GB364304A - Improvements in and relating to resinous compositions - Google Patents

Improvements in and relating to resinous compositions

Info

Publication number
GB364304A
GB364304A GB37546/30A GB3754630A GB364304A GB 364304 A GB364304 A GB 364304A GB 37546/30 A GB37546/30 A GB 37546/30A GB 3754630 A GB3754630 A GB 3754630A GB 364304 A GB364304 A GB 364304A
Authority
GB
United Kingdom
Prior art keywords
liquid
urea
aldehyde
parts
rapidly
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
GB37546/30A
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.)
British Thomson Houston Co Ltd
Original Assignee
British Thomson Houston 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 British Thomson Houston Co Ltd filed Critical British Thomson Houston Co Ltd
Publication of GB364304A publication Critical patent/GB364304A/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)
  • Chemical And Physical Treatments For Wood And The Like (AREA)
  • Investigating Materials By The Use Of Optical Means Adapted For Particular Applications (AREA)

Abstract

Phenol-aldehyde condensation products.--A phenolaldehyde condensation product, which is permanently liquid at ordinary temperature but which solidifies on heating, is produced by condensing a phenol and an aldehyde in presence of an ethanolamine, such as mono-, di- or triethanolamine, a dispersing agent, and urea the reaction mixture being rapidly heated and subsequently rapidly cooled. As dispersing agents are mentioned alkali iodides, bromides, chlorides, nitrates and sulphates, sodium benzoate, salicylate formate and citrate, potassium tartrate and calcium chloride. The aldehyde is preferably used in the solid form, but the commercial liquid can also be used. In an example 30 parts of cresol, 18 parts of paraformaldehyde, 2 parts of triethanolamine, 1 part of potassium bromide, 0,5 part of urea and 0,5 part of guanidine carbonate are rapidly heated to 95-100 DEG C. and then rapidly chilled to room temperature. The liquid product, to which fillers may be added, is stable, but gels at 80 DEG C. in an hour and is fully hardened at 105 DEG C. or higher in 20 hours. The liquid product may be used to impregnate an article such as an electric coil, which is warmed, dipped into the cold or warmed liquid and finally heated; the impregnation may be effected in an evacuated chamber, pressure being applied after the liquid is admitted. Specification 302,609, [Class 2 (iii), Dyes &c.], is referred to. The Specification as open to inspection under Sect. 91 (3) (a) refers to guanidine carbonate as an alternative to urea and uses the expression "a urea body." This subject-matter does not appear in the Specification as accepted.ALSO:A phenol-aldehyde condensation product which is permanently liquid at ordinary temperature but which solidifies on heating, is produced by condensing a phenol such as mono-, di- or triethanolamine and an aldehyde in presence of an ethanolamine, a dispersing agent, and urea, the reaction mixture being rapidly heated and subsequently rapidly cooled. As dispersing agents are mentioned alkali iodides, bromides, chlorides, nitrates and sulphates, sodium benzoate, salicylate, formate, and citrate potassium tartrate and calcium chloride. The aldehyde is preferably used in the solid form but the commercial liquid can also be used. In an example 30 parts of cresol, 18 parts of paraformaldehyde, 2 parts of triethanolamine, 1 part of potassium bromide, 0,5 part of urea, and 0,5 part of guanidine carbonate are rapidly heated to 95-100 DEG C. and then rapidly chilled to room temperature. The liquid product to which fillers may be added is stable, but gels at 80 DEG C. in an hour and is fully hardened at 105 DEG C. or higher in 20 hours. The liquid product may be used to impregnate an article such as an electric coil, which is warmed, dipped into the cold or warmed liquid and finally heated; the impregnation may be effected in an evacuated chamber, pressure being applied after the liquid is admitted. Specification 302,609, [Class 2 (iii), Dyes &c.], is referred to. The Specification as open to inspection under Sect. 91 (3) (a) mentions guanidine carbonate as an alternative to urea, and uses the expression "a urea body." This subject-matter does not appear in the Specification as accepted.
GB37546/30A 1929-12-13 1930-12-12 Improvements in and relating to resinous compositions Expired GB364304A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US364304XA 1929-12-13 1929-12-13

Publications (1)

Publication Number Publication Date
GB364304A true GB364304A (en) 1932-01-07

Family

ID=21888565

Family Applications (1)

Application Number Title Priority Date Filing Date
GB37546/30A Expired GB364304A (en) 1929-12-13 1930-12-12 Improvements in and relating to resinous compositions

Country Status (1)

Country Link
GB (1) GB364304A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0480778A2 (en) * 1990-10-12 1992-04-15 Isover Saint-Gobain Phenolic resin, process for producing this resin, and resin composition for adhering mineral fibres
US5270434A (en) * 1990-10-12 1993-12-14 Isover Saint-Gobain Phenolic resin, procedure for preparation of the resin, and sizing composition for mineral fibers containing this resin

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0480778A2 (en) * 1990-10-12 1992-04-15 Isover Saint-Gobain Phenolic resin, process for producing this resin, and resin composition for adhering mineral fibres
FR2667865A1 (en) * 1990-10-12 1992-04-17 Saint Gobain Isover PHENOLIC RESIN, PROCESS FOR PREPARING THE RESIN AND COMPOSITION FOR THE SIZING OF MINERAL FIBERS CONTAINING THE SAME.
EP0480778A3 (en) * 1990-10-12 1993-09-01 Isover Saint-Gobain Phenolic resin, process for producing this resin, and resin composition for adhering mineral fibres
US5270434A (en) * 1990-10-12 1993-12-14 Isover Saint-Gobain Phenolic resin, procedure for preparation of the resin, and sizing composition for mineral fibers containing this resin

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