WO1989008553A1 - Bandes fibreuses avec encapsulation de polymere de silicone - Google Patents

Bandes fibreuses avec encapsulation de polymere de silicone Download PDF

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Publication number
WO1989008553A1
WO1989008553A1 PCT/US1989/001006 US8901006W WO8908553A1 WO 1989008553 A1 WO1989008553 A1 WO 1989008553A1 US 8901006 W US8901006 W US 8901006W WO 8908553 A1 WO8908553 A1 WO 8908553A1
Authority
WO
WIPO (PCT)
Prior art keywords
web
silicone polymer
fibers
fabric
fluorochemical
Prior art date
Application number
PCT/US1989/001006
Other languages
English (en)
Inventor
James Michael Caldwell
Original Assignee
Sili-Tex, 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
Priority claimed from US07/319,778 external-priority patent/US5004643A/en
Application filed by Sili-Tex, Inc. filed Critical Sili-Tex, Inc.
Priority to KR1019890702108A priority Critical patent/KR970002936B1/ko
Publication of WO1989008553A1 publication Critical patent/WO1989008553A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/51—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
    • A61F13/514—Backsheet, i.e. the impermeable cover or layer furthest from the skin
    • A61F13/51456—Backsheet, i.e. the impermeable cover or layer furthest from the skin characterised by its properties
    • A61F13/51458—Backsheet, i.e. the impermeable cover or layer furthest from the skin characterised by its properties being air-pervious or breathable
    • A61F13/51462—Backsheet, i.e. the impermeable cover or layer furthest from the skin characterised by its properties being air-pervious or breathable being defined by a value or parameter
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A61F13/01—Non-adhesive bandages or dressings
    • A61F13/01008—Non-adhesive bandages or dressings characterised by the material
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/51—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
    • A61F13/514—Backsheet, i.e. the impermeable cover or layer furthest from the skin
    • A61F13/51401—Backsheet, i.e. the impermeable cover or layer furthest from the skin characterised by the material
    • A61F13/51405—Backsheet, i.e. the impermeable cover or layer furthest from the skin characterised by the material treated or coated, e.g. with moisture repellent agent
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/26—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives thereof
    • A—HUMAN NECESSITIES
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    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
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    • A61L15/52—Water-repellants
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05C—APPARATUS FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05C3/00—Apparatus in which the work is brought into contact with a bulk quantity of liquid or other fluent material
    • B05C3/18—Apparatus in which the work is brought into contact with a bulk quantity of liquid or other fluent material only one side of the work coming into contact with the liquid or other fluent material
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/36—After-treatment
    • C08J9/40—Impregnation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/36—After-treatment
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    • C08J9/42—Impregnation with macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C14—SKINS; HIDES; PELTS; LEATHER
    • C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C11/00—Surface finishing of leather
    • C—CHEMISTRY; METALLURGY
    • C14—SKINS; HIDES; PELTS; LEATHER
    • C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C9/00—Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
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    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/425—Cellulose series
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4266—Natural fibres not provided for in group D04H1/425
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
    • D06B15/00—Removing liquids, gases or vapours from textile materials in association with treatment of the materials by liquids, gases or vapours
    • D06B15/08—Removing liquids, gases or vapours from textile materials in association with treatment of the materials by liquids, gases or vapours by scraping
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/244—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
    • D06M15/256—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons containing fluorine
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/356—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms
    • D06M15/3568—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms containing silicon
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
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    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
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    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/653—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain modified by isocyanate compounds
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
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    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, 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
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0002—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
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    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
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    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
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    • A61F2013/00246—Wound bandages in a special way pervious to air or vapours
    • A61F2013/00255—Wound bandages in a special way pervious to air or vapours with pores
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A61F2013/00361—Plasters
    • A61F2013/00727—Plasters means for wound humidity control
    • A61F2013/00731—Plasters means for wound humidity control with absorbing pads
    • A61F2013/00744—Plasters means for wound humidity control with absorbing pads containing non-woven
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A61F2013/00361—Plasters
    • A61F2013/00855—Plasters pervious to air or vapours
    • A61F2013/00863—Plasters pervious to air or vapours with pores
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05C—APPARATUS FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05C11/00—Component parts, details or accessories not specifically provided for in groups B05C1/00 - B05C9/00
    • B05C11/02—Apparatus for spreading or distributing liquids or other fluent materials already applied to a surface ; Controlling means therefor; Control of the thickness of a coating by spreading or distributing liquids or other fluent materials already applied to the coated surface
    • B05C11/04—Apparatus for spreading or distributing liquids or other fluent materials already applied to a surface ; Controlling means therefor; Control of the thickness of a coating by spreading or distributing liquids or other fluent materials already applied to the coated surface with blades
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2205/00—Foams characterised by their properties
    • C08J2205/04—Foams characterised by their properties characterised by the foam pores
    • C08J2205/05—Open cells, i.e. more than 50% of the pores are open
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2427/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2433/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2475/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2483/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02—Natural fibres, other than mineral fibres
    • D06M2101/04—Vegetal fibres
    • D06M2101/06—Vegetal fibres cellulosic
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02—Natural fibres, other than mineral fibres
    • D06M2101/10—Animal fibres
    • D06M2101/12—Keratin fibres or silk
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/16—Synthetic fibres, other than mineral fibres
    • D06M2101/18—Synthetic fibres consisting of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/26—Polymers or copolymers of unsaturated carboxylic acids or derivatives thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/16—Synthetic fibres, other than mineral fibres
    • D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/32—Polyesters
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/16—Synthetic fibres, other than mineral fibres
    • D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/34—Polyamides
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/10—Repellency against liquids
    • D06M2200/12—Hydrophobic properties

Definitions

  • the present invention generally concerns porous fibrous webs (especially fabrics) that are modified in their properties by incorporation thereinto of silicone polymer. Such webs are prepared by impregnation methods that encapsulate at least some of the fibers comprising the web while leaving at least some of the interstices of the web open.
  • U.S. Patents Nos. 3,436,366; 3,639,155; 4,472,470; 4,500,584; and 4,666,765 disclose silicone coated fabrics. Silicone coatings are known to exhibit relative inertness to extreme temperatures of both heat and cold and to be relatively resistant to ozone and ultraviolet light. Also, a silicone coating can selectively exhibit resistance to soiling, strength, enhancement, and/or flame retardancy.
  • Fluorochemical treatment of webs is known to impart properties, such as soil resistance, grease resistance, and the like.
  • Prior art fluorochemical and silicone fabric treatment evidently each can protect only that side of the fabric upon which they are disposed. Such treatments characteristically significantly alter the hand, or tactile feel, of the treated side.
  • Prior silicone fabric coatings typically degrade the tactile finish, or hand, of the fabric and give the coated fabric side a rubberized finish which is not appealing for many fabric uses, particularly garments.
  • U.S. Patent No. 4,454,191 describes a waterproof and moisture-conducting fabric coated with a hydrophilic polymer described as a compressed foam of an acrylic resin modified with polyvinyl chloride or polyurethane. The polymer serves as a sort of "sponge" soaking up excess moisture vapor.
  • microporous polymeric coatings have been used in prior art attempts to make a garment breathable, yet waterproof.
  • Porous webs have been further shown to be surface coated in, for example, U.S. Patent Nos. 4,478,895, 4,112,179, 4,297,265, 2,893,962, 4,504,549, 3,360,394, 4,293,611, 4,472,470, and 4,666,765.
  • These surface coatings impart various characteristics to the surface of a web, but do not substantially impregnate the web fibers. Such coatings remain on the surface and do not provide a film over the individual internal fibers and/or yarn bundles of the web. In addition, such coatings on the web surface tend to wash away quickly.
  • Saturation such as accomplished by padbath immersion, or the like, is capable of producing variable concentrations of a given saturant chemical.
  • a polymer material such as a silicone resin
  • immersion of the flexible web, or fabric, a padbath, or the like using a low viscosity liquid silicone resin so that the low viscosity liquid can flow readily into, and be adsorbed or absorbed therewithin.
  • the silicone resin treated product is typically a rubberized web, or fabric, that is very heavily impregnated with silicone.
  • Such a treated web is substantially devoid of its original tactile and visual properties, and instead has the characteristic rubbery properties of a cured silicone polymer.
  • U.S. Patent No. 2,673,823 teaches impregnating a polymer into the interstices of a fabric and thus fully filling the interstices. This patent provides no control of the saturation of the fabric. It teaches full saturation of the interstices of the fabric.
  • liquid or paste compositions to textiles for purposes of saturation and/or impregnation is typically accomplished by an immersion process.
  • an immersion application of a liquid or paste composition to the web is achieved, for example, by the so-called padding process wherein a fabric material is passed first through a bath and subsequently through squeeze rollers in the process sometimes called single-dip, single-nip padding.
  • the fabric can be passed between squeeze rollers, the bottom one of which carries the liquid or paste composition in a process sometimes called double-dip or double-nip padding.
  • Coating at a predetermined thickness can be achieved by using precision-controlled deposition of coating material followed by passage through a pair of opposed scraping knives.
  • the knives smooth the coating and maintain the thickness of the coating to a desired thickness.
  • a relatively thick silicone liquid elastomer coating to a rough web, typically of fiberglass, in order to make architectural fabric as is taught in U.S. Patent No. 4,666,765.
  • the drag knives are set to a thickness of about 2 to 10 mils thicker than the web thickness. This setting, depending on the coating speed, can yield a base coat thickness of approximately 3 to 12 mils thicker than the web thickness.
  • Various types of coatings, and various coating thicknesses, are possible.
  • One prior art silicone resin composition is taught by U.S. Patent Nos. 4,472,470 and 4,500,584, and includes a vinyl terminated polysiloxane, typically one having a viscosity of up to about 2,000,000 centipoise at 25°C, and a resinous organosiloxane polymer.
  • the composition further includes a platinum catalyst, and an organo ydrogenpolysiloxane crosslinking agent, and is typically liquid.
  • Such composition is curable at temperatures ranging from room temperature to 100°C or higher depending upon such variables as the amount of platinum catalyst present in the composition, and the time and the temperature allowed for curing.
  • Such compositions may additionally include fillers, including finely divided inorganic fillers.
  • Fillers including finely divided inorganic fillers.
  • Silicone resin compositions that are free of any fillers are generally transparent or translucent, whereas silicone resin compositions containing fillers are translucent or opaque depending upon the particular filler employed.
  • Cured silicone resin compositions are variously more resinous, or hard, dependent upon such variables as the ratio of resinous copoly er to vinyl terminated polysiloxane, the viscosity of the polysiloxane, and the like. Curing (including polymerization and cross- linking) can encompass the same reactions. However, in the fabric finishing arts, such terms can be used to identify different phenomena. Thus, controllable and controlled curing, which is taught by the prior art, may not be the same as control of crosslinking.
  • crosslinking In the fabric finishing arts, curing is a process by which resins or plastics are set in, or on, textile materials, usually by heating.
  • Crosslinking may be considered to be a separate chemical reaction from curing in the fabric finishing arts.
  • Crosslinking can occur between substances that are already cured.
  • Crosslinking can stabilize fibers, such as cellulosic fibers through chemical reaction with certain compounds applied thereto.
  • Crosslinking can improve mechanical factors such as wrinkle performance.
  • Polymerization can refer to polymer formation or polymer growth.
  • This invention relates to a silicone polymer composition treated flexible porous web comprised of associated fibers having interstices therebetween. At least some of such fibers are encapsulated with a silicone polymer composition which is preferably cured. At least some of said interstices are open.
  • the silicone polymer composition has a viscosity that is sufficient to achieve encapsulation of the individual fibers in the web. Generally, the viscosity is greater than about 1000 centipoise and less than about 2,000,000 centipoise. Such composition, when cured, is preferably elastomeric.
  • a fluorochemical is impregnated into or coated onto said fibers before the fibers are encapsulated.
  • the quantity of silicone polymer composition can vary widely.
  • the silicone polymer composition is present in an amount that is sufficient to individually encapsulate at least some of the fibers in a web.
  • this amount is in the range of about 5 to about 200 weight percent of the weight of the untreated web or fibers, and preferably is in the range of 5 to 100 weight percent of the weight of the untreated web or fibers.
  • the quantity of fluorochemical is generally in the range of about 0.01 to about 5 weight percent of the weight of the untreated web or fibers, and preferably is in the range of about 0.05 to about 3 weight percent of the weight of the untreated web or fibers.
  • a web incorporates both a fluorochemical and a curable or cured silicone polymer, they are present in an amount sufficient to individually encapsulate at least some of the fibers present in a web.
  • the total weight of fluorochemical and silicone polymer is in the range of about 5 to about 200 weight of the total weight of the untreated web.
  • the porous webs are generally flat or planar.
  • the web fibers can be in the form of monofilaments, yarns, staples, or the like.
  • the webs are preferably a fabric which is woven or non-woven with fibers that can be of any desired composition.
  • the web will generally be tensionable, but not too weak or elastomeric to be processed in accordance with the teachings of the present invention.
  • the web fibers are preferably comprised of a synthetic organic polymer; however, fibers comprised of natural fibrous materials can be used.
  • synthetic polymers include polyamides (nylons) , polyesters, such as polyethylene terephthalate, polyolefins such as polypropylene and polyethylene, acrylics, regenerated cellulose, cellulose acetates, and the like.
  • presently preferred natural fibers include cotton, linen, wool and silk.
  • Blends of these fibers e.g., polyester/cotton can also be used.
  • Webs of the present invention contain a curable or cured silicone polymer impregnant that is present as a film, sheath, coating or layer that encapsulates at least a portion of the web fibers, and, in a presently preferred embodiment, substantially, completely encapsulates the web fibers.
  • the interstices of the web are at least partially unfilled by impregnant, and, in a presently preferred embodiment are substantially completely unfilled by impregnant.
  • the outer surfaces of the web are preferably substantially free of impregnant.
  • the thickness of the film sheath coating or layer is generally in the range of 0.01 to 50 microns.
  • a web of the present invention for example, a fabric
  • a web of the present invention can be regarded as being a complex structure, but generally the discreteness of a major portion of the silicone polymer encapsulated fibers is discernable under microscopic examination as shown in the accompanying scanning electron microscope photographs that will be discussed hereinafter.
  • Silicone polymer which substantially completely encapsulates a web's fibers while leaving the web's interstices substantially completely free of polymer is located mostly upon surface portions of the fibers of the web.
  • a fiber encapsulated web or fabric produced in accordance with the present invention can characteristically and preferably exhibit a soft hand and flexibility that is comparable, essentially equivalent or similar to the hand and flexibility of the untreated fabric.
  • the difference in hand between the treated and untreated webs may not be perceptible. This is particularly surprising in view of the substantial amount of silicone polymer being added to the web.
  • a fiber encapsulated web or fabric has a breathability which, by a present preference, can approach that of the untreated web or fabric notwithstanding the relatively large amounts of silicone polymer present.
  • An encapsulating silicone polymer composition having a viscosity in the range above indicated is used to produce the treated webs.
  • additives can be admixed with such a composition to adjust and improve properties of the composition or web, such as viscosity and/or rheology, combustibility, reflectivity, flexibility, conductivity, light fastness, mildew resistance, rot resistance, stain resistance, grease resistance, and the like.
  • a web of this invention exhibits enhanced durability.
  • a fiber-encapsulated web of the present invention preserves much, or even substantially all, of its original untreated hand even after an extended period of use while demonstrating excellent abrasion resistance.
  • an untreated web typically loses its original hand and displays reduced abrasion resistance after an extended period of use. This is achieved by the encapsulation or sheathing of the fibers so that the silicone and its homogeneously dispersed additives protect the fibers while preserving fluorochemical properties. This encapsulation or sheathing is thought to prevent new fiber surfaces from being exposed, thereby minimizing the amount of new untreated surfaces that degrade much faster than the silicone sheathed fibers.
  • a fiber-encapsulated web of this invention can undergo a large number of machine washings with detergent without experiencing appreciable or significant change or deterioration.
  • the encapsulating silicone polymer composition substantially prolongs the use and service life of a web, usually by at least an order of magnitude, depending on such factors as web type, extent and type of treatment by the teachings of this invention, and the like.
  • agents or additives carried by the silicone polymer composition into a web can be stably fixed in the web with the cured silicone polymer.
  • agents such as ultraviolet light absorbers, dulling agents, reflectivity enhancers, and the like, which modify a web's response to light and radiation are desirably located substantially upon the surface of the web's fibers.
  • This invention is also directed to a viscous silicone polymer composition that contains a substituted benzophenone, as discussed hereinbelow.
  • the present invention is directed to processes for making silicone polymer fiber encapsulated fabrics.
  • Such processes involve tensioning a porous, flexible web, applying a curable silicone polymer composition thereto, and then moving a generally uniformly-applied, localized shear force over and against one surface of the tensioned web.
  • the shear force is sufficient to shear thin the silicone polymer, to distribute the silicone polymer composition within the web, to at least partially individually encapsulate surface portions of at least some of the web component fibers, and to leave at least some of the web interstices open (and not filled with such composition) .
