2018
DOI: 10.1016/j.hydromet.2018.09.007
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Investigation of the kinetics and the morphology of cementation products formed during purification of a synthetic zinc sulfate electrolyte

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Cited by 26 publications
(8 citation statements)
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“…As shown in Fig. 1, it is found that the cementation Cu precipitate consists of fine particles, which shows a good agreement with conventional studies, 19,20) and it contains Cu as main component and Cu 2 O, which resulted from partly oxidized surface.…”
Section: Resultssupporting
confidence: 84%
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“…As shown in Fig. 1, it is found that the cementation Cu precipitate consists of fine particles, which shows a good agreement with conventional studies, 19,20) and it contains Cu as main component and Cu 2 O, which resulted from partly oxidized surface.…”
Section: Resultssupporting
confidence: 84%
“…It is almost impossible to detect Cu + ion during the leaching test because Cu + ions are extremely unstable in sulfuric acid solution. 11,16,18,19) Therefore, the effects of Cu 2+ and O 2 addition on the leaching of Cu were investigated experimentally as follows: Three conditions such as addition of O 2 with 10000 mg/L Cu 2+ , addition of N 2 with 10000 mg/L Cu 2+ , and addition of O 2 without 10000 mg/L Cu 2+ were tested for comparison. Figure 3 shows the leaching behavior of Cu in 1 mol/L sulfuric acid solution at 90°C and 600 rpm with 2% pulp density.…”
Section: Resultsmentioning
confidence: 99%
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“…Almost all the data published [ 2 , 3 , 4 , 5 , 6 ] showed that the activation energy of cobalt removal reaction was higher than 40 kJ/mol, so it must be a chemically controlled process rather than a diffusion-controlled one. The electrochemical reaction for cobalt removal occurs on the microcell surface and is driven by the potential difference between the microcell surface and the solution.…”
Section: Cobalt–hydrogen Electrochemical Competition Model For the Cobalt Removal Processmentioning
confidence: 99%
“…Exposed zinc on the microcell surface undergoes oxidation to become zinc ions while cobalt ions obtain electrons and are reduced to elemental cobalt accompanied by reduction of hydrogen ions to hydrogen molecules. Low pH conditions (pH = 3–5) are usually adopted for cobalt removal to avoid zinc ions from forming basic zinc sulfate, which would deactivate the zinc dust by absorbing it onto its surface [ 5 ]. However, hydrogen ions have greater reactivity than cobalt ions on the zinc surface thereby making high-concentration hydrogen ions compete with cobalt ions for electrons result in a significant drop in the removal rate of cobalt [ 6 ].…”
mentioning
confidence: 99%