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

被引:302
作者
Grossl, PR
Eick, M
Sparks, DL
Goldberg, S
Ainsworth, CC
机构
[1] LOUISIANA STATE UNIV, CTR AGR, LOUISIANA AGR EXPT STN, DEPT AGRON, BATON ROUGE, LA 70803 USA
[2] UNIV DELAWARE, DEPT PLANT & SOIL SCI, NEWARK, DE 19717 USA
[3] USDA ARS, US SALIN LAB, RIVERSIDE, CA 92507 USA
[4] PACIFIC NW LAB, RICHLAND, WA 99352 USA
关键词
D O I
10.1021/es950654l
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
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 far 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 H2AsO4- or HCrO4- with OH ligands at the goethite surface forming an inner-sphere monodentate surface complex. The subsequent step, associated with the slow tau values, involved a second ligand exchange reaction, resulting in the formation of an inner-sphere bidentate surface complex. Overall, the results suggest that chromate may be the more mobile of the two oxyanions in soil systems.
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页码:321 / 326
页数:6
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