Mechanisms of arsenic and lead release from hydrothermally altered rock

被引:106
作者
Tabelin, C. B. [1 ]
Igarashi, T. [1 ]
机构
[1] Hokkaido Univ, Grad Sch Engn, Div Field Engn Environm, Kita Ku, Sapporo, Hokkaido 0608628, Japan
关键词
Arsenic; Lead; Leaching; pH; Redox condition; PYRITE OXIDATION; DISSOLUTION; SPECIATION; KINETICS; SEDIMENTS; BEHAVIOR; METALS;
D O I
10.1016/j.jhazmat.2009.04.049
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This paper describes the effects of pH, dissolved oxygen (DO), redox conditions, and mixing ratio of different rocks on the leaching behaviors of As and Pb from hydrothermally altered rock as well as the functional groups incorporating As and Pb in the rock. Most of As and Pb were incorporated in the residual or crystalline phase although significant amounts were also determined to be exchangeable, with carbonates and with Fe-Mn oxides. Under oxic conditions,As and Pb showed similar leaching behaviors at similar pH values, a higher mobilization in the acidic and alkaline regions and a minimum at circumneutral pH. The absence of DO restricted the oxidation of sulfide minerals that also contained significant quantities of As resulting in a lower As release under these conditions. Strongly reducing conditions favored the release of As by the reductive dissolution of Fe-Mn oxides and prevention of carbonate precipitation while the same conditions immobilized Pb because of its re-precipitation under reducing conditions. In general, depending on the pH, DO, and redox conditions, the major modes of As and Pb release from these sources could be either one or more of the following mechanisms: acid dissolution, reductive dissolution, ion exchange, desorption and sulfide oxidation processes. (c) 2009 Elsevier B.V. Ail rights reserved.
引用
收藏
页码:980 / 990
页数:11
相关论文
共 34 条
[1]   Arsenic release from iron rich mineral processing waste: Influence of pH and redox potential [J].
Al-Abed, Souhail R. ;
Jegadeesan, G. ;
Purandare, J. ;
Allen, D. .
CHEMOSPHERE, 2007, 66 (04) :775-782
[2]  
Appelo CAJ, 2004, GEOCHEMISTRY GROUNDW, DOI DOI 10.1201/9781
[3]   THE ROLE OF OXALATE IN ACCELERATING THE REDUCTIVE DISSOLUTION OF HEMATITE (ALPHA-FE2O3) BY ASCORBATE [J].
BANWART, S ;
DAVIES, S ;
STUMM, W .
COLLOIDS AND SURFACES, 1989, 39 (04) :303-309
[4]   FIXATION, TRANSFORMATION, AND MOBILIZATION OF ARSENIC IN SEDIMENTS [J].
BRANNON, JM ;
PATRICK, WH .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1987, 21 (05) :450-459
[5]   The role of pyrite in controlling metal ion activities in highly reduced soils [J].
Brennan, EW ;
Lindsay, WL .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1996, 60 (19) :3609-3618
[6]   Geochemical cycling of redox-sensitive metals in sediments from Lake Malawi: A diagnostic paleotracer for episodic changes in mixing depth [J].
Brown, ET ;
Le Callonnec, L ;
German, CR .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2000, 64 (20) :3515-3523
[7]   Pyrite oxidation in alkaline solutions: nature of the product layer [J].
Caldeira, CL ;
Ciminelli, VST ;
Dias, A ;
Osseo-Asare, K .
INTERNATIONAL JOURNAL OF MINERAL PROCESSING, 2003, 72 (1-4) :373-386
[8]   Rhenium and molybdenum enrichments in sediments as indicators of oxic, suboxic and sulfidic conditions of deposition [J].
Crusius, J ;
Calvert, S ;
Pedersen, T ;
Sage, D .
EARTH AND PLANETARY SCIENCE LETTERS, 1996, 145 (1-4) :65-78
[9]   Potential role of bicarbonate during pyrite oxidation [J].
Evangelou, VP ;
Seta, AK ;
Holt, A .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (14) :2084-2091
[10]  
Evangelou VP., 1995, Pyrite Oxidation and its Control