GB806195A - Improvements in or relating to the hardening of epoxy resins - Google Patents

Improvements in or relating to the hardening of epoxy resins

Info

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
Application number
GB2430755A
Inventor
Raymond Harold Wright
Mansel David Fisher
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.)
Pressed Steel Co Ltd
SPS Technologies LLC
Original Assignee
Pressed Steel Co Ltd
Standard Pressed Steel 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 Pressed Steel Co Ltd, Standard Pressed Steel Co filed Critical Pressed Steel Co Ltd
Priority to GB2430755A priority Critical patent/GB806195A/en
Priority to FR1157453D priority patent/FR1157453A/en
Publication of GB806195A publication Critical patent/GB806195A/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
    • C08G59/50Amines
    • C08G59/54Amino 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.
GB2430755A 1955-08-24 1955-08-24 Improvements in or relating to the hardening of epoxy resins Expired GB806195A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (3)

* Cited by examiner, † Cited by third party
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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