A catalyst precursor composition for forming a phenol alkylation catalyst, the composition comprising: 70 to 98 weight percent of abase oxide comprising: magnesium oxide with a Brunauer-Emmett-Teller surface area from 75 meter.sup.2/gram to 220 meter.sup.2/gram, preferably from 75 meter.sup.2/gram to 140 meter.sup.2/gram, more preferably from 90 meter.sup.2/gram to 130 meter.sup.2/gram; or magnesium carbonate with a Brunauer-Emmett-Teller surface area of from 100 meter.sup.2/gram to 220 meter.sup.2/gram, preferably from 120 meter.sup.2/gram to 200 meter.sup.2/gram; or a combination thereof; at least one metal promoter precursor comprising an iron precursor, a manganese, a vanadium precursor, or a copper precursor; and a pore former, a lubricant, a coke inhibitor; and optionally, a strength additive; and optionally a binder, and a method of alkylating phenol using a catalyst derived from the catalyst precursor.

A selective hydrogenation catalyst that can be obtained by the process comprising at least the following steps: a) the alumina support is brought into contact with at least one organic additive; b) the alumina support is brought into contact with at least one nickel metal salt, the melting point of said metal salt of which is between 20° C. and 150° C.; c) the solid mixture obtained on conclusion of steps a) and b) is heated with stirring; d) the catalyst precursor on conclusion of step c) is dried; e) a step of heat treatment of the dried catalyst precursor obtained on conclusion of step d) is carried out.

The present invention addresses to obtaining a support of hydrorefining catalysts by an innovative preparation route that reduces the problem of loss (or leaching) of boron over the operating time of industrial units. As the presence of boron in catalysts contributes to increased activity (hydrogenating and acidic) and stability for the hydrorefining reactions (hydrotreating and hydrocracking), its maintenance in the catalyst guarantees the preservation of the properties in operation, throughout the entire cycle of campaign of industrial units.

An object of the present invention is to provide an exhaust gas purification system including a first exhaust gas treatment section provided upstream in an exhaust pathway of an internal-combustion engine, a second exhaust gas treatment section provided upstream in the exhaust pathway of the internal-combustion engine, wherein the exhaust gas purification system allows rhodium element contained in a catalyst layer of the second exhaust gas treatment section to efficiently exhibit the catalytic activity, and the present invention provides an exhaust gas purification system (1) configured to purify exhaust gas emitted from an internal-combustion engine, the exhaust gas purification system (1) including an exhaust gas path (2) through which exhaust gas flows, a first exhaust gas treatment section (3) provided upstream in the exhaust gas path (2), and a second exhaust gas treatment section (4) provided downstream in the exhaust gas path (2); wherein first catalyst layers of the first exhaust gas treatment section (3) each contain cerium element; wherein a percentage of the mass of the cerium element contained in the first catalyst layers in terms of cerium oxide, to the mass of the first catalyst layers, is 5.0% by mass or more and 13.0% by mass or less; and wherein second catalyst layers of the second exhaust gas treatment section (4) each contain rhodium element.

A heterogeneous catalyst comprising a support and a noble metal, wherein said support comprises silicon, and wherein said catalyst comprises from 0.1 to 40 mol % titanium and from 0.1 to 10 mol % of at least one noble metal.

Catalyst containing an active phase which contains a group VIB element, at least one group VIII element and phosphorus, and a support containing alumina, the catalyst being characterized in that at least 80% by weight of the group VIB elements, of the group VIII elements and of the phosphorus are distributed in the form of a crust at the periphery of said support, the thickness of said crust being between 100 and 1200 μm, the content of group VIB element being between 1% and 8% by weight relative to the total weight of the catalyst, the content of group VIII element being between 0.5% and 5% by weight relative to the total weight of the catalyst, and the content of phosphorus being between 0.2% and 3% by weight relative to the total weight of the catalyst, and the support having a specific surface area of between 100 m.sup.2/g and 250 m.sup.2/g.

The present invention provides a catalyst for catalytic reduction of an industrial flue gas SO.sub.2 with CO to prepare sulfur, a method for preparing the same and use thereof. A CeO.sub.2 nanocarrier is prepared by using a hydrothermal method, La and Y are loaded as active components, pre-sulfurization is conducted with 6% of SO.sub.2 and 3% of CO, and finally, the catalyst is prepared. The catalyst has high reactivity and sulfur selectivity and strong stability. The by-product sulfur generated by the reaction is recovered with a solvent CS.sub.2, and the solvent CS.sub.2 is recovered by using a distillation process. The preparation method is low in cost, causes no secondary pollution and is high in sulfur recovery rate. The problem of low sulfur production in China at present is solved.

The present invention relates to: oxygen carrier particles having a metal oxide-perovskite core-shell structure; and a chemical-looping thermochemical water/carbon dioxide splitting process using the same. By using the oxygen carrier particles having a metal oxide-perovskite core-shell structure in the chemical-looping thermochemical water/carbon dioxide splitting process, it is possible to produce hydrogen/carbon monoxide from water/carbon dioxide in high yield by efficiently overcoming the disadvantages of conventionally used oxygen carrier particles.

The present invention provides: an interior material having a surface layer which has visible light-responsive photocatalytic activity and which contains two types of titanium oxide microparticles, the two types of titanium oxide microparticles comprising first titanium oxide microparticles, in which a tin component and a transition metal component for enhancing visible light responsiveness (excluding iron group components) are in solid solution, and second titanium oxide microparticles, in which an iron group component is in solid solution; and a method for manufacturing the interior material. The present invention makes it possible to provide an interior material in which visible light-responsive photocatalytic titanium oxide microparticles, which make it possible to easily produce a surface layer (photocatalyst thin film) having high transparency and expressing photocatalytic activity even in response to visible light (400-800 nm) only, are applied onto a surface, whereby it is possible to obtain, under indoor illumination, excellent photocatalytic properties such as an antimicrobial property and a property of breaking down chemical substances in indoor air without adversely affecting the design quality of the article in question.

Methods of preparing titanated silica catalysts, and titanated silica catalysts. The titanated silica catalysts may include a silica support, which may include spherical beads. Methods of olefin epoxidation, which may include contacting an olefin with a titanated silica catalyst in the presence of an oxidant.