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Influence of Gibbsite Surface Area and Citrate on Ni Sorption Mechanisms at pH 7.5

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Clays and Clay Minerals

Abstract

We investigated the sorption of Ni to gibbsite of two different surface areas at pH 7.5, in the presence and absence of citrate, over a time period of 180 days. Extended X-ray absorption fine-structure spectroscopy was employed to elucidate the sorption mechanisms at the molecular level. In agreement with former results, Ni-Al layered double hydroxide (LDH) formed in the presence of gibbsite of low surface area. However, gibbsite of high surface area suppressed the formation of the surface precipitate. Instead, two Al atoms neighboring Ni at distances of 2.95–2.98 Å indicated formation of an inner-sphere sorption complex, where each NiO6-octahedron shares edges with two AlO6-octahedra. Focused multiple scattering arising from Al atoms at a distance of 6 Å suggest that sorbed Ni(OH)2(OH2)4 monomers epitaxially extend the hexagonal arrangement of Al atoms in gibbsite. Only after 30 days or more was a small amount of LDH formed. The presence of citrate prevented the formation of LDH, while maintaining the formation of inner-sphere sorption complexes.

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Correspondence to Noriko U. Yamaguchi.

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Yamaguchi, N.U., Scheinost, A.C. & Sparks, D.L. Influence of Gibbsite Surface Area and Citrate on Ni Sorption Mechanisms at pH 7.5. Clays Clay Miner. 50, 784–790 (2002). https://doi.org/10.1346/000986002762090182

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  • DOI: https://doi.org/10.1346/000986002762090182

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