2021
DOI: 10.1016/j.chemgeo.2021.120229
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Chemical oxidation of selenite to selenate: Evaluation of reactive oxygen species and O transfer pathways

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Cited by 9 publications
(3 citation statements)
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“…Sharmasarkar and Vance (1995) found Se strongly correlated with clay fractions in Powder River Basin overburden formations. Selenium salts readily dissolve, but the dissolution of Se salts may not contribute substantial soluble Se species (e.g., HSeO3 -or SeO4 2-) if selenite is produced given its preference to readily sorb to sediments (Elrashidi et al 1987;Torres et al 2011;Paydary et al 2021). For the weathering of Powder River Basin waste rock, Se can be modeled as the dissolution of Se-containing gypsum [CaSO4].…”
Section: Arsenic and Selenium Sourcesmentioning
confidence: 99%
“…Sharmasarkar and Vance (1995) found Se strongly correlated with clay fractions in Powder River Basin overburden formations. Selenium salts readily dissolve, but the dissolution of Se salts may not contribute substantial soluble Se species (e.g., HSeO3 -or SeO4 2-) if selenite is produced given its preference to readily sorb to sediments (Elrashidi et al 1987;Torres et al 2011;Paydary et al 2021). For the weathering of Powder River Basin waste rock, Se can be modeled as the dissolution of Se-containing gypsum [CaSO4].…”
Section: Arsenic and Selenium Sourcesmentioning
confidence: 99%
“…Such processes are partially responsible for the significant presence of gypsum in Powder River Basin sedimentary formations [59][60][61][62][63]. Se-bearing salts can readily dissolve, but the dissolution of the salts may not contribute substantial soluble Se species (e.g., selenate (SeO 4 2− )) if selenite is produced because of the preference of selenite to readily sorb to sediments [64][65][66]. The Se released into the leachate appears to be primarily particle release (early and large concentrations) with a contribution from Se salt dissolution that is more visible in the second week when the warm-room leachate indicated higher concentrations of Se.…”
Section: Weathering Processes and Solute Trendsmentioning
confidence: 99%
“…The large, early concentrations for Ca and K suggest the release of Ca-and K-bearing nanoparticles [19], desorption (exchangeable ions) from larger particles [79], and/or loss from roughened surfaces [80], followed by a typical slow release of these elements with bulk aluminosilicate weathering [81,82]. Warm-room leachate shows higher initial concentrations than coldroom leachate for both Ca and K, which is the result of temperature and pH controls on desorption and mineral degradation [62][63][64][65][66][67].…”
Section: Bulk Solid Weatheringmentioning
confidence: 99%