  • the resulting web is then optionally interveningly stored or is immediately subjected to curing conditions (heat, moisture and/or radiation) which converts the liquid polymer composition as deposited in the web into a solid elastomeric polymer sheath.
  • This invention is also directed to an apparatus for carrying out the process of the present invention, as described hereinbelow.
  • Fig. 1 is a graphical plot illustrating the flow of the silicone polymer composition over time upon and in fabrics both pretreated and untreated with water repellent chemicals, such as fluorochemicals;
  • Fig. 2 is a plan view of a prior art silicone polymer treated fabric magnified 150 times;
  • Fig. 3a is a cross section and top field view of a silicone polymer impregnated fabric of the invention magnified 100 times;
  • Fig. 3b is a view of a silicone polymer impregnated fiber of Fig. 3a magnified 6,000 times;
  • Fig. 3c is a view of the side opposite from the side of impregnant application of the silicone polymer impregnated fabric of Fig. 3a magnified 80 times;
  • FIGs. 4a and 4b illustrate diagrammatically one embodiment of an apparatus suitable for use in the practice of the present invention
  • Fig. 5 is a diagrammatic representation illustrating the process in accordance with the present invention.
  • Fig. 6 illustrates diagrammatically another embodiment of an apparatus suitable for use in the practice of the present invention
  • FIG. 7 illustrates diagrammatically another embodiment of an apparatus suitable for use in the practice of the present invention
  • Figs. 8a through 8d are graphs illustrating ways of plotting rheological behavior
  • Fig. 9 is a schematic vector diagram illustrating- surface tension forces
  • Fig. 10 is a graph relating contact angle over a smooth, solid surface
  • Figs. 11a through lid show representative velocity profiles
  • Figs. 12a through 12c illustrate diagrammatically another and presently preferred embodiment of apparatus suitable for use in the practice of the present invention
  • Figs. 13a through 13d are scanning electron photomicrographs that illustrate a representative fiber encapsulated fabric of the present invention.
  • Figs. 14a through 14f are scanning electron photomicrographs that illustrate another representative fiber encapsulated fabric of the present invention.
  • DESCRIPTION OF THE PREFERRED EMBODIMENTS The term "fiber” as used herein refers to a long, pliable, cohesive, natural or man-made (synthetic) thread-like object, such as a monofilament, staple, filament, or the like.
  • a fiber usable in this invention preferably has a length at least 100 times its diameter or width. Fibers can be regarded as being in the form of units which can be formed, by known techniques into yarns, or the like.
  • Fibers can be formed by known techniques into woven or non-woven webs (especially fabrics) , including weaving, knitting, braiding, felting, twisting, matting, needling, pressing, and the like.
  • fibers such as those used for spinning, as into a yarn, or the like, have a lengt of at least about 5 millimeters. Fibers such as those derived from cellulosics of the type produced in paper manufacture can be used in combination with longer fibers as above indicated, as those skilled in the art will readily appreciate.
  • filament refers to a fiber of indefinite length, such as found naturally in silk, or in a synthetic monofilament. Man-made fibers are extruded into filaments which are used to make yarn, staple, tow, or the like.
  • Yarn refers to a continuous strand comprised of a multiplicity of fibers, filaments, or the like in a bundled form, such as may be suitable for knitting, weaving or otherwise used to form a fabric. Yarn occurs as a number of fibers that are twisted together (spun yarn) or a number of filaments that are laid together without twist (a zero-twist yarn) .
  • a flexible porous fibrous web used as a starting material in this invention is generally and typically, essentially planar or flat and has generally opposed, parallel surfaces.
  • Such a web is a three dimensional structure comprised of a plurality of associated or interengaged fibers with interstices therebetween. Interstices exist between the fibers and can be defined as a space, volume or void between the fibers comprising a web.
  • the term "web” as used herein is intended to include fabrics and refers to a sheet-like structure (woven or non-woven) comprised of fibers. Included with the fibers can be non-fibrous elements, such as particulate fillers, binders, dyes, sizes and the like in amounts that do not substantially affect the porosity or flexibility of the web.
  • a web used in the practice of the present invention is fibers
  • more preferred webs have at least about 85 weight percent of their structure as fiber. It is presently preferred that webs be untreated with any sizing agent, coating, or the like, except as taught herein.
  • the web may comprise a laminated fabric and a non-woven porous substrate.
  • the fibers comprising a porous flexible web used in the practice of the present invention can be of natural or synthetic origin. Mixtures of natural fibers and synthetic fibers can also be used. Examples of natural fibers include cotton, wool, silk, jute, linen, and the like. Examples of synthetic fibers include rayon, acetate, polyesters (including polyethyleneterephthalate) , polyamides (including nylon) , acrylics, olefins, aramids, azlons, glasses, modacrylics, novoloids, nytrils, rayons, sarans, spandex, vinal, vinyon, and the like.
  • impregnation or "impregnate”, as used herein, refers to forcing a liquid substance into a porous solid, such as a flexible web or substrate.
  • the term "impregnation” refers to the penetration of such dispersions into a porous web, and to the distribution of such dispersions in a preferably, substantially uniform and controlled manner in such web, particularly as regards the surface portions of the individual web component fibers.
  • the term "impregnation” refers to the penetration of such polymeric compositions into a porous web, to the distribution of such composition in a controlled manner through such web, and to the resultant, at least partial encapsulation of at least a portion of the fibers of such web by such composition in accordance with the present invention.
  • coating refers to a generally continuous film or layer formed by a material over or on a surface.
  • encapsulation refers to the partial or complete surrounding, encasement, or enclosing by a discrete layer, film, coating, or the like, of exposed surface portions of at least some individual fibers of a porous web. Such a layer can sometimes be contiguous or integral with other portions of the same encapsulating material which becomes deposited on internal areas of a web which are adjacent to such encapsulating layer, encapsulated fiber, or the like.
  • elastomeric refers to the ability of a cured silicone polymer impregnated web to stretch and return to its original state.
  • a characteristic of a silicone polymer composition, or impregnant, that is used for impregnation into a web or substrate in accordance with the teachings of this invention is that apparently only a minimum amount of the impregnant appears actually to enter or penetrate into the individual fibers comprising such web or substrate.
  • the exact amount of impregnant which enters into individual fibers is unknown, but is now estimated to be typically below about 10 weight percent of the total quantity of impregnant applied to a web, with the remainder of the impregnant appearing to comprise mainly deposits on and around fibers of a web.
  • curing refers to a change in state, condition, and/or structure in a material, such as a curable silicone polymer composition that is usually, but not necessarily, induced by at least one applied variable, such as time, temperature, radiation, presence and quantity in such material of a curing catalyst or curing accelerator, or the like.
  • the .components of such a composition may experience occurrence of one or more of complete or partial (a) polymerization, (b) cross-linking, or (c) other reaction, depending upon the nature of the composition being cured, application variables, and presumably other factors.
  • the term "filled” as used herein in relation to interstices and the amount of silicone polymer composition therein in a given web, designates the presence of such composition therein. When a given interstice is totally taken up by such composition, it is "completely filled” or "plugged".
  • Measurements of the degree of encapsulation, interstice fillage, plugging, or the like are conveniently made by microscopy, preferably conventional scanning electron microscopy (SEM) techniques. Because of the nature of such measuring by SEM for purposes of the present invention, "a completely filled" interstice can be regarded as a "plugged" interstice.
  • SEM scanning electron microscopy
  • a flexible, porous fibrous web is preferably untreated or scoured before being treated in accordance with the present invention.
  • a web is preliminarily treated, preferably saturated, for example, by padding, to substantially, uniformly impregnate the web fibers with a fluorochemical.
  • the treating composition comprises a dispersion of fluorochemical in a liquid carrier.
  • the liquid carrier is preferably aqueous and can be driven off with heat after application.
  • the treating composition has a low viscosity, typically comparable to the viscosity of water or less. After such a treatment, it is presently preferred that the resulting treated web exhibits a contact angle with water measured on an outer surface of the treated web that is greater than about 90 degrees.
  • the treated web preferably contains fluorochemical substantially uniformly distributed therethrough. Thus, the fluorochemical is believed to be located primarily on and in the individual fibers with the web interstices being substantially free of fluorochemical.
  • a presently preferred concentration of fluorochemical in a treatment composition is typically in the range of about 1 to about 10% fluorochemical by weight of the total composition weight, and more preferably is about 2.5% of an aqueous treating dispersion.
  • Web weight add-ons of the fluorochemical can vary depending upon such factors as the particular web treated, the silicone polymer impregnant to be utilized in the next step of the treatment process of this invention, the ultimate intended use and properties of the treated web of this invention, and the like.
  • the fluorochemical weight add-on is typically in the range of about 0.01 to about 5% of the weight of the untreated fabric.
  • the web is preferably squeezed to remove excess fluorochemical composition after which the web is heated or otherwise dried to evaporate carrier liquid and thereby also accomplish fluorochemical insolubilization or sintering, if permitted or possible with the particular treating composition used.
  • the fluorochemical treated web is thereafter impregnated under pressure, by the procedures taught by this invention, with a predetermined amount of a curable silicone polymer impregnant composition to form a web whose fibers are at least partially encapsulated with the curable silicone polymer impregnant, whose web outer surfaces are substantially free of the curable impregnant, and whose web interstices are not completely filled with the curable impregnant.
  • the curable impregnant composition utilized preferably exhibits a viscosity greater than 1,000 centipoise and less than 2,000,000 centipoise at rest at 25°C at a shear rate of 10 reciprocal seconds.
  • the curable silicone impregnant composition is believed to be typically polymeric, to be usually a mixture of co-curable polymers and oligomers, and to include a catalyst to promote the cure.
  • the silicone polymer impregnant composition can include, as additive components, polyurethanes, fluorosilicones, silicone-modified polyurethanes, acrylics, polytetrafluoroethylene-containing materials, and the like.
  • the web is thereafter cured to convert the curable silicone polymer composition into a solid elastomeric polymer.
  • the depth of silicone polymer impregnation into a web can be controlled by the application procedures herein described to provide selective placement of the silicone polymer impregnant within the web. This placement allows the shear thinning, i.e. viscosity reduction, action to take place selectively throughout the web.
  • the fluorochemical residue that remains after fiber treatment may not be exactly evenly distributed throughout the web, but may be present in the web in certain discontinuities. For example, these discontinuites may be randomly distributed small areas upon an individual fiber's surface. However, the quantity and distribution of fluorochemical through a web is believed to be largely controllable. Some portions of the fluorochemical may become dislodged from the web and migrate through the silicone polymer to cause the shear thinning of the silicone polymer.
  • the silicone polymer composition is theorized to be caused to flow and distribute itself over fibers in a web under the influence of the processing conditions provided by this invention. This flow and distribution is further theorized to be facilitated and
  • Some portion of the residue of fluorochemical resulting from a preliminary web saturating operation is theorized to be present upon a treated fiber's surfaces after encapsulation of fibers by the silicone polymer has been achieved. This is believed to be demonstrated by the fact that a fiber encapsulated fabric or web exhibits an enhanced water and oil repellency, such as is typical of fluorochemicals in porous webs. It is therefore believed that the fluorochemicals are affecting the adherence of the silicone polymer as a thin film encapsulating layer about the treated web fibers as well as facilitating silicone polymer impregnant pressurized flow within and about the interstices of the web being treated so that the silicone polymer can assume its position encapsulating the fibers.
  • the encapsulating silicone polymer film is contiguous, or substantially so, relative to fluorochemical molecules on a fiber surface, and that the layer of silicone polymer on a fiber surface is so thin that any dislodgment of the fluorochemical may release the fluorochemical into the silicone polymer film thereby allowing the fluorine to orient with the required cure temperature of the silicone, reactivating the water surface contact angle so that the water repellant properties of the underlying fluorochemical are exertable through the silicone polymer film.
  • the combination of silicone polymer film and fluorochemical results in a fiber encapsulation of the fibers in a web (or fabric) when this invention is practiced. After curing, the silicone polymer is permanently fixed as a fiber encapsulating material.
  • a curable silicone polymer such as used in the practice of this invention is applied under pressure using shear forces onto and into a web substrate.
  • the shear forces cause the curable silicone polymer to flow into the web.
  • the extent of web fiber encapsulation is believed to be controllable by varying such factors as the selection and applied amount of fluorochemical and curable silicone polymer in combination with the applied compressive and shear forces employed at a given temperature so that fiber encapsulation is achieved while the interstices of the web are not completely filled with such polymer, and the outer opposed surfaces of the web are substantially completely free of silicone polymer coating or residue.
  • the curable silicone polymer impregnant is then cured.
  • the curable silicone polymer impregnant ⁇ is applied in an amount at least sufficient to partially saturate the web and fill some of the interstices of the web. Then, the web, while tensioned, is passed against shearing means or through a compression zone, such as between rollers or against a shear knife. Thus transversely applied shear force and compressive pressure is applied to the web. The combination of tensioning, shearing forces, and web traveling speed is sufficient to cause the curable silicone polymer impregnant to move into the web, out from the interstices and around the web fibers being encapsulated, thereby leaving at least some of the interstices unfilled, and preferably substantially free of silicone polymer impregnant. Excess silicone polymer is removed by the surface wiping action of the shearing means. The curable silicone polymer impregnant encapsulating the fibers is thereafter cured.
  • the desired impregnation or penetration of, and distribution of silicone polymer impregnant in, a web is believed to be achieved by localized pressuring forces exerted on a web surface which are sufficiently high to cause the viscosity of a silicone polymer impregnant composition to be locally reduced, thereby permitting such silicone impregnant to flow, impregnate the web and encapsulate the fibers.
  • the web is preferably at least slightly distorted by tensioning or stretching, while being somewhat transversely compressed at the location of the impregnation. This distortion is believed to facilitate the entrance of the silicone polymer composition into the web. When the compression and tension are released, the silicone polymer composition is believed to be squeezed or compressed within and through the interstitial spaces of the treated web.
  • silicone polymer impregnant composition can be reduced by the pressures and temperatures employed for the impregnation. Alternatively, if the viscosity is excessive, then the impregnating pressure and/or temperature can be increased. Opposite adjustments should be made if silicone polymer impregnant flow is insufficiently viscous.
  • the silicone polymer impregnating composition is resistant to being positioned in a desired location, in a desired amount, in a given web at various viscosities and/or pressures, then the level of fluorochemical pretreatment of the web can be increased, as in the case of overimpregnation, or decreased, as in the case of underimpregnation.
  • the pressured impregnation of a web occurs between two rollers.
  • One such roller bears a silicone polymer impregnant, typically and preferably distributed upon and over a circumferentially extending textured, or gravure surface.
  • Such roller rotates (i) in the same direction as a facing roller and (ii) oppositely to the direction of movement of a continuously moving web traveling past the localized impregnation area achieved between such roller and such moving web.
  • the unidirectional rotation of the two rollers produces a distorting and stretching force or effect upon the web. This force is believed to promote penetration of the silicone polymer impregnant into the web.
  • This form of impregnant application or coating can be termed "reverse roll coating" for convenience.
  • the reverse coating rollers have generally horizontal axes while the web moves generally horizontally.
  • the web is further concurrently both longitudinally tensioned and distorted by being stretched against metering bars, bar knives, and the like which are urged against the web.
  • Such an initial pressured impregnation step is preferably followed by a series of further pressured web treatment steps believed to accomplish impregnant reintroduction, impregnant distribution, impregnant scraping, and excess impregnant removal and recovery.
  • the collective result of such steps gradually produces a web wherein the silicone polymer impregnant encapsulates to a desired extent the fibers comprising the web while not substantially appearing within, or collecting within, or filling beyond a desired extent, the interstices of the web.
  • a silicone polymer composition may be made to substantially completely encapsulate the fibers thereof while substantially not filling the interstices or spaces that are between the fabric's yarn or fiber components.
  • silicone polymer impregnant to a web occurs from a reservoir.
  • This reservoir of viscous silicone impregnant is positioned tightly against the longitudinally tensioned, moving web.
  • the linearly extending, preferably vertically upwardly moving, web (or fabric) constitutes a wall portion of the reservoir.
  • a bar or shear knife is pressed strongly and transversely against and laterally across the longitudinally tensioned web, or fabric.
  • a shear blade or flexible scraper knife is also strongly and transversely forced laterally across and against the tensioned web.
  • More than one shear knife, or more than one flexible co pressive knife, can be successively positioned along the path of web movement.
  • These blade means are believed to reintroduce the silicone impregnant into the web, to distribute the silicone polymer, and to promote and complete the encapsulation of fibers with silicone polymer.
  • These scraper knives or shear blades are also believed to force the viscous silicone polymer impregnant further into the three-dimensional structure of the web. Also, these knives, particularly the scraper knives, wipe or scrape excess silicone polymer impregnant off the surface of the web, thereby regulating the amount of silicone polymer impregnated.
