A kind of method utilizing bisphosphonic acid extractant to recover nickel from electroplating waste liquid
A technology for electroplating waste liquid and extraction agent, applied in the field of nickel recovery, can solve the problems of increasing the amount of post-extraction treatment, many times of extraction, and environmental pollution.
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Embodiment 1
[0025] (1) to contain Ni 2+ The electroplating waste solution is the water phase, and the Ni in the water phase 2+ The concentration is 0.7 g / L, and the pH of the aqueous phase is 4.
[0026] (2) Prepare 0.025mol / L HADMPPA and OADMPPA as the organic phase with diluent, dichloromethane, toluene, dichloroethane and chloroform respectively.
[0027] (3) Mix 5 mL each of the aqueous phase and the organic phase, extract for 10 min, and extract at 25 °C, and measure Ni in the raffinate 2+ See Table 1 for the concentration of the diluent on the extraction rate.
[0028] (4) Use 0.1mol / L dilute hydrochloric acid to carry out organic back-extraction after extraction. The back-extraction time is 20 minutes, the back-extraction temperature is 20°C, and the back-extraction rate is above 99%.
[0029] Table 1
[0030]
Embodiment 2
[0032] (1) to contain Ni 2+ The electroplating waste solution is the water phase, and the Ni in the water phase 2+ The concentration of the solution is 0.8 g / L, and the pH of the aqueous phase is 1.
[0033] (2) Using chloroform as the diluent, prepare 0.0565 mol / L HADMPPA as the organic phase.
[0034] (3) 10 mL of the aqueous phase and organic phase were mixed, the extraction time was 10 min, the extraction temperature was 15 °C, and the Ni in the raffinate was determined 2+ The concentration and extraction rate are shown in Table 2.
[0035] (4) Use 0.1mol / L dilute hydrochloric acid to reverse the organic extraction after extraction. The stripping time is 30 min, the stripping temperature is 30°C, and the stripping rate is over 99%.
Embodiment 3
[0037] (1) to contain Ni 2+ The electroplating waste solution is the water phase, and the Ni in the water phase 2+ The concentration of the solution is 0.8 g / L, and the pH of the aqueous phase is 1.
[0038] (2) Using chloroform as the diluent, prepare 0.0565 mol / L HADMPPA as the organic phase.
[0039] (3) 10 mL of the aqueous phase and organic phase were mixed, the extraction time was 10 min, the extraction temperature was 35 °C, and the Ni in the raffinate was determined 2+ The concentration and extraction rate are shown in Table 2.
[0040] (4) Use 0.1mol / L dilute hydrochloric acid to reverse the organic extraction after extraction. The stripping time is 30 min, the stripping temperature is 30°C, and the stripping rate is over 99%.
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