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Journal of Colloid and Interface Science, Vol.376, 331-333, 2012
Competitive ligand exchange on akaganeite surfaces enriches bulk chloride loadings
Akaganeite (beta-FeOOH) is a nanosized iron oxyhydroxide mineral with a hollandite structure containing chloride ions in 0.4 x 0.4 nm wide channels. Proton and chloride co-sorption into these channels induces variations in bulk O-H stretching vibrations, crystallographic lattice size, and thermal stability, as a result of hydrogen bond formation with chloride ions. In this work, we show that chloride ions bound to akaganeite surfaces can be dislodged into aqueous solutions by competitive adsorption of foreign ions and then transferred alongside co-sorbed protons into the akaganeite bulk. Fourier transform infrared and X-ray photoelectron spectroscopic measurements show that HClO4, H2SO4, and benzoic acid, and thereby, many other anions of various charge-to-size ratios can all effectively contribute to this phenomenon. This linked surface-bulk reactivity should be accounted for in mixed anion systems containing akaganeite-like materials. (C) 2012 Elsevier Inc. All rights reserved.