GB581170A - Copolymers - Google Patents

Copolymers

Info

Publication number
GB581170A
GB581170A GB436342A GB436342A GB581170A GB 581170 A GB581170 A GB 581170A GB 436342 A GB436342 A GB 436342A GB 436342 A GB436342 A GB 436342A GB 581170 A GB581170 A GB 581170A
Authority
GB
United Kingdom
Prior art keywords
fusible
methyl
polymers
ethyl
polymer
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
GB436342A
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.)
PPG Industries Inc
Original Assignee
Pittsburgh Plate Glass 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 Pittsburgh Plate Glass Co filed Critical Pittsburgh Plate Glass Co
Priority to GB436342A priority Critical patent/GB581170A/en
Publication of GB581170A publication Critical patent/GB581170A/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
    • C08F36/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F36/02Homopolymers and copolymers 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
    • C08F36/20Homopolymers and copolymers 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 unconjugated

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

An infusible and insoluble polymer is prepared by polymerizing a mixture of a fusible heat-convertible polymer of an organic oxygen compound containing at least two polymerizable groups and another compound containing at least one of said groups. The fusible polymers may be prepared as described in Specifications 536,807, 540,938 and 540,939. In addition, the polymers made from mono or diisopropenyl carbonate, phthalate, crotonate, maleate, acrylate, malonate or oxalate may be used. Further, the fusible polymer may be prepared as described in Specifications 578,266 and 578,267. The other compound may be vinyl acetate, vinyl chloride, acrylic or a -substituted acrylic acids, methyl, ethyl, propyl, butyl, amyl and lauryl acrylates, methacrylates ethacrylates or a -chloro-acrylates glycol and glycerol monoacrylates or monomethacrylates, glycerol monochloroacrylate, resorcinol monomethacrylate; allyl or crotyl acetate, chloride, benzoate and alcohol; methallyl chloride, acetate, butyrate and benzoate; styrene, vinyl ethyl ether, ethyl allyl ether; methyl, ethyl, propyl, butyl or amyl crotonates, chlorocrotonates, cinnamates or tiglates, methyl, ethyl, propyl or butyl maleates or fumarates; monomethylallyl, monoallyl or monocrotyl phthalates, citrates, tartrates, silicates, adipates, glutarates, lactates, glycollates, suberates, succinates, phosphates, phosphites, sulphates, sulphites or sulphides; butadiene and chlorobutadiene. Mixtures of fusible, heat-convertible polymers, or such polymers incorporated in a monomer capable of forming such polymers may be further polymerized. Preferably, the composition resulting from the polymerization of monomer is concentrated to increase the proportion of fusible polymer relative to monomer. The further polymerization may be catalysed by oxygen, ozone or peroxides under heat, light or pressure. The catalyst may be formed in situ by oxidizing the monomer or polymer by passing air or oxygen through their solutions. In a typical example, a solution of allyl methacrylate and benzoyl peroxide in acetone was refluxed at 63 DEG C. for three hours. Methyl alcohol was added and the mixture added, with stirring, to a methyl alcohol-water mixture. The precipitate of fusible polyallyl methacrylate was mixed with methyl methyacrylate and benzoyl peroxide and heated in a mould at 65 DEG C. for 17 hours. The product was further heated at 100 DEG C. for eight hours to produce an insoluble material.
GB436342A 1942-04-01 1942-04-01 Copolymers Expired GB581170A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB436342A GB581170A (en) 1942-04-01 1942-04-01 Copolymers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB436342A GB581170A (en) 1942-04-01 1942-04-01 Copolymers

Publications (1)

Publication Number Publication Date
GB581170A true GB581170A (en) 1946-10-03

Family

ID=9775756

Family Applications (1)

Application Number Title Priority Date Filing Date
GB436342A Expired GB581170A (en) 1942-04-01 1942-04-01 Copolymers

Country Status (1)

Country Link
GB (1) GB581170A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2615864A (en) * 1947-06-21 1952-10-28 Socony Vacuum Oil Co Inc Esterified allyl ester-polycarboxylic acid copolymers
US5070140A (en) * 1989-12-22 1991-12-03 Basf Corporation Copolymers of vinyl acetate and allyl glycidyl ether capped C12 -C.sub.
US5480954A (en) * 1994-09-21 1996-01-02 Arco Chemical Technology, L.P. Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols
US5605995A (en) * 1994-09-21 1997-02-25 Arco Chemical Technology, L.P. Hydroxy-functional allyl terpolymers

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2615864A (en) * 1947-06-21 1952-10-28 Socony Vacuum Oil Co Inc Esterified allyl ester-polycarboxylic acid copolymers
US5070140A (en) * 1989-12-22 1991-12-03 Basf Corporation Copolymers of vinyl acetate and allyl glycidyl ether capped C12 -C.sub.
US5480954A (en) * 1994-09-21 1996-01-02 Arco Chemical Technology, L.P. Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols
US5519103A (en) * 1994-09-21 1996-05-21 Arco Chemical Company Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols
US5569714A (en) * 1994-09-21 1996-10-29 Arco Chemical Technology, L.P. Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols
US5605995A (en) * 1994-09-21 1997-02-25 Arco Chemical Technology, L.P. Hydroxy-functional allyl terpolymers
US5639827A (en) * 1994-09-21 1997-06-17 Arco Chemical Technology, L.P. Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols

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