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Solution ion effects on the surface exchange of selenite on calcite

Journal Article · · Geochimica et Cosmochimica Acta; (USA)
; ;  [1]
  1. Battelle Pacific Northwest Laboratories, Richland, WA (USA)

The adsorption of SeO{sub 3} on CaCO{sub 3}(s) was evaluated in equilibrium CaCO{sub 3}(aq) suspensions over a range in pH and SeO{sub 3} concentration in the absence and presence of the cosolutes, Mg, SO{sub 4}, and PO{sub 4}. Selenite was adsorbed by CaCO{sub 3}(s) in a manner consistent with its exchange on anionic specific surface sites saturated with CO{sup 2{minus}}{sub 3}/HCO{sup {minus}}{sub 3} that were quantified by H{sup 14}CO{sub 3} isotopic exchange. This exchange process was described very well using the computer program FITEQL and half-reactions for the surface exchange of HCO{sup {minus}}{sub 3}, CO{sup 2{minus}}{sub 3}, HSeO{sup {minus}}{sub 3}. The cosolutes SO{sub 4} and PO{sub 4} decreased SeO{sub 3} sorption by direct competition or site blockage, and these effects were also predicted using the surface exchange model. By contrast, the sorption of SeO{sub 3} was not influenced by Mg because the two ions sorbed over different pH regions and exchanged with different surface sites that appeared to be distinct and noninteractive. Evaluation of SeO{sub 3} sorption over a wide concentration range suggested that the surface of CaCO{sub 3}(s) was heterogeneous and that SeO{sub 3} had access to less than 5% of the total anion specific surface sites.

OSTI ID:
6142461
Journal Information:
Geochimica et Cosmochimica Acta; (USA), Journal Name: Geochimica et Cosmochimica Acta; (USA) Vol. 54:8; ISSN GCACA; ISSN 0016-7037
Country of Publication:
United States
Language:
English