GB848400A - Copolymers of unsaturated polyester resins and process for the production thereof - Google Patents
Copolymers of unsaturated polyester resins and process for the production thereofInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F16/00—Homopolymers 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
- C08F16/12—Homopolymers 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
- C08F16/14—Monomers containing only one unsaturated aliphatic radical
- C08F16/28—Monomers containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/685—Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen
- C08G63/6854—Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/6858—Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D4/00—Coating 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.
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)
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)
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 |
-
0
- DE DENDAT1067210D patent/DE1067210B/en active Pending
-
1958
- 1958-07-29 DE DEB49774A patent/DE1081222B/en active Pending
-
1959
- 1959-06-01 GB GB18537/59A patent/GB848400A/en not_active Expired
- 1959-06-01 FR FR796192A patent/FR1226144A/en not_active Expired
- 1959-07-28 GB GB25823/59A patent/GB887957A/en not_active Expired
Cited By (4)
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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