GB664993A - Improvements in or relating to cellulosic textile materials - Google Patents
Improvements in or relating to cellulosic textile materialsInfo
- Publication number
- GB664993A GB664993A GB2627348A GB2627348A GB664993A GB 664993 A GB664993 A GB 664993A GB 2627348 A GB2627348 A GB 2627348A GB 2627348 A GB2627348 A GB 2627348A GB 664993 A GB664993 A GB 664993A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- ethyl
- vinyl
- compounds
- polymerization product
- 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
- 239000004753 textile Substances 0.000 title abstract 5
- 239000000463 material Substances 0.000 title abstract 4
- 239000000047 product Substances 0.000 abstract 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 6
- 229920001577 copolymer Polymers 0.000 abstract 6
- 239000004744 fabric Substances 0.000 abstract 5
- 238000006116 polymerization reaction Methods 0.000 abstract 5
- 229920001169 thermoplastic Polymers 0.000 abstract 5
- 239000004416 thermosoftening plastic Substances 0.000 abstract 5
- 229920000742 Cotton Polymers 0.000 abstract 4
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 abstract 4
- 229920000297 Rayon Polymers 0.000 abstract 4
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical class NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 abstract 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 2
- 229920000877 Melamine resin Polymers 0.000 abstract 2
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 abstract 2
- 229910000388 diammonium phosphate Inorganic materials 0.000 abstract 2
- 235000019838 diammonium phosphate Nutrition 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 abstract 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 239000002964 rayon Substances 0.000 abstract 2
- -1 styrene Chemical class 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 2
- YWYRVWBEIODDTJ-UHFFFAOYSA-N 1-ethenyl-9h-fluorene Chemical class C1C2=CC=CC=C2C2=C1C(C=C)=CC=C2 YWYRVWBEIODDTJ-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- TVONJMOVBKMLOM-UHFFFAOYSA-N 2-methylidenebutanenitrile Chemical compound CCC(=C)C#N TVONJMOVBKMLOM-UHFFFAOYSA-N 0.000 abstract 1
- BTOVVHWKPVSLBI-UHFFFAOYSA-N 2-methylprop-1-enylbenzene Chemical class CC(C)=CC1=CC=CC=C1 BTOVVHWKPVSLBI-UHFFFAOYSA-N 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical class C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 abstract 1
- ORNUPNRNNSVZTC-UHFFFAOYSA-N 2-vinylthiophene Chemical class C=CC1=CC=CS1 ORNUPNRNNSVZTC-UHFFFAOYSA-N 0.000 abstract 1
- ZWKNLRXFUTWSOY-UHFFFAOYSA-N 3-phenylprop-2-enenitrile Chemical class N#CC=CC1=CC=CC=C1 ZWKNLRXFUTWSOY-UHFFFAOYSA-N 0.000 abstract 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract 1
- 244000198134 Agave sisalana Species 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 abstract 1
- 240000008564 Boehmeria nivea Species 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- KSSJBGNOJJETTC-UHFFFAOYSA-N COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC Chemical compound COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC KSSJBGNOJJETTC-UHFFFAOYSA-N 0.000 abstract 1
- 244000025254 Cannabis sativa Species 0.000 abstract 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 abstract 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 abstract 1
- 240000000491 Corchorus aestuans Species 0.000 abstract 1
- 235000011777 Corchorus aestuans Nutrition 0.000 abstract 1
- 235000010862 Corchorus capsularis Nutrition 0.000 abstract 1
- 239000001856 Ethyl cellulose Substances 0.000 abstract 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- USDJGQLNFPZEON-UHFFFAOYSA-N [[4,6-bis(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(NCO)=NC(NCO)=N1 USDJGQLNFPZEON-UHFFFAOYSA-N 0.000 abstract 1
- YGCOKJWKWLYHTG-UHFFFAOYSA-N [[4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]-(hydroxymethyl)amino]methanol Chemical compound OCN(CO)C1=NC(N(CO)CO)=NC(N(CO)CO)=N1 YGCOKJWKWLYHTG-UHFFFAOYSA-N 0.000 abstract 1
- 150000001242 acetic acid derivatives Chemical class 0.000 abstract 1
