inner yarn core.
  • inner core shall refer to the fire retardant and heat resistant yarn that is encapsulated by the liquid-resistant and strengthening polymer shell comprising the “outer shell”.
  • Fire retardant and heat resistant yarns according to the invention typically comprise at least one type of fire retardant and heat resistant fibers and/or filaments, preferably combined or blended with at least one type of strengthening fibers and/or filaments.
  • Fire retardant and heat resistant fibers can be carded into a thread, either alone or in combination with one or more types of strengthening fibers. Multiple threads can be twisted or braided together to form a yarn strand.
  • One or more fire retardant and heat resistant threads comprising mainly or solely fire retardant and heat resistant fibers or filament(s) can be twisted or braided together with one or more strengthening strands comprising mainly or solely strengthening fibers and/or filament(s). Because a yarn strand typically consists of multiple strands twisted or braded together, it will typically include a substantial amount of interstitial space between the individual strands, at least before being encapsulated by the liquid-shedding polymer.
  • Fabrics comprising the fire retardant and heat resistant yarns can be formed by knitting, weaving or otherwise combining multiple strands of yarn together. Any known method of forming a fabric from a yarn can be utilized to form the inventive fire retardant and heat resistant fabrics. Exemplary fire retardant and heat resistant yarns, fabrics and articles that can be improved according to the present invention are disclosed in U.S. Pat. Nos. 6,287,686, 6,358,608, 6,800,367 and 4,865,906. For purposes of disclosing fire retardant and heat resistant yarns and fabrics capable of being encapsulated according to the invention, the disclosures of the foregoing patents are incorporated by reference.
  • Exemplary fire retardant and heat resistant fibers and filaments are made from oxidized polyacrylonitrile (O-Pan).
  • O-Pan fibers or filaments within the scope of the invention may comprise any type of O-Pan having high fire retardance and heat resistance.
  • O-Pan is obtained by heating polyacrylonitrile (e.g., polyacrylonitrile fibers or filaments) in a cooking process between about 180° C. to about 3000° C. for at least about 120 minutes. This heating/oxidation process is where the polyacrylonitrile receives its initial carbonization.
  • Preferred O-Pan fibers and filaments have an LOI of about 50-65. In most cases, O-Pan made in this way may be considered to be nonflammable.
  • O-Pan fibers examples include LASTAN, manufactured by Ashia Chemical in Japan; PYROMEX, manufactured by Toho Rayon in Japan; PANOX, manufactured by SGL; and PYRON, manufactured by Zoltek. It is also within the scope of the invention to utilize filaments that comprise O-Pan.
  • fire retardant and heat resistant materials can be used in addition to, or in place of, O-Pan so long as they have fire retardant and heat resistance properties that are comparable to those of O-Pan.
  • polymers or other materials having an LOI of at least about 50 and which do not burn when exposed to heat or flame having a temperature of about 3000° F. could be used in addition to, or instead of, O-Pan.
  • the fire retardant and heat resistant yarn comprising the inner core of the overall liquid and gel shedding yarn, fabric or article may consist solely of O-Pan fibers or filaments.
  • O-Pan is preferably included in an amount in a range of about 25% to about 99.9% by weight of the inner core, more preferably in a range of about 40% to about 95% by weight, and most preferably in a range of about 50% to about 90% by weight of the inner core.
  • Strengthening fibers and filaments that may be incorporated into fire retardant and heat resistant yarns, fabrics and articles of the present invention may comprise any fiber or filament known in the art.
  • preferred strengthening fibers will be those that have a relatively high LOI and TPP compared to natural organic fibers such as cotton, although the use of such fibers is within the scope of the invention.
  • the strengthening fibers preferably have an LOI greater than about 20.
  • Strengthening fibers may be carded or otherwise formed into threads, either alone or in combination with other fibers (e.g, O-Pan fibers). Strengthening threads or filaments may be twisted, braided or otherwise combined with fire retardant and heat resistant strands to form a blended yarn.
  • Strengthening fibers and filaments within the scope of the invention include, but are not limited to, polybenzimidazole (PBI), polybenzoxazole (PBO), polyphenylene-2,6-benzobisoxazole (PBO), modacrilic, p-aramid, m-aramid, polyvinyl halides, wool, fire resistant polyesters, fire resistant nylons, fire resistant rayons, cotton, linen, and melamine.
  • PBI polybenzimidazole
  • PBO polybenzoxazole
  • PBO polyphenylene-2,6-benzobisoxazole
  • modacrilic modacrilic
  • p-aramid p-aramid
  • m-aramid polyvinyl halides
  • wool fire resistant polyesters
  • fire resistant nylons fire resistant nylons
  • fire resistant rayons cotton, linen, and melamine
  • Suitable p-aramids include KEVLAR, manufactured by DuPont; TWARON, manufactured by Twaron Products BB; and TECKNORA, manufactured by Teijin.
  • suitable m-aramids include NOMEX, manufactured by DuPont; CONEX, manufactured by Teijin; and P84, an m-aramid yarn with a multi-lobal cross-section made by a patented spinning method, manufactured by Inspec Fiber. For this reason P84 has better fire retardant properties compared to NOMEX.
  • PBO An example of a PBO is ZYLON, manufactured by Toyobo.
  • An example of a PBI fiber is CELAZOLE of PBI Performance Products, Inc.
  • An example of a melamine fiber is BASOFIL.
  • An example of a fire retardant or treated cotton is PROBAN, manufactured by Westex. Another is FIREWEAR.
  • Strengthening fibers and filaments may be incorporated in the yarns of the present invention in at least the following ways: (1) as one or more strengthening filaments twisted, wrapped, braided or otherwise joined together with threads or filaments comprising oxidized polyacrylonitrile; or (2) as fibers blended with O-Pan fibers into one or more threads.
  • strengthening fibers may be added to the inventive yarns in the form of strengthening threads comprising one or more different types of strengthening fibers, a ended thread comprising O-Pan fibers and one or more different types of strengthening fibers, or as a strengthening filament.
  • the strengthening fibers or filaments are preferably included in an amount in a range of about 0.1% to about 75% by weight of the inner core, more preferably in a range of about 5% to about 60% by weight, and most preferably in a range of about 10% to about 50% by weight of the inner core.
  • Yarns according to the invention may include one or more types of metallic or ceramic filaments in order to increase cut resistance, tensile strength and abrasion resistance.
  • Metallic filaments typically have the highest combination of tensile strength and cut resistance but also conduct heat more rapidly.
  • metals used to form high strength filaments include, but are not limited to, stainless steel, stainless steel alloys, other steel alloys, titanium, aluminum, copper, and the like.
  • high strength ceramic filaments include silicon carbide, graphite, silica, aluminum oxide, other metal oxides, and the like.
  • high strength and heat resistant ceramic filaments are set forth in U.S. Pat. Nos. 5,569,629 and 5,585,312 to TenEyck et al., which disclose ceramic filaments that include 62-85% by weight SiO 2 , 5-20% by weight Al 2 O 3 , 5-15% by weight MgO, 0.5-5% by weight TiO x , and 0-5% ZrO 2 .
  • High strength and flexible ceramic filaments based on a blend of one or oxides of Al, Zr, Ti, Si, Fe, Co, Ca, Nb, Pb, Mg, Sr, Cu, Bi and Mn are disclosed in U.S. Pat. No. 5,605,870 to Strom-Olsen et al.
  • Fiberglass filaments can also be used.
  • Strengthening filaments preferably have a diameter in a range of about 0.0001′′ to about 0.01′′, more preferably in a range of about 0.0005′′ to about 0.008′′, and most preferably in a range of about 0.001′′ to about 0.006′′.
  • Yarns containing a high concentration of oxidized polyacrylonitrile fibers that are generally too weak to be used in the manufacture of fire retardant and heat resistant fabrics can be greatly strengthened with even small percentages of one or more metallic filaments, and fabrics manufactured therefrom have been found to be surprisingly strong.
  • the fire retardant and heat resistant yarns and fabrics discussed above can be treated according to the invention by encapsulating the yarn with a liquid-shedding and strengthening polymer coating material.
  • the liquid-shedding and strengthening polymer coating yields yarns, fabrics and articles that are much better at shedding liquids and gels, such as flammable liquids and gels. In this way, thermal protection to the wearer is further increased when used to protect a wearer exposed to flammable liquids or gels.
  • polymer encapsulation significantly increases the tensile strength, abrasion resistance and durability of the first retardant and heat resistant yarns, fabrics and articles of the invention. Increasing the tensile strength, abrasion resistance and durability of a fabric or article also increases the thermal protection of the wearer by reducing the formation of holes or rips through the fabric and increasing the continuity of protection.
  • Exemplary liquid-shedding and strengthening polymer materials are disclosed in U.S. Pat. Nos. 4,666,765, 5,004,643, 5,209,965, 5,418,051, 5,856,245, 5,869,172, 5,935,637, 6,040,251, 6,071,602, 6,083,602, 6,129,978, 6,289,841, 6,312,523, 6,342,280, and 6,416,613.
  • Exemplary liquid-resistant and strengthening polymer coatings include a wide variety of curable silicone-based polymers and polysiloxanes. Such polymers are typically applied as an uncured or partially cured polymer resin and then cured (i.e., cross-linked and/or further polymerized) after encapsulating the yarn being treated.
  • the polymer resins before application typically have a viscosity in a range of about 1000 cps to about 2,000,000 cps at a shear rate of 1/10 s and a temperature of 25° C.
  • the polymer resins preferably have a viscosity in a range of about 5000 cps to about 10,000 cps at a shear rate of 1/10 s and a temperature of 25° C. In a most preferred embodiment, such polymer resins preferably contain less than about 1% by weight of volatile material.
  • the encapsulating polymers are preferably elastomeric in order to yield a generally flexible yarn, fabric or article.
  • a preferred class of liquid curable silicone polymer compositions comprises a curable mixture of the following components: (1) at least one organo-hydrosilane polymer or copolymer; (2) at least one vinyl substituted polysiloxane polymer or copolymer; (3) a platinum or platinum containing catalyst; and (4) optionally fillers and additives.
  • Typical silicone hydrides are polymethylhydrosiloxanes which are dimethyl siloxane copolymers.
  • Typical vinyl terminated siloxanes are vinyl-dimethyl terminated or vinyl substituted polydimethyl siloxanes.
  • Typical catalyst systems include solutions or complexes of chloroplatinic acid in alcohols, ethers, divinylsiloxanes, and cyclic vinyl siloxanes.
  • Particulate fillers can be included to extend and reinforce the cured polymer composition and also improve the thixotropic behavior of the uncured polymer resins.
  • Exemplary silicone polymer resins that may be used to encapsulate fire retardant and heat resistant yarns according to the invention include, but are not limited to, SILOPREN LSR 2530 and SILOPREN LSR 2540/01, which comprise a vinyl-terminated polydimethyl/siloxane with fumed silica and methylhydrogen siloxane, which are available from Mobay Chemical Co.; SILASTIC 595 LSR, a polysiloxane available from Dow Corning; SLE 5100, SLE 5110, SLE 5300, SLE 5500, and SLE 6108, which are polysiloxanes, and SLE 5106, a siloxane resin solution, all available from General Electric; KE 1917 and DI 1940-30, silicone polymers available from Shin-Etsu; LIQUID RUBBER BC-10, a silicone fluid with silicone dioxide filler and curing agents, available from SWS Silicones Corporation.
  • SILOPREN LSR 2530 and SILOPREN LSR 2540/01 which comprise
  • the foregoing silicone polymer resins are characterized as having high viscosity.
  • they In order for such polymer resins to properly encapsulate the yarn, they must typically be thinned in some manner to reduce the viscosity so as to flow around the yarn and at least partially penetrate into the interstitial spaces within the yarn. This may be accomplished in any desired manner.
  • the polymer resins are subjected to high shearing conditions, which causes them to undergo shear thinning and/or thixotropic thinning. Any suitable mixing blade, combination of blades, or other apparatus capable of applying high shear may be introduced into the vessel containing the polymer resin in order to temporarily reduce the viscosity of the resin before or during application to the yarn or fabric.
  • Such polymers are typically encapsulated over the individual yarn strands of a tensioned fabric that is drawn through a bath of shear and/or thixotropically thinned polymer resin. Thereafter, the polymer resin is cured to form the final encapsulated yarn. Curing may be carried out using heat to accelerate polymerization and/or cross-linking or the polymer resin.
  • the process advantageously only encapsulates the yarn strands but leaves spaces between the yarn strands that are woven or knitted together so as to permit the treated fabric to breathe. In this way, the treated fabric still feels and behaves more like an ordinary fabric rather than a laminate sheet or plugged fabric.
  • the silicone polymer resin is blended with a benzophenone (e.g., about 0.3-10 parts by weight of the silicone polymer), examples of which include 2,4-dihydroxybenzophenone (e.g., UVINUL 400, available from BASF), 2-hydroxy-4-methoxybenzophenone (e.g., UVINUL M-40, available from BASF), 2,2′,4,4′-tetrahydroxybenzophenone (e.g., UVINUL D-50, available from BASF), 2,2′-dihydroxy-4,4′-dimethoxybenzophenone (e.g., UVINUL D-49, available from BASF), mixed tetra-substituted benzophenones (e.g., UVINUL 49 D, available from BASF), and 2-ethylhexyl-2-cyano-3,3-diphenylacrylate (e.g., UVINUL N-539, available from BASF).
  • a benzophenone e.g., about 0.3
  • the silicone polymer resin may also be blended with an accelerator (e.g., Dow Corning 7127 accelerator, a proprietary polysiloxane material) (e.g., 5-10 parts by weight of the silicone polymer resin) just before being applied to the yarn or fabric to promote curing.
  • an accelerator e.g., Dow Corning 7127 accelerator, a proprietary polysiloxane material
  • the silicone polymer resin may further include various additives in order to impart desired properties to the yarn or fabric.
  • additives include UV absorbers, flame retardants, aluminum hydroxide, filling agents, blood repellants, flattening agents, optical reflective agents, hand altering agents, biocompatible proteins, hydrolyzed silk, and agents that affect thermal conductivity, radiation reflectivity, and/or electrical conductivity.
  • the yarn is typically encapsulated with the liquid-resistant coating after being woven or knitted into a fabric. Nevertheless, it is within the scope of the invention to encapsulate the yarn before forming it into a fabric.
  • One or more individual yarn strands can be encapsulated by drawing them through a bath of shear thinned polymer composition and then curing the polymer. The treated yarn strands may then be knitted, woven or otherwise joined together to form a desired fabric.
  • the silicone polymer coating is preferably applied to the yarn or fabric in an amount in a range of about 5% to about 200% by weight of the original yarn or fabric inner core, more preferably in an amount in a range of about 10% to about 100% by weight of the original yarn or fabric inner core.
  • Yarns and fabrics may also be advantageously pre-treated with a fluorochemical prior to being encapsulated by the silicone polymer resin in order to further increase the liquid and gel shedding properties of the yarn or fabric.
  • fluorochemical compositions include, but are not limited to, MILEASE F-14N, F-34, F-31 ⁇ and F-53 sold by ICI Americas, Inc.; PHOTOTEX FC104, FC461, FC731, FC208 AND FC232 sold by Ciba/Geigy; TEFLON polymers such as TEFLON G, NPA, SKF, UP, UPH, PPR, N and MLV, sold by DuPont; ZEPEL polymers such as ZEPEL B, D, K, RN, RC, OR, HT, 6700 AND 7040, also from DuPont; SCOTCHGUARD sold by 3M.
  • MILEASE F-14 contains approximately 18% perfluoroacrylate copolymer, 10% ethylene glycol, 7% acetone, and 65% water.
  • MILEASE F-31X is a dispersion of fluorinated resin, acetone and water.
  • ZEPEL 6700 is comprised of 15-20% perfluoroalkyl acrylic copolymer, 1-2% alkoxylated carboxylic acid, 3-5% ethylene glycol, and water, and has a pH of 2-5.
  • ZEPEL 7040 is similar to ZEPEL 6700 but further contains 7-8% acetone.
  • SCOTCHGUARD is comprised of aqueously dispersed fluorochemicals in polymeric form.
  • Liquid repellant fluorochemical compositions are saturated into the fabric or yarn to completely and uniformly wet the fabric or yarn. This may be performed by dipping the fabric or yarn in a bath of liquid composition or padding the composition onto and into the fabric or yarn.
  • the water (or other liquid carrier) and other volatile components of the composition are removed by conventional techniques to provide a treated fabric or yarn that is impregnated with the dried fluorochemical.
  • the saturated fabric or yarn is compressed to remove excess composition. It is then heated to remove the carrier liquid by evaporation (e.g., at a temperature of about 130-160° C. for a period of time about 2-5 minutes). If the fluorochemical is curable, heating may also catalyze Oz or trigger curing.
  • the fluorochemical may also contain a bonding agent in order to strengthen the bond between the fluorochemical and the yarn or fabric to which it is applied.
  • exemplary bonding agents include Mobay SILOPREN bonding agent type LSR Z 3042 and NORSIL 815 primer.
  • the fluorchemical is preferably applied in an amount in a range of about 1% to about 10% by weight of the original yarn or fabric inner core, more preferably in an amount in a range of about 2% to about 4% by weight of the original yarn or fabric inner core.
  • a fire retardant and heat resistant fabric made from a yarn having a 70:30 wt % blend of O-Pan and p-aramid, respectively, is encapsulated with a liquid shedding and strengthening silicone-based polymer as follows. First, the fabric is placed under tension. Second, the tensioned fabric is drawn through a vessel containing a silicone-based polymer resin. Third, the silicone-based polymer resin is subjected to localized shear-thinning forces produced by a rapidly spinning shearing blade adjacent to a surface of the fabric in order for the shear-thinned resin to encapsulate the yarn of the fabric and at least partially penetrate into interstitial spaces of the yarn.
  • the viscosity of the silicone-based polymer resin is sufficiently low that it does not plug the spaces between the individual yarn strands of the fabric.
  • the treated tensioned fabric is removed from the vessel containing the silicone-based polymer resin.
  • the treated fabric is heated in order to cure the silicone-based polymer resin and form the strengthening and liquid-shedding coating over the yarn.
  • the resulting fire retardant and heat resistant fabric comprising silicone polymer encapsulated yarn has increased tensile strength, abrasion resistance, durability and liquid- and gel-shedding capability compared to the fire retardant and heat resistant fabric in the absence of the silicone polymer.
  • the fabric is therefore better able to protect a person wearing the fabric when exposed to fire, heat and a flammable liquid or gel compared to the fire retardant and heat resistant fabric prior to being encapsulated with the silicone polymer by better shedding the flammable liquid or gel and resisting formation of holes through the fabric, thus providing greater continuity of fabric between the wearer's skin and the fire, heat and any remaining flammable liquid or gel. Because the silicone polymer only encapsulates the individual yarn strands comprising the fabric, but does not plug the holes or spaces between the yarn strands, the treated fabric remains porous and is able to breathe.
  • the resulting fabric is somewhat stronger and more durable than the fabric obtained in Example 1 as a result of including a blend of strengthening fibers.
  • a fire retardant and heat resistant fabric made from a yarn consisting of 100% O-Pan is treated in the manner discussed in Example 1. Even though the fabric made from 100% O-Pan is relatively weak and fragile, treatment with the silicone polymer greatly increases the tensile strength, abrasion resistance, and durability so as to be acceptable for applications for which the fabric would otherwise be unacceptable absent the encapsulation treatment.
  • This fabric is significantly stronger to begin with compared to the fabrics of Examples 1-3 as a result of include more strengthening fibers, but is less fire retardant and heat resistant.
  • This fabric is significantly stronger to begin with compared to the fabrics of Example 1 as a result of include more strengthening fibers, but is less fire retardant and heat resistant.
  • This fabric is not as strong as compared to the fabrics of Examples 1, 2, 4 and 5 as a result of including less strengthening fibers, but is more fire retardant and heat resistant as a result of including 10% PBI. Encapsulating this blend with the silicone polymer coating greatly enhances its strength.
  • This fabric is quite stronge as compared to previous examples as a result of including more and more types of strengthening fibers, but is less fire retardant and heat resistant.
  • the fire retardant and heat resistant fabrics of Examples 1-7 are pretreated with a fluorochemical prior to encapsulation with the silicone polymer.
  • the flurochemical is saturated into the fabric as a solution or suspension with a solvent. Excess flurochemical composition is removed from the saturated fabric by applying pressure. Thereafter, the flurochemical composition is heated in order to remove the solvent by evaporation and dry the flurochemical. After applying the silicone polymer according to Example 1, the flurochemical remains at least partially impregnated within the fire retardant and heat resistant fabric.
  • the flurochemical further enhances the liquid- and gel-shedding properties of the fire retardant and heat resistant fabric beyond what is provided by the silicone polymer encapsulation provided in Examples 1-7. Enhancing the liquid- and gel-shedding properties of the fire retardant and heat resistant fabric further protects a wearer of the fabric from fire and heat if doused with a flammable liquid or gel, such as gasoline.
  • Example 1-7 Various treated fire retardant and heat resistant fabrics are manufactured using any of the fabrics utilized in Examples 1-7.
  • the silicone polymer coating used to treat the fire retardant and heat resistant fabric(s) according to Examples 15-33 are set forth in Table I below.
  • the amount of silicone resin in the polymer coating is in all cases 100-parts.
  • the “mixture ratio” refers to the ratio of packaged components as supplied by the manufacturer.
  • R. Grace & Co. is a synthetic amorphous silica 4 Hydral ® 710 (Alcoa) is a hydrated aluminum oxide 5 Silopren ® LSR Z3042 (Mobay) is a silicone primer (bonding agent) mixture 6
  • Flattening Agent OK412 ® (Degussa Corp.) is a wax coated silicon dioxide 7 Nalco ® 1SJ-612 Colloidal Silica (Nalco Chemical Co.) is an aqueous solution of silica and alumina 8 Nalco ® 1SJ-612 Colloidal Alumina (Nalco Chemical Co.) is an aqueous colloidal alumina dispersion 9
  • Fluid (Dow Corning) is a 100 cps viscosity dimethylpolysiloxane 10
  • Zepel ® 7040 (DuPont) is a nonionic fluoropolymer 11 Zonyl ® UR (DuPont) is an anionic fluorosurfactant 12
  • the silicone polymer resin and other components are mixed using a Hockmayer F dispersion blade at low torque and high shear.
  • the fire retardant and heat resistant fabric is tensioned and passed through a bath containing the silicone resin composition. Localized high shear is applied to the silicone resin composition near the surface of the fabric in order to coat the yarn strands comprising the fabric at a rate of 1.0 oz/sq. yd.
  • the fabric is passed through the polymer resin composition several times to ensure thorough impregnation. After impregnation, the impregnated fabric is removed from the silicone polymer composition bath and passed through a line oven of approximately 10 yards in length, as 4-6 yards per minute, and cured at a temperature of 325-350° F.
  • the fire retardant and heat resistant fabric Prior to applying the fluorochemical composition, the fire retardant and heat resistant fabric is washed with detergent, rinsed thoroughly, and hung to air dry. Thereafter, the fabric is soaked in water and then wrung dry to retain 0.8 g water/g fabric. The fabric is then treated with a solution or suspension (e.g., a 2% solution) of the fluorochemical composition, taking into account the water already soaked into the fabric (e.g., using a 2.5% solution of the fluorochemical). The pretreated fabric is wrung through a wringer and air dried. The fabric is then heated in an oven for 1 minute at 350° F. to remove any remaining solvent and sinter the fluorochemical. The fluorochemical treated fabric is then coated with a silicone polymer composition (e.g., a composition from one of Example 15-33.
  • a silicone polymer composition e.g., a composition from one of Example 15-33.
  • the fire retardant and heat resistant fabrics treated according to the foregoing examples have increased tensile strength, abrasion resistance, durability and liquid- and gel-shedding properties compared to the fabrics prior to treating with the silicone-based polymer. Because the silicone-based polymer only encapsulates the individual yarn strands but not the pores or spaces between the overlapping yarn strands, the treated fabrics retain a level of breathability and porosity. In addition, the elastomeric properties of the silicone-based polymer allow the fabrics to retain a level of flexibility and suppleness, which helps maintain the comfort of the fabrics if worn against a person's body.
  • the fabrics can be used in the manufacture of a wide variety of clothing and other articles where high fire retardance, heat resistance, and liquid and gel shedding capabilities are desirable. Examples include, but are not limited to, clothing, jump suits, gloves, socks, welding bibs, fire blankets, padding, protective head gear, linings, undergarments, bedding, drapes, and the like.
  • the treated fabrics and articles are especially useful in the case where the wearer may be coated or doused with a flammable liquid or gel, such as a policemen or soldier hit with a Molotov cocktail or other incendiary device.

