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Dep. of Soil, Crop, and Atmospheric Sciences, Cornell Univ., Ithaca, NY 14853
*Corresponding author (mbm7{at}cornell.edu).
ABSTRACT
Suspensions of natural organic matter and iron oxide (FeOOH) were equilibrated with a wide range of concentrations of added Cu2+ (50–5000 mg kg-1) for as long as 400 d, in order to observe the time-dependent solubility of the free Cu2+ ion. Adsorption was conducted at two pH ranges (5.0–5.5 and 6.5–7.0) and in the presence and absence of phosphate. The Cu2+ activity, measured by ion-selective electrode, was one to two orders of magnitude lower for the organic systems at all Cu loadings investigated when the pH was near 5.5, indicating that the organic matter was a more effective adsorbent for Cu2+ than goethite. Longer reaction times generally caused the Cu2+ activities to decrease due to drifting pH and slow reactions. At higher pH, organic matter again resulted in lower Cu2+ activity than the oxide at all Cu loading levels, but the difference was generally less than at low pH. A downward pH trend in the organic system initially at pH 6.5 caused the Cu2+ activity to increase with longer reaction times. Most of the long-term changes in Cu2+ activity could be attributed to shifting pH, although an aging effect on activity could be discerned. Phosphate added to the oxide or organic matter had little effect on the activity of Cu2+. The EDTA extracted a larger fraction of Cu2+ adsorbed on organic matter than on the oxide, suggesting that strong chelating agents selectively extract metals in quantities not directly related to activity or potential toxicity.
Received for publication November 18, 1997.
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