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Published online 9 August 2006
Published in J Environ Qual 35:1731-1741 (2006)
DOI: 10.2134/jeq2005.0123
© 2006 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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Physicochemical and Mineralogical Characterization of Soil–Saprolite Cores from a Field Research Site, Tennessee

Ji-Won Moona, Yul Rohb,*, Tommy J. Phelpsa, Debra H. Phillipsc, David B. Watsona, Young-Jin Kima and Scott C. Brooksa

a Environmental Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831
b Faculty of Earth System and Environmental Sciences, Chonnam National University, 300 Yongbong-Dong, Buk-Gu, Gwangju, 500-757, Korea
c Environmental Engineering Research Centre, School of Architecture, Civil and Environmental Engineering, and Planning, Queen's University of Belfast, Belfast BT9 5AG, Northern Ireland, UK


Figure 1
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Fig. 1. Site map of NABIR FRC Site 2 and monitoring wells.

 

Figure 2
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Fig. 2. Variation of field measured radioactivity with soil–saprolite pH (mixture with deionized water, 1:1 w/w) and effective cation exchange capacities such as ECEC (Na + K + Mg + Ca + Al) and ECECw/o Ca and (Na + K + Mg + Al).

 

Figure 3
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Fig. 3. (a) Variation of radionuclide, (b) metal, and (c and d) major element concentration levels, which were extracted by oxalate, CBD, and 2 M HNO3 solution.

 

Figure 4
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Fig. 4. The averaged ratio of the concentrations of oxalate-extraction to that of CBD-extraction with maximum and minimum values. The unity (dashed line) means that the oxalate- and CBD-extractable concentrations were similar. The minimum value contacting x axis occurred due to the value of BDL and the data of two orders magnitude were excluded.

 

Figure 5
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Fig. 5. Composite pH–Eh stability diagram for Fe (total dissolved Fe, 4.59 x 10–5 M) and Mn (total dissolved Mn, 1.89 x 10–4 M)–water systems at 25°C. Square symbols denote conditions of pH and Eh at Area 2, FRC site.

 

Figure 6
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Fig. 6. The DXRD patterns of representative bulk samples of (a) 418 cm from the reclaimed soil zone and (b) 778 cm from the saprolite zone. A, anorthite; C, calcite; D, dolomite; Fd, feldspar; Fr, ferrihydrite; G, goethite; H, hydroxy interlayered vermiculite; I, illite; K, kaolinite; M, microcline; Q, quartz; V, vermiculite; *, dioctahedral reflection (0, 2, 11).

 

Figure 7
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Fig. 7. (a) Variation of relative contents of mineral constituents, (b) comparison XRD semiquantification with chemical analysis using XRF.

 

Figure 8
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Fig. 8. Scanning electron microphotograph and XRD pattern of (a and c) Ca-leaching holes of columnar habits of anorthite and (b and d) clay minerals filling crack of saprolite.

 





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