Method for recycling zirconium oxide and yttrium oxide from yttrium oxide steady zirconium oxide solid fused mass waste matter
A yttrium oxide and zirconium oxide technology, applied in zirconium oxide, chemical instruments and methods, rare earth metal compounds, etc., can solve the problems of increasing the amount of waste solution treatment, unfavorable energy saving and emission reduction, long pyrolysis time, etc., and the process is easy to achieve. Control, energy saving, low conversion temperature effect
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Embodiment 1
[0028] (1) Grind to -0.175mm cubic zirconia powder (containing ZrO 2 76.45%, Y 2 o 3 18.54%, SiO 2 2.86%, Fe 2 o 3 0.58%), sulfuric acid and acidifying auxiliary ammonium sulfate are put into a reaction pot according to the solid-liquid ratio of 1:2.5:1.25, mixed evenly, and reacted at a temperature of 200-320° C. for 30 minutes to obtain an acidified frit material.
[0029] (2) Dilute the obtained acidified frit material with water. The mother liquor and eluent produced by step (4) are 1: 2.5 according to the solid-to-liquid ratio, and leached at 85-95° C. for 45-60 minutes of leaching time, and the leaching ends Then carry out solid-liquid separation to obtain zirconium yttrium clear liquid.
[0030] (3) The above clear liquid is evaporated and concentrated, and the concentrated feed liquid is controlled to contain ZrO 2 2.5~2.8mol / L, acidity [H + ]5.8~6.5mol / L, zirconium sulfate crystals were precipitated by cooling.
[0031] (4) The zirconium sulfate crystals ...
Embodiment 2
[0039] Cubic zirconia powder crushed to -0.175mm (chemical composition is the same as in Example 1) and sulfuric acid and acidification auxiliary ammonium sulfate are put into a reaction pot at a solid-to-liquid ratio of 1: 1.75: 1.25 and mixed evenly. Acidification transformation reaction at high temperature for 30 minutes to obtain acidification frit material.
[0040]All the other method steps are the same as in Example 1.
[0041] The zirconia product obtained by the technical scheme provided by the embodiment of the present invention 2 contains ZrO 2 >99.9%, SiO 2 2 o 3 2 o 3 / Re 2 o 3 >99.95%, ZrO 2 2 2 o 3 <0.0022%. The recovery rate of yttrium was 94.5%.
Embodiment 3
[0043] Cubic zirconia powder crushed to -0.175mm (chemical composition is the same as in Example 1) and sulfuric acid and acidification auxiliary ammonium sulfate are put into a reaction pot according to a solid-to-liquid ratio of 1:1.3:1.5 and mixed evenly, at 200-300°C Acidification transformation reaction at high temperature for 50 minutes to obtain acidification frit material.
[0044] All the other method steps are the same as in Example 1.
[0045] The zirconia product obtained by the technical scheme provided by the embodiment of the present invention 3 contains ZrO 2 >99.9%, SiO 2 2 o 3 2 o 3 / Re 2 o 3 >99.9%, ZrO 2 2 2 o 3 <0.0022%. The recovery rate of yttrium was 91.4%.
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