GB1123303A - Production of pigmented resinous compositions - Google Patents
Production of pigmented resinous compositionsInfo
- Publication number
- GB1123303A GB1123303A GB24076/66A GB2407666A GB1123303A GB 1123303 A GB1123303 A GB 1123303A GB 24076/66 A GB24076/66 A GB 24076/66A GB 2407666 A GB2407666 A GB 2407666A GB 1123303 A GB1123303 A GB 1123303A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- ester
- polymer
- methacrylate
- hydroxy
- 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
- C09D157/00—Coating compositions based on unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/006—Preparation of organic pigments
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/44—Carbon
- C09C1/48—Carbon black
- C09C1/56—Treatment of carbon black ; Purification
-
- 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
- C09D157/00—Coating compositions based on unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C09D157/04—Copolymers in which only the monomer in minority is defined
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/22—Rheological behaviour as dispersion, e.g. viscosity, sedimentation stability
-
- 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
- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
- C08F2800/20—Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Abstract
Pigmented compositions comprise a pigment dispersed in a vehicle comprising an iminemodified polymer containing at least 0.1% by weight of carboxylic acid units which have been reacted with an alkylenimine or substituted alkylenimine. Pigments which may be used include carbon black, titanium dioxide, phthalocyanine blue or green, red or yellow iron oxide, transparent orange or red iron oxide, indo red or yellow, molybdate orange, monastral violet, ultramarine blue and cadmium red. The polymer which is iminated is preferably an interpolymer of an ester of an ethylenically unsaturated carboxylic acid; the acid component may be copolymerized with such ester or be present in another polymer which is blended with the ester polymer. Other acid polymers which may be iminated include alkyds, e.g. the product derived from coconut fatty acid, trimethylol ethane, p-t-butylbenzoic acid and phthalic anhydride, and other polycarboxylic acid resins. Suitable acid monomers which may be used in, or with, the ester polymers are acrylic, methacrylic and related a -substituted acrylic acids, maleic acid, fumaric acid and half-esters of such dibasic acids, crotonic acid, 3-butenoic acid, tiglic acid and itaconic acid and its half-esters; copolymerizable fatty acids such as dehydrated castor oil acids may also be used. The ester component of the polymer may be an alkyl methacrylate or an hydroxy alkyl ester of an ethylenically unsaturated carboxylic acid; additional units of the polymer are derived, for example, from alkyl acrylates, acrylonitrile, methacrylonitrile, butadiene, vinyl acetate, vinyl chloride, dibutyl maleate, styrene vinyl toluene, a -alkyl styrenes, dibutyl maleate, glycidyl methacrylate or dimethylbenzyl acrylate. The iminating agent is an alkylenimine which may contain substituents such as aryl, alkaryl, aralkyl, cyano, halo, amino, hydroxy, alkoxy, carbalkoxy and nitrile; preferred compounds are those of 2 to 4 carbon atoms, e.g. ethylenimine, 1,2 - propylenimine and N-(2 - hydroxy ethyl) - ethylenimine. Imination is effected by heating the components, e.g. at 50-150 DEG C. and may take place during or after polymerization. Polymerization of the starting monomers is generally effected using a peroxy catalyst, e.g. cumene hydroperoxide or benzoyl peroxide, or an azo catalyst, and in the presence of an organic solvent, e.g. xylene/butanol or toluene, which remains as part of the dispersing vehicle; a mercaptan may also be present. Additional solvent may also be included in the pigment composition, e.g. butanol, toluene, xylene, acetone, methyl ethyl ketone or ethylene glycol ethyl ether acetate. p-Phenylenediamine may also be added, and in one example a carbon black dispersion is