A method is provided for forming composite of nano-sized zeolite beta and hierarchical zeolite Y. The method includes synthesizing a hierarchical zeolite Y, synthesizing a gel of a nano-sized zeolite beta, forming a slurry of the nano-sized zeolite beta from the gel, and mixing the hierarchical zeolite Y with the slurry to form a composite. The composite is dried and an extrudable paste is formed from the dried composite. The extrudable paste is extruded to form extrudates, which are calcined to form calcined extrudates.

Embodiments of the present disclosure are directed to hydrogen-selective oxygen carrier materials and methods of using hydrogen-selective oxygen carrier materials. The hydrogen-selective oxygen carrier material may comprise a core material, which includes a redox-active transition metal oxide; a shell material, which includes one or more alkali transition metal oxides; and a support material. The shell material may be in direct contact with at least a majority of an outer surface of the core material. At least a portion of the core material may be in direct contact with the support material. The hydrogen-selective oxygen carrier material may be selective to combust hydrogen in an environment that includes hydrogen and hydrocarbons.

A process for hydrodesulfurizing an olefinic naphtha feedstock while retaining a substantial amount of the olefins, which feedstock has a T.sub.95 boiling point below 250° C. and contains at least 50 ppmw of organically bound sulfur and from 5% to 60% olefins, the process including hydrodesulfurizing the feedstock in a sulfur removal stage in the presence of a gas including hydrogen and a hydrodesulfu-rization catalyst, at hydrodesulfurization reaction conditions, to convert at least 60% of the organically bound sulfur to hydrogen sulfide and to produce a desulfurized product stream, with the associated benefit of such a process providing a lower octane loss at all severities above 60% HDS, compared to a process with similar conversion of organic sulfur with a lower gas to oil ratio, as measured by the selectivity slope, while avoiding excessive increase of equipment size by limiting gas to oil ratio.

Provided is a method for preparing a diol. In the method, a saccharide and hydrogen as raw materials are contacted with a catalyst in water to prepare the diol. The employed catalyst is a composite catalyst comprised of a main catalyst and a cocatalyst, wherein the main catalyst is a water-insoluble acid-resistant alloy; and the cocatalyst is a soluble tungstate and/or soluble tungsten compound. The method uses an acid-resistant, inexpensive and stable alloy needless of a support as a main catalyst, and can guarantee a high yield of the diol in the case where the production cost is relatively low.

Provided is a method for preparing a diol. In the method, a saccharide and hydrogen as raw materials are contacted with a catalyst in water to prepare the diol. The employed catalyst is a composite catalyst comprised of a main catalyst and a cocatalyst, wherein the main catalyst is a water-insoluble acid-resistant alloy; and the cocatalyst is a soluble tungstate and/or soluble tungsten compound. The method uses an acid-resistant, inexpensive and stable alloy needless of a support as a main catalyst, and can guarantee a high yield of the diol in the case where the production cost is relatively low.

A method for preparing an SCR catalyst may include: (1) placing a first aqueous solution containing a titanium oxide and a tungstate in an electric field environment, adjusting the pH value of the first aqueous solution, and adjusting the current direction of the electric field environment to obtain a first mixture; (2) providing a second mixture by, in the electric field environment, adding dropwise a second aqueous solution containing a soluble salt of one or more active components, a copper-organic polyamine complex and a dispersant to the first mixture, and adjusting the current direction; and (3) processing the second mixture to obtain the SCR catalyst. The one or more active components may be selected from Ce, Zr, Cu, Fe, Pr and Sc.

Embodiments of the present disclosure are directed to methods of producing a hydrogen- selective oxygen carrier material comprising combining one or more core material precursors and one or more shell material precursors to from a precursor mixture and heat-treating the precursor mixture at a treatment temperature to form the hydrogen-selective oxygen carrier material. The treatment temperature is greater than or equal to 100° C. less than the melting point of a shell material, and the hydrogen- selective oxygen carrier material comprises a core comprising a core material and a shell comprising the shell material. The shell material may be in direct contact with at least a majority of an outer surface of the core material.

Embodiments of the present disclosure are directed to methods of producing a hydrogen- selective oxygen carrier material comprising combining one or more core material precursors and one or more shell material precursors to from a precursor mixture and heat-treating the precursor mixture at a treatment temperature to form the hydrogen-selective oxygen carrier material. The treatment temperature is greater than or equal to 100° C. less than the melting point of a shell material, and the hydrogen- selective oxygen carrier material comprises a core comprising a core material and a shell comprising the shell material. The shell material may be in direct contact with at least a majority of an outer surface of the core material.

A process for hydrodesulfurizing an olefinic naphtha feedstock while retaining a substantial amount of the olefins, which feedstock has a T.sub.95 boiling point below 250° C. and contains at least 50 ppmw of organically bound sulfur and from 5% to 60% olefins, the process including hydrodesulfurizing the feedstock in a sulfur removal stage in the presence of a gas including hydrogen and a hydrodesulfurization catalyst, at hydrodesulfurization reaction conditions, to convert at least 60% of the organically bound sulfur to hydrogen sulfide and to produce a desulfurized product stream wherein the gas to oil ratio and the pressure are configured for the selectivity slope, (% HDS−% OSAT)/(% OSAT*(100−% HDS)), to be above 0.55, and to provide a lower octane loss at all severities above 60% HDS, compared to compared to all prior reported processes with similar conversion of organic sulfur with a lower gas to oil ratio, as measured by the selectivity slope.

A hydroprocessing catalyst has been developed. The catalyst is a crystalline transition metal tungstate material or metal sulfides derived therefrom, or both. The hydroprocessing using the crystalline transition metal tungstate material may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking. A data system comprising at least one processor; at least one memory storing computer-executable instructions; and at least one receiver configured to receive data of a conversion process comprising at least one reaction catalyzed by the catalyst or a metal sulfide decomposition product of the catalyst has been developed.