Process for the preparation of flexible epoxy resin systems

Information

  • Patent Grant
  • 5652318
  • Patent Number
    5,652,318
  • Date Filed
    Tuesday, June 4, 1996
    28 years ago
  • Date Issued
    Tuesday, July 29, 1997
    26 years ago
Abstract
A flexible epoxy resin system is prepared by incorporating a combination of hardeners (A) and (B) in an epoxy resin, wherein the amounts of the two hardeners are varied to adjust the flexibility of the epoxy resin.
Description
Claims
  • 1. A process for preparing a flexible epoxy resin system, comprising:
  • mixing with an epoxy resin a hardener composition comprising a combination of:
  • Hardener (A) which has an NH-active equivalent weight of 100-300 and is prepared by mixing (i) a diamine containing polyether groups and urethane groups (PEDA) of the following composition: ##STR1## wherein R is ##STR2## R.sup.1 is a (cyclo)alkylene radical which has 4-14 carbon atoms, and is optionally substituted by 1-4 CH.sub.3 groups, or units of the formula I or II ##STR3## wherein R.sup.2 is an alkylene radical which has 6-20 carbon atoms, optionally substituted by 1-4 CH.sub.3 groups, wherein 1-3 --CH.sub.2 -- groups can be replaced by --O-- or --NCH.sub.3 -- groups, and (ii) a diamine of the formula:
  • H.sub.2 --R.sup.3 --NH.sub.2 (DA)
  • where
  • R.sup.3 is a (cyclo)alkylene radical which has 2-15 C atoms, optionally substituted by 1-4 CH.sub.3 groups, or units of the formula I or II ##STR4## Hardener (B) which has the same NH-active equivalent weight as Hardener (A) of 100-300, and is prepared by mixing the (i) diamine (PEDA) containing polyether groups and urethane groups and (ii) a monoamine of the composition:
  • H.sub.2 N--R.sup.4
  • where
  • R.sup.4 is an optionally alkyl-substituted alkyl radical having 6-20 C atoms, where 1-3 --CH.sub.2 -- groups can be replaced by --O-- or --NCH.sub.3 -- groups; the weight ratio of hardeners (A) and (B) ranging from 1:99 to 99:1.
  • 2. The process of claim 1, wherein said diamine (ii) is selected from the group consisting of ethylenediamine, 2-methylpentamethylenediamine, 2,2,4-(2,4,4)-trimethylhexamethylenediamine, 3-(Cyclohexylamino)propylamine, 3,3'-Dimethyl-4,4'-diaminodicyclohexylmethane, m-xylylenediamine, 1,2-diaminocyclohexane and isophoronediamine.
  • 3. The process of claim 1, wherein said Hardener (A) has an NH-active equivalent weight of 190.
  • 4. The process of claim 1, wherein monoamine (ii) is a member selected from the group consisting of hexylamine, 2-ethylhexylamine, decylamine, dodecylamine, tridecylamine, butoxypropylamine, hexoxyproylamine, 3-(2-ethylhexoxy)propylamine, lauryloxypropylamine, diethylaminopropylamine and 1-diethyl-amino-4-aminopentane.
  • 5. The process of claim 1, wherein the epoxy resin is based on bisphenol A and bisphenol F.
  • 6. The process of claim 4, wherein said monoamine is selected from the group consisting of hexoxypropylamine, 3-(2-ethylhexoxy)propylamine and lauryloxypropylamine.
  • 7. The process of claim 1, wherein the epoxy resin-hardener composition further contains up to 4% by weight of a catalyst which catalyzes the NH/epoxide reaction.
Priority Claims (1)
Number Date Country Kind
195 21 303.3 Jun 1995 DEX
US Referenced Citations (2)
Number Name Date Kind
3984370 Shinohara et al. Oct 1976
5459204 Lomoelder et al. Oct 1995