Abstract: Process for electrolytically producing metals of Ni, Co, Zn, Cu, Mn, and Cr, comprising, electrolyzing an aqueous solution containing ions of a metal as main component selected from Ni, Co, Zn, Cu, Mn, and Cr in a cathode compartment to deposit the metal electrolytically on a cathode, the cathode compartment being separated by one or more diaphragms from the remainder of the solution where iron or a metal containing iron is used for material of corrosible anode, and maintaining the concentration of iron ion in the solution circulating in the anode compartment at a low level by bringing the whole or a part of the circulating solution into contact with an organic solvent which is prepared by adding petroleum hydrocarbon for dilution of one or more extracting agents selected from the group consisting of carboxylic acids, alkylaryl phosphoric acids, hydroxyoximes, alkyl phosphoric acids, alkylamines, ketones, alkylamides, and neutral phosphoric acid esters, to extract and remove the iron or the chloro-complex ion

Abstract: Process for producing fluorides of Mo, W, Nb, Ta, V, Re, Ti, Zr, Hf, Co, Ni, Cr, Sb, Sn, Zn, Pb, Al and rare earth metals comprising heating fluorine-containing ammonium salts of corresponding metals in a stream of an inert or reducing gas to convert them into fluorides of the metals.

Abstract: A crystallizer comprising a mixing zone of an organic solvent containing ions of a metal extracted therein and an aqueous separating solution provided at the upper part of a main crystallizer body, a lower-part opened organic solvent settling zone provided outside of the mixing zone for receiving and settling the organic solvent overflowing out of the mixing zone, a crystals developing zone having a downwardly narrowing cross section provided at the lower part of the main crystallizer body, a descending pipe extending from the lower end of the mixing zone to the lower part of the crystals developing zone, a crystals fluidizing medium inlet provided at the lower end of the crystals developing zone, a separating solution discharge pipe and a crystals discharge pipe.

Abstract: A process for selectively stripping and separating iron ions from an organic solvent (A) which comprises bringing the organic solvent (A) containing iron and zinc ions, and containing one or more compounds selected from the group consisting of alkyl phosphoric acid, alkyl-aryl phosphoric acid, alkyl thio phosphoric acid and alkyl-aryl thio phosphoric acid together with a petroleum hydrocarbon as a diluent, into contact with an aqueous solution containing NH.sub.4.sup.+ and F.sup.- ions so as to selectively strip the iron ions into the aqueous solution despite the coexistence of zinc ions.

Abstract: The present invention provides for the recovery of gallium from aluminum smelting dust. Aluminum smelting dust is leached with mineral acid, such as sulfuric acid, hydrochloric acid, or nitric acid. Gallium is extracted from the obtained leach liquor with an organic solution containing a liquid cation exchange agent. The resulting loaded organic solution is treated with mineral acid in aqueous solution, either after or before scrubbing with a higher concentration of acid in aqueous solution, to strip gallium. Gallium is extracted from this solution with another organic solution containing an ion-pair extracting type extracting agent. Finally, purified gallium is recovered by stripping the latter loaded organic solution with water or dilute acid in aqueous solution.

Abstract: A process for production of metallic iron by heating ammonium iron fluoride or iron fluoride in hydrogen stream.

Abstract: A recovery process of uranium comprising:(1) extracting uranium ions with an organic solvent containing one or more compounds selected from the group consisting of alkyl phosphoric acid, alkyl-aryl phosphoric acid, alkyl dithio phosphoric acid, aryl dithio phosphoric acid, neutral phosphoric acid ester and alkyl amine together with a petroleum hydrocarbon as a diluent; and(2) stripping the uranium ions in the resultant organic solvent from the step (1) to an aqueous phase with contact of an aqueous solution containing one or more compounds selected from the groups of NH.sub.4 F, NH.sub.4 HF.sub.2, KF or KHF.sub.2.

Abstract: A process for production of metallic iron by heating ammonium iron fluoride or iron fluoride in a hydrogen stream.

Abstract: A process for preparing high purity superfine powders of less than 0.5.mu. diameter of Mo, W, Nb, Zr, Cu, Zn, Co, Ni and In by first producing their fluoride or a double fluoride with ammonium and then decomposing them under heat in a hydrogen-containing stream. Features of the present process are that the double fluoride of the metals with ammonium is faster in crystal growth than their fluoride, recrystallization of these salts can be repeated as desired when a high purity of the metals is required, and particles of a uniform size can be obtained easier.

