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Published in Soil Sci Soc Am J 48:1034-1039 (1984)
© 1984 Soil Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
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Specific Adsorption of Copper on an Hydroxy-Aluminum-Montmorillonite Complex1

J. B. Harsh and H. E. Doner2

ABSTRACT

The adsorption of Na on a prepared hydroxy-aluminum-montmorillonite complex (OH-Al-SWy-l) was investigated as a function of pH, time, and Cu concentration ([Cu]). It was found that Na adsorption from 0.01M NaClO4 increased with pH from 0.015 mol kg–1 at pH 4.5 to 0.33 mol (Na+) kg–1 clay at pH 6.6 Adsorption of 0.16 mol (1/2 Cu2+) kg–1 clay did not affect the amount of Na adsorption, showing that specific sites existed for Cu. Adsorption of Cu was found to increase with pH and both adsorption and resistance to extraction with 0.25M Ba(NO3)2 increased with time. At pH 4.6, Cu adsorption approached a maximum near 0.3 mol (1/2 Cu2+) kg–1 clay of which 0.13 mol (1/2 Cu2+) were extracted with Ba(NO3)2. Electron spin resonance (ESR) of the Cu on OH-Al-SWy-l showed that both physi- and chemisorbed Cu were present and that solubilization as Cu(NH3)2+4 through exposure to NH3 vapor overnight was possible only if the sample had been previously treated with BaCl2. It was concluded that the OH-Al-SWy-l system provided a much more reactive surface toward Cu adsorption than either montmorillonite or hydrous aluminum oxides. In comparison to smectites Cu was less labile to Ba extraction due, in part, to chemisorption by Al-OH groups. Relative to values reported for Al(OH)3 polymorphs, Alx(OH)y3x-y precipitated in the presence of montmorillonite adsorbed more Cu on a mass basis presumably due to a higher surface to mass ratio.


NOTES

1 Contribution from the Dep. of Plant & Soil Biology, Univ. of California, Berkeley, CA 94720.

2 Former Graduate Student, now Assistant Professor, Dep. of Agronomy and Soils, Washington State Univ., Pullman, WA 99164, and Professor of Soil Chemistry, Dep. of Plant & Soil Biology, Univ. of California, Berkeley.

Received for publication November 14, 1983. Accepted for publication April 18, 1984.




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