Abstract: Processes for cracking an alkane reactant to form a lower aliphatic hydrocarbon product and for converting an alkane reactant into a higher aliphatic hydrocarbon product are disclosed, and these processes include a step of contacting the alkane reactant with a supported chromium (II) catalyst. In addition to the formation of various aliphatic hydrocarbons, such as linear alkanes, branched alkanes, 1-alkenes, and internal alkenes, aromatic hydrocarbons and hydrogen also can be produced.

Abstract: Systems and methods are provided for conversion of methanol to gasoline in an integrated system that can also upgrade light paraffins generated by the methanol conversion process to aromatics. In some aspects, the integrated configuration can include integration of the stage for upgrading of light paraffins to aromatics into the product separation sequence for processing of the methanol conversion effluent. In other aspects, the integrated configuration can further include sharing a common catalyst between the methanol conversion stage and the stage for upgrading light paraffins to aromatics.

Abstract: The invention relates to a process for removing dienes from a material stream comprising C3 to C5 hydrocarbons by selective hydrogenation at a specified reaction pressure and a specified reaction temperature in the presence of a hydrogenation catalyst, wherein the reaction pressure and the reaction temperature at the reactor inlet are regulated such that the reaction pressure at the reactor inlet does not deviate by more than 0.01 bar from the specified reaction pressure and the reaction temperature at the reactor inlet does not deviate by more than 0.1° C. from the specified reaction temperature and the proportion of hydrogen supplied to the selective hydrogenation is in the range from 2 to 20 moles per mole of diene present in the material stream comprising C3 to C5 hydrocarbons.

Abstract: Disclosed are a bifunctional catalyst and a preparation method therefor, the bifunctional catalyst being suitable to produce high-value aromatic hydrocarbons by subjecting alkylaromatic hydrocarbons to a disproportionation/transalkylation/dealkylation reaction while suppressing aromatic loss or subjecting C8 aromatic hydrocarbons to an isomerization reaction while suppressing xylene loss.

Abstract: A process and related system for producing para-xylene (PX). In an embodiment, the process includes (a) separating a feed stream comprising C6+ aromatic hydrocarbons into a toluene containing stream and a C8+ hydrocarbon containing stream and (b) contacting at least part of the toluene containing stream with a methylating agent in a methylation unit to convert toluene to xylenes and produce a methylated effluent stream. In addition, the process includes (c) recovering PX from the methylated effluent stream in (b) to produce a PX depleted stream and (d) transalkylating the PX depleted stream to produce a transalkylation effluent stream. The transalkylation effluent stream includes a higher concentration of toluene than the PX depleted stream. Further, the process includes (e) converting at least some ethylbenzene (EB) within the C8+ hydrocarbon containing stream into toluene and (f) flowing the toluene converted in (e) to the contacting in (b).

Abstract: Systems and methods are provided for integration of an aromatic formation process for converting non-aromatic hydrocarbon to an aromatic product and subsequent methylating of a portion of the aromatic product to produce a methylated product, with improvements in the aromatic formation process and/or the methylation process based on integrating portions of the secondary processing trains associated with the aromatic formation process and the methylation process. The aromatic formation process and methylation process can be used, for example, for integrated production of specialty aromatics or gasoline blending components.

Abstract: The application relates to processes and systems that use a furfural compound for producing five-membered carbocyclic rings that are unsaturated, such as cyclopentene and cyclopentadiene. Examples methods for conversion of furfural compounds may include converting a furfural compound to at least a five-membered, saturated carbocyclic ring, and converting the five-membered, saturated carbocyclic ring in a presence of a catalyst to at least a five-membered, unsaturated carbocyclic ring.

Abstract: The present invention relates to a method for producing long-chain alkylbenzene by reacting an aromatic hydrocarbon and a long-chain olefin, wherein the reaction is carried out in the presence of a solid acid catalyst, the aromatic hydrocarbon is selected from the group consisting of benzene, toluene and xylene, the long-chain olefin is selected from the group consisting of C8-C26 alkenes, the catalyst is a HMCM-22 type molecular sieve solid acid catalyst modified with heteroatom(s), the heteroatom(s) is/are selected from the group consisting of boron, gallium, indium, chromium, molybdenum, tungsten, manganese and phosphorus, and the molar ratio of silicon atoms to heteroatoms in the solid acid catalyst is in the range of 1:0.01-0.03. The invention also relates to a method for regenerating the solid acid catalyst used in the reaction.

Abstract: Methods of improving the selectivity of selective hydrogenation of residual 1,3-butadiene in a C4 fraction of a hydrocarbon raffinate stream in a fixed-bed reactor are described. The methods may include co-feeding a competitive chemical species that increases the mechanistic selectivity to 1- and 2-butenes while increasing isomerization selectivity to 2-butene in the product stream. The hydrogenation reactor and competitive chemical species conditions may be tailored to selectively produce butenes over butane or iso-butane, where the butenes comprise 1-butene and/or 2-butene.

Abstract: The invention relates to a process and system arrangement to generate benzene, toluene and xylenes in a refinery. The process relies on recycling a C9+ aromatic bottoms stream from an aromatic recovery complex back to rejoining a hydrotreated naphtha stream as it enters a catalytic reformer. The aromatic bottoms can be further reacted through both the reformer and the subsequent aromatic recovery complex to transform to higher value compounds, thereby reducing waste or reducing bottoms' presence in gasoline pools.

