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GB1040690A - Emulsion polymerization in the presence of selected mercaptan modifier - Google Patents

Emulsion polymerization in the presence of selected mercaptan modifier

Info

Publication number
GB1040690A
GB1040690A GB2058265A GB2058265A GB1040690A GB 1040690 A GB1040690 A GB 1040690A GB 2058265 A GB2058265 A GB 2058265A GB 2058265 A GB2058265 A GB 2058265A GB 1040690 A GB1040690 A GB 1040690A
Authority
GB
United Kingdom
Prior art keywords
mercaptan
carbon atoms
nonyl
decyl
tert
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
GB2058265A
Inventor
Carl Adam Uraneck
John Erickson Burleigh
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.)
Phillips Petroleum Co
Original Assignee
Phillips Petroleum 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 Phillips Petroleum Co filed Critical Phillips Petroleum Co
Priority to DE1965P0036804 priority Critical patent/DE1263309B/en
Priority to GB2058265A priority patent/GB1040690A/en
Publication of GB1040690A publication Critical patent/GB1040690A/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
    • C08F36/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F36/02Homopolymers and copolymers 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
    • C08F36/04Homopolymers and copolymers 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)
  • Polymerisation Methods In General (AREA)

Abstract

A process for producing elastomeric polymers which comprises polymerizing in an aqueous emulsion at least one conjugated diene containing four to twelve carbon atoms, or mixtures of at least one such conjugated diene and at least one monomer containing a vinylidene group in the presence of an open-chain saturated mercaptan containing 8 to 10 carbon atoms or an unsaturated cyclic mercaptan containing from 10 to 12 carbon atoms and one or more olefinic bonds in non-conjugated arrangement and separated by at least two carbon atoms, the mercaptan having a solubilization rate, in an aqueous soap solution of 2.5 to 3.0 weight per cent, of at least 19 x 10-4 g./cm.2/hr. and a depletion rate during polymerization such that not more than 15 weight per cent of the total mercaptan is unreacted at 40% monomer conversion, at least 60% of the mercaptan being introduced at the beginning of the reaction and the remainder being added in one or more increments after about 7% monomer conversion and before 40% conversion. Specified mercaptans are tert.-octyl, tert.-nonyl, 2-nonyl, 4-nonyl, tert.-decyl, 2-decyl, 5-decyl, 4-cyclodecenyl and cyclododecadienyl mercaptans. The elastomers may be polymers of butadiene, isoprene, 2,3-dimethyl butadiene, piperylene, 2-methyl-hexadiene, chloropene, methoxy butadiene and cyanobutadiene or their copolymers with styrene, 3-vinyl toluene 1- or 2-vinylnaphthalene, 3-methylstyrene, 2-methyl-5-vinyl-pyridine, acrylonitrile, methylacrylate or methyl vinyl ether. The usual emulsifiers, catalysts &c. may also be present.
GB2058265A 1965-05-14 1965-05-14 Emulsion polymerization in the presence of selected mercaptan modifier Expired GB1040690A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
DE1965P0036804 DE1263309B (en) 1965-05-14 1965-05-14 Process for the production of elastomeric polymers by polymerizing conjugated dienes
GB2058265A GB1040690A (en) 1965-05-14 1965-05-14 Emulsion polymerization in the presence of selected mercaptan modifier

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2058265A GB1040690A (en) 1965-05-14 1965-05-14 Emulsion polymerization in the presence of selected mercaptan modifier

Publications (1)

Publication Number Publication Date
GB1040690A true GB1040690A (en) 1966-09-01

Family

ID=10148303

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2058265A Expired GB1040690A (en) 1965-05-14 1965-05-14 Emulsion polymerization in the presence of selected mercaptan modifier

Country Status (1)

Country Link
GB (1) GB1040690A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1745417B1 (en) * 1966-10-26 1970-12-23 Aquitaine Petrole Process for the preparation of polymers of conjugated dienes
US4369299A (en) 1977-11-11 1983-01-18 Asahi Kasei Kogyo Kabushiki Kaisha Acrylic resin having excellent solvent resistance and moldability

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1745417B1 (en) * 1966-10-26 1970-12-23 Aquitaine Petrole Process for the preparation of polymers of conjugated dienes
US4369299A (en) 1977-11-11 1983-01-18 Asahi Kasei Kogyo Kabushiki Kaisha Acrylic resin having excellent solvent resistance and moldability

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