GB1100386A - Production of acrylic coatings - Google Patents
Production of acrylic coatingsInfo
- Publication number
- GB1100386A GB1100386A GB1891365A GB1891365A GB1100386A GB 1100386 A GB1100386 A GB 1100386A GB 1891365 A GB1891365 A GB 1891365A GB 1891365 A GB1891365 A GB 1891365A GB 1100386 A GB1100386 A GB 1100386A
- Authority
- GB
- United Kingdom
- Prior art keywords
- weight
- vinyl
- solution
- curing
- copolymer
- 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
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
- C08G18/622—Polymers of esters of alpha-beta ethylenically unsaturated carboxylic acids
- C08G18/6225—Polymers of esters of acrylic or methacrylic acid
-
- 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
- C09D133/00—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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/08—Homopolymers or copolymers of acrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
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)
- Polyurethanes Or Polyureas (AREA)
- Paints Or Removers (AREA)
Abstract
Coated substrates are obtained by applying to the surface of the substrate, e.g. synthetic fabric, metal sheet or wood, a solution comprising an admixture of a polyisocyanate and a copolymer in an inert organic solvent, and curing and/or drying the coating applied; the copolymer used comprising 50-99% by weight of at least one ester of acrylic acid and a C1-C8 alkanol, 1-35% by weight of at least one monomer containing at least one hydroxyl group, at least 50% by weight of this hydroxy-component consisting of at least one bicyclo-[2,2,1]-heptene-(2) derivative having at least one hydroxyl group in the ring or side chains, and 0-25% by weight of at least one further comonomer. The side chains of the bicycloheptene derivative may form another ring system as, for example, in N-b -hydroxyethyl-bicycloheptene - 5,6 - dicarboxylic imide. Suitable hydroxy monomers, additional to the bicycloheptene compounds, include allyl alcohol and diol monoacrylates; optional comonomers include acrylonitrile, styrene and its derivatives, vinyl carbazole, vinyl chloride, vinylidene chloride, vinyl esters, e.g. vinyl acetate, and possibly small amounts of carboxylic acid or amino monomers. Aromatic polyisocyanates are the preferred polyisocyanates. Suitable solvents include ethyl acetate, 2-ethoxyethyl acetate, acetone, tetrahydrofurane, dibutyl ether, toluene and xylene. The coatings may be cured at room or elevated temperature; curing can be accelerated by using tertiary amines, bismuth or lead salts, or tin compounds as catalyst. The coating solution may be pigmented, e.g. with rutile titanium dioxide. Examples illustrate the preparation of the copolymers by solution polymerization in the presence of azodiisobutyronitrile initiator and also, in some cases, diisopropyl xanthic disulphide as chain regulator, part of the reactants being added during the course of polymerization.ALSO:Coated substrates are obtained by applying to the surface of the substrate a solution comprising an admixture of a polyisocyanate and a copolymer in an inert organic solvent, and curing and/or drying the coating applied; the copolymer used comprising 50-99% by weight of at least one ester of acrylic acid and a C1-C8 alkanol, 1-35% by weight of at least one monomer containing at least one hydroxyl group, at least 50% of this hydroxy-component consisting of at least one bicyclo-[2,2,1]-heptene-(2) derivative having at least one hydroxyl group in the ring or side chains (which may form another ring system), and 0-25% by weight of at least one further comonomer. Other hydroxy components of the copolymer include allyl alcohol and diol monoacrylates; further comonomers specified are acrylonitrile, styrene and its derivatives, vinyl carbazole, vinyl chloride, vinylidene chloride, vinyl esters, e.g. vinyl acetate, and small amounts of carboxylic acid or amino monomers. Aromatic polyisocyanates are the preferred polyisocyanates. Suitable solvents include ethyl acetate, thoxy-ethyl acetate, acetone, tetrahydrofurane, dibutyl ether, toluene and xylene. A pigment, e.g. titanium dioxide, may be included in the solution. The solutions may be applied by, e.g. spraying, brushing or knife coating to substrates such as synthetic fibre fabrics, e.g. knitted polyamide fabrics, wood, and sheet metal, e.g. iron. The coatings can be cured at room or elevated temperature; curing can be accelerated by using tertiary amines, bismuth or lead salts, or tin compounds as catalyst.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1964B0076662 DE1238142B (en) | 1964-05-06 | 1964-05-06 | Process for the production of coatings |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1100386A true GB1100386A (en) | 1968-01-24 |
Family
ID=6979170
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1891365A Expired GB1100386A (en) | 1964-05-06 | 1965-05-05 | Production of acrylic coatings |
Country Status (4)
Country | Link |
---|---|
AT (1) | AT255614B (en) |
BE (1) | BE663496A (en) |
DE (1) | DE1238142B (en) |
GB (1) | GB1100386A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011153296A1 (en) * | 2010-06-02 | 2011-12-08 | Lubrizol Advanced Materials, Inc. | Ink/dye receptive films, papers, and fabrics |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55167269A (en) * | 1979-05-29 | 1980-12-26 | Takeda Chem Ind Ltd | Novel triisocyanate compound and its preparation |
-
1964
- 1964-05-06 DE DE1964B0076662 patent/DE1238142B/en active Pending
-
1965
- 1965-05-05 BE BE663496D patent/BE663496A/xx unknown
- 1965-05-05 GB GB1891365A patent/GB1100386A/en not_active Expired
- 1965-05-06 AT AT414365A patent/AT255614B/en active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011153296A1 (en) * | 2010-06-02 | 2011-12-08 | Lubrizol Advanced Materials, Inc. | Ink/dye receptive films, papers, and fabrics |
Also Published As
Publication number | Publication date |
---|---|
AT255614B (en) | 1967-07-10 |
BE663496A (en) | 1965-11-05 |
DE1238142B (en) | 1967-04-06 |
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