Abstract: Embodiments of catalyst systems and methods of synthesizing catalyst systems are provided. The catalyst system may include a core comprising a zeolite; and a shell comprising a microporous fibrous silica. The shell may be in direct contact with at least a majority of an outer surface of the core. The catalyst system may have a Si/Al molar ratio greater than 5. At least a portion of the shell may have a thickness of from 50 nanometers (nm) to 360 nm.

Abstract: Embodiments of catalyst systems and methods of synthesizing catalyst systems are provided. The catalyst system may include a core comprising a zeolite; and a shell comprising a microporous fibrous silica. The shell may be in direct contact with at least a majority of an outer surface of the core. The catalyst system may have a Si/Al molar ratio greater than 5. At least a portion of the shell may have a thickness of from 50 nanometers (nm) to 600 nm.

Abstract: Modified crystalline zeolite materials have a zeolite framework with both tetra-coordinate Lewis aluminum single sites and Brønsted aluminum sites. The tetra-coordinate Lewis aluminum single sites include aluminum atoms covalently bonded to a variable group and to two oxygen atoms and further coordinated to a third oxygen atom. The variable group may be alkyl, hydride, or hydroxyl. Methods for incorporating tetra-coordinate Lewis aluminum single sites into a crystalline zeolite material include contacting the crystalline zeolite material with a dialkylaluminum hydride R2AlH, where each R is alkyl, to react the dialkylaluminum hydride with the zeolite framework and form tetra-coordinate alkyl aluminum single sites. Heating the alkyl-aluminum zeolite induces ?-hydride elimination of the alkyl groups, whereby tetra-coordinate aluminum hydride single sites are formed.

Abstract: Embodiments of catalyst systems and methods of synthesizing catalyst systems are provided. The catalyst system may include a core comprising a zeolite; and a shell comprising a microporous fibrous silica. The shell may be in direct contact with at least a majority of an outer surface of the core. The catalyst system may have a Si/Al molar ratio greater than 5. At least a portion of the shell may have a thickness of from 50 nanometers (nm) to 600 nm.

Abstract: Embodiments of catalyst systems and methods of synthesizing catalyst systems are provided. The catalyst system may include a core comprising a zeolite; and a shell comprising a microporous fibrous silica. The shell may be in direct contact with at least a majority of an outer surface of the core. The catalyst system may have a Si/Al molar ratio greater than 5. At least a portion of the shell may have a thickness of from 50 nanometers (nm) to 360 nm.

Abstract: The invention relates to heterogeneous catalysts comprising an organo-ruthenium complex immobilized to an aluminum-modified inorganic oxide by a chemical bond between a tetra-coordinated aluminum atom on a surface of the aluminum-modified inorganic oxide and an amino or imino nitrogen of the organo-ruthenium complex, methods of preparing the heterogeneous catalysts including immobilizing the organo-ruthenium complex to a tetra-coordinated aluminum atom on a surface of an inorganic oxide by reacting an amino or imino nitrogen of the organo-ruthenium complex and an aluminum-modified inorganic oxide, followed by a defined heat treatment, as well as methods for producing hydrogen from formic acid using the heterogeneous catalysts.

Abstract: Modified crystalline zeolite materials have a zeolite framework with both tetra-coordinate Lewis aluminum single sites and Brønsted aluminum sites. The tetra-coordinate Lewis aluminum single sites include aluminum atoms covalently bonded to a variable group and to two oxygen atoms and further coordinated to a third oxygen atom. The variable group may be alkyl, hydride, or hydroxyl. Methods for incorporating tetra-coordinate Lewis aluminum single sites into a crystalline zeolite material include contacting the crystalline zeolite material with a dialkylaluminum hydride R2AlH, where each R is alkyl, to react the dialkylaluminum hydride with the zeolite framework and form tetra-coordinate alkyl aluminum single sites. Heating the alkyl-aluminum zeolite induces ?-hydride elimination of the alkyl groups, whereby tetra-coordinate aluminum hydride single sites are formed.

Abstract: According to one or more embodiments, cationic polymers may be produced which include one or more monomers containing cations. Such cationic polymers may be utilized as structure directing agents to for mesoporous zeolites. The mesoporous zeolites may include micropores as well as mesopores, and may have a surface area of greater than 350 m2/g and a pore volume of greater than 0.3 cm3/g. Also described are core/shell zeolites, where at least the shell portion includes a mesoporous zeolite material.

Abstract: Embodiments of the present disclosure describe methods of preparing pre-catalysts that may be activated under methane to form catalysts for the hydrogenation of carbon dioxide to form olefins, among other chemical species. Embodiments of the present disclosure also describe methods of preparing catalysts and pre-catalysts, catalyst and pre-catalyst compositions, and methods of producing one or more chemical species using catalysts.

Abstract: According to one or more embodiments, cationic polymers may be produced which include one or more monomers containing cations. Such cationic polymers may be utilized as structure directing agents to for mesoporous zeolites. The mesoporous zeolites may include micropores as well as mesopores, and may have a surface area of greater than 350 m2/g and a pore volume of greater than 0.3 cm3/g. Also described are core/shell zeolites, where at least the shell portion includes a mesoporous zeolite material.

