GB517196A - Improvements in or relating to the production of urea-formaldehyde condensation products - Google Patents

Improvements in or relating to the production of urea-formaldehyde condensation products

Info

Publication number
GB517196A
GB517196A GB21823/38A GB2182338A GB517196A GB 517196 A GB517196 A GB 517196A GB 21823/38 A GB21823/38 A GB 21823/38A GB 2182338 A GB2182338 A GB 2182338A GB 517196 A GB517196 A GB 517196A
Authority
GB
United Kingdom
Prior art keywords
urea
condensation
formaldehyde
thiourea
products
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
GB21823/38A
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.)
ALBERT PRODUCTS Ltd
Original Assignee
ALBERT PRODUCTS 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 ALBERT PRODUCTS Ltd filed Critical ALBERT PRODUCTS Ltd
Publication of GB517196A publication Critical patent/GB517196A/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
    • C08G12/04Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
    • C08G12/10Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with acyclic compounds having the moiety X=C(—N<)2 in which X is O, S or —N
    • C08G12/12Ureas; Thioureas

Landscapes

  • 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)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

517,196. Urea-formaldehyde condensation products. ALBERT PRODUCTS, Ltd. July 22, 1938, No. 21823. Convention date, Aug. 12, 1937. [Class 2 (iii)] Urea and/or thiourea and aqueous formaldehyde are condensed in the presence of a solvent for the condensation product which is insoluble or difficultly-soluble in water so as to form an aqueous phase and a substantially non-aqueous phase containing the product. Suitable solvents are those containing a free OH group, e.g. benzyl', n-butyl and isobutyl alcohols. The yield of the product may be increased by the addition of water-soluble inorganic salts. The condensation, which may be carried out at 90-95‹C., may be commenced at a pH above 5, e.g., 6-9, and completed at ap H below 5, e.g., 3-4.5, the reaction mixture being finally neutralized and cooled ; the molecular proportions of formaldehyde to urea and/or thiourea are 1.5-2.5:1. The products are suitable for the production of lacquers, paints and moulding powders ; or impregnating and stiffening agents for fabric, and as adhesives and packing materials. In examples, urea and aqueous formaldehyde, rendered alkaline with caustic soda, are condensed in the presence of benzyl, n-butyl or isobutyl alcohol, the condensation being completed after acidification with phosphoric acid and the pH finally adjusted to 7 with caustic soda. In example (3) common salt is added to the reaction mixture, and in example (4) a mixture of urea and thiourea is employed.
GB21823/38A 1937-08-12 1938-07-22 Improvements in or relating to the production of urea-formaldehyde condensation products Expired GB517196A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE517196X 1937-08-12

Publications (1)

Publication Number Publication Date
GB517196A true GB517196A (en) 1940-01-23

Family

ID=6549496

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21823/38A Expired GB517196A (en) 1937-08-12 1938-07-22 Improvements in or relating to the production of urea-formaldehyde condensation products

Country Status (1)

Country Link
GB (1) GB517196A (en)

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