formulated into a black enamel by mixing with a butylated melamine-formaldehyde resin, and cured coatings are prepared therefrom.ALSO:In an Example, steel panels are sprayed with a black enamel composition comprising in an organic solvent (a) an interpolymer of n-butyl methacrylate, methyl methacrylate, ethyl acrylate, 2-hydroxy-n-propyl methacrylate and methacrylic acid, wherein the acid groups have been reacted with 1,2-propylenimine (b) carbon black (c) p-phenylene diamine and (d) butylated melamine-formaldehyde resin, and then baked at 250 DEG C. for 30 minutes. In similar Examples (i) the 1, 2-propylenimine is replaced by ethylenimine and (ii) component (c) is omitted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US46049765A | 1965-06-01 | 1965-06-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1123303A true GB1123303A (en) | 1968-08-14 |
Family
ID=23828950
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB24076/66A Expired GB1123303A (en) | 1965-06-01 | 1966-05-31 | Production of pigmented resinous compositions |
Country Status (7)
Country | Link |
---|---|
AT (1) | AT278210B (en) |
BE (1) | BE681937A (en) |
CH (1) | CH465859A (en) |
DE (1) | DE1669253A1 (en) |
GB (1) | GB1123303A (en) |
NL (1) | NL6607487A (en) |
SE (1) | SE324024B (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4451608A (en) * | 1982-06-30 | 1984-05-29 | Union Carbide Corporation | Amphoteric acrylic ester based latexes |
GB2135318A (en) * | 1983-01-29 | 1984-08-30 | Nippon Paint Co Ltd | Resinous composition for coating use |
US4563492A (en) * | 1983-01-29 | 1986-01-07 | Hirotoshi Umemoto | Resinous composition which is useful for the dispersion difficulty dispersible coloring matter |
WO2013083747A1 (en) * | 2011-12-08 | 2013-06-13 | Dow Corning Corporation | Treatment of carbon based filler |
US9000088B2 (en) | 2011-12-08 | 2015-04-07 | Dow Corning Corporation | Hydrolysable silanes and elastomer compositions containing them |
US9080057B2 (en) | 2011-12-08 | 2015-07-14 | Dow Corning Corporation | Treatment of filler with silane |
US9321792B2 (en) | 2011-12-08 | 2016-04-26 | Dow Corning Corporation | Hydrolysable silanes |
US9440997B2 (en) | 2011-12-08 | 2016-09-13 | Dow Corning Corporation | Hydrolysable silanes |
-
1966
- 1966-05-27 SE SE7349/66A patent/SE324024B/xx unknown
- 1966-05-31 GB GB24076/66A patent/GB1123303A/en not_active Expired
- 1966-05-31 NL NL6607487A patent/NL6607487A/xx unknown
- 1966-06-01 CH CH798866A patent/CH465859A/en unknown
- 1966-06-01 AT AT518166A patent/AT278210B/en not_active IP Right Cessation
- 1966-06-01 DE DE19661669253 patent/DE1669253A1/en active Pending
- 1966-06-01 BE BE681937D patent/BE681937A/xx unknown
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4451608A (en) * | 1982-06-30 | 1984-05-29 | Union Carbide Corporation | Amphoteric acrylic ester based latexes |
GB2135318A (en) * | 1983-01-29 | 1984-08-30 | Nippon Paint Co Ltd | Resinous composition for coating use |
US4563492A (en) * | 1983-01-29 | 1986-01-07 | Hirotoshi Umemoto | Resinous composition which is useful for the dispersion difficulty dispersible coloring matter |
WO2013083747A1 (en) * | 2011-12-08 | 2013-06-13 | Dow Corning Corporation | Treatment of carbon based filler |
CN103987795A (en) * | 2011-12-08 | 2014-08-13 | 道康宁公司 | Treatment of carbon based filler |
US9000088B2 (en) | 2011-12-08 | 2015-04-07 | Dow Corning Corporation | Hydrolysable silanes and elastomer compositions containing them |
US9080057B2 (en) | 2011-12-08 | 2015-07-14 | Dow Corning Corporation | Treatment of filler with silane |
US9321792B2 (en) | 2011-12-08 | 2016-04-26 | Dow Corning Corporation | Hydrolysable silanes |
US9440997B2 (en) | 2011-12-08 | 2016-09-13 | Dow Corning Corporation | Hydrolysable silanes |
Also Published As
Publication number | Publication date |
---|---|
NL6607487A (en) | 1966-12-02 |
CH465859A (en) | 1968-11-30 |
AT278210B (en) | 1970-01-26 |
DE1669253A1 (en) | 1970-10-01 |
BE681937A (en) | 1966-12-01 |
SE324024B (en) | 1970-05-19 |
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