GB302737A - Manufacture of artificial resins - Google Patents

Manufacture of artificial resins

Info

Publication number
GB302737A
GB302737A GB37806/28A GB3780628A GB302737A GB 302737 A GB302737 A GB 302737A GB 37806/28 A GB37806/28 A GB 37806/28A GB 3780628 A GB3780628 A GB 3780628A GB 302737 A GB302737 A GB 302737A
Authority
GB
United Kingdom
Prior art keywords
urea
formaldehyde
phenol
derivatives
alcohol
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
GB37806/28A
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.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB302737A publication Critical patent/GB302737A/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
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes

Abstract

302,737. Soc. of Chemical Industry in Baste. Dec. 21, 1927, [Convention date]. Urea-formaldehyde condensation products.- Water-insoluble resins are produced by adding to a urea-formaldehyde reaction mixture before or at any stage in the condensation, in an alkaline medium, a substance capable of forming with formaldehyde or its condensation products with urea or its derivatives in presence of OH ions a water-insoluble resin, and then further heating until on cooling or mixing with water, a waterinsoluble resin separates. The additional substances mentioned are aromatic amines such as aniline and naphthylamine and their derivatives such as anhydroformaldehydeaniline, substituted ureas or urea derivatives such as thiourea and phenyl urea, cyanamide and its derivatives such as dicyandiamide, urea, acid amides of high molecular weight such as biuret, mono- and polyhydric phenols such as phenol, resorcinol, naphthol, pyrogallol and its derivatives such as tannin, phenol-formaldehyde condensation products, and sulphurized phenol resins. For use in Jacquers, the products may be separated at a stage where they are soluble in alcohol. If the agents added are not sufficiently soluble, organic solvents such as alcohol or acetone may be added. The resins may be hardened in alkaline mediums and are therefore suitable for use with basic pigments such as zinc white, white lead, ferric oxide &c. and for application upon basic materials. In the examples, (1) urea, phenyl-urea, and formaldehvde are mixed with caustic soda solution and boiled for 4 hours, the resin being precipitated by water; (2) urea, thiourea, and formaldehyde are heated with caustic soda solution; (3) urea is dissolved in 40 per cent formaldehyde and the solution clarified by active carbon; it is then heated to 100‹ C. until a sample yields a milky precipitate on treatment with water, and it is then boiled with (i) phenyl urea, thiourea, or aniline and caustic soda, (ii) dicyandiamide and ammonia, (iii) urea, biuret, anhydroformaldehydeaniline or #-naphthylamine and caustic soda, (iv) phenol and hexamethylene tetramine, (v) soluble phenol-formaldehyde condensation product, alcohol, and caustic soda, (vi) liquid sulphurized phenol resin, alcohol, and ethylene-diamine, (vii) #-naphthol, alcohol and hexamethylene-tetramine.
GB37806/28A 1927-12-21 1928-12-21 Manufacture of artificial resins Expired GB302737A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH302737X 1927-12-21

Publications (1)

Publication Number Publication Date
GB302737A true GB302737A (en) 1930-01-23

Family

ID=4491480

Family Applications (1)

Application Number Title Priority Date Filing Date
GB37806/28A Expired GB302737A (en) 1927-12-21 1928-12-21 Manufacture of artificial resins

Country Status (1)

Country Link
GB (1) GB302737A (en)

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