GB930467A - Heat-curable copolymers and varnishes prepared therefrom - Google Patents
Heat-curable copolymers and varnishes prepared therefromInfo
- Publication number
- GB930467A GB930467A GB2766560A GB2766560A GB930467A GB 930467 A GB930467 A GB 930467A GB 2766560 A GB2766560 A GB 2766560A GB 2766560 A GB2766560 A GB 2766560A GB 930467 A GB930467 A GB 930467A
- Authority
- GB
- United Kingdom
- Prior art keywords
- parts
- maleic
- monoamide
- styrene
- ethyl acrylate
- 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
- 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
- C09D135/00—Coating compositions based on homopolymers or 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 a carboxyl radical, and containing at least another carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D135/02—Homopolymers or copolymers of esters
-
- 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
- C08F22/00—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 a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
- C08F22/36—Amides or imides
-
- 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
- C08F8/00—Chemical modification by after-treatment
-
- 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
- C09D125/00—Coating compositions based on homopolymers or 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 aromatic carbocyclic ring; Coating compositions based on derivatives of such polymers
- C09D125/02—Homopolymers or copolymers of hydrocarbons
- C09D125/04—Homopolymers or copolymers of styrene
- C09D125/08—Copolymers of styrene
- C09D125/14—Copolymers of styrene with unsaturated esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
A copolymer of (A) a monoamide of a C4-C6 olefinically unsaturated dicarboxylic acid, wherein the carbonamide group may be mono- or di-substituted on the N atom by an aliphatic, cycloaliphatic or aromatic radical; (B) one or more compounds containing a -CH=CH2 or <FORM:0930467/IV(a)/1> group; and (C) one or more alpha-beta olefinically unsaturated mono- or di-carboxylic acids, esters or anhydrides, wherein the mol. ratio of (A):(B+C) is between 0,05 and 1 : 1 and of (B):(C) is between 10 and 0,1 : 1, has the N atoms of the carboxylic acid amide groups substituted by alkoxymethyl groups. The alkoxymethyl groups may be introduced before, during or after polymerization by means of formaldehyde and the appropriate monohydric alcohol. It is also possible to introduce the monoamide groups themselves after polymerization by treating a copolymer derived from a dicarboxylic acid or anhydride with an appropriate amount of an amine. (A) may be a monoamide of maleic or fumaric acid; (B) may be a vinyl ether, vinyl ester, e.g. the acetate, or a vinyl aromatic compound, e.g. styrene or alpha methyl styrene; (C) may be acrylic, maleic or fumaric acid, maleic anhydride, or methyl or ethyl acrylate. In forming the alkoxymethyl groups the alcohol may be used in a 5 to 10 times excess and water of condensation continuously removed to yield a p solution which can be used directly as a varnish. The solutions may also be mixed with other varnish resins, e.g. phenol, urea, melamine, epoxy or alkyd varnish resins. 2 to 20 wt. per cent of epoxy resin is said to donate practically unlimited stability in caustic soda solution. In examples:-(1) 20 parts N-butyl maleic or fumaric acid monoamide, 40 parts styrene and 40 parts ethyl acrylate are polymerized in butanol using benzoyl peroxide as catalyst and subsequently treated with formaldehyde; the resulting solution is used as a varnish alone or mixed with 10% of an epoxy resin based on dihydroxydiphenyldimethylmethane having an epoxy No. of 0,2; (2) the monomers used are 30 parts N-cyclo-hexyl-maleic acid monoamide, 30 parts ethyl acrylate and 40 parts styrene; (3) the monomers are 20 parts N-butyl-maleic acid monoamide, 40 parts styrene, 30 parts ethyl acrylate and 10 parts vinyl ethyl ether; (4) 40 parts styrene, 40 parts ethyl acrylate and 11,5 parts maleic anhydride are polymerized in toluene with benzoyl peroxide as catalyst, precipitated, amidated with 2 parts ammonia, and then treated with excess butanol and formaldehyde. Specification 792,874 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB54399A DE1152820B (en) | 1959-08-12 | 1959-08-12 | Process for the production of thermosetting paint resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB930467A true GB930467A (en) | 1963-07-03 |
Family
ID=6970584
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2766560A Expired GB930467A (en) | 1959-08-12 | 1960-08-10 | Heat-curable copolymers and varnishes prepared therefrom |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1152820B (en) |
GB (1) | GB930467A (en) |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL266400A (en) * | 1955-02-24 |
-
1959
- 1959-08-12 DE DEB54399A patent/DE1152820B/en active Pending
-
1960
- 1960-08-10 GB GB2766560A patent/GB930467A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE1152820B (en) | 1963-08-14 |
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