Abstract

Fire retardant and heat resistant yarns and fabrics include an inner core comprised of oxidized polyacrylonitrile encapsulated by an outer shell comprised of a liquid-resistant and strengthening polymer material. The liquid-resistant and strengthening polymer material includes one or more types of cured silicone polymer resin. A fluorchemical may be at least partially impregnated into the inner core prior to applying the liquid-resistant and strengthening polymer material in order to further enhance the liquid shedding properties of the yarns or fabric. Because the silicone polymer resin only encapsulates the yarn, but does not form a continuous coating over the whole fabric, the treated fabric is still able to breath through pores and spaces between individual yarn strands that make up the fabric. The liquid-resistant and strengthening polymer material increases the strength, abrasion resistance, durability and liquid and gel shedding capability of the fire retardant heat resistant yarn or fabric.

Description

    CROSS-REFERENCE TO RELATED APPLICATION
  • This application claims the benefit under 35 U.S.C. § 119 of U.S. provisional application Ser. No. 60/786,853, filed Mar. 29, 2006, the disclosure of which is incorporated herein in its entirety.
  • BACKGROUND OF THE INVENTION
  • 1. The Field of the Invention
  • The present invention is in the field of fire retardant and heat resistant yarns and fabrics. More particularly, the present invention is in the field of fire retardant and heat resistant yarns comprised of oxidized polyacrylonitrile fibers and encapsulated with a liquid-shedding and strengthening polymer, as well as fabrics and articles of manufacture made therewith.
  • 2. The Relevant Technology
  • Fire retardant clothing is widely used to protect persons who are exposed to fire, particularly suddenly occurring and fast burning conflagrations. These include persons in diverse fields, such as race car drivers, military personnel, and fire fighters, each of which may be exposed to deadly fires and extremely dangerous incendiary conditions. For such persons, the primary line of defense against severe burns and even death is the protective clothing worn over some or all of the body.
  • Even though fire retardant clothing presently exists, such clothing is not always adequate to reliably offset the risk of severe burns, or even death. This is particularly true in the case where a person is not only exposed to flame or high heat but splashed with a flammable hydrocarbon liquid (e.g, gasoline). This could occur, for example, in the case of a vehicle crash or by deliberate sabotage (e.g., a Molotov cocktail or other incendiary device hurled at a policeman or military personnel).
  • A wide variety of different fibers and fibrous blends have been used in the manufacture of fire and heat resistant fabrics. Fire retardance, heat resistance, strength and abrasion resistance all play an important role in the selection of materials used to make such fabrics. However, it is difficult to satisfy all of the foregoing desired properties. There is often a compromise between fire retardance and heat resistance, on the one hand, and strength and abrasion resistance, on the other.
  • Conventional fire retardant fabrics on the market typically rate very high in one, or perhaps two, of the foregoing desired properties. One example is a proprietary fabric aramid fabric sold by DuPont, which rates high in strength and abrasion resistance at room temperature but only provides protection against high temperatures and flame for a relatively short period of time. When exposed to direct flame, the leading m-aramid “fire retardant” fabric begings to shrink and char in as little as 3 seconds, and the degradation of the fabric increases as the duration of exposure increases. Ironically, it is the tendency of m-aramid fabrics to char and shrink that is purported to protect the wearer's skin from heat and flame. M-aramid fabrics may protect the wearer from burns for several seconds, but becomes essentially worthless as a protective shield after it has begun to char, shrink and decompose. Once this occurs, large holes can open up through which flame and heat can pass, thus burning, or even charring, the naked skin of the person wearing the fabric. Fabrics based on p-aramid are also strong and resist abrasion at room temperature but also char and shrink when exposed to flame or high temperature.
  • Flammable fabrics such as cotton, polyester, rayon, and nylon have been treated with a fire retardant finish to enhance fire retardance. While this may temporarily increase the flame retardant properties of such fabrics, typical fire retardant finishes are not permanent. Exposure of the treated fabric to UV radiation (e.g., sun light) as well as routine laundering of the fabric can greatly reduce the fire retardant properties of the fabric. The user may then have a false sense of security, thus unknowingly exposing himself to increased risk of burns. There may be no objective way to determine, short of being caught in a fiery conflagration, whether a treated garment still possesses sufficient fire retardance to offset the risks to which the wearer may be exposed.
  • More recently, a range of highly fire retardant and heat resistant yarns and fabrics comprised of oxidized polyacrylonitrile fibers blended with one or more strengthening fibers were developed. Yarns and fabrics made exclusively from oxidized polyacrylonitrile fibers lack adequate strength for use in many applications. Blending oxidized polyacrylonitrile fibers with one or more types of strengthening fibers yields yarns and fabrics having increased strength and flexibility. U.S. Pat. Nos. 6,287,686 and 6,358,608 to Huang et al. disclose a range of yarns and fabrics that preferably include about 85.5-99.9% by weight oxidized polyacrylonitrile fibers and about 0.1-14.5% by weight of one or more strengthening fibers. U.S. Pat. No. 4,865,906 to Smith, Jr. includes about 25-85% oxidized polyacrylonitrile fibers combined with at least two types of strengthening fibers. For purposes of teaching fire retardant and heat resistant yarns, fabrics and articles of manufacture, the foregoing patents are incorporated herein by reference.
  • Highly flame retardant and heat resistant fabrics made according to the Huang et al. patents are sold under the name CARBONX by Chapman Thermal Products, Inc., located in Salt lake City, Utah. Such fabrics are able to resist burning or charring even when exposed to a direct flame. Fabrics made according to the Huang et al. and Smith, Jr. patents are not only superior to NOMEX as far as providing fire retardance and heat resistance, they are softer, have higher breathability, and are better at absorbing sweat and moisture. CARBONX feels much like an ordinary fabric made from natural or natural feeling synthetic fibers. M-aramid fabric, in contrast, feels more like wearing a plastic sheet than a fabric since it does not breathe well, nor does it wick sweat and moisture but sheds it readily. Unfortunately, the aspect of CARBONX that makes it feel most like an ordinary fabric—its ability to absorb sweat, moisture and liquid—does not aid in shedding a flammable liquid.
  • Some applications may require a level of tensile strength, abrasion resistance, and durability not provided by conventional fire retardant fabrics. One way to improve such features is to incorporate a metallic filament, such as is disclosed in U.S. Pat. No. 6,800,367 to Hanyon et al., the disclosure of which is incorporated by reference. Including a metal filament also increases the cut resistance of the fabric. Nevertheless, adding a metallic filament may increase the ability of a fabric to transfer heat, and it does not appreciably increase the ability of the fabric to shed flammable liquids.
  • Accordingly, it would be an advancement in the art to provide fire retardant and heat resistant yarns that were able to maintain a high level of fire retardance and heat resistance while having improved tensile strength, abrasion resistance, durability, and liquid shedding capabilities.
  • BRIEF SUMMARY OF THE INVENTION
  • The present invention encompasses novel yarns and fabrics that include a high concentration of oxidized polyacrylonitrile (O-Pan) fibers, which maintain a high level of fire retardance and heat resistance, while also possessing improved tensile strength, abrasion resistance, durability, and the ability to shed liquids and gels. The inventive yarns include O-Pan fibers, typically combined with one or more strengthening fibers, and are encapsulated by a liquid-resistant and strengthening coating, such as a silicone polymer. Encapsulating the fire retardant and heat resistant yarn with a silicone polymer increases the tensile strength, abrasion resistance, durability, and liquid and gel shedding capability of the yarn, as well as fabrics and articles made from such yarn. Encapsulating the yarn, rather than coating the whole fabric, not only seals the individual yarn strands in superior fashion, it also maintains breathability of the fabric as a whole rather than forming an impermeable barrier. This greatly improves performance and comfort when worn against a person's body.
  • The present invention combines the tremendous fire retardant and heat resistant characteristics of yarns made from O-Pan fibers with the strengthening and liquid and gel shedding properties imparted by a liquid resistant polymer coating. Simply encapsulating the yarn of a conventional flammable fabric with a silicone polymer coating cannot yield a fabric having a flame retardance and heat resistance that is even remotely similar to the level provided by O-Pan based fabrics. Moreover, encapsulating aramid-based materials with a liquid-resistant and strengthening silicone polymer coating does not alter the inherent tendency of fabrics formed from such materials to char, shrink, and form holes when exposed to direct flame and/or heated to above 600° F. Only by combining the tremendous fire retardant and heat resistant properties of O-Pan based fabrics with the strengthening aspects and liquid and gel shedding capabilities offered by liquid-resistant and strengthening polymer encapsulation can true synergy be obtained (i.e., the ability to provide the highest level of fire retardance and heat resistance to a fabric, while also providing enhanced tensile strength, abrasion resistance, durability, and liquid and gel shedding capabilities, all of which synergistically contribute to the ability of the fabric to protect a wearer from fire and heat).
  • The failure to provide all of these features in a single fabric can greatly undermine the otherwise excellent protection from fire. For example, even though conventional CARBONX fabrics provide superior protection against fire, heat and burns compared to other leading fire resistant fabrics such as the leading aramid “fire retardant” fabrics, such protection can be compromised if the fabric lacks sufficient tensile strength, abrasion resistance and durability for a given application. The fabric will typically only protect the wearer to the extent the fabric is able to maintain its structural integrity when protection is needed most, i.e., a fabric designed to protect the skin advantageously remains positioned between the wearer's body and the heat source to provide maximum protection. An inadvertent hole or tear can provide a conduit through which heat and flame can breach the otherwise continuous protective shield. Because of the generally weaker nature of O-Pan based fabrics compared to conventional fabrics, encapsulating the yarn comprising O-Pan based fabrics with a strengthening polymer provides a much greater incremental benefit with regard to tensile strength, abrasion resistance, and durability compared to conventional fabrics which are stronger to begin with. Encapsulation of the O-Pan based yarn with a liquid-shedding polymer also greatly increases the ability of the O-Pan based fabric to shed liquids and gels, including flammable liquids and gels.
  • Thus, encapsulating the yarn of O-Pan based fabrics with a liquid-resistant and strengthening polymer reduces the tendency of such fabrics to form holes or tears while protecting the wearer from flame and heat, and it helps such fabrics to shed liquids and gels, including flammable liquids and gels that can engulf the wearer in flames if absorbed into the fabric. Encapsulation of the O-Pan based yarn with a liquid-resistant and strengthening polymer coating greatly increases the range of situations where O-Pan based fabrics can provide superior protection from heat and flame as intended, even though the liquid-shedding and strengthening polymer may not itself provide any significant incremental heat or flame resistance beyond that which is already provided by the O-Pan based fabric. The high level of heat and flame resistance is provided mainly or exclusively by the O-Pan based fabric. The encapsulation of the O-Pan yarn comprising the fabric with a liquid-resistant and strengthening polymer coating mainly provides the auxiliary benefits of increased tensile strength, abrasion resistance, durability, and liquid and gel shedding capability (e.g., flammable liquids and gels). Nevertheless, the overall protection to the wearer against flame and heat is greatly enhanced by the auxiliary benefits imparted by encapsulating the yarn with a liquid-resistant and strengthening polymer coating, demonstrating the synergistic effect of combining O-Pan based fabrics with polymer encapsulation of the yarn comprising the fabric.
  • Additional strength and abrasion resistance can be provided by blending one or more types of strengthening fibers with the O-Pan fibers used to make the yarn. Strengthening fibers do not possess the level of fire retardance and heat resistance as 0-Pan fibers but can be used to strengthened the yarn while maintaining an adequate level of fire retardance and heat resistance in the yarn. Exemplary “strengthening fibers” include, but are not limited to, polybenzimidazole (PBI), polybenzoxazole (PBO), polyphenylene-2,6-benzobisoxazole (PBO), modacrilic, p-aramid, m-aramid, polyvinyl halides, wool, fire resistant polyesters, fire resistant nylons, fire resistant rayons, cotton, and melamine. The oxidized polyacrylonitrile fibers and the strengthening fibers are each first preferably carded into respective strands or carded together to form a blended strand. Multiple strands may then be intertwined together to form a yarn. Alternatively, the yarn may include strengthening filaments made from the same materials as the foregoing strengthening fibers. Even ceramic or metal filaments may be included, though they may be unnecessary in view of the greatly increased tensile strength, abrasion resistance and durability imparted by encapsulating the yarn with the liquid-shedding polymer.
