X-ray photoelectron spectroscopy was used to study the surface alterat
ion of olivines (fayalite and forsterite) during acid dissolution (0.0
5 mol l(-1) H2SO4 at room temperature for one day). The abundances of
Fe and Mg, relative to Si, in the near surface of olivines decreased a
fter acid dissolution. The divalent cations in the fayalite were remov
ed more readily than those in the forsterite. After acid dissolution,
the Si 2s and O 1s spectra of fayalite were deconvoluted to contributi
ons from unleached and leached phases. The Si 2s and O Is binding ener
gies were higher for the leached phase relative to the unleached phase
, and comparable to those of silicon dioxide (quartz and silica gel),
indicating that SiO2 . nH(2)O formed on the mineral surface. Scanning
electron micrographs of the leached olivine grains showed a harshly et
ched structure for fayalite and a locally etched structure for forster
ite, indicating that the dissolution proceeded heterogeneously.