Process for reducing hexavalent chromium in oxidic solids, which comprises the steps: a) mixing of the oxidic solid containing Cr(VI) with a carbon-containing compound which is liquid in the range from 20 to 100° C., b) treatment of the mixture obtained after a) in an indirectly heated reactor at a temperature of from 700° C. to 1100° C., particularly preferably at a temperature of from 800° C. to 1000° C., under a protective atmosphere, c) cooling of the reaction product obtained after b) to at least 300° C., preferably at least 150° C., under a protective atmosphere.

In the present invention, nickel is selectively extracted from an acidic solution that contains a high concentration of manganese. This valuable metal extraction agent is represented by the general formula. In the formula, R.sup.1 and R.sup.2 are alkyl groups that may be the same or different, R.sup.3 is a hydrogen atom or an alkyl group, and R.sup.4 is a hydrogen atom or any group, other than an amino group, bonded to an α carbon atom of an amino acid. The general formula preferably has a glycine unit, a histidine unit, a lysine unit, an aspartic acid unit or a n-methylglycine unit. When extracting nickel by using this extraction agent, it is preferable to adjust the pH of the acidic solution to 2.3 to 5.5 inclusive.

A method of treating rare earth metal-bearing permanent magnet scrap, waste or other material in a manner to recover the heavy rare earth metal content separately from the light rare earth metal content. The heavy rare earth metal content can be recovered either as a heavy rare earth metal-enriched iron based alloy or as a heavy rare earth metal based alloy.

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

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.

The invention relates to the metallurgical industry, specifically to the acid treatment of red mud obtained in the process of producing alumina, and can be used in technologies for recycling waste from alumina refinery holding ponds. The method for the acid treatment of red mud involves leaching using a leaching agent comprised of water-soluable aliphatic carbonic acids having fewer than 3 carbon atoms per molecule, filtering the solution, and separating the recoverable end products. To ensure a high level of recovery of valuable components and the increased productivity of the process, leaching is conducted with the addition of red mud in portions and with the control of pH values, and when a target pH value of between 2.3 and 3.8 is reached, no more red mud is added, and once leaching is complete, the solution is kept at a given leaching temperature for no less than one hour.

The disclosure relates to a method for sorting a collection of bodies including cemented carbide bodies and non-cemented carbide bodies. A melt having one or more of bismuth, tin and lead and having a density in the range of 7.0-12.0 g/cm.sup.3 is provided. The collection is subjected to a sorting process based on density difference by providing the collection in the melt and allowing the bodies to be sorted into a first group at a top surface of the melt and a second group at a bottom of the melt. The first group includes non-cemented carbide bodies having a density lower than the density of the melt and the second group includes cemented carbide bodies having a density higher than the density of the melt. The present disclosure also relates to a method for recycling of cemented carbides comprising the sorting method and recycling of the second group.

A method for recovering lead oxide from a pre-desalted lead paste, comprising the following steps: a. dissolving the pre-desalted lead plaster by using a complexing agent solution, and making all of PbO therein react with the complexing agent to generate lead complexing ions, obtaining a lead-containing solution and a filter residue; b. adding a precipitant to the lead-containing solution, and then the precipitant reacting with the lead complexing ions to generate a lead salt precipitate and the regenerated complexing agent; c. calcining the lead salt precipitate to obtain lead oxide and regenerate the precipitant. The final recovery rate of lead oxide of the method can reach 99% or more.

The present disclosure concerns an apparatus suitable for smelting and separating metals in flexible oxido-reduction conditions. More particularly, it concerns an apparatus for smelting metallurgical charges comprising a bath furnace susceptible to contain a molten charge up to a determined level, characterized in that the furnace is equipped with: at least one non-transfer plasma torch for the generation of first hot gases; at least one oxygas burner for the generation of second hot gasses; and, submerged injectors for injecting said first and second hot gases below said determined level.

A process for treating spent catalyst containing heavy metals, e.g., Group VIB metals and Group VIII metals is provided. In one embodiment after deoiling, the spent catalyst is treated with an ammonia leach solution under conditions sufficient to dissolve the group VIB metal and the Group VIII metal into the leaching solution, forming a leach slurry. After solid-liquid separation to recover a leach solution, chemical precipitation and solids repulping is carried out to obtain an effluent stream containing ammonium sulfate (Amsul), ammonium sulfamate, Group VB, Group VIB and Group VIII metals. Following sulfidation, the Group VIII metal is fully removed and Group VB and Group VI metals are partially removed from the Amsul stream. In the additional steps of oxydrolysis and iron precipitation, an effective amount of ferric ion at a pre-select pH is added to form insoluble complexes with the Group VB and Group VIB metals, which upon liquid-solid separation produces an effluent ammonium sulfate stream containing less than 10 ppm each of the Group VB and Group VIB metals.