  • the transversely applied shear forces applied across and against the web are sufficiently high to achieve temporarily and locally, a lowering of the viscosity of the preferably thixotropic viscous silicone polymer impregnant.
  • the silicone polymer impregnant is thus enabled to flow into, and upon, the internal three- dimensional structure of the web. Because the silicone polymer composition that is being applied is subject to cure with heat or radiation and time, and because the pressured impregnation is believed to produce localized heat, the shearing conditions used prior to curing are preferably controlled to minimize premature curing.
  • the properties of the silicone polymer impregnant are preferably selected to be such that cure, or excessive cure, does not occur while the web is being treated with silicone polymer during the pressured impregnation.
  • the cure preferably occurs only after the web impregnation procedure has been completed.
  • the cure temperature of the silicone polymer composition is relatively high (preferably above about 250°F) and the heat exposure time is such as is needed to obtain a desired solid resilient elastomeric silicone polymer.
  • the rheology of the viscous silicone polymer impregnant may be altered or controlled. Characteristics of a fiber encapsulated web are believed to be influenced by rheology, but it is believed that, in general, this invention can be practiced without careful control of rheology while controlling viscosity.
  • the viscosity of the silicone polymer impregnant is preferably lowered by the high pressure (shear) forces exerted during impregnation.
  • curing the activity transpiring at a final step in the practice of a method of this invention is generically referred to herein as curing.
  • Conventional curing conditions known to the prior art for curing silicone polymer compositions are generally suitable for use in the practice of this invention.
  • temperatures in the range of about 250°F to about 350°F are used and times in the range of about 30 seconds to about 1 minute can be used, although longer and shorter curing times and temperatures may be used, if desired, when thermal curing is practiced.
  • Radiation curing as with an electron beam or ultraviolet light can also be used.
  • platinum catalysts to accelerate the cure while using lower temperatures and shorter cure times is preferable.
  • the webs are characteristically air permeable.
  • Sample fabrics that are beneficially impregnated and fiber encapsulated in accordance with the invention are believed to include nylon, cotton, rayon and acrylic fabrics, as well as fabrics that are blends of fiber types.
  • a web is preferably pretreated and impregnated with a fluorochemical prior to being impregnated under pressure with a silicone polymer composition as taught herein.
  • the fluorochemical impregnation is accomplished preferably by first saturating a starting web with a liquid composition which incorporates the fluorochemical, and then, thereafter, removing the excess liquid composition and residual carrier fluid by draining, compression, drying, or some combination thereof from the resulting treated web.
  • a typical fluorochemical of the type used for web treatment can be characterized as a compound having one or more highly fluorinated portions, each portion being a fluoroaliphatic radical or the like, that is (or are) functionally associated with at least one generally non-fluorinated organic portion.
  • organic portion can be part of a polymer, part of a reactive monomer, a moiety with a reactable site adapted to react with a binder, or the like.
  • Such a compound is typically applied to a fabric or other web as a suspension or solution in either aqueous or non-aqueous media.
  • Such an application may be conventionally carried out in combination with a non-fluorine or fluorine containing resin or binder material for the purpose of providing improved durability as regards such factors as laundering, dry cleaning, and the like.
  • Fluorochemicals are sometimes known in the art as durable water repellant (DWR) chemicals, although such materials are typically believed to be not particularly durable and to have a tendency to wash out from a fabric treated therewith.
  • fiber encapsulated webs of this invention which have been pretreated with a fluorochemical display excellent durability and washability characteristics.
  • the combination of fluorochemical pretreatment and silicone polymer fiber encapsulation such as provided by the present invention appears to provide synergistic property enhancement because the effects or properties obtained appear to be better than can be obtained from using either the fluorochemical or the silicone polymer alone for web treatment.
  • Exemplary water repellent fluorochemical compositions include the compositions sold under the name Milease ® by ICI Americas Inc. with the type designations F-14N, F-34, F-31X, F-53. Those compositions with the "F" prefix indicate that they contain a fluorochemical as the principal active ingredient. More particularly, Milease ® F-14 fluorochemical, for example, is said to contain approximately 18 percent perfluoroacrylate copolymer, 10 percent ethylene glycol (CAS 107-21-1) and 7 percent acetone (CAS 67-64-1) dispersed and dissolved in 65 percent water. Milease ® F-31X is said to be a dispersion of a combination of fluorinated resin, acetone, and water.
  • Still another suitable class of water repellent chemicals is the Phobotex ® chemicals of Ciba/Geigy identified as Phototex ® FC104, FC461, FC731, FC208 and FC232 which are each believed to be suitable for use, typically in approximately a 5 percent concentration, in saturating a web for use in the invention.
  • These and many other water repellent fluorochemicals are believed to be capable of creating a surface contact angle with water of greater than about 90 degrees when saturated into a web and to be suitable for use in the practice of this invention.
  • TEFLON ® -based soil and stain repellents of E.I. duPont de Nemours & Co. Inc., 1007 Market Street, Wilmington, DE 19898.
  • Suitable TEFLON ® types for use in the practice of this invention include TEFLON ® G, NPA, SKF, UP, UPH, PPR, N, and MLV.
  • the active water repellent chemical of each composition is believed to be a fluorochemical in polymeric form that is suitable for dispersion in water, particularly in combination with a cationic surfactant as a dispersant. These dispersions are dilutable in all proportions with water at room temperature.
  • One preferred class of fluorochemical treating compositions useful in the practice of this invention comprises about-1 to about 10 weight percent, more preferably about 5 weight percent of one of the above indicated TEFLON ® -type water repellent fluorochemcials in water.
  • Another major group of suitable water repellent fluorochemical compositions useful in the practice of the invention is commercially available under the designation ZEPEL ® rain and stain repellent chemicals of E.I. duPont de Nemours & Co. Inc., such as ZEPEL ® water repellent chemicals types B, D, K, RN, RC, OR, HT, 6700 and 7040.
  • ZEPEL ® water repellent chemicals types B, D, K, RN, RC, OR, HT, 6700 and 7040 Each is believed to be a fluorochemical in polymeric form that is disperible in all proportions at room temperature.
  • the dispersants ZEPEL ® B, D, K, and RN are believed to be cationic, while the d '
  • ZEPEL ® 6700 is said to be comprised of 15 to 20 percent perfluoroalklyl acrylic copolymer, 1 to 2 percent alkoxylated carboxylic acid, and 3 to 5 percent ethylene glycol.
  • Exemplary characteristics of the composition include a boiling point of 100°C at 760mm Hg and a specific gravity of 1.08. The volatiles are approximately 80 percent by weight.
  • the pH is 2 to 5. The odor is mild; the concentrate form is that of a semi-opaque liquid; and the concentrate color is straw white.
  • the composition and characteristics of ZEPEL ® 7040 repellent chemical are believed to be substantially identical to those of ZEPEL ® 6700 except that the former composition additionally contains 7 to 8 percent acetone.
  • Another major group of water repellent fluorochemicals comprises the Scotchgard ® water repellent chemicals of 3M Co. , St. Paul, Minnesota.
  • the Scotchgard ® fluorochemicals are believed to be aqueously dispersed fluorochemicals in polymeric form.
  • the compositions of two suitable Scotchgard ® water repellent fluorochemicals are believed. to be disclosed in U.S. Patent Nos. 3,393,186 and 3,356,628, which patents are incorporated herein by reference.
  • the Scotchgard ® fluorochemical of U.S. Patent No. 3,356,628 consists of copolymers of perfluoroacrylates and hydroxyalkyl acrylates.
  • copolymers are suitable for use as an oil and water repellent coating on a fibrous or porous surface. They have a carbon to carbon main chain and contain recurring monovalent perfluorocarbon groups having from 4 to 18 carbon atoms each and also having recurring hydroxyl radicals. From 20 to 70 percent of the weight of such copolymer is contributed by fluorine atoms in the perfluorocarbon groups and from 0.05 to 2 percent of the weight of the copolymer is contributed by the hydroxyl radicals. Such copolymer is said to have improved surface adherability properties as compared to the homopolymer of a corresponding fluorocarbon monomer.
  • No. 3,393,186 consists of perfluoroalkenylacrylates and polymers thereof.
  • An exemplary fluorinated monomer has the formula:
  • Such a water repellent fluorochemical composition is supplied and saturated into the substrate web as a readily pourable aqueous dispersion.
  • U.S. Patent No. 4,426,476 discloses a fluorochemical textile treating composition containing a water-insoluble fluoroaliphatic radical, an aliphatic chlorine-containing ester and a water insoluble, fluoroaliphatic radical containing polymer.
  • U.S. Patent No. 3,896,251 discloses a fluorochemical textile treating composition containing a fluoroaliphatic radical containing linear vinyl polymer having 10 to 60 weight percent fluorine and a solvent soluble carbodiimide preferably comprising fluoroaliphatic groups.
  • a table in this patent lists a plurality of prior art fluoroaliphatic radical containing polymers useful for the treatment of fabrics and the prior art patents where such polymers are taught.
  • U.S. Patent No. 3,328,661 discloses textile treating solutions of a copolymer of an ethylenically unsaturated fluorocarbon monomer and a ethylenically unsaturated epoxy group containing monomer.
  • U.S. Patent No. 3,398,182 discloses fluorocarbon compounds useful for fabric treatment that contain a highly fluorinated oleophobic and hydrophobic terminal portion and a different non-fluorinated oleophilic portion linked together by a urethane radical.
  • Water repellent fluorochemical compositions are preferably utilized to saturate a starting untreated porous web substrate so that such composition and its constituents wet substantially completely and substantially uniformly all portions of the web. Such a saturation can be accomplished by various well known techniques, such as dipping the web into a bath of the composition, or padding the composition onto and into the web, or the like. Padding is the presently preferred method of fluorochemical application.
  • the water (or liquid carier) and other volatile components of the composition are removed by conventional techniques to provide a treated web that contains the impregnated fluorochemical throughout the web substrate.
  • a web is substantially completely saturated with an aqueous dispersion of a fluorochemical. Thereafter, the resulting impregnated web is compressed to remove excess portions of said dispersion. Finally, the web is heated to evaporate the carrier liquid. If the fluorochemical is curable, then the heating also accomplishes curing. After the fluorochemical treatment, the fluorochemical is found only on or in the web structural elements or fibers and is substantially completely absent from the web interstices.
  • the fluorochemical concentration in the treating composition is such as to permit a treated fluorochemical containing web, after volatiles of the treating composition are removed, to exhibit a contact angle with water applied to an outer web surface which is greater than about 90°. More preferably, the contact angle provided is greater than about 130°.
  • the web weight add-on provided by the fluorochemical after removal of volatiles is usually relatively minor.
  • the weight add on can vary with such factors as the nature of web treated, the type of silicone impregnant utilized in the next step of the process, the temperature at which the impregnant is applied, the ultimate use contemplated for a web, and the like.
  • Typical weight add-ons of fluorochemical are in the range of about 0.01 to about 5 percent of the weight of the untreated web. More preferably, such weight add-ons are about 0.05 to about 3 weight percent of the weight of the untreated web.
  • Durability of a web that has been treated with a fluorochemical and durability of a web that is subsequently treated with a silicone polymer can sometimes be improved by the conventional process of "sintering".
  • the exact physical and chemical processes that occur during sintering are unknown.
  • the so-called sintering temperature utilized is c a function of the fluorochemical composition utilized and such temperature is frequently recommended by fluorochemical manufacturers.
  • sintering is carried out at a temperature of about 130 to about 160°C for a period of time of about 2 to about 5 minutes.
  • Acid catalysts can be added to give improved durability to laundering and dry cleaning solvents.
  • the fluorochemical is believed to provide more than water or other repellent properties to the treated (impregnated) web, particularly since the curable silicone impregnant is often itself a water repellent. Rather, and without wishing to be bound by theory, it is believed that the fluorochemical in a treated web provides relative lubricity for the treated fibers during the pressure application of the curable silicone polymer impregnant.
  • the silicone polymer impregnant is applied under pressures which can be relatively high, and this impregnant is itself relatively viscous, as is discussed herein.
  • the fibers of the web may move over and against each other to a limited extent, thereby to permit entry of the silicone impregnant into and around the fibers. It is thought that the fluorochemical deposits may facilitate such fiber motion and facilitate encapsulation during the pressure impregnation and subsequent shearing processing.
  • the fluorochemical may inhibit deposition of the silicone polymer impregnant at the positions of the fluorochemical deposits which somehow ultimately tends to cause thin encapsulating layers of silicone polymer to form on fibers.
  • a piece of fabric for example the Red Kap Milliken poplin polyester cotton blend fabric, is cut into swatches.
  • One swatch is treated with an adjuvant, for example a three percent solution of the durable water-repellent chemical Milease ® F-31X.
  • the treated swatch and an untreated swatch are each positioned at a 45° angle to plumb.
  • a graphical plot of the flow of the silicone composition respectively upon the untreated and treated swatches over time can be prepared, such as shown in Fig. 1.
  • the viscous composition has typically traveled a distance of about 8.8 centimeters upon the treated swatch, or a rate of about 0.29 centimeters per minute.
  • the viscous composition has typically traveled a lesser distance of about 7.1 centimeters upon the untreated swatch, or a rate of about 0.24 centimeters per minute.
  • Qualitatively commensurate results are obtainable with other DWR fluorochemical adjuvants that facilitate the viscous flow of polymer compositions in accordance with the invention.
  • the fluorochemical pretreated web generally increases the surface contact angle of the silicone polymer while reducing the amount.of saturation of the silicone polymer into the fibers themselves.
  • the fluorochemical treated web is thereafter impregnated under pressure with a predetermined amount of a curable silicone polymer impregnant composition to form a web whose fibers are preferably substantially completely encapsulated with such curable impregnant and whose outer surfaces and interstices are preferably substantially completely free of the curable impregnant.
  • the silicone polymer impregnant is thereafter cured by heat, radiation, or the like. Even room temperature curing can be used.
  • a silicone polymer impregnated, fluorochemical pretreated web can be interveningly stored before being subjected to curing conditions depending upon the so-called pot life of the treating silicone polymer impregnant.
  • a curable silicone polymer impregnant composition utilized in the practice of this invention preferably has a viscosity that is sufficient to encapsulate the fibers of a web.
  • the silicone polymer composition exhibits a viscosity of greater than about 1,000 centipoise and less than about 2,000,000 centipoise at 25°C. at a shear rate of 10 reciprocal seconds. It is presently most preferred that such composition have a viscosity in the range of about 5,000 to about 100,000 centipoise at 25°C. at a shear rate of 10 reciprocal seconds.
  • Such a composition is believed to contain less than about 1% by weight of volatile material.
  • the silicone polymer is believed to be typically polymeric and to be commonly a mixture of co- curable polymers, oligo ers, and/or monomers.
  • a catalyst is usually also present, and, for the presently preferred silicone polymer compositions discussed hereinafter, is platinum or a platinum compound, such as a platinum salt.
  • a preferred class of liquid curable silicone polymer compositions comprises a curable mixture of the following components:
  • Typical silicone hydrides are polymethylhydrosiloxanes which are dimethyl siloxane copolymers.
  • Typical vinyl terminated siloxanes are vinyldimethyl terminated or vinyl substituted polydimethylsiloxanes.
  • Typical catalyst systems include solutions or complexes of chloroplatinic acid in alcohols, ethers, divinylsiloxanes, and cyclic vinyl siloxanes.
  • the polymethylhydrosiloxanes (component A) are used in the form of their dimethyl copolymers because their reactivity is more controllable than that of the homopolymers and because they result in tougher polymers with a lower cross-link density.
  • component B the reaction with vinyl functional silicones
  • the minimum ratio of hydride (component A) to vinyl (component B) in commercial products is reportedly about 2:1 and may be as high as 6:1.
  • Elastomers produced from such a curing reaction are known to demonstrate toughness, tensile strength, and dimensional stability.
  • Particulate fillers are known to be useful additives for incorporation into liquid silicone polymer compositions. Such fillers apparently not only can extend and reinforce the cured compositions produced therefrom, but also can favorably influence thixotropic behavior in such compositions. Thixotropic behavior is presently preferred in compositions used in the practice of this invention.
  • a terminal silanol (Si-OH) group makes such silanol siloxanes susceptible to reaction in curing, as is believed desirable.
  • component B can be replaced with a so called silanol vinyl terminated polysiloxane while using an organotin compound as a suitable curing catalyst as is disclosed in U.S. Patent No. 4,162,356.
  • an organotin compound as a suitable curing catalyst as is disclosed in U.S. Patent No. 4,162,356.
  • vinyl substituted polysiloxanes it is presently preferred to use vinyl substituted polysiloxanes in component B.
  • a silicone composition useful in this invention can contain curable silicone resin, curable polyurethane, curable fluorosilicone, curable modified polyurethane silicones, curable modified silicone polyurethanes, curable acrylics, polytetrafluoro- ethylene, and the like.
