GB409397A - Process for the production of synthetic resins from phenols and aldehydes - Google Patents
Process for the production of synthetic resins from phenols and aldehydesInfo
- Publication number
- GB409397A GB409397A GB31029/32A GB3102932A GB409397A GB 409397 A GB409397 A GB 409397A GB 31029/32 A GB31029/32 A GB 31029/32A GB 3102932 A GB3102932 A GB 3102932A GB 409397 A GB409397 A GB 409397A
- Authority
- GB
- United Kingdom
- Prior art keywords
- heated
- oil
- formaldehyde
- phenol
- product
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/28—Chemically modified polycondensates
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)
- Phenolic Resins Or Amino Resins (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
Abstract
Phenol-aldehyde condensation products capable of being hardened, especially phenolalcohols, are heated with a monohydric aliphatic or aromatic alcohol of boiling point above 80 DEG C., higher oxy-fatty acids or their glycerides being added simultaneously or subsequently, for such a period that the products are still soluble in organic solvents such as benzol hydrocarbons. By further heating the phenol-aldehyde condensation products with the alcohol or by using a larger quantity of alcohol products may be obtained which are soluble in benzine hydrocarbons and may be worked up with fatty acids, fatty oils and neutral resins. The phenol aldehyde products may be derived from phenols such as phenol, naphthol, diphenylolpropane or phenylphenol. The term oxy-fatty acids comprises fatty acids containing more than 10 carbon atoms and at least one hydroxyl group. Fatty oils include drying, semi-drying and non-drying oils such as wood oil, linseed oil, perilla oil, poppy seed oil, soya bean oil, hemp seed oil, nut oil, olive oil, cotton seed oil, earth nut oil and almond oil. Neutral resins include esters of natural or synthetic resin acids urea - formaldehyde and polyhydric alcohol - dicarboxylic acid, condensation products. The new products may be worked up with resins such as shellac, dammar, resin-esters, or artificial resins such as phenol-aldehyde-colophony condensation products. The new products may be hardened by heat with or without a catalyst and with or without pressure. They may be employed with or without fillers, pigments, diluents and softeners as lacquers or varnishes for containers, such as boxes, tubes and tanks, wires, metal bars, pipes such as gas pipes, apparatus parts and casings, chemical, medecinal and other instruments, cooling and heating appliances, electric insulating bodies such as cables, incandescent lamps and machine parts; as binding agents for printing inks, cements, brake-linings, and packings; as impregnating agents for water-proof substances or fabrics; for cold and hot pressed articles and for gramophone records. In examples: (1) p-cresol dialcohol is heated with iso-amylalcohol and mixed with ricinoleic acid; (2) alkaline condensed cresol and formaldehyde is heated with n-butanol and mixed with trioxy stearic acid; (3) the condensation product of dihydroxydiphenyldimethylmethane and formaldehyde is heated with N-butanol and castor oil to give a resin soluble in toluol, butyl acetate, diethyl glycol; (4) alkali condensed phenol and formaldehyde is heated with iso-propyl alcohol and formaldehyde; (5) the condensation product of formaldehyde and the product of treating phenol with acetone is heated with iso-amyl alcohol and ricinoleic acid; (6) the condensation product of p-phenylphenol and formaldehyde is heated with cyclohexanol and castor oil; (7) p-colsol dialcohol is heated with iso-amyl alcohol and the product, mixed with oxidized linseed oil is diluted by means of toluene, benzine or solvent naphtha to give a varnish; (8) the condensation product of dihydroxydiphenyldimethylmethane and formaldehyde is heated with N-butanol and the product is heated with wood oil; (9) the alkaline condensation product of cresol and formaldehyde is heated with iso-propyl alcohol and the product is heated with cotton seed oil; (10) the condensation product of phenol and formaldehyde is heated with N-butanol and the product, heated with coliphony glycerol ester may be used, with or without the