Effect of H2O2 and Ethylene Glycol on Molybdenite Dissolution in H2SO4 Solution

被引:3
|
作者
Bai, Yunlong [1 ,2 ]
Wang, Wei [1 ,2 ]
Xie, Feng [1 ,2 ]
Zhu, Huiping [1 ,2 ]
Lu, Diankun [1 ,2 ]
Jiang, Kaixi [3 ]
机构
[1] Northeastern Univ, Key Lab Ecol Met Multimetall Ores, Minist Educ, Shenyang 110819, Liaoning, Peoples R China
[2] Northeastern Univ, Sch Met, Shenyang 110819, Liaoning, Peoples R China
[3] Fuzhou Univ, Coll Zijin Min, Fuzhou 350108, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Molybdenite; H2O2; Ethylene glycol; Leaching; Kinetics; Electrochemistry; HYDROGEN-PEROXIDE; CATALYTIC DECOMPOSITION; CHALCOPYRITE; KINETICS; CONCENTRATE; OXIDATION; COPPER; MEDIA;
D O I
10.1007/s12666-022-02702-6
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
The leaching behavior of molybdenite was investigated in H2O2-H2SO4 solution in this paper. The results show that H2O2 was an effective oxidant for molybdenite leaching, but it had fast decomposition kinetics. A final molybdenum extraction of 73.0% was obtained under the experimental conditions of 0.5 mol/L H2SO4, 0.5 mol/L H2O2, and the fresh H2O2 addition enhanced molybdenum extraction from 73.0 to 94.5%. The leaching process was controlled by a mixture of surface reactions and diffusion, and the activation energy was 27.98 kJ/mol. Ethylene glycol enhanced molybdenum extraction and improved the stability of H2O2. Electrochemical studies suggested that the decomposition kinetics of H2O2 was faster than that of molybdenite oxidation, and ethylene glycol enhanced recovery by increasing the resistance of H2O2 decomposition and decreasing the resistance of molybdenite oxidation. XRD and XPS analysis confirmed that ethylene glycol did not alter the phase composition and the surface chemical statues of molybdenite.
引用
收藏
页码:39 / 47
页数:9
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