Title
The role of mineralogy on element mobility in two sulfide mine tailings from the Iberian Pyrite Belt (SW Spain)
Date Issued
08 May 2013
Access level
metadata only access
Resource Type
journal article
Author(s)
Pérez-López R.
Acero P.
Ayora C.
Nieto J.
University of Huelva
Abstract
A detailed study of two adjacent mine tailings impoundments comparing mineralogical and geochemical analyses of the solids with geochemical analysis of the pore-water and -gas was carried out in the Monte Romero sulfide mining district (Iberian Pyrite Belt, SW Spain). Since 1978, both facilities have been exposed to weathering in a semi-arid climate with dry-warm and wet-rainy seasons. In these impoundments, sulfide oxidation releases sulfate and contaminants to the pore-water that are transported and concentrated by evaporation in the top surface of the tailings, causing precipitation of soluble iron sulfate salts in dry seasons. These salts act as temporary sinks for minor elements such as Cd, Co, Zn, Ni, Cu and Mn, which are again released during rainfall events in wet seasons. Stored flotation tailings have an average pyrite content of 30. wt.% although average amounts up to 80% are present in the upper 50. cm of one of the impoundments. According to the results of the current study, this difference is key to control the oxidation model in both tailings. In the impoundment containing 30. wt.% of pyrite, pore-water pH increases in wet periods to 3.1 average by rainwater dilution, causing supersaturation and precipitation of secondary Fe(III) phases such as jarosite, goethite and schwertmannite. Consequently, this impoundment shows a 20-25. cm thick yellowish oxidation layer in the top part. In contrast, in the impoundment containing 80. wt.% of pyrite in the top part extremely acidic pore-waters (pH. <. 0.5) are present in both dry and wet seasons, and no precipitation of secondary Fe(III) phases occurs in the oxidation zone. The absence of secondary precipitates explains the apparent unweathered aspect of these tailings, in spite of its much higher remobilization of contaminants to the surface runoff or groundwaters. © 2013 Elsevier B.V.
Start page
119
End page
129
Volume
345
Language
English
OCDE Knowledge area
Geoquímica, Geofísica Geología
Scopus EID
2-s2.0-84877840872
Source
Chemical Geology
ISSN of the container
00092541
Sponsor(s)
This work was financed by the Spanish Ministry of Science and Innovation through the project METODICA (Ref. CGL2010-21956-C02 ). We greatly appreciate the analytical assistance of the technicians from the Research Services of the Institute IDÆA-CSIC in Barcelona and the University of Huelva. R. Pérez-López also thanks the Spanish Ministry of Science and Innovation and the ‘Ramón y Cajal Subprogramme’ ( MICINN-RYC 2011 ). P. Acero is financially supported by a research contract from the ‘Juan de la Cierva Subprogramme’ from the Spanish Ministry of Science and Innovation. We would also like to thank Dr. Jeremy Fein (co-Editor-in-Chief) and two anonymous reviewers for the support and comments that significantly improved the quality of the original paper.
Sources of information: Directorio de Producción Científica Scopus