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GB409397A - Process for the production of synthetic resins from phenols and aldehydes - Google Patents

Process for the production of synthetic resins from phenols and aldehydes

Info

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
Application number
GB31029/32A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CHEMISCHE FAB DR KURT ALBERT
Original Assignee
CHEMISCHE FAB DR KURT ALBERT
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by CHEMISCHE FAB DR KURT ALBERT filed Critical CHEMISCHE FAB DR KURT ALBERT
Publication of GB409397A publication Critical patent/GB409397A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/28Chemically 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.
GB31029/32A 1931-11-07 1932-11-03 Process for the production of synthetic resins from phenols and aldehydes Expired GB409397A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (5)

* Cited by examiner, † Cited by third party
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

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