- UGZICOVULPINFH-UHFFFAOYSA-N acetic acid;butanoic acid Chemical compound CC(O)=O.CCCC(O)=O UGZICOVULPINFH-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 125000005250 alkyl acrylate group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 235000019270 ammonium chloride Nutrition 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- CHCFOMQHQIQBLZ-UHFFFAOYSA-N azane;phthalic acid Chemical compound N.N.OC(=O)C1=CC=CC=C1C(O)=O CHCFOMQHQIQBLZ-UHFFFAOYSA-N 0.000 abstract 1
- 235000009120 camo Nutrition 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 229920002301 cellulose acetate Polymers 0.000 abstract 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 abstract 1
- 235000005607 chanvre indien Nutrition 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 150000001923 cyclic compounds Chemical class 0.000 abstract 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 abstract 1
- 229920001249 ethyl cellulose Polymers 0.000 abstract 1
- 235000019325 ethyl cellulose Nutrition 0.000 abstract 1
- NHWGPUVJQFTOQX-UHFFFAOYSA-N ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethyl-methylamino]ethyl]-dimethylazanium Chemical compound CC[N+](C)(C)CCN(C)CC[N+](C)(C)CC NHWGPUVJQFTOQX-UHFFFAOYSA-N 0.000 abstract 1
- JHHUETYWMKKDLV-UHFFFAOYSA-N ethylazanium;phosphate Chemical compound CC[NH3+].CC[NH3+].CC[NH3+].[O-]P([O-])([O-])=O JHHUETYWMKKDLV-UHFFFAOYSA-N 0.000 abstract 1
- 239000011487 hemp Substances 0.000 abstract 1
- 239000004312 hexamethylene tetramine Substances 0.000 abstract 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 abstract 1
- 238000007689 inspection Methods 0.000 abstract 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical group 0.000 abstract 1
- 125000005394 methallyl group Chemical group 0.000 abstract 1
- 229960004011 methenamine Drugs 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 abstract 1
- GYDSPAVLTMAXHT-UHFFFAOYSA-N pentyl 2-methylprop-2-enoate Chemical class CCCCCOC(=O)C(C)=C GYDSPAVLTMAXHT-UHFFFAOYSA-N 0.000 abstract 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 239000004627 regenerated cellulose Substances 0.000 abstract 1
- 230000000717 retained effect Effects 0.000 abstract 1
- 239000000344 soap Substances 0.000 abstract 1
- 150000003440 styrenes Chemical class 0.000 abstract 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical group CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- 235000005074 zinc chloride Nutrition 0.000 abstract 1
- 239000011592 zinc chloride Substances 0.000 abstract 1
Classifications
-
- 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
- D06M15/263—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
-
- 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
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
-
- 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
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/3188—Next to cellulosic
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2369—Coating or impregnation improves elasticity, bendability, resiliency, flexibility, or shape retention of the fabric
- Y10T442/2393—Coating or impregnation provides crease-resistance or wash and wear characteristics
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Cellulosic textile materials are rendered crease-resistant by impregnating with (a) a melamine-formaldehyde composition, which is at least partly soluble in water, comprising one or more methylol melamines or alkylated methylol melamines, and (b) a film-forming, water-insoluble thermoplastic polymerization product of one or more alkyl acrylates in which the alkyl group contains not more than 5 carbon atoms, with or without one or more monomers containing a CH2: C: group. From 1 to 3 parts of product (b) are used for each part of product (a), and (a) is cured in contact with (b) to a water-insoluble state, the amount of (a) and (b) used being such that the finished textile contains from 8-40 per cent by weight of impregnating composition. Di-, tri-, tetra-, penta- or hexamethylol melamine, or methylated methylol melamines may be used. The thermoplastic polymerization product may be polymerized methyl, ethyl, propyl, tert.