Abstract: Graft copolymers containing:(1) a phenolic resin; and(2) a poly(alkylene oxide) chain pendant to the phenolic resin,selected such that the graft copolymer has a solubility of no more than about 10 g/L in water, are taught. The graft copolymers are useful in coatings compositions with a curing agent, a solvent, and optionally an epoxy resin. The curable compositions have improved flexibility and/or solvent resistance. They are particularly useful in can coatings.

Abstract: Coating formulations which behave as elastic solids having reversible stress-induced fluidity are prepared by creating a fluid having distributed therein effective amounts of ionic charge sites and countercharge sites. For instance, elastic solids having reversible stress-induced fluidity are prepared by combining liquid formulations with a dispersion of a small, but effective, amount of at least one crystalline mixed metal hydroxide conforming substantially to the formulaLi.sub.m D.sub.d T(OH).sub.(m+2d+3+n.multidot.a) (A.sup.n).sub.a .multidot.xH.sub.2 Owhere m is zero to one, D is a divalent metal, d is from zero to 4, T is a trivalent metal, A represents at least one anion or negative-valence radical of valence n and a is the amount of A, where n is 1 or more, (m+2d+3+n.multidot.a) is equal to or greater than 3, (m+d) is greater than zero, and xH.sub.2 O represents excess waters of hydration, if any.

Abstract: The 2-functional component of substituted phenol-aldehyde novolac resins is reduced. Epoxy novolac resins prepared from the novolac resin containing reduced quantities of 2-functional product exhibit increased Tg values when cured.

Abstract: The 2-functional component of substituted phenol-aldehyde novolac resins is reduced. Epoxy novolac resins prepared from the novolac resin containing reduced quantities of 2-functional product exhibit increased Tg values when cured.

Abstract: Phenol-aldehyde novolac resins having reduced quantities of 2-functional material are prepared by removing all or part of the 2-functional material from this product resulting from reacting phenol with an aldehyde. Epoxy novolac resins prepared from the novolac resin containing less 2-functional product exhibit increased Tg values when cured.

Abstract: The 2-functional component of substituted phenol-aldehyde novolac resins is reduced. Epoxy novolac resins prepared from the novolac resin containing reduced quantities of 2-functional product exhibit increased Tg values when cured.

Abstract: Compositions comprising (A) a halogenated phenoxy resin and (B) an advanced epoxy resin are useful in the preparation of electrical laminates when admixed with a suitable curing agent such as dicyandiamide.

Abstract: Phenol-aldehyde novolac resins having reduced quantities of 2-functional material are prepared by removing all or part of the 2-functional material from this product resulting from reacting phenol with an aldehyde. Epoxy novolac resins prepared from the novolac resin containing less 2-functional product exhibit increased Tg values when cured.

Abstract: The 2-functional content of phenol-aldehyde novolac resins is reduced by water extraction. Epoxy novolac resins prepared from the novolac resin containing less 2-functional product exhibit increased Tg values when cured.

Abstract: A water based fluid additive useful in drilling mud used during drilling of an oil or gas well is disclosed, produced by reacting water at temperatures between 210.degree.-280.degree. F. with a mixture comprising in percent by weight:______________________________________ Gilsonite 25-30% Tannin 7-15% Lignite 25-35% Sulfonating Compound 15-25% Water Soluble Base Compound 5-15% Methylene-Yielding Compound 1- 5% ______________________________________and then removing substantially all of the remaining water to produce a dried product.

Abstract: Viscosifiers for addition to high zinc salt brines, used as oil well workover and completion fluids, are prepared from natural polysaccharide gums by treatment with a basic nitrogen reagent, such as a quaternary ammonium compound, hexamethylene tetramine, or dimethylol urea. The treated viscosifiers have improved dispersibility and give increased viscosity effects in the brines. Preferably, the viscosifiers are prepared from carrageenan or locust bean gums.

Abstract: A sulfonated gilsonite used in a drilling mud for drilling a well wherein the sulfonated gilsonite is prepared by reacting at a temperature between 210.degree.-280.degree. F. with a mixture of water, gilsonite having a softening point of at least 300.degree. F., lignite, sulfonating compound and water soluble based compound for a period of time to sulfonate the gilsonite.

Abstract: Compositions containing a relatively low equivalent weight epoxy resin and an advancement catalyst for reacting said epoxy resin with a polyhydric phenol are stable at high storage temperatures when the advancement catalyst is a phosphonium salt of phosphoric acid, phosphorous acid or polyphosphoric acid.

Abstract: High molecular weight epoxy resins containing hydrolyzed epoxy groups are prepared by reacting (A) a low molecular weight epoxy resin, and (B) a hydroxyl-containing compound in the presence of (C) a catalyst therefor and (D) an excess quantity of water and thereafter removing the excess water.

Abstract: Viscosifiers for addition to high zinc salt brines, used as oil well workover and completion fluids, are prepared from polysaccharide gums or gelatin by treatment with formaldehyde and/or an aliphatic dialdehyde containing from 2 to 6 carbons. The treated viscosifiers have improved dispersibility and give increased viscosity effects in the brines. Preferably, the viscosifiers are prepared from carrageenan, locust bean gum, hydroxyethyl cellulose, or gelatin by treatment with a mixture of formaldehyde and glyoxal.

Abstract: A novel composition of matter comprising a color-inhibiting additive, such as sodium bisulfite, and cis-1-(3-chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride or the cis-, trans- mixtures of 1-(3-chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride, is a non-yellowing antimicrobial formulation suitable for the preservation of aqueous organic mixtures such as emulsions, dispersions, latexes and solutions. The color-inhibiting agent may be added as a solid or as an aqueous solution wherein the weight ratio of adamantane to additive is from about 1:0.01 to about 1:4.