U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Multifunctional epoxy resins

Patent 4623701 Issued on November 18, 1986. Estimated Expiration Date: Icon_subject July 10, 2005. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

3240376

3878132

Water-soluble epoxy resins and process for their preparation
Patent #: 4273921
Issued on: 06/16/1981
Inventor: Bertram ,   et al.

Diglycidyl ethers of di-secondary alcohols, their preparation, and curable compositions containing them Patent #: 4284574
Issued on: 08/18/1981
Inventor: Bagga

Inventor

Application

No. 06/753482 filed on 07/10/1985

US Classes:

525/523, Solid polymer contains more than one 1,2-epoxy group or is derived from reactant containing at least one 1,2-epoxy group525/524, Mixed with a reactant containing more than one 1,2-epoxy group per mole or polymer derived therefrom525/533, Mixed with carboxylic acid or derivative reactant or polymer therefrom528/103, Two or more 1,2-epoxy reactants528/87, From 1,2-epoxy-containing phenolic reactant or with 1,2-epoxy-containing reactant528/99, Phenolic reactant contains at least one nitrogen, phosphorus, or sulfur atom549/516Glycidyl ether formed by bonding oxygen directly to an acyclic carbon which is bonded directly to an oxirane ring

Examiners

Primary: Nielsen, Earl

Attorney, Agent or Firm

International Classes

C08G 59/00 (20060101)
C08G 59/04 (20060101)
C08G 59/14 (20060101)
C08G 59/32 (20060101)

Abstract

Multifunctional epoxy resins are prepared by reacting (1) a polyglycidyl ether of a polyhydroxyl-containing material said glycidyl ether having an average of at least 0.05 aliphatic hydroxyl group per molecule and an average of more than one glycidyl ether group per molecule such as a diglycidyl ether of bisphenol A, (2) a hydrolyzed monoglycidyl ether of a material having one aromatic hydroxyl group such as hydrolyzed phenyl glycidyl ether or one aliphatic hydroxyl group such as hydrolyzed butyl glycidyl ether, (3) a hydrolyzed glycidyl ether of a material having an average of more than one aromatic hydroxyl group per molecule such as hydrolyzed diglycidyl ether of bisphenol A or an average of more than one aliphatic hydroxyl group per molecule such as hydrolyzed cyclohexanedimethanol diglycidyl ether, (4) the reaction product of monoglycidyl ether with a polyphenolic compound, or (5) a combination of (1), (2), (3) or (4) with an epihalohydrin such as epichlorohydrin and dehydrohalogenating the resultant halohydrin ether intermediate product with a suitable dehydrohalogenating agent such as sodium hydroxide. These epoxy resins when cured with a suitable curing agent such as methylene dianiline result in an improvement in one or more properties such as toughness, heat distortion temperature, glass transition temperature, acid resistance or the like.

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