GB707425A - Improvements in or relating to synthetic rubber compositions - Google Patents

Improvements in or relating to synthetic rubber compositions

Info

Publication number
GB707425A
GB707425A GB24963/51A GB2496351A GB707425A GB 707425 A GB707425 A GB 707425A GB 24963/51 A GB24963/51 A GB 24963/51A GB 2496351 A GB2496351 A GB 2496351A GB 707425 A GB707425 A GB 707425A
Authority
GB
United Kingdom
Prior art keywords
acids
acid
methyl
specified
acrylic
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
GB24963/51A
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 GB707425A publication Critical patent/GB707425A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F236/00Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F236/02Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F236/04Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated

Landscapes

  • 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)

Abstract

A plastic open-chain aliphatic conjugated diene polymer containing from 0.001 to 0.30 chemical equivalents by weight of combined -COOH groups per hundred parts by weight of polymer, is mixed with a polyvalent metallic oxide, and heated at 125 to 400 DEG F. until salt formation occurs. Specified metallic oxides are those of zinc, magnesium, cadmium, calcium, titanium, aluminium, barium strontium, copper, cobalt and tin. The polymer may be prepared (1) by polymerizing in an acidic aqueous medium, a monomeric mixture of at least 50 per cent. of the diene and an olefinically-unsaturated carboxylic acid, or (2) by reacting a diene polymer with a carboxylating agent or carboxyl-supplying reagent, preferably in the presence of an oxidizing agent, or (3) by reacting with a hydrolysing agent an interpolymer of a diene and an unsaturated copolymerizable material containing a group hydrolysable to a carboxyl group. Specified dienes are butadiene- 1:3, 2 -methyl butadiene-1:3, 2, 3-dimethylbutadiene -1:3, piperylene, 2-neopentyl butadiene- 1:3, 2 -chlorobutadiene 1:3, 2 -cyano -butadiene- 1:3, pentadienes and hexadienes. Specified olefinically unsaturated carboxylic acids are acrylic acid, the alpha-alkyl acrylic acids, b - methyl and b - benzal acrylic acids, crotonic, a - butyl and a - methyld - benzal crotonic acids b - acryloxy propionic acid, a and b - vinyl acrylic acid, a -b -isopropylidene propionic acid, sorbic and hydrosorbic acids, cinnamic acidm- and p-chlorocinnamic, maleic and fumaric acids, undecylenic and ricinoleic acid, linoleic acid and linolenic acid, angelic, umbellic, a - methyl, a - ethyl, a - chloro and a - bromo -sorbic acids, a , b , d or epsilondimethyl sorbic acids, and many others. A third monomer may be present. Specified are acrylonitrile, a -chloroacrylonitrile, methyl, ethyl, butyl, 2- ethylbenzyl, or noctyl acrylate, methyl, butyl or lauryl methacrylate, methyl ethacrylate, styrene, vinylidene chloride, vinyl pyridine and isobutylene. In preparations (1) an emulsifier such as sodium lauryl sulphate, the sodium salts of sulphonated paraffin oil, and lauryl amine hydrochloride (many more listed), a catalyst such as hydrogen peroxide, other peroxides, hydroperoxides, persalts, with or without reducing agents (many specified) and a mercaptan modifier may be present, while the polymerization may be short stopped with hydroquinone or phenyl b -naphthylamine. Among a long list of carboxylating agents for use in (2) are maleic acid, dimethyl maleic anhydride, beta -mercapto propionic acid, bis- (thioglycollic) anhydride, and monopotassium oxalate, which may be reacted by means of catalysts such as benzoyl peroxides, persulphates and perborates (many catalysts specified). Specified copolymerizable materials which may be used in method (3) are esters, amides and nitriles of acrylic and substituted acrylic acids, particularly the alphaalkyl and alpha -halo acrylic acids, maleates and fumarates, vinyl esters of carboxylic acids, alkyl esters of carboxylic acids, the alpha- and betacyano acrylates and related compounds, methyl betaacryloxy propionate, acrylyl chloride and allyl chloride. A third monomer such as vinylidene chloride or chlorofluoride, styrene, ochloro or omethoxy styrene, pdivinyl benzene, vinyl naphthalene, vinyl pyridine or vinyl carbazole may also be present. Here again the usual emulsifiers, catalysts and polymerization modifiers may be used. The hydrolysis method (3) may be carried out in solution in benzene, toluene, acetone, alcohol or methyl ethyl ketone by adding an acidic hydrolysing agent to a cationic aqueous dispersion of the polymer or an alkaline one to an anionic aqueous dispersion, or by reacting the solids together and treating with water or aqueous acid or by adding the hydrolysing agent to the monomer mixture. Hydrolysing agents include strong inorganic and organic acids, alkalihydroxides, quaternary ammonium bases and their salts, primary, secondary and tertiary amines, heterocyclic amines, and salts of a strong base and a weak acid.
GB24963/51A 1950-11-01 1951-10-25 Improvements in or relating to synthetic rubber compositions Expired GB707425A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US707425XA 1950-11-01 1950-11-01

Publications (1)

Publication Number Publication Date
GB707425A true GB707425A (en) 1954-04-14

Family

ID=22097105

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24963/51A Expired GB707425A (en) 1950-11-01 1951-10-25 Improvements in or relating to synthetic rubber compositions

Country Status (1)

Country Link
GB (1) GB707425A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3108709A (en) * 1959-11-27 1963-10-29 Cities Service Res & Dev Co Polymerization and coating processes and products
DE1292377B (en) * 1955-06-29 1969-04-10 Goodrich Co B F Storage-stable aqueous dispersions of copolymers containing carboxyl groups
US4272426A (en) 1979-03-07 1981-06-09 The International Synthetic Rubber Company Ltd. Preparation of latices

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1292377B (en) * 1955-06-29 1969-04-10 Goodrich Co B F Storage-stable aqueous dispersions of copolymers containing carboxyl groups
US3108709A (en) * 1959-11-27 1963-10-29 Cities Service Res & Dev Co Polymerization and coating processes and products
US4272426A (en) 1979-03-07 1981-06-09 The International Synthetic Rubber Company Ltd. Preparation of latices

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