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Process for the manufacture of improved elastomers prepared by reaction of trimellitoyl-functional polymer with epoxy compound

Assignee: Bridgestone Corp
•
Filing: 1974-08-16
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Granted: 1976-08-31
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Expires: 1994-08-16
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Abstract

Abstract The present invention relates to a process for manufacturing a new elastomer having high elasticity, mechanical strength and processability from epoxy compounds, trimellitoyl-functional polymers and a third element. The third element is any of acid anhydride compounds having a molecular weight lower than 700, and having at least one acid anhydride group, such as maleic, phthalic, succinic, adipic, trimellitic, pyromellitic, and benzophenone tetracarboxylic anhydrides. It is, according to another aspect, an improvement of physical properties, especially tensile and tear strengths of the elastomer manufactured by reacting said first two elements according to the copending application Ser. No. 143,643, filed May 14, 1971, while keeping desirably low exothermicity and thermal contraction during the curing.

Inventors

  • 👤 Toshio Yukuta
  • 👤 Takao Moki
  • 👤 Takashi Ohashi
  • 👤 Kouichi Iwami
  • 👤 Akira Suzuki

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 05:08
CPC Classifications
C; C08; C08G; C08G63/00; C08G63/02; C08G63/12; C08G63/40; C08G63/42; C08L; C08L63/00

Claims Analysis

Total Claims: 13
Claim 1
Independent Claim 208 words
Process for the manufacture of an elastomer comprising the steps of mixing (A) at least one trimellitoyl-functional polymer represented by the formula: ##SPC5## in which R represents a residue of an hydroxyl-functional polymer and n is an integer of at least 2, said trimellitoyl-functional polymer being prepared by the reaction of an hydroxyl-functional polymer having a number average molecular weight higher than 700, and having at least two hydroxy groups at the chain ends of the side chain, with trimellitic anhydride or a derivative thereof; (B) at least one polyglycidyl ether of bisphenol A; and (C) at least one acid anhydride compound having a molecular weight lower than 700, and having at least one acid anhydride group, and proceeding with curing at an elevated temperature and wherein the low molecular weight acid anhydride compound is added in the amount of 0.5 to 2.0 equivalents relative to 1 equivalent of the acid anhydride group of the trimellitoyl-functional polymer, and the total amount of the trimellitoyl-functional polymer and the low molecular weight acid anhydride compound is such that the equivalent ratio of total acid anhydride groups of the trimellitoyl-functional polymer and the low molecular weight acid anhydride compound to the epoxy groups of the epoxy compound is 0.5 to 1.5.
Claim 2
Dependent Claim 208 words
Process for the manufacture of an elastomer comprising the steps of mixing (A) at least one trimellitoyl-functional polymer represented by the formula: ##SPC5## in which R represents a residue of an hydroxyl-functional polymer and n is an integer of at least 2, said trimellitoyl-functional polymer being prepared by the reaction of an hydroxyl-functional polymer having a number average molecular weight higher than 700, and having at least two hydroxy groups at the chain ends of the side chain, with trimellitic anhydride or a derivative thereof; (B) at least one polyglycidyl ether of bisphenol A; and (C) at least one acid anhydride compound having a molecular weight lower than 700, and having at least one acid anhydride group, and proceeding with curing at an elevated temperature and wherein the low molecular weight acid anhydride compound is added in the amount of 0.5 to 2.0 equivalents relative to 1 equivalent of the acid anhydride group of the trimellitoyl-functional polymer, and the total amount of the trimellitoyl-functional polymer and the low molecular weight acid anhydride compound is such that the equivalent ratio of total acid anhydride groups of the trimellitoyl-functional polymer and the low molecular weight acid anhydride compound to the epoxy groups of the epoxy compound is 0.5 to 1.5.
Claim 3
Dependent Claim 30 words
An elastomer as claimed in claim 1, in which said hydroxyl-functional polymer is made from polybutadiene, butadiene-styrene copolymer, polyisoprene, butadiene-acrylonitrile copolymer, butadiene-acrylate copolymer ethylene-propylene-diene terpolymer, polyethylene adipate or polytetramethylene ether.
Claim 4
Dependent Claim 20 words
Process as claimed in claim 1, in which the low molecular weight acid anhydride compound has one acid anhydride group.
Claim 5
Dependent Claim 28 words
An elastomer as claimed in claim 1, in which said anhydride is selected from the group consisting of maleic, phthalic, tetrahydrophthalic, hexahydrophthalic, methyltetrahydrophthalic, succinic and adipic acid anhydrides.
Claim 6
Dependent Claim 24 words
Process as claimed in claim 1, in which the low molecular weight acid anhydride compound has one acid anhydride group and a carboxy group.
Claim 7
Dependent Claim 23 words
An elastomer as claimed in claim 1, in which said anhydride is selected from the group consisting of trimellitic and tricarballylic acid anhydrides.
Claim 8
Dependent Claim 20 words
Process as claimed in claim 1, in which the low molecular weight acid anhydride compound has two acid anhydride groups.
Claim 9
Dependent Claim 30 words
An elastomer as claimed in claim 1, in which said anhydride is selected from the group consisting of pyromellitic, benzophenone tetracarboxylic acid anhydrides, ethylene glycol bistrimellitate and xylene glycol bistrimellitate.
Claim 10
Dependent Claim 20 words
Process as claimed in claim 1, in which the low molecular weight acid anhydride compound has three acid anhydride groups.
Claim 11
Dependent Claim 14 words
An elastomer as claimed in claim 1, in which said anhydride is glycerine tristrimellitate.
Claim 12
Dependent Claim 16 words
Process as claimed in claim 1, in which the curing temperature ranges from 100° to 200°C.
Claim 13
Dependent Claim 9 words
The elastomer prepared by the process of claim 1.

References Cited (Backward Citations)

US3140299A Cited
US3437671A Cited
US3609110A Cited
US3555111A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-08-31 1980-03-01 1980-08-31 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-08-31 1984-03-01 1984-08-31 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-08-31 1988-03-01 1988-08-31 $7700.00 Window Closed / Lapsed

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