GB616463A - An improved process for preparing urea formaldehyde lacquer compositions - Google Patents

An improved process for preparing urea formaldehyde lacquer compositions

Info

Publication number
GB616463A
GB616463A GB2657546A GB2657546A GB616463A GB 616463 A GB616463 A GB 616463A GB 2657546 A GB2657546 A GB 2657546A GB 2657546 A GB2657546 A GB 2657546A GB 616463 A GB616463 A GB 616463A
Authority
GB
United Kingdom
Prior art keywords
urea
solvent
water
formaldehyde
alcohol
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
GB2657546A
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.)
REGINALD WILLIAM HENRY WICKING
British Resin Products Ltd
Original Assignee
REGINALD WILLIAM HENRY WICKING
British Resin 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 REGINALD WILLIAM HENRY WICKING, British Resin Products Ltd filed Critical REGINALD WILLIAM HENRY WICKING
Priority to GB2657546A priority Critical patent/GB616463A/en
Publication of GB616463A publication Critical patent/GB616463A/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
    • C08G12/40Chemically modified polycondensates
    • C08G12/42Chemically modified polycondensates by etherifying
    • C08G12/421Chemically modified polycondensates by etherifying of polycondensates based on acyclic or carbocyclic compounds
    • C08G12/422Chemically modified polycondensates by etherifying of polycondensates based on acyclic or carbocyclic compounds based on urea or thiourea

Landscapes

  • Chemical & Material Sciences (AREA)
  • General 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

Coating compositions are prepared by reacting urea with at least 2.7 mols. of formaldehyde per mol. of urea in an aqueous alkaline solution, distilling off most of the water under reduced pressure, then acidifying the mixture and adding a monohydric aliphatic alcohol having four or more carbon atoms or benzyl alcohol or a lower homologue thereof and a solvent inert to the reactants, but which on distillation will entrain alcohol and water to give a two-phase condensate, the amounts added being no more than will yield a product of the desired concentration, then distilling at atmospheric pressure, with separation of the aqueous and solvent phases of the condensate and recycling of the solvent only, until substantially all water is removed. Urea may be partly replaced by thiourea, melamine and their derivatives. Formaldehyde may be used as aqueous solution or as substances which will liberate formaldehyde under the reaction conditions, e.g. paraformaldehyde or hexamethylenetetramine. There are also specified: alkalis-ammonium, sodium and potassium hydroxides and sodium carbonate; alcohols-butyl, amyl, hexyl, octyl, benzyl and mixtures thereof; inert solvents-benzene, toluene, xylene; acids-phthalic anhydride and oxalic, sulphuric and phosphoric acids. There may also be added during the etherification stage minor proportions of methanol, ethanol or n- or iso-propanol or of other resins or resin-forming ingredients, e.g. alkyd resins.
GB2657546A 1946-09-04 1946-09-04 An improved process for preparing urea formaldehyde lacquer compositions Expired GB616463A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2657546A GB616463A (en) 1946-09-04 1946-09-04 An improved process for preparing urea formaldehyde lacquer compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2657546A GB616463A (en) 1946-09-04 1946-09-04 An improved process for preparing urea formaldehyde lacquer compositions

Publications (1)

Publication Number Publication Date
GB616463A true GB616463A (en) 1949-01-21

Family

ID=10245792

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2657546A Expired GB616463A (en) 1946-09-04 1946-09-04 An improved process for preparing urea formaldehyde lacquer compositions

Country Status (1)

Country Link
GB (1) GB616463A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2670341A (en) * 1951-10-19 1954-02-23 Allied Chem & Dye Corp Production of alcohol-modified urea-formaldehyde resins

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2670341A (en) * 1951-10-19 1954-02-23 Allied Chem & Dye Corp Production of alcohol-modified urea-formaldehyde resins

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