Abstract
The sorption of inorganic arsenic species (arsenite and arsenate) from aqueous solutions onto steel-mill waste and waste filter sand, under neutral conditions, was investigated in this study. Additionally, the steel-mill waste material was modified in order to minimize its deteriorating impact on the initial water quality and to meet the drinking water standards. The influence of contact time and initial arsenic concentration was investigated using batch system techniques. To evaluate the application for real groundwater treatment, the capacities of the obtained waste materials were further compared to those exhibited by commercial sorbents, which were examined under the same experimental conditions. Kinetic studies revealed that waste slag materials are the most efficient in arsenic removal, reaching equilibrium arsenic sorption capacities in the range 47.6–55.2 μg/g, while waste filter sand exhibited capacities of 25.4–29.8 μg/g (for an initial arsenic concentration Co=0.5 mg/L). The higher iron content in the slag materials was considered to be responsible for the better removal efficiencies, and the specific arsenic removal efficiency was estimated to be 220 μgAs/gFe. The specific arsenic removal efficiency of the second active substance found in waste filter sand, manganese, was estimated to be 115 μgAs/gMn. Equilibrium studies revealed the occurrence of both chemisorption and physical sorption processes. All the waste materials exhibited higher performances for As(V). The highest maximum sorption capacity was obtained by waste iron slag: 4040 μg/g for As(V). The waste materials reached the arsenic removal capacities of the examined commercial materials, suggesting the feasibility of their application in real groundwater treatment.
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