GB1049462A - Production of oil-modified alkyd resins - Google Patents
Production of oil-modified alkyd resinsInfo
- Publication number
- GB1049462A GB1049462A GB334864A GB334864A GB1049462A GB 1049462 A GB1049462 A GB 1049462A GB 334864 A GB334864 A GB 334864A GB 334864 A GB334864 A GB 334864A GB 1049462 A GB1049462 A GB 1049462A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oil
- acids
- acid
- anhydride
- polyhydric alcohol
- 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
- 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
- C08G63/46—Polyesters chemically modified by esterification
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
An oil-modified alkyd resin is derived from phthalic anhydride, a polyhydric alcohol and a modifying oil comprising at least 50 wt. per cent of cod liver oil. When the oil length exceeds 45% an a ,b -unsaturated dicarboxylic acid or anhydride is also present; when the oil length is less than 45% a monocarboxylic acid or anhydride is added; between 40 and 50%, however, the additional components are not essential. The polyhydric alcohol may be glycerol, pentaerythritol or trimethylolethane, and may include some diol, e.g. diethylene glycol or propylene glycol. Suitable a ,b -unsaturated acids are fumaric, maleic, citraconic and mesaconic acids, and suitable monocarboxylic acids are benzoic, toluic and t-butylbenzoic acids, or aliphatic acids containing up to 10 C-atoms, e.g. caproic and capric acids. Preferably the cod liver oil or oil mixture is first alcoholysed with the polyhydric alcohol, usually in the presence of a catalyst, e.g. Ca(OH)2, and is then condensed with the rest of the starting materials, including any further polyhydric alcohol required. Usually the amounts used of the a ,b -unsaturated acid, or of the monocarboxylic acid, do not exceed 15% or 20% by weight respectively of the phthalic anhydride. The amounts increase as the oil length departs from the 45% value. The polyhydric alcohol is usually in excess, there preferably being 1.1-1.3 OH groups per carboxyl group in free or anhydride form. The condensation may be performed with reactants fused or in solution, e.g. in xylene, preferably at 200-300 DEG C. The product may have an acid value below 10 or 15, and be soluble in solvent naphtha and xylene. The cod liver oil may be mixed with up to 50 wt. per cent of other marine or vegetable oils, and other dicarboxylic acids or anhydrides may be included, e.g. adipic or sebacic acid. In examples an alkali-refined cod liver oil is heated with glycerol and Ca(OH)2 and is then heated with [1] phthalic anhydride, glycerol and benzoic acid, [2], [3] phthalic anhydride, maleic anhydride and xylene, to give alkyds of oil lengths 33%, 55% and 70% respectively. These are milled with TiO2 in xylene to give paints. The paints from resins [1] and [2] are stove-dried, that fro [3] is airdried, after addition of cobalt and lead naphthenate driers.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB334864A GB1049462A (en) | 1964-01-27 | 1964-01-27 | Production of oil-modified alkyd resins |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB334864A GB1049462A (en) | 1964-01-27 | 1964-01-27 | Production of oil-modified alkyd resins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1049462A true GB1049462A (en) | 1966-11-30 |
Family
ID=9756619
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB334864A Expired GB1049462A (en) | 1964-01-27 | 1964-01-27 | Production of oil-modified alkyd resins |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1049462A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10442955B2 (en) * | 2012-05-08 | 2019-10-15 | Dsm Ip Assets B.V. | Resin, composition and use |
-
1964
- 1964-01-27 GB GB334864A patent/GB1049462A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10442955B2 (en) * | 2012-05-08 | 2019-10-15 | Dsm Ip Assets B.V. | Resin, composition and use |
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