TY - JOUR
T1 - Dissolution of albite glass and crystal
AU - Hamilton, James P.
AU - Pantano, Carlo G.
AU - Brantley, Susan L.
N1 - Funding Information:
The authors would like to thank Henry Gong, Shaole Wu, Mark Angelone, and Vince Bojan of the Materials Characterization Laboratory and Don Voigt and Will White of the Department of Geosciences at Penn State University for their assistance with sample characterization and experimental design. This research was supported by the Department of Energy (DE-FG02-95ER14547.A000). We also thank Roland Hellmann and one anonymous reviewer for excellent reviews. Alex Blum and Art White of the U.S. Geological Survey are acknowledged for discussions of natural glass dissolution.
PY - 2000
Y1 - 2000
N2 - When normalized by initial surface area, crystalline and amorphous albite release Si and Al at the same rate within error (±40%) as measured at pH 2, 5.6, and 8.4 at 25°C. Differences in density and tetrahedral ring structure between the glass and crystal structures, however, lead to more extensive Na and Al depletion from the glass surface, especially in acid. X-ray photoelectron spectroscopy (XPS) indicates that the chemistry of the altered layers on glass and crystal must be significantly different at a depth of ~17Å-87Å. Nevertheless, angle-resolved XPS (ARXPS) indicates that the outermost 17Å of the glass and crystal surface are compositionally similar. In neutral and weakly basic conditions, XPS indicates less extensive depletion of Na and Al from reacted glass and crystal surfaces than in acidic conditions. Al enrichment was not observed at any pH on either the crystal or glass surface. At steady state, Al release was stoichiometric for all phases and all pH values, but Na release was always faster than release of Si, especially for the glass. These results are consistent with a model where only the outer surface controls dissolution and the deeper layers of the altered surface do not significantly affect dissolution rate. The similarity in dissolution rate between glass and mineral, if consistent for other phases, may also indicate that some future studies of mineral dissolution could be completed more efficiently by investigation of glass because such studies could reveal the chemical effects in dissolution independent of the microstructure and defects that populate natural mineral samples. Copyright (C) 2000 Elsevier Science Ltd.
AB - When normalized by initial surface area, crystalline and amorphous albite release Si and Al at the same rate within error (±40%) as measured at pH 2, 5.6, and 8.4 at 25°C. Differences in density and tetrahedral ring structure between the glass and crystal structures, however, lead to more extensive Na and Al depletion from the glass surface, especially in acid. X-ray photoelectron spectroscopy (XPS) indicates that the chemistry of the altered layers on glass and crystal must be significantly different at a depth of ~17Å-87Å. Nevertheless, angle-resolved XPS (ARXPS) indicates that the outermost 17Å of the glass and crystal surface are compositionally similar. In neutral and weakly basic conditions, XPS indicates less extensive depletion of Na and Al from reacted glass and crystal surfaces than in acidic conditions. Al enrichment was not observed at any pH on either the crystal or glass surface. At steady state, Al release was stoichiometric for all phases and all pH values, but Na release was always faster than release of Si, especially for the glass. These results are consistent with a model where only the outer surface controls dissolution and the deeper layers of the altered surface do not significantly affect dissolution rate. The similarity in dissolution rate between glass and mineral, if consistent for other phases, may also indicate that some future studies of mineral dissolution could be completed more efficiently by investigation of glass because such studies could reveal the chemical effects in dissolution independent of the microstructure and defects that populate natural mineral samples. Copyright (C) 2000 Elsevier Science Ltd.
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U2 - 10.1016/S0016-7037(00)00388-4
DO - 10.1016/S0016-7037(00)00388-4
M3 - Article
AN - SCOPUS:0033848361
SN - 0016-7037
VL - 64
SP - 2603
EP - 2615
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
IS - 15
ER -