GB1097504A - Elastomeric polyurethanes - Google Patents

Elastomeric polyurethanes

Info

Publication number
GB1097504A
GB1097504A GB681266A GB681266A GB1097504A GB 1097504 A GB1097504 A GB 1097504A GB 681266 A GB681266 A GB 681266A GB 681266 A GB681266 A GB 681266A GB 1097504 A GB1097504 A GB 1097504A
Authority
GB
United Kingdom
Prior art keywords
glycol
glycols
diol
mixture
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
GB681266A
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.)
Pharmacia and Upjohn Co
Original Assignee
Upjohn 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 Upjohn Co filed Critical Upjohn Co
Publication of GB1097504A publication Critical patent/GB1097504A/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
    • C08G18/6633Compounds of group C08G18/42
    • C08G18/6637Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38

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

An elastomeric polyurethane is the reaction product of a diisocyanate, a polyester diol of molecular weight 700-2000, and a mixture of at least two different glycols, in proportions such that the overall ration of isocyanate to hydroxyl groups is about 1:1, while the polyester/glycol ratio ranges from 2:1 to 1:3. The glycol contains between the hydroxy groups a divalent aliphatic group containing 2-10 C atoms, of which 2-6 may form a chain separating the hydroxy groups, and optionally such groups as -O-, <FORM:1097504/C3/1> alkyl, -arylene-, and -O-arylene-O-. Examples are ethylene and tri-, tetra-, penta- and hexamethylene, neopentylene, diethylene, dipropylene, dibutylene glycols, ethyl and methyl diethanolamines, methyl dipropanolamine, p-xylylene diol, p-phenylene diethylene glycol and hydroquinone di-(ethylene glycol) ether. No glycol should comprise less than 20% of a mixture of two glycols, or less than 10% of a mixture of more than two glycols. Many conventional aromatic and aliphatic diisocyanates are listed. Suitable polyester diols may be derived from adipic, succinic, suberic, azelaic, sebacic and terephthalic acids or anhydrides with C2- 10 normal alkylene glycols, or from e -caprolactone polymerized with a glycol or aminoalkanol initiator. Suitable catalysts are metal compounds (lists), phosphines and tertiary amines, in amounts of 0.1-2 weight per cent of the reactants. The preparation preferably proceeds as a one-shot process, but it is possible to form a prepolymer from the diisocyanate and the polyester diol. Conventional pigments, fillers, and colouring agents may be added. In Examples 1, 2, 4 and 5, mixtures of two of trimethylene glycol, tetramethylene glycol and neopentylene glycol are mixed with a poly-(e-caprolactone) diol or a poly-(9:1-ethylenepropylene) adipate diol, then with diphenylmethane diisocyanate. In Example 7 toluenediisocyanate is used, and in Example 8 a mixture of tetramethylene and hexamethylene glycols.
GB681266A 1965-03-09 1966-02-16 Elastomeric polyurethanes Expired GB1097504A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US43842565A 1965-03-09 1965-03-09

Publications (1)

Publication Number Publication Date
GB1097504A true GB1097504A (en) 1968-01-03

Family

ID=23740613

Family Applications (1)

Application Number Title Priority Date Filing Date
GB681266A Expired GB1097504A (en) 1965-03-09 1966-02-16 Elastomeric polyurethanes

Country Status (2)

Country Link
DE (1) DE1645578A1 (en)
GB (1) GB1097504A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3103846A1 (en) 2015-06-10 2016-12-14 UBE Corporation Europe, S.A.U. Self-healing polyurethane polymers

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2161340C3 (en) * 1971-12-10 1982-02-18 Bayer Ag, 5090 Leverkusen Adhesive based on polyurethane
DE2817456A1 (en) * 1978-04-21 1979-10-31 Bayer Ag PROCESS FOR MANUFACTURING THERMOPLASTIC POLYURETHANE ELASTOMERS

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3103846A1 (en) 2015-06-10 2016-12-14 UBE Corporation Europe, S.A.U. Self-healing polyurethane polymers
WO2016198441A1 (en) 2015-06-10 2016-12-15 Ube Corporation Europe, S.A.U. Self-healing polyurethane polymers

Also Published As

Publication number Publication date
DE1645578A1 (en) 1970-10-22

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