GB942839A - Improvements in or relating to a process for the production of alkyd resins - Google Patents
Improvements in or relating to a process for the production of alkyd resinsInfo
- Publication number
- GB942839A GB942839A GB7120/61A GB712061A GB942839A GB 942839 A GB942839 A GB 942839A GB 7120/61 A GB7120/61 A GB 7120/61A GB 712061 A GB712061 A GB 712061A GB 942839 A GB942839 A GB 942839A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diphenylol
- acids
- glycerol
- specified
- propane
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4292—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with monocarboxylic 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/40—Polyesters derived from ester-forming derivatives of polycarboxylic acids or of polyhydroxy compounds, other than from esters thereof
- C08G63/42—Cyclic ethers; Cyclic carbonates; Cyclic sulfites; Cyclic orthoesters
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
A polyhydric alcohol is made by reacting an epoxyalkyl ester of a monocarboxylic acid with an aliphatic, cycloaliphatic or aromatic polyhydroxy compound. Specified epoxy esters are the glycidyl esters of saturated and unsaturated aliphatic monocarboxylic acids having 8-20 carbon atoms (e.g. apric, lauric, palmitic, stearic, oleic, linoleic linolenic and dehydrated castor oil acids) and especially acids in which the carboxy group is directly attached to a tertiary or quaternary carbon atom (Specification 936,808). Specified polyhydroxy compounds are diphenylol methane, diphenylol ethane, diphenylol propane, diphenylol sulphone, hydroquinone, resorcinol, dihydroxy diphenyl and naphthalenes, novalacs and resols, glycols, glycerol, trimethylol propane and pentaerythritol. Reaction is effected at 80 DEG -220 DEG C., possibly in the presence of a catalyst and a solvent. In examples, the glycidyl ester of monocarboxylic acids containing 9-11 carbon atoms and branched in the alpha-position were reacted with diphenylol propane or glycerol. Specification 942,465 also is referred to.ALSO:Alkyd resins are made by reacting (a) a polycarboxylic acid with (b) a polyhydric alcohol formed by reacting an epoxy alkyl ester of a monocarboxylic acid with an aliphatic, cycloaliphatic or aromatic polyhydroxy compound. The reaction mixture may also include free epoxy alkyl ester, and additional polyhydric alcohol (e.g. glycerol, pentaerythritol, trimethylolpropane or 1,2,6-hexanetriol). Specified polycarboxylic acids are maluric, succinic, glutaric, adipic, azelaic, sebacic, maleic, fumaric, phthalic, isophthalic, terephthalic, tetrahydrophthalic, hexahydrophthalic, diglycolic and dimerised fatty acids and Diels-Alder adducts of maleic anhydride with terpenes, cyclopentadiene or hexachloro-cyclopentadiene. Specified epoxyalkyl esters are the glycidyl esters of saturated and unsaturated aliphatic monocarboxylic acids having 8-20 carbon atoms (e.g. capric, lauric, palmitic, stearic oleic, linoleic, linoleinc and dehydrated castor oil acids) and especially acids in which the carboxy group is directly attached to a tertiary and quaternary carbon atom. (Specification 936,808). Specified polyhydroxy compounds are diphenylol methene, diphenylol ethane, diphenylol propane, diphenylol sulphone, hydroquinone, resorcinol, dihydroxy diphenyl and naphthalenes, novolac and resols, glycols, glycerol, trimethylol propane and pentaerythritol. The alkyd resins may be made into coating compositions and components such as pigments (e.g. titanium white), diluents (e.g. xylene), driers or phenol-, urea- or melamine-formaldehyde resins may be added. In examples polyhydric alcohols were made by reacting the glycidyl esters of monocarboxylic acids containing 9-11 carbon atoms and branched at the alpha-position with diphenylol propane or glycerol and the product reacted with glycerol and phthalic anhydride. Specification 942,465 also is referred to.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL248912 | 1960-02-29 | ||
FR853958A FR1289657A (en) | 1960-02-29 | 1961-02-27 | Process for preparing alkyd resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB942839A true GB942839A (en) | 1963-11-27 |
Family
ID=26189449
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7120/61A Expired GB942839A (en) | 1960-02-29 | 1961-02-27 | Improvements in or relating to a process for the production of alkyd resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB942839A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4156665A (en) * | 1977-03-14 | 1979-05-29 | Henkel Kommanditgesellschaft Auf Aktien | Aqueous dispersions of alkyd and/or amino resins containing glycide and ethylene oxide adducts to hydrophobic compounds |
-
1961
- 1961-02-27 GB GB7120/61A patent/GB942839A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4156665A (en) * | 1977-03-14 | 1979-05-29 | Henkel Kommanditgesellschaft Auf Aktien | Aqueous dispersions of alkyd and/or amino resins containing glycide and ethylene oxide adducts to hydrophobic compounds |
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