GB835752A - Diolefine polymers and process for preparing same - Google Patents

Diolefine polymers and process for preparing same

Info

Publication number
GB835752A
GB835752A GB21374/56A GB2137456A GB835752A GB 835752 A GB835752 A GB 835752A GB 21374/56 A GB21374/56 A GB 21374/56A GB 2137456 A GB2137456 A GB 2137456A GB 835752 A GB835752 A GB 835752A
Authority
GB
United Kingdom
Prior art keywords
compound
group
metal
polymers
transition metal
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
GB21374/56A
Inventor
Natta Giulio
Porri Lido
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.)
Montedison SpA
Original Assignee
Montedison SpA
Montecatini Societa Generale per lIndustria Mineraria e Chimica SpA
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 Montedison SpA, Montecatini Societa Generale per lIndustria Mineraria e Chimica SpA filed Critical Montedison SpA
Publication of GB835752A publication Critical patent/GB835752A/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
    • C08F136/06Butadiene

Abstract

Diolefines are polymerized in the presence of a catalyst obtained by reacting an organometallic compound of a metal of Group I, II or III of the Periodic Table with a compound of a transition metal of Group IV, V or VI in which the metal is bound to an organic radical through an oxygen atom. The first compound is preferably triethyl aluminium, the second an alkoxide or acetylacetonate of titanium, vanadium, chromium or molybdenum which is preferably soluble in any solvent present. The two components may be dissolved separately in a hydrocarbon and then mixed. Specifications 810,023 and 834,554 are referred to.ALSO:Linear polymers are prepared from conjugated diolefins having at least one vinyl group by polymerizing in the presence of a catalyst obtained by reacting an organo-metallic compound of a metal of Group I, II or III of the Periodic Table with a compound of a transition metal of Group IV, V or VI in which the metal is bound to an organic radical through an oxygen atom. The transition metal compound is preferably soluble in any solvent present and may be an alkoxide or acetyl-acetonate of titanium, chromium, vanadium or molybdenum. The organo-metallic compound may be triethyl aluminium. The polymerization is preferably carried out in a hydrocarbon solvent and the catalyst is prepared by suspending or dissolving the two components in separate portions of the hydrocarbon and then mixing. The monomer may be added to the suspension or solution of the organo-metallic compound before adding the transition metal compound or may be added to the composite catalyst. Temperatures of -80 DEG to 150 DEG C. may be used. Monomers include butadiene and isoprene. Butadiene yields a mixture of an amorphous and a crystalline polymer which may be separated by dissolving the latter in solvents such as acetone, ether, heptane and toluene. The butadiene polymer has 1,2-enchainment and the isoprene polymer, which is amorphous, 3,4-enchainment. The polymers may be vulcanized. The crystalline polymers can be extruded into filaments and moulded or calendered at temperatures slightly below the melting temperature to obtain sheets with a plane orientation. Oriented films can be obtained by cold-drawing in two directions unoriented sheets obtained by moulding or calendering at above the melting temperature. The amorphous polymers are elastomeric. Specifications 810,023 and 834,554 are referred to.
GB21374/56A 1955-07-15 1956-07-10 Diolefine polymers and process for preparing same Expired GB835752A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT538453 1955-07-15

Publications (1)

Publication Number Publication Date
GB835752A true GB835752A (en) 1960-05-25

Family

ID=11120197

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21374/56A Expired GB835752A (en) 1955-07-15 1956-07-10 Diolefine polymers and process for preparing same

Country Status (8)

Country Link
BE (1) BE549554A (en)
CH (1) CH370245A (en)
DE (1) DE1420558A1 (en)
FR (1) FR1154938A (en)
GB (1) GB835752A (en)
IT (1) IT538453A (en)
LU (1) LU34508A1 (en)
NL (1) NL110776C (en)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4148983A (en) 1978-04-05 1979-04-10 The Goodyear Tire & Rubber Company Polymerization and copolymerization of trans-piperylene and isoprene
US6977281B1 (en) 1999-11-12 2005-12-20 Bridgestone Corporation Modified polymers prepared with lanthanide-based catalysts
US6992147B1 (en) 1999-11-12 2006-01-31 Bridgestone Corporation Modified polymers prepared with lanthanide-based catalysts
US7642322B2 (en) 2000-11-10 2010-01-05 Bridgestone Corporation Functionalized high cis-1,4-polybutadiene prepared using novel functionalizing agents
US7671138B2 (en) 2006-05-26 2010-03-02 Bridgestone Corporation Polymers functionized with hydrobenzamides
US7732534B2 (en) 2006-08-28 2010-06-08 Bridgestone Corporation Polymers functionalized with nitro compounds
US7879952B2 (en) 2005-12-28 2011-02-01 Bridgestone Corporation Functionalized polymers
US7906592B2 (en) 2008-07-03 2011-03-15 Bridgestone Corporation Polymers functionalized with imide compounds containing a protected amino group
US8088868B2 (en) 2006-12-19 2012-01-03 Bridgestone Corporation Polymers functionalized with protected oxime compounds
US8188195B2 (en) 2008-12-31 2012-05-29 Bridgestone Corporation Polymers functionalized with nitroso compounds
US8188201B2 (en) 2007-12-31 2012-05-29 Bridgestone Corporation Bulk polymerization process for producing polydienes
US8268933B2 (en) 2007-12-31 2012-09-18 Bridgestone Corporation Polymers functionalized with polyimine compounds
US8338544B2 (en) 2009-12-21 2012-12-25 Bridgestone Corporation Polymers functionalized with polyoxime compounds and methods for their manufacture
US8344066B2 (en) 2009-01-23 2013-01-01 Bridgestone Corporation Polymers functionalized with nitrile compounds containing a protected amino group
US8748531B2 (en) 2010-12-10 2014-06-10 Bridgestone Corporation Polymers functionalized with oxime compounds containing an acyl group
US8785566B2 (en) 2009-01-23 2014-07-22 Bridgestone Corporation Polymers functionalized with polycyano compounds
US8962766B2 (en) 2011-09-15 2015-02-24 Bridgestone Corporation Polymers functionalized with polyhydrazone compounds

