GB581439A - Curing of polymeric materials - Google Patents

Curing of polymeric materials

Info

Publication number
GB581439A
GB581439A GB2522745A GB2522745A GB581439A GB 581439 A GB581439 A GB 581439A GB 2522745 A GB2522745 A GB 2522745A GB 2522745 A GB2522745 A GB 2522745A GB 581439 A GB581439 A GB 581439A
Authority
GB
United Kingdom
Prior art keywords
diisocyanate
mixtures
acids
glycol
acetone
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
Application number
GB2522745A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2522745A priority Critical patent/GB581439A/en
Publication of GB581439A publication Critical patent/GB581439A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04Polyurethanes

Abstract

Organic diisocyanate modified polyesteramides are cured by heating in uniform admixture with polyvinyl alcohol or a partly hydrolysed polyvinyl acetate, a curing agent, namely, formaldehyde or a formaldehyde-liberating substance or a dichromate, and a curing catalyst, namely, an acid or a substance which is substantially neutral, but which develops acidity under curing conditions. The ingredients are mixed by milling dry or in the presence of water or an organic solvent, and 25 to 175 parts of polyvinyl body are used per 100 parts of modified polyester amides. Additional compounding ingredients are fillers, for example, carbon black, iron oxide, clay, asbestos, blanc fixe, whiting, lithopone and mica; resins, for example, urea-formaldehyde and phenol-formaldehyde resins; other plastic materials, for example, neutral or synthetic rubbers, vulcanized vegetable oils, dark substitute, white substitute, a Cumar resin, wood rosin and pitch; de-tackifying agents, that is to say, materials which reduce the tendency of the mix to stick to the rolls, for example, stearic acid, paraffin wax, oleic acid, lauric acid and dibutyl ammonium oleate; plasticisers, for example, tricresyl phosphate, dibutyl phthalate, butylphthalyl, butyl glycollate, and N-alkyl-toluene-sulphonamides; stabilizers or anti - oxidants, for example, hydroquinone, N : N1-hexamethylene-bis-ortho-hydroxy-benzamide, N-phenyl-a -naphthylamine, N-phenyl-b - naphthylamine and a : a - bis - (2 - hydroxy - 3 : 5-dimethylphenyl)butane, as well as others commonly used in rubber technology. Small quantities of pigments, for example from 1-3 per cent by weight, such as are customarily used in rubber technology or in the coating composition art may also be used to impart colour. The ingredients are mixed and shaped or calendered on to a substrate followed by heating at 100-150 DEG C. Solvents or swelling agents may be incorporated, e.g. acetone, mixtures of benzene and acetone, mixtures of benzene and ethanol, mixtures of benzene and chloroform, mixtures of benzene and methyl-ethyl ketone, mixtures of methyl ethyl ketone and trichlorethylene, and mixtures of acetone and the monoethyl ether of ethylene glycol. Polyester-and polyamide-forming reactants specified are glycols, for example, ethylene glycol, diethylene glycol, trimethylene glycol, pentamethylene glycol, hexamethylene glycol, dodecamethylene glycol, 1 : 12-octadecanediol and pentaglycol; aliphatic or aromatic amino-alcohols having at least one hydrogen atom attached to the amino nitrogen atom and preferably containing an aliphatic chain of at least two carbon atoms separating the amino and hydroxyl groups, for example, b -ethanolamine and 3-aminopropanol; dibasic carboxylic acids or ester-forming derivatives thereof, preferably aliphatic dicarboxylic acids, for example, malonic, succinic, glutaric, adipic, b -methyladipic, pimelic, suberic, azelaic, sebacic, undecanedioic, brassylic, iso-phthalic, hexahydroterephthalic, p-phenylene-diacetic and acetone-dicarboxylic acids; primary and secondary diamines, for example, ethylene diamine, hexamethylenediamine, 3 - methylhexamethy - lenediamine, decamethylenediamine, m-phenylene - diamine, N : N1 - dimethylhexamethylenediamine, N : N1 - diethylhexamethylenediamine and N : N1 - dimethyldecamethylenediamine; monohydroxymonocarboxylic acids or their ester-forming derivatives, for example, glycollic, 6 - hydroxycaproic, 10 - hydroxydecanoic and 12-hydroxystearic acids; polymerizable monoaminomonocarboxylic acids, or their ester-forming derivatives, for example, 6-aminocapoic acid or its lactam, caprolactam, and 9-aminononanoic, 11-aminoundecanoic and 12-aminostearic acids. Diisocyanates specified are ethylene diisocyanate, trimethylene diisocyanate, tetramethylene diisocyanate, hexamethylene diisocyanate, decamethylene diisocyanate, p-phenylene diisocyanate, m-phenylene diisocyanate, p : p1-diphenyl diisocyanate, diphenylmethane-4 : 41-diisocyanate, naphthalene diisocyanates and adipyl diisocyanate. Articles and applications specified are gaskets, packings, hose, diaphragms for pumps, flexible containers, the coating of rollers, blankets and stereos for use in the printing industry, protective sheathings for insulated electric cables and other electrical conductors, the coating of balls for games, tyres and flexible materials generally, including fabrics, protective clothing, leather cloth and floor coverings, and generally in the construction of articles requiring the use of a material having physical properties resembling those of rubber, but also having a good resistance to the action of organic fluids and a low permeability to gases and vapours. The compositions may be used as lacquers or finishing compositions or as substitutes for leather or adhesives for wood, metal, fabrics, paper, leather and regenerated cellulose. In the examples, the organic diisocyanate modified polyesteramide described in example 7 of Specification 580,524 is mixed with a high viscosity partially saponified polyvinyl acetate and water on a rubber mill. The mix is dried and milled with hexamethylol-melamine hexamethyl ether or with ammonium dichromate and 2 : 4-dichloro-1-naphthol. Specifications 553,733, 580,526 and 581,146 also are referred to.
GB2522745A 1944-02-24 1944-02-24 Curing of polymeric materials Expired GB581439A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2522745A GB581439A (en) 1944-02-24 1944-02-24 Curing of polymeric materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2522745A GB581439A (en) 1944-02-24 1944-02-24 Curing of polymeric materials

Publications (1)

Publication Number Publication Date
GB581439A true GB581439A (en) 1946-10-11

Family

ID=10224265

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2522745A Expired GB581439A (en) 1944-02-24 1944-02-24 Curing of polymeric materials

Country Status (1)

Country Link
GB (1) GB581439A (en)

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