Chevron Phillips Chemical Company LP

Chevoron Phillip Chemical Company, LP

Stephen L Kelly

Max P McDaniel

Kathy S Clear

Tin-Tack Peter Cheung

Carlton Edwin Ash

Joseph Bergmeister, Iii

Amanda B Allemand

Maruti Bhandarkar

Wei Wang

William Donald Treleaven

Processes for activating a high-chlorine content aromatization catalyst in a reactor system include the steps of contacting the aromatization catalyst with an inert gas stream in the reactor system at a drying temperature of 300-400° C. to form a treated catalyst, and then contacting the treated catalyst with a reducing gas stream in the reactor system to form an activated catalyst. Subsequently, a hydrocarbon feed can be contacted with the activated catalyst under reforming conditions in the reactor system to produce an aromatic product.

In-reactor activation of a high chloride aromatization catalyst

Silica composites and supported chromium catalysts having a bulk density of 0.08 to 0.4 g/mL, a total pore volume of 0.4 to 2.5 mL/g, a BET surface area of 175 to 375 m/g, and a peak pore diameter of 10 to 80 nm are disclosed herein. These silica composites and supported chromium catalysts can be formed by combining two silica components. The first silica component can be irregularly shaped, such as fumed silica, and the second silica component can be a colloidal silica or a silicon-containing compound, and the second silica component can act as a glue to bind the silica composite together.

Preparation of large pore silicas and uses thereof in chromium catalysts for olefin polymerization

Methods for reinforcing chromium catalysts by the deposition of additional silica are disclosed herein. The resultant silica-reinforced chromium supported catalysts can be used to polymerize olefins to produce, for example, ethylene based homopolymers and copolymers with higher molecular weights and additional long chain branching.

Reinforcement of a chromium/silica catalyst with silicate oligomers

Provided herein are methods of inhibiting polymerization of vinyl aromatic monomers. The methods include distilling a vinyl aromatic monomer in a distillation column to form a vinyl aromatic monomer distillate; removing the vinyl aromatic monomer distillate from the distillation column; combining the vinyl aromatic monomer distillate with 4-tert-butylcatechol (TBC) to form a treated distillate; and adding a reflux liquid that includes the treated distillate to the distillation column liquid of the distillation column. An added oxygen gas may be present in a distillation column liquid in an amount of at least 1 ppmw, based on the weight of the vinyl aromatic monomer.

Methods of inhibiting polymerization of vinyl aromatic monomers

A composition comprising an extruded inorganic support comprising an oxide of a metal or metalloid, and at least one catalytically active metal, wherein the extruded inorganic support has pores, a total pore volume, and a pore size distribution, wherein the pore size distribution displays at least two peaks of pore diameters, each peak having a maximum, wherein a first peak has a first maximum of pore diameters of equal to or greater than about 120 nm and a second peak has a second maximum of pore diameters of less than about 120 nm, and wherein greater than or equal to about 5% of a total pore volume of the extruded inorganic support is contained within the first peak of pore diameters.

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Kingwood, TX, United States of America

Stephen L Kelly