GB972988A - Epoxy resin compositions - Google Patents

Epoxy resin compositions

Info

Publication number
GB972988A
GB972988A GB4324260A GB4324260A GB972988A GB 972988 A GB972988 A GB 972988A GB 4324260 A GB4324260 A GB 4324260A GB 4324260 A GB4324260 A GB 4324260A GB 972988 A GB972988 A GB 972988A
Authority
GB
United Kingdom
Prior art keywords
ketone
diamine
methyl
diimine
isobutyl ketone
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
GB4324260A
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.)
Rohm and Haas Co
Original Assignee
Rohm and Haas Co
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 Rohm and Haas Co filed Critical Rohm and Haas Co
Publication of GB972988A publication Critical patent/GB972988A/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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/4007Curing agents not provided for by the groups C08G59/42 - C08G59/66
    • C08G59/4014Nitrogen containing compounds
    • C08G59/4042Imines; Imides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Epoxy Resins (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

Abstract

Polyimines containing a plurality of imine groups, each N atom of which is joined to two aliphatic or cycloaliphatic carbon atoms one by a single bond and the other by a double bond are prepared by condensing a polyamine with a ketone, if desired in presence of a solvent which may be excess ketone or may be an azeotroping solvent to facilitate removal of water. A catalyst, e.g. iodine or HCl may be used. When using acetone, the polyamine is dissolved in excess acetone and the solution left to stand with HCl as a catalyst. Suitable amines are 1,2,3-triaminopropane; tetrakis (aminomethyl) methane; 1,2-ethylene diamine; 1,2, or 1,3-propylene diamine; 1,4-butylene diamine; 1,5-pentylene diamine; 1,6-hexylene diamineo; 1,8-octylene diamine; m-xylyene diamine; 1,2-diaminocyclohexane; and amines of formula <FORM:0972988/C1/1> in which R1 is a divalent hydrocarbon radical forming part of a cycloalkylene, bicycloalkylene or benzocycloalkylene radical. Suitable ketones are acetone; methyl isobutyl ketone; methyl ethyl ketone; di-isobutyl ketone; methyl benzyl ketone; cyclohexanone; methyl cyclohexyl ketone; cyclopentanone; methyl octyl ketone; methyl decyl ketone. In Example A 1,6-hexane diamine and methyl isobutyl ketone were refluxed in benzene with a water separator. The di-imine boiled at 126 DEG C. at 0.2 mm Hg. Example B describes the preparation of the diimine from m-xylylene diamine and methyl isobutyl ketone. Specifications 518,057, 579,698, 598,447, 853,619 905,725 and U.S.A. Specifications 2,324,483, 2,444,333, 2,606,810, 2,607,754, 2,730,427, 2,752,269, 2,828,313, 2,850,532 are referred to.ALSO:A composition of an epoxy resin and a liquid polyimines latent curing agent which has a plurality of imine groups, each N of which is joined to two aliphatic or cycloaliphatic carbon atoms-one by a single and the other by a double bond, is cured by treatment with water which hydrolyses the polyimine to form amine groups. The polyimines may be made by reaction of a polyamine with a ketone. Any epoxy resin may be used provided it has more than epoxy group per molecule. Many are listed in the Specification. Conventional additives, e.g. pigments, other film-forming materials may be included. In Examples (1), (2), (4) a diimine from hexamethylene diamine and methyl isobutyl ketone is used together with moisture to cure a condensate from epichlorohydrin and bis-(4 hydroxyphenyl)-2, 21-propane. Curing may be at room temperature or in an oven with a humid atmosphere. If desired a condensate of ethylene or butylene glycol with epichloro hydrin may be used alone or together with the first condensate referred to. (3) The latent curing agent is prepared from methyl isobutyl ketone and ethylene diamine. (5) A diimine from methyl isobutyl ketone and xylylene diamine is used to cure the diglycidyl ether of butylene glycol. (6) A diimine from cyclohexanone and hexaethylene diamine or from methylethyl ketone and hexamethylene diamine is used to cure a diglycidyl ether condensate of bis- (4 hydroxyphenyl)-2, 2-propane. (7) A diimine from ethyl isopropyl ketone or methyl isopropyl ketone and tetramethylene diamine is used to cure a copolymer of glycidyl methacrylate and ethyl acrylate in a mono-n-butyl ether of diethylene glycol/ethyl acetate mixture. Specifications 518,057, 579,698, 595,447, 853,619, 905,725 and U.S.A. Specification 2,324,483, 2,444,333, 2,606,810, 2,607,754, 2,730,427, 2,752,269, 2,828,313 and 2,850,532 are referred to.
GB4324260A 1960-01-12 1960-12-15 Epoxy resin compositions Expired GB972988A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US187960A 1960-01-12 1960-01-12

