GB923773A - Improvements in or relating to hardened epoxy resins - Google Patents
Improvements in or relating to hardened epoxy resinsInfo
- Publication number
- GB923773A GB923773A GB2674760A GB2674760A GB923773A GB 923773 A GB923773 A GB 923773A GB 2674760 A GB2674760 A GB 2674760A GB 2674760 A GB2674760 A GB 2674760A GB 923773 A GB923773 A GB 923773A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mol
- alcohol
- specified
- mols
- butanol
- 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
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4223—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof aromatic
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)
- Polyesters Or Polycarbonates (AREA)
Abstract
In examples iron sheets are coated with solutions of an epoxy-resin derived from p,p1-diphenylol-2,2-propane and epichlorhydrin and partial esters of 1 mol. pyromellitic acid dianhydride with (1) 2 mols. n-butanol, (2) 2 mols. of b -ethylhexanol, (3) 1 mol. n-dodecyl alcohol, and (5) as (1). Solvents used are butanol/xylene, and acetone/butanone/xylene. After the solvent is evaporated off the coated sheet is fired at 22 DEG C. for 1 hour.ALSO:Epoxy compounds containing more than one epoxy group per molecule are mixed with the partial ester formed (see Group IV(b)) from a tribasic to hexabasic benzene carboxylic acid or the anhydride thereof and a monohydric alcohol, the partial ester having at least two free carboxyl groups per molecule, and are heated at 100-300 DEG C. to form a hardened resin. Acids specified are trimellitic, trimesic, pyromellitic, benzene pentacarboxylic, and mellitic, and anyhdrides thereof. Alcohols specified are methanol, ethanol, propanols, butanols, pentanols, octanols, dodecanols and oleyl alcohol. Epoxy compounds specified are bisphenol A or polycarboxylic acid/epichlorohydrin condensates. Solvents specified are butanol, xylene, butanone, acetone, and mixtures thereof.ALSO:Partial esters, having at least two free carboxyl groups per molecule, are formed from a trisbasic to hexabasic benzene carboxylic acid or the anhydride thereof and a monohydric alcohol. Acids specified are trimellitic, trimesic, pyromellitic, benzene pentacarboxylic and mellitic and anhydrides thereof. Alcohols specified are methanol, ethanol, propanols, butanols, pentanols, octanols, dodecanols and oleyl alcohol. The reaction is carried out with the appropriate quantity of, and at the boiling temperature of, the appropriate alcohol; if necessary, under pressure. The following reactions were carried out in the examples:-1 mol pyromellitic dianhydride and (1) 2 mols n-butanol, (2) 2 mols b -ethylhexanol, (3) 1 mol n-dodecyl alcohol in the presence of methylethyl and methyl isobutyl ketones, and (4) 1 mol n-dodecyl alcohol, (6) 1 mol trimellitic anhydride and 1 mol n-dodecyl alcohol in the presence of acetone and methyl isobutyl ketone.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB54561A DE1115014B (en) | 1959-08-26 | 1959-08-26 | Process for hardening synthetic resins containing epoxy groups |
Publications (1)
Publication Number | Publication Date |
---|---|
GB923773A true GB923773A (en) | 1963-04-18 |
Family
ID=6970654
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2674760A Expired GB923773A (en) | 1959-08-26 | 1960-08-02 | Improvements in or relating to hardened epoxy resins |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE593934A (en) |
CH (1) | CH413384A (en) |
DE (1) | DE1115014B (en) |
GB (1) | GB923773A (en) |
NL (1) | NL254978A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0050940A1 (en) * | 1980-10-27 | 1982-05-05 | Imperial Chemical Industries Plc | Process of coating using mixed solutions of an epoxy resin and of acid anhydride curing agents |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4527145B2 (en) * | 2007-11-12 | 2010-08-18 | 三菱電機株式会社 | Electric power steering motor |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL79847C (en) * | 1949-08-12 | |||
DE1055812B (en) * | 1955-02-14 | 1959-04-23 | Bergwerksverband Gmbh | Process for the production of polyesters from tri- and polybasic carboxylic acids |
DE1032351B (en) * | 1955-09-26 | 1958-06-19 | Licentia Gmbh | Conductor insulation made from a cast resin based on epoxy resin, especially for winding insulation in electrical machines |
DE1033407B (en) * | 1957-03-12 | 1958-07-03 | Basf Ag | Process for hardening glycidyl polyethers |
DE1040783B (en) * | 1957-09-07 | 1958-10-09 | Henkel & Cie Gmbh | Process for the production of hardened plastics based on polyesters and epoxy compounds |
DE1054705B (en) * | 1958-01-20 | 1959-04-09 | Leuna Werke Veb | Process for optionally multi-stage curing of epoxy resins |
-
0
- BE BE593934D patent/BE593934A/xx unknown
- NL NL254978D patent/NL254978A/xx unknown
-
1959
- 1959-08-26 DE DEB54561A patent/DE1115014B/en active Pending
-
1960
- 1960-07-29 CH CH872260A patent/CH413384A/en unknown
- 1960-08-02 GB GB2674760A patent/GB923773A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0050940A1 (en) * | 1980-10-27 | 1982-05-05 | Imperial Chemical Industries Plc | Process of coating using mixed solutions of an epoxy resin and of acid anhydride curing agents |
Also Published As
Publication number | Publication date |
---|---|
BE593934A (en) | |
CH413384A (en) | 1966-05-15 |
NL254978A (en) | |
DE1115014B (en) | 1961-10-12 |
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