GB1078496A - Bonded fibrous substrates and processes - Google Patents
Bonded fibrous substrates and processesInfo
- Publication number
- GB1078496A GB1078496A GB4915663A GB4915663A GB1078496A GB 1078496 A GB1078496 A GB 1078496A GB 4915663 A GB4915663 A GB 4915663A GB 4915663 A GB4915663 A GB 4915663A GB 1078496 A GB1078496 A GB 1078496A
- Authority
- GB
- United Kingdom
- Prior art keywords
- give
- copolymer
- ester
- fibres
- amide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000758 substrate Substances 0.000 title abstract 7
- 229920001577 copolymer Polymers 0.000 abstract 14
- 239000000049 pigment Substances 0.000 abstract 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 8
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract 8
- 125000004185 ester group Chemical group 0.000 abstract 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 6
- 239000005977 Ethylene Substances 0.000 abstract 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
- 150000001408 amides Chemical class 0.000 abstract 6
- 239000000839 emulsion Substances 0.000 abstract 6
- -1 polyethylene Polymers 0.000 abstract 6
- 125000003368 amide group Chemical group 0.000 abstract 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 4
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 abstract 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 abstract 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 abstract 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 4
- 239000004952 Polyamide Substances 0.000 abstract 4
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract 4
- 125000005250 alkyl acrylate group Chemical group 0.000 abstract 4
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 abstract 4
- 150000001412 amines Chemical class 0.000 abstract 4
- 239000007767 bonding agent Substances 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 4
- 239000002131 composite material Substances 0.000 abstract 4
- 239000004744 fabric Substances 0.000 abstract 4
- 229920002239 polyacrylonitrile Polymers 0.000 abstract 4
- 229920002647 polyamide Polymers 0.000 abstract 4
- 229920000728 polyester Polymers 0.000 abstract 4
- 229920000570 polyether Polymers 0.000 abstract 4
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 4
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 abstract 2
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 abstract 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 2
- 244000198134 Agave sisalana Species 0.000 abstract 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 abstract 2
- 235000017060 Arachis glabrata Nutrition 0.000 abstract 2
- 244000105624 Arachis hypogaea Species 0.000 abstract 2
- 235000010777 Arachis hypogaea Nutrition 0.000 abstract 2
- 235000018262 Arachis monticola Nutrition 0.000 abstract 2
- 241000416162 Astragalus gummifer Species 0.000 abstract 2
- 240000008564 Boehmeria nivea Species 0.000 abstract 2
- 244000025254 Cannabis sativa Species 0.000 abstract 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 abstract 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 abstract 2
- 240000000491 Corchorus aestuans Species 0.000 abstract 2
- 235000011777 Corchorus aestuans Nutrition 0.000 abstract 2
- 235000010862 Corchorus capsularis Nutrition 0.000 abstract 2
- 229920000742 Cotton Polymers 0.000 abstract 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 2
- 239000004471 Glycine Substances 0.000 abstract 2
- 241000219146 Gossypium Species 0.000 abstract 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 abstract 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 abstract 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 2
- 240000006240 Linum usitatissimum Species 0.000 abstract 2
- 235000004431 Linum usitatissimum Nutrition 0.000 abstract 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 2
- 240000000907 Musa textilis Species 0.000 abstract 2
- 241000499877 Phormium Species 0.000 abstract 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 abstract 2
- 239000004698 Polyethylene Substances 0.000 abstract 2
- 239000004743 Polypropylene Substances 0.000 abstract 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 2
- 229920001615 Tragacanth Polymers 0.000 abstract 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 abstract 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 235000010443 alginic acid Nutrition 0.000 abstract 2
- 229920000615 alginic acid Polymers 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 229910021529 ammonia Inorganic materials 0.000 abstract 2
- 235000019270 ammonium chloride Nutrition 0.000 abstract 2
- 239000000908 ammonium hydroxide Substances 0.000 abstract 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 abstract 2
- 150000004056 anthraquinones Chemical class 0.000 abstract 2
- 239000010425 asbestos Substances 0.000 abstract 2
- 239000011230 binding agent Substances 0.000 abstract 2
