A film-forming powder containing a rare earth oxyfluoride has an average particle size D50 of 0.6-15 μm, a total volume of 10 μm pores of 0.51-1.5 cm.sup.3/g as measured by mercury porosimetry, and a BET surface area of 3-50 m.sup.2/g is suitable for forming a dense film in high yields or deposition rates and high productivity. The film-forming powder having a greater pore volume can be prepared by forming a rare earth ammonium fluoride complex salt on surfaces of rare earth oxide particles to provide precursor particles, and heat treating the precursor particles at a temperature of 350 to 700° C.

Provided is an iron oxide powder for a brake friction material which can be suitably used in a brake friction material that is less likely to cause problems regarding brake squealing and that provides superior braking performance. The iron oxide powder for a brake friction material according to a first embodiment of the present invention is characterized by having a sulfur content of 150 ppm or less as measured by combustion ion chromatography, and a saturation magnetization of 20 emu/g or less. The iron oxide powder for a brake friction material according to a second embodiment of the present invention is characterized by having an average particle size of 1.0 μm or more, a chlorine content of 150 ppm or less as measured by combustion ion chromatography, and a saturation magnetization of 20 emu/g or less.

A honeycomb-structured catalyst for decomposing an organic substance, which includes a catalyst particle. The catalyst particle contains a perovskite-type composite oxide represented by A.sub.xB.sub.yM.sub.zO.sub.w, where the A contains at least of Ba and Sr, the B contains Zr, the M is at least one of Mn, Co, Ni, and Fe, y+z=1, 1.001≤x≤1.05, 0.05≤z≤0.2, and w is a positive value that satisfies electrical neutrality. The toluene decomposition rate is greater than 90% when toluene is decomposed using the honeycomb-structured catalyst subjected to a heat treatment at 1200° C. for 48 hours and a gas that contains 50 ppm toluene, 80% nitrogen, and 20% oxygen as a volume concentration as a target at a space velocity of 30,000/h and a catalyst temperature of 400° C.

The present invention concerns a material with a non-stoichiometric spinel-type crystalline structure based on cobalt oxide doped with alkaline elements, its production process for obtaining it by precipitation with controlled washing, and its particular use as a highly active catalyst in the N.sub.2O decomposition reaction. Therefore, we understand that the present invention is in the area of green industry aimed at reducing N.sub.2O emissions into the atmosphere.

This positive electrode active material for nonaqueous electrolyte secondary batteries contains a lithium transition metal composite oxide. This lithium transition metal composite oxide is represented by general formula Li.sub.xMn.sub.yNi.sub.zMe.sub.2-x-y-zO.sub.aF.sub.b (wherein 1≤x≤1.2; 0.4≤y≤0.7; 0.1≤z≤0.4; 0<b≤0.2; 1.9≤a+b≤2.1; and Me represents at least one element selected from among Co, Al, Ti, Ge, Nb, Sr, Mg, Si, P and Sb), while having a BET specific surface area of from 1 m.sup.2/g to 4 m.sup.2/g and an average pore diameter of 100 nm or less.

A nonaqueous electrolyte energy storage device according to one aspect of the present invention is a nonaqueous electrolyte energy storage device including a positive electrode having positive active material particles, in which the positive active material particles contain a lithium transition metal composite oxide having an α-NaFeO.sub.2 structure, the lithium transition metal composite oxide contains at least one of nickel and cobalt, and manganese, a content of lithium with respect to a transition metal in the lithium transition metal composite oxide exceeds 1.0 in terms of a molar ratio, a diffraction peak is present in a range of 20° or more and 22° or less in an X-ray diffraction diagram of the lithium transition metal composite oxide using a CuKα ray, and the positive active material particles contain aluminum.

A cerium-zirconium based mixed oxide composition have: (a) a Ce:Zr molar ratio of 1 or less, and (b) a cerium oxide content of 10-50% by weight. The composition has (i) a surface area of at least 18 m.sup.2/g, and a total pore volume as measured by N.sub.2 physisorption of at least 0.11 cm.sup.3/g, after ageing at 1100° C. in an air atmosphere for 6 hours, (ii) a surface area of at least 42 m.sup.2/g, and a total pore volume as measured by N.sub.2 physisorption of at least 0.31 cm.sup.3/g, after ageing at 1000° C. in an air atmosphere for 4 hours, and (iii) Dynamic Oxygen Storage Capacity (D-OSC) value as measured by H.sub.2-TIR of greater than 500 μmol/g at 600° C. after aging at 800° C. in an air atmosphere for 2 hours. A process contacts the exhaust gas with the composition Another process is for preparing the composition.

The present invention relates to novel sulfur-doped carbonaceous porous materials. The present invention also relates to processes for the preparation of these materials and to the use of these materials in applications such as gas adsorption, mercury and gold capture, gas storage and as catalysts or catalyst supports.

A process for producing a surface-modified particulate lithium nickel metal oxide material is provided. The process comprises the addition of a controlled quantity of a coating liquid comprising a metal-containing compound and a lithium-containing compound to nickel metal precursor particles using an incipient wetness process followed by a calcination step.

A ceramic powder material containing: a first garnet-type compound containing Li, La, and Zr; and a second garnet-type compound containing Li, La, and Zr and having a composition different from a composition of the first garnet-type compound, in which the first garnet-type compound and the second garnet-type compound are represented by Formula [1] Li.sub.7-(3x+y)M1.sub.xLa.sub.3Zr.sub.2-yM2.sub.yO.sub.12, where Ml is Al or Ga, M2 is Nb or Ta, the first garnet-type compound satisfies 0≤(3x+y)≤0.5, and the second garnet-type compound satisfies 0.5<(3x+y)≤1.5.