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A comprehensive characterization of dioctahedral smectites

Authors
  • Wolters, Felicitas1
  • Lagaly, Gerhard2
  • Kahr, Guenter3
  • Nueesch, Rolf
  • Emmerich, Katja1, 4
  • 1 Water and Geotechnology Division, Forschungszentrum Karlsruhe GmbH, Institute for Technical Chemistry, Karlsruhe, 76021, Germany , Karlsruhe (Germany)
  • 2 University of Kiel, Institute of Inorganic Chemistry, Kiel, D-24098, Germany , Kiel (Germany)
  • 3 Institute for Geotechnical Engineering, ETH Zurich, Schafmattstr. 6, Zürich, 8093, Switzerland , Zürich (Switzerland)
  • 4 University of Karlsruhe, Competence Center for Material Moisture, c/o Forschungszentrum Karlsruhe, ITC-WGT, Karlsruhe, 76021, Germany , Karlsruhe (Germany)
Type
Published Article
Journal
Clays and Clay Minerals
Publisher
Springer International Publishing
Publication Date
Feb 01, 2009
Volume
57
Issue
1
Pages
115–133
Identifiers
DOI: 10.1346/CCMN.2009.0570111
Source
Springer Nature
Keywords
License
Yellow

Abstract

The term ‘montmorillonite’ encompasses a wide range of chemical compositions and structures. Comprehensive and reliable characterization is essential for unambiguous classification. Twenty eight purified, Na-exchanged smectites (<0.2 µm) were characterized by layer-charge measurement using the alkylammonium method, by cation exchange capacity (CEC) measurement with Cu-triethylenetetramine, by determination of the chemical composition using X-ray fluorescence analysis, by calculation of the structural formula following determination of the octahedral structure (trans-vacant vs. cis-vacant) by simultaneous thermal analysis, and by X-ray diffraction analysis. Mössbauer spectroscopy was applied to determine the oxidation state and coordination of Fe and changes thereof during purification of the source materials. The charge derived from chemical composition was considerably greater (by up to 30%) than the measured layer charge. The independently measured layer charge was used to calculate the structural formula. The measured CEC values, comprising the permanent charges and the pH-dependent edge charges, were consistent with measured layer charge but not with layer charge derived from the chemical composition. Therefore, the structural formula of smectites should be calculated using the measured layer charge. The dehydroxylation temperature, which conveys information about the structure of the octahedral sheet, was correlated to the amount of Mg and Fe3+ and the location of charges. No relationship was found among the dehydroxylation temperature and the mean layer charge or the Mg content. In contrast, a clear relationship was observed between the Fe content and the dehydroxylation temperature. Montmorillonites with an Fe content <0.3/f.u. are cis-vacant and those containing Fe3+ > 0.3 mol/f.u. are trans-vacant, mostly with additional cis-vacancies. Tetrahedral substitution also appeared to be a function of the number of trans-vacancies. The parameters analyzed provide the basis for a new descriptive classification system.

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