  • Exemplary liquid-resistant and strengthening polymer coatings include a wide variety of curable silicone-based polymers and polysiloxanes. Such polymers are typically encapsulated over the individual yarn strands of a tensioned fabric that is drawn through a bath of shear thinned polymer resin. Thereafter, the polymer resin is cured to form the final encapsulated yarn. The process advantageously only encapsulates the yarn strands but leaves spaces between the yarn strands that are woven or knitted together so as to permit the treated fabric to breathe. In this way, the treated fabric still feels and behaves more like an ordinary fabric rather than a laminate sheet or plugged fabric.
  • In general, the yarn is typically encapsulated with the liquid-resistant and strengthening coating after being woven or knitted into a fabric. Nevertheless, it is within the scope of the invention to encapsulate the yarn before forming it into a fabric. Individual yarn strands can be encapsulated by drawing them through a bath of shear thinned polymer composition and then curing the polymer. The treated yarn strands may then be knitted, woven or otherwise joined together to form a desired fabric.
  • Examples of articles of manufacture made using the liquid-resistant polymer treated O-Pan yarns and fabrics include clothing, jump suits, gloves, socks, welding bibs, fire blankets, padding, protective head gear, linings, undergarments, bedding, drapes, and the like.
  • According to one embodiment, the yarn or fabric may be pre-treated with a fluorochemical prior to encapsulation with the shear thinned polymer coating. Pre-treatment with a fluorochemical may assist in helping the polymer encapsulated yarn or fabric repel or shed liquids and gels, such as water and hydrocarbons. The fluorochemical may advantageously be applied as a suspension or solution in combination with a solvent that is driven off by evaporation. Thereafter, the silicone polymer is applied to the yarn or fabric in order to encapsulate the yarn strands. The fluorochemical is at least partially impregnated into the yarn.
  • These and other objects and features of the present invention will become more fully apparent from the following description and appended claims, or may be learned by the practice of the invention as set forth hereinafter.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS I. Introduction and Definitions.
  • The present invention encompasses fire retardant and heat resistant yarns and fabrics in which the yarn is encapsulated by a liquid-resistant and strengthening coating to yield fabrics and articles that provide better tensile strength, abrasion resistance, durability, and the ability to shed liquids and gels compared to fabrics in the absence of such yarn encapsulation. Encapsulating the individual yarn strands, rather than coating and plugging the whole fabric, not only seals the individual yarn strands in superior fashion, it also maintains breathability of the fabric.
  • By combining the tremendous fire retardant and heat resistant properties of O-Pan based fabrics with the strengthening and liquid-shedding aspects offered by encapsulation a synergistic combination is obtained (i.e., the high level of fire retardance and heat resistance of the fabric, coupled with enhanced tensile strength, abrasion resistance, durability, and liquid-shedding capabilities of the encapsulation, synergistically contribute to the ability of the fabric to protect a wearer from fire and heat). The failure to provide all of these features in a single fabric can greatly undermine the otherwise excellent protection from fire, i.e., the fabric will typically only protect the wearer to the extent the fabric is able to maintain its structural integrity when protection is needed most. Because of the generally weaker nature of O-Pan based fabrics compared to conventional fabrics, encapsulating the yarn comprising O-Pan based fabrics provides a much greater incremental benefit with regard to tensile strength, abrasion resistance, and durability compared to conventional fabrics which are stronger to begin with. Encapsulation of the O-Pan based yarn also greatly increases the ability of the O-Pan based fabric to shed liquids and gels, including flammable liquids and gels.
  • The term “Limiting Oxygen Index” (or “LOI”) is defined as the minimum concentration of oxygen necessary to support combustion of a material. The LOI is primarily a measurement of flame retardancy rather than temperature resistance. Temperature resistance is typically measured as the “continuous operating temperature”.
  • The term “continuous operating temperature” measures the maximum temperature, or temperature range, at which a particular fabric will maintain its strength and integrity over time when exposed to constant heat of a given temperature or range. For instance, a fabric that has a continuous operating temperature of 400° F. can be exposed to temperatures of up to 400° F. for prolonged periods of time without significant degradation of fiber strength, fabric integrity, and protection of the user. In some cases, a fabric having a continuous operating temperature of 400° F. may be exposed to brief periods of heat at higher temperatures without significant degradation. The presently accepted standard for continuous operating temperature in the auto racing industry rates fabrics as being “flame retardant” if they have a continuous operating temperature of between 375° F. to 600° F.
  • The term “fire retardant” refers to a fabric, felt, yarn or strand that is self extinguishing. The term “nonflammable” refers to a fabric, felt, yarn or strand that will not burn.
  • The term “Thermal Protective Performance” (or “TPP”) relates to a fabric's ability to provide continuous and reliable protection to a person's skin beneath a fabric when the fabric is exposed to a direct flame or radiant heat. The TPP measurement, which is derived from a complex mathematical formula, is often converted into an SFI rating, which is an approximation of the time it takes before a standard quantity of heat causes a second degree burn to occur.
  • The term “SFI Rating” is a measurement of the length of time it takes for someone wearing a specific fabric to suffer a second degree burn when the fabric is exposed to a standard temperature. The SFI Rating is printed on a driver's suit. The SFI Rating is not only dependent on the number of fabric layers in the garment, but also on the LOI, continuous operating temperature and TPP of the fabric or fabrics from which a garment is manufactured. The standard SFI Ratings are as follows:
  • SFI Rating Time to Second Degree Burn
    3.2A/1  3 Seconds
    3.2A/3  7 Seconds
    3.2A/5 10 Seconds
    3.2A/10 19 Seconds
    3.2A/15 30 Seconds
    3.2A/20 40 Seconds
  • A secondary test for flame retardance is the after-flame test, which measures the length of time it takes for a flame retardant fabric to self extinguish after a direct flame that envelopes the fabric is removed. The term “after-flame time” is the measurement of the time it takes for a fabric to self extinguish. According to SFI standards, a fabric must self extinguish in 2.0 seconds or less in order to pass and be certifiably “flame retardant”.
  • The term “tensile strength” refers to the maximum amount of stress that can be applied to a material before rupture or failure. The “tear strength” is the amount of force required to tear a fabric. In general, the tensile strength of a fabric relates to how easily the fabric will tear or rip. The tensile strength may also relate to the ability of the fabric to avoid becoming permanently stretched or deformed. The tensile and tear strengths of a fabric should be high enough so as to prevent ripping, tearing, or permanent deformation of the garment in a manner that would significantly compromise the intended level of thermal protection of the garment.
  • The term “abrasion resistance” refers to the tendency of a fabric to resist fraying and thinning during normal wear. Although related to tensile strength, abrasion resistance also relates to other measurements of yarn strength, such as shear strength and modulus of elasticity, as well as the tightness and type of the weave or knit.
  • The terms “fiber” and “fibers” refers to any slender, elongated structure that can be carded or otherwise formed into a thread. Fibers typically have a length of about 2 mm to about 25 mm and an aspect ratio of at least about 100:1. Examples include “staple fibers”, a term that is well-known in the textile art. The term “fiber” differs from the term “filament”, which is defined separately below and which comprises a different component of the inventive yarns.
  • The term “thread”, as used in the specification and appended claims, shall refer to continuous or discontinuous elongated strands formed by carding or otherwise joining together one or more different kinds of fibers.
  • The term “filament” shall refer to a thread of indefinite length, whether comprising multiple fibers or a monofilament.
  • The term “yarn” shall refer to a continuous strand comprises of a multiplicity of fibers, filaments, or the like in bundled form, such as may be suitable for knitting, weaving or otherwise used to form a fabric.
  • The term “fabric” shall refer to an article of manufacture formed by knitting, weaving or otherwise joining a plurality of yarn strands together to form a multi-dimensional structure used to manufacture a wide variety of useful articles.
  • The terms “encapsulate” and “outer shell” shall refer to the positioning or placement of a liquid-shedding polymer material around an inner core comprising a yarn strand, before or after the yarn is formed into a fabric. The terms “encapsulate” and “outer shell” refer to the fact that at least some of the liquid-shedding polymer material is located on an outer perimeter of the yarn strand(s). They do not mean that some of the liquid-shedding polymer material that “encapsulates” the inner yarn core cannot also be located in interstitial spaces or pores within the inner yarn core.
  • The term “inner core” shall refer to the fire retardant and heat resistant yarn that is encapsulated by the liquid-resistant and strengthening polymer shell comprising the “outer shell”.
  • II. Fire Retardant and Heat Resistant Yarns and Fabrics.
  • Fire retardant and heat resistant yarns according to the invention typically comprise at least one type of fire retardant and heat resistant fibers and/or filaments, preferably combined or blended with at least one type of strengthening fibers and/or filaments. Fire retardant and heat resistant fibers can be carded into a thread, either alone or in combination with one or more types of strengthening fibers. Multiple threads can be twisted or braided together to form a yarn strand. One or more fire retardant and heat resistant threads comprising mainly or solely fire retardant and heat resistant fibers or filament(s) can be twisted or braided together with one or more strengthening strands comprising mainly or solely strengthening fibers and/or filament(s). Because a yarn strand typically consists of multiple strands twisted or braded together, it will typically include a substantial amount of interstitial space between the individual strands, at least before being encapsulated by the liquid-shedding polymer.
  • Fabrics comprising the fire retardant and heat resistant yarns can be formed by knitting, weaving or otherwise combining multiple strands of yarn together. Any known method of forming a fabric from a yarn can be utilized to form the inventive fire retardant and heat resistant fabrics. Exemplary fire retardant and heat resistant yarns, fabrics and articles that can be improved according to the present invention are disclosed in U.S. Pat. Nos. 6,287,686, 6,358,608, 6,800,367 and 4,865,906. For purposes of disclosing fire retardant and heat resistant yarns and fabrics capable of being encapsulated according to the invention, the disclosures of the foregoing patents are incorporated by reference.
  • A. Fire Retardant and Heat Resistant Fibers and Filaments
  • Exemplary fire retardant and heat resistant fibers and filaments are made from oxidized polyacrylonitrile (O-Pan). The O-Pan fibers or filaments within the scope of the invention may comprise any type of O-Pan having high fire retardance and heat resistance. In a preferred embodiment, O-Pan is obtained by heating polyacrylonitrile (e.g., polyacrylonitrile fibers or filaments) in a cooking process between about 180° C. to about 3000° C. for at least about 120 minutes. This heating/oxidation process is where the polyacrylonitrile receives its initial carbonization. Preferred O-Pan fibers and filaments have an LOI of about 50-65. In most cases, O-Pan made in this way may be considered to be nonflammable.
  • Examples of suitable O-Pan fibers include LASTAN, manufactured by Ashia Chemical in Japan; PYROMEX, manufactured by Toho Rayon in Japan; PANOX, manufactured by SGL; and PYRON, manufactured by Zoltek. It is also within the scope of the invention to utilize filaments that comprise O-Pan.
  • In general, it is believed that fabrics which include a substantial amount of O-Pan fibers and/or filaments will resist burning, even when exposed to intense heat or flame exceeding 3000° F., because the O-Pan fibers carbonize and expand, thereby eliminating any oxygen content within the fabric necessary for combustion of the more readily combustible strengthening fibers. In this way, the O-Pan fibers or filaments provide a combustion shield that makes the less fire retardant substances in the yarn or fabric act like better fire retardant substances.
  • One of skill in the art will appreciate that other fire retardant and heat resistant materials can be used in addition to, or in place of, O-Pan so long as they have fire retardant and heat resistance properties that are comparable to those of O-Pan. By way of example, polymers or other materials having an LOI of at least about 50 and which do not burn when exposed to heat or flame having a temperature of about 3000° F. could be used in addition to, or instead of, O-Pan.
  • The fire retardant and heat resistant yarn comprising the inner core of the overall liquid and gel shedding yarn, fabric or article may consist solely of O-Pan fibers or filaments. When the O-Pan is blended with one or more strengthening fibers or filaments, O-Pan is preferably included in an amount in a range of about 25% to about 99.9% by weight of the inner core, more preferably in a range of about 40% to about 95% by weight, and most preferably in a range of about 50% to about 90% by weight of the inner core.
  • B. Strengthening Fibers and Filaments
