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GB838007A - Improvements in the production of copolymers from unsaturated polyester resins - Google Patents

Improvements in the production of copolymers from unsaturated polyester resins

Info

Publication number
GB838007A
GB838007A GB1317258A GB1317258A GB838007A GB 838007 A GB838007 A GB 838007A GB 1317258 A GB1317258 A GB 1317258A GB 1317258 A GB1317258 A GB 1317258A GB 838007 A GB838007 A GB 838007A
Authority
GB
United Kingdom
Prior art keywords
ether
glyoxal
alcohol
beta
diureine
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
GB1317258A
Inventor
Herbert Willersinn
Hans Scheuermann
Alfred Woerner
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB838007A publication Critical patent/GB838007A/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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

Ethers of methylol-glyoxal-ureines of the formul <FORM:0838007/IV (b)/1> or <FORM:0838007/IV (b)/2> where R is hydrogen or an aliphatic, cycloaliphatic or aromatic radical, R1 is hydrogen or the radical of a beta, gamma-ethylenically unsaturated alcohol or of a saturated alcohol and R11 is methyl or methylol etherified with a beta, gamma-ethylenically unsaturated alcohol or a saturated, heterocyclic, or aromaticaliphatic alcohol, or an aliphatic, cycloaliphatic, heterocyclic, aromatic or aliphatic aromatic group, are prepared by condensing vicinal dioxo compounds with urea or its derivatives to form the ureines which are reacted with formaldehyde and an alcohol to form the methylol-ether derivative. The desired compounds for use as copolymers (see Group IV (a)) should contain at least two methylol groups etherified with a beta, gamma unsaturated alcohol which may be allyl, methallyl, chlorallyl, crotyl, cyclohexenyl or cyclopentenyl alcohol. Specified compounds are tetraallyl ether of tetramethylol-glyoxal diureine, diallyl ether of dimethylol-glyoxal diureine, trially trimethylol-glyoxal diureine and monobutyldiallyl ether of trimethylol-glyoxal di-ureine.ALSO:Unsaturated polyester resins are copolymerized with a methylol-glyoxal-monoureine which has been etherified with at least 2 mols. of a beta, gamma-ethylenically unsaturated alcohol and, if desired, another copolymerizable monomer. The etherified methylol-glyoxal-monoureines have the formula <FORM:0838007/IV (a)/1> and the diureines the formula <FORM:0838007/IV (a)/2> where R is hydrogen, alkyl, cycloalkyl or aryl, R1 is hydrogen or the radical of a beta, gammaunsaturated alcohol or of a saturated alcohol and R11 is hydrogen, aliphatic, cycloaliphatic, heterocyclic, aromatic or aliphatic-aromatic groups or a beta-gamma ethylenically unsaturated group attached to the nitrogen by an oxymethylene group, provided that at least two of the R11 groups are derived from a beta, gamma unsaturated alcohol. The unsaturated radical may be allyl, methallyl, chlorallyl, crotyl cyclopentenyl or cyclohexenyl. Suitable compounds are tetra-allyl ether of tetramethylol-glyoxal-diureine, diallyl ether of dimethylol-glyoxal-diureine, triallyl ether or monobutyl-diallyl ether of trimethylol-glyoxal-diureine. The polyesters can be formed from ethylene glycol, 1,2- or 1,3-propylene glycol, 2,2-dimethyl-1,3-propanediol, the butylene glycols, 1,6 - hexanediol, 1,8 - octanediol or 1,4 - cyclohexanediol, to which may be added glycerine, trimethylol-propane, pentaerythritol or butanetriol and maleic, fumaric, itaconic, citraconic, aconitic or chlormaleic acid to which may be added up to 70% with reference to unsaturated acid of succinic, glutaric, adipic, pimelic, sebacic, suberic, alpha-methylglutaric, oxadibutyric, sulphone - dibutyric, phthalic, endomethylenetetrahydrophthalic, hexachlorendomethylenetetrahydrophthalic, tetrachlor- or tetrabromphthalic or phenyldibutyric acid. The third, optional, monomer may be styrene, an alkyl or halogenostyrene, divinylbenzene, vinylnaphthalene, vinyl acetate, propionate or succinate, diallyl phthalate or maleate, triallyl phosphate, vinyl methyl ketone, isobutyl vinyl ether, butane-1,4-diol-divinyl ether, glycol diallyl ether, pentaerythritol tetra-allyl ether, ethyl acrylate or methacrylate, glycol dimethacrylate, ethyl alphachloracrylate, acrylo- or methacrylonitrile, acrylamide or methacrylamide, vinyl pyridine, N-vinylcarbazole, N-vinylpyrrolidone, N-vinylcaprolactam, triallyl cyanurate, methyl vinyl sulphone or divinyl sulphone. The polymerizable mixture may contain 5-70% of the ether and 10-70% of the optional monomer. Polymerization may be effected by ultraviolet light or catalysts such as methyl ethyl ketone peroxide, benzoyl peroxide, cyclohexanone peroxide, tertiary butyl hydroperoxide, lauroyl peroxide, azo-bis-isobutyronitrile, azo-bis-isobutyric acid methyl ester or redox systems such as benzoyl peroxide and dimethylaniline or cyclohexanone peroxide and lauryl mercaptan in amounts of 0.5-3%. Temperatures up to 160 DEG C. and pressures up to 10 atmospheres are used. The mixtures can be used to form castings or as lacquers in which latter case metal driers are preferably added e.g. naphthenates, resinates, octoates or linoleates of iron, cobalt, nickel, manganese, chromium, lead, zinc, cerium, aluminium or calcium. Solvents can also be added e.g. toluene, xylene, ethylene glycol monomethyl ether monoacetate, acetone, methyl ethyl ketone, cyclohexanone, methanol, ethanol, propanol, butanol or tetrahydrofuran. A phenol, aminophenol or quinone can also be added in amounts of 0.005-0.1% as inhibitor.
GB1317258A 1957-04-27 1958-04-25 Improvements in the production of copolymers from unsaturated polyester resins Expired GB838007A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB0044429 1957-04-27

Publications (1)

Publication Number Publication Date
GB838007A true GB838007A (en) 1960-06-22

Family

ID=6967326

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1317258A Expired GB838007A (en) 1957-04-27 1958-04-25 Improvements in the production of copolymers from unsaturated polyester resins

Country Status (6)

Country Link
BE (1) BE567009A (en)
CH (1) CH379119A (en)
DE (1) DE1049572B (en)
FR (1) FR1205559A (en)
GB (1) GB838007A (en)
NL (2) NL101648C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3162647A (en) * 1962-07-16 1964-12-22 Sumitomo Chemical Co 4, 5-dialkenyloxy-2-imidazolidinones and method of preparing same

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1156980B (en) * 1960-03-04 1963-11-07 Bayer Ag Process for the production of molded parts or coatings by curing polyester molding compounds
DE1167306B (en) * 1961-01-30 1964-04-09 Saint Gobain Process for the impregnation of fabrics with polymerizable polyesters

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3162647A (en) * 1962-07-16 1964-12-22 Sumitomo Chemical Co 4, 5-dialkenyloxy-2-imidazolidinones and method of preparing same

Also Published As

Publication number Publication date
CH379119A (en) 1964-06-30
BE567009A (en)
DE1049572B (en) 1959-01-29
FR1205559A (en) 1960-02-03
NL101648C (en)
NL227261A (en)

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