A catalyst comprising a microporous crystalline metallosilicate having a Constraint Index of 12, or 10, or 8, or 6 or less, a binder, a Group 1 alkali metal or a compound thereof and/or a Group 2 alkaline earth metal or a compound thereof, a Group 10 metal or a compound thereof, and, optionally, a Group 11 metal or a compound thereof; wherein the catalyst is calcined in a first calcining step before the addition of the Group 10 metal or compound thereof and optionally the Group 11 metal or compound thereof; and wherein the first calcining step includes heating the catalyst to first temperatures of greater than 500° C.; and wherein the catalyst is calcined in a second calcining step after the addition of the Group 10 metal or compound thereof and optionally the Group 11 metal or compound thereof wherein the second calcining step includes heating the catalyst to temperatures of greater than 400° C.

A process for producing olefins comprising introducing butane feed (n-butane, i-butane) and hydrogen to hydrogenolysis reactor comprising hydrogenolysis catalyst to produce a hydrogenolysis product stream (hydrogen, methane, ethane, propane, i-butane, optionally n-butane, optionally C.sub.5+ hydrocarbons); and feeding the hydrogenolysis product stream and hydrogen to hydrocracking reactor comprising a hydrocracking catalyst to produce hydrocracking product stream (hydrogen, methane, ethane, propane, i-butane, optionally n-butane), wherein the amount of i-butane in the hydrocracking product stream is less than in the hydrogenolysis product stream, and wherein the amount of ethane in the hydrocracking product stream is greater than in the hydrogenolysis product stream. The hydrocracking product stream is separated into first hydrogen stream, first methane stream, first C.sub.2+ gas stream (ethane, propane), first C.sub.4s stream (i-butane, optionally n-butane), optionally C.sub.5+ stream; and the first C.sub.2+ gas stream is fed to gas steam cracker to produce a steam cracker product stream comprising olefins (ethylene, propylene).

A catalyst comprising a microporous crystalline aluminosilicate having a Constraint Index less than or equal to 12, a Group 1 alkali metal or a compound thereof and/or a Group 2 alkaline earth metal or a compound thereof, a Group 10 metal or a compound thereof, and optionally a Group 11 metal or a compound thereof; wherein the total amount of Group 1 and/or Group 2 metal is present at a ratio that is optimized for the desirable chemical conversion process.

A catalyst for converting ethane to monoaromatic hydrocarbons including: a zeolite; cesium oxide, wherein cesium of the cesium oxide is present in an amount of 0.01 to 0.5 weight percent, preferably 0.01 to 0.1 weight percent, more preferably 0.03 to 0.07 weight percent, based on a total weight of the catalyst; platinum oxide, wherein platinum of the platinum oxide is present in an amount of 0.01 to 1 weight percent, preferably 0.01 to 0.5 weight percent, more preferably 0.01 to 0.05 weight percent, based on a total weight of the catalyst; and gallium oxide, wherein gallium of the gallium oxide is present in an amount of 0.01 to 1 weight percent, preferably 0.03 to 0.5 weight percent, more preferably 0.05 to 0.2 weight percent, based on a total weight of the catalyst; wherein the monoaromatic hydrocarbons include benzene, toluene, xylene, or a combination including at least one of the foregoing.

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.

The present invention provides a catalyst for aromatization of a long-carbon chain alkane and a preparation method thereof. In the present invention, a molecular sieve containing a BEA structure is taken as an active component and mixed with a carrier, and then the mixture is formed, dried and calcined to obtain the catalyst for aromatization of a long-carbon chain alkane. The active component is prepared by taking a Naβ molecular sieve as a raw material and modifying through the following steps of: first obtaining an Hβ molecular sieve through ammonium ion-exchange, and then conducting dealumination and silicon insertion treatment of the Hβ molecular sieve through first hydrothermal treatment; forming a mesoporous structure in a molecular sieve framework through second hydrothermal treatment; reducing the acidity of the catalyst by potassium ion exchange, and finally using metal modification to improve the capability of the catalyst for catalyzing the aromatization of the long-carbon chain alkane and enhancing the toluene selectivity. The catalyst provided by the present invention shows high stability in the aromatization of the long-chain alkane and has a service life up to 170 h or above and aromatic hydrocarbon selectivity up to 80%, and the selectivity to toluene in aromatic hydrocarbon products can reach 85.5%.

Disclosed herein are embodiments of a method and system for converting ethanol to para-xylene. The method also provides a pathway to produce terephthalic acid from biomass-based feedstocks. In some embodiments, the disclosed method produces p-xylene with high selectivity over other aromatics typically produced in the conversion of ethanol to xylenes, such as m-xylene, ethyl benzene, benzene, toluene, and the like. And, in some embodiments, the method facilitates the ability to use ortho/para mixtures of methylbenzyaldehyde for preparing ortho/para xylene product mixtures that are amendable to fractionation to separate the para- and ortho-xylene products thereby providing a pure feedstock of para-xylene that can be used to form terephthalic anhydride and a pure feedstock of ortho-xylene that can be used for other purposes, such as phthalic anhydride.

Disclosed are a catalyst and a preparation method therefor, the catalyst being able to maintain a high production yield of C8 aromatic hydrocarbons in the process of converting a feedstock containing alkyl aromatics to C8 aromatic hydrocarbons such as mixed xylene through disproportionation/transalkylation/dealkylation while reducing a content of ethylbenzene in the products.

Methods and corresponding catalysts are provided for conversion of an aromatic feed containing C.sub.8+ aromatics (particularly C.sub.9+ aromatics) to form a converted product mixture comprising, e.g., benzene and/or xylenes. The aromatic feed can be converted in the presence of a catalyst that includes a silica binder, a mixture of a first zeolite having an MEL framework (such as ZSM-11 and/or an MFI framework (such as ZSM-5), and a second zeolite having an MOR framework, such as mordenite, particularly a mordenite synthesized using TEA or MTEA as a structure directing agent, and a metal. The catalyst can further include one or more metals supported on the catalyst.

Methods and corresponding catalysts are provided for conversion of an aromatics feed containing C.sub.8+ aromatics, particularly C.sub.9+ aromatics, to form a converted product mixture comprising, e.g., benzene and/or xylenes. The aromatic feed can be converted in the presence of a catalyst that includes a mixture of a first zeolite having an MEL framework, such as ZSM-11, and a second zeolite having a MOR framework, such as mordenite, particularly a mordenite synthesized using TEA or MTEA as a structure directing agent. The weight ratio of the first zeolite to the second zeolite in the catalyst can be from 0.3 to 1.2, or from 0.3 to 1.1, or from 0.3 to 1.0. The catalyst can further include one or more metals supported on the catalyst, such as a combination of metals.