GB1095663A - Polyesterimide resins - Google Patents

Polyesterimide resins

Info

Publication number
GB1095663A
GB1095663A GB2412665A GB2412665A GB1095663A GB 1095663 A GB1095663 A GB 1095663A GB 2412665 A GB2412665 A GB 2412665A GB 2412665 A GB2412665 A GB 2412665A GB 1095663 A GB1095663 A GB 1095663A
Authority
GB
United Kingdom
Prior art keywords
glycol
ethylene glycol
surplus
excess
polycondensation
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
GB2412665A
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.)
Beck & Co Dr GmbH
Original Assignee
Beck & Co Dr GmbH
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 Beck & Co Dr GmbH filed Critical Beck & Co Dr GmbH
Publication of GB1095663A publication Critical patent/GB1095663A/en
Expired legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/303Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups H01B3/38 or H01B3/302
    • H01B3/306Polyimides or polyesterimides
    • 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
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/16Polyester-imides
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/307Other macromolecular compounds

Landscapes

  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Paints Or Removers (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

Thermosetting polyesterimides are prepared by interacting (a) a polybasic carboxylic acid having at least 3 carboxyl groups attached to an aromatic ring or a reactive derivative thereof, (b) a C2- 6 glycol and (c) a poly-primary amine or reactive derivative thereof in the presence of a surplus of the glycol at least part of the surplus being separated by distillation after polycondensation. Polybasic carboxylic acids specified are trimellitic, and pyromellitic. Terephthalic acid may also be present. Pentaerythritol is specified as a polyhydric alcohol. The polyvalent primary amine may be aromatic, e.g. 4,41-diamino-diphenylmethane. Glycols specified are ethylene glycol, propane-1,2 and 1,3-diols, butylene glycol and diethylene glycol. The reactants (a) to (c) may be used in an at least 20% solution in the glycol to give at least 1 mole surplus of glycol for every ester link in the product. The polymerization may be carried out in the presence of hydroxycarboxylic acids, aminocarboxylic acids, amino-alcohols, polyvalent primary amines containing secondary amino-groups and catalysts, e.g. tin oxalate, Sb2O3 or a titanium compound. A fractionating column may be used to ensure that water only is distilled from the system during polycondensation, the glycol being removed afterwards. In the latter case a reduced pressure may be used. Between removal of the water and removal of the glycol a mixture of pigments, e.g. TiO2, Fe2O3, talcum mica, a consolidating agent, e.g. silica gel or dimethyl di-octa-decyl ammonium montmorillonite and a glycol may be added. The product of the reaction is soluble in cresol/xylol/ aromatic hydrocarbon mixtures. It may be used for coating, e.g. wire insulation, mouldings, laminates, films, foils, spin sintering and flame-spraying. The condensed ethylene glycol may be reused as starting material. In Example (3), a condensate of aniline and formaldehyde in the presence of HCl functions both as a polyamine and as a polyhydric alcohol.ALSO:A polyesterimide useful for coating is prepared by reacting a polybasic carboxylic acid having at least 3 carboxyl groups joined to a benzene ring with a C2-6 glycol and a poly-primary amine, the glycol being present in excess and some of the excess being distilled off after polycondensation. The resin may be applied to electrical copper wiring, or woven fibres in solution or by flame spraying or spin sintered spraying. The resin may be hardened at 180 - 200 DEG C. In Examples: (1) a polymer derived from terephthalic acid, pentaerythritol, ethylene glycol, diaminodiphenylmethane and trimellitic anhydride in the presence of tin oxalate and Sb2O3 is applied to metal sheet; (2) the polymer of Example 1 dissolved in a mixture of cresol, xylol and naphtha is applied to copper wire; (3) a condensate of an aniline/formaldehyde resin, ethylene glycol and trimellitic anhydride dissolved in cycolhexane, DMF, DMA and furfuryl alcohol is used to impregnate electrical windings and (4) a polymer of trimellitic anhydride, ethylene glycol and diaminodiphenylmethane dissolved in excess ethylene glycol is also used to impregnate electrical windings.
GB2412665A 1964-06-09 1965-06-08 Polyesterimide resins Expired GB1095663A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE1964B0077166 DE1495182C3 (en) 1964-06-09 1964-06-09 Use of thermosetting polyesterimide resins for solvent-free processing

Publications (1)

Publication Number Publication Date
GB1095663A true GB1095663A (en) 1967-12-20

Family

ID=6979354

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2412665A Expired GB1095663A (en) 1964-06-09 1965-06-08 Polyesterimide resins

