An evaluation of copper remobilization from mine tailings in sulfidic environments

被引:8
|
作者
Simpson, SL
Apte, SC
Hortle, KG
Richards, DG
机构
[1] CSIRO, Div Energy Technol, Ctr Adv Analyt Chem, Bangor, NSW 2234, Australia
[2] PT Freeport Indonesia, Kuala Kencana, Irian Jaya, Indonesia
[3] Rio Tinto Hlth Safety & Environm, Bristol BS99 7YR, Avon, England
关键词
mine tailings; copper; remobilization; sulfide; polysulfides;
D O I
10.1016/S0375-6742(98)00061-2
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
A laboratory-based assessment of copper remobilization from Cu-rich mine tailings exposed to anoxic, sulfide rich waters was performed. The results from incubation experiments, conducted over a 20 day period, were compared to thermodynamic modelling calculations of copper speciation in sulfidic waters. The tailings materials were observed to react rapidly with added sulfide, consuming 159 mu mol HS- g(-1) (dry wt) within a 24 h period. The consumption of sulfide was attributed to a two stage process involving the reduction of Fe-hydroxy phases by sulfide followed by reaction with available Fe2+ and Cu2+ resulting in the formation Fe- and Cu-sulfide phases. During incubation experiments, the dissolved copper concentrations in the absence of sulfide were approximately 0.31. mu mol l(-1), whereas in the presence of sulfide (0.5-5 mM) concentrations were typically 0.24 mu mol l(-1). The experiments did not indicate enhanced solubility owing to the formation of soluble copper sulfide species. The predictions(based on the most recent thermodynamic data for aqueous Cu-sulfide and Cu-polysulfide species) did not accurately explain the laboratory observations. Model predictions were greatly influenced by the assumptions made about the oxidation state of copper under anoxic conditions' and the solid sulfide phase controlling copper solubility. The study emphasizes the limitations of modelling copper speciation in sulfidic waters and the need for laboratory or field verification of predictions. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:203 / 215
页数:13
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