TY - JOUR
T1 - Sorption of Yttrium and Rare Earth Elements by Amorphous Ferric Hydroxide: Influence of Solution Complexation with Carbonate
AU - Quinn, Kelly A.
AU - Byrne, Robert H.
AU - Schijf, Johan
PY - 2006/1/1
Y1 - 2006/1/1
N2 - The influence of solution complexation on the sorption of yttrium and the rare earth elements (YREEs) by amorphous ferric hydroxide was investigated at 25 °C over a range of pH (4.0–7.1) and carbonate concentrations (0M⩽[CO32-]T⩽150μM). Distribution coefficients, defined as iKFeT=[MSi]T/(MT×[Si]), where [MSi]T is the total concentration of sorbed YREE, MT is the total YREE concentration in solution, and [Si] is the concentration of amorphous ferric hydroxide, initially increased in magnitude with increasing carbonate concentration, and then decreased. The initial increase of iKFeT is due to sorption of YREE carbonate complexes (MCO3+), in addition to sorption of free YREE ions (M3+). The subsequent decrease of iKFeT, which is more extensive for the heavy REEs, is due to the increasing intensity of YREE solution complexation by carbonate ions. The competition for YREEs between solution complexation and surface complexation was modeled via the equation: iKFeT=(Sβ1[H+]-1+Sβ2[H+]-2+β1SCO3×β1CO3H[HCO3-]T[H+]-2)(SK1[H+]+1)×(1+HCO3β1[HCO3-]T+β1CO3H[HCO3-]T[H+]-1+β2CO3H[HCO3-]T2[H+]-2) where Sβ1 and Sβ2 are equilibrium constants for free YREE surface species, β1SCO3 is the equilibrium constant for the YREE-carbonate surface species, SK1 is the surface protonation constant for amorphous ferric hydroxide, and HCO3β1, β1CO3H, and β2CO3H are YREE solution complexation constants expressed in terms of bicarbonate concentrations. The equation, which includes (i) a single new constant (β1SCO3) for each YREE, (ii) previously published sorption coefficients (Sβ1 and Sβ2) determined in the absence of carbonate, and (iii) previously published solution complexation constants, precisely predicts both the absolute magnitude of iKFeT and the pattern of iKFeT values over our range of experimental conditions. Experimentally observed iKFeT values, spanning more than five orders of magnitude, are accurately described by our surface/solution complexation model. The logβ1SCO3values determined for each YREE in this work are: Y(−1.30 ± 0.04), La(−0.39 ± 0.02), Ce(−0.21 ± 0.02), Pr(−0.22 ± 0.02), Nd(−0.20 ± 0.02), Sm(−0.20 ± 0.02), Eu(−0.26 ± 0.02), Gd(−0.38 ± 0.02), Tb(−0.40 ± 0.02), Dy(−0.51 ± 0.02), Ho(−0.57 ± 0.02), Er(−0.59 ± 0.02), Tm(−0.56 ± 0.02), Yb(−0.62 ± 0.02), and Lu(−0.59 ± 0.02).
AB - The influence of solution complexation on the sorption of yttrium and the rare earth elements (YREEs) by amorphous ferric hydroxide was investigated at 25 °C over a range of pH (4.0–7.1) and carbonate concentrations (0M⩽[CO32-]T⩽150μM). Distribution coefficients, defined as iKFeT=[MSi]T/(MT×[Si]), where [MSi]T is the total concentration of sorbed YREE, MT is the total YREE concentration in solution, and [Si] is the concentration of amorphous ferric hydroxide, initially increased in magnitude with increasing carbonate concentration, and then decreased. The initial increase of iKFeT is due to sorption of YREE carbonate complexes (MCO3+), in addition to sorption of free YREE ions (M3+). The subsequent decrease of iKFeT, which is more extensive for the heavy REEs, is due to the increasing intensity of YREE solution complexation by carbonate ions. The competition for YREEs between solution complexation and surface complexation was modeled via the equation: iKFeT=(Sβ1[H+]-1+Sβ2[H+]-2+β1SCO3×β1CO3H[HCO3-]T[H+]-2)(SK1[H+]+1)×(1+HCO3β1[HCO3-]T+β1CO3H[HCO3-]T[H+]-1+β2CO3H[HCO3-]T2[H+]-2) where Sβ1 and Sβ2 are equilibrium constants for free YREE surface species, β1SCO3 is the equilibrium constant for the YREE-carbonate surface species, SK1 is the surface protonation constant for amorphous ferric hydroxide, and HCO3β1, β1CO3H, and β2CO3H are YREE solution complexation constants expressed in terms of bicarbonate concentrations. The equation, which includes (i) a single new constant (β1SCO3) for each YREE, (ii) previously published sorption coefficients (Sβ1 and Sβ2) determined in the absence of carbonate, and (iii) previously published solution complexation constants, precisely predicts both the absolute magnitude of iKFeT and the pattern of iKFeT values over our range of experimental conditions. Experimentally observed iKFeT values, spanning more than five orders of magnitude, are accurately described by our surface/solution complexation model. The logβ1SCO3values determined for each YREE in this work are: Y(−1.30 ± 0.04), La(−0.39 ± 0.02), Ce(−0.21 ± 0.02), Pr(−0.22 ± 0.02), Nd(−0.20 ± 0.02), Sm(−0.20 ± 0.02), Eu(−0.26 ± 0.02), Gd(−0.38 ± 0.02), Tb(−0.40 ± 0.02), Dy(−0.51 ± 0.02), Ho(−0.57 ± 0.02), Er(−0.59 ± 0.02), Tm(−0.56 ± 0.02), Yb(−0.62 ± 0.02), and Lu(−0.59 ± 0.02).
UR - https://digitalcommons.usf.edu/msc_facpub/1748
UR - https://doi.org/10.1016/j.gca.2006.06.014
U2 - 10.1016/j.gca.2006.06.014
DO - 10.1016/j.gca.2006.06.014
M3 - Article
VL - 70
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
ER -