- 235000009120 camo Nutrition 0.000 abstract 2
- 239000006229 carbon black Substances 0.000 abstract 2
- 150000007942 carboxylates Chemical class 0.000 abstract 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 2
- 239000005018 casein Substances 0.000 abstract 2
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract 2
- 235000021240 caseins Nutrition 0.000 abstract 2
- 239000003518 caustics Substances 0.000 abstract 2
- 235000005607 chanvre indien Nutrition 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 abstract 2
- 229960001231 choline Drugs 0.000 abstract 2
- 229910000423 chromium oxide Inorganic materials 0.000 abstract 2
- 239000000084 colloidal system Substances 0.000 abstract 2
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 abstract 2
- 150000004985 diamines Chemical class 0.000 abstract 2
- 238000004945 emulsification Methods 0.000 abstract 2
- 239000003995 emulsifying agent Substances 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 2
- 239000011521 glass Substances 0.000 abstract 2
- 210000004209 hair Anatomy 0.000 abstract 2
- 239000011487 hemp Substances 0.000 abstract 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 abstract 2
- 230000001939 inductive effect Effects 0.000 abstract 2
- 230000003993 interaction Effects 0.000 abstract 2
- 229920000609 methyl cellulose Polymers 0.000 abstract 2
- 239000001923 methylcellulose Substances 0.000 abstract 2
- 235000010981 methylcellulose Nutrition 0.000 abstract 2
- 239000011490 mineral wool Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 235000011837 pasties Nutrition 0.000 abstract 2
- 235000020232 peanut Nutrition 0.000 abstract 2
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 abstract 2
- 229920000515 polycarbonate Polymers 0.000 abstract 2
- 239000004417 polycarbonate Substances 0.000 abstract 2
- 229920006149 polyester-amide block copolymer Polymers 0.000 abstract 2
- 229920000573 polyethylene Polymers 0.000 abstract 2
- 229920001155 polypropylene Polymers 0.000 abstract 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 abstract 2
- 229920002635 polyurethane Polymers 0.000 abstract 2
- 239000004814 polyurethane Substances 0.000 abstract 2
- 230000001681 protective effect Effects 0.000 abstract 2
- 235000018102 proteins Nutrition 0.000 abstract 2
- 102000004169 proteins and genes Human genes 0.000 abstract 2
- 108090000623 proteins and genes Proteins 0.000 abstract 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract 2
- 239000004627 regenerated cellulose Substances 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- 229910052895 riebeckite Inorganic materials 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000000377 silicon dioxide Substances 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 abstract 2
- 239000003381 stabilizer Substances 0.000 abstract 2
- 239000010902 straw Substances 0.000 abstract 2
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 abstract 2
- 229950000244 sulfanilic acid Drugs 0.000 abstract 2
- 229920001897 terpolymer Polymers 0.000 abstract 2
- 150000003512 tertiary amines Chemical class 0.000 abstract 2
- 229920001187 thermosetting polymer Polymers 0.000 abstract 2
- 239000002562 thickening agent Substances 0.000 abstract 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 abstract 2
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- 229920001959 vinylidene polymer Polymers 0.000 abstract 2
- 239000007762 w/o emulsion Substances 0.000 abstract 2
- 210000002268 wool Anatomy 0.000 abstract 2
Classifications
-
- 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
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/04—Homopolymers or copolymers of ethene
- C09J123/08—Copolymers of ethene
-
- 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
- D04H1/58—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 by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
- D04H1/587—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 by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives characterised by the bonding agents used
-
- 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
- D04H1/58—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 by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
- D04H1/64—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 by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
-
- 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
-
- 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
- D06M15/267—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof of unsaturated carboxylic esters having amino or quaternary ammonium groups
-
- 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
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/08—Copolymers of ethene
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Dispersion Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Nonwoven Fabrics (AREA)
