Ma. Olazabal et al., PRECIPITATION EQUILIBRIA OF THE CHROMIUM(VI) IRON(III) SYSTEM AND SPECTROSCOPIC CHARACTERIZATION OF THE PRECIPITATES/, Environmental science & technology, 31(10), 1997, pp. 2898-2902
Precipitation equilibria and spectroscopic studies of the Cr-(VI)/Fe(I
II)/H2O system have been performed to identify the aqueous and solid s
peciation of the system in the pH range 1-9. The results suggest that
three different precipitates FeOHCrO4, FeOHCrO4 . 2Fe(OH)(3), and Fe(O
H)(3) exist depending on the pH range. The last two precipitates have
been reported in the literature before, and they are confirmed in this
study. The formation of a new precipitate, FeOHCrO4, that predominate
s in the pH range 1.5-2.5 is being suggested, and its thermodynamic so
lubility constant was estimated to be pK(so) = 22.50 +/- 0.07. The mix
ed precipitate predominated in the 2.5-3.5 pH range and the pure ferri
c iron hydroxide predominated in the pH range grater than 3.5. All thr
ee precipitates were analyzed using X-ray photoelectron spectroscopy (
XPS). The spectroscopic results suggest that the first and second prec
ipitates contain one type of chromium species which corresponds to Cr(
VI) type and one type of Fe species. The third precipitate exhibited t
wo peaks with width greater than 5 eV, indicating the presence of two
chromium species, one of which is closely related to CrOOH type of bin
ding and the other may be attributed to metal-chromate binding. We pos
tulate that in this case chromate was adsorbed onto the iron hydroxide
forming two surface complexes. Since iron is abundant in nature, the
results of this study are important for the understanding of the mobil
ity and reactivity of hexavalent chromium in contaminated groundwater
sites.