Combined DFT and XPS investigation of enhanced adsorption of sulfide species onto cerussite by surface modification with chloride

被引:131
作者
Feng, Qicheng [1 ]
Wen, Shuming [1 ]
Deng, Jiushuai [1 ]
Zhao, Wenjuan [2 ]
机构
[1] Kunming Univ Sci & Technol, Fac Land Resource Engn, State Key Lab Complex Nonferrous Met Resources Cl, Kunming 650093, Yunnan, Peoples R China
[2] Kunming Met Res Inst, Kunming 650031, Yunnan, Peoples R China
基金
中国博士后科学基金;
关键词
Cerussite; Chloride; Sulfide species; Sulfidization products; DFT; XPS; FLOTATION; LEAD; ZINC; SULFIDIZATION; CHALCOPYRITE; SEPARATION; XANTHATE; SULFUR; QUARTZ; ORE;
D O I
10.1016/j.apsusc.2017.07.017
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study systematically investigates the enhanced adsorption of sulfide species onto cerussite by surface modification with chloride through density functional theory calculations and X-ray photoelectron spectroscopy (XPS) measurements. Calculation results demonstrate obvious differences in the surface structures and electronic properties of cerussite after HS- adsorption in the absence and presence of chloride species. Surface modification with chloride promotes the stable adsorption of HS- onto the cerussite surface, and the hybridization of Pb 6p orbital at the surface layer and S 3p orbital from HS- is enhanced. Moreover, the reactivity of cerussite surfaces is enhanced by the occurrence of new DOS peaks of Pb 6p and S 3p near the Fermi level and by the transfer of additional electrons between the bonding atoms in the presence of chloride. Meanwhile, Mulliken population and XPS analysis results indicate that a slight oxidation is involved in the interaction between sulfide species and cerussite surfaces because of the presence of disulfide and polysulfide in the sulfidization products. In addition, a higher proportion of disulfide and polysulfide relative to the overall S is exhibited in the presence of chloride, facilitating the sulfidization flotation of cerussite. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:8 / 15
页数:8
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