GB435762A - Synthetic resins and their applications - Google Patents

Synthetic resins and their applications

Info

Publication number
GB435762A
GB435762A GB8935/34A GB893534A GB435762A GB 435762 A GB435762 A GB 435762A GB 8935/34 A GB8935/34 A GB 8935/34A GB 893534 A GB893534 A GB 893534A GB 435762 A GB435762 A GB 435762A
Authority
GB
United Kingdom
Prior art keywords
resins
hydroxy
oil
acids
methylphenyl
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
GB8935/34A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB435762A publication Critical patent/GB435762A/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
    • C08G8/32Chemically modified polycondensates by organic acids or derivatives thereof, e.g. fatty oils
    • 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
    • C08G8/04Condensation polymers of aldehydes or ketones with phenols only of aldehydes
    • C08G8/08Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
    • 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
    • C08G8/04Condensation polymers of aldehydes or ketones with phenols only of aldehydes
    • C08G8/08Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
    • C08G8/14Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with halogenated phenols
    • 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)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Paints Or Removers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Resinous materials soluble in varnish oils are prepared by reacting in an alkaline medium formaldehyde or a derivative thereof such as methylene chloride, methylal, hexamethylene-tetramine and paraformaldehyde with a binuclear phenol containing at least one but not more than two reactive positions and containing at least four non-aromatic carbon atoms one of which is a secondary or tertiary carbon atom which is directly joined to a benzene ring in one of the o- or p-positions in relation to a phenolic hydroxy group. Suitable phenols include di(4 - hydroxy - 3 - methylphenyl) - dimethylmethane or the corresponding methylethyl-, dipropyl- and ethyl-methane derivatives, di(2 - hydroxy - 5 - methylphenyl) - dimethylmethane or the corresponding methylethyl- or methyl-methane derivative and di(2 - hydroxy - 3 - methylphenyl)propylmethane. In examples: (1) di(4 - hydroxy - 3 - methylphenyl)dimethylmethane is condensed with formaldehyde in the presence of sodium hydroxide and the resinous product, which is soluble in acetone, alcohol and ethoxyethanol, is blended with raw chinawood oil or linseed oil or mixtures thereof and thinned with a mineral thinner and an aromatic hydrocarbon with or without a cobalt drier to yield a varnish; (5) the resin prepared in example 1 is blended with a polyhydric alcohol polybasic acid condensation product containing a drying oil or a fatty acid derived therefrom and thinned with or without the addition of an oil to yield a varnish--suitable polyhydric alcohols include glycerol, ethylene glycol, diethylene glycol, pentaerythritol and monoethylin, suitable polycarboxylic acids include phthalic anhydride, adipic, sebacic, dilactylic, maleic, diphenic, tetrahydrophthalic and quinolinic acids and suitable modifying agents which may be used in addition to the drying oils or drying oil acids include natural resins such as rosin, kauri, congo and ester gums, monocarboxylic acids such as butyric, oleic, stearic, salicylic, benzoic acids and semi- and non-drying oil acids and monohydric alcohols such as amyl, ethoxyethyl, lauryl, benzyl and cyclohexyl alcohols. The products may be blended with cellulose derivatives such as nitrocellulose, cellulose acetate, benzyl cellulose and ethyl cellulose; natural resins and ester gums such as rosin, kauri, copal and rosin glyceride; synthetic resins or synthetic resin forming material such as metastyrene, coumarone-indene resins, amine-aldehyde resins, acrylic ester resins, vinyl resins, casein plastics, polyhydric alcohol-polybasic acid resins unmodified by drying oils or drying oil acids; bitumens such as asphalts; natural or synthetic waxes such as beeswax, candelilla wax, montan wax, carnauba wax and lauryl stearate; other ester-like bodies such as stearin, castor oil, hydrogenated castor oil, tricresyl phosphate, dibutyl phthalate, triethylin, animal fats and waxes; pigments; solvents; plasticizers, antioxidants, fillers and lakes for use in the manufacture of coating compositions, moulding plastics, impregnating agents for paper, wood, cloth, stone, or rubberized fabrics, adhesives for safety glass, linoleum, adhesives, cements, sealing waxes, insulating materials together with mica or asbestos and laminated sheet or tubes from cellulose derivatives such as cellulose acetate. Specification 199,528, [Class 2 (iii)], is referred to. Di(4 - hydroxy - 3 - methylphenyl)dimethylmethane is prepared by condensing acetone with o-cresol in the presence of dry hydrochloric acid gas. The Specification as open to inspection under Sect. 91 refers also to the subject-matter of Specifications 435,796 and 435,797. This subject-matter does not appear in the Specification as accepted.
GB8935/34A 1933-03-21 1934-03-21 Synthetic resins and their applications Expired GB435762A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US435796XA 1933-03-21 1933-03-21
US435762XA 1933-03-21 1933-03-21

Publications (1)

Publication Number Publication Date
GB435762A true GB435762A (en) 1935-09-23

Family

ID=62529113

Family Applications (2)

Application Number Title Priority Date Filing Date
GB8935/34A Expired GB435762A (en) 1933-03-21 1934-03-21 Synthetic resins and their applications
GB19654/35A Expired GB435796A (en) 1933-03-21 1934-03-21 Synthetic resins and their applications

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB19654/35A Expired GB435796A (en) 1933-03-21 1934-03-21 Synthetic resins and their applications

Country Status (1)

Country Link
GB (2) GB435762A (en)

Also Published As

Publication number Publication date
GB435796A (en) 1935-09-23

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