GB806195A - Improvements in or relating to the hardening of epoxy resins - Google Patents
Improvements in or relating to the hardening of epoxy resinsInfo
- Publication number
- GB806195A GB806195A GB2430755A GB2430755A GB806195A GB 806195 A GB806195 A GB 806195A GB 2430755 A GB2430755 A GB 2430755A GB 2430755 A GB2430755 A GB 2430755A GB 806195 A GB806195 A GB 806195A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- polyamine
- acids
- ethyl
- mol
- 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
- C08G59/50—Amines
- C08G59/54—Amino amides>
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
Abstract
Epoxide resins are cured by heating the epoxy resin with a liquid condensation product of an aliphatic polyamine and a saturated aliphatic monocarboxylic acid or corresponding amino acid, containing 2-10 carbon atoms in the molecule, the condensate containing free amino groups and being obtained by mixing the polyamine and acid in proportions of at least one mol. polyamine per mol. acid and heating the mixture to first remove the elements of water and then further under reduced pressure to remove residual polyamine. Acids specified are acetic, propionic, butyric, valeric, caproic, enanthic, caprylic, pelargonic, capric, 2-ethyl hexoic, amino-caproic; their acid halides or alcoholic esters may also be used; dicarboxylic acids may be present in minor amounts. 2 mols. triethylene tetramine and 1 mol. 2-ethyl hexoic acid were heated to 235 DEG C. in an atmosphere of nitrogen; a low vacuum was applied and the temperature allowed to fall to 180 DEG C. during which period a syrupy distillate was removed; distillation was continued under a vacuum of 26 inches, 15 gs. of the residual liquid was mixed with 45 gs. of an epoxy resin and 7 gs. dibutyl phthalate; the mixture set in four days to a tough solid.ALSO:Liquid amides containing free amino radicals are prepared by reacting at least one mol., preferably one to two mols., of an aliphatic polyamine with a C2-10 saturated aliphatic monocarboxylic acid or an amide-forming derivative thereof, e.g. an acid halide or an aliphatic alcohol ester, subjecting the resulting salt to heat treatment to remove the elements of water and to further heat treatment under reduced pressure to remove any residual polyamine. The heat treatment is preferably carried out under nitrogen and the recovered polyamine is recycled for re-use. The polyamine is such as to furnish liquid reaction products and is exemplified by triethylene tetramine. The carboxylic acid may be a fatty acid, such as acetic, propionic, butyric, valeric, caproic, enanthic, caprylic, pelargonic and capric acids, a branched-chain acid, such as 2-ethyl-hexoic acid, or an amino acid, such as aminocaproic acid. Mixtures of the above acids may be employed and the above acids may also contain minor amounts of dicarboxylic acids such as sebacic acid. In examples triethylene tetramine is condensed with (1) acetic acid; (2) capric acid; and (3) 2-ethyl-hexoic acid. The Provisional Specification refers to the use of ethylene diamine and diethylene triamine as polyamine reactants and to the use of linoleic acid to form mono- and diamide derivatives.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2430755A GB806195A (en) | 1955-08-24 | 1955-08-24 | Improvements in or relating to the hardening of epoxy resins |
FR1157453D FR1157453A (en) | 1955-08-24 | 1956-08-23 | Epoxy resin curing enhancements |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2430755A GB806195A (en) | 1955-08-24 | 1955-08-24 | Improvements in or relating to the hardening of epoxy resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB806195A true GB806195A (en) | 1958-12-23 |
Family
ID=10209628
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2430755A Expired GB806195A (en) | 1955-08-24 | 1955-08-24 | Improvements in or relating to the hardening of epoxy resins |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR1157453A (en) |
GB (1) | GB806195A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3478089A (en) * | 1966-05-06 | 1969-11-11 | Takeda Chemical Industries Ltd | Liquid carboxylic acid salts of diamines as curing agents |
EP1103776A2 (en) * | 1999-11-24 | 2001-05-30 | Sammet Dampers OY | Corrosion-protected construction in a pipe heat exchanger and a method for forming the construction |
-
1955
- 1955-08-24 GB GB2430755A patent/GB806195A/en not_active Expired
-
1956
- 1956-08-23 FR FR1157453D patent/FR1157453A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3478089A (en) * | 1966-05-06 | 1969-11-11 | Takeda Chemical Industries Ltd | Liquid carboxylic acid salts of diamines as curing agents |
EP1103776A2 (en) * | 1999-11-24 | 2001-05-30 | Sammet Dampers OY | Corrosion-protected construction in a pipe heat exchanger and a method for forming the construction |
EP1103776A3 (en) * | 1999-11-24 | 2003-08-27 | Sammet Dampers OY | Corrosion-protected construction in a pipe heat exchanger and a method for forming the construction |
Also Published As
Publication number | Publication date |
---|---|
FR1157453A (en) | 1958-05-29 |
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