GB739634A - Improvements in chemically modified elastomers - Google Patents

Improvements in chemically modified elastomers

Info

Publication number
GB739634A
GB739634A GB4483/54A GB448354A GB739634A GB 739634 A GB739634 A GB 739634A GB 4483/54 A GB4483/54 A GB 4483/54A GB 448354 A GB448354 A GB 448354A GB 739634 A GB739634 A GB 739634A
Authority
GB
United Kingdom
Prior art keywords
elastomers
esters
adducts
isoprene
ketone
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
GB4483/54A
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.)
Uniroyal Inc
Original Assignee
United States Rubber 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 United States Rubber Co filed Critical United States Rubber Co
Publication of GB739634A publication Critical patent/GB739634A/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
    • C08C19/28Reaction with compounds containing carbon-to-carbon unsaturated bonds

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)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Synthetic elastomers are dry mixed with maleic anhydride and the mixture is heated, in the absence of organic peroxide or solvent and in the presence of an inhibitor of free radical polymerization, to at least 150 DEG C., preferably while mechanically mixing and desirably in the substantial absence of oxygen. Elastomers specified are copolymers of butadiene, isoprene, piperylene and 2,3-dimethylbutadiene, with styrene, methylstyrenes, acrylonitrile, methacrylonitrile, acrylic and methacrylic acids and their alkyl esters, acrylamide, N-substituted acrylamides, vinyl pyridines, fumarate esters, methylene malonic acid esters, vinylidine chloride, methyl vinyl ketone and methyl isopropenyl ketone. The examples also include a terpolymer of isoprene, butadiene and styrene (11) and mixtures of elastomers (10). The inhibitors of which many are listed belong to the following classes: phenol derivatives, aromatic amines and their quinonoid derivatives, condensation products of aromatic amines with aldehydes or ketones, organic phosphites and phosphate esters including those specified in U.S.A. Specification 2,587,477. To obtain a product having substantially no cross-linking a mixture of inhibitors, one of which inhibits self cross-linking at 150 DEG C. (e.g. aryl phosphites), is desirably used. Ingredients which may be included before, during or after the reaction are further inhibitor; softeners such as pine tar, coal tar (Bardol) and petroleum oil; plasticizers such as polyesters (Paraflux), dinitrochlorobenzene and xylyl mercaptans; and inert fillers or pigments such as carbon black, clay, titanium dioxide, lithopone, blanc fixe and diatomaceous earth. The adducts may be cold milled to reduce their viscosity, they may be blended together and they are of equal or lower viscosity than the original elastomer and are soluble in the same solvents, e.g. benzene and methyl ethyl ketone. The adducts may be vulcanized with the oxides, hydroxides and carbonates of zinc, magnesium, calcium, barium and divalent lead and are useful as water-resistant coatings or for making composite articles of metal and rubber.
GB4483/54A 1953-03-16 1954-02-16 Improvements in chemically modified elastomers Expired GB739634A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US739634XA 1953-03-16 1953-03-16

Publications (1)

Publication Number Publication Date
GB739634A true GB739634A (en) 1955-11-02

Family

ID=22116874

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4483/54A Expired GB739634A (en) 1953-03-16 1954-02-16 Improvements in chemically modified elastomers

Country Status (3)

Country Link
DE (1) DE1066024B (en)
FR (1) FR1095954A (en)
GB (1) GB739634A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3090715A (en) * 1958-08-25 1963-05-21 Exxon Research Engineering Co Chemically modified polydiolefin resin as an adhesive
US4341837A (en) 1978-08-11 1982-07-27 Kureha Kagaku Kogyo Kabushiki Kaisha Laminar thermoplastic resin structure
US4426498A (en) 1981-04-07 1984-01-17 Toa Nenryo Kogyo Kabushiki Kaisha Polyethylene composition comprising lldpe and rubber

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2265553C2 (en) * 1972-12-09 1987-02-05 Hoechst Ag, 6230 Frankfurt, De
DE2358722A1 (en) * 1972-12-09 1975-05-28 Hoechst Ag Polymers from diolefins, phenols and dicarboxylic acids - with good adhesion and physical props
DE2260376C2 (en) * 1972-12-09 1983-04-28 Hoechst Ag, 6230 Frankfurt Reaction products of diolefin polymers with a phenol and an olefinically unsaturated dicarboxylic acid or its anhydride and the use of these products
DE2366332C2 (en) * 1973-11-26 1989-02-09 Hoechst Ag, 6230 Frankfurt, De
GB9000907D0 (en) * 1990-01-16 1990-03-14 Bp Chem Int Ltd Process

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3090715A (en) * 1958-08-25 1963-05-21 Exxon Research Engineering Co Chemically modified polydiolefin resin as an adhesive
US4341837A (en) 1978-08-11 1982-07-27 Kureha Kagaku Kogyo Kabushiki Kaisha Laminar thermoplastic resin structure
US4426498A (en) 1981-04-07 1984-01-17 Toa Nenryo Kogyo Kabushiki Kaisha Polyethylene composition comprising lldpe and rubber

Also Published As

Publication number Publication date
FR1095954A (en) 1955-06-08
DE1066024B (en) 1959-09-24

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