addition of a fatty oil as a varnish or as a binder in the manufacture of grinding wheels or discs; (11) the condensation product of the compound obtained by treating phenol with acetone and formaldehyde is heated with iso-amyl alcohol and the product heated with the condensation product of phthalic acid, ricinoleic acid and glycerol; (12) the condensation product of p-phenylphenol and formaldehyde is heated with cyclohexanol and then heated with the resin derived from phthalic anhydride, succinic acid, linseed oil and glycerol. Specifications 259,030, 261,522, and 298,680, [all in Class 2 (iii)], are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE409397X | 1931-11-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB409397A true GB409397A (en) | 1934-05-03 |
Family
ID=6422413
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31029/32A Expired GB409397A (en) | 1931-11-07 | 1932-11-03 | Process for the production of synthetic resins from phenols and aldehydes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB409397A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE748932C (en) * | 1941-07-17 | 1944-11-14 | Process for the production of curable synthetic resins | |
US2457738A (en) * | 1946-04-02 | 1948-12-28 | Monsanto Chemicals | Thermoplastic aminoplasts |
US2470130A (en) * | 1945-02-07 | 1949-05-17 | Bakelite Corp | Caustic resistant etherified phenolformaldehyde resins |
US4634758A (en) * | 1984-10-12 | 1987-01-06 | Acme Resin Corporation | Process for preparing alkoxy-modified phenolic resole resins |
US4723592A (en) * | 1984-10-12 | 1988-02-09 | Acme Resin Corporation | Process for preparing foundry cores and molds |
-
1932
- 1932-11-03 GB GB31029/32A patent/GB409397A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE748932C (en) * | 1941-07-17 | 1944-11-14 | Process for the production of curable synthetic resins | |
US2470130A (en) * | 1945-02-07 | 1949-05-17 | Bakelite Corp | Caustic resistant etherified phenolformaldehyde resins |
US2457738A (en) * | 1946-04-02 | 1948-12-28 | Monsanto Chemicals | Thermoplastic aminoplasts |
US4634758A (en) * | 1984-10-12 | 1987-01-06 | Acme Resin Corporation | Process for preparing alkoxy-modified phenolic resole resins |
US4723592A (en) * | 1984-10-12 | 1988-02-09 | Acme Resin Corporation | Process for preparing foundry cores and molds |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US1975246A (en) | Alkyd resin | |
US2275843A (en) | Condensation product and method | |
US2091965A (en) | Phenol resin ester and method of preparing | |
GB409397A (en) | Process for the production of synthetic resins from phenols and aldehydes | |
US1888849A (en) | Ebwabjd s | |
US2111762A (en) | Resinous compositions from oxalic acid and polyhydric alcohols and process of makingsame | |
US2069314A (en) | Process for making bituminous compositions | |
US3108978A (en) | Preparation of addition products of fatty acid compounds with phenol aldehyde condensation products | |
US2135976A (en) | Composition of matter and method of | |
US1969761A (en) | Polyhydric alcohol-carboxylic organic acid-weak polybasic inorganic phenol-aldehyde condensation product | |
US2027337A (en) | Manufacture of resins | |
US2028908A (en) | Polyhydric alcohol-polybasic acidmonobasic aliphatic acid anhydride condensation product and process of making the same | |
US1853049A (en) | Resinous condensation product | |
US2146012A (en) | Synthetic resins and method of producing | |
US2373177A (en) | Wrinkle finish drying compositions | |
US3028348A (en) | Process for the manufacture of synthetic resins obtained by condensation and esterification | |
US2064950A (en) | Resinous condensation product and method of producing same | |
GB355281A (en) | Improvements in the manufacture and production of artificial resins | |
US2088035A (en) | Synthetic resin composition | |
US2142833A (en) | Resinous composition and method of making the same | |
US2027338A (en) | Manufacture of varnish bases | |
US1982788A (en) | Synthetic resin | |
US2079606A (en) | Process for producing resins | |
US2081154A (en) | Artificial resin and method of making the same | |
US2027339A (en) | Manufacture of varnish resins, varnishes, and like coating compositions |