- Coloring (AREA)
Abstract
The fibres of a fibrous substrate are bonded to one another by a bonding agent comprising a modified copolymer of ethylene and an alkyl acrylate. This copolymer contains 0.01 to 0.5 mol of acrylate units per mol of ethylene units and has an emulsification-inducing proportion of the acrylate units in hydrophilic form, so that it can form a stable aqueous emulsion without emulsifying agents but is water-insoluble. The same binder may serve also to bond pigments to the substrate. The bonding agent is formed by treating a copolymer of ethylene and an alkyl acrylate or methacrylate, with a caustic alkali to hydrolyse some or all of the ester groups. Ammonia or an amine may also be present to convert some of the ester groups to amide groups, and some ester groups to amide groups, and some ester groups may remain unchanged. A tertiary amine, such as choline can be used to provide a quaternary ammonium salt. Alternatively, the copolymer can be reacted with: an aminoaliphatic carboxylic acid (e.g. glycine) or an aminosulphonic acid (e.g. sulphanilic acid) to give a substituted amide with an acid group in the side chain; an unsaturated amine or alcohol (e.g. allylamine or allyl alcohol) to give an ester or amide with an unsaturated side chain, which can then be further reacted to give e.g. a salt of a sulphate half-ester; a diamine (e.g. ethylendiamine) to give an amide with an amino-substituted side chain; a polyether (e.g. a polyethylene oxide) to give a half-ester of the polyether, which may then be treated to give a sulphate half-ester salt. The emulsion may also contain methanol, ethanol or isopropanol. When used to bond a pigment, it may also include thickening agents, such as gum tragacanth, alginates, methylcellulose, hydroxyethylcellulose, aqueous gasoline or aqueous oil emulsions, protective colloids, catalysts, stabilizers or thermosetting resins such as urea- or melamine-aldehyde, or may be a water-in-oil emulsion of pasty consistency, which may be applied by printing. The copolymer can be cross-linked by using such agents as aldehydes, or by the interaction of carboxylate and amide groups if both be present. Catalysts that can be used are ammonium chloride and ammonium hydroxide. The substrate may be of staple fibres, yarn, filament, card sliver or twisted continuous filaments and may be woven, knitted, felted or fused or may be a pile fabric or a paper fabric. The fibres may be natural e.g. cotton, flax, hemp, jute, ramie, sisal, abaca, phormium, silk, wool, fur, hair, animal bristles or straw, or synthetic, e.g. of polyamide, polyester, polyacrylonitrile, copolymers of acrylonitrile with vinyl acetate, vinyl chloride, methyl acrylate, vinylpyridine or sodium styrenesulphonate, terpolymer of acrylonitrile, methyl acrylate and sodium styrensulphonate, vinyl or vinylidene polymer or copolymer, polycarbonate, polyurethane, polyesteramide, polyethylene, polypropylene, polytetrafluorethylene, celluse acetate or triacetate, composite filament, e.g. a sheath of polyamide around a core of polyester, self-crimped composite filaments, e.g. two acrylonitrile polymers differing in ionizable-group content spun as sheath and core, regenerated cellulose, fibres made from casein or peanut protein, glass, asbestos, rock wool or silica. They may be crimped, drawn or bulked; blends of two or more fibres may be used. Pigments referred to are carbon black, phthalo-cyanine blue, phthalocyanine green, azo pigments, vat pigments of the indigoid and anthraquinone types, chromium oxide, and titanium oxide.ALSO:The fibres of a fibrous substrate are bonded to one another by a bonding agent comprising a modified copolymer of ethylene and an alkyl acrylate. This copolymer contains 0.01 to 0.5 mol of acrylate units per mol of ethylene units and has an emulsification-inducing proportion of the acrylate units in hydrophilic form, so that it can form a stable aqueous emulsion without emulsifying agents but is water-insoluble. The same binder may serve also to bond pigments to the substrate. The bonding agent is formed by treating a copolymer of ethylene and an alkyl acrylate or methacrylate, with a caustic alkali to hydrolyse some or all of the ester groups. Ammonia or an amine may also be present to convert some of the ester groups to amide groups, and some ester groups may remain unchanged. A tertiary amine, such as choline can be used to provide a quaternary ammonium salt. Alternatively, the copolymer can be reacted with: an aminoaliphatic carboxylic acid (e.g. glycine) or an aminosulphonic acid (e.g. sulphanilic acid) to give a substituted amide with an acid group in the side chain; an unsaturated amine or alcohol (e.g. allylamine or allyl alcohol) to give an ester or amide with an unsaturated side chain, which can then be further reacted to give e.g. a salt of a sulphate half-ester; a