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Published in J Environ Qual 18:479-482 (1989)
© 1989 American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
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Self-Diffusion of Selenate and Selenite in Overburden

J. S. Ahlrichs*

Cenex/Land O'Lakes, P.O. Box 64089, St. Paul, MN 55164;

L. R. Hossner

Dep. of Soil and Crop Sciences, Texas A&M Univ., College Station, TX 77843.

* Corresponding author.

ABSTRACT

Self-diffusion coefficients (D) for selenate (SeO2–4) and selenite (HSeO3) were evaluated as a function of overburden pH (2, 3, 5, 7, 9) and volumetric water content ({Theta}v = 0.22, 0.28, 0.34). Selenate self-diffusion coefficients were least (D = 0.23 x 10–6 cm2 s–1 in overburden adjusted to pH 3 and {Theta}v = 0.22 and greatest (D = 1.8 x 10–6 cm2 s–1 and 1.7 x 10–6 cm2 s–1) in overburden adjusted to pH 9 and {Theta}v = 0.28 and 0.34. Self-diffusion coefficients for HSeO3 were 2 to 3 orders of magnitude slower than for SeO2–4. The most rapid HSeO3 diffusion was observed at pH 2 and {Theta}v = 0.34 (D = 53.2 x 10–9 cm2 s–1). The slowest was at pH 3 and {Theta}v = 0.22 (D = 0.2 x 10–9 cm2 s–1). For both SeO2–4 and HSeO3 the self-diffusion coefficients increased with increasing water content and were related to adsorption characteristics of the soil and the Se species present at each soil pH.


Received for publication March 7, 1988.


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S. Deore, F. Xu, and A. Navrotsky
Oxide-melt solution calorimetry of selenides: Enthalpy of formation of zinc, cadmium, and lead selenide
American Mineralogist, May 1, 2008; 93(5-6): 779 - 783.
[Abstract] [Full Text] [PDF]




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