GB656138A - Improvements in or relating to high molecular weight polyesters - Google Patents

Improvements in or relating to high molecular weight polyesters

Info

Publication number
GB656138A
GB656138A GB26480/47A GB2648047A GB656138A GB 656138 A GB656138 A GB 656138A GB 26480/47 A GB26480/47 A GB 26480/47A GB 2648047 A GB2648047 A GB 2648047A GB 656138 A GB656138 A GB 656138A
Authority
GB
United Kingdom
Prior art keywords
acid
maleic
esters
acids
fumaric
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
GB26480/47A
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.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid 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 American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB656138A publication Critical patent/GB656138A/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
    • C08G63/16Dicarboxylic acids and dihydroxy compounds
    • C08G63/20Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
    • 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
    • C08G63/60Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
    • 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
    • C08G63/78Preparation processes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

A dihydric alcohol and an alpha beta unsaturated dicarboxylic acid are reacted until a resin having a low acid number not exceeding 50 is produced, about 0.5 to 2.0 per cent of an acid, an hydroxy acid or an alcohol with a total of at least 3 hydroxyl and carboxyl groups and no CH2=C= groups is added and the reaction continued until a polyester of high molecular weight is obtained. It may be copolymerized with a compatible polymerizable substance having a CH2=C group, a boiling-point of at least 60 DEG C., and no conjugated double bonds. The dihydric alcohols are preferably those containing only primary hydroxyl groups, e.g. the glycols. The alpha beta unsaturated acids include maleic, fumaric, itaconic, citraconic, mesaconic, halogenated maleic and may in part be substituted by acrylic, beta-benzoyl acrylic, methacrylic, cinnamic, and crotonic acids. The compound with at least 3 carboxyl and hydroxyl groups may be any such alcohol, acid or hydroxy acid as pentaerythritol, glycerol, pentaglycerol, sorbitol, mannitol, trimethylol benzene; citric, malic, dihydroxystearic, tartaric, trihydroxyglutaric, methylol phthalic, or benzene tricarboxylic, fumaric or maleic acid or adducts of higher fatty acids with a conjugated double bond such as linseed fatty acids. The compatible polymerizable substance may be styrene or a styrene derivative, an isopropenyl toluene or benzene, styrene with nuclear-substituted fluorine, bromine or chlorine, vinyl-naphthalene, -mesitylene, -diphenyl, -carbazole, -phenol, or -furane, dialkyl esters of maleic, fumaric and itaconic acid, diallyl esters of high boiling-point various specified allyl esters and compounds, acrylic and methacrylic acids, methyl methacrylate, methyl acrylate and ether esters. Polymerization catalysts such as various specified peroxides may be employed in the copolymerization and polymerization inhibitors may be used during the preparation of the preliminary alkyd resin or during copolymerization. An inert solvent such as xylol or toluene may be included in the reaction mixture to remove water of esterification and thus reduce esterification temperature. Eight examples are given in seven of which a saturated aliphatic dibasic acid and in the other phthalic anhydride, is included in the reacting mixture in higher molecular proportion than the unsaturated acid. Samples have been furnished under Sect. 2 (5) of polyesters in which the reacting mixture (1) does not include such a saturated acid; (2) includes phthalic anhydride in lesser molecular proportion.
GB26480/47A 1946-10-02 1947-10-01 Improvements in or relating to high molecular weight polyesters Expired GB656138A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US656138XA 1946-10-02 1946-10-02

Publications (1)

Publication Number Publication Date
GB656138A true GB656138A (en) 1951-08-15

Family

ID=22063921

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26480/47A Expired GB656138A (en) 1946-10-02 1947-10-01 Improvements in or relating to high molecular weight polyesters

Country Status (1)

Country Link
GB (1) GB656138A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3044978A (en) * 1958-05-21 1962-07-17 Herberts & Co Gmbh Dr Kurt New addition polymers from monomeric vinyl compounds and unsaturated cross-linked polyester resins and a process for preparing the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3044978A (en) * 1958-05-21 1962-07-17 Herberts & Co Gmbh Dr Kurt New addition polymers from monomeric vinyl compounds and unsaturated cross-linked polyester resins and a process for preparing the same

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