A porous silicon manufacturing method according to the present invention comprises the steps of: pretreating a silicon precursor and a heat dispersant; and conducting a thermal reduction reaction between the heat dispersant-pretreated silicon precursor and a metal reducing agent by using a rotary reaction chamber. When porous silicon manufactured by the manufacturing method is contained in a secondary battery anode active material and used in secondary batteries, the batteries exhibit high capacity and long lifespan characteristics. The present invention relates to a method for manufacturing porous silicon and a method for manufacturing a secondary battery anode active material containing the porous silicon manufactured thereby, with the aim of solving the problems with silicon materials under development for anode active materials for lithium secondary batteries, including excessive volume expansion during charge/discharge and resultant electrode fracture and lifespan shortening.

A supported catalyst for decomposing an organic substance that includes a support and a catalyst particle supported on the support. 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 one selected from Ba and Sr, the B contains Zr, the M is at least one selected from Mn, Co, Ni and Fe, y+z=1, x≥0.995, z≤0.4, and w is a positive value satisfying electrical neutrality. A film thickness of a catalyst-supporting film supported on the support and containing the catalyst particle is 5 μm or more, or a supported amount as determined by normalizing a mass of the catalyst particle supported on the support by a volume of the support is 45 g/L or more.

Sintering is an important issue in creating crystalline metal oxides with high porosity and surface area, especially in the case of high-temperature materials such as metal aluminates. Herein we report a rationally designed synthesis of metal aluminates that diminishes the surface area loss due to sintering. Metal aluminate (e.g. MeAl.sub.2O.sub.4or MeAlO.sub.3−Me=Mg, Mn, Fe, Ni, Co, Cu, La, or Ce; or mixture thereof) supported on γ-Al.sub.2O.sub.3 with ultralarge mesopores (up to 30 nm) was synthesized through microwave-assisted peptization of boehmite nanoparticles and their self-assembly in the presence of a triblock copolymer (Pluronic P123) and metal nitrates, followed by co-condensation and thermal treatment. The resulting materials showed the surface area up to about 410 m.sup.2.Math.g.sup.−1, porosity up to about 2.5 cm.sup.3.Math.g.sup.−1, and very good thermal stability. The observed enhancement in their thermomechanical resistance is associated with the faster formation of the metal aluminate phases. The nanometer scale path diffusion and highly defective interface of γ-alumina facilitate the counter diffusion of Me.sup.X+ and Al.sup.3+ species and further formation of the metal aluminate phase.

A carbon-sulfur composite including a carbonized metal-organic framework (MOF); and a sulfur compound introduced to at least a part of an outside surface and an inside of the carbonized metal-organic framework, wherein the carbonized metal-organic framework has a specific surface area of 2500 m.sup.2/g to 4000 m.sup.2/g, and the carbonized metal-organic framework has a pore volume of 0.1 cc/g to 10 cc/g, and a method for preparing the same.

Particulate composite materials and devices comprising the same are provided.

A sheet-shaped member is provided and includes a porous carbon material including a material obtained from carbonization of a raw material including rice husk, the raw material having a silicon content of at least 5 wt %, the raw material is heat treated before carbonization, and the raw material is treated by an alkali treatment after carbonization to reduce the silicon content, the porous carbon material having a specific surface area of at least 10 m2/g as measured by the nitrogen BET method, a pore volume of at least 0.1 cm3/g as measured by the BJH method and MP method, and an R value of 1.5 or greater, wherein the porous carbon material includes mesopores having pore sizes from 2 nm to 50 nm and obtained from the alkali treatment of the raw material after carbonization, the porous carbon material further includes macropores and micropores, the R value is expressed as R=B/A, the A referring to an intensity at an intersection between the baseline of a diffraction peak of the (002) plane as obtained based on powdery X-ray diffractometry of the porous carbon material and a perpendicular line downwardly drawn from the diffraction peak of the (002) plane, and the B referring to the intensity of the diffraction peak of the (002) plane.

A powder for coating or sintering exhibits a peak assigned to orthorhombic YAlO.sub.3 in an X-ray diffractometry. Of peaks exhibited in the X-ray diffractometry, the peak assigned to the (112) plane of orthorhombic YAlO.sub.3 is a peak that has the highest peak intensity. Preferably, the value of the ratio of S2 to S1, S2/S1, is less than 1 in an X-ray diffractometry using CuKα radiation, where SI represents the peak intensity of the peak assigned to the (112) plane of orthorhombic YAlO.sub.3 and S2 represents the peak intensity of the peak assigned to the (104) plane of trigonal Al.sub.2O.sub.3.

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 hydrogenation catalyst with a small amount of supported metal that is excellent in stability and inhibition of side reactions is provided. The catalyst hydrogenates an aromatic hydrocarbon compound into an alicyclic hydrocarbon compound, and a Group X metal represented by nickel is supported in a composite support including at least alumina and titania. The composite support preferably includes at least an alumina substrate coated with titania. It is also preferable that the Group X metal is prereduced by hydrogen. In the case that the Group X metal is nickel, the nickel content is preferably 5-35 wt % as nickel oxide in the catalyst. The substrate includes, for example, a porous structure formed by a plurality of needle-shaped or column-shaped intertwined three-dimensionally.

A negative electrode material for a lithium-ion secondary battery containing a composite (C) that contains a porous carbon (A) and a Si-containing compound (B). The porous carbon (A) satisfies V.sub.1/V.sub.0>0.80 and V.sub.2/V.sub.0<0.10. When a total pore volume at the maximum value of a relative pressure P/P.sub.0 is defined as V.sub.0 and P.sub.0 is a saturated vapor pressure, a cumulative pore volume at a relative pressure P/P.sub.0=0.1 is defined as V.sub.1, and a cumulative pore volume at a relative pressure P/P.sub.0=10.sup.−7 is defined as V.sub.2 in a nitrogen adsorption test. Further, the porous carbon (A) has a BET specific surface area of 800 m.sup.2/g or more, and the Si-containing compound (B) is contained in pores of the porous carbon (A). Also disclosed is a negative electrode sheet including the negative electrode material and a lithium-ion secondary battery including the negative electrode sheet.