There is provided one-solution type photocatalyst-containing coating suspension comprising: 100 parts by weight of an aqueous solution including deionized water; 2 to 15 parts by weight of photocatalyst powders, wherein each of the photocatalyst powders receives light from an outside and exhibits a photocatalytic effect; 10 to 20 parts by weight of a negatively charged surfactant, wherein the surfactant surrounds the photocatalyst powders such that the photocatalyst powers are micellized into micelles dispersed in the aqueous solution; 5 to 15 parts by weight of colloidal inorganic binders dispersed in the aqueous solution.

A powdered catalyst material on a titanium oxide basis. The powdered catalyst material includes a combined content of at least 90 wt.-% of a hydrated titanium oxide having the general formula TiO.sub.(2-x)(OH).sub.2x, with 0<x?1, (calculated as TiO.sub.2), and a silicon dioxide and hydrated precursors of the silicon dioxide (calculated as SiO.sub.2). A weight ratio of TiO.sub.2/SiO.sub.2, determined for TiO.sub.2 and SiO.sub.2 respectively, is at least 3 and less than 30. The wt.-% is based on a total weight of the catalyst material after the catalyst material has been dried at 105? C. for at least 2 hours. The powdered catalyst material has a specific surface area of >300 m.sup.2/g and an isoelectric point of from 4.0 to 7.0.

A method provides for valorization of naturally abundant organic solid biomass under a specified gas atmosphere with the existence of a catalyst structure. The method effectively converts the organic solid feedstock while producing valuable liquid hydrocarbon products, as well as utilizing methane rich resources, providing an economical and environmental benefit in the oil and gas industry.

An oxidative dehydrogenation catalyst having: a structure having a formula Mo.sub.vV.sub.wNb.sub.yBi.sub.zO.sub.x, where v is 1, w is from 0.1 to 0.5, y is from 0.001 to 0.3, z is from 0.01 to 0.3, and x is the oxygen content required to charge-balance the structure. The oxidative dehydrogenation catalyst has a Pba2-32 space group, characterized by reflections determined with CuK.sub. X-ray diffraction (XRD) as follows.

Disclosed herein is a catalyzed soot filter (CSF) containing a porous wall flow substrate, a lean NOx trap (LNT) catalyst, and a catalyst for selective catalytic reduction (SCR). Also disclosed is a method of preparing the catalyzed soot filter, an emissions treatment system containing the catalyzed soot filter, and processes for treating exhaust gas emissions employing the catalyzed soot filter.

The present invention relates to a bimetallic mercaptan conversion catalyst for sweetening liquefied petroleum gas at a low temperature, which is prepared by using an Al.sub.2O.sub.3SiO.sub.2 composite oxide as a carrier to support bimetallic active components vanadium and nickel. The bimetallic mercaptan conversion catalyst has a proper specific surface area and more metal active center sites, and has advantages of simple preparation, an efficient mercaptan conversion ability even at a low temperature, and causing no saturation and polymerization of olefins. The bimetallic mercaptan conversion catalyst exhibits superior mercaptan conversion performance in LPG sweetening, has strong adaptability to starting materials, and can also nearly completely remove trace carbonyl sulfide contained in LPG.

The present invention relates to a magnesium oxide (MgO) catalyst for isomerisation of olefins with defined physical properties. The present invention further relates to a catalyst for conversion of olefins having a first catalyst component and a second catalyst component. The first catalyst component has a metathesis catalyst. The second catalyst component has the magnesium oxide catalyst. A process for obtaining an olefin is also disclosed.

A process and catalyst is disclosed for converting heavy hydrocarbon feed into lighter hydrocarbon products using multifunctional catalysts. Multifunctional catalysts enable use of less expensive metal by substituting expensive metals for less expensive metals with no loss or superior performance in slurry hydrocracking. Less available and expensive ISM can be replaced effectively.

A mixed oxide, a catalytic composition, a catalytic wall-flow monolith, the use of the mixed oxide and the process of the preparation of the mixed oxide. The mixed oxide comprises zirconium, cerium, lanthanum and optionally at least one rare earth element other than cerium and other than lanthanum. The catalytic composition and the wall-flow monolith comprise the particles of the mixed oxide. The use of the mixed oxide is in the preparation of a coating on a filter. The process of preparation of the mixed oxide consists jet milling. The mixed oxide is a compromise between a calibrated size and a low viscosity when in the form of an aqueous slurry while retaining a high specific surface area and a high pore volume.

A method of and system for recirculating a fluid in a particle production system. A reactor produces a reactive particle-gas mixture. A quench chamber mixes a conditioning fluid with the reactive particle-gas mixture, producing a cooled particle-gas mixture that comprises a plurality of precursor material particles and an output fluid. A filter element filters the output fluid, producing a filtered output. A temperature control module controls the temperature of the filtered output, producing a temperature-controlled, filtered output. A content ratio control module modulates the content of the temperature-controlled, filtered output, thereby producing a content-controlled, temperature-controlled, filtered output. A channeling element supplies the content-controlled, temperature-controlled, filtered output to the quench chamber, wherein the content-controlled, filtered output is provided to the quench chamber as the conditioning fluid to be used in cooling the reactive particle-gas mixture.