A precipitated silica is disclosed. Said precipitated silica has a BET/CTAB in a range of 0.8-1.35; a DBP oil absorption in a range of 240-320 ml/100 g; and a CDBP coefficient (DA) in range of 0.4 to 0.9.

A process of preparing precipitated silica is disclosed. Said process comprises of reacting an aqueous solution of a metal silicate with a mineral acid in the presence of a surfactant solution comprising gelatin and C8-C20 sulfosuccinate blend, at a reaction temperature in a range of about 70 to 100 C. with constant stirring such that a reaction mixture having a pH of about 10.Math.0.3 is obtained; optionally, allowing the reaction mixture to age at a temperature in a range of about 70 to 100 C. for a time period in range of 10 to 100 minutes; adjusting the pH of the reaction mixture to about 4, followed by aging said mixture at a temperature in a range of about 70 to 100 C. for a time period in a range of 10 minutes to 2 hours; and recovering the precipitated silica from the reaction mixture.

There is disclosed a layered article that can be used in indirect printing, in analog or digital processes. The layered article, when configured as a transfer member, may serve to receive an ink in any form, allow the ink to be treated so as to form an ink image, and permit the application of the ink image on a substrate. The transfer member comprises a support layer and an imaging layer, which may be formed of a silicon matrix including dispersed carbon black particles. Methods for preparing the same are also disclosed.

Amorphous aluminosilicates are disclosed, and these amorphous aluminosilicates are characterized by a unique combination of high surface area, low oil absorption, and a significant fraction of the total pore volume resulting from micropores. These amorphous aluminosilicates can be used in various paint and coating applications, with the resultant dried or solid film capable of removing VOC's from the surrounding air.

Carbon black having a specific surface area of 150 m.sup.2/g or more and 400 m.sup.2/g or less, and a ratio (Lc/SSA) of a crystallite size (Le ()) to a specific surface area (SSA (m.sup.2/g)) of 0.15 or less.

The invention relates to a novel process for the preparation of a precipitated silica, in which: a silicate is reacted with an acidifying agent, so as to obtain a suspension of precipitated silica, said suspension of precipitated silica is filtered, so as to obtain a filtration cake, said filtration cake is subjected to a liquefaction operation comprising the addition of an aluminum compound, after the liquefaction operation, a drying stage is carried out,
characterized in that a mixture of polycarboxylic acids is added to the filtration cake, during or after the liquefaction operation. It also relates to novel precipitated silicas and to their uses.

A positive electrode active material for a nonaqueous electrolyte secondary battery is used for a nonaqueous electrolyte secondary battery. The positive electrode active material includes a composite oxide containing at least lithium, nickel, and manganese and contains aggregated particles of primary particles having an average particle diameter of 1.0 m or more. The primary particles have a layered crystal structure and a spinel crystal structure.

The present invention relates to iron oxide red pigments having improved color values, a process for producing these improved iron oxide red pigments by the Penniman red process using nitrate (also referred to as nitrate process or direct red process) and an apparatus for the production thereof.

Apparatus for reducing a particle size of a precursor powder material by fluid energy impact according to one embodiment of the invention may include a housing defining an interior milling cavity therein having a peripheral wall. A powder feed inlet operatively associated with the housing introduces the precursor powder material into the interior milling cavity. A feed gas inlet operatively associated with the powder feed inlet introduces a feed gas into the interior milling cavity. A product discharge outlet operatively associated with the housing removes a milled powder product from the interior milling cavity. An oil injection nozzle assembly operatively associated with the product discharge outlet injects oil into a particle-laden product stream from the product discharge outlet.

An electrode material for a lithium ion battery including an active material represented by LiMPO.sub.4 (M is at least one selected from the group consisting of Fe, Mn, Co, Ni, Zn, Al, Ga, Mg, and Ca), in which an oil absorption amount for which diethyl carbonate is used (DEC oil absorption amount) is 50 cc/100 g or more and 80 cc/100 g or less, and a ratio (DEC/NMP) of the DEC oil absorption amount to an oil absorption amount for which N-methyl-2-pyrrolidinone is used (NMP oil absorption amount) is 1.3 or more and 1.8 or less.