Provided are a dielectric, a capacitor and a semiconductor device that include the dielectric, and a method of preparing the dielectric, the dielectric including: a composition represented by Formula 1; and an oxide including a perovskite type crystal structure having a polar space group or a non-polar space group other than a Pbnm space group:

<Formula 1>

A.sub.xB.sub.yO.sub.3- wherein, in Formula 1, A is a monovalent, divalent, or trivalent cation, B is a trivalent, tetravalent, or pentavalent cation, and 0.5x1.5, 0.5y1.5, and 00.5.

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.

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 are compositions comprising inorganic UV-absorbing agents and the use of such compositions, in particular for protecting a subject or the surface of an inanimate object against a harmful effect of ultraviolet radiation.

Disclosed are compositions comprising inorganic UV-absorbing agents and the use of such compositions, in particular for protecting a subject or the surface of an inanimate object against a harmful effect of ultraviolet radiation.

Provided is a novel polyoxometalate and a method for producing the polyoxometalate. The polyoxometalate is represented by the compositional formula: M.sub.xO.sub.y in which M is tungsten, molybdenum or vanadium; 4x1000; and 2.5y/x7.

Provided is an anode particulate, having a dimension from 10 nm to 100 m, for use in an alkali metal battery, the particulate comprising (i) an anode active material capable of reversibly absorbing and desorbing lithium ions or sodium ions, (ii) an electron-conducting material, and (iii) a lithium ion-conducting or sodium ion-conducting electrolyte, wherein the electron-conducting material forms a three dimensional network of electron-conducting pathways in electronic contact with the anode active material and the electrolyte forms a three dimensional network of lithium ion- or sodium ion-conducting channels in ionic contact with the anode active material. The particulate can be of any shape, but preferably spherical or ellipsoidal in shape. Also provided is a cathode in a particulate form containing a cathode active material, an electron-conducting material forming a three dimensional network of electron-conducting pathways, and a lithium ion-conducting or sodium ion-conducting electrolyte forming a three dimensional network of ion-conducting channels.

A method for treating a liquid redox electrolyte solution for use in a flow battery includes feeding a liquid redox electrolyte solution into a first half-cell of an electrochemical cell and feeding a gaseous reductant into a second half-cell of the electrochemical cell, and electrochemically reducing at least a portion of the liquid redox electrolyte solution in the electrochemical cell using the gaseous reductant.

A method for treating a liquid redox electrolyte solution for use in a flow battery includes feeding a liquid redox electrolyte solution into a first half-cell of an electrochemical cell and feeding a gaseous reductant into a second half-cell of the electrochemical cell, and electrochemically reducing at least a portion of the liquid redox electrolyte solution in the electrochemical cell using the gaseous reductant.

In a garnet-type or garnet-like LLZ-based lithium ion-conductive oxide material, a high ion conductivity is realized. Specifically, the lithium ion-conductive oxide material contains each element of Li, La, Zr and O and at least an A element, the A element has a d electron, and is in a cation state where regular octahedral coordination preference in stabilization of an anion of oxygen by a ligand field becomes 50 kJ/mol or more, and a mole ratio A/La of the A element to La is 0.01 or more and 0.45 or less.