  • Such a composition comprises in combination: (i) a liquid vinyl chainterminated polysiloxane having the formula,
  • R and R 1 are monovalent hydrocarbon radicals free of aliphatic unsaturation with at least 50 mole percent of the R 1 groups being methyl, and where n has a value sufficient to provide a viscosity of about 500 centipoise to about 2,000,000 centipoise at 25°C;
  • a resinous organopolysiloxane copolymer comprising: (i) (R 2 ) 3 SiO o 5 units and Si0 2 units, or
  • R 2 and R 3 are selected from the group consisting of vinyl radicals and monovalent hydrocarbon radicals free of aliphatic unsaturation, where from about 1.5 to about 10 mole percent of the silicon atoms contain silicon-bonded vinyl groups, where the ratio of monofunctional units to tetrafunctional units is from about 0.5:1 to about 1:1, and the ratios of difunctional units to tetrafunctional units ranges up to about 0.1:1; (iii) a platinum or platinum containing catalyst; and
  • R a is a monovalent hydrocarbon radical free of aliphatic unsaturation
  • a has a value of from about 1.0 to about 2.1
  • b has a value of from about 0.1 to about 1.0
  • the sum of a and b is from about 2.0 to about 2.7, there being at least two silicon- bonded hydrogen atoms per molecule.
  • such a composition can contain a finely divided inorganic filler (identified herein for convenience as component (v) ) .
  • such a composition can comprise on a parts by weight basis: (a) 100 parts of above component (i) ;
  • a catalytically effective amount of above component (iii) which, for present illustration purposes, can range from about 0.01 to about 3 parts of component
  • component (e) 0-50 parts of above component (v) .
  • Embodiments of such starting composition are believed to be available commercially from various manufacturers under various trademarks and trade names. As commercially available, such a composition is commonly in the two-package form (which are combined before use) .
  • the component (iv) above is maintained apart from the components (i) and (ii) to prevent possible gelation in storage before use, as those skilled in the art appreciate.
  • one package can comprise components (i) and (ii) which can be formulated together with at least some of component (ii) being dissolved in component (i) , along with component (iii) and some or all of component (v) (if employed)
  • the second package can comprise component (iv) and optionally a portion of component (v) (if employed) .
  • the quantity of catalyst component (iii) required to produce a desired curable composition is achieved.
  • component (iii) and component (iv) are not included together in the same package.
  • the distribution of the components between the two packages is preferably such that from about 0.1 to 1 part by weight of the second package is employed per part of the first package.
  • the two packages are merely mixed together in suitable fashion at the point of use.
  • U.S. Patent No. 4,032,502 provide compositions containing a linear polydiorganosiloxane having two siloxane bonded vinyl groups per molecule, organosiloxane that is soluble in such linear polydiorganosiloxane and comprised of a mixture of a polyorganosiloxane and a polydiorganosiloxane, platinum- containing catalyst, a platinum catalyst inhibitor, and a reinforcing silica filler whose surface has been treated with an organosilicone compound.
  • U.S. Patent No. 4,108,825 discloses a composition comprising a triorganosiloxy end-blocked polydiorganosiloxane, an organohydrogensiloxane having an average of at least 2.1 silcon-bonded hydrogen atoms per molecule, a reinforcing silica filler having a surface treated with an organosilicone compound, a platinum catalyst, and eerie hydrate.
  • Such silicone polymer composition is desirable when a web is being prepared which has flame retardant properties.
  • U.S. Patent No. 4,162,243 discloses a silicone composition of 100 parts by weight triorganosiloxy endblocked polydimethylsiloxane, reinforcing amorphous silica that is surface treated with organosiloxane groups, organohydrogensiloxane, and platinum catalyst.
  • U.S. Patent No. 4,250,075 discloses a liquid silicone polymer composition that comprises vinyldiorganosiloxy endblocked polydiorganosiloxane, polyorganohydrogensiloxane, platinum catalyst, platinum catalyst inhibitor, and carbonaceous particles. Such a silicone polymer composition is useful when a web of this invention is being prepared that has electrically conductive properties.
  • 4,427,801 discloses a curable organopolysiloxane of liquid triorganosiloxy endblocked polydiorganosiloxane wherein the triorganosiloxy groups are vinyl dimethylsiloxy or vinylmethylphenylsiloxy, finely divided amorphous silica particles treated with mixed trimethylsiloxy groups and vinyl-containing siloxy groups, organopolysiloxane resin containing vinyl groups, organohydrogensiloxane, and a platinum containing catalyst.
  • U.S. Patent No. 4,500,659 discloses a silicone composition of liquid triorganosiloxy endblocked polydimethylsiloxane wherein the triorganosiloxy units are dimethyl inylsiloxy or methylphenylvinylsiloxy, a reinforcing filler whose surface has been treated with a liquid hydroxyl end-blocked polyorganosiloxane which is fluorine-substituted, a liquid methylhydrogensiloxane, and a platinum-containing catalyst.
  • U.S. Patent No. 4,585,830 discloses an organosiloxane composition of a triorganosiloxy- endblocked polydiorganosiloxane containing at least two vinyl radicals per molecule, an organohydrogensiloxane containing at least two silicone-bonded hydrogen atoms per molecule, a platinum-containing hydrosilation catalyst, optionally a catalyst inhibitor, a finely divided silica filler, and a silica treating agent which is at least partially immiscible with said polydiorganosiloxane.
  • U.S. Patent No. 4,753,978 discloses an organosiloxane composition of a first diorganovinylsiloxy terminated polydiorganosiloxane exhibiting a specified viscosity and having no ethylenically unsaturated hydrocrabon radicals bonded to non-terminal silicon atoms, a second diorganovinylsiloxy terminated polydiorganosiloxane that is iscible with the first polydiorganosiloxane and contains a vinyl radical, an organohydrogensiloxane, a platinum hydrosilation catalyst, and a treated reinforcing silica filler.
  • U.S. Patent No. 4,785,047 discloses silicone elastomers having a mixture of a liquid polydiorganosiloxane containing at least two vinyl or other ethylenically unsaturated radicals per molecule and a finely divided silica filler treated with a hexaorganodisilazane which mixture is then compounded with additional hexaorganodisiloxane.
  • 4,329,274 discloses viscous liquid silicone polymer compositions that are believed to be suitable and are comprised of vinyl containing diorganopolysiloxane (corresponding to component B) , silicon hydride siloxane (corresponding to component A) and an effective amount of a catalyst which is a halogenated tetrameric platinum complex.
  • U.S. Patent No. 4,442,060 discloses a mixture of 100 parts by weight of a viscous diorganopolysiloxane oil, 10 to 75 parts by weight of finely divided reinforcing silica, 1 to 20 parts by weight of a structuring inhibitor, and 0.1 to 4 parts by weight of 2,4-dichlorobenzoyl peroxide cross-linking agent.
  • Silicone resin compositions shown in Table I below have all been used in the practice of this invention. Such compositions of Table I are believed to involve formulations that are of the type hereinabove characterized.
  • Identified components do not represent complete composition of the individual products shown.
  • the combination of silicone polymer compositions with a benzophenone, preferably a substituted benzophenone, is believed to be novel and inventive and is presently preferred for purposes of practicing the present invention.
  • a polymer composition of viscous liquid silicone polymer and substituted benzophenone is impregnated into a porous web as taught herein, protection of such web against ultraviolet radiation is improved, and the degradation effects upon such web associated with ultraviolet light exposure are inhibited, as may be expected from prior art teachings concerning the behavior of substituted benzophenones.
  • silicone polymer compositions such as used in this invention that contain a substituted benzophenone are believed to display improved viscosity characteristics, particularly thixotropic characteristics, and also improved curing acceleration, as when such a composition is subjected to high shear forces such as are experienced, for example, when a silicone polymer composition is used in the practice of the process described and taught herein.
  • a presently preferred benzophenone additive for use in this invention is 2,4-dihydroxybenzophenone.
  • the regulation of internal and external rheology, and of viscosity, achieved in a characteristically highly viscous polymer composition of the invention is believed to be an important and desirable feature of the benzophenone and silicone polymer compositions which find use in fiber encapsulated web manufacture as taught herein.
  • compositions of the present invention a control of compositional rheology, and particularly of complex viscosity, is believed to be accomplishable, if desired, by the selective addition of diluent and additives.
  • These polymer compositions characteristically exhibit performance curves indicating substantially level and constant loss modulus, storage modulus, and complex viscosity over extended temperature ranges.
  • the graphic plots of loss modulus, storage modulus, and complex viscosity versus temperature all are believed to characteristically exhibit a sharp knee that shows the moduli to increase in value rapidly at cure temperatures.
  • compositions of this invention are controllably curable into polymeric materials which are preferably not sticky or tacky, and which have desirable elastomeric, flexural, strength and resiliency characteristics.
  • a silicone polymer composition which incorporates a benzophenone
  • the benzophenone component can be regarded as, or identified herein for convenience as, component (vi) .
  • a composition of this invention preferably contains from about 0.3 to about 10 parts of component (vi) , although larger and smaller amounts can be used, if desired, without departing from the spirit and scope of the invention.
  • One class of substituted benzophenones useful in the practice of this invention is characterized by the generic formula:
  • R 1 and R 2 are each selected from the group consisting of hydroxyl, lower alkoxy, and hydrogen, and n and are each an integer of 1 or 2
  • Examples of substituted benzophenones of formula (3) include: Table II
  • R 3 is a lower alkyl radical.
  • An example of a derivitized benzophenone of formula (4) is: 2-ethylhexyl-2-cyano-3,3- diphenylacrylate (available from BASF under the trademark "Uvinul N-539”) .
  • the contact angle exhibited by a silicone impregnant composition of this invention varies with the particular web which is to be saturated therewith. However, the contact angle of water is generally lower for the non-impregnated side than the impregnated side.
  • the combination of the processed web, the silicone polymer and the fluorochemical generally produces higher water contact angles than the web treated only with fluorochemicals.
  • the performance of an impregnant composition may be determined by the nature of a previously applied saturant such as a fluorochemical.
  • Suitable starting compositions include 100% liquid curable silicone rubber compositions, such as SLE5600 A/B from General Electric, Mobay LSR 2580A/B, Dow Corning "Silastic ® 595 LSR” and “Silastic ® 590" which when formulated with substituted benzophenones as taught herein will form a contact angle of much greater than 70 degrees, and typically of 90+ degrees, with typical porous webs (such as fabrics) that have a residue of fluorochemical upon (and within) the web from a prior saturation.
  • 100% liquid curable silicone rubber compositions such as SLE5600 A/B from General Electric, Mobay LSR 2580A/B, Dow Corning "Silastic ® 595 LSR” and “Silastic ® 590" which when formulated with substituted benzophenones as taught herein will form a contact angle of much greater than 70 degrees, and typically of 90+ degrees, with typical porous webs (such as fabrics) that have a residue of fluorochemical upon (and within) the web from
  • the silicone polymer composition of this invention can also carry additives into the three- dimensional structure of the web during the pressured impregnation. Further, it is preferable, that any additives be bound into the cured composition permanently as located in the three-dimensional structure of the web. Particularly in the case of fabrics, this desirably positions the additives mainly on surface portions of the treated yarns and fibers in positions where they typically are beneficially located and maintained.
  • Control of the pressurized impregnation step can be provided at a number of areas since the. impregnation is sensitive to the viscosity of the impregnant both at atmospheric pressure and at superatmospheric pressure.
  • the ambient temperature affecting the impregnant as it is applied, and the pressure-induced temperature changes occurring during application of the impregnant also play roles in viscosity and therefore the shear process.
  • the chemical composition of the silicone polymer impregnant composition of this invention also plays a role in the shear process and assists in assuring that the treated web fibers are encapsulated while, the interstices remain open.
  • the amount of silicone polymer impregnant utilized and the weight add-on thereof are again variable and dependent upon several things such as the treated web, the desired end use of the web, cost and the like.
  • Web weight add-ons can be as little as about 5 weight percent up to about 200 weight percent of the untreated web.
  • weight add-ons are preferably in the range of about 10 to about 100 weight percent of the weight of the untreated web.
  • the fluorochemical saturant composition may also contain a bonding agent. The bonding agent can facilitate the bonding of the water repellant chemical and/or the impregnate to the three-dimensional structure of the web within which it is saturated.
  • Mobay Silopren ® bonding agent type LSR Z 3042, and Norsil tm 815 primer are representative compositions that can be used to facilitate bonding of the water repellant chemicals and/or impregnant to and within the web.
  • Use of the bonding agents is not essential to the practice of this invention, but may improve bonding of the fluorochemical and/or the silicone polymer composition to fibers.
  • the fluorochemical particularly, and also the bonding agents when used, are preferably affixed to the three-dimensional structure of the web prior to a subsequent pressured impregnation. Complete affixing is not necessary for the fluorochemical.
  • the fluorochemical will apparently facilitate the pressured impregnation of a silicone polymer composition even if the fluorochemical is not preliminarily fixed within or located within the web being treated.
  • fixing especially by sintering, causes the water repellant chemicals to flow and to become better attached to the three-dimensional structure of the web.
  • a lesser amount of fluorochemical will remain in place better, and will better facilitate the subsequent pressure impregnation of the silicone polymer, if the sintering or insolubilizing step is performed prior to a pressured impregnation.
  • a web may have a surface contact angle of greater than about 70 degrees, and more typically greater than about 90 degrees.
  • Web impregnation pressures can involve transverse force or pressure in the range of tens to hundreds of pounds per square inch of web surface.
  • the silicone impregnant introduced by the pressured impregnation step can be defined by its functional qualifications.
  • the silicone polymer impregnant produces a contact angle with a fluorocarbon treated web of greater than about 70 degrees.
  • the contact angle of a fluorochemical will be within a range of about 90 degrees to about 180 degrees while the contact angle of the silicone polymer will be within a range of about 70 degrees to about 180 degrees.
  • the contact angle exhibited by the silicone polymer impregnant can be, if desired, qualified against the particular web as saturated with the particular fluorochemical saturant.
  • the selection of a suitable silicone polymer composition may be determined by the nature of a previously applied fluorochemical saturant.
  • the fluorochemical saturants and silicone polymer compositions are, however, not critical to the practice of this invention since wide respective compositional ranges may be involved.
  • a substantially undiluted liquid silicone rubber which is available from suppliers such as GE, Dow Corning, and Mobay-Bayer will characteristically form a contact angle of much greater than about 70 degrees, and typically greater than about 90 degrees, with typical porous webs (such as fabrics) that have a residue of fluorochemical upon (and within) the web resulting from a prior saturation.
  • the silicone polymer composition can carry additives into the three-dimensional structure of the web in the pressured impregnation step of the method of the invention. Further, the silicone polymer composition, when cured, is capable of adhering both to fibers, yarns, and the like, and any additives dispersed therein. , Thus, additives are positioned adjacent to or on surfaces of yarns, fibers, and the like, in a position where they can be beneficial.
  • additives that are dispersible in effective amounts in a viscous silicone polymer composition typically at a concentration of about 0.1 to 20 weight percent (based on total composition weight) include ultraviolet absorbers, flame retardants, aluminum hydroxide, filling agents, blood repellents, flattening agents, optical reflective agents, hand altering agents, bioco patible proteins, hydrolyzed silk, and the like.
  • Hydrolyzed silk is a texturing agent that imparts a substantially silky feel to a fabric treated in accordance with the method of the invention regardless of whether or not such fabric is itself silk.
  • silicone polymer dispersible agents include those affecting thermal conductivity, radiation reflectivity, electrical conductivity, and other properties. For example, if a metallic sheen and/or thermal or electrical conductivity or infrared background blending is desired, powdered metals may be dispersed therein.
  • the impregnation is sensitive to the viscosity of the silicone polymer composition.
  • the impregnation temperature affects the silicone polymer composition by reducing or altering its viscosity. Shear-induced temperature changes occurring during application or during subsequent shear processing of the silicone polymer can affect viscosity.
  • the chemical composition of the silicone polymer also plays a role in the treating process and can assist in the treatment of web fibers and the regulation of the interstices voids.
  • FIG. 4a An embodiment of a machine suitable for accomplishing pressured impregnation in accordance with this invention is illustrated in side elevational view in Figure 4a.
  • Two blades 200 and 210 in opposed relationship to one another are provided in functional combination with means for providing a precisely adjustable gap therebetween through which a web or fabric 300 is drawn while having a silicone polymer composition 220 applied to either one or both surfaces thereof.
  • An enlarged side view of a typical blade 200 or 210 is shown in Figure 4b.
  • Dimensions A, B, C, D, and E are typically and exemplarily illustrated as, respectively, about 3-1/2 inches, about 1-1/2 inches, about 2 inches, about 1/2 inch, and about 5/16 inch.
  • the narrow edge is preferably milled to a tolerance of about 1/10,000 inch continuously along the edge surface of each blade which is typically and illustratively about 38 inches long.
  • Each of the corners of the narrow edge is preferably and illustratively a hard (not beveled or ground) angular edge.
  • Each blade 200 or 210 is typically and illustratively made from carbon steel or stainless steel.
