Applications of the continuous‐flow stirred‐cell (CFSC) technique: II. The adsorption behaviour of Na, Cs, Sr, Cu, Ni and Pb on humic acids

Abstract

SummaryThe first part of this paper deals with the sorption of Na, Cs, Sr, Ni, Cu and Pb on two humic fractions derived from a soil. The sorption data for individual elements were obtained using the continuous‐flow stirred‐cell (CFSC) technique, in which the metal sorptive solution is pumped through a cell containing a known mass of the humic acid retained by a filter and the solution emerging from the cell was analysed by either atomic absorption spectrometry (Cu, Ni and Pb) or by the combined use of radioisotope dilution and gamma‐ray spectroscopy (Na, Cs and Sr). Sorption isotherms were determined at two flow rates. It was found that, in general, the sorption isotherms for all the metals studied could be described by the Langmuir equation and parameters derived from the fitted line provided information on the metal‐humate binding strengths and the maximum amount of metal sorbed per unit mass of humic acid. Caesium showed anomalous behaviour at certain flow rates in both its sorption and desorption behaviour.In the second part of the paper we discuss the sequential sorption and desorption of one metal by another on the same humic fraction, using Na, Cs, Zn and Cd. The aim was to elucidate the nature of the binding process when several metals were competing simultaneously for the functional groups on the humic acids. In addition, at the end of the experiment, the humic material was isolated and analysed by gamma‐ray spectroscopy to determine the metals still bound in this fraction. Some tentative conclusions concerning the nature of the metal‐humate complexes are made on the basis of these data.