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GB1298134A - Fiber filled urethane elastomer compositions - Google Patents

Fiber filled urethane elastomer compositions

Info

Publication number
GB1298134A
GB1298134A GB5231770A GB5231770A GB1298134A GB 1298134 A GB1298134 A GB 1298134A GB 5231770 A GB5231770 A GB 5231770A GB 5231770 A GB5231770 A GB 5231770A GB 1298134 A GB1298134 A GB 1298134A
Authority
GB
United Kingdom
Prior art keywords
urethane
fibres
diisocyanate
intermediate polymer
resin
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
GB5231770A
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.)
Atlantic Richfield Co
Original Assignee
Atlantic Richfield Co
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 Atlantic Richfield Co filed Critical Atlantic Richfield Co
Publication of GB1298134A publication Critical patent/GB1298134A/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
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67Unsaturated compounds having active hydrogen
    • C08G18/69Polymers of conjugated dienes
    • 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
    • C08L75/14Polyurethanes having carbon-to-carbon unsaturated bonds

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)
  • Polyurethanes Or Polyureas (AREA)

Abstract

1298134 Elastomeric compositions ATLANTIC RICHFIELD CO 3 Nov 1970 [18 Nov 1969] 52317/70 Heading C3P Elastomeric compositions comprise fibres incorporated into a urethane made by reacting a diisocyanate with a hydroxy-containing intermediate polymer derived from 25-100% of a C 4-12 conjugated diene and 0-75% of a C 2-12 olefinic monomer, the amount of fibres being 0À1-50 wt. per cent based on the intermediate polymer. The intermediate polymer is a liquid polymer defined as containing an average of at least 1À8 predominantly primary terminal allylic hydroxyl groups per average molecule, having a viscosity at 30‹ C. of 5-20,000 poises, a number average M.W. of 400-25,000, and more than 50% of its unsaturation in the main carbon chain. The urethane formation may take place in the additional presence of a polyhydroxy reactant and/or a diamine, the latter resulting in a urea-urethane. The urethane or urea-urethane resin may be formed in situ, or the fibres may be added to pre-formed resin, both alternatives being exemplified. In specific examples, the fibres are of glass; the hydroxycontaining liquid intermediate polymer is derived from butadiene or butadiene-styrene; the diisocyanate used is tolylene diisocyanate or diphenylmethane diisocyanate; the additional polyhydroxy reactant (when used) is N,N-bis-(2- hydroxy-propyl) aniline; the additional diamine reactant (when used) is 3,3<SP>1</SP>-dichlorobenzidine or N,N - bis - (1,4 - dimethylpentyl) - p - phenylene diamine; and carbon black and naphthenic extender oil are present in some cases. In those examples in which the urethane or ureaurethane resin is produced in situ, stannous octoate or dibutyl tin laurate is present as catalyst.
GB5231770A 1969-11-18 1970-11-03 Fiber filled urethane elastomer compositions Expired GB1298134A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US87782769A 1969-11-18 1969-11-18

Publications (1)

Publication Number Publication Date
GB1298134A true GB1298134A (en) 1972-11-29

Family

ID=25370807

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5231770A Expired GB1298134A (en) 1969-11-18 1970-11-03 Fiber filled urethane elastomer compositions

Country Status (5)

Country Link
BE (1) BE759129A (en)
DE (1) DE2056740A1 (en)
FR (1) FR2069618A5 (en)
GB (1) GB1298134A (en)
NL (1) NL7016917A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4456707A (en) * 1982-04-23 1984-06-26 Bayer Aktiengesellschaft Process for the production of fiber-containing polyurethane moldings having inhomogeneously colored surfaces
GB2141722A (en) * 1983-06-20 1985-01-03 Secretary Industry Brit Urethane composites

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4456707A (en) * 1982-04-23 1984-06-26 Bayer Aktiengesellschaft Process for the production of fiber-containing polyurethane moldings having inhomogeneously colored surfaces
GB2141722A (en) * 1983-06-20 1985-01-03 Secretary Industry Brit Urethane composites

Also Published As

Publication number Publication date
BE759129A (en) 1971-05-18
NL7016917A (en) 1971-05-21
FR2069618A5 (en) 1971-09-03
DE2056740A1 (en) 1971-05-27

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee