GB528479A - A process for the manufacture of resinous condensation products - Google Patents

A process for the manufacture of resinous condensation products

Info

Publication number
GB528479A
GB528479A GB1373639A GB1373639A GB528479A GB 528479 A GB528479 A GB 528479A GB 1373639 A GB1373639 A GB 1373639A GB 1373639 A GB1373639 A GB 1373639A GB 528479 A GB528479 A GB 528479A
Authority
GB
United Kingdom
Prior art keywords
urea
butanol
mols
formaldehyde
gram
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
GB1373639A
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.)
Beck Koller and Company England Ltd
Original Assignee
Beck Koller and Company England 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
Application filed by Beck Koller and Company England Ltd filed Critical Beck Koller and Company England Ltd
Priority to GB1373639A priority Critical patent/GB528479A/en
Publication of GB528479A publication Critical patent/GB528479A/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
    • C08G12/40Chemically modified polycondensates
    • C08G12/42Chemically modified polycondensates by etherifying
    • C08G12/421Chemically modified polycondensates by etherifying of polycondensates based on acyclic or carbocyclic compounds
    • C08G12/422Chemically modified polycondensates by etherifying of polycondensates based on acyclic or carbocyclic compounds based on urea or thiourea

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)

Abstract

528,479. Urea-formaldehyde condensation products. BECK, KOLLER & CO. (ENGLAND), Ltd., (Hodgins, T. S., and Hovey, A. G.). May 8, 1939, Nos. 13736 and 28137. [Class 2 (iii)] Urea-formaldehyde condensation products, suitable for use in preparing coating compositions, are prepared by condensing aqueous formaldehyde with urea in the presence of butanol, undersuperatmospheric pressures reflux, a temperature of 100‹C. and initial pH between 8 and 9, in presence of an alkaline-reacting catalyst, and thereafter further condensing by heating in an acid medium, until the nitrogen content is approximately 18 per cent., at least 2¢ mols. formaldehyde and 3 mols. butanol per mol. urea being employed. In examples : (1) urea 24 gram mols. aqueous formaldehyde, 7.2 gram mols. butanol and 8 gram mols. urea, together with a little ammonia, giving pH between 8 and 9 are heated to 100‹C. in one hour and maintained for about 1 hour under 2 atmospheres pressure ; further butanol, making a total of 24 gram molecules is then added and the reaction completed in an acid medium either under vacuum or atmospheric pressure (2) urea, aqueous formaldehyde and butanol in molecular ratios 1:3:3 are worked up with potassium hydroxide, under reflux, then acidified with phosphoric acid and the reaction completed by distilling off the azeotrope of butanol and water. The products are soluble in alcohols, ketones, aromatic hydrocarbons and tolerate straight-chain aliphatic hydrocarbons, and are compatible with oil modified alkyd resins. Specifications 256,248, 261,029, 309,849, 327,673, [all in Class 2 (iii)], 344,626, 442,054, 484,200, 491,857, 494,700 and 511,087 U.S.A. Specification 2,108,113 and Re-issue 19463, and German Specification 403,645 are referred to.
GB1373639A 1939-05-08 1939-05-08 A process for the manufacture of resinous condensation products Expired GB528479A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1373639A GB528479A (en) 1939-05-08 1939-05-08 A process for the manufacture of resinous condensation products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1373639A GB528479A (en) 1939-05-08 1939-05-08 A process for the manufacture of resinous condensation products

Publications (1)

Publication Number Publication Date
GB528479A true GB528479A (en) 1940-10-30

Family

ID=10028425

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1373639A Expired GB528479A (en) 1939-05-08 1939-05-08 A process for the manufacture of resinous condensation products

Country Status (1)

Country Link
GB (1) GB528479A (en)

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