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Protonation of different goethite surfaces: unified models for NaNO3 and NaCl media
Institut für Nukleäre Entsorgung, Forschungszentrum Karlsruhe.
Pacific Northwest National Laboratory , Richland, WA.
Luleå University of Technology, Department of Civil, Environmental and Natural Resources Engineering, Sustainable Process Engineering.
Department of Chemistry, Umeå University.
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2008 (English)In: Journal of Colloid and Interface Science, ISSN 0021-9797, E-ISSN 1095-7103, Vol. 317, no 1, p. 155-165Article in journal (Refereed) Published
Abstract [en]

Acid–base titration data for two goethites samples in sodium nitrate and sodium chloride media are discussed. The data are modeled based on various surface complexation models in the framework of the multi site complexation (MUSIC) model. Various assumptions with respect to the goethite morphology are considered in determining the site density of the surface functional groups. The results from the various model applications are not statistically significant in terms of goodness of fit. More importantly, various published assumptions with respect to the goethite morphology (i.e., the contributions of different crystal planes and their repercussions on the “overall” site densities of the various surface functional groups) do not significantly affect the final model parameters within simple 1-pK approximations. The simultaneous fit of the chloride and nitrate data results in electrolyte binding constants, which are applicable over a wide range of electrolyte concentrations including mixtures of chloride and nitrate. Model parameters for the goethite sample with 90 m2/g specific surface area are in excellent agreement with parameters that were independently obtained by another group on different goethite titration data sets.

Place, publisher, year, edition, pages
2008. Vol. 317, no 1, p. 155-165
National Category
Physical Chemistry
Research subject
Chemistry of Interfaces
Identifiers
URN: urn:nbn:se:ltu:diva-3352DOI: 10.1016/j.jcis.2007.08.055ISI: 000251283100019Scopus ID: 2-s2.0-36048930175Local ID: 12b5f370-c82d-11dc-b13a-000ea68e967bOAI: oai:DiVA.org:ltu-3352DiVA, id: diva2:976210
Note
Validerad; 2008; 20080121 (pafi)Available from: 2016-09-29 Created: 2016-09-29 Last updated: 2018-07-10Bibliographically approved

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