TY - JOUR
T1 - Stoichiometry of smectite dissolution reaction
AU - Metz, Volker
AU - Amram, Keren
AU - Ganor, Jiwchar
N1 - Funding Information:
This research was supported by The Israel Science Foundation (grant No. 174/01), by the Israeli Ministry of Energy and Infrastructure (grant No. ES-66-96) and by the Belfer Foundation for Energy and Environmental Research. We gratefully acknowledge thorough reviews by the associate editor, David J. Wesolowski, and by James I. Drever and two other anonymous reviewers. We thank Michael Dvorchak (Geological Survey of Israel, Jerusalem) and Klaus Spieler (INE) for their technical assistance during the SEM measurements, Prof. Amitai Katz (Hebrew University Jerusalem) for carrying out the ICP-AES analyses, and Dr. Dieter Schild (INE) for performing the XPS analyses. The technical assistance of Ester Shani, Adva Avital, Boaz Kfir, Gefen Ronen and Emmanuelle Roueff (Ben-Gurion University of the Negev) is greatly acknowledged.
PY - 2005/4/1
Y1 - 2005/4/1
N2 - The dissolution stoichiometry of smectite-rich bentonites SAz-1, STx-1 and SWy-1 was studied at 50°C and pH 2 and 3 using flow-through reactors. In addition to smectite, these samples contain considerable amounts of silica phases (quartz, cristobalite and/or amorphous silica). As a result, the molar Al/Si ratios of the bulk samples are significantly lower than those of the pure smectite. Smectite dissolution was highly incongruent during the first few hundred to few thousand hours of the experiments. Release rates of Si, Mg, Ca and Na underwent a distinct transition from an initial period of rapid release to significantly lower release rate at steady state. A reversed trend was observed for release of Al, which gradually increased from very low starting release rate to higher release rate at steady state. At steady state the ratio of released Al to released Si was found to be constant and independent of the experimental conditions. We suggest that this ratio represents the Al/Si ratio of the smectite itself, and it is not influenced by the presence of accessory phases in the sample. The rapid release of calcium, sodium and magnesium from the interlayer sites is explained by ion-exchange reactions, whereas the fast release of silicon is explained by dissolution of amorphous silica. We interpret the initial slow release of Al as the result of inhibition of smectite dissolution due to coating or cementation of the smectite aggregates by amorphous silica. As the silica is dissolved, the aggregates fall apart and more smectite surfaces are exposed, resulting in an increase in the smectite dissolution rate. Thereafter, the system approaches steady state, in which the major tetrahedral and octahedral cations of smectite are released congruently.
AB - The dissolution stoichiometry of smectite-rich bentonites SAz-1, STx-1 and SWy-1 was studied at 50°C and pH 2 and 3 using flow-through reactors. In addition to smectite, these samples contain considerable amounts of silica phases (quartz, cristobalite and/or amorphous silica). As a result, the molar Al/Si ratios of the bulk samples are significantly lower than those of the pure smectite. Smectite dissolution was highly incongruent during the first few hundred to few thousand hours of the experiments. Release rates of Si, Mg, Ca and Na underwent a distinct transition from an initial period of rapid release to significantly lower release rate at steady state. A reversed trend was observed for release of Al, which gradually increased from very low starting release rate to higher release rate at steady state. At steady state the ratio of released Al to released Si was found to be constant and independent of the experimental conditions. We suggest that this ratio represents the Al/Si ratio of the smectite itself, and it is not influenced by the presence of accessory phases in the sample. The rapid release of calcium, sodium and magnesium from the interlayer sites is explained by ion-exchange reactions, whereas the fast release of silicon is explained by dissolution of amorphous silica. We interpret the initial slow release of Al as the result of inhibition of smectite dissolution due to coating or cementation of the smectite aggregates by amorphous silica. As the silica is dissolved, the aggregates fall apart and more smectite surfaces are exposed, resulting in an increase in the smectite dissolution rate. Thereafter, the system approaches steady state, in which the major tetrahedral and octahedral cations of smectite are released congruently.
UR - http://www.scopus.com/inward/record.url?scp=13144262911&partnerID=8YFLogxK
U2 - 10.1016/j.gca.2004.09.027
DO - 10.1016/j.gca.2004.09.027
M3 - Article
AN - SCOPUS:13144262911
SN - 0016-7037
VL - 69
SP - 1755
EP - 1772
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
IS - 7
ER -