James L. Bertram - Lake Jackson TX Louis L. Walker - Clute TX Van I. W. Stuart - Missouri City TX
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
B01J 3112 B01J 3102
US Classification:
502154
Abstract:
Latent catalysts for epoxy reactions are prepared by reacting a tetrasubstituted onium compound such as tetrabutylphosphonium acetate acetic acid complex with an acid or metal salt of an acid having a weak-nucleophilic anion such as fluoboric acid. These catalysts provide stable latent catalysts for epoxy resins for advancement or curing reactions.
Latent, Curable, Catalyzed Mixtures Of Epoxy-Containing And Phenolic-Hydroxyl-Containing Compounds Containing Compounds Or Complexes Formed From Contacting Organic Phosphines Or Arsines With Weak Nucleophilic Acids
John W. Muskopf - Lake Jackson TX Louis L. Walker - Clute TX James L. Bertram - Lake Jackson TX
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
C08G 5968
US Classification:
525482
Abstract:
The products resulting from contacting an organic phosphine or arsine with an inorganic acid having a weak nucleophilic anion provide for relatively stable compositions when admixed with a compound containing an average of more than one vicinal epoxide group per molecule and which optionally contains a compound containing an average of more than one phenolic hydroxyl group per molecule.
Curable Composition Which Comprises Adducts Of Heterocyclic Compounds
James L. Bertram - Lake Jackson TX Louis L. Walker - Clute TX John W. Muskopf - Lake Jackson TX
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
C08G 5962 C08G 5914
US Classification:
428414
Abstract:
A curable composition which comprises: (1) a compound which contains on average more than 1 epoxy group per molecule; (2) a compound which contains on average more than 1 phenolic hydroxyl group per molecule; and (3) a catalytic amount of a catalyst compound which contains: (a) a cation containing at least one heterocyclic nitrogen-containing ring, and (b) an anion which is a conjugate base of fluoroarsenic acid, fluoroantimonic acid, fluorophosphoric acid, chloroarsenic acid, chloroantimonic acid, chlorophosphoric acid, nitric acid, hydrofluoric acid, trifluoroacetic acid, trifluoromethane sulfonic acid, picric acid, fluoboric acid, or an acid represented by the Formula: HBR. sub. 3 R' wherein each R is independently a hydrocarbyl or substituted hydrocarbyl group and R' is a halogen, a hydrocarbonoxy group, a hydrocarbonamino group, or a hydrocarbonphosphino group.
Amide Modified Epoxy Resins From A Dialkanolamine, A Monoalkanolamine, An Anhydride And (An) Unsaturated Monomer(S)
James L. Bertram - Lake Jackson TX Willie L. Myles - Sweeny TX
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
C08G 5958
US Classification:
523417
Abstract:
Curable amide modified epoxy resins are prepared by polymerizing (I) the reaction product of (A) the reaction product of (1) an epoxy resin having an average of more than one 1,2-epoxy group per molecule and an average of from about 0 to about 30 aliphatic hydroxyl groups per molecule such as a diglycidyl ether of bisphenol A and (2) (a) a material having only one primary amine group per molecule such as monoethanolamine and (b) a material having only one secondary amine group per molecule such as diethanolamine wherein (a) and (b) are added sequentially with (a) being added first, or as a mixture with (B) an anhydride of an unsaturated dicarboxylic acid such as maleic anhydride with (II) a polymerizable ethylenically unsaturated monomer or mixture of monomers such as styrene and methacrylic acid. The resultant resin can be employed as is in the preparation of organic solvent borne coatings or it can be neutralized with a base so as to improve its stability in the preparation of aqueous coatings.
James L. Bertram - Lake Jackson TX William Davis - Lake Jackson TX Louis L. Walker - Clute TX
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
C08G 5902
US Classification:
528 93
Abstract:
Epoxy resin compositions are disclosed which are the reaction products resulting from reacting (A) the reaction product of a cyanuric halide and at least one dihydric or polyhydric phenol with (B) at least one dihydric or polyhydric phenol and (C) at least one epoxy resin having an average of more than one epoxy group per molecule. These epoxy resin compositions are suitable for use as electrical laminates, structural laminates, coatings, castings, electrical encapsulation and the like.
Latent Catalysts, Epoxy Compositions Incorporating Same, And Coating, Impregnating And Bonding Methods Employing The Compositions
James L. Bertram - Lake Jackson TX Louis L. Walker - Clute TX Charlie Z. Hotz - Walnut Creek CA
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
C09J 502
US Classification:
1563074
Abstract:
Products resulting from contacting (1) at least one compound selected from the group consisting of (a) at least one onium compound of the element nitrogen, phosphorus, sulfur or arsenic; (b) at least one amine compound; and (c) a mixture of any two or more of the (a) and (b) components; with (2) either (a) boric acid or (b) a mixture of boric acid and at least one acid having a weak nucleophilic anion are suitable catalysts for reacting vicinal epoxy-containing compounds with aromatic hydroxyl-containing compounds.
Triazine Containing Epoxy Resins Having Improved Thermal Stability
James L. Bertram - Lake Jackson TX Louis L. Walker - Clute TX
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
C08G 5932
US Classification:
528 96
Abstract:
The thermal stability of epoxy resins prepared by dehydrohalogenating the reaction product of an epihalohydrin with an adduct prepared from a cyanuric halide and a polyhydric aromatic compound is improved by employing as the polyhydric aromatic compound one which is substituted with a hydrocarbyl group, a halogen atom or a nitro group at each ortho position relative to each aromatic hydroxyl group. These epoxy resins are useful in coating and molding compositions and in the preparation of laminates and composites.
Weldable coatings containing, an electro-conductive pigment such as zinc, an epoxy resin binder and solvent are improved by employing as the epoxy resin binder, the reaction product of a relatively low molecular weight epoxy resin such as the diglycidyl ether of bisphenol A and an amine compound having two amine hydrogen atoms such as ethanolamine.