To provide a catalyst capable of hydrotreating a hydrocarbon oil with high desulfurization activity. A hydrotreating catalyst for a hydrocarbon oil includes: an inorganic composite oxide carrier including alumina as a main component; and an active metal component supported on the carrier, the active metal component including, as active metal species, a first metal which is at least one of molybdenum and tungsten, and a second metal which is at least one of cobalt and nickel, the hydrotreating catalyst for having a Lewis acid amount and a Brnsted acid amount per unit surface area of 0.80 mol/m.sup.2 or more and 0.03 mol/m.sup.2 or less, respectively, as measured by pyridine desorption at 250 C. and a BET single-point method.

A Pd-supporting Zr-based composite oxide wherein by having a Zr-containing composite oxide support and Pd supported thereon and by showing, upon XAFS (X-ray absorption fine structure) analysis, a maximum peak in a Pd bond distance range of 2.500-3.500 , the maximum peak being located in a position of 3.050-3.110 .

Provided is a catalyst that can exhibit high activity. The catalyst is an electrode catalyst having catalytic metals supported on a catalyst support, in which the catalytic metals include platinum and a metal component other than platinum; the electrode catalyst has mesopores having a mode radius of pore distribution of mesopores having a radius of 1 nm or more, of 1 nm or more and less than 2.5 nm; alloy microparticles of platinum and the metal component other than platinum are supported inside the mesopores; and a molar content ratio of platinum with respect to the metal component other than platinum in the alloy microparticles supported inside the mesopores is 1.0 to 10.0.

Provided is a methanation catalyst processing method capable of suppressing degradation of a catalyst performance. A methanation catalyst processing method of the present disclosure includes oxidizing nickel through a heat treatment of a methanation catalyst by supplying an oxygen gas containing oxygen to a reactor, the reactor housing the methanation catalyst containing the nickel as a catalyst component. In the oxidizing, the oxygen gas is supplied to the reactor such that the oxygen is supplied to 1 g of the methanation catalyst at a supply rate in a range of from 0.0213 mmol-O.sub.2/sec.Math.g-cat. to 0.0638 mmol-O.sub.2/sec.Math.g-cat., and a time period of the heat treatment of the methanation catalyst by supplying the oxygen gas to the reactor is set to 30 minutes or more.

The present invention relates to zeolite containing Cu2+ (?) and Cu2+ (?) having different NO adsorption capacities loaded at a specific ratio, wherein the zeolite is chabazite (CHA)-type zeolite, particularly chabazite (CHA)-type zeolite loaded with divalent copper ions in which the NO adsorption area ratio of Cu2+ (?)/Cu2+ (?) after exposure to NO (nitrogen oxide) for 180 sec is 80% or more. In addition, the present invention relates to a method of preparing zeolite that is ion-exchanged in a slurry state and to a catalyst including the specified chabazite (CHA)-type zeolite.

Active catalysts for the treatment of a low temperature exhaust gas stream are provided containing copper oxides dispersed on a spinel oxide for the direct, lean removal of nitrogen oxides from the exhaust gas stream. The low temperature, direct decomposition is accomplished without the need of a reductant molecule. In one example, CuO.sub.x may be dispersed as a monolayer on a metal oxide support, such as Co.sub.3O.sub.4 spinel oxide, synthesized using an incipient wetness impregnation technique. The CuO.sub.x/Co.sub.3O.sub.4 catalyst system converts nitric oxide to nitrogen gas with high product specificity, avoiding the production of a significant concentration of the undesirable N.sub.2O product.

The present invention relates to a catalyst composition and a process for preparing thereof, wherein the catalyst composition is specifically active for hydro-conversion of LCO involving mainly the partial ring opening of multi-ring aromatics leading to the production of petrochemical feedstock. The catalyst composition comprises of a carrier comprising ultra-stable Y zeolite and binder alumina, group VIB and VIIIB metal species, and organic additives. The carrier is impregnated with metal solution to form active sites of WS.sub.2 slabs of dimensions in the range of 35-45 .

This invention relates to an aqueous dispersion of particles, the dispersion having a particle content of 10-70 wt %, and the particles comprising, on an oxide basis: (a) 10-98 wt % in total of ZrO.sub.2+HfO.sub.2, and (b) 2-90 wt % in total of Al.sub.2O.sub.3, CeO.sub.2, La.sub.2O.sub.3, Nd.sub.2O.sub.3, Pr.sub.6O.sub.11, Y.sub.2O.sub.3, or a transition metal oxide, wherein the dispersion has a Z-average particle size of 100-350 nm and the particles have a crystallite size of 1-9 nm. The invention also relates to a substrate coated with the aqueous dispersion of particles.

A catalyst, including silica and iron. The silica is in the form of a mesoporous spherical particle. The iron is in the form of nanoparticles evenly distributed and encapsulated in the silica. The particle size of the silica is between 140 and 160 nm, and the silica includes pores between 2 and 9 nm in diameter.

A metal/-MoC.sub.1-x load-type single-atomic dispersion catalyst, a synthesis method therefor, and applications thereof. The catalyst uses -MoC.sub.1-x as carrier, and has metal that has the mass fraction ranging from 1-100% and that is dispersed on carrier -MoC.sub.1-x in the single atom form. The catalyst provided in the present application can be adapted to a wide alcohol/water proportion in hydrogen production based on aqueous-phase reforming of alcohols, outstanding hydrogen production performance can be obtained at a variety of proportions, and catalysis performance of the catalyst is much higher than that of metal loaded with an oxide carrier. Especially when the metal is Pt, catalysis performance of the catalyst provided in the present application in the hydrogen production based on aqueous-phase reforming of alcohols is much higher than that of a Pt/-MoC.sub.1-x load-type catalyst on the -MoC.sub.1-x carrier on which Pt is disposed on a layer form in the prior art. The hydrogen production performance of the catalyst provided in the present application can be higher than 20,000 h.sup.1 at the temperature of 190 C.