The present invention provides a process for preparing furfural and furfural derivatives using a furfural-derived solvent.

The present invention provides a process for preparing furfural and furfural derivatives using a furfural-derived solvent.

An exhaust gas purification catalyst containing a CeO.sub.2 particle supported on the surface of an MnO.sub.2 particle, wherein the Ce amount relative to the total amount of Mn and Ce (Ce/(Mn+Ce)) in the catalyst is more than 0 mol % and 40 mol % or less; and a method for producing the exhaust gas purification catalyst above, including mixing an aqueous solution containing a manganese ion and a cerium ion in a ratio of more than 0 mol % and 40 mol % or less in terms of the Ce amount relative to the total amount of Mn and Ce (Ce/(Mn+Ce)) and an aqueous solution having dissolved therein a carbonate ion-containing reducing agent, thereby precipitating a particle, and firing the particle, are provided.

An exhaust gas purification catalyst containing a CeO.sub.2 particle supported on the surface of an MnO.sub.2 particle, wherein the Ce amount relative to the total amount of Mn and Ce (Ce/(Mn+Ce)) in the catalyst is more than 0 mol % and 40 mol % or less; and a method for producing the exhaust gas purification catalyst above, including mixing an aqueous solution containing a manganese ion and a cerium ion in a ratio of more than 0 mol % and 40 mol % or less in terms of the Ce amount relative to the total amount of Mn and Ce (Ce/(Mn+Ce)) and an aqueous solution having dissolved therein a carbonate ion-containing reducing agent, thereby precipitating a particle, and firing the particle, are provided.

The present technology relates to perovskite materials for oxygen storage. In one aspect, the perovskite material includes at least one platinum group metal (PGM) andat least one perovskite compound selected from the group consisting of formula (a): La.sub.xMO.sub.3 and formula (b): La.sub.(1-y)Sr.sub.yMO.sub.3, wherein: M is selected from the group consisting of Co, Cu, Fe, Mn and Ni; x is about 0.7 to about 1.1; and y is 0 to about 0.8, and wherein M, x, and y are independently variable for each one of said perovskite compounds. In one exemplary method, the perovskite materials of the technology are employed to treat automotive exhaust gas. In one embodiment, the perovskite materials are included in the washcoat of an automotive catalytic converter.

The present technology relates to perovskite materials for oxygen storage. In one aspect, the perovskite material includes at least one platinum group metal (PGM) andat least one perovskite compound selected from the group consisting of formula (a): La.sub.xMO.sub.3 and formula (b): La.sub.(1-y)Sr.sub.yMO.sub.3, wherein: M is selected from the group consisting of Co, Cu, Fe, Mn and Ni; x is about 0.7 to about 1.1; and y is 0 to about 0.8, and wherein M, x, and y are independently variable for each one of said perovskite compounds. In one exemplary method, the perovskite materials of the technology are employed to treat automotive exhaust gas. In one embodiment, the perovskite materials are included in the washcoat of an automotive catalytic converter.

An object of the present invention is to provide a process for producing an oxide catalyst used in a vapor-phase catalytic oxidation or vapor-phase catalytic ammoxidation reaction of propane or isobutene, which enables a catalyst demonstrating favorable yield to be stably produced. According to the present invention, there is provided a process for producing an oxide catalyst used in a vapor-phase catalytic oxidation or vapor-phase catalytic ammoxidation reaction of propane or isobutane, comprising the steps of: (i) preparing a catalyst raw material mixture containing Mo, V and Nb and satisfying the relationships of 0.1≦a≦1 and 0.01≦b≦1 when atomic ratios of V and Nb to one atom of Mo are defined as a and b, respectively; (ii) drying the catalyst raw material mixture; and (iii) calcining a particle, in which a content of the particle having a particle diameter of 25 μm or less is 20% by mass or less and a mean particle diameter is from 35 to 70 μm, in an inert gas atmosphere.

An object of the present invention is to provide a process for producing an oxide catalyst used in a vapor-phase catalytic oxidation or vapor-phase catalytic ammoxidation reaction of propane or isobutene, which enables a catalyst demonstrating favorable yield to be stably produced. According to the present invention, there is provided a process for producing an oxide catalyst used in a vapor-phase catalytic oxidation or vapor-phase catalytic ammoxidation reaction of propane or isobutane, comprising the steps of: (i) preparing a catalyst raw material mixture containing Mo, V and Nb and satisfying the relationships of 0.1≦a≦1 and 0.01≦b≦1 when atomic ratios of V and Nb to one atom of Mo are defined as a and b, respectively; (ii) drying the catalyst raw material mixture; and (iii) calcining a particle, in which a content of the particle having a particle diameter of 25 μm or less is 20% by mass or less and a mean particle diameter is from 35 to 70 μm, in an inert gas atmosphere.

A composite including: a carbonaceous material; and a solid solution including a first metal and a cerium oxide, wherein the solid solution is disposed on the carbonaceous material.

A composite including: a carbonaceous material; and a solid solution including a first metal and a cerium oxide, wherein the solid solution is disposed on the carbonaceous material.