Method for direct production of ultra-pure manganese sulfate by non-carbon reduction of manganese dioxide
A technology of manganese dioxide and manganese sulfate, applied in the direction of manganese sulfate, etc., can solve problems such as high production costs, environmental pollution, and indicators that cannot meet the requirements, and achieve the effect of saving concentration costs
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[0012] The specific embodiment of the present invention is: a kind of method of directly producing ultra-high-purity manganese sulfate by carbon-free reduction of manganese dioxide, 1. at first manganese dioxide powder and pyrite powder are washed with dilute sulfuric acid in a stirring tank to the fullest calcium, Magnesium impurities are then filtered and washed respectively; ②The washed manganese dioxide powder and pyrite powder are put into another stirring tank for water washing according to the ratio of Mn:S of 1:0.4, and then press-filtered until dry; ③The press-filtered The mixed powder is dried and roasted; ④The roasted product is leached in a non-open container with dilute sulfuric acid, and then the pH of the leaching solution is adjusted to 6 with hydrogen peroxide; Pure manganese sulfate solution can be obtained; ⑥ evaporate and crystallize the obtained pure manganese sulfate solution to obtain pure manganese sulfate crystals, concentrate the mother liquor to prepa...
example 1
[0020] Wash and dry 1000g containing MnO 2 Mix 45% manganese powder, 200g pyrite powder containing 45% S and a small amount of catalyst evenly, then put it into a metal container with a cover, and then put the container into a high-temperature furnace at 450°C and keep it warm for 30 minutes. Then take it out and cool it, get 300g calcined sand and 500ml distilled water and put them into a three-neck flask with stirring, introduce a small amount of gas generated by the reaction into the lye from one mouth with a small tube, and add 75ml of concentrated sulfuric acid dropwise from the other mouth with a separatory funnel, After reacting for 90 minutes, adjust the pH to 6 with hydrogen peroxide, and filter after standing for 3 hours. After standing for 24 hours, filter the filtrate again with slow filter paper. The fine filtrate was tested, and the harmful impurities:
[0021] K=300μg / ml, Na=30μg / ml, Ca=225μg / ml, Mg=265μg / ml, Zn=30μg / ml, Pb=2μg / ml, Cd=4μg / ml, Cu<2μg / ml, As< 1μg...
example 2
[0026] 1000g of pickled and dried MnO-containing 2 Add 35% manganese powder, 150g pyrite powder containing 41% S, and 20g combustion accelerant into a special heating furnace with stirring at the same time, react at 500°C for 60 minutes and cool down to detect that the calcine has not reduced MnO 2 6%, take 500 grams of calcined sand and leaching with 10% dilute sulfuric acid under ventilated conditions, control the pH value of the reaction end point to 4.5, then neutralize with hydrogen peroxide to pH = 6, filter after standing for 3 hours, and filter the filtrate after standing for 24 hours Filter again with slow filter paper, the fine filtrate is tested, harmful impurities:
[0027] K=345μg / ml, Na=42μg / ml, Ca=305μg / ml, Mg=345μg / ml, Zn=35μg / ml, Pb=1.5μg / ml, Cd=3μg / ml, Cu<2μg / ml, As <1μg / ml,
[0028] Concentrate and recrystallize to obtain qualified high-purity manganese sulfate.
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