An adsorption material which includes a carbon nanohorn aggregate in which a plurality of single-walled carbon nanohorns aggregate in a fibrous state, particularly coexisting a globular carbon nanohorn aggregate and some of the single-walled carbon nanohorns included in the carbon nanohorn aggregate have an opening portion, is used. The adsorption material including such a fibrous carbon nanohorn aggregate is produced by a method including: preparing an inert gas atmosphere, a nitrogen gas atmosphere or a mixed atmosphere in a vessel in which a catalyst-containing carbon target is placed; and evaporating the target to obtain a carbon nanohorn aggregate including a fibrous carbon nanohorn aggregate in which a plurality of single-walled carbon nanohorns aggregate in a fibrous state.

Provided is a method for preparing a catalyst for a dehydrogenation reaction of formate and a hydrogenation reaction of bicarbonate, the method including: adding a silica colloid to a polymerization step of polymerizing aniline and reacting the resulting mixture to form a poly(silica-aniline) composite; carbonizing the corresponding poly(silica-aniline) composite under an atmosphere of an inert gas; removing silica particles from the corresponding poly(silica-aniline) composite to form a polyaniline-based porous carbon support; and fixing palladium particles on the corresponding polyaniline-based porous carbon support to prepare the catalyst.

The present disclosure recognizes a correlation between zeolitic surface area (ZSA) of a catalyst composition and its catalytic activity. Particularly, the disclosure provides catalyst articles for diesel NO.sub.x abatement, including a substrate and a washcoat layer containing metal-promoted molecular sieves, wherein the zeolitic surface area (ZSA) of the catalyst article is about 100 m.sup.2/g or greater, the volumetric surface area is about 900 m.sup.2/in.sup.3 or greater, and/or the total zeolitic surface area (tZSA) is about 1200 m.sup.2 or greater. The disclosure further relates to methods for evaluating ZSA, volumetric ZSA, and tZSA, e.g., including the steps of coating a catalyst composition comprising metal-promoted molecular sieves onto a substrate; calcining and aging the catalyst composition; determining the ZSA (or volumetric ZSA or tZSA) thereof; and correlating the ZSA (or volumetric ZSA or tZSA) with catalyst composition NO.sub.x abatement activity to determine whether the catalyst composition is suitable for an intended use.

Disclosed herein are metal-organic frameworks and methods of making and use thereof.

Hydrogenation catalysts for aromatic hydrogenation including an organosilica material support, which is a polymer comprising independent units of a monomer of Formula [Z.sup.1OZ.sup.2OSiCH.sub.2].sub.3 (I), wherein each Z.sup.1 and Z.sup.2 independently represent a hydrogen atom, a C.sub.1-C.sub.4 alkyl group or a bond to a silicon atom of another monomer; and at least one catalyst metal are provided herein. Methods of making the hydrogenation catalysts and processes of using, e.g., aromatic hydrogenation, the hydrogenation catalyst are also provided herein.

The present invention relates to a method for the selective hydrogenation of polyunsaturated compounds containing at least two carbon atoms per molecule in the presence of a catalyst comprising an active phase made from at least one group VIII metal and a support in the form of a ceramic or metal foam, the catalyst having a geometric surface area of between 1000 and 7000 m.sup.2/m.sup.3 and a pore diameter of between 0.2 and 1.5 mm.

The present invention relates to a method for preparing size-modulated UiO-66, which is achieved by modulating the concentrations of reactants, and a catalyst with improved activity of hydrolyzing chemical warfare agents prepared by the method.

A catalytic converter, including a substrate formed of an open cell carbon foam having a geometric surface area of at least about 5000 m.sup.2/m.sup.3 and a permeability of at least about 8.0 darcys, wherein the carbon foam has catalytic metals incorporated thereinto.

A catalyst includes a support, where the support includes an external surface, about 60 wt % to about 99 wt % silica, and about 1.0 wt % to about 5.0 wt % alumina. A catalytic layer is disposed within the support adjacent to the external surface, where the catalytic layer further includes Pd, Au, and potassium acetate (KOAc). In the catalyst, (a) the KOAc is from about 60 kg/m.sup.3 to about 150 kg/m.sup.3 of the catalyst; or (b) the catalytic layer has an average thickness from about 50 m to about 150 m; or (c) both (a) and (b). The catalyst also possesses a Brunauer-Emmett-Teller surface area of about 130 m.sup.2/g to about 300 m.sup.2/g and a geometric surface area per packed bed volume from about 550 m.sup.2/m.sup.3 to about 1500 m.sup.2/m.sup.3. The catalyst is highly active for the synthesis of vinyl acetate monomer and exhibits a high selectivity for vinyl acetate monomer.

A substrate for a catalytic converter, comprising an open cell carbon foam having a geometric surface area of at least about 5000 m.sup.2/m.sup.3 and a permeability of at least about 8.0 darcys, wherein the substrate has a catalytic material which includes non-noble metal nano-scale catalyst particles.