GB592400A - Improvements in and relating to the manufacture of synthetic resins - Google Patents
Improvements in and relating to the manufacture of synthetic resinsInfo
- Publication number
- GB592400A GB592400A GB579/44A GB57944A GB592400A GB 592400 A GB592400 A GB 592400A GB 579/44 A GB579/44 A GB 579/44A GB 57944 A GB57944 A GB 57944A GB 592400 A GB592400 A GB 592400A
- Authority
- GB
- United Kingdom
- Prior art keywords
- castor oil
- heating
- mols
- acid
- pyridine
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
1-3 mols. of an unsaturated dicarboxylic acid are reacted with 1 mol. of castor oil to form an ester in which half the carboxyl group of the acid are unesterified, and the unesterified carboxyl groups are removed by heating with pyridine, quinoline, nicotine, or piperidine to yield a viscous resin which is polymerized to a solid resin with the aid of a peroxide catalyst. The decarboxylated product may be copolymerized with styrene or a higher methacrylic ester, e.g. butyl methacrylate. A mixture of the decarboxylated product with castor oil with or without butyl or another methacrylate is also useful. Suitable dicarboxylic acids are maleic, fumaric or itaconic. The compositions are suitable for casting, as filling compounds, or particularly when mixed with siccatives, as coating, impregnating or insulating compositions, with or without fillers such as wood flour, asbestos, glass fibre, sand or paper. In the examples: (1) 1.6 mols. of maleic anhydride and 0.8 mols. of castor oil were heated till the acid value dropped from 200 to 101. A little pyridine was added and heating continued at 110 DEG C. to 200 DEG C. with a further addition of pyridine. A viscous resin with acid value 36.4 was formed. Heated on a steam bath with benzoyl peroxide it set to a solid, flexible state. A solution of the viscous resin in butyl methacrylate also set to an infusible flexible gel when heated at 80 DEG C. with castor oil containing benzoyl peroxide. Examples (2) and (3) are similar, employing different proportions, Example (4) describes the copolymerization of butyl methacrylate with the de-carboxylated castor oil-maleic anhydride esterification product and benzoyl peroxide. Example (5) describes the copolymerization of styrene with a similar esterification product and tertiary butyl peroxide. Heating for 15 hours at 60 DEG C. yielded a flexible gel which became rigid on further heating at higher temperature. The Specification as open to inspection under Sect. 91 covers generally the use of any hydroxylated fatty oil, and refers generally to unsaturated polycarboxylic acids. Aconitic acid is mentioned as suitable. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US592400XA | 1943-01-20 | 1943-01-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB592400A true GB592400A (en) | 1947-09-17 |
Family
ID=22021696
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB579/44A Expired GB592400A (en) | 1943-01-20 | 1944-01-12 | Improvements in and relating to the manufacture of synthetic resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB592400A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2024115988A1 (en) * | 2022-12-02 | 2024-06-06 | Apollo Tyres Ltd. | Environment-friendly rubber composition |
-
1944
- 1944-01-12 GB GB579/44A patent/GB592400A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2024115988A1 (en) * | 2022-12-02 | 2024-06-06 | Apollo Tyres Ltd. | Environment-friendly rubber composition |
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