diamine (e.g. ethylendiamine) to give an amide with an amino-substituted side chain; a polyether (e.g. a polyethylene oxide) to give a half-ester of the polyether, which may then be treated to give a sulphate half-ester salt. The emulsion may also contain methanol, ethanol or isopropanol. When used to bond a pigment, it may also include thickening agents, such as gum tragacanth, alginates, methylcellulose, hydroxyethylcellulose, aqueous gasoline or aqueous oil emulsions, protective colloids, catalysts, stabilizers or thermosetting resins such as urea- or melamine-aldehyde, or may be a water-in-oil emulsion of pasty consistency, which may be applied by printing. The copolymer can be cross-linked by using such agents as aldehydes, or by the interaction of carboxylate and amide groups if both be present. Catalysts that can be used are ammonium chloride and ammonium hydroxide. The substrate may be of staple fibres, yarn, filament, card sliver or twisted continuous filaments and may be woven, knitted, felted or fused or may be a pile fabric or a paper fabric. The fibres may be natural e.g. cotton, flax, hemp, jute, ramie, sisal, abaca, phormium, silk, wool, fur, hair, animal bristles or straw, or synthetic, e.g. of polyamide, polyester, polyacrylonitrile, copolymers of acrylonitrile with vinyl acetate, vinyl chloride, methyl acrylate, vinylpyridine or sodium styrenesulphonate, terpolymer of acrylonitrile, methyl acrylate and sodium styrensulphonate, vinyl or vinylidene polymer or copolymer, polycarbonate, polyurethane, polyesteramide, polyethylene, polypropylene, polytetrafluorethylene, celluse acetate or triacetate, composite filament, e.g. a sheath of polyamide around a core of polyester, self-crimped composite filaments, e.g. two acrylonitrile polymers differing in ionizable-group content spun as sheath and core, regenerated cellulose, fibres made from casein or peanut protein, glass, asbestos, rock wool or silica. They may be crimped, drawn or bulked; blends of two or more fibres may be used. Pigments referred to are carbon black, phthalo-cyanine blue, phthalocyanine green, azo pigments, vat pigments of the indigoid and anthraquinone types, chromium oxide, and titanium oxide.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24829762A | 1962-12-31 | 1962-12-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1078496A true GB1078496A (en) | 1967-08-09 |
Family
ID=22938503
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4915663A Expired GB1078496A (en) | 1962-12-31 | 1963-12-12 | Bonded fibrous substrates and processes |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JPS5113800B1 (en) |
| DE (1) | DE1292129B (en) |
| FR (1) | FR1519502A (en) |
| GB (1) | GB1078496A (en) |
| SE (2) | SE316145B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN120925133A (en) * | 2025-10-14 | 2025-11-11 | 徐州虹纬智能纺织有限公司 | Deodorant bio-based wool blended yarn and preparation method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3951691A (en) * | 1974-10-07 | 1976-04-20 | W. R. Grace & Co. | Wettable battery separator and process therefor |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE634597C (en) * | 1933-02-19 | 1936-08-31 | I G Farbenindustrie Akt Ges | Process for the production of fibrous filling material for upholstery purposes |
| US2765228A (en) * | 1955-03-03 | 1956-10-02 | Rohm & Haas | Cellulosic fibrous products and methods of producing them |
| US2982682A (en) * | 1956-08-13 | 1961-05-02 | Rohm & Haas | Non-woven bonded fibrous products and methods for their production |
| GB866049A (en) * | 1956-08-13 | 1961-04-26 | Parsons C A & Co Ltd | Improvements in and relating to nuclear reactors and fuel elements therefor |
| NL219660A (en) * | 1956-08-13 | 1900-01-01 | ||
| NL108558C (en) * | 1956-08-13 | |||
| FR1181170A (en) * | 1956-08-13 | 1959-06-12 | Rohm & Haas | Fibrous products and their manufacture |
| NL275178A (en) * | 1961-02-24 | |||
| DE1243633B (en) * | 1963-02-01 | 1967-07-06 | Hoechst Ag | Process for crease-proof finishing of textiles containing native or regenerated cellulose |
-
1963
- 1963-12-12 GB GB4915663A patent/GB1078496A/en not_active Expired
- 1963-12-27 FR FR958597A patent/FR1519502A/en not_active Expired
- 1963-12-30 JP JP7146563A patent/JPS5113800B1/ja active Pending
- 1963-12-30 DE DEC31783A patent/DE1292129B/en active Pending
-
1967
- 1967-06-30 SE SE1007767A patent/SE316145B/xx unknown
- 1967-06-30 SE SE1007667A patent/SE316144B/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN120925133A (en) * | 2025-10-14 | 2025-11-11 | 徐州虹纬智能纺织有限公司 | Deodorant bio-based wool blended yarn and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| SE316145B (en) | 1969-10-20 |
| FR1519502A (en) | 1968-04-05 |
| DE1292129B (en) | 1969-04-10 |
| SE316144B (en) | 1969-10-20 |
| JPS5113800B1 (en) | 1976-05-04 |
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