Abstract: A main object of the present disclosure is to provide a cathode active material with excellent capacity properties. In order to achieve the object, the present disclosure provides a cathode active material to be used in a fluoride ion battery wherein the cathode active material mainly contains a metal element M and a metal element M?; the metal element M is at least one kind of Cu, Fe and Mn; and the metal element M? is at least one kind of Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho and Yb.

Abstract: A main object of the present disclosure is to provide an anode active material with excellent capacity properties. The present disclosure achieves the object by providing an anode active material to be used in an alkaline storage battery, the anode active material including: a base material containing Ti and Cr, and including a BCC structure as a metastable phase; and a coating layer that coats the base material, and contains a catalyst metal and a metal with oxygen affinity that is more than oxygen affinity of Ti; wherein an oxide film is present in an interface between the coating layer and the base material; and when a first thickness TA (nm) and a second thickness TB(nm) of the oxide film are determined by Auger electron spectroscopy, a rate of the TA with respect to the TB, which is TA/TB is, for example, 1.50 or more.

Abstract: A main object of the present disclosure is to provide a cathode active material with excellent capacity properties. In order to achieve the object, the present disclosure provides a cathode active material to be used in a fluoride ion battery wherein the cathode active material mainly contains a metal element M and a metal element M?; the metal element M is at least one kind of Cu, Fe and Mn; and the metal element M? is at least one kind of Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho and Yb.

Abstract: To provide a hydrogen absorbing alloy having a BCC (body-centered cubic structure) as a crystal structure, and particularly a hydrogen-absorbing alloy for a nickel-hydride cell having excellent discharge capacity and durability (cycle characteristics), said hydrogen-absorbing alloy having a composition expressed by the general formula Ti(100-a-b-c-d)CraVbNicXd, where X is at least one member selected from the group consisting of Y (yttrium), lanthanoids, Pd and Pt, and each of a, b, c and d is represented, in terms of at %, by the relations 8≦a≦50, 30<b≦60, 5≦c≦15, 2≦d≦10 and 40≦a+b+c+d≦90, wherein the crystal structure of a principal phase is a body-centered cubic structure, and further, the alloy contains at least one of Mo and W in place of V and at least one member selected from the group consisting of Y (yttrium), lanthanoids, Pd and Pt, and its crystal structure is converted to the body-centered cubic structure by heat-treatment.

Abstract: To provide a hydrogen absorbing alloy having a BCC (body-centered cubic structure) as a crystal structure, and particularly a hydrogen-absorbing alloy for a nickel-hydride cell having excellent discharge capacity and durability (cycle characteristics), said hydrogen-absorbing alloy having a composition expressed by the general formula Ti(100-a-b-c-d)CraVbNicXd, where X is at least one member selected from the group consisting of Y (yttrium), lanthanoids, Pd and Pt, and each of a, b, c and d is represented, in terms of at %, by the relations 8≦a≦50, 30 <b≦60, 5≦c≦15, 2≦d≦10 and 40≦a+b+c+d≦90, wherein the crystal structure of a principal phase is a body-centered cubic structure, and further, the alloy contains at least one of Mo and W in place of V and at least one member selected from the group consisting of Y (yttrium), lanthanoids, Pd and Pt, and its crystal structure is converted to the body-centered cubic structure by heat-treatment.

Abstract: To provide a hydrogen absorbing alloy having a BCC (body-centered cubic structure) as a crystal structure, and particularly a hydrogen-absorbing alloy for a nickel-hydride cell having excellent discharge capacity and durability (cycle characteristics), said hydrogen-absorbing alloy having a composition expressed by the general formula Ti(100−a−b−c−d)CraVbNicXd, where X is at least one member selected from the group consisting of Y (yttrium), lanthanoids, Pd and Pt, and each of a, b, c and d is represented, in terms of at %, by the relations 8≦a≦50, 30<b≦60, 5≦c≦15, 2≦d≦10 and 40≦a+b+c+d≦90, wherein the crystal structure of a principal phase is a body-centered cubic structure, and further, the alloy contains at least one of Mo and W in place of V and at least one member selected from the group consisting of Y (yttrium), lanthanoids, Pd and Pt, and its crystal structure is converted to the body-centered cubic structure by heat-treatment.

Abstract: The present invention relates to a surface treatment for hydrogen-absorbing alloy. More particularly, the present invention relates to a surface treatment for hydrogen-absorbing alloy by which the poisoning resistance of a surface of alloy powder with respect to oxide film, water or absorbing gas can be enhanced so that activation treatment can be easily conducted on alloy powder. In the method, the poisoning resistance is enhanced by forming a protective film, which contains at least one of sulfide and fluoride, on the surface of hydrogen-absorbing alloy powder in an atmosphere containing SF6 gas when hydrogen-absorbing alloy is crushed or hydrogen-absorbing alloy is in a state of powder or when hydrogen-absorbing alloy is made into powder by rapidly cooling and solidifying.