  • Strengthening fibers and filaments that may be incorporated into fire retardant and heat resistant yarns, fabrics and articles of the present invention may comprise any fiber or filament known in the art. In general, preferred strengthening fibers will be those that have a relatively high LOI and TPP compared to natural organic fibers such as cotton, although the use of such fibers is within the scope of the invention. The strengthening fibers preferably have an LOI greater than about 20.
  • Strengthening fibers may be carded or otherwise formed into threads, either alone or in combination with other fibers (e.g, O-Pan fibers). Strengthening threads or filaments may be twisted, braided or otherwise combined with fire retardant and heat resistant strands to form a blended yarn.
  • Strengthening fibers and filaments within the scope of the invention include, but are not limited to, polybenzimidazole (PBI), polybenzoxazole (PBO), polyphenylene-2,6-benzobisoxazole (PBO), modacrilic, p-aramid, m-aramid, polyvinyl halides, wool, fire resistant polyesters, fire resistant nylons, fire resistant rayons, cotton, linen, and melamine. By way of comparison with O-Pan, which has an LOI of about 50-65, the LOI's of selected strengthening fibers are as follows:
  • PBO 68
    PBI 35–36
    modacrylic 28–32
    m-Aramid 28–36
    p-Aramid 27–36
    wool 23
    polyester 22–23
    nylon 22–23
    rayon 16–17
    cotton 16–17
  • Examples of suitable p-aramids include KEVLAR, manufactured by DuPont; TWARON, manufactured by Twaron Products BB; and TECKNORA, manufactured by Teijin. Examples of suitable m-aramids include NOMEX, manufactured by DuPont; CONEX, manufactured by Teijin; and P84, an m-aramid yarn with a multi-lobal cross-section made by a patented spinning method, manufactured by Inspec Fiber. For this reason P84 has better fire retardant properties compared to NOMEX.
  • An example of a PBO is ZYLON, manufactured by Toyobo. An example of a PBI fiber is CELAZOLE of PBI Performance Products, Inc. An example of a melamine fiber is BASOFIL. An example of a fire retardant or treated cotton is PROBAN, manufactured by Westex. Another is FIREWEAR.
  • Strengthening fibers and filaments may be incorporated in the yarns of the present invention in at least the following ways: (1) as one or more strengthening filaments twisted, wrapped, braided or otherwise joined together with threads or filaments comprising oxidized polyacrylonitrile; or (2) as fibers blended with O-Pan fibers into one or more threads.
  • In short, strengthening fibers may be added to the inventive yarns in the form of strengthening threads comprising one or more different types of strengthening fibers, a ended thread comprising O-Pan fibers and one or more different types of strengthening fibers, or as a strengthening filament. When O-Pan is blended with one or more strengthening fibers or filaments, the strengthening fibers or filaments are preferably included in an amount in a range of about 0.1% to about 75% by weight of the inner core, more preferably in a range of about 5% to about 60% by weight, and most preferably in a range of about 10% to about 50% by weight of the inner core.
  • C. Metallic and Ceramic Filaments
  • Yarns according to the invention may include one or more types of metallic or ceramic filaments in order to increase cut resistance, tensile strength and abrasion resistance. Metallic filaments typically have the highest combination of tensile strength and cut resistance but also conduct heat more rapidly. Examples of metals used to form high strength filaments include, but are not limited to, stainless steel, stainless steel alloys, other steel alloys, titanium, aluminum, copper, and the like.
  • Examples of high strength ceramic filaments include silicon carbide, graphite, silica, aluminum oxide, other metal oxides, and the like. Examples of high strength and heat resistant ceramic filaments are set forth in U.S. Pat. Nos. 5,569,629 and 5,585,312 to TenEyck et al., which disclose ceramic filaments that include 62-85% by weight SiO2, 5-20% by weight Al2O3, 5-15% by weight MgO, 0.5-5% by weight TiOx, and 0-5% ZrO2. High strength and flexible ceramic filaments based on a blend of one or oxides of Al, Zr, Ti, Si, Fe, Co, Ca, Nb, Pb, Mg, Sr, Cu, Bi and Mn are disclosed in U.S. Pat. No. 5,605,870 to Strom-Olsen et al. For purposes of disclosing high strength ceramic filaments, the foregoing patents are incorporated herein by reference. Fiberglass filaments can also be used. Strengthening filaments preferably have a diameter in a range of about 0.0001″ to about 0.01″, more preferably in a range of about 0.0005″ to about 0.008″, and most preferably in a range of about 0.001″ to about 0.006″. Yarns containing a high concentration of oxidized polyacrylonitrile fibers that are generally too weak to be used in the manufacture of fire retardant and heat resistant fabrics can be greatly strengthened with even small percentages of one or more metallic filaments, and fabrics manufactured therefrom have been found to be surprisingly strong.
  • In general, where it is desired to maximize the strength of the material, it will be preferable to maximize the volume of strengthening filaments that are added to the yarn. However, it will be appreciated that as the amount of strengthening filaments increases in the yarn, the heat resistance generally declines. As a practical matter, the fire retardant and heat resistant requirements of the resulting yarn, fabric or other fibrous blend will determine the maximum amount of strengthening filaments that can be added to the yarn.
  • III. Liquid-Shedding and Strengthened Fire Retardant and Heat Resistant Yarns and Fabrics.
  • The fire retardant and heat resistant yarns and fabrics discussed above can be treated according to the invention by encapsulating the yarn with a liquid-shedding and strengthening polymer coating material. The liquid-shedding and strengthening polymer coating yields yarns, fabrics and articles that are much better at shedding liquids and gels, such as flammable liquids and gels. In this way, thermal protection to the wearer is further increased when used to protect a wearer exposed to flammable liquids or gels. In addition, polymer encapsulation significantly increases the tensile strength, abrasion resistance and durability of the first retardant and heat resistant yarns, fabrics and articles of the invention. Increasing the tensile strength, abrasion resistance and durability of a fabric or article also increases the thermal protection of the wearer by reducing the formation of holes or rips through the fabric and increasing the continuity of protection.
  • Exemplary liquid-shedding and strengthening polymer materials, optional compositions applied to yarns in addition to the liquid-shedding and strengthening polymer materials, as well as methods for encapsulating yarns with the liquid-shedding and strengthening polymer materials, are disclosed in U.S. Pat. Nos. 4,666,765, 5,004,643, 5,209,965, 5,418,051, 5,856,245, 5,869,172, 5,935,637, 6,040,251, 6,071,602, 6,083,602, 6,129,978, 6,289,841, 6,312,523, 6,342,280, and 6,416,613. For purposes of disclosing liquid-shedding and strengthening polymer coating materials, as well as methods of applying such materials to a fabric, the disclosures of the foregoing patents are incorporated by reference.
  • Exemplary liquid-resistant and strengthening polymer coatings include a wide variety of curable silicone-based polymers and polysiloxanes. Such polymers are typically applied as an uncured or partially cured polymer resin and then cured (i.e., cross-linked and/or further polymerized) after encapsulating the yarn being treated. The polymer resins before application typically have a viscosity in a range of about 1000 cps to about 2,000,000 cps at a shear rate of 1/10 s and a temperature of 25° C. The polymer resins preferably have a viscosity in a range of about 5000 cps to about 10,000 cps at a shear rate of 1/10 s and a temperature of 25° C. In a most preferred embodiment, such polymer resins preferably contain less than about 1% by weight of volatile material. When cured, the encapsulating polymers are preferably elastomeric in order to yield a generally flexible yarn, fabric or article.
  • A preferred class of liquid curable silicone polymer compositions comprises a curable mixture of the following components: (1) at least one organo-hydrosilane polymer or copolymer; (2) at least one vinyl substituted polysiloxane polymer or copolymer; (3) a platinum or platinum containing catalyst; and (4) optionally fillers and additives.
  • Typical silicone hydrides (component 1) are polymethylhydrosiloxanes which are dimethyl siloxane copolymers. Typical vinyl terminated siloxanes are vinyl-dimethyl terminated or vinyl substituted polydimethyl siloxanes. Typical catalyst systems include solutions or complexes of chloroplatinic acid in alcohols, ethers, divinylsiloxanes, and cyclic vinyl siloxanes.
  • Particulate fillers can be included to extend and reinforce the cured polymer composition and also improve the thixotropic behavior of the uncured polymer resins.
  • Exemplary silicone polymer resins that may be used to encapsulate fire retardant and heat resistant yarns according to the invention include, but are not limited to, SILOPREN LSR 2530 and SILOPREN LSR 2540/01, which comprise a vinyl-terminated polydimethyl/siloxane with fumed silica and methylhydrogen siloxane, which are available from Mobay Chemical Co.; SILASTIC 595 LSR, a polysiloxane available from Dow Corning; SLE 5100, SLE 5110, SLE 5300, SLE 5500, and SLE 6108, which are polysiloxanes, and SLE 5106, a siloxane resin solution, all available from General Electric; KE 1917 and DI 1940-30, silicone polymers available from Shin-Etsu; LIQUID RUBBER BC-10, a silicone fluid with silicone dioxide filler and curing agents, available from SWS Silicones Corporation.
  • The foregoing silicone polymer resins are characterized as having high viscosity. In order for such polymer resins to properly encapsulate the yarn, they must typically be thinned in some manner to reduce the viscosity so as to flow around the yarn and at least partially penetrate into the interstitial spaces within the yarn. This may be accomplished in any desired manner. According to one embodiment, the polymer resins are subjected to high shearing conditions, which causes them to undergo shear thinning and/or thixotropic thinning. Any suitable mixing blade, combination of blades, or other apparatus capable of applying high shear may be introduced into the vessel containing the polymer resin in order to temporarily reduce the viscosity of the resin before or during application to the yarn or fabric.
  • Such polymers are typically encapsulated over the individual yarn strands of a tensioned fabric that is drawn through a bath of shear and/or thixotropically thinned polymer resin. Thereafter, the polymer resin is cured to form the final encapsulated yarn. Curing may be carried out using heat to accelerate polymerization and/or cross-linking or the polymer resin. The process advantageously only encapsulates the yarn strands but leaves spaces between the yarn strands that are woven or knitted together so as to permit the treated fabric to breathe. In this way, the treated fabric still feels and behaves more like an ordinary fabric rather than a laminate sheet or plugged fabric.
  • According to one embodiment, the silicone polymer resin is blended with a benzophenone (e.g., about 0.3-10 parts by weight of the silicone polymer), examples of which include 2,4-dihydroxybenzophenone (e.g., UVINUL 400, available from BASF), 2-hydroxy-4-methoxybenzophenone (e.g., UVINUL M-40, available from BASF), 2,2′,4,4′-tetrahydroxybenzophenone (e.g., UVINUL D-50, available from BASF), 2,2′-dihydroxy-4,4′-dimethoxybenzophenone (e.g., UVINUL D-49, available from BASF), mixed tetra-substituted benzophenones (e.g., UVINUL 49 D, available from BASF), and 2-ethylhexyl-2-cyano-3,3-diphenylacrylate (e.g., UVINUL N-539, available from BASF).
  • The silicone polymer resin may also be blended with an accelerator (e.g., Dow Corning 7127 accelerator, a proprietary polysiloxane material) (e.g., 5-10 parts by weight of the silicone polymer resin) just before being applied to the yarn or fabric to promote curing.
  • The silicone polymer resin may further include various additives in order to impart desired properties to the yarn or fabric. Exemplary additives include UV absorbers, flame retardants, aluminum hydroxide, filling agents, blood repellants, flattening agents, optical reflective agents, hand altering agents, biocompatible proteins, hydrolyzed silk, and agents that affect thermal conductivity, radiation reflectivity, and/or electrical conductivity.
  • In general, the yarn is typically encapsulated with the liquid-resistant coating after being woven or knitted into a fabric. Nevertheless, it is within the scope of the invention to encapsulate the yarn before forming it into a fabric. One or more individual yarn strands can be encapsulated by drawing them through a bath of shear thinned polymer composition and then curing the polymer. The treated yarn strands may then be knitted, woven or otherwise joined together to form a desired fabric.
  • The silicone polymer coating is preferably applied to the yarn or fabric in an amount in a range of about 5% to about 200% by weight of the original yarn or fabric inner core, more preferably in an amount in a range of about 10% to about 100% by weight of the original yarn or fabric inner core.
  • Yarns and fabrics may also be advantageously pre-treated with a fluorochemical prior to being encapsulated by the silicone polymer resin in order to further increase the liquid and gel shedding properties of the yarn or fabric. Exemplary fluorochemical compositions include, but are not limited to, MILEASE F-14N, F-34, F-31× and F-53 sold by ICI Americas, Inc.; PHOTOTEX FC104, FC461, FC731, FC208 AND FC232 sold by Ciba/Geigy; TEFLON polymers such as TEFLON G, NPA, SKF, UP, UPH, PPR, N and MLV, sold by DuPont; ZEPEL polymers such as ZEPEL B, D, K, RN, RC, OR, HT, 6700 AND 7040, also from DuPont; SCOTCHGUARD sold by 3M.
  • MILEASE F-14 contains approximately 18% perfluoroacrylate copolymer, 10% ethylene glycol, 7% acetone, and 65% water. MILEASE F-31X is a dispersion of fluorinated resin, acetone and water. ZEPEL 6700 is comprised of 15-20% perfluoroalkyl acrylic copolymer, 1-2% alkoxylated carboxylic acid, 3-5% ethylene glycol, and water, and has a pH of 2-5. ZEPEL 7040 is similar to ZEPEL 6700 but further contains 7-8% acetone. SCOTCHGUARD is comprised of aqueously dispersed fluorochemicals in polymeric form.
