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a Formerly with Dep. of Plant Biology and Pathology, Rutgers Univ., New Brunswick, NJ 08901
b Currently at: Water Resources Research Center, Univ. of Hawaii at Manoa, Honolulu, HI 96822
c Dep. of Plant Biology and Pathology, Rutgers Univ. New Brunswick, NJ 08901
* Corresponding author (zinati{at}aesop.rutgers.edu).
Little information is available about the changes of the proton charge of goethite in the presence of phosphate (P) and humic acid (HA). The objectives of this study were to systematically measure the proton charge of the ternary mixture and adsorption of HA and P on goethite. The potentiometric titration method was used to measure proton charges in single, binary, and ternary mixtures of goethite, HA, and P as a function of pH and ionic strengths. Results showed that proton charge in the ternary mixture became more negative with increasing pH and the loadings of HA and P. The point of zero charge (PZC) decreased linearly with the initial concentrations of HA and P. At low to intermediate pH, little variation was observed in adsorption of P on goethite in the presence of HA. A small reduction in the adsorption of P in the presence of HA was observed when compared with the control (without HA loading) at high pH. In 2008, Weng et al. developed a model describing the electrostatic interaction between HA and P at the 1-plane of the compact part of the electrical double layer (EDL). In this study, Weng et al.'s model was used to interpret the effect of adsorbed HA on the adsorption of P on goethite as well as the nonsignificant interaction of PZC between HA and P.
Abbreviations: EDL, electrical double layer FA, fulvic acid HA, humic acid P, phosphate PPZC, pristine point of zero charge PZC, point of zero charge PZSE, point of zero salt effect
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