A nickel hydroxide includes stacked nickel hydroxide layers. Each of the nickel hydroxide layers includes Ni.sup.2+ and OH.sup.−. At least one of the nickel hydroxide layers further includes a type of polyatomic anions. The polyatomic anions include a type of anions that are not SO.sub.4.sup.2− or CO.sub.3.sup.2−.

Provided is a lithium ion battery whose manufacturing process is simple and which has high energy density and heat resistance. A lithium ion battery capable of storing and releasing lithium ions, and being provided with a separator between a positive electrode and a negative electrode having irreversible capacity at the initial charge/discharge, and having a structure in which void portions in the separator are filled with a nonaqueous electrolytic solution including lithium ions, wherein a positive electrode active material contained in the positive electrode has a first charge-discharge efficiency of 80% to 90% when charged/discharged using metal Li as an counter electrode; a negative electrode active material contained in the negative electrode includes a mixed material of a silicon compound and a carbon material; in the negative electrode, lithium corresponding to an irreversible capacity at the initial charge/discharge is not doped; a capacity ratio of the negative electrode to the positive electrode at the initial electric charge capacity of the positive electrode and the negative electrode is 0.95 or more and 1 or less; the positive electrode binder contained in the positive electrode is an aqueous binder; the negative electrode binder contained in the negative electrode is a polyimide; and the nonaqueous electrolyte contains lithium bis(oxalate) borate.

A lead-based alloy containing alloying additions of bismuth, antimony, arsenic, and tin is used for the production of doped leady oxides, lead-acid battery active materials, lead-acid battery electrodes, and lead-acid batteries.

The present invention relates to an electrode material of formula LiFe.sub.1-xCo.sub.xBO.sub.3, where 0<x<1, and to a method of preparing the same comprising independently preparing an iron borate and a cobalt borate and then simultaneously thermally treating them under an inert atmosphere, in the presence of a precursor of lithium and of boric acid.

Disclosed is a boron recovering device including: an aeration-type water-channel reactor including a water channel; at least one aeration unit disposed in the water channel and aerating a boron-containing solution by passing it through the water channel to deposit boron in the form of borax; and a precipitation bath precipitating the deposited borax in the boron-containing solution having passed through the aeration-type water-channel reactor and separating a filtrate by overflowing, a boron recovering device, a method of recovering boron, and a boron recovering system.

The present invention relates to an electrode material of formula LiMn.sub.xCo.sub.1-xBO.sub.3, where 0<x<1, and to a method of preparing the same comprising independently preparing a manganese borate and a cobalt borate and then simultaneously thermally treating them under an inert atmosphere, in the presence of a precursor of lithium and of boric acid.

A method of forming a dissolvable part of amorphous borate includes: preparing a mixture comprising one or more boron compounds and one or more alkali compounds, at least one of the one or more boron compounds and the one or more alkali compounds being hydrous; heating the mixture to a melting temperature for a predetermined time to melt the mixture and release water from the mixture to form an anhydrous boron compound that is moldable, wherein the amount of alkali compound being selected to achieve an alkali oxide content of between about 10 to 25%; with the anhydrous boron compound at a molding temperature, molding the anhydrous boron compound in a mold; and cooling the anhydrous boron compound to form a solid.

Provided is a positive electrode active material that has high output characteristics and battery capacity when used for a positive electrode of a nonaqueous electrolyte secondary battery and can inhibit gelation of positive electrode mixture paste. A method for producing the positive electrode active material is also provided. A positive electrode active material for a nonaqueous electrolyte secondary battery contains a lithium-nickel-cobalt-manganese composite oxide represented by General Formula (1): Li.sub.i+sNi.sub.xCo.sub.yMn.sub.zB.sub.tM1.sub.uO.sub.2+β and having a hexagonal layered crystal structure. The lithium-nickel-cobalt-manganese composite oxide contains a secondary particle formed of a plurality of flocculated primary particles and a boron compound containing lithium present at least on part of surfaces of the primary particles. A water-soluble Li amount present on the surfaces of the primary particles is up to 0.1% by mass relative to the entire amount of the positive electrode active material.

Provided is a positive electrode active material that has high output characteristics and battery capacity when used for a positive electrode of a nonaqueous electrolyte secondary battery and can inhibit gelation of positive electrode mixture paste. A method for producing the positive electrode active material is also provided. A positive electrode active material for a nonaqueous electrolyte secondary battery contains a lithium-nickel-cobalt-manganese composite oxide represented by General Formula (1): Li.sub.i+sNi.sub.xCo.sub.yMn.sub.zB.sub.tM1.sub.uO.sub.2+β and having a hexagonal layered crystal structure. The lithium-nickel-cobalt-manganese composite oxide contains a secondary particle formed of a plurality of flocculated primary particles and a boron compound containing lithium present at least on part of surfaces of the primary particles. A water-soluble Li amount present on the surfaces of the primary particles is up to 0.1% by mass relative to the entire amount of the positive electrode active material.

A powder boronizing composition comprising: a. 0.5 to 4.5 wt % of a boron source selected from B.sub.4C, amorphous boron, calcium hexaboride, borax or mixtures thereof; b. 45.5 to 88.5 wt % of a diluent selected from SiC, alumina or mixtures thereof; c. 1.0 to 20.0 wt % of an activator selected from KBF.sub.4, ammonia chloride, cryolite or mixtures thereof; and d. 10.0 to 30.0 wt % of a sintering reduction agent selected from carbon black, graphite or mixtures thereof.