GB828814A - Improvements in or relating to elastomeric addition products - Google Patents

Improvements in or relating to elastomeric addition products

Info

Publication number
GB828814A
GB828814A GB21163/56A GB2116356A GB828814A GB 828814 A GB828814 A GB 828814A GB 21163/56 A GB21163/56 A GB 21163/56A GB 2116356 A GB2116356 A GB 2116356A GB 828814 A GB828814 A GB 828814A
Authority
GB
United Kingdom
Prior art keywords
styrene
methyl
iron
addition product
para
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
GB21163/56A
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.)
Goodyear Tire and Rubber Co
Original Assignee
Goodyear Tire and 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 Goodyear Tire and Rubber Co filed Critical Goodyear Tire and Rubber Co
Publication of GB828814A publication Critical patent/GB828814A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L15/00Compositions of rubber derivatives
    • 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
    • C08C19/20Incorporating sulfur atoms into the molecule
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L21/00Compositions of unspecified rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/01Hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L11/00Compositions of homopolymers or copolymers of chloroprene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L17/00Compositions of reclaimed rubber
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L7/00Compositions of natural rubber
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/02Copolymers with acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/06Copolymers with styrene

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

An elastomeric addition product having a Mooney plasticity on the large motor at 100 DEG C. of not less than 35 is obtained by reacting in the presence of a catalyst system and in the absence of substantial amounts of oxygen (A), at least 30% of the double bonds present in at least one synthetic rubber latex containing an emulsion polymerized polymer of at least one conjugated diolefin having 4-6 carbon atoms with from none to an equal amount by weight of at least one monomer containing a reactive component selected from the group consisting of vinyl and vinylidene radicals which are polymerizable with the diolefin with (B) at least one aliphatic monomercaptan having 1-6 carbon atoms, removing unreacted mercaptan from the reaction mixture and isolating the addition product. The latex may be obtained by polymerizing butadiene, isoprene, dimethyl butadiene, methyl pentadiene, piperylene or 2-chlorobutadiene 1,3; or copolymers of these monomers with styrene, para methyl styrene, ortho-para dimethyl styrene, para methoxy styrene, chloro and bromo styrenes, alpha methyl styrene, alpha-para dimethyl styrene, acrylic and methacrylic acid, methyl and ethyl acrylate, methyl or ethyl methacrylate, vinyl pyridines, 2-vinyl pyridine, 2 - methyl - 5 - vinyl pyridine, vinylidene chloride, acrylonitrile and methacrylonitrile. The latices may be prepared according to the "hot rubber" processes using as emulsifying agent an ammonium or alkali metal salt of stearic, palmitic or oleic acids, or hydrogenated tallow acids or hydrogenated rosin acids or sodium salts of alkylated benzene, or naphthalene sulphonic acids and sodium lauryl sulphate, and using as catalyst potassium persulphate, alkali metal salts of perborates, benzoyl peroxide or hydrogen peroxide, octyl, dodecyl, hexadecyl, octadecyl or benzyl mercaptan, according to the "cold process" using as catalyst sodium formaldehyde sulphoxylate, an organic hydroperoxide and an iron salt, a mixture of a polyethylene polyamine, an iron salt and an organic hydroperoxide, a mixture of an iron-pyrophosphate complex and an organic hydroperoxide, or a mixture of an iron-ethylenediamine tetra-acetic acid complex and an organic hydroperoxide at 41-55 DEG F. The mercaptans used in the manufacture of the addition product may be methyl, ethyl, propyl, isopropyl, butyl, isobutyl, amyl, isoamyl and hexyl mercaptans. The catalysts which may be used in the preparation of the addition product may be azodi-isobutyronitrile, dimethyl azo isobutyrate, or cumene hydroperoxide or para-menthane hydroperoxide alone or in admixture with (1) sodium formaldehyde sulphoxylate and an iron salt (2) a polyethylene polyamine (3) an iron-ethylene diamine tetra-acetic acid complex or (4) an iron-pyrophosphate complex. The addition is preferably effected at 50-65 DEG C. A processing oil may be used in an amount of 5 to 100 parts of the addition product, and natural rubber, reclaimed rubber, butadiene-styrene copolymer, butadiene-acrylonitrile copolymer and polymerized 2-chlorobutadiene, polystyrene resins, copolymers of styrene and monomethyl styrene, copolymers of styrene and anthracene, copolymers of styrene and actylonitrile, phenolformaldehyde resins and melamine resins may also be added. The compounded addition product may then be mixed with zinc oxide stearic acid, sulphur, mercaptobenzthiazole and styrenated phenol and the whole cured for 90 minutes at 275 DEG F.
GB21163/56A 1955-10-28 1956-07-09 Improvements in or relating to elastomeric addition products Expired GB828814A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US828814XA 1955-10-28 1955-10-28

Publications (1)

Publication Number Publication Date
GB828814A true GB828814A (en) 1960-02-24

Family

ID=22174049

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21163/56A Expired GB828814A (en) 1955-10-28 1956-07-09 Improvements in or relating to elastomeric addition products

Country Status (1)

Country Link
GB (1) GB828814A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0213568A2 (en) * 1985-09-03 1987-03-11 Agfa-Gevaert AG Electrostatographic suspension developer
WO2018075175A1 (en) * 2016-10-19 2018-04-26 Contitech Usa, Inc. Severely hydrotreated naphthenic distillate containing rubber compositions

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0213568A2 (en) * 1985-09-03 1987-03-11 Agfa-Gevaert AG Electrostatographic suspension developer
EP0213568A3 (en) * 1985-09-03 1988-07-27 Agfa-Gevaert Ag Electrostatographic suspension developer
WO2018075175A1 (en) * 2016-10-19 2018-04-26 Contitech Usa, Inc. Severely hydrotreated naphthenic distillate containing rubber compositions
US10597519B2 (en) 2016-10-19 2020-03-24 Contitech Usa, Inc. Severely hydrotreated naphthenic distillate containing rubber compositions

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