The present invention provides a carbon black molded body having different pore structure from conventional carbon black. A carbon black molded body of the present invention includes a peak M of a pore volume being exist in a specified pore diameter in the specified Log differential pore volume distribution; a specified half band width of the peak M; a specified ratio of the half band width/an area-based median diameter; and a specified difference between a maximum value and a minimum value of a Log differential pore volume.

The present invention relates to a method for manufacturing a structure of a titanium compound selected from the group consisting of sheets, wires and tubes. The present invention also relates to intermediate products and structures comprising titanium dioxide obtainable by the method. The invention provides an improved method giving improved yield as well as other advantages.

This invention relates to azirconium hydroxideor zirconium oxide comprising, on an oxide basis, up to 30 wt % of a dopant comprising one or more of silicon, sulphate, phosphate, tungsten, niobium, aluminium, molybdenum, titanium or tin, and having acid sites, wherein the majority of the acid sites are Lewis acid sites. In addition, the invention relates to a catalyst, catalyst support or precursor, binder, functional binder, coating or sorbent comprising the zirconium hydroxide or zirconium oxide. The invention also relates to a process for preparing zirconium hydroxide, the process comprising the steps of:(a) dissolving a zirconium salt in an aqueous acid, (b) addingone or more complexing agents to the resulting solution or sol, the one or more complexing agents being an organic compound comprising at least one of the following functional groups: an amine, an organosulphate, a sulphonate, a hydroxyl, an ether or a carboxylic acid group, (c) heating the solution or sol formed in step (b), (d) adding a sulphating agent, and (e) adding a base to form a zirconium hydroxide, and (f) optionally adding a dopant.

Provided is an alumina-based composite oxide having a large initial specific surface area and a small initial mean pore size, with excellent heat resistance of the specific surface area and pore volume; and a production method therefor. Specifically, provided is an alumina-based composite oxide wherein the initial crystallite diameter is 10 nm or less and the initial specific surface area is 80 m.sup.2/ml or more; after calcination at 1200° C. for 3 hours in air, the specific surface area is 10 m.sup.2/ml or more; the initial mean pore size is 10 nm or more and 50 nm or less; and after calcination at 1200° C. for 3 hours in air, the pore volume retention rate is 10% or more, which is determined by (P.sub.1/P.sub.0)×100 wherein P.sub.0 represents an initial pore volume (ml/g), and P.sub.1 represents a pore volume (ml/g) after calcination at 1200° C. for 3 hours in air.

A method for manufacturing a carbon dioxide adsorbent includes preparing an amine aqueous solution having an amine compound concentration ranging from 5% to 70% inclusive and a temperature ranging from 10° C. to 100° C. inclusive, impregnating silica gel with the amine aqueous solution, and aeration-drying the silica gel carrying the amine compound. The silica gel has a particle size ranging from 1 mm to 5 mm inclusive, an average pore diameter ranging from 10 nm to 100 nm inclusive, and a pore volume ranging from 0.1 cm.sup.3/g to 1.3 cm.sup.3/g inclusive.

The present invention is directed to a solid and substantially amorphous active pharmaceutical ingredient, to an oral pharmaceutical formulation comprising said substantially amorphous active pharmaceutical ingredient, as well as to a method for the manufacture of the same. The invention is also directed to a particulate anhydrous and substantially amorphous mesoporous magnesium carbonate (MMC), to a method for the manufacture thereof, and the use of said particulate anhydrous and substantially amorphous mesoporous magnesium carbonate (MMC) to stabilize an active pharmaceutical ingredient (API).

Disclosed is a lithium complex oxide sintered plate for use in a positive electrode of a lithium secondary battery. The lithium complex oxide sintered plate has a structure where a plurality of primary grains having a layered rock-salt structure are bonded, and has a porosity of 3 to 30%, a mean pore diameter of 15 μm or less, an open pore rate of 70% or more, and a thickness of 40 to 200 μm. The primary grains have a primary grain diameter of 20 μm or less, the primary grain diameter being a mean diameter of the primary grains, and a pore diameter distribution includes a first peak corresponding to a pore diameter of more than 0 μm to 1.2 μm or less and a second peak corresponding to a pore diameter which is larger than the pore diameter corresponding to the first peak and is 20 μm or less.

Provided are a halloysite powder and a method for producing the halloysite powder. The halloysite powder contains granules in which halloysite including halloysite nanotubes is aggregated. The granules have first pores derived from the tube holes in the halloysite nanotubes and second pores that are different from the first pores.

A flexible boron nitride nanoribbon aerogel has an interconnected three-dimensional porous network structure which is formed by mutually twining and contacting boron nitride nanoribbons and consists of macropores having a pore diameter of more than 50 nm, mesopores having a pore diameter of 2-50 nm and micropores having a pore diameter of less than 2 nm. The preparation method of the flexible boron nitride nanoribbon aerogel includes the following steps: performing high-temperature dissolution on boric acid and a nitrogen-containing precursor to form a transparent precursor solution, preparing the transparent precursor solution into precursor hydrogel, subsequently drying and performing high-temperature pyrolysis to obtain the flexible boron nitride nanoribbon aerogel. The boron nitride nanoribbon aerogel has excellent flexibility and resilience and can withstand different forms of loads from the outside within a wide temperature range.

A hierarchical porous honeycombed nickel oxide microsphere and a preparation method thereof are disclosed. The method includes mixing nickel sulfate hexahydrate, urea, water and glycerol, to obtain a mixed solution; subjecting the mixed solution to a hydrothermal reaction, to obtain a precursor; and calcining the precursor, to obtain the hierarchical porous honeycombed nickel oxide microspheres.