GB278698A - Improvements in the manufacture and production of condensation products of urea and formaldehyde - Google Patents

Improvements in the manufacture and production of condensation products of urea and formaldehyde

Info

Publication number
GB278698A
GB278698A GB25475/27A GB2547527A GB278698A GB 278698 A GB278698 A GB 278698A GB 25475/27 A GB25475/27 A GB 25475/27A GB 2547527 A GB2547527 A GB 2547527A GB 278698 A GB278698 A GB 278698A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
urea
added
condensation products
condensed
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
GB25475/27A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB278698A publication Critical patent/GB278698A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08L61/22Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
    • C08L61/24Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with urea or thiourea

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

278,698. I. G. Farbenindustrie Akt.- Ges. Oct. 8, 1926, [Convention date]. Addition to 258,289. Urea-formaldehyde condensation products.-In the production of urea-formaldehyde condensation products by the process of the parent Specification, materials capable of furnishing acids during the heat treatment required for hardening are added to the condensation products prior to the hardening stage, i.e. either during or after the practically complete removal of the water. Both inorganic and organic materials may be employed, e.g. magnesium chloride and formic esters; formamide may also be used, for its hydrolysis yields ammonium formate, which becomes converted by excess formaldehyde into hexamethylenetetramine and formic acid. The modifi cation is also applicable to the process of Speci fication 288 346. in which urea and formaldehyde are first condensed in an aqueous acid solution of pH between 4 and 6, and the products then concentrated while maintaining pH between 6 and 7. According to the examples, (1) urea is condensed with formaldehyde in the presence of primary sodium phosphate: after the addition ol a mixture of secondary and tertiary sodium phosphate to reduce the pH to 6.6, the solution is partly concentrated in vacuo; formamide is then added and after the concentration has proceeded further, the viscous product is hardened in a mould by prolonged heat treatment: (2) urea and formaldehyde are condensed in the presence or a buffer mixture of sodium acetate and acetic acid: sodium acetate solution is added and the whole concentrated in vacuo; towards the end of the concentration stage, magnesium chloride is added, and the viscous end product then completely hardened by prolonged heat treatment.
GB25475/27A 1926-10-08 1927-09-27 Improvements in the manufacture and production of condensation products of urea and formaldehyde Expired GB278698A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE278698X 1926-10-08

Publications (1)

Publication Number Publication Date
GB278698A true GB278698A (en) 1928-12-27

Family

ID=6028552

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25475/27A Expired GB278698A (en) 1926-10-08 1927-09-27 Improvements in the manufacture and production of condensation products of urea and formaldehyde

Country Status (1)

Country Link
GB (1) GB278698A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2839506A (en) * 1953-11-16 1958-06-17 American Cyanamid Co Antistatic treatment for hydrophobic synthetic fiber-containing materials

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2839506A (en) * 1953-11-16 1958-06-17 American Cyanamid Co Antistatic treatment for hydrophobic synthetic fiber-containing materials

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