Publications (1)

Publication Number Publication Date
GB972988A true GB972988A (en) 1964-10-21

Family

ID=21698243

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4324260A Expired GB972988A (en) 1960-01-12 1960-12-15 Epoxy resin compositions

Country Status (3)

Country Link
BE (1) BE599022A (en)
GB (1) GB972988A (en)
NL (1) NL259945A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4391958A (en) 1980-11-28 1983-07-05 Takeda Chemical Industries, Ltd. Aldimines and ketimines of 1,3,5-(aminomethyl)benzene or cyclohexane and their use as curing agents for epoxy and poylurethane resins
WO2002062908A2 (en) * 2001-02-02 2002-08-15 Battelle Memorial Institute Single component room temperature curable low voc epoxy coatings
CN103524716A (en) * 2013-08-31 2014-01-22 苏州保力瑞生物材料科技开发有限公司 Ketimine and preparation method thereof
WO2013135378A3 (en) * 2012-03-14 2014-07-24 Kienle + Spiess Gmbh Stack of laminations and method for the production thereof
CN109574874A (en) * 2018-02-04 2019-04-05 山东富源新材料技术有限公司 A kind of benzaldehyde and its latent solid agent of derivative imines
CN109734624A (en) * 2018-02-12 2019-05-10 济南大学 Latent solid agent of one kind and its preparation method and application
CN109734858A (en) * 2019-01-21 2019-05-10 济南大学 A kind of Novel submarine consolidates agent and its preparation method and application
US20200247937A1 (en) * 2018-09-06 2020-08-06 Mallinda Anhydrous routes to highly processable covalent network polymers and blends

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4391958A (en) 1980-11-28 1983-07-05 Takeda Chemical Industries, Ltd. Aldimines and ketimines of 1,3,5-(aminomethyl)benzene or cyclohexane and their use as curing agents for epoxy and poylurethane resins
WO2002062908A2 (en) * 2001-02-02 2002-08-15 Battelle Memorial Institute Single component room temperature curable low voc epoxy coatings
WO2002062908A3 (en) * 2001-02-02 2002-09-26 Battelle Memorial Institute Single component room temperature curable low voc epoxy coatings
US6649673B2 (en) 2001-02-02 2003-11-18 Battelle Memorial Institute Single component room temperature curable low VOC epoxy coatings
CN104508955A (en) * 2012-03-14 2015-04-08 金勒+施皮斯有限公司 Stack of laminations and method for the production thereof
WO2013135378A3 (en) * 2012-03-14 2014-07-24 Kienle + Spiess Gmbh Stack of laminations and method for the production thereof
US9531223B2 (en) 2012-03-14 2016-12-27 Kienle + Spiess Gmbh Method for manufacturing stack of laminations
US11476739B2 (en) 2012-03-14 2022-10-18 Kienle + Spiess Gmbh Method for the production of a stack of laminations
CN103524716A (en) * 2013-08-31 2014-01-22 苏州保力瑞生物材料科技开发有限公司 Ketimine and preparation method thereof
CN103524716B (en) * 2013-08-31 2016-02-03 苏州保力瑞生物材料科技开发有限公司 A kind of ketoimine and preparation method thereof
CN109574874A (en) * 2018-02-04 2019-04-05 山东富源新材料技术有限公司 A kind of benzaldehyde and its latent solid agent of derivative imines
CN109734624A (en) * 2018-02-12 2019-05-10 济南大学 Latent solid agent of one kind and its preparation method and application
US20200247937A1 (en) * 2018-09-06 2020-08-06 Mallinda Anhydrous routes to highly processable covalent network polymers and blends
US11530288B2 (en) * 2018-09-06 2022-12-20 Mallinda Anhydrous routes to highly processable covalent network polymers and blends
CN109734858A (en) * 2019-01-21 2019-05-10 济南大学 A kind of Novel submarine consolidates agent and its preparation method and application

Also Published As

Publication number Publication date
NL259945A (en)
BE599022A (en)

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