Shell Oil Comapny

Anne H Zuzich

George C Blytas

Harry Frank

Eugene L Holloway

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.

Polyethercyclipolyols from epihalohydrins, polyhydric alcohols, and

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.

Polycondensation of phenolic hydroxyl-containing compounds and

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.

Polyethercyclicpolyols from epihalohydrins, polyhydric alcohols, and

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.

Polyethercyclicpolyols from epihalohydrins, polyhydric alcohols and

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.

Thermal condensation of polyhydric alcohols to form

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.

Polycondensation of epoxy alcohols with polyhydric alcohols and thermal

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.

Polycondensation of epoxy alcohols with polyhdric alcohols and thermal

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.

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Houston, TX, United States of America

Anne H Zuzich