Recovery process for valuable metals in tungsten residues
A technology for valuable metals and tungsten slag, which is applied to the recovery process of valuable metals in tungsten slag, can solve the problems of high energy consumption and large environmental pollution in pyrometallurgy, achieve good environmental benefits, reduce recycling costs, and low costs Effect
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Embodiment 1
[0037] Such as figure 1 Shown, the present invention comprises the steps:
[0038] 1) Preparation of tungsten
[0039] 1) Melting material
[0040] First add hydrochloric acid with a calculated concentration of 15-25% into the tank, heat to 60°C, slowly add black and white mixed tungsten slag under stirring, after adding black and white mixed tungsten slag, add 0.2% of the first hydrochloric acid amount 15-25% hydrochloric acid about twice as much, after heating and boiling, add 20kg / t NaF, 10kg / t NaNO3; when the pH value reaches about 1.0, add 15-25% of 0.4-0.5 times the amount of hydrochloric acid for the first time Hydrochloric acid, make S:L=1:4.5, boil until the mud turns reddish brown, stop heating, continue to stir, add 2t / t of water, stir for 0.5h;
[0041] 2) Press filter
[0042] When the temperature of the material liquid prepared in step 1) is below 80°C, carry out plate and frame filter press, add water to wash after press filter, and blow dry; put the filtrat...
Embodiment 2
[0087] 1) Preparation of tungsten
[0088] 1) Melting material
[0089] Add tungsten slag to the tank body with water or acid leaching and filtered washing water under slow stirring, and the liquid-solid ratio is 1:1; steam is heated to 60°C and then added according to the mass ratio of tungsten slag and sulfuric acid 1:1.2 8% sulfuric acid, keep the reaction temperature for 1.5 hours, then add 15% to 25% HCl 0.25 times the amount of sulfuric acid, heat to boil, then add 20kg / t NaF, 10kg / t NaNO 3 ;When the pH value reaches about 1.0, put in 15-25% hydrochloric acid that is 0.4-0.5 times the amount of sulfuric acid to make S:L=1:4.5, boil until the mud turns reddish brown, stop heating, continue stirring, add water 2t / t, stirring for 0.5h; when the temperature of the feed liquid reaches 80°C, pour the feed liquid into a filter for filtration while stirring, then wash and dry it, put the filtrate in a storage tank and let it stand for at least 12 hours, and then finely filter ...
Embodiment 3
[0136] Except for 7) the step of extracting W in the step of 1) the preparation of tungsten, the other steps are the same as those in Example 1 and will not be repeated here. The specific operation of the extraction step of this embodiment is as follows:
[0137] After the finely filtered filtrate produced in step 2) is reduced, put it into the extraction tank according to O / A=1 / 20-30, stir for 2 minutes, and add a concentration of 0.01% citric acid or stearic acid, grade 4 Countercurrent extraction, then add water according to the ratio O / A=1 / 1, stir for 3 minutes, and wash in 6 stages; then add hot 2mol / L NaOH solution according to the ratio O / A=2 / 1, stir for 15-20 Minutes; 3-stage reverse extraction and countercurrent, filter the stripping solution; then add water for backwashing according to O / A=1 / 3~5, stir for 5~10 minutes, clarify, and return the water phase to alkali dissolution; then press the comparison O / A=3~5 / 1 Add 6mol / L hydrochloric acid to acidify, stir for 3~5 ...
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