GB256711A - A new synthetic resin product - Google Patents

A new synthetic resin product

Info

Publication number
GB256711A
GB256711A GB1270725A GB1270725A GB256711A GB 256711 A GB256711 A GB 256711A GB 1270725 A GB1270725 A GB 1270725A GB 1270725 A GB1270725 A GB 1270725A GB 256711 A GB256711 A GB 256711A
Authority
GB
United Kingdom
Prior art keywords
urea
phenol
formaldehyde
dehydration
weight
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
GB1270725A
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.)
DAMARD LACQUER Co Ltd
Original Assignee
DAMARD LACQUER Co 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 DAMARD LACQUER Co Ltd filed Critical DAMARD LACQUER Co Ltd
Priority to GB1270725A priority Critical patent/GB256711A/en
Publication of GB256711A publication Critical patent/GB256711A/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
    • C08G14/00Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
    • C08G14/02Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
    • C08G14/04Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
    • C08G14/06Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols and monomers containing hydrogen attached to nitrogen
    • C08G14/08Ureas; Thioureas

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

256,711. Fleet, W. F., Potter, H. V., and Damard Lacquer Co., Ltd. May 15, 1925. Samples furnished. Urea-phenol-aldehyde condensation products.- Resinous compounds are prepared by condensing urea or a substitution product with aldehydes in the presence of an amount of phenol or a homologue which varies between one-third and five times the quantity of the urea. Thiourea is mentioned as a substitution product of urea, whilst formaldehyde, acetaldehyde, and furfuraldehyde are specified as aldehydes. The best results are obtained bv condensing 33<1>/3- 100 parts by weight of phenol with 20-100 parts by weight of urea and 150-313 parts by volume of a 40 per cent solution of formaldehyde. In any case, the volume of 40 per cent solution of formaldehyde employed should be X+2.5Y, where X and Y represent the weight of phenol and urea respectively employed. An accelerator such as ammonia may be present. The reacting materials are heated together, preferably at the boiling point of the mixture, for some time, and the product then dehydrated either by boiling in an open pan or by evaporation in vacuo. After dehydration in an open pan, the viscous product is soluble in such solvents as o-toluidine, pyridine, aniline, tetrachlorethane, and ethyl lactate, and can be used either in this form or in the bard resinous form in varnish manufacture or for the preparation of moulding mixtures. After dehydration in vacuo, the resulting syrup is soluble in alcohol, acetone, butyl alcohol, and methylated spirit. Either of the dehydration products can be hardened in the usual manner. Examples are given. The Provisional Specification refers also to cresol as a starting material and to caustic soda or mineral acids as accelerators.
GB1270725A 1925-05-15 1925-05-15 A new synthetic resin product Expired GB256711A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1270725A GB256711A (en) 1925-05-15 1925-05-15 A new synthetic resin product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1270725A GB256711A (en) 1925-05-15 1925-05-15 A new synthetic resin product

Publications (1)

Publication Number Publication Date
GB256711A true GB256711A (en) 1926-08-16

Family

ID=10009629

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1270725A Expired GB256711A (en) 1925-05-15 1925-05-15 A new synthetic resin product

Country Status (1)

Country Link
GB (1) GB256711A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE767062C (en) * 1937-10-30 1951-08-16 Albert Ag Chem Werke Process for the manufacture of hardened synthetic resin products
US4239881A (en) * 1978-12-27 1980-12-16 C.P. Chemical Company, Inc. Phenal-urea-formaldehyde condensation product
US4345061A (en) * 1978-12-27 1982-08-17 C.P. Chemical Co., Inc. Process for the preparation of phenol-urea-formaldehyde condensation products

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE767062C (en) * 1937-10-30 1951-08-16 Albert Ag Chem Werke Process for the manufacture of hardened synthetic resin products
US4239881A (en) * 1978-12-27 1980-12-16 C.P. Chemical Company, Inc. Phenal-urea-formaldehyde condensation product
US4345061A (en) * 1978-12-27 1982-08-17 C.P. Chemical Co., Inc. Process for the preparation of phenol-urea-formaldehyde condensation products

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