-butyl or amyl acrylate or copolymers of these acrylates with monovinyl compounds such as vinyl acetate, propionate and butyrate; monovinyl substituted cyclic compounds such as styrene, mono-and dimethyl-styrenes, halogenated styrenes, cyano styrenes and a -p-dimethyl styrene; vinyl pyridines, vinyl thiophenes, vinyl fluorenes and vinyl and vinylidene halides; acrylic acid and its amides, for example acrylamide, N-methyl acrylamide and N-diethyl acrylamide; acrylonitrile; alkacrylic compounds such as methacrylic and ethacrylic acids, methacrylamide and ethacrylamide, methacrylonitrile and ethacrylonitrile; methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl and amyl methacrylates and ethacrylates; allyl and methallyl esters such as the acetates, propionates and laurates; and 1,3-butadiene and similar compounds. Preferred copolymers are those of ethyl acrylate and styrene or acrylonitrile. The curing of the melamine-formaldehyde or similar reaction product may be accelerated by addition of a catalyst such as oxalic, acetic or phosphoric acid, diammonium hydrogen phosphate, ethyl ammonium phosphate, diammonium phthalate and ammonium or zinc chloride. Textile materials which may be treated are cotton, linen, hemp, jute, ramie, sisal, regenerated cellulose, cellulose acetate or acetate-butyrate rayons, saponified acetate rayons, viscose rayons, cuprammonium rayons and ethyl cellulose, or mixtures of such materials. Mercerized cotton cloth is especially mentioned. In one example an aqueous impregnating bath is prepared containing 10 per cent of methylated methylol melamine, 20 per cent of a thermoplastic polymerization product and 0.35 per cent of a mixture of diammonium hydrogen phosphate and hexamethylene tetramine. The fabric is soaked in this bath and then squeezed through a padder so that 90 per cent of the liquid (by weight of the dry fabric) is retained by the fabric. The fabric is then heated for 6 minutes at 290 DEG F. and the dried and cured textile washed in an aqueous solution containing 0.1 per cent soap and 0.1 per cent sodium bicarbonate, rinsed in water and dried. Cotton percale and mercerized cotton twill may be treated in this way, using as the thermoplastic polymerization product various additives such as a copolymer of 70 per cent ethyl acrylate and 30 per cent styrene, a copolymer of 90 per cent ethyl acrylate and 10 per cent acrylonitrile, or a copolymer of 79 per cent ethyl acrylate and 21 per cent a -para-dimethylstyrene. The Specification as open to inspection under Sect. 91 refers also to the use as the thermoplastic polymerization product of polymers or copolymers of the monomeric compounds mentioned above. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US785188A US2536050A (en) | 1947-11-10 | 1947-11-10 | Treatment of cellulosic textile materials and products thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
GB664993A true GB664993A (en) | 1952-01-16 |
Family
ID=25134704
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2627348A Expired GB664993A (en) | 1947-11-10 | 1948-10-08 | Improvements in or relating to cellulosic textile materials |
Country Status (7)
Country | Link |
---|---|
US (1) | US2536050A (en) |
BE (1) | BE485717A (en) |
DE (1) | DE936029C (en) |
ES (1) | ES185807A1 (en) |
FR (1) | FR974362A (en) |
GB (1) | GB664993A (en) |
NL (1) | NL71547C (en) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2862901A (en) * | 1958-12-02 | Aqueous solution of amino-aldehyde | ||
BE506631A (en) * | 1950-10-24 | 1900-01-01 | ||
US2780562A (en) * | 1950-10-30 | 1957-02-05 | Bayer Ag | Process of decorating textile materials |
US2719831A (en) * | 1951-01-20 | 1955-10-04 | Basf Ag | Production of pigmented prints and coatings on fibrous material |
US2674741A (en) * | 1951-03-21 | 1954-04-13 | Cluett Peabody & Co Inc | Shirt collar |
