Abstract: A method for producing an epoxy polyetherpolyol having 15 to 75 wt % epoxy comprising heating a polyol and catalyst to initiate condensation, removing water, introducing sufficient epoxy into the reaction mixture to give 15 to 75 wt % epoxy in the product. Generally, between 0.5 and 1.19 moles of water per mole of polyol are removed. In one embodiment at least 95 wt % of all of the polyol is introduced initially into the reaction zone. In another embodiment the condensation is terminated prior to 93 percent completion. Also provided are novel compositions suitable for drilling fluids, adhesives and coatings.

Abstract: Method for preparing polyethercyclicpolyol by heating alkali and/or alkaline earth hydroxide optionally with polyol, its precursors or derivatives, admixing epoxy alcohol or epihalohydrin therewith to initiate an addition reaction, and thermally condensing the product of the addition reaction.

Abstract: Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and controlling process conditions to avoid substantial undesirable degeneration. Lower molecular weight polyethercyclicpolyols are polycondensed with phenolic hydroxyl-containing compounds to form higher molecular weight polyethercyclicpolyols.

Abstract: A process for producing lower alcohols is presented in which an olefinic feed and H.sub.2 SO.sub.4 react to form a mixture comprising alkyl sulfates, alkyl disulfates, fat acid, and nonpolar hydrocarbons. The mixture is separated into two phases, a nonpolar phase comprising nonpolar hydrocarbons and a polar phase comprising alkyl sulfates, alkyl disulfates, and fat acids. A rag-layer that forms between the nonpolar and polar phases comprising carbonaceous particulate material is removed by contact with an extraction reagent. This can be a slip stream comprising an etheric derivative of the olefinic feed and an oligomeric derivative of the feed which is withdrawn from a subsequent step the process. This forms a separate hydrocarbon phase which is then extracted. The sulfates are then hydrolyzed to form alcohol.

Abstract: Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and controlling process conditions to avoid substantial undesirable degeneration. Lower molecular weight polyethercyclicpolyols are copolymerized with epoxy resins to form higher molecular weight polyethercyclicpolyols.

Abstract: Method for preparing polyethercyclicpolyol by heating a reaction mixture of an alkali or alkaline earth metal hydroxide with a polyol, adding epihalohydrin to initiate an addition reaction, and heating the mixture until the reaction is complete.

Abstract: Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and controlling process conditions to avoid substantial undesirable degeneration. Lower molecular weight polyethercyclicpolyols are polycondensed ith dihydric alcohols to form higher molecular weight polyethercyclicpolyols.

Abstract: Method for preparing polyethercyclicpolyol by heating an alkali or alkaline earth metal hydroxide with a polyol and epihalohydrin or epoxy alcohol to initiate an addition reaction, and adding epoxy resin to the addition reaction mixture prior to the addition reaction going to completion.

Abstract: Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and controlling process conditions to avoid substantial undesirable degeneration.

Abstract: Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the glycol, cyclic derivatives of the polyol, or mixtures thereof, and controlling process conditions to avoid substantial undesirable degeneration. Lower molecular weight polyethercyclicpolyols are polycondensed with epoxy alcohols to form higher molecular weight polyethercyclicpolyols.

Abstract: Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and controlling process conditions to avoid substantial undesirable degeneration. Lower molecular weight polyethercyclicpolyols are polycondensed with phenolic hydroxyl-containing compounds to form higher molecular weight polyethercyclicpolyols.

Abstract: Method for preparing polyethercyclicpolyol by heating an alkali or alkaline earth metal hydroxide with a polyol and epihalohydrin or epoxy alcohol to initiate an addition reaction, and adding epoxy resin to the addition reaction mixture prior to the addition reaction going to completion.

Abstract: An aqueous base drilling fluid additive composed of salt and lime or gypsum, and including an acyclic polyol and/or cyclicetherpolyol and salt.

Abstract: Drilling fluid properties are enhanced by incorporation thereinto of a cyclicetherpolyol such as a cyclic dimer of glycerol and, optionally, a polyol such as glycerol or a monoalicyclicpolyol, and/or salt.

Abstract: Oil in water emulsion drilling fluid properties are enhanced by incorporation thereinto of an alcohol such as glycerol or polycyclicpolyetherpolyol and salt.

Abstract: Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and controlling process conditions to avoid substantial undesirable degeneration. Lower molecular weight polyethercyclicpolyols are copolymerized with epoxy resins to form higher molecular weight polyethercyclicpolyols.

Abstract: Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and controlling process conditions to avoid substantial undesirable degeneration. Lower molecular weight polyethercyclicpolyols are polycondensed with epoxy alcohols to form higher molecular weight polyethercyclicpolyols.

Abstract: An invert oil emulsion drilling fluid containing oil, an emulsifier such as a fatty acid soap, clay or polymer, and an alcohol such as glycerol or cyclicetherpolyol as the internal phase of the emulsion. A method using substantially water-free drilling fluid and monitoring the influx of formation water into the drilling fluid.

Abstract: Polyethercyclicpolyols are prepared by thermally condensing a polyol having at least three hydroxyl groups of which at least two of the hydroxyl groups are vicinal, precursors of the polyol, cyclic derivatives of the polyol, or mixtures thereof, and controlling process conditions to avoid substantial undesirable degeneration. Lower molecular weight polyethercyclicpolyols are polycondensed with epihalohydrins to form higher molecular weight polyethercyclicpolyols.

Abstract: A process for removal of H.sub.2 S from gas streams is described, the process being characterized by use of a novel iron chelate treating solution containing a specified ferric to ferrous chelate ratio, aqueous ammonia, and thiosulfate ion.