GB967552A - Polymerization process - Google Patents

Polymerization process

Info

Publication number
GB967552A
GB967552A GB3677360A GB3677360A GB967552A GB 967552 A GB967552 A GB 967552A GB 3677360 A GB3677360 A GB 3677360A GB 3677360 A GB3677360 A GB 3677360A GB 967552 A GB967552 A GB 967552A
Authority
GB
United Kingdom
Prior art keywords
acrylate
ester
poly
methacrylate
copolymer
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
GB3677360A
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 GB967552A publication Critical patent/GB967552A/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
    • C08F20/16Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F20/18Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • 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

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)

Abstract

Polymerizing at least one ester of acrylic and/or methacrylic acid by forming, at a temperature between -20 DEG and 40 DEG C., a solution of the ester and from 0.2 to 1.5 moles of an organomagnesium compound per mole of ester, mixing the solution with the same or different ester in such an amount as to provide a mixture containing from 0.01 to 0.2 moles of organomagnesium compound per mole of ester, and maintaining the mixture at a temperature between 0 DEG and -100 DEG C. until the polymer is formed. The magnesium compound has preferably the formula RMgY, where R represents an alkyl, cycloalkyl, aralkyl, aryl, alkenyl, aralkenyl, or alkynyl group, and Y is bromine, or R. Exemplified compounds are phenyl magnesium bromide, diphenyl magnesium, and etherates thereof. The solvent for the monomers may be a hydrocarbon or an ether, or mixtures. The Specification mentions many monomers. In the examples the preparation of the following polymers is described polyisopropyl acrylate, polyallyl acrylate, poly 2-ethylhexyl acrylate, polyphenyl methacrylate, polystearyl methacrylate, polybenzyl methacrylate, poly sec-butyl acrylate, polymethyl methacrylate, poly cyclohexyl acrylate, poly tert.-butyl acrylate, polyisobornyl acrylate, a copolymer of cyclohexyl and isobornyl acrylate, a copolymer of isopropyl acrylate and isobornyl acrylate, and a copolymer of isopropyl acrylate and 2-ethyl-hexyl acrylate. The reaction is generally terminated by the addition of methyl alcohol, and the polymer recovered and purified by conventional techniques such as treatment with water, methanol, and hydrochloric acid. Specifications 841,338, 837,227, 884,733 and 967,551 are referred to.
GB3677360A 1959-10-30 1960-10-26 Polymerization process Expired GB967552A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US84976259A 1959-10-30 1959-10-30

Publications (1)

Publication Number Publication Date
GB967552A true GB967552A (en) 1964-08-26

Family

ID=25306461

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3677360A Expired GB967552A (en) 1959-10-30 1960-10-26 Polymerization process

Country Status (6)

Country Link
BE (1) BE596602A (en)
CH (1) CH414168A (en)
DE (1) DE1131017B (en)
FR (1) FR1279307A (en)
GB (1) GB967552A (en)
NL (2) NL257229A (en)

Also Published As

Publication number Publication date
FR1279307A (en) 1961-12-22
CH414168A (en) 1966-05-31
DE1131017B (en) 1962-06-07
BE596602A (en) 1961-05-02
NL257229A (en)
NL122333C (en)

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