Abstract: According to one or more embodiments disclosed herein, methods for operating dehydrogenation processes during non-normal operating conditions, such as at start-up, shut-down, system recycle, or unit trip, are described. The methods may include contacting a feed stream with a catalyst in a reactor portion of a reactor system to form a reactor effluent stream, separating at least a portion of the reactor effluent stream from the catalyst, passing the catalyst to a catalyst processing portion and processing the catalyst, wherein processing the catalyst comprises contacting the catalyst with oxygen, passing the catalyst from the processing portion to the reactor portion, wherein the catalyst exiting the processing portion comprises at least 0.001 wt. % oxygen, and contacting the catalyst with supplemental hydrogen, the contacting removing at least a portion of the oxygen from the catalyst by a combustion reaction.

Abstract: The present invention relates to a system and process for preparing aromatics from syngases, which has advantages of shortened flow process and reduced investment. The process comprises reforming the liquefied gas, separated dry gas with a water steam to produce carbon monoxide and hydrogen, which return, as raw materials, to the aromatization system, so that the problem of by-product utilization is solved, and the syngas unit consumption per ton of aromatic products is reduced. The problem of utilization of a dry gas as a by-product is also solved in the present invention from the perspective of recycling economy, which reduces the water consumption in the process, and conforms to the concept of green chemistry.

Abstract: Methods of producing 1-butene from a 2-butene-containing feedstock include feeding a hydrocarbon feed comprising 2-butene to a reactor, the reactor containing an isomerization catalyst and contacting the hydrocarbon feed with the isomerization catalyst in the reactor at a temperature from 150° C. to 350° C. to produce an isomerization reaction effluent comprising 1-butene. Further, the isomerization catalyst comprises a MCM-48 catalyst with WO3 incorporated into a silica framework of the MCM-48 catalyst.

Abstract: A process for blending a hydrocarbon-based composition that includes combining a first heated water stream with a first hydrocarbon-based composition comprising asphaltene to create a first combined feed stream and allowing the first heated water stream and the first hydrocarbon-based composition to interact such that the second combined feed stream comprises micelles and reverse micelles, thereby preventing asphaltene aggregation. The process further includes similarly combining a second heated water stream with a second hydrocarbon-based composition to form a second combined feed stream. The process further includes introducing the first combined feed stream and the second combined stream into a supercritical blending vessel operating at a temperature greater than a critical temperature of water and a pressure greater than a critical pressure of water, and blending the first combined feed stream and the second combined stream to form a blended hydrocarbon-based composition.

Abstract: A facility and method for membrane permeation treatment of a feed gas flow containing at least methane and carbon dioxide that includes a compressor, a pressure measurement device, at least one valve, and first, second, third, and fourth membrane separation units for separation of CO2 from CH4 to permeates enriched in CO2 and retentates enriched in CH4, respectively. A temperature of the first retentate is adjusted at an inlet of the second membrane separation unit with at least one heat exchanger as a function of the measured CH4 concentration in such a way so as to reduce the determined difference.

Abstract: Provided in this disclosure is a process for the oxidative dehydrogenation of a lower alkane into a corresponding alkene. The process includes providing a gas stream comprising the lower alkane to a reactor; contacting, in the oxidative dehydrogenation reactor, the lower alkane with a catalyst that includes a mixed metal oxide; and providing to the last 50% of the oxidative dehydrogenation reactor a stream comprising from 0.01 vol. % to 10 vol. % of a C1-C3 alcohol.

Abstract: The present invention relates to a method for preparing paraffin, and can provide a method for preparing paraffin including a hydrogenation step of by-products of a process for preparing linear alpha olefins. Since the method for preparing paraffin of the present invention can convert the by-products of the process for preparing linear alpha olefins to paraffin at a high conversion ratio, it is possible to increase the added value of the by-products.

Abstract: A method for processing a chemical stream includes contacting a feed stream with a catalyst in a reactor portion of a reactor system causing a reaction which forms a product stream. The method includes separating the product stream from the catalyst, passing the catalyst to a catalyst processing portion of the reactor system, processing the catalyst in the catalyst processing portion, and passing a portion of the catalyst from the catalyst processing portion of the reactor system into a catalyst withdrawal system that includes a catalyst withdrawal vessel and a transfer line coupling the catalyst withdrawal vessel to the catalyst processing portion. Each of the catalyst withdrawal vessel and the transfer line include an outer metallic shell and an inner refractory lining. The method further includes cooling the catalyst in the catalyst withdrawal vessel from greater than or equal to 680° C. to less than or equal to 350° C.

Abstract: A method for converting an alcohol to a jet-diesel hydrocarbon fraction, comprising contacting the alcohol with a pillared two-dimensional zeolite catalyst at a temperature of at least 200° C. and up to 500° C. to convert the alcohol to hydrocarbons comprising: (a) a first mixed olefin fraction containing a mixture of C2-C5 olefins; (b) a first paraffin fraction containing C3-C5 paraffins; and (c) a gasoline fraction containing C6+ hydrocarbons; and the conversion of the alcohol is energy neutral or exothermic. The first mixed olefin fraction may be subjected to an oligomerization process to result in a second paraffin fraction containing C3-C6 paraffins along with a C7+ partially unsaturated fraction, and the first and second paraffin fractions combined into a total C3-C6 paraffin fraction, which can in turn be subjected to a dehydrogenation or aromatization process with hydrogen gas as byproduct, and the hydrogen gas recycled for use in producing the jet-diesel fraction.

Abstract: The present invention provides a production method for indene, comprising a dehydrogenation step of obtaining a reaction product containing indene by contacting a raw material gas containing indane and molecular hydrogen with a dehydrogenation catalyst, wherein the dehydrogenation catalyst comprises a support containing aluminum, and a supported metal supported on the support, the supported metal contains a group 14 metal element and platinum, and an atomic ratio of the group 14 metal element to the platinum in the dehydrogenation catalyst is 8.0 or less.