The invention relates to a method for producing functionalised bimodal periodic mesoporous organosilicates (PMOs) by means of pseudomorphic transformation, to functionalised bimodal periodic mesoporous organosilicates (PMOs) that comprise at least one organosilicate and at least one functional component, and to the use of the PMO as a filter material, adsorption means, sensor material or carrier material for pharmaceutical products, insecticides or pesticides.

Provided is a method of preparing a metal oxide-silica composite aerogel and a metal oxide-silica composite aerogel having an excellent weight reduction property prepared by the method. The method comprises adding an acid catalyst to a first water glass solution to prepare an acidic water glass solution (step 1); adding a metal ion solution to the acidic water glass solution to prepare a precursor solution (step 2); and adding a second water glass solution to the precursor solution and performing a gelation reaction (step 3).

The present invention relates to an activated carbon, having a pore volume (A) of 0.3 to 0.7 mL/g at a pore diameter of 6.5 to 50 nm as determined by mercury intrusion porosimetry, a pore volume (B) of 0.23 mL/g or less at a pore diameter of 750 to 4,000 nm as determined by mercury intrusion porosimetry, and a pore volume ratio (A)/(B) of 1.7 or higher.

A molded sintered body containing a mayenite type compound, an inorganic binder sintered material, and a transition metal, wherein a content of the inorganic binder sintered material is 3 to 30 parts by mass with respect to 100 parts by mass of the molded sintered body, and the molded sintered body has at least one pore peak in each of a pore diameter range of 2.5 to 20 nm and a pore diameter range of 20 to 350 nm. A method for producing the molded sintered body, including mixing a precursor of a mayenite type compound and a raw material of an inorganic binder sintered material to prepare a mixture; molding the mixture to prepare a molded body of the mixture; firing the molded body to prepare a fired product; and supporting a transition metal on the fired product to produce a molded sintered body.

Provided is a nickel composite hydroxide that was excellent in reactivity to a lithium compound and a positive electrode active material using the nickel composite hydroxide as a precursor. The nickel composite hydroxide, having an average diameter of pores of 50 Å or larger and 60 Å or smaller in pore distribution measurement by a nitrogen adsorption method and an integrated intensity ratio of a diffraction peak appearing in a range of 2θ=51.9±1.0°/a diffraction peak appearing in a range of 2θ=19.1±1.0° in powder X-ray diffraction using CuKα rays of 0.40 or more and 0.50 or less.

A method for producing mesoporous magnesium hydroxide nanoplates involving solvothermal treatment of a solution of a magnesium salt, a base, a glycol, and water is disclosed. The method does not use a surfactant or template in the solvothermal treatment. The method yields mesoporous nanoparticles of magnesium hydroxide having a plate-like morphology with a diameter of 20 nm to 100 nm, a mean pore diameter of 2 to 10 nm, a surface area of 50 to 70 m.sup.2/g, and a type-III nitrogen adsorption-desorption BET isotherm with a H3 hysteresis loop. An antibacterial composition containing the mesoporous magnesium hydroxide nanoplates is also disclosed. A method for reducing nitroaromatic compounds with a reducing agent and the mesoporous magnesium hydroxide nanoplates as a catalyst is also disclosed.

A process for producing a porous alpha-alumina catalyst support, comprising i) preparing a precursor material comprising, based on inorganic solids content, at least 50 wt.-% of a transition alumina having a loose bulk density of at most 600 g/L, a pore volume of at least 0.6 mL/g and a median pore diameter of at least 15 nm; and at most 30 wt.-% of an alumina hydrate; ii) forming the precursor material into shaped bodies; and iii) calcining the shaped bodies to obtain the porous alpha-alumina catalyst support. The catalyst support has a high overall pore volume, thus allowing for impregnation with a high amount of silver, while keeping its surface area sufficiently large so as to provide optimal dispersion of catalytically active species, in particular metal species. The invention further relates to a shaped catalyst body for producing ethylene oxide by gas-phase oxidation of ethylene, comprising at least 15 wt.-% of silver, relative to the total weight of the catalyst, deposited on a porous alpha-alumina catalyst support obtained in the process described above. The invention also relates to a process for preparing a shaped catalyst body as described above comprising impregnating a porous alpha-alumina catalyst support obtained in the process described above with a silver impregnation solution, preferably under reduced pressure; and optionally subjecting the impregnated porous alumina support to drying; and b) subjecting the impregnated porous alpha-alumina support to a heat treatment; wherein steps a) and b) are optionally repeated. The invention further relates to a process for producing ethylene oxide by gas-phase oxidation of ethylene, comprising reacting ethylene and oxygen in the presence of a shaped catalyst body as described above.

A process for the conversion of hardwood and bamboo to engineered carbon is disclosed. The biomass feedstock of hardwood and bamboo is placed into a holding canister, and the holding canister is lowered into the sealable reactor vessel. The biomass feedstock is ignited, and superheated stream and/or water is metered, or alternately steam is created in situ by introduction of water, into the process. The process is controlled by supplying compressed air and steam, or in situ water, and releasing process gases. The process is performed in an oxygen deprived state. Steam, or in situ water, is injected at the end of the cycle to end the thermal conversion and clean the resulting engineered carbon.

There is provided herein a porous silica particle characterized by having a hierarchical pore structure wherein at least about 20% of the pores of the silica particle are of a size in the range of from about 7.0 to about 13.0 nm, and at least about 10% of the pores of the silica particle are of a size in the range of from about 0.5 to about 5.0 nm, and by having a particle size of from about 0.1 μm to about 10.0 μm. There is also provided compositions comprising such silica particles, process for their preparation, and medical and non-medical uses thereof.

An adsorbent consisting of iron oxyhydroxide, having a high adsorption rate and high adsorption efficiency compared with conventional products. The adsorbent particle is an adsorbent particle having a crystal structure of β-iron oxyhydroxide, having an average crystallite diameter of 10 nm or less as measured by X-ray diffraction, wherein 90% or more of volume of adsorbent particle is constituted of granular crystals having crystal particle diameter of 20 nm or less, or columnar crystals having width of 10 nm or less and length of 30 nm or less. The adsorbent particle have at least either of the following characteristics: (A) the adsorbent particle contains metal element other than iron in amount of 0.1 to 20% by mass with respect to iron element, or (B) the adsorbent particle contains sulfur oxoacid ions in an amount of 0.01 to 20% by mass in terms of sulfur element with respect to iron element.