Abstract: A BCC type hydrogen-absorbing alloy, which uses a ferroalloy, is advantageous from the aspect of the production cost and exhibits excellent hydrogen absorption and desorption characteristics due to a fine structure constituted by spinodal decomposition even when the iron component is increased. The hydrogen-absorbing alloy is expressed by the general formula AxVayBz, where A is at least one of Ti and Zr, Va is at least one member of the Group Va elements of the Periodic Table consisting of V, Nb and Ta, and B contains at least Fe and is at least one member selected from the group consisting of Cr, Mn, Co, Ni, Cu, Al, Mo and W, each of x, y and z satisfies the relation, in terms of of the atomic number ratio, 0≦x≦70, 0≦y≦50, x+y+z=100, and x/z=0.25 to 2.0, the phase of the body-centered cubic structure is at least 50% in terms of the phase fraction and its lattice constant is at least 0.2950 nm but not greater than 0.3100 nm.

Abstract: A hydrogen-absorbing alloy capable of controlling the very fine structure formed by a spinodal decomposition for improving flatness of an emission equilibrium pressure in a practical temperature/pressure range and excellent in activation and hydrogen absorption/desorption amounts, and a production method thereof. The hydrogen-absorbing alloy has a composition expressed by the general formula Ti.sub.x Cr.sub.y V.sub.z (where each of x, y and z represents an atomic percent and satisfies the relation x+y+z=100), wherein the composition has a body-centered cubic structural phase as a principal phase, the principal phase exists within the range in which the body-centered cubic structure appears and a spinodal decomposition occurs with the exception of a C14 (a typical structure of the Laves phase; a MgZn.sub.2 type crystal structure) mono-phase range, and has a regular periodical structure formed by the spinodal decomposition, and its apparent lattice constant is at least 0.2950 nm but is not greater than 0.

Abstract: This invention relates to a hydrogen-absorbing alloy, and particularly provides a hydrogen-absorbing alloy having a body-centered cubic structure which has a periodical structure formed by spinodal decomposition, has a large hydrogen storage amount, has excellent hydrogen desorption characteristics and can mitigate activation conditions, the alloy comprises at least two elements of alloy components, wherein the relational curve between chemical free energy of solid solutions and an alloy composition has a shape describing an upwardly convexed curve, or said alloy comprises two solid solutions having a regular periodical structure formed by spinodal decomposition within a region satisfying the relation d.sup.2 G/dX.sub.B.sup.2 <0 (where G is chemical free energy and X.sub.B is a solute alloy concentration) as the principal phase.

Abstract: A magnesium alloy includes 0.1 to 6.0% by weight of Al, 0.25 to 6.0% by weight of Zn, 0.1 to 4.0% by weight of rare earth element (hereinafter referred to as "R.E."), and balance of Mg and inevitable impurities. Preferably, it includes 1.0 to 3.0% by weight of Al ("a"), 0.25 to 3.0% by weight of Zn ("b") and 0.5 to 4.0% by weight of R.E.: wherein when "b" is in a range, 0.25.ltoreq."b".ltoreq.1.0, "a" and "c" satisfy a relationship, "c".ltoreq."a"+1.0; and when "b" is in a range, 1.0.ltoreq."b".ltoreq.3.0, "a," "b" and "c" satisfy a relationship, "c".ltoreq."a"+"b".ltoreq.(1/2)"c"+4.0; in order to further improve creep properties at elevated temperatures while maintaining enhanced tensile strength at room temperature and up to 100.degree. C. at least.

Abstract: A magnesium alloy includes 0.1 to 6.0% by weight of Al, 1.0 to 6.0% by weight of Zn, 0.1 to 3.0% by weight of rare earth element (hereinafter referred to as "R.E."), and balance of Mg and inevitable impurities. By thusly adding Al and Zn, the castability, especially the die-castability, is improved. At the same time, the room temperature strength can be improved because the Mg-Al-Zn crystals having a reduced brittleness are dispersed uniformly in the crystal grains. Further, by adding R.E. as aforementioned, the high temperature strength is improved because the Mg-Al-Zn-R.E. crystals having a higher melting point and being less likely to melt are present in the crystal grain boundaries between the Mg-Al-Zn crystals. This magnesium alloy is excellent in castability, can be die-cast, has a higher tensile strength at room temperature, and is satisfactory in high temperature properties and creep properties. Moreover, when the magnesium alloy includes R.E. in a reduced amount of 0.1 to 2.