GB813198A - Improvements in polymerization of isoprene - Google Patents

Improvements in polymerization of isoprene

Info

Publication number
GB813198A
GB813198A GB28627/56A GB2862756A GB813198A GB 813198 A GB813198 A GB 813198A GB 28627/56 A GB28627/56 A GB 28627/56A GB 2862756 A GB2862756 A GB 2862756A GB 813198 A GB813198 A GB 813198A
Authority
GB
United Kingdom
Prior art keywords
lithium
dilithium
mol
benzene
isoprene
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
GB28627/56A
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.)
Bridgestone Firestone Inc
Original Assignee
Firestone 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 Firestone Tire and Rubber Co filed Critical Firestone Tire and Rubber Co
Publication of GB813198A publication Critical patent/GB813198A/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
    • C08F136/00Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F136/02Homopolymers 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
    • C08F136/04Homopolymers 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
    • C08F136/08Isoprene

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)
  • Polymerization Catalysts (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

Abstract

Isoprene is polymerized in the presence of a hydrocarbon lithium or polylithium to give a rubbery essentially cis 1,4-polyisoprene. Specified catalysts are methyl-, ethyl-, butyl-, amyl-, hexyl-, 2-ethyl hexyl-, n-dodecyl- and n-hexadecyl-lithium; allyl- and methallyl-lithium; phenyl-, tolyl- and xylyl-lithium; alpha- and beta-naphthyl lithium; methylene-, ethylene-, trimethylene-, pentamethylene-, hexamethylene-, decamethylene-, octadecamethylene-dilithium; 1,2-dilithium propane; 1,4-dilithium benzene, 1,5-dilithium naphthalene, and 1,2-dilithium-1,3-diphenyl propane; 1,3,5-trilithium pentane, 1,3,5-trilithium benzene and the compound of the formula <FORM:0813198/IV (a)/1> Mixtures of such compounds may be used and the mixture obtained by treating 1 mol. of an alkyl lithium with 2/3 mol. of an alcohol and thereafter with an olefine for a period of two hours, e.g. treating amyl lithium with isopropanol and propylene. The polymerization is preferably carried out in bulk, solvents particularly hydrocarbons such as pentane, hexane, heptane, petroleum ether, benzene or cyclopentane may be used. The monomer should be at least 90 mol. per cent pure and may be submitted to a final purification by passing through silica gel into the reaction vessel. Oxygen and water should be excluded and final traces of air are removed by venting a portion of the monomer before sealing the reaction vessel; inert gases may be used during and before charging. The amount of catalyst may be 0.005-0.5 gram of carbon-linked lithium per 100 grams of isoprene. Temperatures of 0 DEG to 100 DEG C. for small-scale and 150 DEG C. for large-scale operations may be used for reaction times of 3 to 60 hours. Polymerization may be stopped by adding an alcohol. The polymer should be washed to remove catalyst and an antioxidant added. Numerous examples are given.
GB28627/56A 1955-09-19 1956-09-19 Improvements in polymerization of isoprene Expired GB813198A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US813198XA 1955-09-19 1955-09-19

Publications (1)

Publication Number Publication Date
GB813198A true GB813198A (en) 1959-05-13

Family

ID=22163426

Family Applications (1)

Application Number Title Priority Date Filing Date
GB28627/56A Expired GB813198A (en) 1955-09-19 1956-09-19 Improvements in polymerization of isoprene

Country Status (3)

Country Link
DE (1) DE1040796B (en)
FR (1) FR1206628A (en)
GB (1) GB813198A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017150199A1 (en) 2016-02-29 2017-09-08 日本ゼオン株式会社 Method for manufacturing polymer latex
US9840574B2 (en) 2014-05-16 2017-12-12 Kraton Polymers U.S. Llc Branched broad MWD conjugated diene polymer

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB910227A (en) * 1960-09-02 1962-11-14 Firestone Tire & Rubber Co Polymerization of diolefins
US3157604A (en) * 1960-10-24 1964-11-17 Phillips Petroleum Co Polymerization initiators
DE1177157B (en) * 1960-11-21 1964-09-03 Phillips Petroleum Co Process for the production of organolithium compounds
GB945122A (en) * 1961-09-11 1963-12-23 Phillips Petroleum Co Polymerization of monomeric material
US3520858A (en) * 1967-09-06 1970-07-21 Texas Us Chem Co Polymerization process
US6748840B2 (en) * 2002-08-07 2004-06-15 Blount, Inc. Saw chain having drive link with guard feature
US7836808B2 (en) 2006-01-23 2010-11-23 Szymanski David A Safety chain and rotational devices and replaceable teeth therefor

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9840574B2 (en) 2014-05-16 2017-12-12 Kraton Polymers U.S. Llc Branched broad MWD conjugated diene polymer
WO2017150199A1 (en) 2016-02-29 2017-09-08 日本ゼオン株式会社 Method for manufacturing polymer latex
EP3424984B1 (en) 2016-02-29 2023-04-19 Zeon Corporation Method for manufacturing polymer latex

Also Published As

Publication number Publication date
DE1040796B (en) 1958-10-09
FR1206628A (en) 1960-02-10

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