  • Liquid repellant fluorochemical compositions are saturated into the fabric or yarn to completely and uniformly wet the fabric or yarn. This may be performed by dipping the fabric or yarn in a bath of liquid composition or padding the composition onto and into the fabric or yarn. After applying the fluorochemical composition to the fabric or yarn, the water (or other liquid carrier) and other volatile components of the composition are removed by conventional techniques to provide a treated fabric or yarn that is impregnated with the dried fluorochemical. In one embodiment, the saturated fabric or yarn is compressed to remove excess composition. It is then heated to remove the carrier liquid by evaporation (e.g., at a temperature of about 130-160° C. for a period of time about 2-5 minutes). If the fluorochemical is curable, heating may also catalyze Oz or trigger curing.
  • The fluorochemical may also contain a bonding agent in order to strengthen the bond between the fluorochemical and the yarn or fabric to which it is applied. Exemplary bonding agents include Mobay SILOPREN bonding agent type LSR Z 3042 and NORSIL 815 primer.
  • When included, the fluorchemical is preferably applied in an amount in a range of about 1% to about 10% by weight of the original yarn or fabric inner core, more preferably in an amount in a range of about 2% to about 4% by weight of the original yarn or fabric inner core.
  • IV. EXAMPLES
  • The following examples are provided in order to illustrate various embodiments of the invention. Although the examples are written in present tense and are therefore hypothetical in nature, they are based on testing of a fabric comprising a 70:30 wt % blend of O-Pan and p-aramid that was coated with a proprietary silicone-based polymer coating owned by Nextec Applications Inc., based in Vista, Calif. at the request of the inventor. The examples therefore have a high degree of predictive value based on test results conducted by the inventor.
  • Example 1
  • A fire retardant and heat resistant fabric made from a yarn having a 70:30 wt % blend of O-Pan and p-aramid, respectively, is encapsulated with a liquid shedding and strengthening silicone-based polymer as follows. First, the fabric is placed under tension. Second, the tensioned fabric is drawn through a vessel containing a silicone-based polymer resin. Third, the silicone-based polymer resin is subjected to localized shear-thinning forces produced by a rapidly spinning shearing blade adjacent to a surface of the fabric in order for the shear-thinned resin to encapsulate the yarn of the fabric and at least partially penetrate into interstitial spaces of the yarn. The viscosity of the silicone-based polymer resin is sufficiently low that it does not plug the spaces between the individual yarn strands of the fabric. Fourth, the treated tensioned fabric is removed from the vessel containing the silicone-based polymer resin. Fifth, the treated fabric is heated in order to cure the silicone-based polymer resin and form the strengthening and liquid-shedding coating over the yarn.
  • The resulting fire retardant and heat resistant fabric comprising silicone polymer encapsulated yarn has increased tensile strength, abrasion resistance, durability and liquid- and gel-shedding capability compared to the fire retardant and heat resistant fabric in the absence of the silicone polymer. The fabric is therefore better able to protect a person wearing the fabric when exposed to fire, heat and a flammable liquid or gel compared to the fire retardant and heat resistant fabric prior to being encapsulated with the silicone polymer by better shedding the flammable liquid or gel and resisting formation of holes through the fabric, thus providing greater continuity of fabric between the wearer's skin and the fire, heat and any remaining flammable liquid or gel. Because the silicone polymer only encapsulates the individual yarn strands comprising the fabric, but does not plug the holes or spaces between the yarn strands, the treated fabric remains porous and is able to breathe.
  • Example 2
  • A fire retardant and heat resistant fabric made from a yarn having a 60:20:20 wt % blend of O-Pan, p-aramid, and m-aramid, respectively, is treated in the manner discussed in Example 1. The resulting fabric is somewhat stronger and more durable than the fabric obtained in Example 1 as a result of including a blend of strengthening fibers.
  • Example 3
  • A fire retardant and heat resistant fabric made from a yarn consisting of 100% O-Pan is treated in the manner discussed in Example 1. Even though the fabric made from 100% O-Pan is relatively weak and fragile, treatment with the silicone polymer greatly increases the tensile strength, abrasion resistance, and durability so as to be acceptable for applications for which the fabric would otherwise be unacceptable absent the encapsulation treatment.
  • Example 4
  • A fire retardant and heat resistant fabric made from a yarn having a 40:20:20:20 wt % blend of O-Pan, p-aramid, fire retardant wool, and PBI, respectively, is treated in the manner discussed in Example 1. This fabric is significantly stronger to begin with compared to the fabrics of Examples 1-3 as a result of include more strengthening fibers, but is less fire retardant and heat resistant.
  • Example 5
  • A fire retardant and heat resistant fabric made from a yarn having a 60:40 wt % blend of O-Pan and m-aramid, respectively, is treated in the manner discussed in Example 1. This fabric is significantly stronger to begin with compared to the fabrics of Example 1 as a result of include more strengthening fibers, but is less fire retardant and heat resistant.
  • Example 6
  • A fire retardant and heat resistant fabric made from a yarn having a 90:10 wt % blend of O-Pan and PBI, respectively, is treated in the manner discussed in Example 1. This fabric is not as strong as compared to the fabrics of Examples 1, 2, 4 and 5 as a result of including less strengthening fibers, but is more fire retardant and heat resistant as a result of including 10% PBI. Encapsulating this blend with the silicone polymer coating greatly enhances its strength.
  • Example 7
  • A fire retardant and heat resistant fabric made from a yarn having a 60:10:15:15 wt % blend of O-Pan, p-aramid, polyvinyl chloride, and m-aramid, respectively, is treated in the manner discussed in Example 1. This fabric is quite stronge as compared to previous examples as a result of including more and more types of strengthening fibers, but is less fire retardant and heat resistant.
  • Examples 8-14
  • The fire retardant and heat resistant fabrics of Examples 1-7 are pretreated with a fluorochemical prior to encapsulation with the silicone polymer. The flurochemical is saturated into the fabric as a solution or suspension with a solvent. Excess flurochemical composition is removed from the saturated fabric by applying pressure. Thereafter, the flurochemical composition is heated in order to remove the solvent by evaporation and dry the flurochemical. After applying the silicone polymer according to Example 1, the flurochemical remains at least partially impregnated within the fire retardant and heat resistant fabric.
  • The flurochemical further enhances the liquid- and gel-shedding properties of the fire retardant and heat resistant fabric beyond what is provided by the silicone polymer encapsulation provided in Examples 1-7. Enhancing the liquid- and gel-shedding properties of the fire retardant and heat resistant fabric further protects a wearer of the fabric from fire and heat if doused with a flammable liquid or gel, such as gasoline.
  • Examples 15-33
  • Various treated fire retardant and heat resistant fabrics are manufactured using any of the fabrics utilized in Examples 1-7. The silicone polymer coating used to treat the fire retardant and heat resistant fabric(s) according to Examples 15-33 are set forth in Table I below. The amount of silicone resin in the polymer coating is in all cases 100-parts. The “mixture ratio” refers to the ratio of packaged components as supplied by the manufacturer.
  • TABLE I
    Mix- Substituted
    Exam- Silicone ture Benzo- Other
    ple Resin Ratio phenone Parts Additives Part
    15 Silopren ® 1:1 Uvinul 400 5 7127 5/10
    LSR 2530 Accelerator1
    16 Silastic ® 1:1 Uvinul 400 5 Syl-off ® 50
    595 LSR 76112
    17 SLE 5100, 10:1  Uvinul 400 5 Sylox ® 23 8
    Liquid BC- 1:1
    10
    18 Silopren ® 1:1 Uvinul 400 5 Hydral ® 10
    LSR 2530 7104
    19 Silopren ® 1:1 Uvinul 400 5 Silopren ® 1
    LSR 1530 LSR Z30425
    20 SLE 5500 10:1  Uvinul 400 5
    21 Silopren ® 1:1 Uvinul 400 5
    2430
    22 SLE 5300 10:1  Uvinul 400 5
    23 SLE 5106 10:1  Uvinul 400 5
    24 Silopren ® 1:1 Uvinul 400 5 Flattening 4
    LSR 2530 Agent
    OK412 ®6
    25 Silopren ® 1:1 Uvinul 400 5 Nalco ® 50
    LSR 2530 1SJ-612
    Colloidal
    Silica7
    26 Silopren ® 1:1 Uvinul 400 5 Nalco ® 50
    LSR 2530 1SJ-612
    Colloidal
    Alumina8
    27 Silastic ® 1:1 Uvinul 400 5 200 Fluid9 7
    595 LSR
    28 Silopren ® 1:1 Uvinul 400 5
    LSR 2530
    29 Silastic ® 1:1 Uvinul 400 5 Zepel ® 3
    595 LSR 704010
    30 Silastic ® 1:1 Uvinul 400 5 Zonyl ® 1/10
    595 LSR UR11
    31 Silastic ® 1:1 Uvinul 400 5 Zonyl ® 1/10
    595 LSR FSN-10012
    32 Silopren ® 1:1 Uvinul 400 5 DLX- 5
    LSR 2530 600 ®13
    33 Silopren ® 1:1 Uvinul 400 5 TE- 5
    LSR 2530 3608 ®14
    17127 Accelerator (Dow Corning) is a polysiloxane
    2Syl-off ® (Dow Corning) is a cross-linker
    3Sylox ® 2 (W. R. Grace & Co.) is a synthetic amorphous silica
    4Hydral ® 710 (Alcoa) is a hydrated aluminum oxide
    5Silopren ® LSR Z3042 (Mobay) is a silicone primer (bonding agent) mixture
    6Flattening Agent OK412 ® (Degussa Corp.) is a wax coated silicon dioxide
    7Nalco ® 1SJ-612 Colloidal Silica (Nalco Chemical Co.) is an aqueous solution of silica and alumina
    8Nalco ® 1SJ-612 Colloidal Alumina (Nalco Chemical Co.) is an aqueous colloidal alumina dispersion
    9200 Fluid (Dow Corning) is a 100 cps viscosity dimethylpolysiloxane
    10Zepel ® 7040 (DuPont) is a nonionic fluoropolymer
    11Zonyl ® UR (DuPont) is an anionic fluorosurfactant
    12Zonyl ® FSN-100 (DuPont) is a nonionic fluorosurfactant
    13DLX-600 ® (DuPont) is a polytetrafluoroethylene micropowder
    14TE-3608 ® (DuPont) is a polytetrafluoroethylene micropowder
  • The silicone polymer resin and other components are mixed using a Hockmayer F dispersion blade at low torque and high shear. The fire retardant and heat resistant fabric is tensioned and passed through a bath containing the silicone resin composition. Localized high shear is applied to the silicone resin composition near the surface of the fabric in order to coat the yarn strands comprising the fabric at a rate of 1.0 oz/sq. yd. The fabric is passed through the polymer resin composition several times to ensure thorough impregnation. After impregnation, the impregnated fabric is removed from the silicone polymer composition bath and passed through a line oven of approximately 10 yards in length, as 4-6 yards per minute, and cured at a temperature of 325-350° F.
  • Examples 34-60
  • Various treated fire retardant and heat resistant fabrics are manufactured according to any of Examples 8-14. The fluorochemical compositions used to pretreat the fire retardant and heat resistant fabric(s) according to Examples 34-60 prior to application of the silicone resin composition (which may comprise any of the compositions of Examples 15-33 in Table I) are set forth in Table II below.
  • TABLE II
    Example Flurochemical
    34 Milease ® F-14N
    35 Milease ® F-34
    36 Milease ® F-31X
    37 Milease ® F-53
    38 Phobotex ® FC104
    39 Phobotex ® FC461
    40 Phobotex ® FC731
    41 Phobotex ® FC208
    42 Phobotex ® FC232
    43 Teflon ® G
    44 Teflon ® NPA
    45 Teflon ® SKF
    46 Teflon ® UP
    47 Teflon ® UPH
    48 Teflon ® PPR
    49 Teflon ® N
    50 Teflon ® MLV
    51 Zepel ® B
    52 Zepel ® D
    53 Zepel ® K
    54 Zepel ® RN
    55 Zepel ® RC
    56 Zepel ® OR
    57 Zepel ® HT
    58 Zepel ® 6700
    59 Zepel ® 7040
    60 Scotchguard ®
  • Prior to applying the fluorochemical composition, the fire retardant and heat resistant fabric is washed with detergent, rinsed thoroughly, and hung to air dry. Thereafter, the fabric is soaked in water and then wrung dry to retain 0.8 g water/g fabric. The fabric is then treated with a solution or suspension (e.g., a 2% solution) of the fluorochemical composition, taking into account the water already soaked into the fabric (e.g., using a 2.5% solution of the fluorochemical). The pretreated fabric is wrung through a wringer and air dried. The fabric is then heated in an oven for 1 minute at 350° F. to remove any remaining solvent and sinter the fluorochemical. The fluorochemical treated fabric is then coated with a silicone polymer composition (e.g., a composition from one of Example 15-33.
  • Example 61
  • Various treated liquid- and gel-shedding and strengthened fire retardant and heat resistant fabrics are manufactured using the fabrics disclosed in Examples 1-7, the silicone resin compositions of Examples 15-33, and the fluorochemical compositions of Examples 34-60 (i.e., a wide range of different liquid- and gel-shedding and strengthened fire retardant and heat resistant fabrics are manufactured using every possible combination of fabrics, silicone resin compositions, and fluorochemical compositions of Examples 1-7, 15-33 and 34-60, respectively).
  • The fire retardant and heat resistant fabrics treated according to the foregoing examples have increased tensile strength, abrasion resistance, durability and liquid- and gel-shedding properties compared to the fabrics prior to treating with the silicone-based polymer. Because the silicone-based polymer only encapsulates the individual yarn strands but not the pores or spaces between the overlapping yarn strands, the treated fabrics retain a level of breathability and porosity. In addition, the elastomeric properties of the silicone-based polymer allow the fabrics to retain a level of flexibility and suppleness, which helps maintain the comfort of the fabrics if worn against a person's body.
  • The fabrics can be used in the manufacture of a wide variety of clothing and other articles where high fire retardance, heat resistance, and liquid and gel shedding capabilities are desirable. Examples include, but are not limited to, clothing, jump suits, gloves, socks, welding bibs, fire blankets, padding, protective head gear, linings, undergarments, bedding, drapes, and the like. The treated fabrics and articles are especially useful in the case where the wearer may be coated or doused with a flammable liquid or gel, such as a policemen or soldier hit with a Molotov cocktail or other incendiary device.
  • The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.

