GB972988A - Epoxy resin compositions - Google Patents
Epoxy resin compositionsInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates 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
- C08G59/18—Macromolecules 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
- C08G59/40—Macromolecules 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
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4014—Nitrogen containing compounds
- C08G59/4042—Imines; 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.
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)
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 |
-
0
- BE BE599022D patent/BE599022A/xx unknown
- NL NL259945D patent/NL259945A/xx unknown
-
1960
- 1960-12-15 GB GB4324260A patent/GB972988A/en not_active Expired
Cited By (15)
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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