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UNDERSTANDING VARIATION IN PARTITION COEFFICIENT, Kd ...

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2- 2- -<br />

competing anions such as SO4 , and CO3 /HCO3 . The adsorption data developed by these<br />

investigators was used to calculate the <strong>Kd</strong> values (Appendix E). These <strong>Kd</strong> values were used as the<br />

basis to develop the look-up Table 5.7.<br />

5.4.6.2.1 Limits of K d Values with Respect to pH<br />

Natural soil pH typically ranges from about 4 to 11 (Richards, 1954). The 2 most common<br />

methods of measuring soil pH are either using a soil paste or a saturation extract. The standard<br />

procedure for obtaining saturation extracts from soils has been described by Rhoades (1996). The<br />

saturation extracts are obtained by saturating and equilibrating the soil with distilled water<br />

followed by collection using vacuum filtration. Saturation extracts are usually used to determine<br />

the pH, the electrical conductivity, and dissolved salts in soils.<br />

The narrow pH ranges in the look-up table (Table 5.7) were selected from the observed rate of<br />

change of K d with pH. The K d values for all 4 soils were observed to decline with increasing pH<br />

and at pH values beyond about 9, K d values for Cr(VI) are #1 ml/g (see Appendix E).<br />

5.4.6.2.2 Limits of K d Values with Respect to Extractable Iron Content<br />

The soil characterization data provided by Rai et al. (1988) indicate the soils with DCB<br />

extractable iron contents above ~0.3 mmol/g can reduce Cr(VI) to Cr(III). Therefore the<br />

measured K d values for such soils reflect both redox-mediated precipitation and adsorption<br />

phenomena. The data also show that soils with DCB extractable iron contents of about<br />

0.25 mmol/g or less do not appear to reduce Cr(VI). Therefore, 3 ranges of DCB extractable iron<br />

contents were selected which represent the categories of soils that definitely reduce ($0.3<br />

mmol/g), probably reduce (0.26 - 0.29 mmol/g), and do not reduce (#0.25 mmol/g) Cr(VI) to<br />

Cr(III) form.<br />

5.4.6.2.3 Limits of K d Values with Respect to Competing Anion Concentrations<br />

The adsorption data (Rai et al., 1988) show that when total sulfate concentration in solution is<br />

about 2 x 10 -3 M (191.5 mg/l), the chromium K d values are reduced by about an order of<br />

magnitude as compared to a noncompetitive condition. Therefore, a sulfate concentration of<br />

about 2 x 10 -3 M (191.5 mg/l) has been used as a limit at which an order of magnitude reduction<br />

in K d values are expected. Four ranges of soluble sulfate concentrations (0 - 1.9, 2 -18.9, 19 -<br />

189, and $190 mg/l) have been used to develop the look-up table. The soluble sulfate<br />

concentrations in soils can be assessed from saturation extracts (Richards, 1954).<br />

5.23

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