Claims (21)

1. A liquid-shedding fire retardant and heat resistant yarn, comprising:
a fire retardant and heat resistant inner core comprised of:
one or more types of fire retardant and heat resistant polymer fibers and/or filaments having an LOI of at least about 50 and that do not burn when exposed to heat or flame having a temperature of about 3000° F.; and
one or more types of strengthening fibers and/or filaments; and
an outer liquid-shedding and strengthening shell encapsulating at least a portion of the inner core comprised of a liquid-resistant and strengthening polymer coating,
wherein the liquid-shedding fire retardant and heat resistant yarn has increased strength, abrasion resistance, durability and liquid shedding ability compared to a yarn consisting exclusively of the fire retardant and heat resistant inner core.
2. A liquid-shedding fire retardant and heat resistant yarn as defined in claim 1, wherein the fire retardant and heat resistant polymer fibers and/or filaments comprise oxidized polyacrylonitrile.
3. A liquid-shedding fire retardant and heat resistant yarn as defined in claim 1, wherein the fire retardant and heat resistant inner core includes oxidized polyacrylonitrile in an amount in a range of about 25% to about 99.9% by weight of the inner core.
4. A liquid-shedding fire retardant and heat resistant yarn as defined in claim 1, wherein the fire retardant and heat resistant inner core includes oxidized polyacrylonitrile in an amount in a range of about 40% to about 95% by weight of the inner core.
5. A liquid-shedding fire retardant and heat resistant yarn as defined in claim 1, wherein the fire retardant and heat resistant inner core includes oxidized polyacrylonitrile in an amount in a range of about 50% to about 90% by weight of the inner core.
6. A liquid-shedding fire retardant and heat resistant yarn as defined in claim 1, wherein the strengthening fibers and/or filaments comprise at least one of p-aramid, m-aramid, polybenzimidazole, polybenzoxazole, polyphenylene-2,6-benzobisoxazole, modacrilic, polyvinyl halide, wool, fire resistant polyester, nylon, rayon, cotton, or melamine.
7. A liquid-shedding fire retardant and heat resistant yarn as defined in claim 1, wherein the inner core comprises at least one metallic strengthening filament selected from steel, stainless steel, steel alloy, titanium, titanium alloy, aluminum, aluminum alloy, copper, or copper alloy.
8. A liquid-shedding fire retardant and heat resistant yarn as defined in claim 1, wherein the inner core further comprises at least one ceramic strengthening filament selected from silicon carbide, graphite, or a high strength ceramic that includes at least one oxide of Al, Zr, Ti, Si, Fe, Co, Ca, Nb, Pb, Mg, Sr, Cu, Bi, or Mn.
9. A liquid-shedding fire retardant and heat resistant yarn as defined in claim 1, wherein the liquid-resistant and strengthening polymer coating comprises at least one type of cured silicone polymer resin.
10. A liquid-shedding fire retardant and heat resistant yarn as defined in claim 1, further comprising at least one fluorochemical at least partially impregnated within the inner core that further imparts liquid shedding capability to the liquid-shedding fire retardant and heat resistant yarn.
11. A liquid-shedding fire retardant and heat resistant yarn as defined in claim 1, wherein the yarn also has flammable gel shedding ability.
12. A liquid shedding fire retardant and heat resistant fabric comprising:
a plurality of liquid shedding fire retardant and heat resistant yarns (according to claim 1 that have been woven, knitted, or otherwise joined together into a fabric.
13. A liquid shedding fire retardant and heat resistant article of manufacture formed from the liquid shedding fire retardant and heat resistant fabric according to claim 11.
14. A liquid shedding fire retardant and heat resistant article of manufacture as defined in claim 12, wherein the article of manufacture is selected from the group consisting of clothing, jump suit, glove, sock, welding bib, fire blanket, padding, protective head gear, lining, undergarment, bedding, and drape.
15. A liquid-shedding fire retardant and heat resistant yarn, comprising:
a fire retardant and heat resistant inner core comprised of polyacrylonitrile fibers and/or filaments;
at least one fluorochemical at least partially impregnated within the inner core; and
an outer liquid-shedding and strengthening shell encapsulating at least a portion of the inner core comprised of a liquid-resistant and strengthening silicone polymer coating,
wherein the liquid-shedding fire retardant and heat resistant yarn has increased strength, abrasion resistance, durability and liquid shedding ability compared to a yarn consisting exclusively of the fire retardant and heat resistant inner core.
16. A liquid shedding fire retardant and heat resistant yarn as defined in claim 15, the fire retardant and heat resistant inner core further comprising one or more types of strengthening fibers and/or filaments selected from the group consisting of p-aramid, m-aramid, polybenzimidazole, polybenzoxazole, polyphenylene-2,6-benzobisoxazole, modacrilic, polyvinyl halide, wool, fire resistant polyester, nylon, rayon, cotton, and melamine.
17. A liquid-shedding fire retardant and heat resistant fabric, comprising:
a plurality of liquid-shedding fire retardant and heat resistant yarn strands woven, knitted or otherwise joined together to form the fabric, wherein the fire retardant and heat resistant yarn strands are comprised of polyacrylonitrile fibers and/or filaments, wherein the fabric includes spaces between the yarn strands; and
a liquid-shedding and strengthening shell encapsulating at least a portion of the yarn strands, wherein the liquid-shedding and strengthening shell is comprised of a liquid-resistant and strengthening polymer coating that is applied so that the fabric maintains spaces between the yarn strands and remains porous and breathable,
wherein the liquid-shedding fire retardant and heat resistant fabric has increased strength, abrasion resistance, durability and liquid shedding ability compared to a fabric consisting exclusively of the fire retardant and heat resistant yarn strands.
18. A liquid shedding fire retardant and heat resistant fabric as defined in claim 17, the fire retardant and heat resistant yarn strands further comprising one or more types of strengthening fibers and/or filaments selected from the group consisting of p-aramid, m-aramid, polybenzimidazole, polybenzoxazole, polyphenylene-2,6-benzobisoxazole, modacrilic, polyvinyl halide, wool, fire resistant polyester, nylon, rayon, cotton, and melamine.
19. A liquid-shedding fire retardant and heat resistant fabric as defined in claim 17, wherein the liquid-resistant and strengthening polymer coating comprises at least one type of cured silicone polymer resin.
20. A liquid-shedding fire retardant and heat resistant fabric as defined in claim 17, further comprising at least one fluorochemical at least partially impregnated within the fire retardant and heat resistant yarn strands that further imparts liquid shedding capability to the liquid-shedding fire retardant and heat resistant yarn strands.
21. A liquid shedding fire retardant and heat resistant fabric as defined in claim 17, wherein the fabric forms at least part of an article of manufacture selected from the group consisting of clothing, jump suit, glove, sock, welding bib, fire blanket, padding, protective head gear, lining, undergarment, bedding, and drape.
US11/691,248 2006-03-29 2007-03-26 Fire retardant and heat resistant yarns and fabrics treated for increased strength and liquid shedding Abandoned US20070231573A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US11/691,248 US20070231573A1 (en) 2006-03-29 2007-03-26 Fire retardant and heat resistant yarns and fabrics treated for increased strength and liquid shedding
EP07006546A EP1847638B1 (en) 2006-03-29 2007-03-29 Fire retardant and heat resistant yarns and fabrics treated for increased strength and liquid shedding
US12/627,911 US20100071119A1 (en) 2006-03-29 2009-11-30 Yarns and fabrics that shed liquids, gels, sparks and molten metals and methods of manufacture and use
US14/067,089 US9630031B2 (en) 2006-03-29 2013-10-30 Lightweight protective fabrics and clothing for protection against hot or corrosive materials
US15/641,696 US20180127903A1 (en) 2006-03-29 2017-07-05 Breathable Fire Resistant Fabrics

