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GB644829A - Curing polymeric materials - Google Patents

Curing polymeric materials

Info

Publication number
GB644829A
GB644829A GB709448A GB709448A GB644829A GB 644829 A GB644829 A GB 644829A GB 709448 A GB709448 A GB 709448A GB 709448 A GB709448 A GB 709448A GB 644829 A GB644829 A GB 644829A
Authority
GB
United Kingdom
Prior art keywords
hexamethylene
chloroprene
toluene
phenylene
modified polyester
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
GB709448A
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 GB709448A priority Critical patent/GB644829A/en
Publication of GB644829A publication Critical patent/GB644829A/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
    • C08L11/00Compositions of homopolymers or copolymers of chloroprene
    • 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
    • C08L75/06Polyurethanes from polyesters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

Chloroprene polymers and interpolymers are cured in admixture with an organic polyisocyanate-modified polyester, for example, by heating with magnesium oxide or zinc oxide. Specified as starting materials are glycols: ethylene, 1 : 2 - propylene, diethylene, trimethylene, pentamethylene, hexamethylene, decamethylene, and dodecamethylene glycols 1 : 12-octadecanediol, and pentaglycol; carboxylic acids: malonic, succinic, glutaric, adipic, b -methylapidic, pimeleic, suberic, azelaic, sebacic, undecanedioic, brassylic, isophthalic, terephthalic, hexahydroterephthalic, p-phenylene diacetic acids, and acetone dicarboxylic acid; polyisocyanates: ethylene, tri-methylene, tetramethylene, hexamethylene, decamethylene, p-phenylene, m-phenylene, and naphthalene di-isocyanates, benzene 1 : 3 : 5-, toluene 2 : 4 : 6-, ethylbenzene 2 : 4 : 6-, triphenylmethane 4 : 41 : 411 -, and diphenyl-2 : 4 : 41-tri-isocyanates. Preferably the modified polyester has an intrinsic viscosity in chloroform solution of more than 0.6. The chloroprene polymer and modified polyester may be admixed either by milling or in solution in chloroform, carbon tetrachloride, trichlorethylene, acetone, benzene, or toluene, or the unmodified polyester may be admixed with the polychloroprene and then reacted with the polyisocyanate. Before curing there may be mixed with the compositions carbon black, iron oxides, clay, asbestos, blanc fixe, lithopone, pigments, plasticizers, e.g. tricresyl phosphate, dibutyl phthalate, butyl phthalyl butyl glycollate, N-alkyl-toluene sulphonamides, and stabilizers, e.g. hydroquinone, N : N1-hexamethylene - bis - o - hydroxy - benzamide, N-phenyl - a or b - naphthylamine, and a : a bis - (2 - hydroxy - 3 : 5 - dimethylphenyl)-butane. The products may be used as gaskets, diaphragms for pumps, fuel containers, balls for games, tyres, protective clothing, leather cloth, floor coverings and in coating compositions. Examples describe (1) milling together polyethylene sebacate modified by hexamethylene di-isocyanate and a chloroprene polymer, with and without the addition of magnesium oxide and zinc oxide; (2) using an interpolymer of chloroprene and isoprene in processes as in (1).
GB709448A 1948-03-08 1948-03-08 Curing polymeric materials Expired GB644829A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB709448A GB644829A (en) 1948-03-08 1948-03-08 Curing polymeric materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB709448A GB644829A (en) 1948-03-08 1948-03-08 Curing polymeric materials

Publications (1)

Publication Number Publication Date
GB644829A true GB644829A (en) 1950-10-18

Family

ID=9826500

Family Applications (1)

Application Number Title Priority Date Filing Date
GB709448A Expired GB644829A (en) 1948-03-08 1948-03-08 Curing polymeric materials

Country Status (1)

Country Link
GB (1) GB644829A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2782172A (en) * 1953-01-22 1957-02-19 Goodyear Tire & Rubber White factice and isocyanate-modified polyester composition
US3049505A (en) * 1958-09-24 1962-08-14 Borg Warner Mechanical blend of a polyurethane rubber with blends of a graft copolymer of polybutadiene, styrene, and acrylonitrile
US3110615A (en) * 1957-09-30 1963-11-12 Congoleum Nairn Inc Urethane coating for cork surface and process therefor
US3136681A (en) * 1959-10-14 1964-06-09 Minnesota Mining & Mfg Adhesive composition and method of applying same
US3196035A (en) * 1960-07-16 1965-07-20 Fuji Tsushinki Seizo Kk Method of bonding an epoxy coating to a polyisocyanate treated polyester fiber base
US3429948A (en) * 1964-12-22 1969-02-25 Gen Etablissements Michelin Ra Polyesterurethane elastomers vulcanizable in live steam

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2782172A (en) * 1953-01-22 1957-02-19 Goodyear Tire & Rubber White factice and isocyanate-modified polyester composition
US3110615A (en) * 1957-09-30 1963-11-12 Congoleum Nairn Inc Urethane coating for cork surface and process therefor
US3049505A (en) * 1958-09-24 1962-08-14 Borg Warner Mechanical blend of a polyurethane rubber with blends of a graft copolymer of polybutadiene, styrene, and acrylonitrile
US3136681A (en) * 1959-10-14 1964-06-09 Minnesota Mining & Mfg Adhesive composition and method of applying same
US3196035A (en) * 1960-07-16 1965-07-20 Fuji Tsushinki Seizo Kk Method of bonding an epoxy coating to a polyisocyanate treated polyester fiber base
US3429948A (en) * 1964-12-22 1969-02-25 Gen Etablissements Michelin Ra Polyesterurethane elastomers vulcanizable in live steam

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