US2908658A (en) * | 1951-08-22 | 1959-10-13 | Bayer Ag | Printing paste and process of decorating textile therewith |
DE1062206B (en) * | 1952-09-03 | 1959-07-30 | Freudenberg Carl Kg | Process for the production of non-woven, porous surface structures of textile-like character |
US2819237A (en) * | 1953-09-22 | 1958-01-07 | American Cyanamid Co | Aqueous dispersions of a copolymer of an ethylenically unsaturated monomer containing a primary hydroxy group and a thermosetting resin forming reaction product |
US2864093A (en) * | 1954-10-20 | 1958-12-16 | Chicopec Mfg Corp | Washable garment part |
US2987421A (en) * | 1955-09-19 | 1961-06-06 | Goodrich Co B F | Composition for treating textile materials, method, and article produced thereby |
US2998326A (en) * | 1956-04-04 | 1961-08-29 | Nat Starch Products Inc | Cleaning and sizing of fabrics |
BE577868A (en) * | 1958-04-18 | |||
US3068121A (en) * | 1958-09-29 | 1962-12-11 | Johnson & Johnson | Pressure sensitive adhesive tape and paper backing element impregnated with an acrylic ester copolymer and a water-dispersible aldehyde resin |
BE585717A (en) * | 1958-12-23 | 1900-01-01 | ||
BE588503A (en) * | 1959-03-13 | 1900-01-01 | ||
US3068183A (en) * | 1959-07-20 | 1962-12-11 | Du Pont | Coating compositions containing styrene, ethyl acrylate, methacrylic acid interpolymers |
US3252932A (en) * | 1959-08-10 | 1966-05-24 | Minnesota Mining & Mfg | Resin compositions comprising a segmented fluorine-containing copolymer and an aminoplast |
US3087905A (en) * | 1960-05-03 | 1963-04-30 | American Cyanamid Co | Durable fluorochemical-melamine resin textile finish |
US3095320A (en) * | 1960-10-24 | 1963-06-25 | Geigy Chem Corp | Low temperature pigment binder compositions for textile fabrics |
US3214488A (en) * | 1961-08-24 | 1965-10-26 | American Cyanamid Co | Composition comprising polymethyl ether of polymethylol melamine and copolymer of olefin and carboxyl monomer |
US3316123A (en) * | 1964-01-28 | 1967-04-25 | American Cyanamid Co | Paper carrying non-blocking flexible grease-proof vinyl polymer coating |
US3448462A (en) * | 1964-09-14 | 1969-06-10 | Deering Milliken Res Corp | Collar and cuff-like garment member and method of making it |
CH1615668D (en) * | 1964-09-15 | |||
CH1357464D (en) * | 1964-09-21 | 1900-01-01 | ||
US3473948A (en) * | 1966-09-29 | 1969-10-21 | Burlington Industries Inc | Method of improving resin finished textiles |
US7063895B2 (en) | 2001-08-01 | 2006-06-20 | National Starch And Chemical Investment Holding Corporation | Hydrophobically modified solution polymers and their use in surface protecting formulations |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2187383A (en) * | 1936-06-13 | 1940-01-16 | Rohm & Haas | Process of laminating with a urea formaldehyde resin |
US2378365A (en) * | 1940-10-31 | 1945-06-12 | American Cyanamid Co | Coating compositions containing methyl methacrylate |
US2339203A (en) * | 1941-08-30 | 1944-01-11 | American Cyanamid Co | Treatment of cellulosic textile material |
FR905762A (en) * | 1943-01-27 | 1945-12-13 | Ig Farbenindustrie Ag | Process for improving the water resistance of products containing fibrous materials and organic binders |
US2499653A (en) * | 1946-10-17 | 1950-03-07 | American Cyanamid Co | Treatment of protein-containing textile materials and products thereof |
-
0
- BE BE485717D patent/BE485717A/xx unknown
- NL NL71547D patent/NL71547C/xx active
-
1947
- 1947-11-10 US US785188A patent/US2536050A/en not_active Expired - Lifetime
-
1948
- 1948-10-08 GB GB2627348A patent/GB664993A/en not_active Expired
- 1948-10-27 FR FR974362D patent/FR974362A/en not_active Expired
- 1948-11-03 ES ES0185807A patent/ES185807A1/en not_active Expired
-
1950
- 1950-09-30 DE DEA3923A patent/DE936029C/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE936029C (en) | 1955-12-01 |
FR974362A (en) | 1951-02-21 |
NL71547C (en) | 1900-01-01 |
ES185807A1 (en) | 1949-02-01 |
BE485717A (en) | 1900-01-01 |
US2536050A (en) | 1951-01-02 |
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