GB641703A - Manufacture of unpolymerized urea-formaldehyde reaction products - Google Patents

Manufacture of unpolymerized urea-formaldehyde reaction products

Info

Publication number
GB641703A
GB641703A GB6870/48A GB687048A GB641703A GB 641703 A GB641703 A GB 641703A GB 6870/48 A GB6870/48 A GB 6870/48A GB 687048 A GB687048 A GB 687048A GB 641703 A GB641703 A GB 641703A
Authority
GB
United Kingdom
Prior art keywords
urea
formaldehyde
temperature
liquid
proportion
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
GB6870/48A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB641703A publication Critical patent/GB641703A/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)
  • Chemical And Physical Treatments For Wood And The Like (AREA)

Abstract

Liquid urea-formaldehyde compositions are made by admixing a liquid mixture of formaldehyde and water containing from 50-70 per cent of formaldehyde by weight, the temperature of said liquid having been maintained above 45 DEG C. since its preparation, with urea at a pH of 7-9, in the proportion of one molecule of urea per 3.9-10 molecules of formaldehyde and maintaining the temperature of the resulting liquid at least momentarily at from 70-90 DEG C. The proportion of formaldehyde to urea is preferably from 4.5 : 1 to 7.0 : 1, and most preferred at 6.0 : 1. Additional amounts of urea may be added subsequently to reduce the formaldehyde-urea ratio to not less than 3.9 : 1, the temperature being preferably lowered below 50 DEG C. prior to the second addition of urea. The formaldehyde solution may be prepared by liquefying a gaseous formaldehyde-watervapour mixture of corresponding composition having a temperature above 90 by cooling to 60-90 DEG C. The compositions obtained may be used for impregnating lignocellulosic and cellulosic materials, e.g. wood, and in the manufacture of lacquers, moulded products and finishes. Further additions of urea may be made immediately before such use. The pH is preferably adjusted by the use of buffer mixtures, e.g. phosphoric acid or boric acid and sodium hydroxide. Examples are given, giving details of procedures carried out in accordance with the above.ALSO:Liquid urea-formaldehyde compositions are made by admixing a liquid mixture of formaldehyde and water containing from 50-70 per cent of formaldehyde by weight, the temperature of said liquid having been maintained above 45 DEG C. since its preparation, with urea at a pH of 7-9, in the proportion of one molecule of urea per 3.9-10 molecules of formaldehyde and maintaining the temperature of the resulting liquid at least momentarily at from 70-90 DEG C. The proportion of formaldehyde to urea is preferably from 4.5 : 1 to 7.0 : 1, and most preferred at 6.0 : 1. Additional amounts of urea may be added subsequently to reduce the formaldehyde-urea ratio to not less than 3.9 : 1, the temperature being preferably lowered below 50 DEG C. prior to the second addition of urea. The formaldehyde solution may be prepared by liquefying a gaseous formaldehyde-water-vapour mixture of corresponding composition having a temperature above 90 by cooling to 60-90 DEG C. The compositions obtained may be used for impregnating lignocellulosic and cellulosic materials, e.g. wood, and in the manufacture of lacquers, moulded products, and finishes. Further additions of urea may be made immediately before such use. The pH is preferably adjusted by the use of buffer mixtures, e.g. phosphoric acid or boric acid and sodium hydroxide. Examples are given, giving details of procedures carried out in accordance with the above.
GB6870/48A 1947-03-06 1948-03-05 Manufacture of unpolymerized urea-formaldehyde reaction products Expired GB641703A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US641703XA 1947-03-06 1947-03-06

Publications (1)

Publication Number Publication Date
GB641703A true GB641703A (en) 1950-08-16

Family

ID=22054037

Family Applications (1)

Application Number Title Priority Date Filing Date
GB6870/48A Expired GB641703A (en) 1947-03-06 1948-03-05 Manufacture of unpolymerized urea-formaldehyde reaction products

Country Status (1)

Country Link
GB (1) GB641703A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1239290B (en) * 1957-10-30 1967-04-27 Montedison Spa Continuous process for the production of concentrated permanent aqueous solutions of urea, formaldehyde and urea-formaldehyde condensation products

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1239290B (en) * 1957-10-30 1967-04-27 Montedison Spa Continuous process for the production of concentrated permanent aqueous solutions of urea, formaldehyde and urea-formaldehyde condensation products

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