Method for preparing high-purity cobalt nitrate by utilizing alumina-supported cobalt-based spent catalyst for Fischer-Tropsch synthesis
An alumina-loaded, waste catalyst technology, applied in inorganic chemistry, cobalt compounds, chemical instruments and methods, etc., can solve the problems of high cost and environmental pollution of waste catalysts, and achieve the effect of high recovery rate
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Embodiment 1
[0018] Embodiment 1: see figure 1 , using Co / Al for Fischer-Tropsch synthesis 2 o 3 Spent catalyst is ground into uniform powder, and the result of elemental analysis is: the mass percentage of cobalt is 10.68%; Take by weighing 5.00g this powder, place in beaker, add 60mL mass fraction and be the concentrated hydrochloric acid heating of 35%~37%, keep slight Boil to dissolve it, stop heating when the amount of insoluble matter remains unchanged, filter to remove insoluble matter after cooling, and obtain CoCl 2 with AlCl 3 mixed solution. Under constant stirring, add saturated NaOH solution dropwise to the above solution until the pH is 2.3, then add 60 mL of acetic acid buffer solution with a concentration of 2 mol / L and pH 3.0, mix well and add 5.44 g of NaOH in four times 2 S·9H 2 O solid, shake for 10min after addition and let stand for 24h. The CoS precipitate was separated by filtration, and the precipitate was washed with a small amount of 2 mol / L pH 3.0 acetic a...
Embodiment 2
[0019] Embodiment 2: Fischer-Tropsch synthesis with Co / Al 2 o 3 Spent catalyst is ground into uniform powder, and the result of elemental analysis is: the mass percentage of cobalt is 19.08%, takes by weighing 7.26g this powder, is placed in beaker, adds 87mL mass fraction and is the concentrated hydrochloric acid heating of 35%~37%, keeps slight Boil to dissolve it, stop heating when the amount of insoluble matter remains unchanged, filter to remove insoluble matter after cooling, and obtain CoCl 2 with AlCl 3 mixed solution. Under continuous stirring, add saturated KOH solution dropwise to the above solution until the pH is 2.3, then add 87 mL of acetic acid buffer solution with a concentration of 2 mol / L and pH 3.0, mix well and add 14.10 g of Na in four times 2 S·9H 2 O solid, shake for 10min after addition and let stand for 24h. The CoS precipitate was separated by filtration, and the precipitate was washed with a small amount of 2 mol / L pH 3.0 acetic acid buffer sol...
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