  • a reservoir of silicone polymer composition is formed preferably on one upper surface of the fabric 300 behind (relative to the direction of fabric movement) an upper one of the blades 200 and 210 which are mounted on a frame (not shown) so as to extend horizontally.
  • the slit orifice gap is chosen preferably and illustratively to be slightly smaller than the relaxed thickness of the starting web or fabric. Referring to Fig.
  • a second pressured impregnation station is seen to be positioned downstream (relative to the direction of fabric movement) from the pair of opposed blades 200 and 210.
  • a knife blade 230 is provided which has an edge that presses against the web or fabric 300 to reintroduce the silicone polymer composition into the fabric 300.
  • One side of blade 230 adjacent the edge thereof is strongly biased against an adjacent cylinder or bar 240, which, in the embodiment shown, does not rotate. If desired, bar 240 can be journaled for rotational movement.
  • the compression force is in the range of about 10 to about 500 inch pounds, although higher and lower forces can be employed.
  • the fabric 300 passes over the edge of blade 230, it is drawn away at an angle from the blade edge under longitudinal tension.
  • longitudinal tension in the range of from about 0.5 to 10 pounds per inch can be employed.
  • Such pressured impregnation serves to distribute and reintroduce the polymer composition in the web. Excess polymer composition is removed by blade scraping. Passage of the fabric 300 between the blade 230 and the bar 240 and over the edge of the blade 230 is believed to produce shear forces in the impregnant 220 (within the fabric 300) that facilitate flow and distribution thereof within the three-dimensional matrix of the fabric 300. Concurrently, blade 230 also scrapes excess silicone polymer composition impregnant off the fabric's surface in contact with the edge of blade 230.
  • Both the steps of fluorochemical saturation and of subsequent silicone polymer composition impregnation are performable, if desired, in production volumes, and at speeds which can be typical of the so called high end range of fabric finishing lines.
  • the fluorochemical saturation is conveniently accomplished conventionally by using a padbath in which the fabric is run through a dilute treating bath followed by squeeze rollers to remove excess liquid and overdrying. In general, any method of applying the fluorochemical would ' be acceptable.
  • FIG. 5 Another embodiment of a machine suitable for accomplishing pressurized impregnation in accordance with this invention is shown diagrammatically in Fig. 5 which also illustrates a process embodiment of this invention.
  • pressurized introduction of the silicone polymer composition into the web is first carried out.
  • controlled pressure reintroduction, distribution, and metering of the silicone polymer impregnant and recovery of excess liquid impregnant transpires using a shear knife or blade which applies transverse force against the impregnated web laterally across the web.
  • further controlled pressure reintroduction and metering takes place by means of a flexible blade, such as a so-called flex-knife or Spanish knife.
  • Such silicone polymer composition is then reintroduced, distributed, and metered in a controlled manner in the web with the aid of transversely applied shearing force and compressive force such that the impregnated composition becomes distributed in the web so that the fibers are at least partially encapsulated while the interstices are not completely filled with the silicone polymer composition.
  • the web is longitudinally tensioned and the pressurized application and impregnation and the subsequent shearing and compressive actions are successively accomplished in localized zones preferably extending generally laterally across the web (that is, generally perpendicularly to the direction of such longitudinal web tensioning) using transversely applied force exerted locally against surface portions of the web during each impregnation and shearing operation.
  • the web is conveniently and preferably, but not necessarily, moved longitudinally relative to such laterally extending web processing zones.
  • the impregnation, shearing and compressing steps are preferably carried out successively or sequentially.
  • Such zones are themselves preferably at stationary locations while the web is moved, but if desired, the web can be stationary while the zones are moved, or both. The result is that the silicone polymer composition flows into the web and is distributed therethrough generally uniformly to a predeterminable and controllable extent.
  • FIG. 6 A schematic side elevational view of another embodiment of a suitable pressurized impregnation machine for use in the practice of the invention is shown in Figure 6.
  • This machine continuously moves a longitudinally tensioned web 60 successively through a pressure impregnation station which incorporates a reverse roll coater having rollers 10 and 11, a shear station which incorporates a shear knife 20, and a finishing station which employs at least one so called flex-knife (or Spanish knife) 30.
  • flex-knife or Spanish knife
  • a silicone resin impregnant 50 is contained within reservoir 51.
  • Roller 12 rotates in the indicated direction so that its circumferential surface, preferably a textured or gravure surface, picks up liquid 50 from reservoir 51 and deposits it on the circumferential surface of roller 10 across a controlled width gap 13 between rollers 10 and 12.
  • gap 13 is actually less than the unencumbered thickness of the starting web 60.
  • roller 10 also preferably has a textured or gravure surface.
  • Roller 10 rotating in the roller arrow indicated direction, which is opposite to the direction of travel of web 60, applies the silicone polymer impregnant to one surface of the moving web 60, which is typically a fabric.
  • Roller 11 is urged with a compressive force against the back or opposed surface of web 60 and roller
  • roller 11 rotates in a direction which is the same as that in which web 60 travels. Roller 11 aids in achieving the desired pressured impregnation of web 60 by the silicone polymer impregnant from the surface of roller 10.
  • the impregnant is believed to be introduced into the fibers and the interstices of the web 60 by the aid of a back-pulling or shearing action resulting from the distorting and pressuring of web 60 caused by rollers 10 and 11 rotating in the same direction.
  • This direction may be the indicated direction with roller 10 rotating against the linear movement of web 60 indicated by web directional arrow 61, or all rollers 10, 11 and 12 may be reversed in respective rotational directions so as to cause each roll to turn in an opposite direction relative to that direction which is illustrated by the respective roller arrows in Fig. 6.
  • the web 60 is stretched and distorted to pull open the interstices of the web and to aid in impregnating web 60 with silicone polymer impregnant 50. This distorting, and particularly this stretching, is believed to facilitate the full and deep introduction of the impregnating liquid into the moving web 60.
  • the extent of pressured impregnation of the silicone polymer impregnant 50 into the web 60 which occurs between rotating rollers 10 and 11 is controllable to some extent by such variables as the speed of roller rotation, the pressure exerted by rollers 10 and 11 on web 60, the duro eter hardness and surface characteristics of each roll 10 and 11
  • the pressurized impregnation may also be carried out with rollers 10 and 11 which have finely milled, smooth circumferential surfaces.
  • the viscosity of impregnant 50 and the amount of impregnant liquid 50 transferred from roll 12 to roll 10 across gap 13 may also be varied to regulate impregnation.
  • Feed roller 12 preferably rotates counter to application roller 10.
  • the impregnant 50 can be monitored to assure that its homogeneous composition is maintained. If desired, the impregnant 50 formulation can be altered to adjust to process needs during a continuous treating operation.
  • the impregnation extent can be such that spaces (or interstices) both between the fabric's fibers/filaments, or between the fabric's yarn members (as the case may be) are filled with impregnant 50.
  • the amount of impregnant can be such that spaces (or interstices) both between the fabric's fibers/filaments, or between the fabric's yarn members (as the case may be) are filled with impregnant 50.
  • the amount of impregnant can be such that spaces (or interstices) both between the fabric's fibers/filaments, or between the fabric's yarn members (as the case may be) are filled with impregnant 50.
  • the impregnant 50 which is thus introduced into web 60 can be much less than such a saturation level; for example, the amount introduced can be insufficient even to coat or encapsulate completely individual fibers of the web.
  • the impregnant 50 can be relatively non- uniformly distributed in the web after such pressurized impregnation.
  • the action of the shear knife 20 in the next zone of processing is such as to smooth out and to make uniform the distribution of impregnant 50 in web 60. Also, the shear knife 20 helps regulate the amount of. impregnant 50 that is allowed to remain in web 60.
  • a top coat polymer can additionally be introduced; for example, just before or after flex knife 30.
  • a top coat polymer can additionally be introduced; for example, just before or after flex knife 30.
  • the top coating can comprise a dilute dispersion of a fluorochemical fabric treating composition. In a web treated therewith, such treatment enhances the surface properties of the web, such as by increasing grease or chemical penetration resistance, soil resistance, or the like.
  • the dilute fluorochemical dispersion ' can be applied by spraying, misting, or the like.
  • Both treating agents then enter a curing stage, which can be accomplished conveniently by passing the treated web through an oven wherein the temperature and web residence time are sufficient to cure both the fluorochemical and silicone polymer impregnant to a desired extent, or by radiation, if desired.
  • the amount of silicone polymer impregnant actually introduced through the pressured impregnation, and into the preferably stretched openings of the interstices of the web 60 is influenced by such factors as the velocity of movement of web 60, the viscosity characteristics of impregnant 50, the compressive pressure exerted by roll 10 against roll 11, the longitudinal tension exerted upon the tensioned web 60, the impregnant distribution achieved by shear blade 20 and scraper flex knive(s) 30, and the like.
  • the impregnant reintroduction and distribution believed to be achieved by bar or shear knife 20 is achieved by the exertion of a pressure against moving tensioned web 60.
  • the shear force and the temperature elevation due to such shear force results in the impregnant 50 flowing upon the three dimensional structure of the web 60 and the knife 20.
  • the liquid impregnant 50 is thixotropic.
  • the flowing of the impregnant 50 into the web 60 using controlled liquid rheology preferably does not result, at the time of impregnation, in a fluid viscosity which is so low as to cause the liquid impregnant to spread into and be distributed substantially uncontrolled throughout the web 60.
  • the flowing activity of the viscous impregnant is preferably accomplished using an impregnant 50 which has controllable rheology and viscosity such that impregnant-50 will achieve a desired encapsulation of individual fibers of the web 60.
  • impregnant 50 which has controllable rheology and viscosity such that impregnant-50 will achieve a desired encapsulation of individual fibers of the web 60.
  • this encapsulation results in the fabric's individual fibers being surrounded with a localized layer or film of silicone polymer.
  • a plurality of web tension control devices 70 can be used in the region of metering bar or shear knife 20 and in the region of reintroduction scraper flex knives 30 along web 60 in order to provide the capacity for precision control of the tension exerted on web 60 and of the compressive pressures and shear forces exerted on web 60 at metering bar or shear knife 20 and flexible knives 30.
  • the machine preferably includes an impregnant 50 recovery and recycling system which more preferably also includes a filtering subsystem, such system being diagrammatically represented and indicated by dashed line path 40.
  • This system includes a collection tray, or pan, 41, positioned under and behind the moving web 60 to collect along the sides of web 60, the excess impregnating liquid as it is wiped from the web surface contacted by the metering bar 20 and/or by the recovery knives 30 and passed laterally into pan or tray 41.
  • the excess impregnant 50 is pumped back through filter 42 into the reservoir 51 of the reverse roll coater for loading and distribution on the surface of roller 12, transfer to roller 10, and reapplication to portions of continuously moving web 60.
  • the ability to reuse the excess impregnant 50 wiped from the moving web 60 rather than losing such impregnant within the process makes the entire process more economically attractive.
  • FIG. 7 Another embodiment of a machine suitable for use in the practice of this invention is shown - 5 schematically in side elevation in Figure 7.
  • rollers 10 and 11 of the Figure 6 apparatus are replaced with a combination of a reservoir 51, and a bar or shear knife 100.
  • the reintroduction bar or shear knife 100 pressurizes the impregnant 50 which is applied
  • the web 60 in effect constitutes a retaining wall for a part of the reservoir 51.
  • the reservoir 51 thus functions to hold a pool of the silicone polymer composition impregnant 50 against a
  • the bar or shear knife 100 functions to apply pressure or force upon the silicone polymer composition impregnant 50 that was deposited on the web 60, thereby causing the impregnant
  • the knife 100 also serves to distribute and move the impregnant in the web and to encapsulate the fibers thereof. Excess impregnant 50 is also scraped away by knife 100.
  • one or more of flex knives 100 function to further reintroduce, 25 distribute the impregnant 50 and encapsulate fibers of web 60.
  • the knives 110 can be considered to function in a manner which is equivalent to the knives 30 on the treated surface of web 50 in the Fig. 6 apparatus.
  • the Fig. 6 embodiment is believed to exhibit a wider degree of control in the practice of the present impregnation process. Particularly, both the initial applied amount and the successive pressurings of, a silicone polymer impregnant 50 are precisely controllable.
  • the Fig. 7 embodiment is characterized by the capability for operation at higher web 60 transport speeds, typically at speeds characteristic of higher end commercial fabric finishing line operations. The embodiment shown in Fig.
  • Top roller pressure 0 to 500 lbs/ Delivery quantity, down and in at an linear inch depth, residue angle or in front of presence both at lower roller yarn level and a fiber or filament level
  • Metered Film Thickness .05 mil thick Contiguous film on top roller non-contiguous delivery quantity film to 10 mil controlling thicker on roller film presence and allows more impregnant to dam at either second or third stage
  • Lower roller surface Low durometer Low durometer and composition material material allows surface to high pressure from upper strength metals roller to be agitation of yarn bundles or filament's metal surface causes more complete distortion and agitation of yarn and fiber/filament
  • Adjustment Parameters to Adjustment adjustment of Web Angle of bar knife Bar knife faces Angle effects shear forward to meet forces on impregnate web coming to and determines bar; bar knife distortion or vertical to web, bar agitation as it faces away or relates to causing racked back from flow of impregnate; web run direc ⁇ can determine tion reintroduction of impregnate by dammed quantity of impregnate
  • Edge Shape Knife very Sharpness of knife sharp affects shear forces. The sharper and thinner the edge, the greater the shear forces at the contact edge
  • FIG. 12a A schematic, side elevational view of another and preferred suitable pressurized impregnation system or apparatus 73 for practicing the present invention is shown in Fig. 12a.
  • a continuous web 74 is moved along a web pathway from a supply roll 76 to a take-up roll 77.
  • a liquid silicone polymer composition is applied to one face (here, the upper face 79) of web 74 by a conventional reverse roll coater apparatus 81 wherein such composition is applied to the surface of a reversely rotating (relative to the direction of travel for web 74) coating roll 82 from a nip region reservoir 83 formed between the coating roll 82 and a transfer roll 84 (which rotates in the direction of travel for web 74, but whose surface does not contact web 74) .
  • the web 74 is transversely compressed between coating ' roll 82 and drive roll 86 as it passes through station 78.
  • the polymer composition is applied under a positive pressure against face 79 by coating roll 82 which functions to cause the composition to be impregnated into web 74.
  • a present preference is to use a coating roll 82 which has smooth, chrome plated surfaces.
  • the web 74 is pretensioned by coacting clutching rolls 87, 88 and 89. After it passes over guide roller 91 on the web pathway from supply roll 76, the web 74 passes over roll 87, between rolls 87 and 88, around roll 88, and between rolls 88 and 89.
  • the clutching rolls 87, 88 and 89 are components of a conventional web clutching mechanism (not detailed) which provides for adjustments between rolls 87, 88 and 89 so that selective tensioning of web 74 is achieved along the web pathway between the clutching rolls 87, 88 and 89 and the nip region 92 defined between rolls 82 and 86 with the intervening roller roll 93 being used for guidance of web 74.
  • the clutching rollers 87, 88 and 89 also function to smooth out and extend the web 74 before it enters the coater apparatus 81 so that in the apparatus 81, the web will have polymer composition uniformly applied thereto.
  • the web 74 After passing nip region 92 the web 74 is preferably highly longitudinally tensioned along the web pathway extending from nip region 92 to compensating and regulating coacting tension rollers 94, 95 and 96.
  • the tension rollers 94, 95 and 96 are components of a conventional web tension adjusting and regulating mechanism (not detailed) which provides for on-line, in- stream operator controlled adjustments between rollers 94, 95 and 96 that permit selective control of the tautness of web 74 particularly in the web pathway region from nip region 92 to rollers 94, 95 and 96.
  • the web 74 successively passes through each one of a series of processing stations 98, 99 and 100.
  • a substantially non-flexible shear knife 101 and 102 extends laterally across web 74 with the web 74 being entirely unsupported on the lower face 101 thereof which is opposed to upper face 79 and to the respective blades of each shear knife 101 and 102.
  • the web 74 passes over each knife edge in a contacting relationship and three idler rolls 105, 106 and 107 that are provided in a typically fixed (but off-line adjustable) relationship relative to knives 101 and 102 as apparatus 73 is operated.
  • each blade 101 and 102 Relative to the direction of web 74 travel, idler rolls 105 and 106 thus are positioned so that roll 105 is on the lead side, and roll 106 on the trailing side, of knife 101 while idler rolls 106 and 107 are positioned so that roll 106 is on the lead side, and roll 107 is on the trailing side of knife 102.
  • the angle of inclination or tilt of each blade 101 and 102 relative to the vertical is adjustable over a wide range, but it is presently preferred to adjust the blade inclination angle for each blade between about ⁇ 45° relative to the vertical with the web 74 being horizontal.
  • each respective blade is functionally associated with a knife back support 108 and 109, respectively.
  • Each support 108 and 109 permits its associated blade 101 and 102 to be adjustably inclined in relation to the vertical relative to a supporting frame (not shown) .
