GB912902A - Amine-modified urea-formaldehyde resin and method of making same - Google Patents

Amine-modified urea-formaldehyde resin and method of making same

Info

Publication number
GB912902A
GB912902A GB875559A GB875559A GB912902A GB 912902 A GB912902 A GB 912902A GB 875559 A GB875559 A GB 875559A GB 875559 A GB875559 A GB 875559A GB 912902 A GB912902 A GB 912902A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
urea
acid
point
mixture
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
GB875559A
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.)
Kimberly Clark Tissue Co
Original Assignee
Scott Paper 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 Scott Paper Co filed Critical Scott Paper Co
Publication of GB912902A publication Critical patent/GB912902A/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)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

Abstract

Cationic amine-modified urea-formaldehyde resins are made by the acid condensation of a mixture of urea, formaldehyde and at least one polyalkylene polyamine of formula <FORM:0912902/IV(a)/1> x being one or more and n being 2 or 3, a watersoluble non-ionic aliphatic viscosity-lowering additive which is hydroxylated in aqueous solution being introduced into the reaction mixture at the point of incipient gelation thereof, and the reaction being then continued until the point of incipient gelation is again reached. Viscosity-lowering additives mentioned are formaldehyde, paraldehyde, methyl, ethyl, n-propyl, iso-propyl, or tert.-butyl alcohol, ethylene glycol, glycerine, diethylene glycol, triethylene glycol, glucose, or furfuryl alcohol. Suitable polyamines mentioned are triethylene tetramine, tetraethylene pentamine. The reaction medium may be rendered acid with diglycolic, maleic, oxalic, phthalic, acetic, phosphoric, hydrochloric or sulphuric acid. In a typical Example (1) Ammonium sulphate, urea, triethylene tetramine and 37% formaldehyde were refluxed with stirring for 10-15 minutes. Diglycolic acid was added and heating continued to the point of incipient gelation. Further formaldehyde was added and heating continued until the mixture again began to gel. This process was repeated twice and the reaction mixture was then neutralized, and diluted with water to 31% solids. The resin syrups are useful for addition to paper pulp in the beater to increase the wet strength of the treated paper.
GB875559A 1958-03-20 1959-03-13 Amine-modified urea-formaldehyde resin and method of making same Expired GB912902A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US72264258A 1958-03-20 1958-03-20

Publications (1)

Publication Number Publication Date
GB912902A true GB912902A (en) 1962-12-12

Family

ID=24902733

Family Applications (1)

Application Number Title Priority Date Filing Date
GB875559A Expired GB912902A (en) 1958-03-20 1959-03-13 Amine-modified urea-formaldehyde resin and method of making same

Country Status (2)

Country Link
BE (1) BE576866A (en)
GB (1) GB912902A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2505895A1 (en) * 1981-05-14 1982-11-19 Sandoz Sa PRECONDENSAT AND METHOD FOR IMPROVING SOLIDITY AT THE WET OF OPTICAL DYES AND DYURANTS ON SUBSTRATES CONTAINING HYDROXY GROUPS

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2505895A1 (en) * 1981-05-14 1982-11-19 Sandoz Sa PRECONDENSAT AND METHOD FOR IMPROVING SOLIDITY AT THE WET OF OPTICAL DYES AND DYURANTS ON SUBSTRATES CONTAINING HYDROXY GROUPS
US4452606A (en) * 1981-05-14 1984-06-05 Sandoz Ltd. Compositions useful for improving the fastness of dyeings on cellulosic substrates: precondensates of N-methylol compound with polyalkylene polyamine-epihalohydrin product

Also Published As

Publication number Publication date
BE576866A (en) 1959-09-19

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