ES249853A1 - Modified alkyd resin compositions and process of preparing the same - Google Patents
Modified alkyd resin compositions and process of preparing the sameInfo
- Publication number
- ES249853A1 ES249853A1 ES0249853A ES249853A ES249853A1 ES 249853 A1 ES249853 A1 ES 249853A1 ES 0249853 A ES0249853 A ES 0249853A ES 249853 A ES249853 A ES 249853A ES 249853 A1 ES249853 A1 ES 249853A1
- Authority
- ES
- Spain
- Prior art keywords
- epoxy
- acid
- stearate
- ester
- acids
- 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
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A film-forming alkyd ester composition comprises (1) a monobasic acid-modified alkyd ester which is the reaction product of a monocarboxylic acid, a polyol and a dicarboxylic acid or anhydride, this reaction product having an acid value of 45-90 before being further reacted with a dicarboxylic acid anhydride to form a partial ester of acid number 80-120, (2) an epoxidized unsaturated fatty acid ester containing 6-26 carbon atoms in the fatty acid chains and (3) a volatile neutralizing agent in a proportion sufficient to inhibit reaction between free carboxylic acid groups of the modified alkyd and the epoxy groups of the epoxidized ester. Specified are monocarboxylic acids numerous unsaturated and saturated fatty acids derived from fatty oils of vegetable, animal and marine origin (the oils themselves may be used reacting by alcoholysis) and benzoic, p-tert. butyl benzoic, 2-ethyl hexoic and pelargonic acids polyols pentaerythritol, trimethylolethane, trimethylolpropane, sorbitol, diethylene glycol, propylene glycol, ethylene glycol, glycerol, 1,2,6-hexanetriol, copolymers of styrene and allyl alcohol and glycol etherified phenols dicarboxylic acids and anhydrides phthalic, tetrahydrophthalic, hexahydrophthalic, tetrachlorophthalic, maleic, chlorendic and succinic anhydrides and isophthalic, terephthalic, adipic and fumaric acids for the initial condensation with tetrachlorophthalic, monochlorophthalic, chlorendic, phthalic, tetrahydrophthalic and hexahydrophthalic anhydrides for the subsequent reaction volatile neutralizing agents triethylamine, dimethyl formamide, diethanolamine, ammonia, dimethylethanolamine, mono-ethanolamine, dipropylamine and diisopropylamine and epoxidized unsaturated fatty acid esters epoxidized unsaturated glyceride oils and synthetic esters and dimer and trimer polymers derived therefrom of which there are particularly mentioned epoxidized linseed, segregated soybean, safflower and fish oils, epoxy-stearyl acetate, epoxy-stearyl epoxy-stearate, butyl epoxy-stearate, octyl epoxy-behenate, methyl di-eposy-stearate, di-(epoxy-lauryl) adipate, propyl tri-epoxy-stearate and allyl epoxy-stearate. A solvent, e.g. xylene or toluene, is incorporated into the composition during its preparation and usually a small proportion of a secondary solvent, e.g. butanol, mono- or di-butyl ether of ethylene or diethylene glycol or mono- or di-ethyl ether of ethylene or diethylene glycol, is also incorporated. The composition may be dispersed in water by use of excess of the neutralizer. A compatible resinous material, e.g. a phenol-formaldehyde or melamine-formaldehyde condensation product, an acrylic emulsion or a natural or synthetic rubber latex such as a butadiene-styrene copolymer, may also be included. The composition may also be pigmented, e.g. with titanium dioxide. Specification 921,622 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US74302758A | 1958-06-19 | 1958-06-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES249853A1 true ES249853A1 (en) | 1960-01-16 |
Family
ID=24987227
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES0249853A Expired ES249853A1 (en) | 1958-06-19 | 1959-06-05 | Modified alkyd resin compositions and process of preparing the same |
Country Status (4)
Country | Link |
---|---|
ES (1) | ES249853A1 (en) |
FR (1) | FR1227620A (en) |
GB (1) | GB921623A (en) |
NL (1) | NL240377A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009006527A1 (en) * | 2007-07-03 | 2009-01-08 | Georgia-Pacific Chemicals Llc | Chemical modification of maleated fatty acids |
CN111944132A (en) * | 2020-07-21 | 2020-11-17 | 江苏三木化工股份有限公司 | Primer alkyd resin and preparation method and application thereof |
-
0
- NL NL240377D patent/NL240377A/xx unknown
-
1959
- 1959-06-05 ES ES0249853A patent/ES249853A1/en not_active Expired
- 1959-06-12 FR FR797397A patent/FR1227620A/en not_active Expired
- 1959-06-12 GB GB2024959A patent/GB921623A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
NL240377A (en) | |
FR1227620A (en) | 1960-08-22 |
GB921623A (en) | 1963-03-20 |
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