Abstract: Embodiments of the present disclosure describe a treated iron ore catalyst. Embodiments of the present disclosure further describe a method of preparing a treated iron ore catalyst comprising dehydrating an iron ore, milling the iron ore to a selected particle size, and reducing the iron ore to form a treated iron ore catalyst. Another embodiment of the present disclosure is a method of using a treated iron ore catalyst comprising contacting a feed gas with a treated iron ore catalyst to produce hydrogen and graphene.

Abstract: According to one or more embodiments, cationic polymers may be produced which include one or more monomers containing cations. Such cationic polymers may be utilized as structure directing agents to for mesoporous zeolites. The mesoporous zeolites may include micropores as well as mesopores, and may have a surface area of greater than 350 m2/g and a pore volume of greater than 0.3 cm3/g. Also described are core/shell zeolites, where at least the shell portion includes a mesoporous zeolite material.

Abstract: According to one or more embodiments, cationic polymers may be produced which include one or more monomers containing cations. Such cationic polymers may be utilized as structure directing agents to for mesoporous zeolites. The mesoporous zeolites may include micropores as well as mesopores, and may have a surface area of greater than 350 m2/g and a pore volume of greater than 0.3 cm3/g. Also described are core/shell zeolites, where at least the shell portion includes a mesoporous zeolite material.

Abstract: According to one or more embodiments, a mesoporous zeolite may included a microporous framework that includes a plurality of micropores having diameters of less than or equal to 2 nm, and a plurality of mesopores having diameters of greater than 2 nm and less than or equal to 50 nm. The mesoporous zeolite may included an aluminosilicate material, a titanosilicate material, or a pure silicate material. The mesoporous zeolite may included a surface area of greater than 350 m2/g and a pore volume of greater than 0.3 cm3/g.

Abstract: Embodiments of the present disclosure describe a catalyst and/or a precatalyst, in particular a single site catalyst and/or a single site precatalyst, for the oxidation and/or ammoxidation of olefins to produce aldehydes and/or nitriles, methods of preparing a corresponding catalyst and/or precatalyst, in particular single site catalyst and/or single site precatalyst, and methods of using said catalyst and/or precatalyst, in particular said single site catalyst and/or single site precatalyst, to produce aldehydes and/or nitriles.

Abstract: Embodiments of the present disclosure describe a catalyst for dehydrocyclisation of hydrocarbons comprising a suitable support and an organometallic complex or a coordination compound including at least a dehydrogenation metal, wherein the dehydrogenation metal of the organometallic complex or coordination compound is grafted to a selected site of the suitable support. Embodiments of the present disclosure further describe a method of preparing a dehydrocyclisation catalyst for hydrocarbons comprising grafting a dehydrogenation metal of an organometallic complex or coordination compound to a selected site of a suitable support to form the dehydrocyclisation catalyst. Another embodiment of the present disclosure is a method of dehydrocyclisation of hydrocarbons comprising contacting a hydrocarbon with a dehydrocyclisation catalyst to convert the hydrocarbon to an aromatic compound, wherein the dehydrocyclisation catalyst includes a dehydrogenation metal grafted to a selected site of a suitable support.

Abstract: Provided herein are bi-metallic catalysts, methods of making, and uses thereof. In some embodiments, the bi-metallic catalyst contains two different metal catalysts that can be used in hydrocarbon metathesis reactions, in some embodiments, the methods of making the bi-metallic catalysts can include two steps utilizing a surface organometallic chemistry approach in which the two different metal catalysts are sequentially grafted onto a support.

Abstract: Embodiments of the present disclosure provide for supported Ni/Pt bimetallic nanoparticles having a Ni core and a Pt layer disposed on the surface of the Ni core, compositions including supported NiPt nanoparticles, methods of making supported NiPt nanoparticles, methods of using supported NiPt nanoparticles, and the like.

Abstract: The present invention uses a cobalt catalyst for carbon dioxide reforming of lower alkanes to synthesis gas having a cobalt catalyst on an oxide support where the supported cobalt catalyst has been modified with a boron precursor. The boron-treated cobalt catalyst systems as described herein show significant increases in the conversion of CH4 and CO2 during the dry reforming of methane (DRM) reaction as compared to traditional catalysts. Described herein are supported catalysts and methods of using the catalysts for the dry reforming of methane to synthesis gas, with the supported catalysts in the present invention include a boron-treated cobalt catalyst disposed on an oxide support. Also described herein are processes for preparing the supported catalysts.

Abstract: Embodiments of the present disclosure provide for methods that can be used to produce carbon nanotubes (hereinafter CNT) having an inner diameter about 5-55 nm, methods of tuning the inner diameter of CNTs (e.g., by adjusting reaction pressure), CNTs having an inner diameter of greater than 20 nm or more, and the like.