GB543096A - Improved resinous condensation products and methods of producing same - Google Patents

Improved resinous condensation products and methods of producing same

Info

Publication number
GB543096A
GB543096A GB12632/40A GB1263240A GB543096A GB 543096 A GB543096 A GB 543096A GB 12632/40 A GB12632/40 A GB 12632/40A GB 1263240 A GB1263240 A GB 1263240A GB 543096 A GB543096 A GB 543096A
Authority
GB
United Kingdom
Prior art keywords
condensation products
aldehyde
products
resins
condensation
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
GB12632/40A
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 GB543096A publication Critical patent/GB543096A/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
    • 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
    • C08G12/22Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with carboxylic acid amides
    • 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

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)

Abstract

543,096. Resinous condensation products ; proofing permeable materials. BRITISH THOMSON-HOUSTON CO., Ltd. Aug. 6, 1940, No. 12632. Convention date, Aug. 10, 1939. [Class 2 (iii)] [Also in Group VIII] Resinous condensation products are prepared by heating together an aliphatic aldehyde and a diamide of an unsaturated dicarboxylic acid containing a CH 2 =C # grouping and in which the carboxyl groups are attached to different carbon atoms. Specified diamides are itaconic diamide, methyl itaconic diamide and glutaric diamide, and the condensation may be carried out under acid, alkaline or neutral conditions. Inter-condensates may be produced by adding other aliphatic-aldehyde-reactable organic compounds capable of forming a methylol derivative as an intermediate during the resin formation, e.g. urea, phenols or acetone. The products may be used alone, or mixed with fillers, pigments, dyes or lubricants, as moulding compositions. The liquid condensates may be used in the production of paints, varnishes, lacquers or enamels, and as adhesives. The products may also be used as fire-retardants and water-repellents when applied to wood or to fabrics. Examples are given of the preparation of resinous condensates from itaconic diamide and formaldehyde, with or without phenol or urea. Curing catalysts may be incorporated with the condensates, or self-curing characteristics may be imparted to the resins by inter-condensing into the initial condensation products such substances as chloroacetamide, mono-chloroacetyl urea, chloroacetonitrile, chloral hydrate, chloroacetone, nitrourea, sodium nitrourea, methylene diamino monohydrochloride, aminoacetamide hydrochloride and diethanolamine hydrochloride. The resins of this invention may be modified by introducing before, during or after condensation, partially hydrolysed wood products, lignin, proteins, protein-aldehyde condensation products, phenol-aldehyde condensation products, aniline-aldehyde condensation products, furfural condensation products, alkyd resins, sulphonamide-aldehyde resins, water-soluble cellulose derivatives, natural gums and resins such as copal, shellac or rosin, polyvinyl compounds and super-polyamides. Specified optional additions to the condensation products are alpha cellulose flock, barium sulphate, zinc sulphide, titanium oxides, flaked aluminium or copper, stearates or palmitates of tin and zinc, and waxes such as carnauba and paraffin wax. An example is given of the preparation of a laminated article by dipping paper sheets into an acidified condensation syrup, drying at 80‹ C., superposing the sheets, and beating under pressure. Specifications 519,349 and 542,513 are referred to.
GB12632/40A 1939-08-10 1940-08-06 Improved resinous condensation products and methods of producing same Expired GB543096A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US543096XA 1939-08-10 1939-08-10

Publications (1)

Publication Number Publication Date
GB543096A true GB543096A (en) 1942-02-10

Family

ID=21990173

Family Applications (1)

Application Number Title Priority Date Filing Date
GB12632/40A Expired GB543096A (en) 1939-08-10 1940-08-06 Improved resinous condensation products and methods of producing same

Country Status (1)

Country Link
GB (1) GB543096A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4429075A (en) 1982-05-17 1984-01-31 Chem-Nuclear Systems, Inc. Cross-linked urea-formaldehyde polymer matrix compositions containing cyclic intermediate structures
US4499200A (en) * 1982-05-17 1985-02-12 Chem-Nuclear Systems, Inc. Compound catalyst system usable for the polymerization or curing of urea-formaldehyde polymeric condensation systems

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4429075A (en) 1982-05-17 1984-01-31 Chem-Nuclear Systems, Inc. Cross-linked urea-formaldehyde polymer matrix compositions containing cyclic intermediate structures
US4499200A (en) * 1982-05-17 1985-02-12 Chem-Nuclear Systems, Inc. Compound catalyst system usable for the polymerization or curing of urea-formaldehyde polymeric condensation systems

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