Laboratory evaluation of zero-valent iron to treat water impacted by acid mine drainage

被引:159
作者
Wilkin, RT [1 ]
McNeil, MS [1 ]
机构
[1] US EPA, Robert S Kerr Environm Res Lab, Natl Risk Management Res Lab, Off Res & Dev, Ada, OK 74820 USA
关键词
zero-valent iron; groundwater remediation; permeable reactive barrier; acid mine drainage; PERMEABLE REACTIVE BARRIER; LONG-TERM PERFORMANCE; ZEROVALENT IRON; HEAVY-METALS; REMOVAL; KINETICS; IONS; GROUNDWATER; PYRITE;
D O I
10.1016/S0045-6535(03)00512-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study examines the applicability and limitations of granular zero-valent iron for the treatment of water impacted by mine wastes. Rates of acid-neutralization and of metal (Cu, Cd, Ni, Zn, Hg, Al, and Mn) and metalloid (As) uptake were determined in batch systems using simulated mine drainage (initial pH 2.3-4.5; total dissolved solids 14000-16000 mg l(-1)). Metal removal from solution and acid-neutralization occurred simultaneously and were most rapid during the initial 24 h of reaction. Reaction half-lives ranged from 1.50 +/- 0.09 h for Al to 8.15 +/- 0.36 h for Zn. Geochemical model results indicate that metal removal is most effective in solutions that are highly undersaturated with respect to pure-metal hydroxides suggesting that adsorption is the initial and most rapid metal uptake mechanism. Continued adsorption onto or co-precipitation with iron corrosion products are secondary metal uptake processes. Sulfate green rust was identified as the primary iron corrosion product, which is shown to be the result of elevated [SO42-]/[HCO3-] ratios in solution. Reversibility studies indicate that zero-valent iron will retain metals after shifts in redox states are imposed, but that remobilization of metals may occur after the acid-neutralization capacity of the material is exhausted. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:715 / 725
页数:11
相关论文
共 39 条
[1]  
Baes C.F., 1976, The Hydrolysis of Cations
[2]  
BARNES I, 1964, 473A GEOL SURV
[3]   Geochemistry of a permeable reactive barrier for metals and acid mine drainage [J].
Benner, SG ;
Blowes, DW ;
Gould, WD ;
Herbert, RB ;
Ptacek, CJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1999, 33 (16) :2793-2799
[4]   A full-scale porous reactive wall for prevention of acid mine drainage [J].
Benner, SG ;
Blowes, DW ;
Ptacek, CJ .
GROUND WATER MONITORING AND REMEDIATION, 1997, 17 (04) :99-107
[5]  
Bernal JD., 1959, Clay Minerals Bulletin, V4, P15
[6]  
Blowes D.W., 1994, Environmental chemistry of sulphide mine wastes, P271
[7]   Treatment of inorganic contaminants using permeable reactive barriers [J].
Blowes, DW ;
Ptacek, CJ ;
Benner, SG ;
McRae, CWT ;
Bennett, TA ;
Puls, RW .
JOURNAL OF CONTAMINANT HYDROLOGY, 2000, 45 (1-2) :123-137
[8]   Iron control by equilibria between hydroxy-Green Rusts and solutions in hydromorphic soils [J].
Bourrié, G ;
Trolard, F ;
Génin, JMR ;
Jaffrezic, A ;
Maître, V ;
Abdelmoula, M .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1999, 63 (19-20) :3417-3427
[9]   ZERO-VALENT IRON FOR THE IN-SITU REMEDIATION OF SELECTED METALS IN GROUNDWATER [J].
CANTRELL, KJ ;
KAPLAN, DI ;
WIETSMA, TW .
JOURNAL OF HAZARDOUS MATERIALS, 1995, 42 (02) :201-212
[10]   HYDROTALCITE-TYPE ANIONIC CLAYS: PREPARATION, PROPERTIES AND APPLICATIONS [J].
Cavani, F. ;
Trifiro, F. ;
Vaccari, A. .
CATALYSIS TODAY, 1991, 11 (02) :173-301