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a Railroad Commission of Texas, Surface Mining and Reclamation Division, P.O. Box 12967 Austin, TX 78711-2967
b USDA-ARS, 808 East Blackland Road, Temple, TX 76502
c Department of Soil and Crop Sciences, MS 2474, Texas A&M University, College Station, TX 77843-2474
* Corresponding author (gn-white{at}tamu.edu)
Received for publication May 12, 2005. Siderite (FeCO3) is commonly found in coal overburden and, when present, can cause interference in the determination of neutralization potential (NP). Under acidic testing conditions, FeCO3 reacts to neutralize acid, which contributes to the NP. However, continued weathering of FeCO3 (oxidation of Fe2+ and hydrolysis of Fe3+) produces a neutral to slightly acidic solution. The effects of hydrogen peroxide (H2O2), potassium permanganate (KMnO4), and O2 on the laboratory measurement of NP of siderite samples taken from overburden were examined. All oxidation treatments lowered the NP values of the siderite samples as compared with the standard USEPA method. However, oxidation with H2O2 produced variable results depending on the amount of H2O2 added. Neutralization potential values obtained after oxidation treatments were highly correlated with Mn concentration. Reaction products (i.e., 2-line ferrihydrite) of siderite samples with H2O2 and KMnO4 were not representative of natural siderite weathering. Oxidation with O2 produced the lowest NP values for siderite samples. The reaction products produced by oxidation with O2 most closely represent those intermediate products formed when siderite is exposed to atmospheric weathering conditions. Oxidation with O2 also proved to be the most reproducible method for accurately assessing NP when siderite is present in overburden samples.
Abbreviations: AAS, atomic adsorption spectroscopy ABA, acidbase account AFM, acid-forming materials EA, exchangeable acidity GR1(CO3), green rust NP, neutralization potential PA, potential acidity XRD, X-ray diffraction analysis
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