GB500357A - Improvements in or relating to the production of resinous compositions - Google Patents
Improvements in or relating to the production of resinous compositionsInfo
- Publication number
- GB500357A GB500357A GB21792/37A GB2179237A GB500357A GB 500357 A GB500357 A GB 500357A GB 21792/37 A GB21792/37 A GB 21792/37A GB 2179237 A GB2179237 A GB 2179237A GB 500357 A GB500357 A GB 500357A
- Authority
- GB
- United Kingdom
- Prior art keywords
- resin
- urea
- alkyd resin
- aldehyde
- prepared
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08L61/22—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
- C08L61/24—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with urea or thiourea
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
Abstract
500,357. Synthetic resin compositions. BAKELITE, Ltd. Aug. 7, 1937, No. 21792. Convention date, Aug. 18, 1936. [Class 2 (iii)] A resinous composition comprises a mixture of a heat-hardenable urea-aldehyde resin with finely-divided C-stage alkyd resin, the latter constituting 3 to 50 per cent by weight of the mixture. The alkyd resin is preferably prepared by repeated heating and grinding. 10-30 per cent by weight (calculated on the mixture) of alkyd resin may be added to a urea-aldehyde syrup or varnish and used for impregnating absorbent cellulosic material, e.g. paper or textiles, which may be formed into laminated panels by hot-pressing. The alkyd resin may be prepared by condensing a polyhydric alcohol, e.g. glycerol, sorbitol, or pentaerythritol, with a polybasic acid or anhydride, e.g. phthalic anhydride, succinic, malic, or maleic acid, to incipient gelation, then cooling in thin layers and repeatedly grinding and heating at 140‹ C. to a total of 100 to 120 hours' treatment. The resin may then be refluxed with an organic solvent, e.g. acetone, ethyl acetate, or ethyleneglycel mono- or di-ethyl ether; soaked in warm acetone; or boiled in water at atmospheric or higher pressure. The alkyd resin may be added to the urea-aldehyde resin by grinding them together or by stirring the alkyd resin into the liquid-stage, molten, or dissolved urea-aldehyde resin. In examples : (1) urea and formaldehyde are condensed in the presence of ammonium hydroxide to the viscous stage, and ethyl alcohol, ethyl lactate, alkyd resin prepared as above, lithopone, and carnauba wax added, the composition being used to coat sheets of alpha-cellulose paper, which are then dried, superimposed, and hot-pressed; (2) urea and formalin are condensed in the presence of ethylenediamine to a syrup, and ethyl alcohol and alkyd resin prepared as above are added, the composition being used as in example 1. The Specification as open to inspection under Sect. 91 refers also to mixtures of finely-divided C-stage alkyd resins in any proportions, with urea-aldehyde or phenol-aldehyde resins. In an example, a fusible resin is prepared by condensing phenol and formalin in the presence of barium hydroxide, and is incorporated with an alkyd resin prepared as above and treated with water under pressure at 140‹ C., either by adding the latter in alcoholic suspension during condensation or by grinding the resins together. The products may be moulded or cast and may be used for the preparation of dentures. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US500357XA | 1936-08-18 | 1936-08-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB500357A true GB500357A (en) | 1939-02-07 |
Family
ID=21963046
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB21792/37A Expired GB500357A (en) | 1936-08-18 | 1937-08-07 | Improvements in or relating to the production of resinous compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB500357A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1147038B (en) * | 1957-10-07 | 1963-04-11 | Ohio Commw Eng Co | Process for the production of higher molecular weight mixed condensates |
WO2010000781A1 (en) * | 2008-07-01 | 2010-01-07 | Kaindl Decor Gmbh | Impregnation with hybrid resins |
-
1937
- 1937-08-07 GB GB21792/37A patent/GB500357A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1147038B (en) * | 1957-10-07 | 1963-04-11 | Ohio Commw Eng Co | Process for the production of higher molecular weight mixed condensates |
WO2010000781A1 (en) * | 2008-07-01 | 2010-01-07 | Kaindl Decor Gmbh | Impregnation with hybrid resins |
CN102076764B (en) * | 2008-07-01 | 2013-05-01 | 凯得装饰有限公司 | Impregnation with hybrid resins |
US8877873B2 (en) | 2008-07-01 | 2014-11-04 | Kaindl Decor Gmbh | Impregnation with hybrid resins |
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