GB622235A - Alkyd copolymers - Google Patents

Alkyd copolymers

Info

Publication number
GB622235A
GB622235A GB24415/46A GB2441546A GB622235A GB 622235 A GB622235 A GB 622235A GB 24415/46 A GB24415/46 A GB 24415/46A GB 2441546 A GB2441546 A GB 2441546A GB 622235 A GB622235 A GB 622235A
Authority
GB
United Kingdom
Prior art keywords
allyl
peroxide
glycol
alcohol
acids
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
GB24415/46A
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.)
Wingfoot Corp
Original Assignee
Wingfoot Corp
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 Wingfoot Corp filed Critical Wingfoot Corp
Publication of GB622235A publication Critical patent/GB622235A/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
    • C08F283/00Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/01Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters

Abstract

Low pressure laminating compositions are prepared by copolymerizing, e.g. by heating, preferably in the presence of a catalyst, up to 150 DEG C., an unsaturated alkyd resin with an ester of carbamic acid or an N-alkyl derivative thereof and an alcohol having a double bond between the second and third carbon atoms from the hydroxyl group. The alkyd resins are those obtained by condensing a polyhydric alcohol, e.g. ethylene glycol, diethylene glycol, triethylene glycol, tetramethylene glycol, pentaerythritol, glycerine, trimethylene glycol, thiodiglycol, monoethylin, and 1,2-propylene glycol, with a polycarboxylic acid, e.g. maleic, acetylene dicarboxylic, fumaric, mesaconic, itaconic, aconitic, monochloromaleic, monochlorofumaric, citraconic, alpha-methyl itaconic and alpha-ethyl itaconic acids or their anhydrides, partly replaced by a non-ethylenic polycarboxylic acid, e.g. succinic, phthalic, benzoylphthalic, adipic, sebacic, suberic, and pimelic, up to 75 mol. per cent. Modifiers may be included, e.g. monohydric alcohols such as propyl, isopropyl, butyl, isobutyl, amyl, isoamyl, allyl, methallyl, crotyl alcohols, monocarboxylic acids such as acetic, propionic, butyric, benzoic, acrylic, methacrylic acids and drying or semi-drying oils, e.g. tung, soya, castor and linseed. The carbamates have the general formula RR1NCO2R11, R and R1 being H or alkyl and R11 being the residue of the unsaturated alcohol, e.g. allyl, 3-chloro-allyl, methallyl, crotyl, a -ethyl allyl, b -ethyl allyl, 2-chloro-allyl, tiglyl or b -propyl-allyl alcohol. Catalysts for the copolymerization are benzoyl peroxide, hydrogen peroxide, ammonium persulphate, sodium perborate, barium peroxide, sodium peroxide, acetyl peroxide, lauroyl peroxide or stearyl peroxide. In the example, diethylene glycol and maleic anhydride were condensed to an alkyd resin which was mixed with allyl carbamate containing dissolved benzoyl peroxide. A multi-ply structure of glass cloth was impregnated with the mixture, was enveloped in "Cellophane" (Registered Trade Mark), pressed between glass sheets and heated to 80 DEG C. The mixture was also polymerized in a mould to form a clear sheet. The products are insoluble in common organic solvents and resistant to acids and alkalis. The mixture to be polymerized may include fillers, e.g. carbon black, textile flocs, e.g. cotton, rayon, silk, nylon, wool, or hemp, dyes, plasticizers, pigments and resins.
GB24415/46A 1946-03-05 1946-08-16 Alkyd copolymers Expired GB622235A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US622235XA 1946-03-05 1946-03-05

Publications (1)

Publication Number Publication Date
GB622235A true GB622235A (en) 1949-04-28

Family

ID=22041013

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24415/46A Expired GB622235A (en) 1946-03-05 1946-08-16 Alkyd copolymers

Country Status (1)

Country Link
GB (1) GB622235A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2813086A (en) * 1954-05-04 1957-11-12 Hooker Electrochemical Co Sulfur-containing crosslinked polyester elastomers
US2981713A (en) * 1957-10-28 1961-04-25 Fairbanks Company Polyester molding composition
US3227778A (en) * 1960-03-30 1966-01-04 Reichhold Chemicals Inc Hardened shaped articles and method of making the same
US6464257B1 (en) 1997-04-10 2002-10-15 Senior Investments Ag Vibration decoupler apparatus

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2813086A (en) * 1954-05-04 1957-11-12 Hooker Electrochemical Co Sulfur-containing crosslinked polyester elastomers
US2981713A (en) * 1957-10-28 1961-04-25 Fairbanks Company Polyester molding composition
US3227778A (en) * 1960-03-30 1966-01-04 Reichhold Chemicals Inc Hardened shaped articles and method of making the same
US6464257B1 (en) 1997-04-10 2002-10-15 Senior Investments Ag Vibration decoupler apparatus

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