Antimony distribution and environmental mobility at an historic antimony smelter site, New Zealand

被引:173
|
作者
Wilson, NJ [1 ]
Craw, D [1 ]
Hunter, K [1 ]
机构
[1] Univ Otago, Chem & Geol Dept, Dunedin, New Zealand
关键词
antimony; arsenic; oxidation; adsorption; stibnite; arsenopyrite; senarmontite; metalloids; mining;
D O I
10.1016/j.envpol.2003.10.014
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A historic antimony smelter site at Endeavour Inlet, New Zealand has smelter residues with up to 17 wt.% antimony. Residues include coarse tailings (cm scale particles, poorly sorted), sand tailings (well sorted) and smelter slag (blocks up to 30 cm across). All of this material has oxidised to some degree over the ca. 100 years since the site was abandoned. Oxidation has resulted in acidification of the residues down to pH 2-5. Smelter slag contains pyrrhotite (FeS) and metallic antimony, and oxidation is restricted to surfaces only. The coarse tailings are the most oxidised, and few sulfide grains persist. Unoxidised sand tailings contain 10-20 vol.% stibnite (Sb2S3) containing up to 5% As, with subordinate arsenopyrite (FeAsS), and minor pyrite (FeS2). The sand tailings are variably oxidised on a scale of 2-10 cm, but original depositional layering is preserved during oxidation and formation of senarmontite (Sb2O3). Oxidation of sand tailings has resulted in localised mobility of both Sb and As on the cm scale, resulting in redistribution of these metalloids with iron oxyhydroxide around sand grain boundaries. Experiments demonstrate that Sb mobility decreases with time on a scale of days. Attenuation of both As and Sb occurs due to adsorption on to iron oxyhydroxides which are formed during oxidation of the smelter residues. There is no detectable loss of Sb or As from the smelter site into the adjacent river, <50 in away, which has elevated Sb (ca. 20 mug/l) and As (ca. 7 mug/l) from mineralised rocks upstream. Despite the high concentrations of Sb and As in the smelter residues, these metalloids are not being released into the environment. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:257 / 266
页数:10
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