GB884706A - Polymerization with organo aluminum compounds - Google Patents

Polymerization with organo aluminum compounds

Info

Publication number
GB884706A
GB884706A GB10241/58A GB1024158A GB884706A GB 884706 A GB884706 A GB 884706A GB 10241/58 A GB10241/58 A GB 10241/58A GB 1024158 A GB1024158 A GB 1024158A GB 884706 A GB884706 A GB 884706A
Authority
GB
United Kingdom
Prior art keywords
polymerization
butyl
esters
reaction
cycloalkyl
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
GB10241/58A
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.)
Rohm and Haas Co
Original Assignee
Rohm and Haas 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 Rohm and Haas Co filed Critical Rohm and Haas Co
Publication of GB884706A publication Critical patent/GB884706A/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
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/10Esters
    • C08F20/12Esters of monohydric alcohols or phenols

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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polymerization Catalysts (AREA)

Abstract

Esters of acrylic and methacrylic acids are polymerized with the aid, as a catalyst, of an organo aluminium compound of the formula <FORM:0884706/IV (a)/1> where R, R11 and R111 represent hydrocarbon groups, although one R may represent hydrogen, the polymerization being carried out in the substantial absence of water, oxygen, or any other substance which would interfere with the reaction. Polymerization may be carried out in bulk or in solution in an inert solvent such as benzene, toluene, xylene, naphtha or diethyl or dibutyl ether. Organo aluminium compounds specified are those in which the hydrocarbon groups are alkyl, cycloalkyl, aralkyl or aryl groups, e.g. trimethyl, triethyl, tripropyl, triisopropyl, tributyl, tricyclohexyl, triphenyl, tritolyl, trinaphthyl and tribenzyl aluminiums, and diethyl, diisopropyl and diphenyl aluminium hydrides. Preferred polymerizable esters are those of the formula CH2 = C(R)COOR DEG where R is hydrogen and R DEG is an alkyl, alkenyl, cycloalkyl, phenyl or aralkyl group, e.g. methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, octyl, 2-ethylhexyl, 3,5,5-trimethylhexyl, dodecyl, tetradecyl, hexadecyl, octadecyl, cyclopentyl, cyclohexyl, methlcyclohexyl, phenyl, benzyl, methyl benzyl, allyl, pentenyl, undecenyl and oleyl groups. The process may be employed to homopolymerize the above esters or to copolymerize them with one another. At the end of the reaction, and before the destruction of catalyst, the tendency for the polymer to cross-link on exposure to oxygen may be overcome by treating the reaction product with a compound having a reactive hydrogen atom, e.g. a C1-C4 alkanol, a methanolic solution of hydrochloric or acetic acid, an ethanolic solution of acetic acid, a nitroparaffin, a malonic ester or an acetoacetic ester.
GB10241/58A 1957-04-11 1958-03-31 Polymerization with organo aluminum compounds Expired GB884706A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US884706XA 1957-04-11 1957-04-11

Publications (1)

Publication Number Publication Date
GB884706A true GB884706A (en) 1961-12-13

Family

ID=22211568

Family Applications (1)

Application Number Title Priority Date Filing Date
GB10241/58A Expired GB884706A (en) 1957-04-11 1958-03-31 Polymerization with organo aluminum compounds

Country Status (4)

Country Link
BE (1) BE566622A (en)
DE (1) DE1067218B (en)
FR (1) FR1212059A (en)
GB (1) GB884706A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3172868A (en) * 1965-03-09 Process for forming a z-hydroxyethyl methacrylate foam
US3293198A (en) * 1963-11-20 1966-12-20 Grace W R & Co Foamed products and process therefor

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB883973A (en) * 1958-10-06 1961-12-06 American Cyanamid Co Method of producing pigmented paper
US3019157A (en) * 1958-10-06 1962-01-30 American Cyanamid Co Web-forming fibrous suspensions of improved freeness
FR1357679A (en) * 1963-02-13 1964-04-10 Saint Gobain Process for the preparation of polymers and copolymers of phenylacrylic acid esters

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3172868A (en) * 1965-03-09 Process for forming a z-hydroxyethyl methacrylate foam
US3293198A (en) * 1963-11-20 1966-12-20 Grace W R & Co Foamed products and process therefor

Also Published As

Publication number Publication date
FR1212059A (en) 1960-03-22
DE1067218B (en) 1959-10-15
BE566622A (en)

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