Method for recovering high-purity molybdenum from molybdenum-containing dead catalyst
A waste catalyst, high-purity technology, applied in the direction of improving process efficiency, etc., can solve the problems of low molybdenum recovery rate, insufficient purity of molybdenum, high treatment cost, etc., and achieve the effect of easy complete conversion, simple equipment and high purity
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Embodiment 1
[0027] 500 g of the spent hydrogenation catalyst FDS-4 was roasted at 400° C. for 3 hours, and then pulverized to 120 mesh after cooling. Obtained 432.6g, the content of molybdenum and cobalt (based on oxide weight) was analyzed to be 15.4% and 4.8%, respectively. Alkaline preparation, NH in ammonia water (concentration about 28%) 4 The weight ratio of OH to molybdenum in the spent catalyst is 4:1 (the weight is about 270g), and the weight ratio of ammonium bicarbonate to the spent catalyst is 1:1 (the weight is about 70g) in the ammonia water, and the hydrogen peroxide is added to the mixed solution. 6% by weight (weight is about 20g). Add the pulverized powder into the prepared alkaline solution, and mix thoroughly at 40° C. for 2 hours. Filtration, solid-liquid separation, solid roasting at 400°C for 2 hours, impregnation and separation in the same way. Mix the two solutions and adjust the pH to 7.5 with high-concentration nitric acid. If there is aluminum precipitation,...
Embodiment 2
[0029] 500 g of the FDS-4 hydrogenation catalyst was calcined at 500° C. for 4 hours, and then pulverized to 180 mesh after cooling. The obtained 414.2 g were analyzed to have molybdenum and cobalt contents (calculated as oxides) of 16.8% and 5.2%, respectively. Alkaline preparation, NH in ammonia water (about 30% by weight) 4 The weight ratio of OH and molybdenum in the spent catalyst is 6:1 (about 420g in weight), and the weight ratio of molybdenum (by element weight) in ammonium bicarbonate and spent catalyst is added in ammoniacal liquor to 1.5:1 (about 105g in weight), Add hydrogen peroxide and be about 6% (weight is about 26g) of mixed solution weight. Add the pulverized powder into the prepared alkaline solution, and mix thoroughly at 40° C. for 2 hours. Filtration, solid-liquid separation, the solid was roasted at 400°C for 2 hours, and then impregnated and separated by the same method. Mix the two filtrates and add high-concentration nitric acid to adjust the pH to...
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