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 hydrogenolysis bimetallic supported catalyst comprising a first metal, a second metal, and a zeolitic support; wherein the first metal and the second metal are different; and wherein the first metal and the second metal can each independently be selected from the group consisting of iridium (Ir), platinum (Pt), rhodium (Rh), ruthenium (Ru), palladium (Pd), molybdenum (Mo), tungsten (W), nickel (Ni), and cobalt (Co).

A catalyst for the carbonylation of dimethyl ether to methyl acetate. The catalyst comprises a zeolite, such as a mordenite zeolite, at least one Group IB metal, such as copper, and/or at least one Group VIII metal, such as iron, and at least one Group IIB metal, such as zinc. Such a catalyst with combined metals provides enhanced catalytic activity, improved stability, and improved selectivity to methyl acetate, and does not require a halogen promoter, as compared to a metal-free or copper only zeolite.

A process for producing xylene from C.sub.9+ aromatic hydrocarbons comprises contacting a first feedstock comprising C.sub.9+ aromatic hydrocarbons with a first catalyst in the presence of hydrogen under effective vapor phase dealkylation conditions to dealkylate part of the C.sub.9+ aromatic hydrocarbons and produce a first product comprising benzene and unreacted C.sub.9+ aromatic hydrocarbons. A second feedstock comprising toluene is contacted with a second catalyst in the presence of hydrogen under effective vapor phase toluene disproportionation conditions to disproportionate at least part of the toluene and produce a second product comprising para-xylene. A third feedstock comprising C.sub.9+ aromatic hydrocarbons and benzene and/or toluene is contacted with a third catalyst in the presence of hydrogen under effective liquid phase C.sub.9+ transalkylation conditions to transalkylate at least part of the C.sub.9+ aromatic hydrocarbons and produce a third product comprising xylenes.

A composite media for non-oxidative C.sub.2H.sub.6 dehydrogenation comprises an aluminosilicate zeolite matrix, and an EDH catalyst on one or more of an external surface of the aluminosilicate zeolite matrix and internal surfaces within pores of the aluminosilicate zeolite matrix. The EDH catalyst comprises one or more of Fe, Zn, Pt, Ga, alloys thereof, and oxides thereof. A C.sub.2H.sub.6 activation system, and a method of processing a C.sub.2H.sub.6-containing stream are also described.

The present disclosure provides an aromatization catalyst, a preparation method, a regeneration method and an aromatization method thereof. The preparation method comprises steps of: mixing a zeolite molecular sieve with a binder to obtain a catalyst precursor; the catalyst precursor is successively subjected to an ion exchange modification and a first modification treatment, and then subjected to a hydrothermal treatment, and further subjected to active metal loading and a second modification treatment, to obtain the aromatization catalyst. The aromatization catalyst has good carbon deposition resistance and high aromatization activity, and enables an aromatization reaction to be completed under mild conditions, and has high aromatic selectivity, and the liquid yield is above 98.5%.

Disclosed are processes for conversion of a feedstock comprising C.sub.8+ aromatic hydrocarbons to lighter aromatic products in which the feedstock and optionally hydrogen are contacted in the presence of the catalyst composition under conversion conditions effective to dealkylate and transalkylate said C.sub.8+ aromatic hydrocarbons to produce said lighter aromatic products comprising benzene, toluene and xylene. The catalyst composition comprises a zeolite, a first metal, and a second metal, and is treated with a source of sulfur and/or a source of steam.

A process for producing methyl tert-butyl ether (MTBE) comprising introducing a butane feed stream (n-butane, i-butane) and hydrogen to a hydrogenolysis reactor comprising a hydrogenolysis catalyst to produce a hydrogenolysis product stream comprising hydrogen, methane, ethane, propane, i-butane, and optionally n-butane; separating the hydrogenolysis product stream into a first hydrogen-containing stream, an optional methane stream, a C.sub.2 to C.sub.3 gas stream (ethane, propane), and a butane stream (i-butane, optionally n-butane); feeding the butane stream to a dehydrogenation reactor to produce a dehydrogenation product stream, wherein the dehydrogenation reactor comprises a dehydrogenation catalyst, and wherein the dehydrogenation product stream comprises hydrogen, i-butane, and isobutylene; and feeding the dehydrogenation product stream and methanol to an etherification unit to produce an unreacted methanol stream, an unreacted isobutylene stream, and an MTBE stream.

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.

Catalytic methods for synthesis of super linear alkenyl arenes and alkyl arenes are provided. The methods are capable of synthesizing super linear alkyl and alkenyl arenes from simple arene and olefin starting materials and with high selectivity for linear coupling. Methods are also provided for making a 2,6-dimethylnapthalene (DMN) or 2,6-methylethylnapthalene (MEN).