Preparation method of analytically pure nickel sesquioxide
A technology of nickel trioxide and nickel nitrate, which is applied in the direction of nickel oxide/nickel hydroxide, etc., can solve the problems of high impurity content and low purity of nickel trioxide, and achieve low impurity content, easy control, and improved competitiveness Effect
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Embodiment 1
[0017] A preparation method for analyzing pure nickel sesquioxide, the steps are:
[0018] (1), nickel nitrate iron removal:
[0019] Dissolve 1kg of nickel nitrate in 3000mL of distilled water, add 10g of hydrogen peroxide to oxidize, heat to 80°C, slowly add 85g / L sodium carbonate solution while stirring, control the pH value of the solution to 1.7, add dropwise for 1.5 hours, continue to add sodium carbonate to the solution When the pH value reaches 4.0, there is no iron ion in the solution, filter to obtain solution A;
[0020] (2) Calcium removal and magnesium ion removal:
[0021] Heat solution A to 85°C, slowly add ammonium fluoride, control the pH value of the solution to 5.0, let it stand for 2 hours, and filter to obtain solution B;
[0022] (3), synthetic nickel oxalate:
[0023] Heat and concentrate solution B at 50°C to a relative density of 15°Be, add 1.04g / L oxalic acid solution while stirring, control the pH value of the solution to 4.5, and form a nickel ox...
Embodiment 2
[0027] A preparation method for analyzing pure nickel sesquioxide, the steps are:
[0028] (1), nickel nitrate iron removal:
[0029] Dissolve 1.2kg nickel nitrate in 3600mL distilled water, add 12g hydrogen peroxide to oxidize, heat to 85°C, slowly add 90g / L sodium carbonate solution while stirring, control the pH value of the solution to 2.0, add dropwise for 2 hours, continue to add sodium carbonate to The pH value of the solution reaches 4.5, and there is no iron ion in the solution, and is filtered to obtain solution A;
[0030] (2) Calcium removal and magnesium ion removal:
[0031] Heat solution A to 90°C, slowly add ammonium fluoride, control the pH value of the solution to 6.0, let it stand for 2.5 hours, and filter to obtain solution B;
[0032] (3), synthetic nickel oxalate:
[0033] Heat and concentrate solution B at 60°C to a relative density of 18°Be, add 1.05g / L oxalic acid solution while stirring, control the pH value of the solution to 5.0, and form a nicke...
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