TY - JOUR
T1 - Schwertmannite and Fe oxides formed by biological low-pH Fe(II) oxidation versus abiotic neutralization
T2 - Impact on trace metal sequestration
AU - Burgos, William D.
AU - Borch, Thomas
AU - Troyer, Lyndsay D.
AU - Luan, Fubo
AU - Larson, Lance N.
AU - Brown, Juliana F.
AU - Lambson, Janna
AU - Shimizu, Masayuki
N1 - Funding Information:
This work was supported by the National Science Foundation (NSF) under Grant No. CHE-0431328 , by the Pennsylvania Department of Environmental Protection, Bureau of Abandoned Mine Reclamation , by the Office of Surface Mining under Cooperative Agreement S11AC20005, and by an NSF CAREER Award ( EAR 0847683 ) to Thomas Borch. Janna Lambson was supported by NSF EAR 0525503 (REU Supplement) to Jenn L. Macalady. Portions of this research were carried out at the Stanford Synchrotron Radiation Lightsource (SSRL), a national user facility operated by Stanford University on behalf of the U.S. Department of Energy, Office of Basic Energy Sciences. We thank Brent Means from the US Office of Surface Mining, and Malcolm Crittenden from the Pennsylvania Department of Environmental Protection for directing us to the Lower Red Eyes site. We thank the associate editor and three anonymous reviewers for the helpful suggestions to improve this work.
PY - 2012/1/15
Y1 - 2012/1/15
N2 - Three low-pH coal mine drainage (CMD) sites in central Pennsylvania were studied to determine similarities in sediment composition, mineralogy, and morphology. Water from one site was used in discontinuous titration/neutralization experiments to produce Fe(III) minerals by abiotic oxidative hydrolysis for comparison with the field precipitates that were produced by biological low-pH Fe(II) oxidation. Even though the hydrology and concentration of dissolved metals of the CMD varied considerably between the three field sites, the mineralogy of the three iron mounds was very similar. Schwertmannite was the predominant mineral precipitated at low-pH (2.5-4.0) along with lesser amounts of goethite. Trace metals such as Zn, Ni and Co were only detected at lmol/g concentrations in the field sediments, and no metals (other than Fe) were removed from the CMD at any of the field sites. Metal cations were not lost from solution in the field because of unfavorable electrostatic attraction to the iron mound minerals. Ferrihydrite was the predominant mineral formed by abiotic neutralization (pH 4.4-8.4, 4 d aging) with lesser amounts of schwertmannite and goethite. In contrast to low-pH precipitation, substantial metal removal occurred in the neutralized CMD. Al was likely removed as hydrobasaluminite and Al(OH)3, and as a co-precipitate into schwertmannite or ferrihydrite. Zn, Ni and Co were likely removed via adsorption onto and co-precipitation into the freshly formed Fe and Al solids. Mn was likely removed by co-precipitation and, at the highest final pH values, as a Mn oxide. Biological low-pH Fe(II) oxidation can be cost-effectively used to pretreat CMD and remove Fe and acidity prior to conventional neutralization techniques. A further benefit is that solids formed under these conditions may be of industrial value because they do not contain trace metal or metalloid contaminants.
AB - Three low-pH coal mine drainage (CMD) sites in central Pennsylvania were studied to determine similarities in sediment composition, mineralogy, and morphology. Water from one site was used in discontinuous titration/neutralization experiments to produce Fe(III) minerals by abiotic oxidative hydrolysis for comparison with the field precipitates that were produced by biological low-pH Fe(II) oxidation. Even though the hydrology and concentration of dissolved metals of the CMD varied considerably between the three field sites, the mineralogy of the three iron mounds was very similar. Schwertmannite was the predominant mineral precipitated at low-pH (2.5-4.0) along with lesser amounts of goethite. Trace metals such as Zn, Ni and Co were only detected at lmol/g concentrations in the field sediments, and no metals (other than Fe) were removed from the CMD at any of the field sites. Metal cations were not lost from solution in the field because of unfavorable electrostatic attraction to the iron mound minerals. Ferrihydrite was the predominant mineral formed by abiotic neutralization (pH 4.4-8.4, 4 d aging) with lesser amounts of schwertmannite and goethite. In contrast to low-pH precipitation, substantial metal removal occurred in the neutralized CMD. Al was likely removed as hydrobasaluminite and Al(OH)3, and as a co-precipitate into schwertmannite or ferrihydrite. Zn, Ni and Co were likely removed via adsorption onto and co-precipitation into the freshly formed Fe and Al solids. Mn was likely removed by co-precipitation and, at the highest final pH values, as a Mn oxide. Biological low-pH Fe(II) oxidation can be cost-effectively used to pretreat CMD and remove Fe and acidity prior to conventional neutralization techniques. A further benefit is that solids formed under these conditions may be of industrial value because they do not contain trace metal or metalloid contaminants.
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U2 - 10.1016/j.gca.2011.10.015
DO - 10.1016/j.gca.2011.10.015
M3 - Article
AN - SCOPUS:84855889676
SN - 0016-7037
VL - 76
SP - 29
EP - 44
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
ER -