Dissolution of albite glass and crystal

Citation
Jp. Hamilton et al., Dissolution of albite glass and crystal, GEOCH COS A, 64(15), 2000, pp. 2603-2615
Citations number
65
Categorie Soggetti
Earth Sciences
Journal title
GEOCHIMICA ET COSMOCHIMICA ACTA
ISSN journal
00167037 → ACNP
Volume
64
Issue
15
Year of publication
2000
Pages
2603 - 2615
Database
ISI
SICI code
0016-7037(200008)64:15<2603:DOAGAC>2.0.ZU;2-Z
Abstract
When normalized by initial surface area, crystalline and amorphous albite r elease Si and Al at the same rate within error (+/-40%) as measured at pH 2 , 5.6, and 8.4 at 25 degrees 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 a ltered layers on glass and crystal must be significantly different at a dep th of similar to 17 Angstrom-87 Angstrom. Nevertheless, angle-resolved XPS (ARXPS) indicates that the outermost 17 Angstrom of the glass and crystal s urface 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 rele ase 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 dissoluti on and the deeper layers of the altered surface do not significantly affect dissolution rate. The similarity in dissolution rate between glass and min eral, if consistent for other phases, may also indicate that some future st udies of mineral dissolution could be completed more efficiently by investi gation of glass because such studies could reveal the chemical effects in d issolution independent of the microstructure and defects that populate natu ral mineral samples. Copyright (C) 2000 Elsevier Science Ltd.