The disclosure provides a method of producing hydrogen. The method comprises conducting a thermochemical reaction by contacting a metal, or an alloy thereof, with steam to produce a metal oxide and/or a metal hydroxide and hydrogen. The method then comprises contacting the metal oxide and/or the metal hydroxide produced in the thermochemical reaction with water or a basic aqueous solution to produce a solution comprising a metal ion. Finally, the method comprises conducting an electrochemical reaction by applying a voltage across an anode and a cathode, whereby at least a portion of the cathode contacts the solution comprising the metal ion, to produce hydrogen, oxygen and the metal, or the alloy thereof.

A method of recovering metals from electronic waste comprises providing a powder comprising electronic waste in at least a first reactor and a second reactor and providing an electrolyte comprising at least ferric ions in an electrochemical cell in fluid communication with the first reactor and the second reactor. The method further includes contacting the powders within the first reactor and the second reactor with the electrolyte to dissolve at least one base metal from each reactor into the electrolyte and reduce at least some of the ferric ions to ferrous ions. The ferrous ions are oxidized at an anode of the electrochemical cell to regenerate the ferric ions. The powder within the second reactor comprises a higher weight percent of the at least one base metal than the powder in the first reactor. Additional methods of recovering metals from electronic waste are also described, as well as an apparatus of recovering metals from electronic waste.

A method of recovering metals from electronic waste comprises providing a powder comprising electronic waste in at least a first reactor and a second reactor and providing an electrolyte comprising at least ferric ions in an electrochemical cell in fluid communication with the first reactor and the second reactor. The method further includes contacting the powders within the first reactor and the second reactor with the electrolyte to dissolve at least one base metal from each reactor into the electrolyte and reduce at least some of the ferric ions to ferrous ions. The ferrous ions are oxidized at an anode of the electrochemical cell to regenerate the ferric ions. The powder within the second reactor comprises a higher weight percent of the at least one base metal than the powder in the first reactor. Additional methods of recovering metals from electronic waste are also described, as well as an apparatus of recovering metals from electronic waste.

An electrochemical process comprises a step E.sup.l of electrolysis of an electrolyte in order to produce gaseous oxygen and a step of converting oxidation-reduction chemical energy into electrical energy with production of H.sub.2. The electrolyte comprises M.sup.m+ ions of a metal M corresponding to the redox pair (M.sup.m+/M), and A.sup.a+ ions of a depolarization additive A corresponding to a redox pair (A.sup.a+/A). Current is supplied between the anode and the cathode, A.sup.a+ and M.sup.m+ are deposited on the cathode respectively in the form of A and M during the electrolysis and gaseous oxygen is released at the anode. The supply of current between the anode and the cathode is then cut off. Depolarization occurs corresponding to the conversion step C°, with production of H.sub.2 and dissolution of M and A into M.sup.m+ and A.sup.a+ at the electrode acting as the cathode during step E.sup.l and the produced H.sub.2 is collected.

An electrochemical process comprises a step E.sup.l of electrolysis of an electrolyte in order to produce gaseous oxygen and a step of converting oxidation-reduction chemical energy into electrical energy with production of H.sub.2. The electrolyte comprises M.sup.m+ ions of a metal M corresponding to the redox pair (M.sup.m+/M), and A.sup.a+ ions of a depolarization additive A corresponding to a redox pair (A.sup.a+/A). Current is supplied between the anode and the cathode, A.sup.a+ and M.sup.m+ are deposited on the cathode respectively in the form of A and M during the electrolysis and gaseous oxygen is released at the anode. The supply of current between the anode and the cathode is then cut off. Depolarization occurs corresponding to the conversion step C°, with production of H.sub.2 and dissolution of M and A into M.sup.m+ and A.sup.a+ at the electrode acting as the cathode during step E.sup.l and the produced H.sub.2 is collected.

A method for extracting metal ions from water is provided that includes disposing two electrically conductive electrodes in water, where the water includes a target ion species in solution, where at least one of the electrically conductive electrodes is a functionalized electrode having species-specific adsorption of the target ion species, and providing electrical current to the electrically conductive electrodes such that the one or more target ion species are deposited to metallic form or metal oxides at the functionalized electrode by one or more electrochemical reactions.

A method for extracting metal ions from water is provided that includes disposing two electrically conductive electrodes in water, where the water includes a target ion species in solution, where at least one of the electrically conductive electrodes is a functionalized electrode having species-specific adsorption of the target ion species, and providing electrical current to the electrically conductive electrodes such that the one or more target ion species are deposited to metallic form or metal oxides at the functionalized electrode by one or more electrochemical reactions.

An electrochemical process implements, in a decoupled manner, a first step of electrolysis of an electrolyte to produce gaseous oxygen in a chamber and a second step of electrochemical conversion of H+ ions into gaseous hydrogen in a chamber which contains a liquid phase and a gas phase not dissolved in the liquid phase. Gaseous hydrogen produced in the conversion step is partly present in the gaseous headspace of chamber and as bubbles in the electrolyte, and partly dissolved in the electrolyte which is saturated with hydrogen. The electrolyte has at least one redox pair (A/B) forming at least one intermediate vector enabling the decoupling of the first and second steps. The interface between the gas and liquid phases is increased during the second step to accelerate the diffusion, from liquid phase to gas phase, of the dissolved hydrogen able to supersaturate the electrolyte. Pressurized gaseous hydrogen is then collected.

The method includes two technological segments (i) a reduction segment and (ii) an oxidation segment that are interconnected by various support technological processes for the regeneration of solutions and gases and heat recuperation. The reduction segment includes an electrolysis that is performed from a solution of chloride salts of an energy carrier. During the electrolysis, these elements reduce to a lower oxidation state, solidify on the electrodes or precipitate to a solid state. The solid substance thus obtained is the energy carrier that can be stored outside of the electrolyser until a need for additional energy emerges. During the electrolysis, chlorine gas develops that is collected and dissolved in water. An HCl solution is regenerated, which is used in the oxidation segment. Oxygen is released in this process. The energy that has thus been stored in the oxidation potential of the energy carrier is released during a spontaneous chemical reaction between the energy carrier and the HCl solution in the oxidation segment. In this chemical reaction, the oxidation state of the chemical elements which constitute the energy carrier is increased to an oxidation state identical to that from before the beginning of the electrolysis. The reaction product hydrogen is formed that represents a high calorific fuel. This fuel can be immediately converted to heat or electrical energy, without a need for intermediate storage, by known methods. Only water enters the entire method, oxygen and hydrogen leave, while the cycle is closed/cyclic for the remaining substances.

A zinc production method further includes chlorine-concentration adjusting processes 101, 101, and 105 of using an alkali hydroxide aqueous solution as an extraction solvent for selectively extracting zinc components in a zinc-containing aqueous-solution generating process 102, and separating chlorine components contained in electric arc furnace dust or secondary dust to decrease the chlorine concentration of a zinc-containing aqueous solution at a stage prior to an electrolyzing process 103.