An electrode catalyst material includes graphite particles and catalyst particles. Each of the graphite particles has a hollow structure that includes an outer shell, and the outer shell has at least one of a through-hole and a recess. Each of the catalyst particles is supported by the at least one of through-hole and recess.

The present invention relates to a Cracking Catalyst composition for cracking of heavy hydrocarbon feed stocks and process for preparing the catalyst. The catalyst is prepared by incorporating 1-10 wt % phosphate treated USY zeolite in which phosphate is present in the range of 10 to 50 wt % on the basis of phosphated zeolite, in a mixture of 10-50 wt % dispersible alumina, 0-30 wt % non-dispersal alumina, 5-30 wt % colloidal silica, 15-50 wt % clay and 5-15 wt % phosphate.

A composite hollow particle comprising titanium dioxide and a metal ion in the shell which covers a hollow core. A method of making the composite hollow particle and a method of employing the composite hollow particle in production of hydrogen gas under visible light are provided.

Disclosed is a direct synthesis method of nanostructured catalyst particles on surfaces of various supports. In the disclosed synthesis method of a catalyst structure having a plurality of nanostructured catalyst particles dispersed in a support by a one-step process using a high-temperature high-pressure closed reactor, the one-step process includes supplying the support and a catalyst source into the high-temperature high-pressure closed reactor; supplying an atmosphere forming gas of the reactor into the reactor; perfectly sealing the high-temperature high-pressure closed reactor and heating the reactor to produce the catalyst structure in the reactor under self-generated pressure and synthesis temperature conditions, the catalyst structure including the plurality of nanostructured catalyst particles dispersed in the support; removing internal gases of the reactor to allow the reactor to be in a high-temperature, atmospheric pressure state and supplying an inert gas into the reactor to remove unreacted materials and byproducts remaining in the reactor; and cooling the reactor to room temperature while supplying the inert gas to synthesize the catalyst structure.

The invention is directed to a CO to CO.sub.2 combustion promoter comprising microsphere sized porous silica and/or alumina comprising particles further comprising on or more Group VIII noble metals wherein the noble metal is distributed in the particle as an eggshell such that a higher content of noble metal is present in the outer region of the particle as compared to the content of noble metal in the center of the particle.

The invention is directed to a CO to CO.sub.2 combustion promoter comprising microsphere sized porous silica and/or alumina comprising particles further comprising on or more Group VIII noble metals wherein the noble metal is distributed in the particle as an eggshell such that a higher content of noble metal is present in the outer region of the particle as compared to the content of noble metal in the center of the particle.

A method of synthesizing an Au(TiO.sub.2-y/WO.sub.3-x) semiconductor composite, the method comprising: loading tungsten oxide (WO.sub.3) powder in a fluidized bed reactor followed by H.sub.2 treatment to produce reduced tungsten oxide (WO.sub.3) nanoparticles or WO.sub.3-x nanoparticles; producing reduced titanium dioxide (TiO.sub.2) nanoparticles or TiO.sub.2-y (containing defect states) nanoparticles in-situ; coupling the TiO.sub.2-y nanoparticles with the WO.sub.3-x nanoparticles to provide a titanium dioxide/tungsten oxide nanocomposite (TiO.sub.2-y/WO.sub.3-x); and simultaneous substitutional doping of TiO.sub.2-y and WO.sub.3-x in the titanium dioxide/tungsten oxide nanocomposite (TiO.sub.2-y/WO.sub.3-x) with gold ions (Au) to obtain the Au(TiO.sub.2-y/WO.sub.3-x) semiconductor composite; wherein x has a value between 0.33 and 0.37. The thus produced composite can be used as a photocatalyst.

A method of synthesizing an Au(TiO.sub.2-y/WO.sub.3-x) semiconductor composite, the method comprising: loading tungsten oxide (WO.sub.3) powder in a fluidized bed reactor followed by H.sub.2 treatment to produce reduced tungsten oxide (WO.sub.3) nanoparticles or WO.sub.3-x nanoparticles; producing reduced titanium dioxide (TiO.sub.2) nanoparticles or TiO.sub.2-y (containing defect states) nanoparticles in-situ; coupling the TiO.sub.2-y nanoparticles with the WO.sub.3-x nanoparticles to provide a titanium dioxide/tungsten oxide nanocomposite (TiO.sub.2-y/WO.sub.3-x); and simultaneous substitutional doping of TiO.sub.2-y and WO.sub.3-x in the titanium dioxide/tungsten oxide nanocomposite (TiO.sub.2-y/WO.sub.3-x) with gold ions (Au) to obtain the Au(TiO.sub.2-y/WO.sub.3-x) semiconductor composite; wherein x has a value between 0.33 and 0.37. The thus produced composite can be used as a photocatalyst.

The present invention relates (i) to a method for producing a doped copper-tetraammine-salt-based hydrogenation catalyst suitable for the hydrogenation of an aromatic nitro compound such that an aromatic amine is obtained, the hydrogenation catalyst comprising copper in metal form or in oxidic form and a doping metal selected from iron, cobalt, manganese, vanadium, zinc or a mixture of two or more thereof in metal form or in oxidic form on a carrier, the carrier comprising silicon dioxide shaped bodies and/or silicon carbide shaped bodies, (ii) to a doped copper-tetraammine-salt-based hydrogenation catalyst obtainable using the aforementioned method according to the invention, and (iii) to a method for producing an aromatic amine, comprising the hydrogenation of an aromatic nitro compound in the presence of a doped copper-tetraammine-salt-based hydrogenation catalyst comprising copper in metal form or in oxidic form and comprising a doping metal in metal form or in oxidic form on a carrier as hydrogenation catalyst, the carrier comprising silicon dioxide shaped bodies and/or silicon carbide shaped bodies, and the hydrogenation catalyst being, more particularly, the aforementioned hydrogenation catalyst according to the invention.

The present invention relates (i) to a method for producing a doped copper-tetraammine-salt-based hydrogenation catalyst suitable for the hydrogenation of an aromatic nitro compound such that an aromatic amine is obtained, the hydrogenation catalyst comprising copper in metal form or in oxidic form and a doping metal selected from iron, cobalt, manganese, vanadium, zinc or a mixture of two or more thereof in metal form or in oxidic form on a carrier, the carrier comprising silicon dioxide shaped bodies and/or silicon carbide shaped bodies, (ii) to a doped copper-tetraammine-salt-based hydrogenation catalyst obtainable using the aforementioned method according to the invention, and (iii) to a method for producing an aromatic amine, comprising the hydrogenation of an aromatic nitro compound in the presence of a doped copper-tetraammine-salt-based hydrogenation catalyst comprising copper in metal form or in oxidic form and comprising a doping metal in metal form or in oxidic form on a carrier as hydrogenation catalyst, the carrier comprising silicon dioxide shaped bodies and/or silicon carbide shaped bodies, and the hydrogenation catalyst being, more particularly, the aforementioned hydrogenation catalyst according to the invention.