A process for the chemical conversion of contaminated magnesium hydroxide to high purity solutions of magnesium bicarbonate include steps of providing an impure reagent including at least 40% and less than 95% by total weight of total metals of magnesium in a form of solid magnesium hydroxide and at least 10% by weight of total metals of calcium carbonate, combining the impure reagent containing the solid magnesium hydroxide with carbonic acid in water, thereby generating magnesium bicarbonate and water and then filtering out solid calcium carbonate leaving a solution of magnesium bicarbonate in water having a by weight ratio of Mg/(Mg+Ca) in the solution of greater than 95%. Heating and/or drying the magnesium bicarbonate solution produces correspondingly high purity magnesium carbonate.

The invention is directed to a process and apparatus for metal refining, in particular for refining a mixture of conductive particles, such as heavy non-ferrous particles. In accordance with the invention a feed containing a mixture of conductive particles is fed to a dissolution unit, wherein the less noble metal is separated from a metal of interest in the presence of one or more acids or complexing agents, thus producing a stream having a concentrated less noble metal and producing a conductive stream containing a metal of interest. The conductive stream is then fed to a refining unit, wherein the conductive stream is separated in a stream of concentrated metal(s) of interest and a stream of concentrated conductive particles.

A nickel recovery process capable of decreasing nickel remaining in a byproduct by recovering nickel from the byproduct of electrolytic nickel manufacturing process by chlorine-leaching, and also, capable of simplifying a cementation step simultaneously, is provided. In a nickel recovery step S60, a nickel recovery step S70 and a nickel recovery step S80, nickel is recovered in each step from S.sup.0 slurry, residue flaker and chlorine-leached residue, which are byproducts of electrolytic nickel manufacturing process by chlorine-leaching, by using an aqueous solution containing 80 g/L to 390 g/L of chlorine and 30 g/L to 70 g/L of copper.

The present invention relates to a method and a process of preparing precipitated calcium carbonate of high purity by extracting calcium ion contained in an alkali ion-containing inorganic material such as mineral, steelmaking slag and waste concrete with the use of an acidic aqueous solution, separating other metal ions from the extracted solution, preparing an alkaline earth metal hydroxide using an alkaline aqueous solution and then contacting the same with carbon dioxide.

A method for producing metal zinc by liquid/liquid extraction, comprising leaching of a zinc-bearing solid raw material containing antimony with a slightly acid aqueous solution, at a pH value maintained above 3 and less than or equal to 5, with formation of a suspension, drawing-off from the suspension of an aqueous phase containing zinc in solution to be subject to the extraction, additional leaching of the remaining suspension with an acid aqueous solution, at a pH value maintained below 3.5 and greater than or equal to 1, with formation of a pulp, introduction of a neutralizing agent in this pulp with coprecipitation of antimony and other impurities and separation from this neutralized pulp of a zinc-bearing aqueous solution which is recycled to the step for leaching the zinc-bearing solid raw material.

Cathode material from exhausted lithium ion batteries are dissolved in a solution for extracting the useful elements Co (cobalt), Ni (nickel), Al (Aluminum) and Mn (manganese) to produce active cathode materials for new batteries. The solution includes compounds of desirable materials such as cobalt, nickel, aluminum and manganese dissolved as compounds from the exhausted cathode material of spent cells. Depending on a desired proportion, or ratio, of the desired materials, raw materials are added to the solution to achieve the desired ratio of the commingled compounds for the recycled cathode material for new cells. The desired materials precipitate out of solution without extensive heating or separation of the desired materials into individual compounds or elements. The resulting active cathode material has the predetermined ratio for use in new cells, and avoids high heat typically required to separate the useful elements because the desired materials remain commingled in solution.

A variety of systems, methods and compositions are disclosed, including, in one method for recycling a spent alkaline battery comprising: dissolving insoluble metal ions in aqueous solution thereby producing pregnant leach solution; extracting zinc sulfate from aqueous solution thereby producing zinc sulfate product and raffinate solution comprising manganese sulfate and potassium sulfate; separating manganese hydroxide from raffinate solution thereby producing manganese sulfate product and aqueous potassium sulfate solution; crystallizing aqueous potassium sulfate solution to produce solid potassium sulfate product. A system for recycling spent alkaline battery comprising: first liquid-solid extraction unit capable of dissolving insoluble metal ions in aqueous solution thereby producing pregnant leach solution; liquid-liquid extraction unit capable of extracting zinc from pregnant leach solution; second liquid-solid extraction unit capable of precipitating manganese hydroxide from raffinate produced by liquid-liquid extraction unit; and third liquid-solid extraction unit capable of crystallizing aqueous potassium sulfate solution produced by second liquid-solid extraction unit.

The invention discloses Method for whole component microwave fast digestion and precious metal extraction from ionic liquid of waste circuit board, and belongs to the field of hydrometallurgy. Based on the theory that microwaves can directly penetrate through a leaching medium to directly heat a circuit board, microwave-assisted leaching can reinforce mass transfer and heat transfer in the traditional leaching process, the leaching time is greatly shortened, and the leaching efficiency is improved. Before leaching, a waste circuit board does not need to be smashed, and environmental protection is achieved while energy is saved. The temperature rising process and reaction time of the reaction can be controlled, the whole process is conducted under the airtight condition, heat loss in the leaching process is avoided, the valuable leaching rate is high, the selectivity is high, and efficient leaching of valuable metal can be achieved. Precious metal leachate is extracted through imidazolium ionic liquid, the selectivity of the imidazolium ionic liquid to gold is high, and the co-extraction phenomenon of gold, nickel, copper and other ions is avoided. The method for extracting the precious metal leachate through ionic liquid is a green and clean recycling method, and the overall recycling rate of gold, nickel and copper can reach 99% or above

Disclosed is a method for enhancing leaching of metals in zinc hypoxide powder by mechanochemistry coupling with sonochemistry, comprising the following: mechanical activation: a raw material containing zinc hypoxide powder is mechanically activated so that an activated material is obtained; and ultrasonic treatment: the activated material is mixed with an acidic leaching solution to obtain a mixture, the mixture is subjected to ultrasonic treatment, and a liquid phase is obtained as the leachate. Mechanochemical activation and ultrasonic chemistry synergistically enhance the leaching efficiency and leaching rate of multiple metals through the destruction and cavitation of the zinc oxide powder structure. This process can indirectly reduce the concentration of the used acidic leaching solution and shorten the leaching duration. In practical production, the specific application of the process can reduce the anticorrosion cost and running cost of reaction equipment, indirectly leading to excellent production benefit.

A method to be used in conjunction with a single-stage or multi-stage process for leaching ash originating from the recovery boiler of a pulp mill, particularly when the ash contains a significant amount of carbonate, wherein calcium compounds, such as calcium oxide (CaO) or calcium hydroxide (Ca(OH).sub.2), are employed as additives in one or more leaching stages, a liquid fraction formed in the leaching process is utilized outside the main chemical recovery cycle, such as a substitute for purchased sodium hydroxide in the bleaching line of the pulp mill, and a solids fraction may be mixed with a black-liquor stream of the mill or subjected to further processing to separate calcium compounds for recycle.