Comprehensive utilization method for iron ore sintering smoke ash leaching liquid
A technology for extracting liquid and dust, applied in chemical instruments and methods, bismuth compounds, improving process efficiency, etc., can solve problems such as ineffective use of sodium, complex leachate components, loss of calcium and carbonate, etc., and achieve good promotion Application prospects, increasing the added value of raw materials, and the effect of efficient recycling
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Embodiment 1
[0024] a. According to the liquid-solid mass ratio of 2.0:1, add water and sintering soot into the reactor, leaching the sintering soot with water for 1.0 hour at room temperature and a stirring speed of 300 rpm, and obtain the leaching solution and leaching slag;
[0025] b. According to the content of bismuth in the leaching solution obtained in step a, add 100% sodium oxalate in a theoretical amount according to stoichiometry, and precipitate and react for 1.5 hours at 80° C. and a stirring speed of 300 rpm, separate and obtain bismuth oxalate precipitation and filtrate; oxalic acid The bismuth precipitate was washed, dried and calcined at 800°C for 1.0 hour to obtain bismuth trioxide product.
[0026] C, step b gained filtrate, according to the content of lead in the solution, add the sodium chromate of theoretical quantity 120% by stoichiometry, precipitation reaction 1.0h under stirring condition at room temperature 300rpm, separate, wash and obtain lead chromate product...
Embodiment 2
[0034] a. According to the liquid-solid mass ratio of 1.0:1, add water and sintering soot into the reactor, leaching the sintering soot with water for 2.0 hours at room temperature and a stirring speed of 500 rpm, and obtain the leaching solution and leaching slag;
[0035] b. According to the content of bismuth in the leaching solution obtained in step a, add 100% sodium oxalate in a theoretical amount according to stoichiometry, and precipitate and react for 1.0 hour at 60° C. and a stirring speed of 500 rpm, separate and obtain bismuth oxalate precipitation and filtrate; oxalic acid The bismuth precipitate was washed, dried and calcined at 600°C for 2.0 hours to obtain bismuth trioxide product.
[0036] C, step b gained filtrate, according to the content of lead in the solution, add the sodium chromate of theoretical quantity 100% by stoichiometry, precipitation reaction 0.75h under room temperature 200rpm stirring conditions, separation, washing obtain lead chromate produc...
Embodiment 3
[0044] a. According to the liquid-solid mass ratio of 1.5:1, add water and sintering soot into the reactor, and leaching the sintering soot with water for 0.5 hour under the conditions of room temperature and stirring speed of 400rpm, and obtain the leaching solution and leaching slag;
[0045] b. According to the content of bismuth in the leaching solution obtained in step a, add theoretically 100% sodium oxalate according to stoichiometry, and precipitate and react for 2.0 hours at 90°C and a stirring speed of 400rpm, separate and obtain bismuth oxalate precipitate and filtrate; oxalic acid The bismuth precipitate was washed, dried and calcined at 700°C for 1.5 hours to obtain bismuth trioxide product.
[0046] C, step b gained filtrate, according to the content of lead in the solution, add the sodium chromate of theoretical quantity 110% by stoichiometry, precipitation reaction 0.5h under room temperature 400rpm stirring conditions, separation, washing obtain lead chromate ...
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