Temporal geochemical variations in above- and below-drainage coal mine discharge. (November 2015)
- Record Type:
- Journal Article
- Title:
- Temporal geochemical variations in above- and below-drainage coal mine discharge. (November 2015)
- Main Title:
- Temporal geochemical variations in above- and below-drainage coal mine discharge
- Authors:
- Burrows, Jill E.
Peters, Stephen C.
Cravotta, Charles A. - Abstract:
- Highlights: Water quality has improved at below-drainage discharges. Above-drainage discharges exhibited less change in water quality. The Fe geochemistry in these CMDs is limited by oxygenation. Effective treatment design and priority may be anticipated based on drainage type. Abstract: Water quality data collected in 2012 for 10 above- and 14 below-drainage coal mine discharges (CMDs), classified by mining or excavation method, in the anthracite region of Pennsylvania, USA, are compared with data for 1975, 1991, and 1999 to evaluate long-term (37 year) changes in pH, SO4 2−, and Fe concentrations related to geochemistry, hydrology, and natural attenuation processes. We hypothesized that CMD quality will improve over time because of diminishing quantities of unweathered pyrite, decreased access of O2 to the subsurface after mine closure, decreased rates of acid production, and relatively constant influx of alkalinity from groundwater. Discharges from shafts, slopes, and boreholes, which are vertical or steeply sloping excavations, are classified as below-drainage; these receive groundwater inputs with low dissolved O2, resulting in limited pyrite oxidation, dilution, and gradual improvement of CMD water quality. In contrast, discharges from drifts and tunnels, which are nearly horizontal excavations into hillsides, are classified as above-drainage; these would exhibit less improvement in water quality over time because the rock surfaces continue to be exposed to air, whichHighlights: Water quality has improved at below-drainage discharges. Above-drainage discharges exhibited less change in water quality. The Fe geochemistry in these CMDs is limited by oxygenation. Effective treatment design and priority may be anticipated based on drainage type. Abstract: Water quality data collected in 2012 for 10 above- and 14 below-drainage coal mine discharges (CMDs), classified by mining or excavation method, in the anthracite region of Pennsylvania, USA, are compared with data for 1975, 1991, and 1999 to evaluate long-term (37 year) changes in pH, SO4 2−, and Fe concentrations related to geochemistry, hydrology, and natural attenuation processes. We hypothesized that CMD quality will improve over time because of diminishing quantities of unweathered pyrite, decreased access of O2 to the subsurface after mine closure, decreased rates of acid production, and relatively constant influx of alkalinity from groundwater. Discharges from shafts, slopes, and boreholes, which are vertical or steeply sloping excavations, are classified as below-drainage; these receive groundwater inputs with low dissolved O2, resulting in limited pyrite oxidation, dilution, and gradual improvement of CMD water quality. In contrast, discharges from drifts and tunnels, which are nearly horizontal excavations into hillsides, are classified as above-drainage; these would exhibit less improvement in water quality over time because the rock surfaces continue to be exposed to air, which facilitates sustained pyrite oxidation, acid production, and alkalinity consumption. Nonparametric Wilcoxon matched-pair signed rank tests between 1975 and 2012 samples indicate decreases in Fe and SO4 2− concentrations were highly significant ( p < 0.05) and increases in pH were marginally significant ( p < 0.1) for below-drainage discharges. For above-drainage discharges, changes in Fe and SO4 2− concentrations were not significant, and increases in pH were highly significant between 1975 and 2012. Although a greater proportion of above-drainage discharges were net acidic in 2012 compared to below-drainage discharges, the increase in pH between 1975 and 2012 was greater for above- (median pH increase from 4.4 to 6.0) compared to below- (median pH increase from 5.6 to 6.1) drainage discharges. For cases where O2 is limited, transformation of aqueous Fe II species to Fe III may be kinetically limited. In contrast, where O2 is abundant, aqueous Fe concentrations may be limited by Fe III mineral precipitation; thus, trends in Fe may not follow those for SO4 2− . In either case, when the supply of alkalinity is sufficient to buffer decreased acidity, the pH could increase by a step trend from strongly acidic (3–3.5) to near neutral (6–6.5) values. Modeled equilibrium with respect to Fe III precipitates varies with pH and Fe and SO4 2− reconcentrations: increasing pH promotes the formation of ferrihydrite, while decreasing concentrations of Fe limit the formation of ferrihydrite, and decreasing Fe and SO4 2− concentrations limit the precipitation of schwertmannite and favor formation of Fe III hydroxyl complexes and uncomplexed Fe 2+ and Fe 3+ . The analysis of the long-term geochemical changes in CMDs in the anthracite field and the effect of the hydrologic setting on water quality presented in this paper can help prioritize CMD remediation and facilitate selection and design of the most appropriate treatment systems. … (more)
- Is Part Of:
- Applied geochemistry. Volume 62(2015:Nov.)
- Journal:
- Applied geochemistry
- Issue:
- Volume 62(2015:Nov.)
- Issue Display:
- Volume 62 (2015)
- Year:
- 2015
- Volume:
- 62
- Issue Sort Value:
- 2015-0062-0000-0000
- Page Start:
- 84
- Page End:
- 95
- Publication Date:
- 2015-11
- Subjects:
- Environmental geochemistry -- Periodicals
Water chemistry -- Periodicals
Geochemistry -- Social aspects -- Periodicals
Geochemistry -- Periodicals
551.9 - Journal URLs:
- http://www.elsevier.com/journals ↗
- DOI:
- 10.1016/j.apgeochem.2015.02.010 ↗
- Languages:
- English
- ISSNs:
- 0883-2927
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1572.585000
British Library DSC - BLDSS-3PM
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