Chemical Fractionation and Contamination Intensity of Trace Elements in Stream Sediments at the Sarcheshmeh Porphyry Copper Mine, SE Iran

This paper presents chemical fractionation and contamination intensities of trace elements in stream sediments at the Sarcheshmeh mine, southeastern Iran, which is one of the world’s largest Oligo-Miocene porphyry copper deposits. Evaluation of environmental pollution indices and maximum probable ba...

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Veröffentlicht in:Mine water and the environment 2012-09, Vol.31 (3), p.199-213
Hauptverfasser: Khorasanipour, Mehdi, Tangestani, Majid H., Naseh, Reza, Hajmohammadi, Hamid
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Sprache:eng
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Zusammenfassung:This paper presents chemical fractionation and contamination intensities of trace elements in stream sediments at the Sarcheshmeh mine, southeastern Iran, which is one of the world’s largest Oligo-Miocene porphyry copper deposits. Evaluation of environmental pollution indices and maximum probable background concentrations revealed that As, Cu, Cd, Mo, Pb, Sb, Se, S, and Zn are highly concentrated in the contaminated sediments, while Cr, Co, Ni, Fe, and Mn show lower enrichment values. Discharges of industrial effluents (especially those contaminated by tailings), reject waste from the semi-autogenous mill, and rock waste drainages are the main anthropogenic contaminant sources. High values of As, Cu, Fe, Mo, Pb, and Zn were associated with the oxidizable, primary sulfide, and residual sediment fractions. Relatively high percentages of Co (>92 %), Cr (>58 %), Cu (>79 %), Fe (>40 %), Mn (>97 %), Ni (>87 %), and Zn (>83 %) in the sediments associated with the rock waste drainages were readily released during the extraction of water-soluble, exchangeable, and carbonate fractions. Sediments that received reject waste drainages were also polluted by As (>351.7 mg kg −1 ), Cu (>1.58 %), Mo (>91.8 mg kg −1 ), Pb (>291.8 mg kg −1 ), and Zn (>762.4 mg kg −1 ). A large percentage of these contaminants were found to be adsorbed and co-precipitated with amorphous Fe-oxides and carbonate phases. The chemical fractionation pattern of the potentially hazardous trace elements corresponded well with the mineralogical composition of the contaminated sediments.
ISSN:1025-9112
1616-1068
DOI:10.1007/s10230-012-0198-0