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Arsenate and chromate retention mechanisms on goethite. 2. Kinetic evaluation using a pressure-jump relaxation technique

Journal Article · · Environmental Science and Technology
DOI:https://doi.org/10.1021/es950654l· OSTI ID:460035
 [1];  [2];  [3];  [4];  [5]
  1. Utah State Univ., Logan, UT (United States)
  2. Louisiana State Univ., Baton Rouge, LA (United States)
  3. Univ. of Delaware, Newark, DE (United States)
  4. Salinity Lab., Riverside, CA (United States)
  5. Pacific Northwest Lab., Richland, WA (United States)
The kinetics of arsenate and chromate adsorption/desorption on goethite ({alpha}-FeOOH) were investigated using a pressure-jump (p-jump) relaxation technique. Information provided by this technique was used to elucidate the fate of arsenate and chromate in natural environments. Chemical relaxations resulting from rapidly induced pressure changes were monitored via conductivity detection. The adsorption/desorption of these oxyanions on goethite involved a double relaxation event. The proposed mechanism for the adsorption of arsenate and chromate on goethite is a two-step process resulting in the formation of an inner-sphere bidentate surface complex. The first step, associated with the fast {tau} values, involved an initial ligand exchange reaction of aqueous oxyanion species H{sub 2}AsO{sub 4}{sup -} or HCrO{sub 4}{sup -} with OH ligands at the goethite surface forming an inner-sphere monodentate surface complex. The subsequent step, associates with the slow {tau} values, involved a second ligand exchange reaction, resulting in the formation of a inner-sphere bidentate surface complex. Overall, the results suggest that chromate may be the more mobile of the two oxyanions in soil systems. 23 refs., 10 figs., 2 tabs.
OSTI ID:
460035
Journal Information:
Environmental Science and Technology, Journal Name: Environmental Science and Technology Journal Issue: 2 Vol. 31; ISSN ESTHAG; ISSN 0013-936X
Country of Publication:
United States
Language:
English

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