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US78685306P 2006-03-29 2006-03-29
US11/691,248 US20070231573A1 (en) 2006-03-29 2007-03-26 Fire retardant and heat resistant yarns and fabrics treated for increased strength and liquid shedding

Related Child Applications (3)

Application Number Title Priority Date Filing Date
US12/627,911 Continuation-In-Part US20100071119A1 (en) 2006-03-29 2009-11-30 Yarns and fabrics that shed liquids, gels, sparks and molten metals and methods of manufacture and use
PCT/US2010/057854 Continuation-In-Part WO2011066308A2 (en) 2006-03-29 2010-11-23 Method of protecting a person from hot high heat capacity materials and hot corrosive materials
US14/067,089 Continuation-In-Part US9630031B2 (en) 2006-03-29 2013-10-30 Lightweight protective fabrics and clothing for protection against hot or corrosive materials

Publications (1)

Publication Number Publication Date
US20070231573A1 true US20070231573A1 (en) 2007-10-04

Family

ID=38255202

Family Applications (1)

Application Number Title Priority Date Filing Date
US11/691,248 Abandoned US20070231573A1 (en) 2006-03-29 2007-03-26 Fire retardant and heat resistant yarns and fabrics treated for increased strength and liquid shedding

Country Status (2)

Country Link
US (1) US20070231573A1 (en)
EP (1) EP1847638B1 (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090181588A1 (en) * 2008-01-15 2009-07-16 Brookwood Companies, Inc. Breathable, Fire Resistant Fabric Having Liquid Barrier and Water-Repellant Properties
US20100071119A1 (en) * 2006-03-29 2010-03-25 Chapman Therman Products, Inc. Yarns and fabrics that shed liquids, gels, sparks and molten metals and methods of manufacture and use
US20100223717A1 (en) * 2009-03-05 2010-09-09 Davis Llp Fire resistant materials and methods for making same
US20100316822A1 (en) * 2009-06-12 2010-12-16 Malloy Cassie M Textile sleeve with high temperature abrasion resistant coating and methods of assembly, construction and curing thereof
WO2011050257A2 (en) * 2009-10-23 2011-04-28 Invista Technologies S.A R.L. Blended fiber yarns and fabrics including oxidized polymeric fibers
WO2011056467A2 (en) * 2009-10-28 2011-05-12 Invista Technologies S.A.R.L. Nylon -- cotton fabric having high durability and breathability
US20130045358A1 (en) * 2009-09-11 2013-02-21 Cte Pty Ltd Protective coating composition
US20150165745A1 (en) * 2012-07-19 2015-06-18 Daewoo International Corporation Method for manufacturing synthetic leather using different liquid silicone rubber coating solutions
US20160076845A1 (en) * 2014-09-16 2016-03-17 Gian Almazan Temperature reduction protective wrap
US9630031B2 (en) 2006-03-29 2017-04-25 Chapman Thermal Products, Inc. Lightweight protective fabrics and clothing for protection against hot or corrosive materials
US20170291331A1 (en) * 2016-04-11 2017-10-12 Soon Kie JUNG Method for producing synthetic leather and synthetic leather produced by the same
US10036135B2 (en) 2015-10-23 2018-07-31 Philip S. Dunlap Methods and systems to contain pollution and hazardous environments (CPHE)
US10094052B1 (en) 2009-08-26 2018-10-09 National Safety Apparel, Inc. Fire retardant material and method of making the same

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1398314B1 (en) * 2010-02-23 2013-02-22 I S O P R A M S N C Di Sergio E Fulvio Alberico SAFETY FABRIC, PARTICULARLY USABLE IN AIRCRAFT AND IN GENERAL VEHICLES.
IT1398313B1 (en) * 2010-02-23 2013-02-22 Textil Plast S R L COVER STRUCTURE, PARTICULARLY FOR AIRCRAFT AND VEHICLES IN GENERAL.
FR2975710B1 (en) * 2011-05-23 2013-05-31 Mdb Texinov Sa TRICOTE TEXTILE STRUCTURE BASED ON SILICONE
RU2565185C2 (en) * 2014-02-21 2015-10-20 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Саратовский государственный технический университет имени Гагарина Ю.А." (СГТУ имени Гагарина Ю.А.) Composition for fire-proof finishing of polyacrylonitrile fibres
TWI551229B (en) * 2015-03-04 2016-10-01 Ching-Hui Tsai Suspension structure of fire pants
WO2020100066A1 (en) * 2018-11-14 2020-05-22 3M Innovative Properties Company Flame-resistant nonwoven fabric
CN113039065A (en) * 2018-11-14 2021-06-25 3M创新有限公司 Flame retardant nonwoven fiber assembly
CN109629060B (en) * 2019-01-10 2021-01-15 军事科学院系统工程研究院军需工程技术研究所 High-strength flame-retardant anti-dripping wear-resistant anti-static blending wrapping core-spun yarn and preparation method thereof
US20230295844A1 (en) * 2022-03-18 2023-09-21 Federal-Mogul Powertrain Llc Flexible, high temperature resistant, fluid resistant, abrasion resistant, multilayered wrappable textile sleeve and method of construction thereof

Citations (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2673823A (en) * 1949-08-26 1954-03-30 Owens Corning Fiberglass Corp Method of producing vapor permeable fluid impermeable fabric and product
US2759900A (en) * 1954-12-23 1956-08-21 Eastman Kodak Co Textile coating compositions containing polyacrylates with carboxyalkyl ethers
US3265529A (en) * 1962-11-20 1966-08-09 Eastman Kodak Co Breathable fabric with a layer of water-sweliable elastomer
US3326713A (en) * 1964-01-29 1967-06-20 Burlington Industries Inc Breathable and waterproof coated fabric and process of making same
US4181769A (en) * 1976-06-17 1980-01-01 Rohm And Haas Company Heteropolymer acrylic latices and textiles treated therewith
US4287261A (en) * 1978-09-25 1981-09-01 Reeves Brothers, Inc. Fabric coating process and product thereof
US4293611A (en) * 1979-10-22 1981-10-06 Sws Silicones Corporation Silicone polyether copolymers
US4297265A (en) * 1979-11-23 1981-10-27 Otto Fabric, Inc. Silicone rubber coating material having reduced surface tension
US4478895A (en) * 1982-08-11 1984-10-23 Toray Silicone Co., Ltd. Method of manufacture of silicone elastomer coated cloth
US4540617A (en) * 1984-08-22 1985-09-10 Teikoku Sen-I Co., Ltd. Fabric articles having a flame-resistant coating on at least one surface thereof
US4548859A (en) * 1984-10-12 1985-10-22 The Boeing Company Breather material and method of coating fabric with silicone rubber
US4666765A (en) * 1985-10-02 1987-05-19 Caldwell James M Silicone coated fabric
US4678681A (en) * 1984-10-05 1987-07-07 Hiraoka & Co. Ltd. Process for preparation of water-proof sheets
US4778544A (en) * 1985-05-06 1988-10-18 Bulrington Industries, Inc. Low toxic navy board facing
US4865906A (en) * 1988-01-22 1989-09-12 Smith Novis W Jr Flame retardant yard blend
US4943475A (en) * 1986-07-23 1990-07-24 Membrane Technology & Research, Inc. Multilayer composite protective fabric material and use in protective clothing
US4994317A (en) * 1988-12-21 1991-02-19 Springs Industries, Inc. Flame durable fire barrier fabric
US5004643A (en) * 1988-03-14 1991-04-02 Sili-Tex, Inc. Silicone polymer-internally coated webs
US5091243A (en) * 1989-04-04 1992-02-25 Springs Industries, Inc. Fire barrier fabric
US5209965A (en) * 1988-03-14 1993-05-11 Sili-Tex, Inc. Internally coated webs
US5242744A (en) * 1991-10-11 1993-09-07 General Electric Company Silicone flame retardants for thermoplastics
US5279878A (en) * 1990-03-23 1994-01-18 Carl Freudenberg Flame barrier made of nonwoven fabric
US5292575A (en) * 1990-08-21 1994-03-08 Aerospatiale Societe Nationale Industrielle Sheet material for constructing high performance thermal screens
US5322727A (en) * 1992-10-21 1994-06-21 Alliedsignal Inc. Plasma spray masking tape
US5401566A (en) * 1993-08-26 1995-03-28 Wacker Silicones Corporation Coated fabrics for air bags
US5506043A (en) * 1989-08-18 1996-04-09 Norfab Corporation Thermal protective fabric and core-spun heat resistant yarn for making the same, said yarns consisting essentially of a fiberglass core and a cover of modacrylic fibers and at least one other flame retardant fiber
US5569348A (en) * 1994-03-30 1996-10-29 Kufner Textilwerk Gmbh Method for the raster-pattern coating of fabrics with hot melt adhesive
US5607758A (en) * 1995-06-21 1997-03-04 Bgf Industries, Inc. Smoke containment curtain
US5856245A (en) * 1988-03-14 1999-01-05 Nextec Applications, Inc. Articles of barrier webs
US5869172A (en) * 1988-03-14 1999-02-09 Nextec Applications, Inc. Internally-coated porous webs with controlled positioning of modifiers therein
US5935637A (en) * 1989-03-10 1999-08-10 Nextec Applications, Inc. Method of feedback control for the placement of a polymer composition into a web
US6040251A (en) * 1988-03-14 2000-03-21 Nextec Applications Inc. Garments of barrier webs
US6071602A (en) * 1995-06-07 2000-06-06 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US6083602A (en) * 1988-03-14 2000-07-04 Nextec Applications, Inc. Incontinent garments
US6129978A (en) * 1988-03-14 2000-10-10 Nextec Applications, Inc. Porous webs having a polymer composition controllably placed therein
US20010006865A1 (en) * 1999-01-22 2001-07-05 Frisby Technologies, Inc. Gel-coated materials with incereased flame retardancy
US6287686B1 (en) * 2000-05-31 2001-09-11 Chapman Thermal Products, Inc. Fire retardant and heat resistant yarns and fabrics made therefrom
US6312523B1 (en) * 1988-03-14 2001-11-06 Nextec Applications, Inc. Apparatus of feedback control for the placement of a polymer composition into a web
US6342280B1 (en) * 1998-06-23 2002-01-29 Nextec Applications, Inc. Products of and methods for improving adhesion between substrate and polymer layers
US6416613B1 (en) * 1998-06-23 2002-07-09 Nextec Applications, Inc. Products of and method for improving adhesion between substrate and polymer layers
US20020182967A1 (en) * 2001-03-21 2002-12-05 Tex Tech Industries Inc. Fire blocking fabric
US6670291B1 (en) * 2000-10-18 2003-12-30 3M Innovative Properties Company Laminate sheet material for fire barrier applications
US20040018787A1 (en) * 1996-08-07 2004-01-29 Hi-Tex, Inc. Treated textile fabric
US20050255772A1 (en) * 2004-05-17 2005-11-17 Fung Duncan C Composite fabric/silicone structure
US7087300B2 (en) * 2002-04-25 2006-08-08 Chapman Thermal Products, Inc. Fire retardant and heat resistant yarns and fabrics incorporating metallic or other high strength filaments
US20080096001A1 (en) * 2004-08-04 2008-04-24 Lightex Limited Breathable Fabric
US20100071119A1 (en) * 2006-03-29 2010-03-25 Chapman Therman Products, Inc. Yarns and fabrics that shed liquids, gels, sparks and molten metals and methods of manufacture and use
US20110145984A1 (en) * 2009-11-30 2011-06-23 Chapman Thermal Products, Inc. Methods of protecting a person from hot high heat capacity materials and hot corrosive material

