Ion exchange catalyzed bisphenol synethesis
AssigneeGeneral Electric Company
InventorAshok K. Mendiratta
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Abstract
An improved bis-phenol synthesis reactor system is provided using multiple acetone injection in an ion exchange catalyzed BPA synthesis process. This process results in an improved reactant effluent product distribution and color.
Claims7
A process for the preparation of bisphenol-A comprising reacting 5-10 moles of phenol per mole of acetone at a temperature of about 50.degree. C. to about 120.degree. C. in the presence of a cation exchange resin catalyst in a series of reactors wherein all of said phenol and from about 25% to about 75% by weight of said acetone necessary for the reaction is charged to a first reactor and the remainder of said acetone is charged to a subsequent reactor whereby a reduction in color bodies and by-products in the bisphenol-A effluent is achieved and the ratio of phenol to acetone necessary to produce an optimized yield of bisphenol-A is reduced.
A process for the production of bis(hydroxyphenyl) alkanes such that a phenolic compound having at least one replaceable hydrogen atom attached directly to a carbon atom in a phenolic ring is reacted at a temperature of about 50.degree. C. to about 120.degree. C. with an aliphatic ketone in the presence of a cation exchange resin catalyst in a reactor or a series of reactors wherein all of said phenolic compound and a portion of said aliphatic ketone necessary for the reaction is charged at the beginning of the reactor and the remainder of said aliphatic ketone is injected along the reactor length or in a subsequent reactor.
The process for the preparation of 2,2'-di(hydroxyphenyl)propane comprising reacting phenol and acetone in the presence of a 2-mercapto-ethyl amine modified microreticular sulfonated polystyrene divinyl benzene ion-exchange resin catalyst at the temperature of between about 60.degree. C. and about 80.degree. C. in a reactor or a series of reactors wherein all of said phenol and a portion of said acetone necessary is charged at the beginning of the reactor or the first reactor and the remainder of said acetone is injected along the reactor length or in a subsequent reactor.
Dependencies are inferred from the claim text.