Trace metal(loid) mobility in waste deposits and soils around Chadak mining area, Uzbekistan
- 1. Institute of Geology and Geophysics, Academy of Sciences of Uzbekistan, Olimlar, 49, 100041 Tashkent (Uzbekistan)
- 2. Geosciences Institute, Johannes Gutenberg University, Mainz 55099 (Germany)
- 3. Department of Soil Sciences, Faculty of Sciences, University of Granada, Campus Fuentenueva s/n, 18002 Granada (Spain)
Description
Highlights: • Total concentrations of As and Sb strongly exceed the intervention values in abandoned wastes. • Selective extractions showed As and Sb with relatively high potential mobility. • Zn and Pb mobility was controlled by cation exchange capacity of clay particles. • Precipitation of Ca–Fe(III)–AsO4 phases was first observed in Chadak mine wastes. • Long-term pollution will be mainly controlled by tailing oxidations processes. The assessment of potential trace metal(loid) contamination in tailing dumps and soils was characterized in the Chadak mining area (Uzbekistan). Concentrations of trace elements (V, Cr, Co, Ni, Cu, Zn, As, Cd, Sb, Pb) were determined by X-ray fluorescence analysis and compared with background and intervention values (IV). The concentrations of As, Zn, Sb, and Pb were higher in the abandoned than in the active tailing dump, ranging from 42–1689 mg/kg for As, 73–332 mg/kg for Zn, 14–1507 mg/kg for Sb, and 27–386 mg/kg for Pb. Selective extractions were applied in order to assess the mobility and availability of trace metal(loid)s in samples. Oxyanion-forming elements such as As and Sb were immobilized by Fe oxides, although to some extent also extractable with acetic acid and soluble-in-water forms were detected, indicating potential bioavailability that can impose a potential toxicity risk for the environment. Selective extractions data also showed that Zn and Pb were relatively immobile, although in higher contamination sites significant amounts of these elements were also extractable with acetic acid. In tailing materials Zn and Pb mobility were negatively correlated by the cation-exchange capacity (CEC) and clay content, indicating the importance of these factors in the reduction of the potential toxicity for these elements. Total concentration of As, Sb, and Pb were also negatively correlated with soil pH, indicating that the oxidation process of sulphide tailings and thus the generation of acidic conditions may lead to release of contaminants over time. However, due to the calcium carbonate content, the acid neutralization capacity of the tailings is not yet exhausted and contaminant concentrations in soil-pore water are still relatively low. The results of our investigation suggest that environmental risk associated with these wastes in semi-arid climate is therefore not a short-term problem but rather requires constant monitoring and additional ecotoxicological studies.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2017.10.049Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2017.10.049;
- PII
- S0048969717327511;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 622
- Journal Page Range
- p. 1658-1667
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53011493
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- ACETIC ACID; ARSENATES; BIOLOGICAL AVAILABILITY; CATIONS; CLAYS; ECOLOGICAL CONCENTRATION; ION EXCHANGE; IRON OXIDES; MINERAL WASTES; OXIDATION; PH VALUE; POLLUTION; SOILS; TAILINGS; TOXICITY; TRACE AMOUNTS; UZBEKISTAN; WATER; X-RAY FLUORESCENCE ANALYSIS
- Descriptors DEC
- ARSENIC COMPOUNDS; ASIA; CARBOXYLIC ACIDS; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL ANALYSIS; CHEMICAL REACTIONS; HYDROGEN COMPOUNDS; IONS; IRON COMPOUNDS; MINERALS; MONOCARBOXYLIC ACIDS; NONDESTRUCTIVE ANALYSIS; ORGANIC ACIDS; ORGANIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; SILICATE MINERALS; SOLID WASTES; TRANSITION ELEMENT COMPOUNDS; WASTES; X-RAY EMISSION ANALYSIS
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier B.V. All rights reserved.