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Sorption of cesium and iodide ions onto KENTEX-bentonite

By: Contributor(s): Material type: TextTextSeries: Environmental earth sciences ; Volume , number ,Verlag Springer 2013Content type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
Subject(s): Online resources: Summary: The sorption of cesium and iodide ions onto KENTEX-bentonite was investigated using batch test and in-diffusion test methods. The cesium ions were highly sorbed on the bentonite, and the experimental data fit the Freundlich isotherm well. The distribution coefficient, K d, of the cesium ions was variably affected by the chemical conditions of the solution (initial ion concentration, pH, salinity) and temperature. An increasing pH of solution increased the K d. However, there were different K d values that decrease with an increase in the initial ion concentration, salinity, and temperature. The iodide ions, on the contrary, were negligibly sorptive. The K d values obtained from the in-diffusion tests were quite lower than those from the batch tests, which could be explained by changes in the pore water chemistry and surface area available for sorption.
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Journal Article Journal Article Main Library - Special Collections GE105 ENV (Browse shelf(Opens below)) Vol.70 , No.5 (Nov 2013) Not for loan For In House Use Only

The sorption of cesium and iodide ions onto KENTEX-bentonite was investigated using batch test and in-diffusion test methods. The cesium ions were highly sorbed on the bentonite, and the experimental data fit the Freundlich isotherm well. The distribution coefficient, K d, of the cesium ions was variably affected by the chemical conditions of the solution (initial ion concentration, pH, salinity) and temperature. An increasing pH of solution increased the K d. However, there were different K d values that decrease with an increase in the initial ion concentration, salinity, and temperature. The iodide ions, on the contrary, were negligibly sorptive. The K d values obtained from the in-diffusion tests were quite lower than those from the batch tests, which could be explained by changes in the pore water chemistry and surface area available for sorption.

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