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 catalytic composition is built up from a ceramic material including a catalytic material and a first inorganic binder and a second inorganic binder and a catalytic structure made thereof. Preferably, the structure is made by a colloidal ceramic shaping technique. The structure is usable for catalytic or ion exchange applications as well. It is demonstrated that the catalytic structures have excellent mechanical, physicochemical and catalytic properties.

Porous zeolite monolith compositions for the catalytic cracking of alkanes. The compositions may be prepared layer by layer using a 3D printer such that the compositions comprise a plurality of micropores and a plurality of mesopores and may be characterized by macro-meso-microporosity.

Embodiments of zeolite composite catalysts and methods of producing the zeolite composite catalysts are provided, where the methods comprise dissolving in an alkaline solution a catalyst precursor comprising at least one mesoporous zeolite while heating, stirring, or both to yield a dissolved zeolite solution, where the mesoporous zeolite has a molar ratio of SiO.sub.2/Al.sub.2O.sub.3 of at least 30, where the mesoporous zeolite comprises zeolite beta, adjusting the pH of the dissolved zeolite solution, aging the pH adjusted dissolved zeolite solution to yield solid zeolite composite from the dissolved zeolite solution, and calcining the solid zeolite composite to produce the zeolite composite catalyst, where the zeolite composite catalyst has a mesostructure comprising at least one disordered mesophase and at least one ordered mesophase, and where the zeolite composite catalyst has a surface area defined by the Brunauer-Emmett-Teller (BET) analysis of at least 600 m.sup.2/g.

A process for conversion of hydrocarbon feedstock into lighter olefins of C.sub.2 to C.sub.4 carbons, the process comprising of cracking the hydrocarbon feedstock in a reactor in the presence of a catalyst. The catalyst for short contact time catalytic cracking process of heavy hydrocarbons having contact time less than 1 second to produce light olefins of C.sub.2 to C.sub.4 carbon in the range of 40 to 60 wt % on fresh feed basis in a fluidized bed reactor which is concentric downflow reactor in presence of catalyst consisting of ultra-stable Y zeolite in the range of 5-10 wt %, 4 to 8 wt % of pentasil zeolite, 2.5-5 wt % of bottom selective material, 0.5-2 wt % of rare earth and 75-88 wt % of support material.

Novel MEL framework type zeolites can be made to have small crystallite sizes and desirable silica/SiO.sub.2 molar ratios. Catalyst compositions comprising such MEL framework type zeolites can be particularly advantageous in isomerization C8 aromatic mixtures. An isomerization process for converting C8 aromatic hydrocarbons can advantageously utilize a catalyst composition comprising a MEL framework type zeolite.

Novel MEL framework type zeolites can be made to have small crystallite sizes and desirable silica/SiCb molar ratios. Catalyst compositions comprising such MEL framework type zeolites can be particularly advantageous in isomerization C8 aromatic mixtures. An isomerization process for converting C8 aromatic hydrocarbons can advantageously utilize a catalyst composition comprising a MEL framework type zeolite.

Catalyst composition which comprises a first zeolite having a BEA* framework type and a second zeolite having a MOR framework type and a mesopore surface area of greater than 30 m.sup.2/g is disclosed. These catalyst compositions are used to remove catalyst poisons from untreated feed streams having one or more impurities which cause deactivation of the downstream catalysts employed in hydrocarbon conversion processes, such as those that produce mono-alkylated aromatic compounds.

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.