GB549303A - Improvements in or relating to the manufacture of oil-soluble polystyrene resinous products - Google Patents

Improvements in or relating to the manufacture of oil-soluble polystyrene resinous products

Info

Publication number
GB549303A
GB549303A GB6140/41A GB614041A GB549303A GB 549303 A GB549303 A GB 549303A GB 6140/41 A GB6140/41 A GB 6140/41A GB 614041 A GB614041 A GB 614041A GB 549303 A GB549303 A GB 549303A
Authority
GB
United Kingdom
Prior art keywords
oil
resinous products
styrene
resin
oxalic
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
GB6140/41A
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.)
Bakelite Ltd
Original Assignee
Bakelite Ltd
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
Priority claimed from US335322A external-priority patent/US2374316A/en
Application filed by Bakelite Ltd filed Critical Bakelite Ltd
Publication of GB549303A publication Critical patent/GB549303A/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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • 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
    • C08G8/30Chemically modified polycondensates by unsaturated compounds, e.g. terpenes

Abstract

549,303. Polystyrene resinous products. BAKELITE, Ltd. May 12, 1941, No. 6140. Convention date, May 15, 1940. [Class 2 (iii)] Oil-soluble polystyrene resinous products suitable for use in varnishes, moulding compositions, laminated articles, brake linings and for insulating purposes are obtained by polymerizing a mixture of styrene and an oil-soluble phenolic resin. prepared from an alkyl or aryl substituted phenol. Catalysts which may be used comprise benzoyl peroxide and boron compounds such as the halides ; the latter may be used together with a dicarboxylic acid, particularly acids having hydroxy and carboxylic groups attached to the same or adjacent carbon atoms e.g. oxalic, tartaric, lactic, salicylic acids. The polymerization can be carried out in the presence of an inert solvent e.g. toluol, xylol and naphtha, and mixtures of oilsoluble phenolic resins may be used, whilst additional natural or synthetic resins may also be incorporated. Inhibitors e.g. sulphur, tertbutyl phenol, hydroquinone, catechol, resorcinol, and methoxy compounds such as guaiacol may be present during the polymerization but must be removed before making the product into a varnish. Crude styrene may be used and the reaction can be carried out in the presence of drying or semi-drying oils, e.g. tung, oiticica, linseed, perilla and soya. Oils containing double bonds, e.g. tung, oiticica, must not exceed 25 per cent. of the mass. In examples resinous products from which varnishes could be obtained by heating with china wood oil and mineral spirits, were produced from styrene and (1) pphenylphenol-formaldehyde resin, oxalic and boric acids ; (3) a resin made from tert-butyl phenol or p-phenylphenol and formaldehyde, china wood oil, oxalic and boric acids ; (4) the resin of (3), rosin or rosin-glycerol ester, triamyl borate and salicylic acid. The varnish of Ex. 3 is compatible with ethyl cellulose and chlorinated rubbers to form quick-drying lacquers. In example (5) a crude styrene mixture, 50 per cent. in xylene, was used together with the materials specified in (1) above. Fillers, e.g. .asbestos, ground cork and pigments such as titanium dioxide may be included in the reaction mass. Coating compositions may be applied to wood, metals, e.g. steel, tinplate, rubber, fabrics, paper, leather and the material known under the Registered Trade Mark " Cellophane."
GB6140/41A 1940-05-15 1941-05-12 Improvements in or relating to the manufacture of oil-soluble polystyrene resinous products Expired GB549303A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US549303XA 1940-05-15 1940-05-15
US335322A US2374316A (en) 1940-05-15 1940-05-15 Oil soluble resins

Publications (1)

Publication Number Publication Date
GB549303A true GB549303A (en) 1942-11-16

Family

ID=26733655

Family Applications (1)

Application Number Title Priority Date Filing Date
GB6140/41A Expired GB549303A (en) 1940-05-15 1941-05-12 Improvements in or relating to the manufacture of oil-soluble polystyrene resinous products

Country Status (1)

Country Link
GB (1) GB549303A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2507665A (en) * 1947-10-30 1950-05-16 Brogdex Co Protective coating compositions
US2563784A (en) * 1946-08-22 1951-08-07 Sherwin Williams Co Interpolymerization of vinyl aromatic compound and oil-modified alkyd in the presence of sulfur
US3188235A (en) * 1960-10-03 1965-06-08 Continental Can Co China-wood oil and amine resin compositions
US3544519A (en) * 1967-03-30 1970-12-01 Ici Ltd Sulfonated styrene-phenol resins

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2563784A (en) * 1946-08-22 1951-08-07 Sherwin Williams Co Interpolymerization of vinyl aromatic compound and oil-modified alkyd in the presence of sulfur
US2507665A (en) * 1947-10-30 1950-05-16 Brogdex Co Protective coating compositions
US3188235A (en) * 1960-10-03 1965-06-08 Continental Can Co China-wood oil and amine resin compositions
US3544519A (en) * 1967-03-30 1970-12-01 Ici Ltd Sulfonated styrene-phenol resins

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