Staff Publications

Staff Publications

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    'Staff publications' is the digital repository of Wageningen University & Research

    'Staff publications' contains references to publications authored by Wageningen University staff from 1976 onward.

    Publications authored by the staff of the Research Institutes are available from 1995 onwards.

    Full text documents are added when available. The database is updated daily and currently holds about 240,000 items, of which 72,000 in open access.

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Record number 62835
Title The relationship between molecular structure and ion adsorption on variable charge minerals
Author(s) Rietra, R.P.J.J.; Hiemstra, T.; Riemsdijk, W.H. van
Source Geochimica et Cosmochimica Acta 63 (1999)19-20. - ISSN 0016-7037 - p. 3009 - 3015.
DOI http://dx.doi.org/10.1016/S0016-7037(99)00228-8
Department(s) Sub-department of Soil Quality
Publication type Refereed Article in a scientific journal
Publication year 1999
Keyword(s) mineralen - structuur - adsorptie - minerals - structure - adsorption
Categories Geology (General)
Abstract Ion adsorption modeling is influenced by the presumed binding structure of surface complexes. Ideally, surface complexes determined by modeling should correspond with those derived from spectroscopy, thereby assuring that the mechanistic description of ion binding scales from the nanoscopic molecular structure to the macroscopic adsorption behavior. Here we show that the structure of adsorbed species is a major factor controlling the pH dependency of adsorption. An important aspect of the pH dependency is the macroscopic proton-ion adsorption stoichiometry. A simple and accurate experimental method was developed to determine this stoichiometry. With this method, proton-ion stoichiometry ratios for vanadate, phosphate, arsenate, chromate, molybdate, tungstate, selenate and sulfate have been characterized at 1 or 2 pH values. Modeling of these data shows that the macroscopic proton-ion adsorption stoichiometry is almost solely determined by the interfacial charge distribution of adsorbed complexes. The bond valence concept of Pauling can be used to estimate this charge distribution from spectroscopic data. Conversely, the experimentally determined proton-ion adsorption stoichiometry allows us to successfully predict the spectroscopically identified structures of, for example, selenite and arsenate on goethite. Consequently, we have demonstrated a direct relationship between molecular surface structure and macroscopic adsorption phenomena.
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