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filingDate 1968-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1972-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1259595-A
abstract 1,259,595. Treating fabric articles comprising keratinous fibres. I.W.S. NOMINEE CO. Ltd. 31 Jan., 1969 [9 Feb., 1968], No. 6621/68. Heading D1P. A garment piece of made-up garment, e.g. trousers, skirt or shirt, or other fabric article, made from keratinous fibres, e.g. wool, hair, fur fibres, alpaca, cashmere, vicuna, guanaco, camel hair or llama, alone or in admixture with cotton, polyester, polyamide or acrylic fibres, is rendered dimensionally stable to agitation in the presence of water by setting it in a desired configuration by the action of steam at super atmospheric pressure or of steam and a reducing or basic setting agent for keratinous fibres, and then treating is with a solution of a resin or resin-forming material, which will confer shrink resistance on keratinous fibres, in an organic solvent, e.g. perchloroethylene, trichloroethylene, carbon tetrachloride, 1,1,2 - trichloro - 1,2,2 - trifluoroethane or 1,1,1 - trichloroethane. The material may be set in a flat, creased or pleated configuration. As setting agent there is used a reducing agent, e.g. an alkali metal sulphite, bisulphite, borohydride or hydrosulphite, sodium or zinc formaldehyde sulphoxylate, thioglycollic acid and its alkali metal and ammonium salts, 2 - mercaptoethanol, 2 - aminothioethanol, tetrakis (hydroxymethyl) phosphonium chloride, thiourea dioxide, tris (hydroxymethyl) phosphine, 1,4-thiothreitol or an aliphatic amine or alkanolamine sulphite or bisulphite, or basic agent, a lower alkanolamine, ethylene diamine, hexamethylene diamine, an alkanolamine carbonate or bicarbonate or hydrazine, which may be used in conjunction with a wetting agent, e.g. an ethylene oxide condensation product or sodium salt of a sulphated or sulphonated fatty acid. Setting may be improved by the use of a humectant or swelling agent, e.g. urea or guanidine or a derivative thereof, ethylene glycol, glycerol, dimethyl formamide or dimethyl sulphoxide. The resin may be self crosslinkable or may be cross-linked by cross linking agents, e.g. compounds containing thiol, hydroxy, amino, amide, isothiocyanate or isocyanate groups or epoxide or epichlorohydrin resins. Suitable resins are a copolymer of ethylene, vinyl acetate and methacryloyl chloride, a prepolymer obtained by the reaction of a polyhydroxy compound, an alkylene oxide and a polyfunctional isocyanate, a polyamide, a polyacrylate, a resin formed by the catalytic oxidation of unsaturated fatty acid esters and a carboxylated polybutadiene, polyamides optionally being formed on the material by an interfacial polymerisation technique by first treating it with a diamine and then treating it with a solution of a carboxylic acid in an organic solvent. The resin may be cured at ambient temperatures of 30‹-170‹C. A softener, e.g. a quaternary ammonium compound containing saturated or unsaturated hydrocarbon chains having 8-18 carbon atoms, lanolin or polypropylene-oxy-glycols, may be applied to the materials together with or after the application of the resin. Treatment with the resin solution may be effected in a dry cleaning apparatus.
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