GB466096A - Manufacture of aldehyde condensation products and manufacture of lacquers therewith - Google Patents

Manufacture of aldehyde condensation products and manufacture of lacquers therewith

Info

Publication number
GB466096A
GB466096A GB988537A GB988537A GB466096A GB 466096 A GB466096 A GB 466096A GB 988537 A GB988537 A GB 988537A GB 988537 A GB988537 A GB 988537A GB 466096 A GB466096 A GB 466096A
Authority
GB
United Kingdom
Prior art keywords
lacquer
formaldehyde
manufacture
hydrochloric acid
melamine
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
GB988537A
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
Priority to GB988537A priority Critical patent/GB466096A/en
Publication of GB466096A publication Critical patent/GB466096A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D161/00Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
    • C09D161/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C09D161/26Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Lacquers are prepared containing a condensation product of an aldehyde or a substance that yields an aldehyde with an aminotriazine or a derivative thereof containing at least one replaceable hydrogen atom. Suitable aminotriazines include melamine, melam, melem, melone, ammelin, ammelide, formoguanamine, 2-chloro-or 2-(p-oxyphenyl)-4-6-diamino - 1 - 3 - 5 - triazine, 2 - phenyl - 4-amino - 6 - oxy - 1 - 3 - 5 - triazine, alkyl-, aryl- and arylmelamines or the iso-derivatives of the aminotriazines. Suitable aldehydes include formaldehyde, paraformaldehyde, benaldehyde and furfurol. Other substances p capable of condensation with aldehydes to form resins such as phenols, urea, thiourea or aniline may be present in the resin-forming condensation, or performed condensates may be added to the aminotriazine condensates before or after their formation. Other substances such as dyestuffs, water-repelling agents, filling materials or softeners may be added at any time. In examples: (1) a methylolmethamine is dissolved in butyl alcohol containing hydrochloric acid and heated to yield a lacquer which may be mixed with a nitrocellulose lacquer; (2) an alcoholic solution prepared by condensing melamine and alcoholic formaldehyde in the presence of hydrochloric acid is mixed with a paste obtained by mixing nitro cellulose, tricresyl phosphate, butyl alcohol, ethyl acetate and toluene, and the mixture diluted for use as a lacquer with a mixture of toluene, alcohol and ethyl acetate; (3) formoguanamine is condensed with aqueous formaldehyde to produce a solution that may be used as a lacquer; (4) melamine is condensed with alcoholic formaldehyde in the presence of hydrochloric acid and the monoglyceride of linoleic acid to yield a solution which on dilution with benzene may be used as a lacquer. Specifications 455,008, 468,677, and 468,746 are referred to.
GB988537A 1935-10-08 1935-10-08 Manufacture of aldehyde condensation products and manufacture of lacquers therewith Expired GB466096A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB988537A GB466096A (en) 1935-10-08 1935-10-08 Manufacture of aldehyde condensation products and manufacture of lacquers therewith

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB988537A GB466096A (en) 1935-10-08 1935-10-08 Manufacture of aldehyde condensation products and manufacture of lacquers therewith

Publications (1)

Publication Number Publication Date
GB466096A true GB466096A (en) 1937-05-10

Family

ID=9880598

Family Applications (1)

Application Number Title Priority Date Filing Date
GB988537A Expired GB466096A (en) 1935-10-08 1935-10-08 Manufacture of aldehyde condensation products and manufacture of lacquers therewith

Country Status (1)

Country Link
GB (1) GB466096A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2437691A (en) * 1948-03-16 Manufacture of
US2459397A (en) * 1941-08-30 1949-01-18 American Cyanamid Co Amino aliphatic guanamines
US2474194A (en) * 1941-08-30 1949-06-21 American Cyanamid Co N-heterocyclic substituted guanamines
US4262033A (en) 1978-10-04 1981-04-14 Ciba-Geigy Corporation Process for advancing highly methylated methylolguanamines with triazines ureas or biscarbamates

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2437691A (en) * 1948-03-16 Manufacture of
US2459397A (en) * 1941-08-30 1949-01-18 American Cyanamid Co Amino aliphatic guanamines
US2474194A (en) * 1941-08-30 1949-06-21 American Cyanamid Co N-heterocyclic substituted guanamines
US4262033A (en) 1978-10-04 1981-04-14 Ciba-Geigy Corporation Process for advancing highly methylated methylolguanamines with triazines ureas or biscarbamates

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