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3232920A (en) * 1958-03-06 1966-02-01 Phillips Petroleum Co Preparation of rubbery polymers of butadiene
DE1106962B (en) * 1958-07-16 1961-05-18 Stamicarbon Process for polymerizing diolefins
NL272366A (en) * 1961-03-13
US3823121A (en) * 1972-11-09 1974-07-09 Goodyear Tire & Rubber Polymerization process
MXPA01011985A (en) * 1999-06-09 2002-08-12 Bridgestone Corp Molybdenum-based catalyst composition for polymerizing conjugated dienes.

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4148983A (en) 1978-04-05 1979-04-10 The Goodyear Tire & Rubber Company Polymerization and copolymerization of trans-piperylene and isoprene
US6977281B1 (en) 1999-11-12 2005-12-20 Bridgestone Corporation Modified polymers prepared with lanthanide-based catalysts
US6992147B1 (en) 1999-11-12 2006-01-31 Bridgestone Corporation Modified polymers prepared with lanthanide-based catalysts
US7671136B2 (en) 1999-11-12 2010-03-02 Bridgestone Corporation Modified polymers prepared with lanthanide-based catalysts
US7750087B2 (en) 1999-11-12 2010-07-06 Bridgestone Corporation Modified polymers prepared with lanthanide-based catalysts
US7642322B2 (en) 2000-11-10 2010-01-05 Bridgestone Corporation Functionalized high cis-1,4-polybutadiene prepared using novel functionalizing agents
US9644052B2 (en) 2000-11-10 2017-05-09 Bridgestone Corporation Functionalized high cis-1,4-polybutadiene prepared using novel functionalizing agents
US8362126B2 (en) 2000-11-10 2013-01-29 Yoichi Ozawa Functionalized high cis-1,4-polybutadiene prepared using novel functionalizing agents
US7879952B2 (en) 2005-12-28 2011-02-01 Bridgestone Corporation Functionalized polymers
US7671138B2 (en) 2006-05-26 2010-03-02 Bridgestone Corporation Polymers functionized with hydrobenzamides
US7732534B2 (en) 2006-08-28 2010-06-08 Bridgestone Corporation Polymers functionalized with nitro compounds
US8088868B2 (en) 2006-12-19 2012-01-03 Bridgestone Corporation Polymers functionalized with protected oxime compounds
US8188201B2 (en) 2007-12-31 2012-05-29 Bridgestone Corporation Bulk polymerization process for producing polydienes
US8268933B2 (en) 2007-12-31 2012-09-18 Bridgestone Corporation Polymers functionalized with polyimine compounds
US8426609B2 (en) 2008-07-03 2013-04-23 Bridgestone Corporation Polymers functionalized with imide compounds containing a protected amino group
US7906592B2 (en) 2008-07-03 2011-03-15 Bridgestone Corporation Polymers functionalized with imide compounds containing a protected amino group
US9127100B2 (en) 2008-12-31 2015-09-08 Bridgestone Corporation Polymers functionalized with nitroso compounds
US8188195B2 (en) 2008-12-31 2012-05-29 Bridgestone Corporation Polymers functionalized with nitroso compounds
US9670299B2 (en) 2008-12-31 2017-06-06 Bridgestone Corporation Polymers functionalized with nitroso compounds
US8735494B2 (en) 2009-01-23 2014-05-27 Bridgestone Corporation Polymers functionalized with nitrile compounds containing a protected amino group
US8785566B2 (en) 2009-01-23 2014-07-22 Bridgestone Corporation Polymers functionalized with polycyano compounds
US8344066B2 (en) 2009-01-23 2013-01-01 Bridgestone Corporation Polymers functionalized with nitrile compounds containing a protected amino group
US9447213B2 (en) 2009-01-23 2016-09-20 Bridgestone Corporation Polymers functionalized with polycyano compounds
US10081688B2 (en) 2009-01-23 2018-09-25 Bridgestone Corporation Polymers functionalized with polycyano compounds
US8338544B2 (en) 2009-12-21 2012-12-25 Bridgestone Corporation Polymers functionalized with polyoxime compounds and methods for their manufacture
US8748531B2 (en) 2010-12-10 2014-06-10 Bridgestone Corporation Polymers functionalized with oxime compounds containing an acyl group
US8962766B2 (en) 2011-09-15 2015-02-24 Bridgestone Corporation Polymers functionalized with polyhydrazone compounds

Also Published As

Publication number Publication date
CH370245A (en) 1963-06-30
IT538453A (en) 1900-01-01
BE549554A (en) 1957-01-14
NL110776C (en) 1965-03-15
LU34508A1 (en) 1958-01-13
DE1420558A1 (en) 1968-10-24
FR1154938A (en) 1958-04-18

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