GB1189997A - Polyether-Urethanes - Google Patents

Polyether-Urethanes

Info

Publication number
GB1189997A
GB1189997A GB4323366A GB4323366A GB1189997A GB 1189997 A GB1189997 A GB 1189997A GB 4323366 A GB4323366 A GB 4323366A GB 4323366 A GB4323366 A GB 4323366A GB 1189997 A GB1189997 A GB 1189997A
Authority
GB
United Kingdom
Prior art keywords
triol
glycol
reaction
liquid
prepolymers
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
GB4323366A
Inventor
John Young Lewis
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.)
Pfizer Ltd
Original Assignee
Pfizer 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 Pfizer Ltd filed Critical Pfizer Ltd
Priority to GB4323366A priority Critical patent/GB1189997A/en
Priority to DE19671745276 priority patent/DE1745276A1/en
Priority to FR122335A priority patent/FR1538174A/en
Publication of GB1189997A publication Critical patent/GB1189997A/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
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666Compounds of group C08G18/48 or C08G18/52
    • C08G18/667Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6674Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

1,189,997. Polyetherurethanes. PFIZER Ltd. 27 Sept., 1967 [28 Sept., 1966], No. 43233/66. Headings C3C and C3R. Liquid polyetherurethane prepolymers having a free isocyanate content are prepared by reacting, in the absence of a catalyst: (A) an aromatic diisocyanate; (B) a linear, liquid alpha-omega glycol having an hydroxyl equivalent weight below 250; and (C) a liquid polyoxyalkylene triol having an hydroxyl equivalent weight of at least 250, the ratio of isocyanate groups in (A) to hydroxyl groups in (B) plus (C) being greater than one and the proportion of triol (C) to glycol (B) being such that the reaction product is a stable liquid, i.e. a liquid which does not crystallize within 24 hours at ambient temperatures. The compounds (A), (B) and (C) are those conventionally used in the art. Especially preferred as glycol (B) is diethylene glycol which may be used such that the weight ratio of triol (C) to diethylene glycol is at least 4 to 1, preferably 6 to 1. The reaction between (A), (B) and (C) is preferably carried out at temperatures of 55‹ to 90‹ C. Elastomers may be prepared from the prepolymers by reaction with further amounts of glycol (B) and/or triol (C) in the presence of an organometallic catalyst such that the ratio of isocyanate groups to hydroxyl groups is in the range of 0À95 to 1 to 1À2 to 1. Alternatively the prepolymer may be reacted with other compounds containing two or more hydroxyl and/or primary amine groups or may be dissolved in a solvent with a tertiary amine catalyst and allowed to cure by reaction with moisture in the atmosphere. Microcellular elastomers may be prepared from the prepolymers by reaction with further amounts of (B) and/or (C) in the presence of small amounts of air and/or water and, if desired, a nucleating agent. The additional triol (C) may be partially or entirely replaced by an inert plasticizer such as phthalic acid esters and chlorinated hydrocarbons. Numerous examples are given of the polyetherurethane prepolymers and elastomers prepared therefrom.
GB4323366A 1966-09-28 1966-09-28 Polyether-Urethanes Expired GB1189997A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB4323366A GB1189997A (en) 1966-09-28 1966-09-28 Polyether-Urethanes
DE19671745276 DE1745276A1 (en) 1966-09-28 1967-09-23 Polyaether urethanes and processes for their preparation
FR122335A FR1538174A (en) 1966-09-28 1967-09-26 Improvements in processes for the preparation and use of polyetherurethanes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4323366A GB1189997A (en) 1966-09-28 1966-09-28 Polyether-Urethanes

Publications (1)

Publication Number Publication Date
GB1189997A true GB1189997A (en) 1970-04-29

Family

ID=10427849

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4323366A Expired GB1189997A (en) 1966-09-28 1966-09-28 Polyether-Urethanes

Country Status (2)

Country Link
DE (1) DE1745276A1 (en)
GB (1) GB1189997A (en)

Also Published As

Publication number Publication date
DE1745276A1 (en) 1971-08-12

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Legal Events

Date Code Title Description
PS Patent sealed
PLNP Patent lapsed through nonpayment of renewal fees