  • Another adjustable variable is the amount of angular web depression, which in the embodiment shown, extends downwardly, achieved by web in its passage over the circumferential edges of adjacent rolls 105 and 106 relative to knife 101, and in its passage over the circumferential edges of rolls 106 and 107 relative to knife 102.
  • the angle of the knife 101 or knife 102 relative to the web can be in the range of about 30° to about 140°.
  • shear knives 101 and 102 which have straight edges
  • shear knives having somewhat curved edges can be used, if desired.
  • shear knives 101 and 102 which have sharp edges, more preferably edges which are sharpened to a micro edge uniformity of at least about root mean squared (RMS) 8
  • shear knives can be used which have dull or rounded edges.
  • shear knives 101 and 102 which are formed of steel, other materials of knife construction could be used if desired, such as metal alloys, non-metallic composites, and the like.
  • the amount of shear force applied by a shear knife 101 or 102 transversely against a web 74 is a function of many variables with probably the most important or principal variables being the fluorochemical pretreatment, the silicone polymer viscosity and the longitudinal web tension (assuming a fixed spatial position for idler rolls 105, 106 and 107 and shear knives 101 and 102 during operation) .
  • a suitable and preferred level of applied shear force and web tensioning has been achieved to produce a product having encapsulated fibers, one can usually hear a distinctive sound in the region of a shear blade 101 and 102. This sound can also be heard in the vicinity of shear blades being used in the operation of other processes described herein. This sound can in fact be used by an operator as a rough guide as to whether or not he is succeeding in producing a silicone polymer impregnated product containing encapsulated fibers.
  • Idler roll 105 also functions as a compensator roll for mechanically adjusting and controlling web tension after coating apparatus 81 and before knife processing begins. Also, conveniently and preferably the web tension is sensed electronically, and then roll 105 is automatically raised or lowered to achieve web tensioning adjustments so as to maintain a preset tension in web 74.
  • the web 74 is passed over the circumferential surface of a conventional padder roll 111.
  • a flexible so-called “flex-knife” or “Spanish knife” 100 is positioned between the idler roll 107 and the padder roll 111.
  • the blade of this flexible knife 100 is inclined at an angle with respect to the web 74 passing thereagainst so that the knife 100 exerts a compressive force against the face 79 of web 74 with opposed face 103 being entirely unsupported.
  • the angle with respect to a (hypothetical) perpendicular line extending into a (hypothetical) straight line extending from the circumferential edge of roll 107 to the circumferential edge of roll 111 can range from about 30° to about 140° for the adjustment of the inclination angle of the flex knife.
  • knife 100 is functionally associated with a mounting bracket or back support 113 which in turn is adjustable relative to an apparatus frame (not shown) .
  • the padder roll 111 is not employed as a web 74 treating means.
  • web 74 After leaving the mechanical tension compensator rolls 94, 95 and 96, web 74 is under reduced or preferably minimal tension and is led along a pathway which extends over spacer rolls 113 and 114.
  • a platform 116 In the region over spacer rolls 113 and 114, and generally between tension roll 96 and idler roll 117, a platform 116 is conveniently positioned which can incorporate suitable instrumentation panels, operating controls and the like so that an operator can observe the operation of the apparatus 73 in the practice of the process of this invention and then control and regulate the same.
  • a position which is suitable for operator observation of a web in progress that is located in the vicinity of the tenter frame 118 is desirable because it has been observed that a web being processed can experience some distortion owing to the forces exerted thereon.
  • the tenter frame 118 adjusted by the operator so that, as the web passes therethrough, the web can be straightened or shaped either longitudinally or laterally, as desirable or considered necessary for an individual web. If desired, the tenter frame 118 can be automatically operated to apply tensioning forces to a web in accordance with a predetermined program, or the like.
  • the tenter frame 118 also provides the start of a new zone of limited longitudinal and transverse tensioning which extends forwardly along the web pathway from tenter frame 118 through oven 119 to a tension compensator, here shown as utilizing three tension rolls 121, 122 and 123 which are part of a conventional mechanical tension compensator subassembly which is similar in structure and function to the compensator subassembly incorporating the previously described tension rolls 94, 95 and 96.
  • the tensioning longitudinally of web 74 as it passes through oven 119 is employed to control the web 74 as it passes through oven 119 as regards web dimensional limits. This tensioning is chosen to be at a level which does not introduce significant distortion into the web, yet web sagging is avoided, as from thermal expansion and elongation.
  • Rollers can be used in the oven 119 to avoid sagging and to maintain uniform heat exposure.
  • the rolls 121, 122 and 123 also serve to provide a cooling pathway for the web 74 as it emerges from the oven 119 before it passes over guide roller 124 and into take-up roll 77.
  • the oven 119 functions to cure the silicone polymer composition impregnated into web 74.
  • Oven 119 can be operated with gas or some other energy source. Oven 119 can extend for from about 12 to 20 yards, a 15 yard long oven being convenient. Curing temperatures of from about 320° to about 500°F, applied for times of from about 2 minutes to about 30 seconds (depending upon the temperature) are desirable. If a curing accelerator is present in the silicone polymer, curing temperatures can be dropped down to temperatures of about 265°F or even lower (with times remaining in the range indicated) .
  • a source of radiation can be employed (electron beams, ultraviolet light, or the like) to accomplish curing, if desired.
  • the full heating capacity of the oven 119 can be used, if desired, or if full oven capacity is not needed, either longitudinally or vertically.
  • full heating capacity can be used, if desired, or if full oven capacity is not needed, either longitudinally or vertically.
  • only top heating or only bottom heating with respect to the web can sometimes be used as compared to a combination of both top and bottom heating.
  • the take-up roll 77 operates at approximately the same speed as the supply roll 76.
  • the tension roll combination of rolls 121, 122 and 123 can be used to take up or reduce web slack, as the case may be.
  • Web transport speeds can vary widely; for example, from about 2 yards per minute to about 90 yards per minute.
  • Figs. 12b and 12c two alternate variations or modes are seen. In such views, similar components are similarly numbered but with the addition of single prime marks thereto in the case of Fig. 12b and double prime marks thereto in the case of Fig. 12c.
  • Fig. 12b a further stage of web pressurization is introduced after the flex knife 112' and before the tenter frame 118'.
  • the web 74' after passage through the flex knife 112' is passed through the nip region 126 existing between padder roll 111' and associated transfer roll 127 where the web 74' is subjected to compression between rolls 127 and 111' for the purpose of achieving a better distribution of silicone polymer composition on web 74'.
  • the web 74' After leaving nip region 126, the web 74' is- retained under some compression against roll 127 by means of retaining bar or roll 128 for similar purposes.
  • the roll 128 can be replaced by a flex knife (not shown) over whose edge the web 74' passes after departure or preparation from roll 127.
  • the flex knife can accomplish substantial further polymer distribution in web 74 • .
  • Fig. 12c there is seen an embodiment where the web 74 ' ' is passed through the nip region of rolls 111 1 ' and 127*'.
  • the rolls 111 11 and 127'' serve to end the region of high longitudinal tension in the stages of blade or knife application to web 74'' and to provide the desired reduced pressure for web passage through a curing station, here illustrated by oven 119'' which the desirable and preferred intervening tenter 118' ' .
  • webs of this invention are characterized by having fiber encapsulation layers which range from about 0.1 to about 50 microns.
  • a presently preferred web which is both fluorochemical and silicone resin treated and is breathable, water resistant and rewashable is characterized as being a longitudinally tensionable porous fibrous web having opposed, substantially parallel surfaces that is comprised of associated * individual fibers with interstices existing between adjacent fibers.
  • the web is substantially uniformly impregnated with a fluorochemical and thereafter impregnated with a silicone polymer composition to individually encapsulate the fibers.
  • the application side of the web is virtually indistinguishable from the opposite side of the web with complete fiber definition. All fiber interstices remain defined and/or substantially open.
  • the polymer is preferably selected from the group consisting of polyamides, polyesters, regenerated cellulose, cellulose acetate, and mixtures thereof.
  • Preferred webs of this invention are more specifically characterized by having a water drop contact angle in the range of about 90° to about 160°; a rewash capability of at least about 3; a breathability of at least about 35% of the untreated web; and a water repellency rating of at least about 80 prior to washing.
  • a general process for making a porous web of this invention which is a silicone resin fiber encapsulated web comprises the steps of: tensioning a flexible, porous web as above characterized, applying a curable silicone polymer composition having a viscosity sufficient to encapsulate the fibers of the web to at least one web surface and then moving a uniformly applied localized shear force over and against the surface of the web while tensioned to: distribute the silicone polymer composition within the web generally uniformly, at least partially individually encapsulate surface portions of at least some of the fibers with the silicone polymer composition, and leave at least some of the interstices open. Thereafter, the web is subjected to conditions sufficient to cure the silicone polymer composition in the web. Curing is accomplished by heat, by radiation, or both.
  • a silicone polymer composition is pressured under force into a porous substrate that is distorted at the location of the pressuring in order to facilitate entrance of the polymer composition into the substrate.
  • the viscosity of the polymer composition is reduced by shear forces occurring during the pressuring and the polymer composition impregnates the substrate.
  • the distorting is accomplished by stretching the web, preferably by passing the tensioned web under a bar knife.
  • the substrate is also scraped to remove excess polymer composition from its surface, preferably while the web is under tension so that further pressure is exerted against the polymer composition so as to further reduce its viscosity and again force it under this additional pressure to further impregnate the porous web.
  • the pressurized scraping simultaneously and sequentially transpires at a plurality of locations along the tensioned substrate as it moves under tension past a plurality of scrapers.
  • the process may be said to comprise the steps of:
  • a presently preferred process for making a fluorochemical and silicone resin treated web having breathability, water resistance and rewashability comprises the successive steps of: impregnating the associated fibers of a flexible porous fibrous web having interstices between fibers with a fluorochemical, longitudinally tensioning the fluorochemical impregnated web while sequentially first applying to one surface thereof a curable silicone polymer composition and concurrently applying a transversely exerted localized compressive force against said surface, and moving a substantially rigid shearing means over said surface of the web to transversely exert an applied, localized shear force against said surface and wipe away exposed portions of said silicone polymer composition on said surface, thereby individually encapsulating at least some of said fibers with said silicone polymer composition; and curing the silicone polymer composition in the web.
  • the fluorochemical impregnation operation is conveniently and preferably carried out by the steps of: substantially completely saturating the web with a solution or dispersion of a curable fluorochemical composition in a carrier liquid; compressing the saturated web to remove therefrom excess portions of said dispersion; and heating said web to evaporate the carrier liquid therefrom.
  • any convenient process can be used for accomplishing fluorochemical pretreatment of a web to be used in this invention.
  • the presently preferred polymer impregnant used in the pressure impregnation and knife blade treatment of webs by this invention is a non-Newtonian liquid exhibiting thixotropic, pseudo-plastic behavior. Such a liquid is temporarily lowered in viscosity by high pressure shear forces.
  • One aspect of the invention is a recognition that when high forces are applied to curable silicone polymer compositions, such as those as viscous as bathtub caulk, then the viscosities of these materials can be lowered perhaps up to 99% or more. Conversely, when cured (polymerized and/or cross-linked) these compounds increase in viscosity up to perhaps 1,000,000% or more.
  • the internal and external rheological control of viscous silicone impregnant materials achieved by the present invention is believed to be of an extreme level even for thixotropes. When subjected to shear force, the silicone polymer composition can flow more readily, perhaps comparably, to water. When subsequently subjected to curing, the same composition sets to a solid form which can have a consistency comparable to that of a hard elastomeric rubber.
  • the invention preferably employs a combination of: (i) mechanical pressure to squeeze a silicone polymer composition impregnant into a porous web; (ii) a porous web pretreatment with a water repellent chemical, such as a fluorochemical, which is theorized to reduce the surface tension characteristics of the web and create a favorable surface contact angle between the silicone polymer composition and the treated substrate fiber surfaces which subsequently allows, under pressure and shear force exerted upon an applied silicone polymer composition, the production and creation of thin enveloping or encapsulating film to form as a result of impregnant flow over fiber surfaces in a porous web; and (i ⁇ ) a silicone polymer composition impregnant preferably having favorable rheological and viscosity properties which responds to such working pressures and forces, and is controllably impregnated into, and distributed in a web.
  • a water repellent chemical such as a fluorochemical
  • This combination produces a fiber encapsulated web having a high degree of performance.
  • This product is achieved through pressure impregnation and applied shear forces brought to bear upon a treated web so as to cause controlled movement and flow of a silicone polymer composition into and through a web.
  • pressure impregnation and applied shear forces brought to bear upon a treated web so as to cause controlled movement and flow of a silicone polymer composition into and through a web.
  • repeated compressive applications of pressure or successive applications of localized shear forces upon the impregnant in the treated web are employed.
  • the impregnant responds to a water repellent fluorochemical pretreatment of the web so as to permit enhanced flow characteristics of the impregnant over the web and the development of silicone polymer composition encapsulated fibers in a treated web.
  • the boundary or edge of the impregnant is moved, preferably repeatedly, in response to applied suitable forces into the interior region of a porous web so as to cause thin films of the impregnant to develop on the fiber surfaces.
  • thixotropy refers herein to liquid flow behavior in which the viscosity of a liquid is reduced by shear agitation or stirring. It is theorized to be caused by the breakdown of some loosely knit structure in the starting liquid that is built up during a period of rest (storage) and that is torn down during a period of suitable applied stress. Thixotropic behavior is preferably built into an impregnant used in the invention by either polymer design or additive/filler design. For example, it now appears that thixotropic behavior can be accentuated by introducing into a silicone polymer composition certain additives that are believed to impart enhanced thixotropy to the resulting composition.
  • a lower viscosity at high shear rates (during application to a web) is believed to faciliate impregnant flow and application to a web, whereas an impregnant with high viscosity, or applied at a low shear rate (before and/or after application) actually may retard or prevent fiber encapsulation.
  • stage 1 silicone polymer composition impregnant is prepared which can be purchased commercially and comes in typically two parts, designated as A and B.
  • a and B a base vinyl terminated polysiloxane
  • B a liquid organohydrogensiloxane crosslinking agent
  • Certain remaining components, such as a resinous organopolysiloxane copolymer and a platinum catalyst may (or can) apparently initially be in either part A or part B.
  • Stage 2 can be considered to involve the mixing of such a product's parts with or without additives.
  • Changes in viscosity can be obtained and measured based on applied shear rates and shear stresses. Such changes can be experienced by an impregnant with or without additives. Up to a 99% reduction in viscosity of a liquid silicone polymer composition is believed to be obtainable by the shear forces involved in the mixing or infusion of a silicone polymer composition impregnant into a web during,, the elapsed applied combination of processing time, temperature, radiation, and/or chemical changes involved. Thereafter, a very substantial increase in impregnant viscosity is believed to be obtainable taking into account these same factors.
  • Stage 3 can be considered to be the pressure introduction stage. Up to a 99% reduction of the impregnant viscosity is believed to be obtainable due to the applied shear forces, elapsed time, temperature, radiation and/or chemical changes. Thereafter, a 10,000% increase or even more in the resulting impregnant viscosity is believed to be obtainable. In this stage, curing of the impregnant can take place. Most commonly, impregnant viscosity is decreased during the pressure introduction stage 3 by the application of shear forces.
  • Stage 4 can be considered to be the first stage internal matrix dispersing and reintroduction with metering, and also recovery and recycle of excess impregnant.
  • the shear forces cause a temporary lowering of impregnant viscosity, causing it to flow upon and into the three- dimensional structure of the web.
  • the initial visco- elastic character of the impregnant is typically ⁇ theorized to be recovered almost immediately after shear forces are removed.
  • Stage 5 can be considered to be a second stage internal matrix dispersing and reintroduction with metering and also recovery and recycling of excess impregnant.
  • the variations in the viscosity of the impregnant are equivalent to stage 4.
  • the viscosity of the impregnant is again lowered causing it to flow within the web. Because of the application of repeated shear force induced reductions in viscosity, the thixotropic behavior of an impregnant may not undergo complete recovery, following each application of shear force and the viscosity of the impregnant may not revert to its pre-impregnation values.
  • the silicone polymer composition impregnant is believed to have the capacity to form a thin film upon the surfaces of components comprising a porous three-dimensional matrix such as a web during time intervals that the impregnant is caused to flow under pressure in and about matrix components. In between these times, the impregnant may recover substantially all of its initial high viscosity, although perhaps slightly less so with each repeated application of shearing pressure or force.
  • Stage 6 can be considered to be occurring just as curing is begun, and just as heat is introduced.
  • Stage 7 can be considered to be occurring with regard to the exertion of control of curing.
  • at least a partial curing (including cross-linking and/or polymerizing) , is obtained by relatively low temperatures applied for relatively short times, for example, temperatures under about 350°F applied for under about 3 minutes, when, for example, light cotton, nylon or like fabrics are being impregnated.
  • Fig. 8 shows four graphs illustrating four ways that could be used for plotting impregnant rheological behavior: (a) shear rate versus shear stress (uniform scales) , (b) shear rate versus shear stress (log scales) , (c) viscosity versus shear rate (uniform scales) , and (d) viscosity versus shear rate (log scales) , if desired, in the practice of this invention. Only the log versus log scales are believed to be capable of encompassing a full range of values for the three indicated variables.
  • the graphs represent some broad ranges of viscosity changes relative to shear stress that could be undergone by a given silicone polymer composition impregnant during execution of a given pressured impregnation procedure as taught herein.
  • surface tension can be considered to have reference to a single factor consisting of such variables as intermolecular, or secondary, bonding forces, such as permanent dipole forces, induced forces, dispersion or nonpolar van der Waals forces, and hydrogen bonding forces.
  • bonding forces such as permanent dipole forces, induced forces, dispersion or nonpolar van der Waals forces, and hydrogen bonding forces.
  • the strong primary bonding forces at an interface due to a chemical reaction are theorized to be excluded from surface tension effects; however, it is noted that even a small degree of chemical reactivity can have a tremendous influence on wetting effects and behavior affected by surface tension.
  • adhesion is theorized to be a wetting effect.
  • Spontaneous adhesion always occurs for contact angles less than about 90°. However, for a combination of a rough surface and a contact angle over 90°, adhesion may or may not occur. In fact, roughness becomes antagonistic to adhesion, and adhesion becomes less probable as roughness increases.
  • penetration is theorized to be a wetting effect. Spontaneous penetration occurs for contact angles less than about 90°, and does not occur for contact angles over about 90°. The roughness of a solid surface accentuates either the penetration or the repellency action, but has no influence on which type of wetting takes place.
  • Fig. 9 is a schematic vector diagram illustrating the surface tension forces acting at the vertex boundary line of a liquid contact angle on a planar solid surface. It illustrates how surface tension forces might be measured between a silicone polymer composition impregnant and a fiber of a web (or a fabric) as treated by the invention.
  • Fig. 10 is a graph relating the contact angle over a smooth solid surface as a function of " ⁇ + and i that apply respectively, to adhesion (i cos ⁇ + 1) , penetration (i cos ⁇ ) , and spreading (i cos ⁇ - 1) .
  • Fig. 10 illustrates what is theorized to be the relationship of a silicone polyer composition impregnant to silicone polymer composition solids in a treated web as regards such factors as adhesion, penetration, spreading, and retraction.
  • Fig. 11 consisting of Figs. 11a through lid, shows representative viscosity profiles plotted on log viscosity versus log shear rate graphs for (a) pseudoplastic flow, (b) distant flow, (c) pseudoplastic flow with superimposed thixotropic behavior, and (d) laminar Newtonian flow that erupts into turbulent flow at a critical transition point.
  • Figs. 11a through lid show a broad range of illustrative flow characteristics that could be demonstrated by silicone polymer composition impregnants suitable for use in this invention using pressured impregnation of a web as taught herein.
  • the term "wetting" is used to designate such processes as adhesion, penetration, spreading, and cohesion. If wetting transpires as a spontaneous process, then adhesion and penetration are assured when the solid surface tension exceeds the liquid surface tension. Surface roughness promotes these spontaneous wetting actions. On the other hand, no such generalizations can be made when the solid surface tension is less than the liquid surface tension.
  • Example 2-19 Liquid Silicone Polymer Preparation The procedure of Example 1 was repeated with various other curable viscous liquid silicone polymer composition commercially available. To this product system is added a substituted benzophenone and other additives, the result of which are shown in Table VI below. All parts are by weight. Table VI Illustrative Silicone Resin Compositions
  • Ratio listed is that recommended by the manufacturer.
  • Syl-off ® (registered trademark of Dow Corning) is a cross-linker.
  • Sylox ® 2 (registered trademark of W.R. Grace & Co.) is a synthetic amorphous silica.
  • Hydral ® 710 (registered trademark of Alcoa) is a hydrated aluminum oxide.
  • Silopren ® LSR Z/3042 registered trademark of
  • Mobay is a silicone primer (bonding agent) mixture.
  • Flattening Agent OK412 ® (registered trademark of Degussa Corp.) is a wax coated silicon dioxide.
  • Nalco ® 1SJ-612 Colloidal Silica (registered trademark of Nalco Chemical Company) is an aqueous solution of silica and alumina.
  • Nalco ® 1SJ-614 Colloidal Alumina (registered trademark of Nalco Chemical Company) is an aqueous colloidal alumina dispersion.
  • Zonyl ® UR (registered trademark of duPont) is an anionic fluorosurfactant.
  • Zonyl ® FSN-100 (registered trademark of duPont) is a nonionic fluorosurfactant.
  • DLX-6000 ® (registered trademark of duPont) is a polytetrafluoroethylene micropowder.
  • TE-3608 ® (registered trademark of duPont) is a polytetrafluoroethylene micropowder.
  • Example 20 Fiber Encapsulated Fabric Preparation A complete, stepwise, application of the inventive method in the production of an encapsulated- fiber fabric was as follows. The selected base fabric was Utopia Poplin available from Red Kap, Inc. This fabric was plainweave, 65%/35% polyester/cotton. If desired, this and other fabrics may be calendered to modify surface texture. The fabric was weighed and measured. Its initial weight is 5.1 ounces per square yard. Its thickness equals 11 mils.
  • the fabric was run through a typical industrial padder assembly consisting of a spreader roller, a submersion roller, a solution reservoir, and nip padder.
  • the nip padder pressure was set at 5.5 tons or 50 psi.
  • the linespeed was 15 yards per minute.
  • the water retained was 0.53 g water/g fabric.
  • the fabric was then treated with a water repellant fluorochemical, a 3% solution by weight of
  • the fabric was then run as in the preferred production embodiment (Fig. 12C) and as described below, the fabric was run from a free spinning roll with no braking mechanism to a clutching mechanism that sets up an initial tension for controlled alignment into the reverse roll coater.
  • the material runs through the reverse roll coater, over an idler roller, under a shear blade at 90° to the floor, over an idler roller and under a second shear blade at 60° to the floor, over an idler roller, under a flex blade at 45° to the floor, over a stationary roller to establish the correct web geometry coming off the flex blade and then onto the tenter frame.
  • the material was run directly from the last shear station to the tenter frame instead of through an intermediate tensioning station such as the nip padder described in the preferred embodiment (Fig. 12C) .
  • the tenter frame acts as a part of the tensioning assembly so the desired product can be produced but this is not the preferred method as most tenter assemblies are not designed to handle the tension produced in the processing method.
  • the material was run through the line oven, cured and rolled on a take-up reel at nominal tension.
  • the impregnant was Mobay 2530 A/B in a 1:1 ratio and can be considered to be a visco- elastic liquid that flows only under the shear forces resulting from the pressured impregnation.
  • the impregnant was believed to return very substantially to its original viscous condition almost immediately upon release of the pressure.
  • the impregnant was believed to flow a short distance within the matrix of the fabric during the short time that it was, because of pressure shearing forces, of lowered viscosity. Therefore, a number of "flows" may be usefully generated in a number of passes in order to properly distribute the impregnant in its preferred position substantially encapsulating the surfaces of the fabric's fibers.
  • the impregnated fabric was run- through the oven at a rate of 12 yards per minute, and was cured at 380°F.
  • the resultant fabric had a non- tacky thin film of silicone substantially encapsulating the fabric fibers.
  • Example 21 Evaluation of Fiber Encapsulated Fabric Properties The test results of the original versus the fiber encapsulated fabric of Example 20 were as follows:
  • Impregnated 1.1 oz/yd * Environmental chamber at 104°F and 47% humidity. Laundering Test Times ; Washed (spray ratings) Initial 5X 10X 15X impregnated side 100 90 90 90 reverse side 100 90 90 90 90 90 unimpregnated, treated fabric 100 80 80 40
  • the spray test was conducted in accordance with AATCC 22-1974. It measures water repellency of a fabric sample on a scale of 0-100, with a reading of 100 designating a completely water repellent fabric.
  • the rain test was conducted in accordance with AATCC 35-1985. It measures resistance of a fabric sample to penetration of water under static pressure from a shower head of 3 feet/5 minutes. A fabric is stormproof when less than 1.0 gram of water is absorbed by a standardized blotter used in the test.
  • Abrasion resistance is measured by mounting a fabric sample on a Taber Abraser Model 174 and measuring the number of cycles before the fabric begins tearing apart.
  • the hydrostatic resistance test was conducted in accord with Fed. Test Method Std. 191A, Method 5512. The test measures a fabric sample's resistance to water under pressure using the Mullen's Burst Test apparatus. Test results are expressed in pounds per square inch at which water beads penetrate the fabric.
  • MVTR moisture vapor transmission
  • Figures 3a, 3b, and 3c are photomicrographs taken using a Cambridge 360 scanning electron microscope displaying various aspects of the fiber encapsulated fabric.
  • the samples were cut using teflon coated razor blades mounted on 1/2 inch diameter aluminum stubs, and coated with a gold/palladium alloy.
  • Figure 3a shows the Utopia poplin of Example 21 magnified 100 times and shows a combination cross section and top field view of the fabric sample.
  • the sample was both impregnated and encapsulated as demonstrated by the presence of a thin film of the silicone polymer impregnant substantially on the surface filaments and in the yarn bundles. While the silicone was substantially encapsulating the surface filaments, they remained individual and distinct. Additionally, the interstices between each filament and between each fiber bundle remain substantially open.
  • Example 23 Fiber Encapsulated Fabric Preparation A complete, stepwise, application of the inventive method in the production of an encapsulated- fiber fabric was as follows.
  • the selected base fabric was 100% woven nylon oxford cloth (white color) #60609-1 available from Travis Textiles. If desired, this and other fabrics may be calendered to modify surface texture.
  • the fabric was weighed and measured. Its average intial weight is 3.0 ounces per square yard. Its average thickness equals 5.4 mils.
  • the fabric was then heated in an oven for 2 minutes at 320°F. This heating sinters the water repellant fluorochemical.
  • the fluorochemical treated fabric was clamped to the impregnation apparatus at one end, while the other end was tensioned manually at a pressure of about 1 inch pounds.
  • the silicone impregnation material (a 1:1 mixture of Dow Corning LSR 595 A/B) was spread on the fabric with a spatula. Normally the impregnant was put on only the upper side.”
  • the impregnant was manually sheared into the fabric using a blade with one straight side and one beveled side, tapered to a point, held at approximately a 65° angle, relative to the floor. Two passes were done at this angle, after which the blade was wiped clean.
  • the impregnant can be considered to be a visco-elastic liquid that flow ' s under the shear forces resulting from the pressured impregnantion.
  • the impregnant was believed to flow a short distance within the matrix of the fabric during the short time that it was, because of pressure shearing forces, of lowered viscosity. Therefore, a number of "flows" may be usefully generated in a number of passes in order to properly distribute the impregnant in its preferred position substantially encapsulating the surfaces of the fabric's fibers.
  • Figures 13a, 13b, 13c and 13d are scanning electron microphotographs of the product of Example 23 and were taken using a Cambridge 360 scanning electron microscope. The samples were cut using a teflon coated razor blade, mounted on 1/2 inch diameter aluminun stubs, and coated with an alloy of gold and palladium.
  • Figure 13a shows the side of the fabric opposite to that of silicone application. Silicone is present on this side, as the flow was controlled in order to teach this side. While there is residue present on this opposite side, substantial fibers are distinct and encapsulated, as evidenced by their rough surface texture.
  • the cross section shows approximately 50% silicone impregnation, with the remainder of the yarn interstices left open, indicating at least partial encapsulation. This impregnation/ ncapsulation is also seen in the cross-section in Figure 13b.
  • Figures 13c and 13d are further evidence of individual fiber encapsulation.
  • the sheath of silicone was dragged down over the end of the fiber during cutting. Silicone is also visible along the length of each of these fibers. The thickness of the silicone encapsulating one fiber was measured as being 126nm ( Figure 13d) .
  • Example 25 Fiber Encapsulated Fabric Preparation
  • the selected base fabric was Utooia poplin available from Red Kap, Inc. This (plainweave) fabric was 65%/35% polyester/cotton. If desired, this and other fabrics may be calendered to modify surface texture.
  • the fabric was weighed and measured. Its initial weight is 5.1 ounces per square yard. Its thickness equals 11 mils.
  • the fabric was soaked in water, wrung dry, and weighed. The water retained was equal to 0.64 g water/g fabric. The fabric was then treated with a water repellant chemical fluorochemical, a 2% solution by weight of Milease ® F31X. In order to do so the fabric must be soaked in a 3.13% solution of Milease ® F31X water-repel1ant chemical in distilled water. This was because
  • the silicone (Mobay 2530, no Uvinal) impregnant material mixed to a 1:1 ratio was manually applied at ambient room temperature as follows. A one-half inch bead of the impregnant was laid across the width of the sample at one end. It was then sheared into the material by drawing a blade, held at 75° to the floor, down the length of the material. This is repeated twice. The excess impregnant is then removed by drawing the same blade that has been wiped clean down the length of the material, twice. The blade is held at 90° to the floor. Normally the impregnant was put on only the upper side.
  • the impregnant can be considered to be a visco-elastic liquid that flows only under the shear forces resulting from the pressure impregnation.
  • the impregnant was believed to return very substantially to its original viscous condition almost immediately upon release of the pressure.
  • the impregnant was believed to flow a short distance within the matrix of ⁇ the fabric during the short time that it was, because of pressure shearing forces, of lowered viscosity. Therefore, a number of "flows" may be usefully generated in a number of passes in order to properly distribute the impregnant in its preferred position substantially encapsulating the surfaces of the fabric's fibers.
  • Example 26 Evaluation of Fiber Encapsulated Fabric Properties Using the test procedures of Example 21, the test results of the original versus the produced fiber encapsulated fabric of Example 25 were as follows:
  • Amount Impregnated 0.7 oz/yd 2 * Environmental chamber at 104°F and 47% humidity.
  • the spray test was conducted in accordance with AATCC 22-1974. It measures water repellancy on a scale of 0-100, with a reading of 100 being completely water repellant.
  • the rain test was conducted in accordance with
  • AATCC 35-1985 It measures resistance to penetration of water under static pressure from shower head of 3 feet/5 minutes.
  • a fabric is stormproof if less than 1.0 gram of water is absorbed by a blotter used in the test. The amount impregnated was determined by ASTM
  • the hydrostatic resistance was determined by AATCC Test 127-1980.
  • the test measures fabric's resistance to water under pressure using the Suters apparatus. Test results are in mm of water at which three water beads penetrate the fabric.
  • the moisture vapor transmission rate was measured in accordance with ASTM E96-B.
  • the test measures amount of moisture vapor passing through fabric in a controlled environment during a 24 hour period.
  • the obtained MVTR figure is grams of water/square meter of surface/24 hour day.
  • Example 27 Fiber Encapsulated Fabric Preparation A complete, stepwise, application of the inventive method in the production of an encapsulated- fiber fabric was as follows.
  • the selected base fabric was 100% woven nylon, plain weave, (white color), #90208, obtained from a local fabric store. If desired, this and other fabrics may be calendered to modify surface texture. To remove any finish present, the fabric was next washed five times with Tide detergent, rinsed thoroughly, and tumbled dry after the fifth washing. The fabric was weighed and measured. Its initial weight was 2.03 ounces per square yard. Its thickness was 5 mils.
  • the fabric was soaked in water, wrung dry, and weighed. The water retained was equal to 0.44 g water/g fabric. Three fabric samples were then treated with a water repellant fluorochemical, a 2% solution by weight of Milease ® F-31X. In order to do so the fabric was soaked in a 4.5 % solution of Milease ® water-repellant chemical in distilled water. This was because
  • the treated fabric was then run through a wringer and tumble dried.
  • the fabric was heated in an oven for 2 minutes at 310°F. This heating sinters the water repellant fluorochemical.
  • the silicone impregnation material (Mobay 2530 A&B) was spread on the fabric with a spatula. Normally the impregnant was put on one only, upper, side. The impregnant was then manually sheared into the fabric twice, using a blade with one straight side and one beveled side, tapered to a point. The blade was held at approximately a 65° angle to the floor. To remove residual surface impregnant the blade was wiped clean and passed over the fabric once more at a 90° angle to the floor. Multiple process stages of pulling the blade with applied impregnant across the fabric were preferably made.
  • the impregnant can be considered to be a visco-elastic liquid that flows only under the shear forces resulting from the pressured impregnation.
  • the impregnant was believed to return very substantially to its original viscous condition almost immediately upon release of the pressure.
  • the impregnant was believed to flow a short distance within the matrix of the fabric during the short time that it was, because of pressure shearing forces, of lowered viscosity. Therefore, a number of "flows" may be usefully generated in a number of passes in order to properly distribute the impregnant in its preferred position substantially encapsulating the surfaces of the fabric's fibers.
