2009
DOI: 10.1021/es902164n
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Surface Complexation Modeling of U(VI) Adsorption by Aquifer Sediments from a Former Mill Tailings Site at Rifle, Colorado

Abstract: A study of U(VI) adsorption by aquifer sediment samples from a former uranium mill tailings site at Rifle, Colorado, was conducted under oxic conditions as a function of pH, U(VI), Ca, and dissolved carbonate concentration. Batch adsorption experiments were performed using <2 mm size sediment fractions, a sand-sized fraction, and artificial groundwater solutions prepared to simulate the field groundwater composition. To encompass the geochemical conditions of the alluvial aquifer at the site, the experimental … Show more

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Cited by 47 publications
(50 citation statements)
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References 25 publications
(56 reference statements)
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“…Calculation of U(VI) distributions between the sediment and aqueous phase were based on the equilibrium surface complexation model of Hyun et al (2009). A porosity of 27% in the aquifer was used to determine the ratio of groundwater to sediments.…”
Section: U(vi) Adsorption Calculations and Modelingmentioning
confidence: 99%
“…Calculation of U(VI) distributions between the sediment and aqueous phase were based on the equilibrium surface complexation model of Hyun et al (2009). A porosity of 27% in the aquifer was used to determine the ratio of groundwater to sediments.…”
Section: U(vi) Adsorption Calculations and Modelingmentioning
confidence: 99%
“…Although the reduced sediments may be a relatively small fraction of the total mass of the aquifer sediment, their ability to seasonally sequester and/or release U may affect the overall behavior of the contaminant in the aquifer . Estimates of sediment composition, mineralogy, and natural attenuation capacity are often based on representative aquifer sediment samples (e.g., Hyun et al, 2009), but the heterogeneity caused by naturally reduced zones may be an overlooked yet important component in understanding long-term U behavior.…”
Section: Introductionmentioning
confidence: 99%
“…The distribution coefficient is sometimes portrayed as a constant (Weber and DiGiano, 1996). However, in this system, as in others (e.g., Fox et al, 2006;Hyun et al, 2009), the distribution coefficient varied as a function of pH and concentration of the solute. At pH 7 and pH 9, the value of K d is essentially independent of the SSR.…”
Section: Methodsmentioning
confidence: 57%