GB753142A - Improvements in or relating to cationic urea-formaldehyde resin and process therefor - Google Patents

Improvements in or relating to cationic urea-formaldehyde resin and process therefor

Info

Publication number
GB753142A
GB753142A GB2350/54A GB235054A GB753142A GB 753142 A GB753142 A GB 753142A GB 2350/54 A GB2350/54 A GB 2350/54A GB 235054 A GB235054 A GB 235054A GB 753142 A GB753142 A GB 753142A
Authority
GB
United Kingdom
Prior art keywords
urea
formaldehyde
resin
under acid
acid conditions
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
GB2350/54A
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.)
Hercules Powder Co
Original Assignee
Hercules Powder 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 Hercules Powder Co filed Critical Hercules Powder Co
Publication of GB753142A publication Critical patent/GB753142A/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
    • C08G12/043Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with at least two compounds covered by more than one of the groups C08G12/06 - C08G12/24
    • C08G12/046Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with at least two compounds covered by more than one of the groups C08G12/06 - C08G12/24 one being 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)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

A cationic polyalkylene-polyamine modified urea-formaldehyde resin for producing paper of improved wet strength is prepared by cooling to at least 10 DEG C. an aqueous solution of the resin and separating the resulting precipitate. The resin is prepared by reacting 1.90 to 2.10 moles of formaldehyde with 0.90 mol. of urea and modifying with 3 to 30 per cent by weight, based on the urea, of a polyalkylenepolyamine of the general formula H2N(CnH2nHN)xH, where n is 2 or more and x is 2 or more, e.g. diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine and the corresponding polypropylene and polybutylene polyamines. The ingredients may be heated for a short time under alkaline conditions and then under acid conditions, or entirely under acid conditions until the required viscosity is obtained. Alternatively the urea and formaldehyde may be reacted under alkaline conditions followed by the addition of the nitrogen base and final reaction under acid conditions to the required viscosity. In an example the resin solution was cooled by the addition of ice and a viscous gummy precipitate obtained. After the separation of the resin by usual methods the filtrate may be concentrated and the urea-formaldehyde ratio adjusted, or paraformaldehyde, dimethylolurea or a concentrated formaldehyde solution added directly and then the ratio again adjusted and the modifier added. Specification 663,736 is referred to.
GB2350/54A 1953-10-12 1954-01-26 Improvements in or relating to cationic urea-formaldehyde resin and process therefor Expired GB753142A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US753142XA 1953-10-12 1953-10-12

Publications (1)

Publication Number Publication Date
GB753142A true GB753142A (en) 1956-07-18

Family

ID=22124900

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2350/54A Expired GB753142A (en) 1953-10-12 1954-01-26 Improvements in or relating to cationic urea-formaldehyde resin and process therefor

Country Status (1)

Country Link
GB (1) GB753142A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1092195B (en) * 1957-04-18 1960-11-03 Boehme Fettchemie Gmbh Process for the production of textile auxiliaries
DE1187794B (en) * 1958-11-12 1965-02-25 Basf Ag Process for the production of solution-stable, cation-active condensation products from urea, ethylene diamine and formaldehyde

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1092195B (en) * 1957-04-18 1960-11-03 Boehme Fettchemie Gmbh Process for the production of textile auxiliaries
DE1187794B (en) * 1958-11-12 1965-02-25 Basf Ag Process for the production of solution-stable, cation-active condensation products from urea, ethylene diamine and formaldehyde

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