  • the spray test was conducted in accordance with AATCC 22-1974. It measures water repellancy on a scale of 0-100, with a reading of 100 being completely water repellant.
  • the rain test was conducted in accordance with AATCC 35-1985. It measures resistance to penetration of water under static pressure from shower head of 3 feet/5 minutes. A fabric is stormproof if less than 1.0 gram of water is absorbed by a blotter used in the test.
  • the amount impregnated was determined by ASTM D-3776-85. Determination of weight of fabric samples of known area for impregnated and unimpregnated fabrics allows calculation of amount of material impregnated in ounces per square yard.
  • Abrasion resistance is measured by placing fabric sample on Taber Abraser Model 174 and measuring number of cycles before fabric begins tearing apart.
  • the hydrostatic resistance was determined by AATCC Test 127-1980.
  • the test measures fabric's resistance to water under pressure using the Suters apparatus. Test results are in mm of water at which three water beads penetrate the fabric.
  • the moisture vapor transmission rate was measured in accordance with ASTM E96-B.
  • the test measures amount of moisture vapor passing through fabric in a controlled environment during a 24 hour period.
  • the obtained MVTR figure is grams of water/square meter of surface/24 hour day.
  • the accelerated weathering test was conducted in accordance with ASTM G-53. Samples of original and impregnated fabrics are placed in the QUV weatherometer and results are compared.
  • Fig. 2 The fabric resulting from a conventional application of a viscous liquid curable silicone polymer composition is shown in Fig. 2.
  • the photographic view of Fig. 2 is at 150X magnifica ion. It shows a polyester and cotton cloth blend into which Dow Corning 590 LSR silicone polymer composition has been coated by a conventional procedure of the prior art.
  • the fabric side shown in Fig. 2 is the top, or treatment, side, which was the fabric side upon which coating was accomplished.
  • the prior art impregnated fabric is characterized by a high degree of disorder.
  • a large number of particulates (typical) appear to litter the surface of the fabric.
  • a substantial portion of the area of the surface, which appears to be a solid layer, is silicone polymer composition.
  • Certain yarn fragments can be observed to protrude through the surface of this silicone polymer composition.
  • the silicone polymer composition on either the polyester or the cotton fibers is not an encapsulation layer, but rather a matrix with the coated fibers being in general disarray, probably from forces occurring during the prior art silicone polymer composition application procedure.
  • silicone polymer composition is present upon the yarn or fiber surfaces of the substrate, and certainly is present as a layer upon the exterior surface of the three-dimensional fabric body, the silicone polymer composition has not controllably and individually encapsulated the fibers and left the interstices between fibers largely devoid of such polymer.
  • placement of silicone polymer composition in a fabric is not controlled to such a degree so as to produce a product in accordance with the present invention.
  • the fabric was tensioned between two fixed points, using a torque wrench to yield a longitudinal tension of 5.7 lbs/in.
  • the silicone was placed across the width at one end of the fabric.
  • the silicone was subsequently drawn the length of the fabric two times with a coating knife held at an angle of approximately 65°. A third pass of the knife held at 90°, was then utilized to remove excess silicone on the fabric surface.
  • the tension was released, and the sample was cured for two minutes at 320°F.
  • Figs. 14a, 14b, 14c, 14d, 14e, 14f, 14g, and 14h are scanning electron photomicrographs at various magnifications ranging from 120 times to 2,500 times.
  • Fig. 14a is a scanning electron photomicrograph at 120x showing a view of the fabric of Example 30. The surface being that surface from which the silicone coating material was applied.
  • Fig. 14b is a scanning electron photomicrograph at 12Ox showing a view of the fabric of Example 30. The surface being that surface that is opposite the surface from which the silicone coating material was applied.
  • Fig. 14c is a scanning electron photomicrograph at 45Ox showing a cross sectional view of the fabric of Example 30. The upper face being that side from which the silicone coating material was applied.
  • Fig. 14d is a scanning electron photomicrograph at 450x showing a cross sectional view of the fabric of Example 30.
  • the upper face being that side that is opposite from the side to which the silicone coating material was applied.
  • Fig 14e is a scanning electron photomicrograph at 2,500x of a portion of Fig. 14c.
  • Fig 14f is a scanning electron photomicrograph at 2,500x of a portion of Fig. 14d.
  • the side of the fabric from which the silicone coating material was applied is virtually indistinguishable from the opposite side of the fabric, the individual fibers being encapsulated with silicone and having open interstices between the fibers.
  • X-ray analysis of the cross sectional views confirmed that the individual fibers of the fabric were encapsulated with silicone.
  • the preceding examples demonstrate the impressive performance of the fiber encapsulated fabric of the fabric's invention in diverse areas. Yet, the results of each of these tests and performance capabilities expressed individually fails to capture the comprehensively enhanced range of performance capabilities of the fiber encapsulated fabric of the invention.
  • the impregnation process of the this invention produces a fiber encapsulated breathable waterproof fabric that produces equal, or superior, test results over a broad range of different performances at a lighter, more insubstantial fabric weight compared, for example, to the untreated fabric. In other words, less fabric can be used, or worn in the case of garments, in order to obtain equal or superior performance.
  • "Comprehensive composite fabric performance” is defined herein as the equally weighted criteria of spray rating, rain test pass/fail, and abrasion cycles, as such are, respectively, obtained by the above indicated spray, rain, and abrasion tests.
  • the fiber encapsulated fabric of the present invention is clearly superior to unimpregnated (untreated) fabrics for a broad fabric range, and perhaps in fact for substantially all fabrics.
  • the present invention is thus of good utility for use with Aramid cloth, although not particularly for adding strength to such a cloth (which is already extremely strong) . It should be understood that the above defined comprehensive composite performance (based on spray, rain, and abrasion resistance) is enhanced by the fiber encapsulation of fabric as taught by the present invention even as applied to Aramid fiber encapsulated fabric.

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Abstract

Dans une bande poreuse flexible (de préférence un tissu) constituée de fibres associées, les fibres sont au moins partiellement encapsulées avec un polymère de silicone. De préférence, au moins 50 % de toutes les fibres de la bande ont au moins environ 25 % de leurs surfaces exposées encapsulées dans une couche d'un polymère de silicone d'une épaisseur comprise entre 0,1 et 50 microns. La plupart des interstices entre les fibres restent ouverts mais sont partiellement remplis du polymère de silicone. La bande traitée présente des caractéristiques que l'on ne peut obtenir avec les bandes de l'art antérieur traitées soit avec du polymère fluorochimique soit avec du polymère de silicone, caractéristiques telles qu'un plus grand angle de contact aux gouttelettes d'eau, une plus grande résistance à l'abrasion et une meilleure aptitude au relavage à l'eau, tout en conservant d'excellentes respirabilité et imperméabilité. La bande traitée possède des caractéristiques de toucher semblables à celles d'une bande non-traitée. Eventuellement et préférablement, une bande est imprégnée uniformément au préalable avec un produit fluorochimique. Eventuellement, une bande peut subir un traitement postérieur avec un produit fluorochimique pour améliorer des caractéristiques telles que la pénétration d'huile et la résistance aux souillures. La bande traitée est produite en utilisant une technique d'imprégnation par pression d'une composition polymérisable d'un polymère de silicone. Une classe préférée de compositions polymérisables de polymère de silicone comprend un benzophénone substitué. Un procédé et un appareil préférés de traitement sont également décrits.
PCT/US1989/001006 1988-03-14 1989-03-13 Bandes fibreuses avec encapsulation de polymere de silicone WO1989008553A1 (fr)

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US16763088A 1988-03-14 1988-03-14
US16764388A 1988-03-14 1988-03-14
US16779788A 1988-03-14 1988-03-14
US167,643 1988-03-14
US167,630 1988-03-14
US167,869 1988-03-14
US167,797 1988-03-14
US31977689A 1989-03-10 1989-03-10
US31977789A 1989-03-10 1989-03-10
US319,776 1989-03-10
US319,777 1989-03-10
US319,778 1989-03-10
US07/319,778 US5004643A (en) 1988-03-14 1989-03-10 Silicone polymer-internally coated webs

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Cited By (24)

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WO1996036757A2 (fr) * 1995-05-17 1996-11-21 Nextec Applications, Inc. Tissus de protection
WO1996036758A2 (fr) * 1995-05-17 1996-11-21 Nextec Applications, Inc. Bandes a revetement interne poreux et a modificateurs positionnes de maniere modulable dans la bande
US5698303A (en) * 1988-03-14 1997-12-16 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5856245A (en) * 1988-03-14 1999-01-05 Nextec Applications, Inc. Articles of barrier webs
EP0893530A1 (fr) * 1997-07-24 1999-01-27 Polymer Group, Inc. Etoffe non-tissée perméable à la vapeur et imperméable aux liquides et méthode
US5874164A (en) * 1988-03-14 1999-02-23 Nextec Applications, Inc. Barrier webs having bioactive surfaces
US5876792A (en) * 1988-03-14 1999-03-02 Nextec Applications, Inc. Methods and apparatus for controlled placement of a polymer composition into a web
US5912116A (en) * 1988-03-14 1999-06-15 Nextec Applications, Inc. Methods of measuring analytes with barrier webs
US5954902A (en) * 1988-03-14 1999-09-21 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5958137A (en) * 1989-03-10 1999-09-28 Nextec Applications, Inc. Apparatus 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
WO2000049221A1 (fr) * 1999-02-22 2000-08-24 Milliken & Company Tissu de protection contre les fluides recouvert de silicone
WO2001066851A1 (fr) * 2000-03-10 2001-09-13 W.L. Gore & Associates Gmbh Vetement nettoyable resistant aux salissures
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
EP2034088A1 (fr) * 2007-09-10 2009-03-11 W.L.Gore & Associates Gmbh Étoffe et stratifié d'étoffe
WO2009050312A1 (fr) * 2007-10-16 2009-04-23 Comersan, S.A. Procédé pour l'obtention d'un tissu présentant l'aspect de la peau apprêtée ou du cuir, tissu obtenu au moyen de ce procédé et son utilisation
WO2014049390A1 (fr) * 2012-09-25 2014-04-03 Mas Research And Innovation (Private) Limited Ensemble textile pourvu d'un revêtement élastomère perméable à l'air et à la vapeur d'eau
EP3153040A1 (fr) 2015-10-07 2017-04-12 Mast Industries (Far East) Limited Partie de soutien-gorge et soutien-gorge pourvu de zones de modules d'élasticité variable
CN107033596A (zh) * 2010-11-25 2017-08-11 史密夫及内修公开有限公司 组合物i – ii及其产品和用途
CN109789440A (zh) * 2016-09-27 2019-05-21 富士胶片株式会社 膜的制造方法

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US4973510A (en) * 1987-09-02 1990-11-27 Teijin Limited Coated sheet material and process for producing same
US5112545A (en) * 1990-02-14 1992-05-12 Airfoil Textron Inc. Composite preforms and articles and methods for their manufacture
GB9024596D0 (en) * 1990-11-13 1991-01-02 Sherman Aaron Foamed products
GB2276336B (en) * 1990-11-13 1995-07-19 Aaron Sherman Foamed products
US5183702A (en) * 1991-04-03 1993-02-02 Dover Corporation Barrier fabrics
JP3354220B2 (ja) * 1993-07-09 2002-12-09 日清紡績株式会社 メラミン系樹脂発泡体
FR2715411B1 (fr) * 1994-01-24 1996-04-26 Celta Matériau compact résistant à l'eau et repulpable, à base de matériaux cellulosiques broyés, et son procédé de fabrication.

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Cited By (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6040251A (en) * 1988-03-14 2000-03-21 Nextec Applications Inc. Garments of barrier webs
US5954902A (en) * 1988-03-14 1999-09-21 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5874164A (en) * 1988-03-14 1999-02-23 Nextec Applications, Inc. Barrier webs having bioactive surfaces
US6083602A (en) * 1988-03-14 2000-07-04 Nextec Applications, Inc. Incontinent garments
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
US6129978A (en) * 1988-03-14 2000-10-10 Nextec Applications, Inc. Porous webs having a polymer composition controllably placed therein
US5698303A (en) * 1988-03-14 1997-12-16 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5846604A (en) * 1988-03-14 1998-12-08 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5856245A (en) * 1988-03-14 1999-01-05 Nextec Applications, Inc. Articles of barrier webs
US5912116A (en) * 1988-03-14 1999-06-15 Nextec Applications, Inc. Methods of measuring analytes with barrier webs
US5876792A (en) * 1988-03-14 1999-03-02 Nextec Applications, Inc. Methods and apparatus for controlled placement of a polymer composition into a web
US6289841B1 (en) 1989-03-10 2001-09-18 Nextec Applications, Inc. Method and apparatus for controlled placement of a polymer composition into a web
US5958137A (en) * 1989-03-10 1999-09-28 Nextec Applications, Inc. Apparatus of feedback control for the placement of a polymer composition into a web
WO1996036761A2 (fr) * 1995-05-17 1996-11-21 Nextec Applications, Inc. Procede d'obtention de la permeabilite et de la porosite desirees pour un voile de fibres
WO1996036757A3 (fr) * 1995-05-17 1997-04-03 Nextec Applications Inc Tissus de protection
WO1996036758A3 (fr) * 1995-05-17 1997-02-13 Nextec Applications Inc Bandes a revetement interne poreux et a modificateurs positionnes de maniere modulable dans la bande
WO1996036758A2 (fr) * 1995-05-17 1996-11-21 Nextec Applications, Inc. Bandes a revetement interne poreux et a modificateurs positionnes de maniere modulable dans la bande
WO1996036761A3 (fr) * 1995-05-17 1997-02-06 Nextec Applications Inc Procede d'obtention de la permeabilite et de la porosite desirees pour un voile de fibres
WO1996036757A2 (fr) * 1995-05-17 1996-11-21 Nextec Applications, Inc. Tissus de protection
US6071602A (en) * 1995-06-07 2000-06-06 Nextec Applications, Inc. Controlling the porosity and permeation of a web
EP0893530A1 (fr) * 1997-07-24 1999-01-27 Polymer Group, Inc. Etoffe non-tissée perméable à la vapeur et imperméable aux liquides et méthode
US6416613B1 (en) 1998-06-23 2002-07-09 Nextec Applications, Inc. Products of and method for improving adhesion between substrate and polymer layers
US6342280B1 (en) 1998-06-23 2002-01-29 Nextec Applications, Inc. Products of and methods for improving adhesion between substrate and polymer layers
WO2000049221A1 (fr) * 1999-02-22 2000-08-24 Milliken & Company Tissu de protection contre les fluides recouvert de silicone
EP1143062A1 (fr) * 2000-03-10 2001-10-10 W.L. GORE & ASSOCIATES GmbH Vêtement nettoyable résistant aux salissures
WO2001066851A1 (fr) * 2000-03-10 2001-09-13 W.L. Gore & Associates Gmbh Vetement nettoyable resistant aux salissures
EP2034088A1 (fr) * 2007-09-10 2009-03-11 W.L.Gore & Associates Gmbh Étoffe et stratifié d'étoffe
WO2009033626A1 (fr) * 2007-09-10 2009-03-19 W.L.Gore & Associates Gmbh Tissu et stratifié de tissu
CN101796245B (zh) * 2007-09-10 2014-06-25 W.L.戈尔有限公司 织物与织物叠层
WO2009050312A1 (fr) * 2007-10-16 2009-04-23 Comersan, S.A. Procédé pour l'obtention d'un tissu présentant l'aspect de la peau apprêtée ou du cuir, tissu obtenu au moyen de ce procédé et son utilisation
ES2319065A1 (es) * 2007-10-16 2009-05-01 Comersan, S.A. Procedimiento para la obtencion de un tejido con aspecto de piel curtida o cuero, tejido obtenido a partir de el y su uso.
CN107033596A (zh) * 2010-11-25 2017-08-11 史密夫及内修公开有限公司 组合物i – ii及其产品和用途
WO2014049390A1 (fr) * 2012-09-25 2014-04-03 Mas Research And Innovation (Private) Limited Ensemble textile pourvu d'un revêtement élastomère perméable à l'air et à la vapeur d'eau
EP3153040A1 (fr) 2015-10-07 2017-04-12 Mast Industries (Far East) Limited Partie de soutien-gorge et soutien-gorge pourvu de zones de modules d'élasticité variable
US9883702B2 (en) 2015-10-07 2018-02-06 Mast Industries (Far East) Limited Portion of bra and bra having zones of varying elastic moduli
CN109789440A (zh) * 2016-09-27 2019-05-21 富士胶片株式会社 膜的制造方法

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AU3346089A (en) 1989-10-05
AU689799B2 (en) 1998-04-09
AU3440689A (en) 1989-10-05
AU3436889A (en) 1989-10-05
WO1989008554A1 (fr) 1989-09-21
WO1989008555A1 (fr) 1989-09-21
KR970002936B1 (ko) 1997-03-13
AU7592594A (en) 1995-05-04
KR900700284A (ko) 1990-08-13

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