Mechanistic insights into the interfacial adsorption behaviors of Cr(VI) on ferrihydrite: Effects of pH and naturally coexisting anions in the environment
Changjin Liang, Honghai Wu, Jing Chen, Yanfu Wei
Abstract
Interfacial interaction of hexavalent chromium (Cr[VI]) with ferrihydrite (Fh) plays a key role in the behavior of Cr(VI) in the environment. In this study, H2PO4−, SO42−, NO3−, Cl−, and HCO3− were chosen as coexisting anions to explore their inhibition of the capacity of Fh to adsorb Cr(VI). We employed X-ray diffraction, scanning electron microscopy, attenuated total reflection Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy to thoroughly characterize Fh reaction products before and after adsorption of Cr(VI). The results clearly revealed that pH has a marked effect on the extent of Cr(VI) adsorption onto Fh, and this process is also highly dependent on the types of anions present. H2PO4− exhibited the most evident inhibition of Cr(VI) adsorption, even at low concentrations. Similarly, the inhibition of Cr(VI) adsorption by HCO3− increased markedly with increasing pH. In contrast, SO42− only slightly competed with Cr(VI) for reactive Fh surface sites. The anions Cl− and NO3− exhibited almost no inhibitory effect on Cr(VI) adsorption. The differential order of adsorptive affinity of all six anions for Fh was as follows: H2PO4− > HCO3− > SO42− ≈ HCrO4− > NO3− ≈ Cl−. Based on these results, we further provide mechanistic insights into the complexities of Cr(VI) adsorption/desorption behaviors on Fh surfaces. Using Fh as a geosorbent, these interfacial properties could be exploited to mediate the immobilization and release of chromate from and/or into contaminated environments such as aquifers.