GB876129A - Improvements in or relating to co-polymerisation processes - Google Patents

Improvements in or relating to co-polymerisation processes

Info

Publication number
GB876129A
GB876129A GB13430/60A GB1343060A GB876129A GB 876129 A GB876129 A GB 876129A GB 13430/60 A GB13430/60 A GB 13430/60A GB 1343060 A GB1343060 A GB 1343060A GB 876129 A GB876129 A GB 876129A
Authority
GB
United Kingdom
Prior art keywords
diols
vinyl
diol
trans
acid
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
GB13430/60A
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.)
Rhone Poulenc SA
Original Assignee
Rhone Poulenc SA
Societe des Usines Chimiques Rhone Poulenc SA
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 Rhone Poulenc SA, Societe des Usines Chimiques Rhone Poulenc SA filed Critical Rhone Poulenc SA
Publication of GB876129A publication Critical patent/GB876129A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/52Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
    • C08G63/56Polyesters derived from ester-forming derivatives of polycarboxylic acids or of polyhydroxy compounds other than from esters thereof
    • C08G63/58Cyclic ethers; Cyclic carbonates; Cyclic sulfites ; Cyclic orthoesters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

Polymerization products are prepared by copolymerizing at least one monomer containing a terminal ethylenic group with an ethylenically unsaturated polyester derived at least in part by reaction of an unsaturated aliphatic dicarboxylic acid or anhydride thereof with cyclododeca-5, 9-diene-1, 2-diol, cyclododecane-1, 2- diol or the 1, 2-epoxide of either diol. The polyesters may be derived from maleic, fumaric, itaconic, citraconic, mesaconic or glutaconic acid, optionally together with adipic or phthalic acid and other diols, e.g. ethylene glycol, its homologues, di- and polyethers of such glycols, cycloaliphatic diols, alkylaromatic diols and diphenols. Specified monomers are styrene, a -chlorostyrene, a -methyl styrene, vinyl naphthalene, vinyl acetate, vinyl butyrate, allyl phthalate, allyl succinate, vinyl ethers, vinyl ketones, acrylic esters and nitriles and vinyl pyridine. Polymerization may be effected in the presence of catalysts, e.g. methyl ethyl ketone peroxide and organic salts of metals such as cobalt octanoate or naphthenate and manganese naphthenate. The products may be used in containers for the chemical industry and laminates based on glass fabrics.ALSO:Cyclododeca-5,9-diene-1,2-diols may be prepared by trimerising butadiene to trans-transcis or trans-trans-trans cyclododeca-1,5,9-triene and hydroxylating the products with organic peracids, e.g. a mixture of formic acid and hydrogen peroxide, or by converting the products to the 1,2-epoxides and hydrolysing the epoxides with aqueous sulphuric acid or aqueous-acetone solutions of perchloric acid. The diols may be hydrogenated to cyclododecane-1,2-diol.
GB13430/60A 1959-04-21 1960-04-14 Improvements in or relating to co-polymerisation processes Expired GB876129A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR876129X 1959-04-21

Publications (1)

Publication Number Publication Date
GB876129A true GB876129A (en) 1961-08-30

Family

ID=9360461

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13430/60A Expired GB876129A (en) 1959-04-21 1960-04-14 Improvements in or relating to co-polymerisation processes

Country Status (1)

Country Link
GB (1) GB876129A (en)

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