GB1096569A - Copolymerisation process - Google Patents

Copolymerisation process

Info

Publication number
GB1096569A
GB1096569A GB5304965A GB5304965A GB1096569A GB 1096569 A GB1096569 A GB 1096569A GB 5304965 A GB5304965 A GB 5304965A GB 5304965 A GB5304965 A GB 5304965A GB 1096569 A GB1096569 A GB 1096569A
Authority
GB
United Kingdom
Prior art keywords
vinyl
preferred
vinyl ether
water
sodium
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
GB5304965A
Inventor
Keith Julian
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB5304965A priority Critical patent/GB1096569A/en
Publication of GB1096569A publication Critical patent/GB1096569A/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
    • C08F218/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
    • C08F218/02Esters of monocarboxylic acids
    • C08F218/04Vinyl esters
    • 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
    • C08F16/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
    • C08F16/12Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical

Abstract

An emulsion of a copolymer of a vinyl ester and a vinyl ether is prepared by continuously introducing the vinyl ester, the vinyl ether and a polymerization initiator to an agitated solution comprising water, and a protective colloid and/or a surface-active agent, the introduction of the vinyl ether being begun after that of the vinyl ester and the pH of the solution being maintained at a value of at least 4. Preferred surface-active agents are sodium lauryl sulphate, sodium dodecylobenzene sulphonate, sodium dioctylsulphosuccinate, cetyl pyridinium bromide and a condensation product of ethylene and/or propylene oxide either alone or with an alcohol or phenol Preferred protective colloids are gum acacia, starch or a modified starch, dextrin, a water-soluble salt of a polyacrylic acid, a hydroxy alkyl cellulose and a polyvinyl alcohol containing 10 to 30% by weight of residual acetate groups. Preferred vinyl esters are vinyl esters of aliphatic carboxylic acids containing up to 20 carbon atoms, particularly vinyl acetate and vinyl propionate, and vinyl chloride. Preferred vinyl ethers, are alkyl vinyl ethers in which the alkyl group contains up to 20 carbon atoms particularly methyl vinyl ether and isobutyl vinyl ethers. The pH may be maintained at the desired figure by the addition of a buffer salt, particularly an alkali metal phosphate, borate or carbonate, or alkali. The preferred initiator is a water soluble peroxide or persalt e.g. potassium persulphate.
GB5304965A 1965-12-14 1965-12-14 Copolymerisation process Expired GB1096569A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB5304965A GB1096569A (en) 1965-12-14 1965-12-14 Copolymerisation process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB5304965A GB1096569A (en) 1965-12-14 1965-12-14 Copolymerisation process

Publications (1)

Publication Number Publication Date
GB1096569A true GB1096569A (en) 1967-12-29

Family

ID=10466433

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5304965A Expired GB1096569A (en) 1965-12-14 1965-12-14 Copolymerisation process

Country Status (1)

Country Link
GB (1) GB1096569A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0682045A2 (en) * 1994-05-09 1995-11-15 Rohm And Haas Company Method for making a polymer
US6826331B2 (en) 2001-09-28 2004-11-30 Bookham Technology Plc Method of extracting spectral parameters of channels from non-channelized light

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0682045A2 (en) * 1994-05-09 1995-11-15 Rohm And Haas Company Method for making a polymer
EP0682045A3 (en) * 1994-05-09 1995-11-29 Rohm And Haas Company Method for making a polymer
US5652293A (en) * 1994-05-09 1997-07-29 Rohm And Haas Company Method for making an aqueous emulsion polymer
US6826331B2 (en) 2001-09-28 2004-11-30 Bookham Technology Plc Method of extracting spectral parameters of channels from non-channelized light

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