Sorption kinetics of isotopically labelled divalent mercury (196Hg2+) in soil

Abstract

Understanding the sorption kinetics of Hg²⁺ is the key to predicting its reactivity in soils which is indispensable for environmental risk assessment. The temporal change in the solubility of ¹⁹⁶Hg²⁺ spikes (6 mg kg^-1) added to a range of soils with different properties was investigated and modelled. The sorption of ¹⁹⁶Hg²⁺ displayed a biphasic pattern with a rapid initial (short-term) phase followed by a slower (time-dependent) one. The overall reaction rate constants ranged from 0.003 to 4.9 h^-1 and were significantly correlated (r = 0.94) to soil organic carbon (SOC). Elovich and Spherical Diffusion expressions compellingly fitted the observed ¹⁹⁶Hg²⁺ sorption kinetics highlighting their flexibility to describe reactions occurring over multiple phases and wide timeframes. A parameterized Elovich model from soil variables indicated that the short-term sorption is solely controlled by SOC while the time-dependent sorption appeared independent of SOC and decreased at higher pH values and Al(OH)₃ and MnO₂ concentrations. This is consistent with a rapid chemical reaction of Hg²⁺ with soil organic matter (SOM) which is followed by a noticeably slower phase likely occurring through physical pathways e.g. pore diffusion of Hg²⁺ into spherical soil aggregates and progressive incorporation of soluble organic-Hg into solid phase. The model lines predicted that in soils with >4% SOC, Hg²⁺ is removed from soil solution over seconds to minutes; however, in soils with <2% SOC and higher pH values, Hg²⁺ may remain soluble for months and beyond with a considerable associated risk of re-emission or migration to the surrounding environments.

Keywords: Environmental pollution; Heavy metals; Kinetic modelling; Stable isotopes.