Competitive adsorption-desorption reactions of two hazardous heavy metals in contaminated soils.

Investigating the interactions of heavy metals is imperative for sustaining environment and human health. Among those, Cd is toxic for organisms at any concentration. While Ni acts as a micronutrient at very low concentration but is hazardous toxic above certain threshold value. In this study, the chemical adsorption and desorption reactions of Ni and Cd in contaminated soils were investigated in both single and binary ion systems. Both Ni and Cd experimental data demonstrated Langmuir type adsorption. In the competitive systems, an antagonistic effect was observed, implying that both ions compete for same type of adsorption sites. Adverse effect of Cd on Ni adsorption was slightly stronger than that of opposite system, consistent with adsorption isotherms in single ion systems. Variation in ionic strength indicated that Ca, a much weaker adsorbate, could also compete with Cd and Ni for adsorption on soil particles. Desorption data indicated that Cd and Ni are adsorbed very tightly such that after four successive desorption steps, less than 0.5 % of initially adsorbed ions released into the soil solution. This implies that Ca, at concentration in equilibrium with calcite mineral, cannot adequately compete with and replace adsorbed Ni and Cd ions. This adsorption behavior was led to considerable hysteresis between adsorption and desorption in both single and binary ion systems. In the binary ion systems, desorption of Cd and Ni was increased by increase in both equilibrium concentration of adsorbed ion and concentration of competitor ion. The overall results obtained in this research indicate that Cd and Ni are strongly adsorbed in calcareous soil and Ca, the major dissolved ion, insignificantly influences metal ions adsorption. Consequently, the contaminated soils by Ni and Cd can simultaneously be remediated by environmentally oriented technologies such as phytoremediation.

An analytical deterministic model for simultaneous phytoremediation of Ni and Cd from contaminated soils.

Soil contamination by heavy metals, due to human activities, is not often limited to a single contaminant. The objective of this study was to develop a simple model for phytoextracting separate and combined Ni and Cd from contaminated soils. The study was further aimed to study phytoextraction potential of ornamental kale and land cress grown in soils contaminated with separate and combined Ni and Cd metals. The results indicated that elevated Ni and Cd concentrations in soil inhibit growth of both ornamental kale and land cress plants. In Ni + Cd treatments, growth and development of both plants were more affected than in either Ni or Cd treatments. Further, in Ni + Cd treatments, Ni concentration in tissues of both plants was increased by increasing soil Ni concentration under various Cd concentrations. At constant Ni concentration, addition of Cd did not appreciably changed Ni content of plant tissues. Land cress demonstrated higher tolerance to soil contamination by Ni and Cd compared to ornamental kale. It also demonstrated higher phytoextraction potential for soil Cd than ornamental kale. Enhanced bioavailability of Ni and Cd ions, due to competitive adsorption and desorption reactions, had no reasonable effect on metal ion accumulation in plant tissues. This indicates that at relatively high soil contamination, metal ion adsorption is no longer a limiting factor for phytoremediation. The newly proposed model, which assumes that metal uptake rate inversely depends on total soil metal ion concentration, reasonably well predicted the cleanup time of Ni, Cd, and Ni at the presence of Cd from the contaminated soils. The model also predicts that phytoremediation process takes much longer time when soil is contaminated by multi-metal ions.