Country Status (6)

Country Link
AT (2) AT283548B (en)
DE (1) DE1495182C3 (en)
DK (1) DK121629B (en)
FR (1) FR1436978A (en)
GB (1) GB1095663A (en)
SE (1) SE338164B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4650839A (en) * 1986-01-23 1987-03-17 Allied Corporation Thermosettable modified phenolic imide resins
US4757118A (en) * 1986-01-23 1988-07-12 Allied Corporation Thermosettable modified phenolic polyester imide resins
US4771113A (en) * 1986-01-23 1988-09-13 Allied Corporation Thermosettable modified phenolic polyester imide resins

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3880812A (en) * 1974-01-11 1975-04-29 Standard Oil Co Poly(alkylenetrimellitate imides) and method of preparation
DE2522386C3 (en) * 1975-05-21 1984-09-27 Chemische Fabrik Dr.Wiedeking, 4152 Kempen Electrical insulating varnish
AT349113B (en) * 1976-03-25 1979-03-26 Herberts & Co Gmbh PROCESS FOR MANUFACTURING HIGH HEAT-RESISTANT INSULATING COVERINGS ON ELECTRIC LADDERS AND MEANS FOR CARRYING OUT THE PROCESS
DE3121306A1 (en) * 1981-05-29 1982-12-23 Dr. Beck & Co Ag, 2000 Hamburg METHOD FOR PRODUCING AQUEOUS HEAT-CURABLE ELECTRO-INSULATING LACQUER AND THE USE THEREOF
DE102011052518A1 (en) * 2011-08-09 2013-02-14 Elantas Gmbh Solvent-free wire enamel composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4650839A (en) * 1986-01-23 1987-03-17 Allied Corporation Thermosettable modified phenolic imide resins
US4757118A (en) * 1986-01-23 1988-07-12 Allied Corporation Thermosettable modified phenolic polyester imide resins
US4771113A (en) * 1986-01-23 1988-09-13 Allied Corporation Thermosettable modified phenolic polyester imide resins

Also Published As

Publication number Publication date
FR1436978A (en) 1966-04-29
DE1495182B2 (en) 1976-12-02
DK121629B (en) 1971-11-08
SE338164B (en) 1971-08-30
AT267186B (en) 1968-12-10
AT283548B (en) 1970-08-10
DE1495182A1 (en) 1969-08-28
DE1495182C3 (en) 1978-03-09

Similar Documents

Publication Publication Date Title
US3968135A (en) Chromium salt catalysts
US3962182A (en) Imide oxirane reactions
RU2129570C1 (en) Phosphorus-modified epoxy resin, methods of preparation and application thereof
US3428486A (en) Polyamide-imide electrical insulation
JP2002540238A (en) Esteralkylamide-condensation polymers containing acid groups
US4017429A (en) Preparation of 2-hydroxyalkyl esters
US2956613A (en) Treated glass cloth insulation making
JPS621967B2 (en)
JP2000080251A (en) Phosphorus-modified flame-retardant epoxy resin composition and its production and molded product and laminate using the phosphorus-modified flame-retardant epoxy resin composition
GB1095663A (en) Polyesterimide resins
US2953545A (en) Process for curing glycidyl polyethers and products produced thereby
TW316918B (en)
BR0008834B1 (en) metal conductor coating composition, coating process involving use thereof, use of said composition as well as coated electrical conductor.
US2884406A (en) Production of cured epoxide resins
JPH04233935A (en) Thermosetting composition for producing epoxide network structure, and manufacture and use thereof
GB1069150A (en) Improvements in or relating to the production of polyesterimide resins
US3293248A (en) Isocyanurate-trianhydride polymer
GB1046756A (en) Improvements in or relating to electrical conductors and processes for producing thesame
US3798242A (en) N,n'-diglycidyl-dicarboxylic acid dianilides
GB866402A (en) Improvements in or relating to the insulation of electrical apparatus
US3931058A (en) Polyglycidyl compounds, processes for their manufacture and use
ES2534875T3 (en) Resin compositions containing epoxy resins modified with sorbic acid
US3072737A (en) Polyglycidyl ether and electrical conductor insulated therewith
US3281495A (en) Processes for hardening polyepoxides
US3052647A (en) Heat hardenable composition comprising an alkyd resin, an epoxy polyester resin, anda dipentene:maleic acid anhydride adduct and process of preparing same