Highly heat-resistant anatase-type titanium oxide particles stably retard an anatase-type crystal phase having excellent reactivity in a temperature range of 700° C., and have fine particles and a uniform particle size distribution. The highly heat-resistant anatase-type titanium oxide includes titanium oxide particles having a content of an anatase crystal phase in the total crystal phases of 85% or more and a modification layer provided on the surfaces of the titanium oxide particles. The modification layer is obtained by modifying an organic acid having a molecular weight of 200 or less with an acidic solution containing 1.5×10.sup.−4 mol/L or more and 0.12 mol/L or less. The pH of the acidic solution is 0.2 to 5.

The present invention relates to inorganic fibres having a composition comprising: 61.0 to 70.8 wt % SiO.sub.2; 28.0 to 39.0 wt % CaO; 0.10 to 0.85 wt % MgO other components, if any, providing the balance up to 100 wt %,

The sum of SiO.sub.2 and CaO is greater than or equal to 98.8 wt % and the other components comprise less than 0.70 wt % Al.sub.2O.sub.3, if any.

An object of the present invention is to provide an AFX zeolite having a novel structure. An AFX zeolite having a lattice spacing d of a (004) plane being not less than 4.84 Å and not greater than 5.00 Å, and a molar ratio of silica to alumina being not less than 10 and not higher than 32. Such an AFX zeolite can be produced by a production method comprising a crystallization step of crystallizing a composition at a temperature of not lower than 160° C.; the composition containing a silicon source, an aluminum source, a 1,3-di(1-adamantyl)imidazolium cation, and an alkali metal; a molar ratio of hydroxide ions to silica being less than 0.25 or a molar ratio of silica to alumina being not higher than 27; and a molar ratio of the 1,3-di(1-adamantyl)imidazolium cation to silica being less than 0.20.

Provided is a granular activated carbon that can be used for applications similar to wood-based steam-activated carbons; and also provided is a method for manufacturing the same. The granular activated carbon is obtained in the following manner. An activated carbon raw material is carbonized, and then pulverized. The pulverized product is then mixed with a calcium component, and the mixture is molded. Subsequently, the molded product is carbonized and activated, followed by washing.

A titanium oxide powder of the present invention has a BET specific surface area of 5 m.sup.2/g or more and 15 m.sup.2/g or less and contains polyhedral-shaped titanium oxide particles having eight or more faces, in which a mass reduction rate in a case of being heated at 800° C. for 1 hour in an air atmosphere is 0.03% by mass or more and 0.5% by mass or less.

The present invention relates to inorganic fibres having a composition comprising: 65.7 to 70.8 wt % SiO.sub.2; 27.0 to 34.2 wt % CaO; 0.10 to 2.0 wt % MgO; and optional other components providing the balance up to 100 wt %,
wherein the sum of SiO.sub.2 and CaO is greater than or equal to 97.8 wt %; and the other components, when present, comprise no more than 0.80 wt % Al.sub.2O.sub.3; and wherein the amount of MgO and other components are configured to inhibit the formation of surface crystallite grains upon heat treatment at 1100° C. for 24 hours, wherein said surface crystallite grains comprise an average crystallite size in a range of from 0.0 to 0.90 μm.

Single crystals of a new noncentrosymmetric polar oxysulfide SrZn.sub.2S.sub.2O (s.g. Pmn2.sub.1) grown in a eutectic KF-KCl flux with unusual wurtzite-like slabs consisting of close-packed corrugated double layers of ZnS.sub.3O tetrahedra vertically separated from each other by Sr atoms and methods of making same.

Provided are a preparation method for insoluble sulfur and an anti-reversion stabilizer used thereby. Methane is used as the anti-reversion stabilizer. The methane is added to liquid sulfur at sulfur gasification stage, and is cracked into active free radicals under the action of sulfur vapor active free radicals; in the quenching process of sulfur vapor mixed with methane, the active free radicals generated by methane cracking carry out end capping on insoluble sulfur end groups generated by sulfur vapor polymerization, thus completing insoluble sulfur stabilization. The methane is added at liquid sulfur gasification stage, and after sulfur gasification, the methane is mixed with sulfur vapor in a gaseous form, rather than being added to the product in a solid or liquid manner at a later stage, so that the insoluble sulfur and the stabilizer can be uniformly contacted and mixed to the greatest extent.

A lithium composite transition metal oxide includes nickel (Ni), cobalt (Co), and manganese (Mn), wherein the lithium composite transition metal oxide includes two or more kinds of first dopants selected from the group consisting of Zr, Al, V, Co, and Mg and two or more kinds of second dopants selected from the group consisting of Ti, Y, Sr, Nb, Ba, and Ca, and particles of the lithium composite transition metal oxide has a crystallite size of 170-300 nm.

The purpose of the present invention is to provide an industrially advantageous method for producing α-lithium aluminate which has physical properties that are suitable for use as an electrolyte holding plate of a MCFC having excellent thermal stability, even if the α-lithium aluminate is a fine material having a BET specific surface area of 10 m.sup.2/g or higher in particular. Provided is a method for producing α-lithium aluminate characterized by subjecting a mixture (a), which is obtained by mixing transitional alumina and lithium carbonate at an Al/Li molar ratio of 0.95-1.01, to a first firing reaction so as to obtain a fired product, and subjecting a mixture (b), which is obtained by adding an aluminum compound to the obtained fired product at quantities whereby the molar ratio of aluminum atoms in the aluminum compound relative to lithium atoms in the fired product (Al/Li) is 0.001-0.05, to a second firing reaction.