GB848400A - Copolymers of unsaturated polyester resins and process for the production thereof - Google Patents

Copolymers of unsaturated polyester resins and process for the production thereof

Info

Publication number
GB848400A
GB848400A GB18537/59A GB1853759A GB848400A GB 848400 A GB848400 A GB 848400A GB 18537/59 A GB18537/59 A GB 18537/59A GB 1853759 A GB1853759 A GB 1853759A GB 848400 A GB848400 A GB 848400A
Authority
GB
United Kingdom
Prior art keywords
acid
vinyl
ether
unsaturated
alcohol
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
GB18537/59A
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 GB848400A publication Critical patent/GB848400A/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
    • C08F16/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
    • C08F16/12Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
    • C08F16/14Monomers containing only one unsaturated aliphatic radical
    • C08F16/28Monomers containing nitrogen
    • 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
    • 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
    • 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
    • C08G63/68Polyesters containing atoms other than carbon, hydrogen and oxygen
    • C08G63/685Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen
    • C08G63/6854Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/6858Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D4/00Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

A hard glossy copolymer is obtained by copolymerising through unsaturated ethylenic linkages a homogenous mixture of (A) an unsaturated polyester resin of an alpha-betaunsaturated polycarboxylic acid and a saturated polyhydric alcohol and (B) a solvent-soluble condensation product of an ether from a beta gamma-ethylenically unsaturated alcohol and a methylol glyoxal diureine, with itself or with a compound containing at least, and preferably two reactive groups which are hydroxy and/or carboxy groups, the condensation product containing at least, and preferably two diureine units per molecule and having at least two beta gamma ethylenically unsaturated ether groups per diureine unit. The preferred initial materials prior to their polycondensation with each other or with a minor proportion of saturated polyhydroxy or polycarboxy compounds have the formula : <FORM:0848400/IV(a)/1> where R is hydrogen, lower alkyl, cycloalkyl or phenyl radical and R1 is the hydrocarbon residue of a beta gamma ethylenically unsaturated monohydric alcohol. The nitrogen atom of the diureine is attached to the methylene group, this with the oxygen, and this in term with the radical of the beta gamma unsaturated alcohol remaining after etherification by splitting off water between the hydroxyl group of the beta-gamma unsaturated alcohol and the hydroxyl group of the methylol group. Suitable radicals of the betagamma unsaturated alcohol are allyl, methallyl, crotyl, cyclohexenyl or cyclopentenyl radicals. Condensation may be effected between 40 and 180 DEG C using as catalyst, hydrochloric acid, nitric acid, phosphoric acid, sulphuric acid, sulphurous acid, para-toluene sulphonic acid, phthalic acid, formic acid, oxalic acid, acetic acid, chlorinated acetic acid, sodium hydrogen sulphate, primary sodium phosphate, ammonium nitrate or ammonium phosphate. The polymerisable mixture of unsaturated polyester resin and condensation products from beta gamma unsaturated ethers of methylol duireines may be copolymerised with styrene, alkyl styrene, halogen styrenes, divinyl benzenes, vinyl naphthalene, vinyl pyridine, N-vinyl carbazole, vinyl methyl ketone, methyl vinyl sulphone, divinyl sulphone, vinyl acetate, vinyl propionate, succinic acid, divinyl ester, N-vinyl pyrrolidone, N-vinyl captrolactam, isobutyl vinyl ether, butane diol- 1,4-divinyl ether, ethyl acrylate, methyl methacrylate, glycol dimethacrylate, ethyl alpha-chloroacrylate, acrylonitrile, methacrylonitrile, acrylamide, methacrylamide, diallyl phthalate, diallyl maleate, triallyl cyanurate, triallyl phosphate, glycol diallyl ether or pentacrythritol tetra allyl ether. Polymerisatio may be effected by the action of ultra violet light, or in the presence of a catalyst such as methyl ethyl ketone peroxide, cyclohexanone peroxide, cumene hydroperoxide, tertiary butyl hydroperoxide, tertiary-butyl permaleates, ditertiary butyl peroxide, azo-bisisobutyronitrile, azo-bis-isobutyric acid, dibutyl ester or redox systems containing one of the peroxides and a tertiary amine such as dimethylaniline, diethylaniline or dodecylmercaptan. Metal driers such as naphthenates, octoates, or, linoleates of iron, cobalt, nickel, manganese, chromium, lead, zinc, cerium, aluminium or calcium may be added and also polymerisation inhibitors such as monohydric or polyhydric phenols such as hydroquinone, resorcinol, pyrocatechol, 2,6-ditertiary-butyl para cresols, or phenylnaphthylamine. In examples, the tetra-allyl ether of tetramethylol glyoxal diureine is condensed with succinic acid or allyl alcohol and then reacted with the unsaturated polyester resin derived from maleic acid and propylene glycol or from maleic acid, 2,2-dimethyl-1,3 and is then copolymerised with styrene. The product is a hard tack free polymer and may be moulded to form carriage bodies and boat hulls.
GB18537/59A 1958-05-31 1959-06-01 Copolymers of unsaturated polyester resins and process for the production thereof Expired GB848400A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE848400X 1958-05-31
DEB49774A DE1081222B (en) 1958-05-31 1958-07-29 Process for the production of polymerisation products based on unsaturated polyester resin compositions

Publications (1)

Publication Number Publication Date
GB848400A true GB848400A (en) 1960-09-14

Family

ID=25950180

Family Applications (2)

Application Number Title Priority Date Filing Date
GB18537/59A Expired GB848400A (en) 1958-05-31 1959-06-01 Copolymers of unsaturated polyester resins and process for the production thereof
GB25823/59A Expired GB887957A (en) 1958-05-31 1959-07-28 Condensation products and polymerizable compositions

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB25823/59A Expired GB887957A (en) 1958-05-31 1959-07-28 Condensation products and polymerizable compositions

Country Status (3)

Country Link
DE (2) DE1081222B (en)
FR (1) FR1226144A (en)
GB (2) GB848400A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3711746A (en) * 1971-06-16 1973-01-16 Maxwell Lab High voltage energy storage capacitor
US5180835A (en) * 1991-06-25 1993-01-19 American Cyanamid Company Process for the preparation of monomeric tetramethoxymethylglycoloril
WO2002024798A2 (en) * 2000-09-21 2002-03-28 Ppg Industries Ohio, Inc. Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers

Families Citing this family (3)

* 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
DE2256496C2 (en) * 1972-11-17 1983-01-20 Will, Günther, Dr., 6100 Darmstadt Process for the production of molded parts with a cell structure
EP2583995B1 (en) 2011-10-20 2015-12-16 Ulrich Hüther Metal-filled cast resin for producing a porous, resin-bonded moulding

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3711746A (en) * 1971-06-16 1973-01-16 Maxwell Lab High voltage energy storage capacitor
US5180835A (en) * 1991-06-25 1993-01-19 American Cyanamid Company Process for the preparation of monomeric tetramethoxymethylglycoloril
WO2002024798A2 (en) * 2000-09-21 2002-03-28 Ppg Industries Ohio, Inc. Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers
WO2002024798A3 (en) * 2000-09-21 2002-06-13 Ppg Ind Ohio Inc Aminoplast-based crosslinkers and powder coating compositions containing such crosslinkers

Also Published As

Publication number Publication date
DE1081222B (en) 1960-05-05
DE1067210B (en) 1959-10-15
GB887957A (en) 1962-01-24
FR1226144A (en) 1960-07-08

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