Item talk:Q251203

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Revision as of 00:23, 21 August 2024 by Sky (talk | contribs) (Created page with "{ "USGS Publications Warehouse": { "@context": "https://schema.org", "@type": "Article", "additionalType": "Journal Article", "name": "Quantifying differences in the impact of variable chemistry on equilibrium uranium(VI) adsorption properties of aquifer sediments", "identifier": [ { "@type": "PropertyValue", "propertyID": "USGS Publications Warehouse IndexID", "value": "70005002", "url": "https://pubs.usgs.gov/...")
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 "USGS Publications Warehouse": {
   "@context": "https://schema.org",
   "@type": "Article",
   "additionalType": "Journal Article",
   "name": "Quantifying differences in the impact of variable chemistry on equilibrium uranium(VI) adsorption properties of aquifer sediments",
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       "value": "10.1021/es202677v",
       "url": "https://doi.org/10.1021/es202677v"
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   "journal": {
     "@type": "Periodical",
     "name": "Environmental Science & Technology",
     "volumeNumber": "45",
     "issueNumber": "20"
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   "inLanguage": "en",
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   "datePublished": "2011",
   "dateModified": "2020-01-11",
   "abstract": "Uranium adsorption-desorption on sediment samples collected from the Hanford 300-Area, Richland, WA varied extensively over a range of field-relevant chemical conditions, complicating assessment of possible differences in equilibrium adsorption properties. Adsorption equilibrium was achieved in 500-1000 h although dissolved uranium concentrations increased over thousands of hours owing to changes in aqueous chemical composition driven by sediment-water reactions. A nonelectrostatic surface complexation reaction, >SOH + UO22+ + 2CO32- = >SOUO2(CO3HCO3)2-, provided the best fit to experimental data for each sediment sample resulting in a range of conditional equilibrium constants (logKc) from 21.49 to 21.76. Potential differences in uranium adsorption properties could be assessed in plots based on the generalized mass-action expressions yielding linear trends displaced vertically by differences in logKc values. Using this approach, logKc values for seven sediment samples were not significantly different. However, a significant difference in adsorption properties between one sediment sample and the fines (<0.063 mm) of another could be demonstrated despite the fines requiring a different reaction stoichiometry. Estimates of logKc uncertainty were improved by capturing all data points within experimental errors. The mass-action expression plots demonstrate that applying models outside the range of conditions used in model calibration greatly increases potential errors.",
   "description": "8 p.",
   "publisher": {
     "@type": "Organization",
     "name": "ACS Publications"
   },
   "author": [
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       "@type": "Person",
       "name": "Kent, Douglas B. dbkent@usgs.gov",
       "givenName": "Douglas B.",
       "familyName": "Kent",
       "email": "dbkent@usgs.gov",
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           "@type": "Organization",
           "name": "WMA - Earth System Processes Division",
           "url": "https://www.usgs.gov/mission-areas/water-resources"
         }
       ]
     },
     {
       "@type": "Person",
       "name": "Stoliker, Deborah L. dlstoliker@usgs.gov",
       "givenName": "Deborah L.",
       "familyName": "Stoliker",
       "email": "dlstoliker@usgs.gov",
       "affiliation": [
         {
           "@type": "Organization",
           "name": "National Research Program - Western Branch",
           "url": "https://www.usgs.gov/centers/arizona-water-science-center"
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     },
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       "@type": "Person",
       "name": "Zachara, John M.",
       "givenName": "John M.",
       "familyName": "Zachara"
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   "funder": [
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       "@type": "Organization",
       "name": "Branch of Regional Research-Western Region",
       "url": "https://www.usgs.gov/mission-areas/water-resources"
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       "@type": "Organization",
       "name": "Toxic Substances Hydrology Program",
       "url": null
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   "archivedAt": "http://dx.doi.org/10.1021/es202677v",
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       "name": "Washington"
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       "name": "Benton County"
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