GB1409817A - Dyeable polyurethane elastomer and its production - Google Patents

Dyeable polyurethane elastomer and its production

Info

Publication number
GB1409817A
GB1409817A GB5434372A GB5434372A GB1409817A GB 1409817 A GB1409817 A GB 1409817A GB 5434372 A GB5434372 A GB 5434372A GB 5434372 A GB5434372 A GB 5434372A GB 1409817 A GB1409817 A GB 1409817A
Authority
GB
United Kingdom
Prior art keywords
residues
diols
dyeable
isocyanate
nov
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
GB5434372A
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.)
Toyobo Co Ltd
Original Assignee
Toyobo Co 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
Priority claimed from JP46094722A external-priority patent/JPS5017237B2/ja
Priority claimed from JP47025032A external-priority patent/JPS5017520B2/ja
Application filed by Toyobo Co Ltd filed Critical Toyobo Co Ltd
Publication of GB1409817A publication Critical patent/GB1409817A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C08G18/12Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step

Abstract

1409817 Dyeable segmented polyurethane elastomers TOYO BOSEKI KK 24 Nov 1972 [25 Nov 1971 10 March 1972] 54343/72 Heading C3A A dyeable segmented polyurethane elastomer contains the copolymerized residues of:-(i) an isocyanate - terminated polyurethane containing residues of (a) an organic polyisocyanate and (b) a polyol of M.W. 500 to 6000 and M.P. not above 60‹ C.; (ii) an isocyanate-terminated polyurethane containing residues of (a) as in (i), (c) a diol containing tertiary nitrogen and (b) at least 7 mol. per cent based on (c) of (b) as in (i); and (iii) a monomeric polyfunctional compound selected from diamines, hydrazine, dihydrazides, glycol and water. Residues (ii) are preferably present in proportions providing 10 to 150 mmole/kg. of polymer. Specified t-N- containing diols are those of formula where R 1 to R 4 are optionally substituted alkyl or cycloalkyl or R 1 and R 2 may be H; R 5 to R 7 are optionally substituted alkylene or cycloalkylene; and n is 1 to 10, and salts thereof. In examples various diols (ii) (c) are used; (i) and (ii) (a) is 4,4<SP>1</SP>-diisocyanato-methane; (i) and (ii) (b) is a polytetramethylene glycol of M.W. 800, 1000, 1300 or 1320, polylactone diol of M.W. 1250, or a polyester of M.W. 1785 of adipic acid and a mixture of 1,4-butane- and 2,2-dimethylpropane-1,3-diols; and (iii) is 1,1- propylene diamine.
GB5434372A 1971-11-25 1972-11-24 Dyeable polyurethane elastomer and its production Expired GB1409817A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP46094722A JPS5017237B2 (en) 1971-11-25 1971-11-25
JP47025032A JPS5017520B2 (en) 1972-03-10 1972-03-10

Publications (1)

Publication Number Publication Date
GB1409817A true GB1409817A (en) 1975-10-15

Family

ID=26362629

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5434372A Expired GB1409817A (en) 1971-11-25 1972-11-24 Dyeable polyurethane elastomer and its production

Country Status (1)

Country Link
GB (1) GB1409817A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20220161528A1 (en) * 2020-11-24 2022-05-26 Chance Line Industrial Co., Ltd. Filament made from cutting membrane material and being thinned to improve physical properties and manufacturing method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20220161528A1 (en) * 2020-11-24 2022-05-26 Chance Line Industrial Co., Ltd. Filament made from cutting membrane material and being thinned to improve physical properties and manufacturing method thereof

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Legal Events

Date Code Title Description
PS Patent sealed
PE20 Patent expired after termination of 20 years