A nitrous oxide (N.sub.2O) removal catalyst composite is provided, comprising a N.sub.2O removal catalytic material on a substrate, the catalytic material comprising a rhodium (Rh) component supported on a ceria-based support, wherein the catalyst composite has a H.sub.2-consumption peak of about 100° C. or less as measured by hydrogen temperature-programmed reduction (H.sub.2-TPR). Methods of making and using the same are also provided.

A nitrous oxide (N.sub.2O) removal catalyst composite is provided, comprising a N.sub.2O removal catalytic material on a substrate, the catalytic material comprising a rhodium (Rh) component supported on a ceria-based support, wherein the catalyst composite has a H.sub.2-consumption peak of about 100° C. or less as measured by hydrogen temperature-programmed reduction (H.sub.2-TPR). Methods of making and using the same are also provided.

A metal trap for an FCC catalyst include pre-formed microspheres impregnated with a salt of calcium and/or magnesium and an organic acid salt of a rare earth element.

The invention provides a process for preparing a cobalt-containing catalyst precursor. The process includes calcining a loaded catalyst support comprising a silica (SiO.sub.2) catalyst support supporting cobalt nitrate to convert the cobalt nitrate into cobalt oxide. The calcination includes heating the loaded catalyst support at a high heating rate, which does not fall below 10° C./minute, during at least a temperature range A. The temperature range A is from the lowest temperature at which calcination of the loaded catalyst support begins to 165° C. Gas flow is effected over the loaded catalyst support during at least the temperature range A. The catalyst precursor is reduced to obtain a Fischer-Tropsch catalyst.

A nitrous oxide (N.sub.2O) removal catalyst composite is provided, comprising a N.sub.2O removal catalytic material on a substrate, the catalytic material comprising a rhodium (Rh) component supported on a ceria-based support, wherein the catalyst composite has a H.sub.2-consumption peak of about 100° C. or less as measured by hydrogen temperature-programmed reduction (H.sub.2-TPR). Methods of making and using the same are also provided.

A nitrous oxide (N.sub.2O) removal catalyst composite is provided, comprising a N.sub.2O removal catalytic material on a substrate, the catalytic material comprising a rhodium (Rh) component supported on a ceria-based support, wherein the catalyst composite has a H.sub.2-consumption peak of about 100° C. or less as measured by hydrogen temperature-programmed reduction (H.sub.2-TPR). Methods of making and using the same are also provided.

A photocatalyst laminate which is composed of an undercoat layer provided on a substrate and a photocatalyst layer laminated on the surface of the undercoat layer. The undercoat layer contains (A) 100 parts by mass of a resin component and (B) 0.1-50 parts by mass of fine core-shell particles, each of which has a core that is formed of a fine tetragonal titanium oxide solid solution particle wherein tin and manganese are solid-solved and a shell that is formed from silicon oxide on the outside of the core. This photocatalyst laminate is not susceptible to decrease in the photocatalyst function even under outdoor exposure for a long period of time, and is thus capable of providing a coated article that exhibits excellent weather resistance.

A photocatalyst laminate which is composed of an undercoat layer provided on a substrate and a photocatalyst layer laminated on the surface of the undercoat layer. The undercoat layer contains (A) 100 parts by mass of a resin component and (B) 0.1-50 parts by mass of fine core-shell particles, each of which has a core that is formed of a fine tetragonal titanium oxide solid solution particle wherein tin and manganese are solid-solved and a shell that is formed from silicon oxide on the outside of the core. This photocatalyst laminate is not susceptible to decrease in the photocatalyst function even under outdoor exposure for a long period of time, and is thus capable of providing a coated article that exhibits excellent weather resistance.

Provided is an exhaust gas purification catalyst that suppresses phosphorus poisoning and improves long-term durability. The exhaust gas purification catalyst includes a phosphorus collection layer and a catalyst layer containing at least one precious metal element MP selected from the group consisting of Pt, Pd, and Rh, wherein the phosphorus collection layer is arranged on the upper layer side and/or the upstream side with respect to the catalyst layer; the phosphorus collection layer contains a composite oxide containing Al and an alkaline earth metal element M.sup.a that includes Mg and that may include at least one selected from the group consisting of Ca, Sr, and Ba, and having a cubic spinel structure belonging to the space group Fd-3m; the composite oxide has a M.sup.a/A1 molar ratio in a range of 0.02 or more and 0.60 or less; and the composite oxide has a peak derived from the cubic spinel structure belonging to the space group Fd-3m of the composite oxide between a diffraction angle 2θxm.sup.ao that is a position of a peak derived from an alkaline earth metal oxide M.sup.aO and a diffraction angle 2θx.sub.Al203 that is a position of a peak derived from an aluminum oxide Al.sub.2O.sub.3 in an X-ray diffraction spectrum.

Provided is an exhaust gas purification catalyst that suppresses phosphorus poisoning and improves long-term durability. The exhaust gas purification catalyst includes a phosphorus collection layer and a catalyst layer containing at least one precious metal element MP selected from the group consisting of Pt, Pd, and Rh, wherein the phosphorus collection layer is arranged on the upper layer side and/or the upstream side with respect to the catalyst layer; the phosphorus collection layer contains a composite oxide containing Al and an alkaline earth metal element M.sup.a that includes Mg and that may include at least one selected from the group consisting of Ca, Sr, and Ba, and having a cubic spinel structure belonging to the space group Fd-3m; the composite oxide has a M.sup.a/A1 molar ratio in a range of 0.02 or more and 0.60 or less; and the composite oxide has a peak derived from the cubic spinel structure belonging to the space group Fd-3m of the composite oxide between a diffraction angle 2θxm.sup.ao that is a position of a peak derived from an alkaline earth metal oxide M.sup.aO and a diffraction angle 2θx.sub.Al203 that is a position of a peak derived from an aluminum oxide Al.sub.2O.sub.3 in an X-ray diffraction spectrum.