GB915702A - Coating composition and resin therefor - Google Patents
Coating composition and resin thereforInfo
- Publication number
- GB915702A GB915702A GB727358A GB727358A GB915702A GB 915702 A GB915702 A GB 915702A GB 727358 A GB727358 A GB 727358A GB 727358 A GB727358 A GB 727358A GB 915702 A GB915702 A GB 915702A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- polyamide
- diamine
- ethylene diamine
- oil
- 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
-
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-amides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
-
- 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
- C09D177/00—Coating compositions based on polyamides obtained by reactions forming a carboxylic amide link in the main chain; Coating compositions based on derivatives of such polymers
- C09D177/06—Polyamides derived from polyamines and polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (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)
- Oil, Petroleum & Natural Gas (AREA)
- Polyamides (AREA)
Abstract
A film-forming thixotropic composition comprises an ester body in which has been dissolved a polyamide resin derived from a polymerized fatty acid which may be replaced wholly or in part by an aliphatic dicarboxylic acid in which the carboxyl groups are separated by at least 4 carbon atoms together with a substantial excess of monocarboxylic acid and an alkylene polyamine and having a molecular weight below 3,000. Specified polyamines are ethylene diamine, 1:3-propane diamine, tetramethylene diamine, diethylene triamine, and N-(isopropyl)-2-methyl-1:2-propane diamine which may be replaced in part by 3-amino-propane-1-ol, 2-amino ethanol, phenylene diamine or xylylene diamine. The molecular weight of the polyamide may be controlled by the presence in the polyamide-forming composition of monofunctional acids or amines. The examples describe the preparation of polyamides from:-(1) ethylene diamine, dimer acid and soyabean oil fatty acids; (2) hexamethylene diamine, dimer acid and sunflower seed oil fatty acids; (3) ethylene diamine, dimer acid and soyabean oil fatty acids; (4) ethylene diamine, dimer acid and oleic acid; (5) ethylene diamine and dimer acid; (6) ethylene diamine, dimer acid and lauric acid; (7) ethylene diamine, sebacic acid and linseed oil fatty acids; (8) ethylene diamine, dimer acid, oleic acid and sebacic acid and (9) ethylene diamine, dimer acid, oleic acid and diethylene triamine. Examples (10) to (15) describe the preparation of thixotropic compositions by dissolving:- (10) the polyamide of Example (1) in varnish linseed oil; (11) the polyamide of Example (1) in an alkyd resin derived from soyabean oil, pentaerythritol and phthalic anhydride; (12) the polyamide of Example (1) in a mixture of linseed stand oil and ester gum; (13) the polyamide of Example (2) in a solution in xylol of an alkyd resin derived from linseed oil, glycerol and phthalic anhydride; (14) the polyamide of Example (3) in ester gum in the presence of white spirits, the product being incorporated into oils, alkyd resins or oleo resinous vehicles and (15) the polyamide of Example (7) in linseed stand oil, the product being thinned with white spirit. In Examples (16) to (18):-(16) and (17) a polyamide made from sebacic acid, oleic acid and hexamethylene diamine is dissolved in linseed stand oil, the product being thinned with white spirit and (18) a polyamide made from adipic acid, oleic acid and hexamethylene diamine is dissolved in linseed stand oil. U.S.A. Specifications 2,482,761 and 2,663,669 are referred to.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL107200D NL107200C (en) | 1958-03-06 | ||
NL236629D NL236629A (en) | 1958-03-06 | ||
GB727358A GB915702A (en) | 1958-03-06 | 1958-03-06 | Coating composition and resin therefor |
CH7039759A CH397718A (en) | 1958-03-06 | 1959-03-05 | Composition thixotropique format des films |
BE576415A BE576415A (en) | 1958-03-06 | 1959-03-06 | Resin and coating compound containing it. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB727358A GB915702A (en) | 1958-03-06 | 1958-03-06 | Coating composition and resin therefor |
Publications (1)
Publication Number | Publication Date |
---|---|
GB915702A true GB915702A (en) | 1963-01-16 |
Family
ID=9829935
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB727358A Expired GB915702A (en) | 1958-03-06 | 1958-03-06 | Coating composition and resin therefor |
Country Status (3)
Country | Link |
---|---|
CH (1) | CH397718A (en) |
GB (1) | GB915702A (en) |
NL (2) | NL107200C (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0959066A2 (en) * | 1998-05-20 | 1999-11-24 | Basf Aktiengesellschaft | Use of amides of polymerised fatty acids as thickening agent |
US6630541B1 (en) | 1997-11-03 | 2003-10-07 | Akzo Nobel N.V. | Thixotropic agent based on an alkyd resin |
US6870011B2 (en) | 2001-01-24 | 2005-03-22 | Arizona Chemical Company | Hydrocarbon-terminated polyether-polyamide block copolymers and uses thereof |
CN112979933A (en) * | 2021-04-07 | 2021-06-18 | 安庆瑞泰化工有限公司 | Biomass polyacid modified polyester resin and preparation method thereof |
-
0
- NL NL236629D patent/NL236629A/xx unknown
- NL NL107200D patent/NL107200C/xx active
-
1958
- 1958-03-06 GB GB727358A patent/GB915702A/en not_active Expired
-
1959
- 1959-03-05 CH CH7039759A patent/CH397718A/en unknown
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6630541B1 (en) | 1997-11-03 | 2003-10-07 | Akzo Nobel N.V. | Thixotropic agent based on an alkyd resin |
EP0959066A2 (en) * | 1998-05-20 | 1999-11-24 | Basf Aktiengesellschaft | Use of amides of polymerised fatty acids as thickening agent |
EP0959066A3 (en) * | 1998-05-20 | 2003-08-20 | Basf Aktiengesellschaft | Use of amides of polymerised fatty acids as thickening agent |
US6870011B2 (en) | 2001-01-24 | 2005-03-22 | Arizona Chemical Company | Hydrocarbon-terminated polyether-polyamide block copolymers and uses thereof |
US7745546B2 (en) | 2001-01-24 | 2010-06-29 | Arizona Chemical Company | Hydrocarbon-terminated polyether-polyamide block copolymers and uses thereof |
US8013021B2 (en) | 2001-01-24 | 2011-09-06 | Arizona Chemical Company, Llc | Hydrocarbon-terminated polyether-polyamide block copolymer and uses thereof |
CN112979933A (en) * | 2021-04-07 | 2021-06-18 | 安庆瑞泰化工有限公司 | Biomass polyacid modified polyester resin and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
NL107200C (en) | |
NL236629A (en) | |
CH397718A (en) | 1965-08-31 |
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