Abstract: A process for the production of aluminum oxide from aluminum compounds containing fluorine comprising:(1) extracting aluminum ions with an organic solvent containing one or more compounds selected from the groups of alkyl phosphoric acid, alkyl and aryl thio phosphoric acid, carboxylic acid and hydroxime together with a petroleum hydrocarbon as a diluent;(2) preparing aluminum compounds containing fluorine by stripping the aluminum ions in the resultant organic solvent from the step (1) in contact with an aqueous solution containing one or more compounds selected from the groups of HF, NH.sub.4 HF.sub.2, NH.sub.4 F or KHF.sub.2 and simultaneously regenerating the organic solvent; and(3) producing aluminum oxide by heating the resultant aluminum compounds containing fluorine from the step (2) in gas stream containing oxygen or H.sub.2 O.

Abstract: A process for recovery of reusable chromic acid from waste chromic acid solution containing impurities, which process comprises a first step in which the solution containing chromic acid is introduced into the cathode compartment in an electro-dialysis process and free chromic acid or chromate ions in the above solution are transferred to the anode compartment, a second step in which H.sub.2 SO.sub.4 is added in at least equivalent amounts to the heavy metallic ion contained in the outlet solution, in which chromic acid ion concentration is reduced, in order to convert chemical species of the contained metallic ion and increase the H.sup.+ ion concentration and then chromate ions in the resultant solution are extracted into an organic phase with contact of an organic solvent (A), and a third step in which residual amounts of chromic acid ion remaining in the aqueous raffinate from the second step are extracted into an organic phase with contact of an organic solvent (B).

Abstract: This invention relates to a process for recovery of waste H.sub.2 SO.sub.4 and HCl which are used for pickling metallic materials and articles and contain a large quantities of Fe ions. Furthermore, it offers a process for the recovery of H.sub.2 SO.sub.4 and HCl from waste H.sub.2 SO.sub.4 which contains large amounts of Fe ions after removal of Ti ions by a hydrolysis process in the production of TiO.sub.2 and also for the recovery of high-purity electrolytic iron or iron hydroxide.

Abstract: This invention relates to a process for recovery of waste H.sub.2 SO.sub.4 and HCl which are used for pickling metallic materials and articles and contain a large quantities of Fe ions. Furthermore, it offers a process for the recovery of H.sub.2 SO.sub.4 and HCl from waste H.sub.2 SO.sub.4 which contains large amounts of Fe ions after removal of Ti ions by a hydrolysis process in the production of TiO.sub.2 and also for the recovery of high-purity electrolytic iron or iron hydroxide.

Abstract: A process for treating an acid waste liquid containing Fe ions which has been used for acid washing of metallic materials or articles, comprising the first stage where an organic solvent (A) is added to the acid waste liquid to extract Fe ions, the second stage where an acid is added to the resulting acid waste liquid to convert chemical species of remaining metal salts and increase the hydrogen ion concentration followed by addition of an organic solvent (B) to recover the mineral acid of concern by extraction, the third stage where an organic solvent (C) is added to the resulting acid waste liquid to extract and recover other required mineral acids, and regenerating each of the organic solvents (A), (B) and (C) in respective stages.

Abstract: A process for recovery of reusable chromic acid from waste chromic acid solution containing impurities, which process comprises a first step in which the solution containing chromic acid is introduced into the cathode compartment in an electro-dialysis process and free chromic acid or chromate ions in the above solution are transferred to the anode compartment, a second step in which H.sub.2 SO.sub.4 is added in at least equivalent amounts to the heavy metallic ion contained in the outlet solution, in which chromic acid ion concentration is reduced, in order to convert chemical species of the contained metallic ion and increase the H.sup.+ ion concentration and then chromate ions in the resultant solution are extracted into an organic phase with contact of an organic solvent (A), and a third step in which residual amounts of chromic acid ion remaining in the aqueous raffinate from the second step are extracted into an organic phase with contact of an organic solvent (B).

Abstract: This invention relates to a process for recovery of waste H.sub.2 SO.sub.4 and HCl which are used for pickling metallic materials and articles and contain a large quantities of Fe ions. Furthermore, it offers a process for the recovery of H.sub.2 SO.sub.4 and HCl from waste H.sub.2 SO.sub.4 which contains large amounts of Fe ions after removal of Ti ions by a hydrolysis process in the production of TiO.sub.2 and also for the recovery of high-purity electrolytic iron or iron hydroxide.

Abstract: Production of titanium dioxide which is characterized by recovery of reusable H.sub.2 SO.sub.4, highly pure Fe oxide and hydroxide and fractional recovery of Mn, V and Cr, etc., from FeSO.sub.4. nH.sub.2 O and waste acid of 20 - 40% H.sub.2 SO.sub.4 containing abundant heavy metallic ions, which are by-produced in the production of TiO.sub.2 by dissolution of Ti raw materials such as ilmenite, steel production slag, such as electric furnace slag, convertor slag with H.sub.2 SO.sub.4.