GB723456A - Improvements in or relating to a process for producing synthetic rubbery compositions - Google Patents

Improvements in or relating to a process for producing synthetic rubbery compositions

Info

Publication number
GB723456A
GB723456A GB16750/52A GB1675052A GB723456A GB 723456 A GB723456 A GB 723456A GB 16750/52 A GB16750/52 A GB 16750/52A GB 1675052 A GB1675052 A GB 1675052A GB 723456 A GB723456 A GB 723456A
Authority
GB
United Kingdom
Prior art keywords
methacrylic acid
butadiene
mixing
weight
acrylic acid
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
GB16750/52A
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.)
Goodrich Corp
Original Assignee
BF Goodrich Corp
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 BF Goodrich Corp filed Critical BF Goodrich Corp
Publication of GB723456A publication Critical patent/GB723456A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08CTREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
    • C08C19/00Chemical modification of rubber
    • C08C19/30Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
    • C08C19/34Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups
    • C08C19/36Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups with carboxy radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

Synthetic rubbery compositions are prepared by mixing a synthetic rubbery polymeric material comprising predominantly linear carbon chains to which are attached from 0.001 to 0.30 chemical equivalents by weight of combined carboxyl ( - COOH) per 100 parts by weight of polymer with an amount of curing agent sufficient to react with at least 1/10 of the carbonyl groups, the curing agent being selected from primary and secondary aliphatic and heterocyclic polyamines and their salts containing at least two amino- or imino-nitrogen groups and heating at from 100 DEG to 450 DEG F. until an elastic condition is produced. The polymeric material may be prepared by any of the methods of Specification 707,425, and may be any of those specified therein. Preferred polymers are those of an open-chain unsaturated aliphatic diene (e.g. butadiene-1 : 3), of an alkyl ester of acrylic acid, which is then hydrolysed, of a mixture of an olefinically unsaturated carboxylic acid (e.g. methacrylic acid) with either of the above; specified are butadiene-sorbic acid copolymer, butadiene-acrylonitrile-methacrylic acid terpolymer, ethyl acrylate-acrylic acid-methacrylic acid terpolymer (this polymerization may take place in two stages) and ethylacrylate-acrylic acid-methacrylic acid-divinyl benzene tetrapolymer. The mixing may be done in any conventional manner such as mill-mixing, preferably below 175 DEG to 200 DEG F. Preferred curing agents are the polymethylene diamines and the polyethylene diamines, e.g. hexamethylene diamine, its carbonate and its borate and the preferred proportions vary from 1 to 30 per cent based on the weight of polymer. The heating may be carried out until the product has properties comparable to metallocarboxylates (e.g. 150-300 DEG F.) or more drastically to form diamide- or imido-type cross-linkages (e.g. 250-450 DEG F.).
GB16750/52A 1951-07-25 1952-07-03 Improvements in or relating to a process for producing synthetic rubbery compositions Expired GB723456A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US723456XA 1951-07-25 1951-07-25

Publications (1)

Publication Number Publication Date
GB723456A true GB723456A (en) 1955-02-09

Family

ID=22107000

Family Applications (1)

Application Number Title Priority Date Filing Date
GB16750/52A Expired GB723456A (en) 1951-07-25 1952-07-03 Improvements in or relating to a process for producing synthetic rubbery compositions

Country Status (1)

Country Link
GB (1) GB723456A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0023084A1 (en) * 1979-06-26 1981-01-28 The British Petroleum Company p.l.c. Cross-linked polymer compositions and production thereof
US4812242A (en) * 1984-05-31 1989-03-14 The British Petroleum Company P.L.C. Method of encapsulating organic material

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0023084A1 (en) * 1979-06-26 1981-01-28 The British Petroleum Company p.l.c. Cross-linked polymer compositions and production thereof
US4812242A (en) * 1984-05-31 1989-03-14 The British Petroleum Company P.L.C. Method of encapsulating organic material

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