Patent Citations (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2673823A (en) * 1949-08-26 1954-03-30 Owens Corning Fiberglass Corp Method of producing vapor permeable fluid impermeable fabric and product
US2759900A (en) * 1954-12-23 1956-08-21 Eastman Kodak Co Textile coating compositions containing polyacrylates with carboxyalkyl ethers
US3265529A (en) * 1962-11-20 1966-08-09 Eastman Kodak Co Breathable fabric with a layer of water-sweliable elastomer
US3326713A (en) * 1964-01-29 1967-06-20 Burlington Industries Inc Breathable and waterproof coated fabric and process of making same
US4181769A (en) * 1976-06-17 1980-01-01 Rohm And Haas Company Heteropolymer acrylic latices and textiles treated therewith
US4287261A (en) * 1978-09-25 1981-09-01 Reeves Brothers, Inc. Fabric coating process and product thereof
US4293611A (en) * 1979-10-22 1981-10-06 Sws Silicones Corporation Silicone polyether copolymers
US4297265A (en) * 1979-11-23 1981-10-27 Otto Fabric, Inc. Silicone rubber coating material having reduced surface tension
US4478895A (en) * 1982-08-11 1984-10-23 Toray Silicone Co., Ltd. Method of manufacture of silicone elastomer coated cloth
US4540617A (en) * 1984-08-22 1985-09-10 Teikoku Sen-I Co., Ltd. Fabric articles having a flame-resistant coating on at least one surface thereof
US4678681A (en) * 1984-10-05 1987-07-07 Hiraoka & Co. Ltd. Process for preparation of water-proof sheets
US4548859A (en) * 1984-10-12 1985-10-22 The Boeing Company Breather material and method of coating fabric with silicone rubber
US4778544A (en) * 1985-05-06 1988-10-18 Bulrington Industries, Inc. Low toxic navy board facing
US4666765A (en) * 1985-10-02 1987-05-19 Caldwell James M Silicone coated fabric
US4943475A (en) * 1986-07-23 1990-07-24 Membrane Technology & Research, Inc. Multilayer composite protective fabric material and use in protective clothing
US4865906A (en) * 1988-01-22 1989-09-12 Smith Novis W Jr Flame retardant yard blend
US6312523B1 (en) * 1988-03-14 2001-11-06 Nextec Applications, Inc. Apparatus of feedback control for the placement of a polymer composition into a web
US5856245A (en) * 1988-03-14 1999-01-05 Nextec Applications, Inc. Articles of barrier webs
US6040251A (en) * 1988-03-14 2000-03-21 Nextec Applications Inc. Garments of barrier webs
US5209965A (en) * 1988-03-14 1993-05-11 Sili-Tex, Inc. Internally coated webs
US5869172A (en) * 1988-03-14 1999-02-09 Nextec Applications, Inc. Internally-coated porous webs with controlled positioning of modifiers therein
US5004643A (en) * 1988-03-14 1991-04-02 Sili-Tex, Inc. Silicone polymer-internally coated webs
US6129978A (en) * 1988-03-14 2000-10-10 Nextec Applications, Inc. Porous webs having a polymer composition controllably placed therein
US5418051A (en) * 1988-03-14 1995-05-23 Fabric Coating Corporation Internally coated webs
US6083602A (en) * 1988-03-14 2000-07-04 Nextec Applications, Inc. Incontinent garments
US4994317A (en) * 1988-12-21 1991-02-19 Springs Industries, Inc. Flame durable fire barrier fabric
US6289841B1 (en) * 1989-03-10 2001-09-18 Nextec Applications, Inc. Method and apparatus for controlled placement of a polymer composition into a web
US5935637A (en) * 1989-03-10 1999-08-10 Nextec Applications, Inc. Method of feedback control for the placement of a polymer composition into a web
US5091243A (en) * 1989-04-04 1992-02-25 Springs Industries, Inc. Fire barrier fabric
US5506043A (en) * 1989-08-18 1996-04-09 Norfab Corporation Thermal protective fabric and core-spun heat resistant yarn for making the same, said yarns consisting essentially of a fiberglass core and a cover of modacrylic fibers and at least one other flame retardant fiber
US5279878A (en) * 1990-03-23 1994-01-18 Carl Freudenberg Flame barrier made of nonwoven fabric
US5292575A (en) * 1990-08-21 1994-03-08 Aerospatiale Societe Nationale Industrielle Sheet material for constructing high performance thermal screens
US5242744A (en) * 1991-10-11 1993-09-07 General Electric Company Silicone flame retardants for thermoplastics
US5322727A (en) * 1992-10-21 1994-06-21 Alliedsignal Inc. Plasma spray masking tape
US5401566A (en) * 1993-08-26 1995-03-28 Wacker Silicones Corporation Coated fabrics for air bags
US5569348A (en) * 1994-03-30 1996-10-29 Kufner Textilwerk Gmbh Method for the raster-pattern coating of fabrics with hot melt adhesive
US6071602A (en) * 1995-06-07 2000-06-06 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5607758A (en) * 1995-06-21 1997-03-04 Bgf Industries, Inc. Smoke containment curtain
US20040018787A1 (en) * 1996-08-07 2004-01-29 Hi-Tex, Inc. Treated textile fabric
US6342280B1 (en) * 1998-06-23 2002-01-29 Nextec Applications, Inc. Products of and methods for improving adhesion between substrate and polymer layers
US6416613B1 (en) * 1998-06-23 2002-07-09 Nextec Applications, Inc. Products of and method for improving adhesion between substrate and polymer layers
US20010006865A1 (en) * 1999-01-22 2001-07-05 Frisby Technologies, Inc. Gel-coated materials with incereased flame retardancy
US6287686B1 (en) * 2000-05-31 2001-09-11 Chapman Thermal Products, Inc. Fire retardant and heat resistant yarns and fabrics made therefrom
US6670291B1 (en) * 2000-10-18 2003-12-30 3M Innovative Properties Company Laminate sheet material for fire barrier applications
US20020182967A1 (en) * 2001-03-21 2002-12-05 Tex Tech Industries Inc. Fire blocking fabric
US7087300B2 (en) * 2002-04-25 2006-08-08 Chapman Thermal Products, Inc. Fire retardant and heat resistant yarns and fabrics incorporating metallic or other high strength filaments
US20050255772A1 (en) * 2004-05-17 2005-11-17 Fung Duncan C Composite fabric/silicone structure
US20080096001A1 (en) * 2004-08-04 2008-04-24 Lightex Limited Breathable Fabric
US20100071119A1 (en) * 2006-03-29 2010-03-25 Chapman Therman Products, Inc. Yarns and fabrics that shed liquids, gels, sparks and molten metals and methods of manufacture and use
US20110145984A1 (en) * 2009-11-30 2011-06-23 Chapman Thermal Products, Inc. Methods of protecting a person from hot high heat capacity materials and hot corrosive material

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Dixit, B.. "Performance of Protective Clothing: Development and Testingof Asbestos substitutes,"" Performance of Protective Clothing. ASTM STP 900, R. L.Barker and G. C. Colette, Eds., American Society for Testing and Materials, Philadelphia, 1986. pp. 446-460 *

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100071119A1 (en) * 2006-03-29 2010-03-25 Chapman Therman Products, Inc. Yarns and fabrics that shed liquids, gels, sparks and molten metals and methods of manufacture and use
US9630031B2 (en) 2006-03-29 2017-04-25 Chapman Thermal Products, Inc. Lightweight protective fabrics and clothing for protection against hot or corrosive materials
US7666802B2 (en) 2008-01-15 2010-02-23 Brookwood Companies, Inc. Breathable, fire resistant fabric having liquid barrier and water-repellant properties
US20090181588A1 (en) * 2008-01-15 2009-07-16 Brookwood Companies, Inc. Breathable, Fire Resistant Fabric Having Liquid Barrier and Water-Repellant Properties
US20100223717A1 (en) * 2009-03-05 2010-09-09 Davis Llp Fire resistant materials and methods for making same
US20100316822A1 (en) * 2009-06-12 2010-12-16 Malloy Cassie M Textile sleeve with high temperature abrasion resistant coating and methods of assembly, construction and curing thereof
US10094052B1 (en) 2009-08-26 2018-10-09 National Safety Apparel, Inc. Fire retardant material and method of making the same
US20130045358A1 (en) * 2009-09-11 2013-02-21 Cte Pty Ltd Protective coating composition
US20110104466A1 (en) * 2009-10-23 2011-05-05 Invista North America S.A R.L. Blended fiber yarns and fabrics including oxidized polymeric fibers
WO2011050257A2 (en) * 2009-10-23 2011-04-28 Invista Technologies S.A R.L. Blended fiber yarns and fabrics including oxidized polymeric fibers
US11261546B2 (en) 2009-10-23 2022-03-01 National Safety Apparel, Inc. Blended fiber yarns and fabrics including oxidized polymeric fibers
CN102656303A (en) * 2009-10-23 2012-09-05 英威达技术有限公司 Blended fiber yarns and fabrics including oxidized polymeric fibers
WO2011050257A3 (en) * 2009-10-23 2011-09-15 Invista Technologies S.A R.L. Blended fiber yarns and fabrics including oxidized polymeric fibers
TWI486494B (en) * 2009-10-23 2015-06-01 Invista Tech Sarl Blended fiber yarns and fabrics including oxidized polymeric fibers
RU2552248C2 (en) * 2009-10-23 2015-06-10 Инвиста Текнолоджиз С.А Р.Л. Yarn and fabrics of fibre mixture containing oxidized polymer fibres
US10240263B2 (en) 2009-10-23 2019-03-26 National Safety Apparel, Inc. Blended fiber yarns and fabrics including oxidized polymeric fibers
WO2011056467A2 (en) * 2009-10-28 2011-05-12 Invista Technologies S.A.R.L. Nylon -- cotton fabric having high durability and breathability
WO2011056467A3 (en) * 2009-10-28 2011-09-22 Invista Technologies S.A.R.L. Nylon -- cotton fabric having high durability and breathability
WO2011066308A3 (en) * 2009-11-30 2011-10-06 Chapman Thermal Products, Inc. Method of protecting a person from hot high heat capacity materials and hot corrosive materials
US9925752B2 (en) * 2012-07-19 2018-03-27 Jeongsan International Co., Ltd Method for manufacturing synthetic leather using different liquid silicone rubber coating solutions
US20150165745A1 (en) * 2012-07-19 2015-06-18 Daewoo International Corporation Method for manufacturing synthetic leather using different liquid silicone rubber coating solutions
US10024619B2 (en) * 2014-09-16 2018-07-17 Gian Almazan Temperature reduction protective wrap
US20160076845A1 (en) * 2014-09-16 2016-03-17 Gian Almazan Temperature reduction protective wrap
US10036135B2 (en) 2015-10-23 2018-07-31 Philip S. Dunlap Methods and systems to contain pollution and hazardous environments (CPHE)
US20170291331A1 (en) * 2016-04-11 2017-10-12 Soon Kie JUNG Method for producing synthetic leather and synthetic leather produced by the same
US10456958B2 (en) * 2016-04-11 2019-10-29 Soon Kie JUNG Method for producing synthetic leather and synthetic leather produced by the same

Also Published As

Publication number Publication date
EP1847638B1 (en) 2013-02-20
EP1847638A2 (en) 2007-10-24
EP1847638A3 (en) 2009-03-25

Similar Documents

Publication Publication Date Title
EP1847638B1 (en) Fire retardant and heat resistant yarns and fabrics treated for increased strength and liquid shedding
US20100071119A1 (en) Yarns and fabrics that shed liquids, gels, sparks and molten metals and methods of manufacture and use
US9630031B2 (en) Lightweight protective fabrics and clothing for protection against hot or corrosive materials
CA2410619C (en) Fire retardant and heat resistant yarns and fabrics made therefrom
EP3231906B1 (en) Flame resistant garment and fabric
CA2478417C (en) Fire retardant and heat resistant yarns and fabrics incorporating metallic or other high strength filaments
US20180127903A1 (en) Breathable Fire Resistant Fabrics
US20090209155A1 (en) Layered thermally-insulating fabric with thin heat reflective and heat distributing core
US8793814B1 (en) Flame resistant fabric made from a fiber blend
JP7128365B2 (en) flame retardant fabric
KR20130131382A (en) Flame resistant fabric for protective clothing
ES2382121T3 (en) Flame resistant mixtures.
JP6464044B2 (en) Laminated fabric and textile products
US20110145984A1 (en) Methods of protecting a person from hot high heat capacity materials and hot corrosive material
RU2705605C2 (en) Fire-resistant fabric
JP6595224B2 (en) Fabrics and textile products
US20060201128A1 (en) Fireproof composite yarn comprising three types of fibers
JP2023504513A (en) Flame-retardant fibers formed from long staple yarns and filament yarns

Legal Events

Date Code Title Description
AS Assignment

Owner name: CHAPMAN THERMAL PRODUCTS, INC., UTAH

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:THATCHER, TYLER M.;REEL/FRAME:019276/0687

Effective date: 20070508

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION