The Role of Silica in the Chlorination-Volatilization of Cobalt Oxide by Using Calcium Chloride

被引:1
|
作者
Han, Peiwei [1 ,2 ]
Li, Zhengchen [1 ,2 ]
Liu, Xiang [1 ,2 ]
Yan, Jingmin [1 ,2 ]
Ye, Shufeng [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Innovat Acad Green Manufacture, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
chlorination-volatilization; cobalt oxide; calcium chloride; phases of calcines; SPENT HYDROREFINING CATALYSTS; RICH PYRITE CINDER; SELECTIVE CHLORINATION; NICKEL; EXTRACTION; RECOVERY; COPPER; KINETICS; REMOVAL;
D O I
10.3390/met11122036
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The role of silica in the chlorination-volatilization of cobalt oxide, using calcium chloride, is investigated in this paper. It is found that the Co volatilization percentage of the CoO-Fe2O3-CaCl2 system is not larger than 12.1%. Silica plays an important role in the chlorination-volatilization of cobalt oxide by using calcium chloride. In the CoO-SiO2-Fe2O3-CaCl2 system, the Co volatilization percentage is initially positively related to the molar ratio of SiO2 to CaCl2, and remains almost constant when the molar ratio of SiO2 to CaCl2 rises from zero to eight. The critical molar ratios of SiO2 to CaCl2 are 1 and 2 when the molar ratios of CaCl2 to CoO are 8.3 and 16.6, respectively. The Co volatilization percentage remains almost constant with the increase in CaO concentration, and decreases when Al2O3 and MgO are added. Ca2SiO3Cl2 is determined after roasting at 1073 K and 1173 K, and disappears at temperatures in excess of 1273 K in the calcines from the CoO-SiO2-CaCl2 system. CaSiO3 always exists in the calcines at temperatures in excess of 973 K.
引用
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页数:10
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