A process for synthesizing a Mn.sup.4+ doped phosphor of formula I by electrolysis is presented. The process includes electrolyzing a reaction solution comprising a source of manganese, a source of M and a source of A. One aspect relates to a phosphor composition produced by the process. A lighting apparatus including the phosphor composition is also provided. A.sub.x[MF.sub.y]:Mn.sup.4+ (I) where, A is Li, Na, K, Rb, Cs, or a combination thereof; M is Si, Ge, Sn, Ti, Zr, Al, Ga, In, Sc, Hf, Y, La, Nb, Ta, Bi, Gd, or a combination thereof; x is the absolute value of the charge of the [MF.sub.y] ion; and y is 5, 6 or 7.

The present invention relates to a transition metal complex that exhibits high activity in the polymerization reaction of olefin monomers and improved copolymerization activity, thus enabling the preparation of a low density, high molecular weight polyolefin, a catalyst composition including the same, and a method for preparing a polyolefin using the composition.

A method (100) for producing a sintered component being a solid electrolyte and/or an electrode including titanium and sulfur for an all-solid state battery, the method including mixing powders (102) so as to obtain a powder mixture comprising titanium and sulfur, pressing (106) a component with the powder mixture, sintering (108) the component under a partial pressure of sulfur comprised between 200 Pa and 0.2 MPa so as to obtain an intermediate sintered component comprising titanium and sulfur, and sintering (114) the intermediate sintered component under a partial pressure of sulfur equal to or smaller than 150 Pa at a temperature plateau comprised between 200 C. and 400 C. so as to obtain a sintered component comprising titanium and sulfur, the solid electrolyte exhibiting the peaks in positions of 2=15.08 (0.50), 15.28 (0.50), 15.92 (0.50), 17.5 (0.50), 18.24 (0.50), 20.30 (0.50), 23.44 (0.50), 24.48 (0.50), and 26.66 (0.50) in a X-ray diffraction measurement using CuK line.

Provided is an alkali metal titanate which, when used as a constituent material of a friction material, is excellent in heat resistance and friction force and capable of effectively suppressing wear of a mating material disposed to face the friction material. The alkali metal titanate includes a sodium atom and a silicon atom. The content of the sodium atom is 2.0 to 8.5 mass %. The content of the silicon atom is 0.2 to 2.5 mass %. The ratio of the content of an alkali metal atom other than the sodium atom to the content of the sodium atom is 0 to 6.

The present application describes a process for the preparation of titanium-based compounds having an anatase type structure with cationic vacancies arising from a partial substitution of oxygen atoms by fluorine atoms and hydroxyl groups. Electrochemically active materials comprising the titanium-based compounds for use in lithium-ion battery electrodes are also described.

The present disclosure broadly relates to a process for recovering vanadium, iron, titanium and silica values from vanadiferous feedstocks. More specifically, but not exclusively, the present disclosure relates to a metallurgical process in which vanadium, iron, titanium and silica values are recovered from vanadiferous feedstocks such as vanadiferous titanomagnetite, iron ores, vanadium slags and industrial wastes and by-products containing vanadium. The process broadly comprises digesting the vanadiferous feedstocks into sulfuric acid thereby producing a sulfation cake; dissolving the sulfation cake and separating insoluble solids thereby producing a pregnant solution; reducing the pregnant solution thereby producing a reduced pregnant solution; and crystallizing ferrous sulfate hydrates from the reduced pregnant solution, producing an iron depleted reduced solution. The process further comprises removing titanium compounds from the iron depleted reduced solution thereby producing a vanadium-rich pregnant solution; concentrating vanadium and recovering vanadium products and/or a vanadium electrolyte.

Disclosed is a method of regenerating a nitric and hydrofluoric acid bath contained in a machining vessel, the method including, when the etching bath is spent, performing steps of: transferring a portion of the spent etching bath, referred to as the spent solution, from the machining vessel into a reactor; adding NaF and NaNO.sub.3 to the spent solution, to form HF, HNO.sub.3, and Na.sub.2TiF.sub.6; separating the resulting precipitate from the supernatant; transferring the supernatant, which is a regenerated solution, into a tank; measuring the concentrations of HF, of HNO.sub.3, and of dissolved titanium in the tank and in the machining vessel; and determining the volume of regenerated solution that can be added to the spent etching bath to obtain a regenerated bath in which the concentrations of HF, of HNO.sub.3, and of dissolved titanium lie in acceptable concentration ranges, and transferring the regenerated solution into the machining vessel.

The present disclosure provides a calcium copper titanate film preparation method and a calcium copper titanate film, where the calcium copper titanate film has excellent step coverage, film thickness uniformity and film continuity, is particularly suitable for a high aspect ratio structure. The calcium copper titanate film preparation method includes: forming a layered deposition structure on a substrate, where the layered deposition structure includes at least one titanium dioxide layer, at least one copper oxide layer and at least one calcium oxide or calcium carbonate layer; and subjecting the layered deposition structure to high-temperature annealing treatment in an oxygen-containing atmosphere to obtain a calcium copper titanate film.

According to one embodiment, an active material is provided. The active material includes particles. The particles have a crystal structure belonging to a monoclinic niobium-titanium composite oxide. A ratio of a crystallite size Dc corresponding to a (020) plane with respect to an average primary particle size Dp of the particles is not less than 35%.

A material of formula Li.sub.aTi.sub.b(A.sub.xS.sub.3-x).sub.c wherein A is a metalloid element chosen from selenium, tellurium and mixtures thereof, and the stoichiometric coefficients a, b, c and x are such that 0<x<2.2; 0.4a4.5; 0.9b1.1; and 0.9c1.1.