Abstract: A process for dehydrogenating a paraffinic feedstock, producing olefins and/or dienes. The process includes feeding a paraffinic hydrocarbon feedstock comprising one or more C2+ paraffinic hydrocarbons and a fuel gas stream to a dehydrogenation reactor preheater, combusting the fuel gas stream in the dehydrogenation reactor preheater and heating the paraffinic hydrocarbon feedstock to a temperature in the range of 500-650° C., producing a heated paraffinic feedstock, feeding the heated paraffinic feedstock to a first dehydrogenation reactor operating in a reaction mode and containing an active dehydrogenation catalyst and at least one first electrical heating element, heating the heated paraffinic feedstock in the first dehydrogenation reactor using the at least one first electrical heating element, and contacting the heated paraffinic feedstock with the active dehydrogenation catalyst and the at least one electrical heating element thereby producing an olefinic product stream comprising one or more olefins.

Abstract: A method of performing an oxidative coupling of methane (OCM) reaction to produce C2+ compounds using a low temperature gas mixture feed is provided. The method includes introducing a gas mixture feed containing methane, oxygen, hydrogen, and carbon monoxide at a temperature of less than or equal to 300° C. to an inlet of an OCM reactor, which contains a combustion catalyst and an OCM catalyst. At least a portion of the gas mixture feed is combusted using the combustion catalyst to generate a heated gas mixture having a temperature of at least 450° C. The heated gas mixture contacts the OCM catalyst to initiate an OCM reaction and produce an OCM effluent that includes C2+ compounds. A system for performing an OCM reaction using a low temperature feedstock gas mixture is also provided.

Abstract: Various biomass reactors systems and methods of pyrolyzing biomass are disclosed. One type of biomass reactor system comprises a plurality of biomass processing stations configured in series, each station comprising an auger reactor including an auger inlet for receiving biomass and a transfer screw for conveying the biomass through the auger reactor.

Abstract: Various biomass reactors systems and methods of pyrolyzing biomass are disclosed. One type of biomass reactor system comprises a plurality of biomass processing stations configured in series, each station comprising an auger reactor including an auger inlet for receiving biomass and a transfer screw for conveying the biomass through the auger reactor.

Abstract: A fluid cracked naphtha stream is subjected to hydrodesulfurization and fractionation, preferably simultaneously in catalytic distillation reactors. The overheads and a portion of the bottoms from the fractionation are recombined to produce a naphtha blend having an ASTM D-86 95% point greater than the end point of the overheads and less than the ASTM D-86 95% point of the bottoms.

Abstract: A selected boiling range fluid catalytically cracked naphtha stream is subjected to simultaneous splitting, thioetherification of a light boiling range naphtha and selective hydrogenation of the dienes in a medium boiling range naphtha.

Abstract: A process for the production of propylene from the metathesis of ethylene and 2-butene is disclosed wherein a mixed C4 stream is first treated to enrich and separate the 2-butene from 1-butene and isobutene by isomerization of 1-butene and concurrent fractional distillation of the 2-butene and isobutene to provide the 2-butene feed the metathesis with ethylene. In addition the mixed C4 stream may be treated to remove mercaptans and dienes prior to 2-butene enrichment.

Abstract: A process for concurrently fractionating and hydrotreating a full range naphtha stream.

Abstract: A process is disclosed for preparing a C4 stream for feeding to an alkylation process which reacts isobutane with butene to produce isooctane. The C4 stream is treated in a first distillation column reactor to remove dienes and mercaptans and separate out any C5's which might be present. The treated C4's are then fed to a second distillation column reactor that concurrently isomerizes 1-butene to 2-butene and splits the normal C4's from the iso C4's. The iso C4's are then fed to a third distillation column reactor where a portion of the isobutene is saturated to isobutane. The C4's from the isomerization/splitter are combined with the C4's from the hydrogenation unit and fed to a cold acid alkylation unit. The third distillation column may also oligomerize a portion of the isobutene to diisobutene in the upper end which is saturated in the bottom of the column to isooctane.