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1 Dipartimento di Scienze della Terra, Sapienza Università di Roma, P.le A. Moro, 5, I-00185 Rome, Italy
2 CNR-IGAG, Istituto di Geologia Ambientale e Geoingegneria, Sede di Roma, Via Bolognola 7, I-00138 Rome, Italy
3 CNR-IGG, Istituto di Geoscienze e Georisorse, Sede di Roma, P.le A. Moro, 5, I-00185 Rome, Italy
4 Department of Geological Engineering, Hacettepe University, Ankara, Turkey
5 Department of Geological Engineering, Ankara University, Ankara, Turkey
6 Department of Chemical and Biochemical Engineering, The University of Iowa, Iowa City, Iowa 52242, U.S.A.
Correspondence: * E-mail: umran-dogan{at}uiowa.edu
A complete crystal-chemical characterization of erionite-K from Rome, Oregon, was obtained by combining field emission scanning electron microscopy, laboratory parallel-beam transmission powder diffraction, and 57Fe Mössbauer spectroscopy. Rietveld refinement results evidenced that the most striking difference in comparison with the structure of erionite-Ca is significant K at a K2 site(
, 0, 0), which is empty in erionite-Ca. In addition, site Ca1 shows low occupancy and Ca3 is vacant. The oxidation and coordination state of Fe, whose occurrence was revealed by chemical analysis, have been clarified by exploiting room- and low-temperature 57Fe Mössbauer spectroscopy. The majority of Fe (95%) was attributed to Fe3+-bearing, superparamagnetic, oxide-like nanoparticles with dimensions between 1 and 9 nm, and the remaining 5% was attributed to hematite particles with size
10 nm, both located on the crystal surface.
Key Words: Oregon erionite erionite-K crystal structure iron topochemistry field emission scanning electron microscopy laboratory parallel-beam transmission powder diffraction Rietveld refinement 57Fe Mössbauer spectroscopy
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