TY - JOUR
T1 - The Influence of Ionic Strength on Yttrium and Rare Earth Element Complexation by Fluoride Ions in NaClOsub4/sub, NaNOsub3/sub and NaCl Solutions at 25 °C
AU - Luo, Yu-Ran
AU - Byrne, Robert H.
PY - 2007/1/1
Y1 - 2007/1/1
N2 - Stability constants of the form F β 1 (M)=[MF 2+ ][M 3+ ] −1 [F − ] −1 (where [MF 2+ ] represents the concentration of a yttrium or a rare earth element (YREE) complex, [M 3+ ] is the free YREE ion concentration, and [F − ] is the free fluoride ion concentration) were determined by direct potentiometry in NaNO 3 and NaCl solutions. The patterns of log 10 F β 1 (M) in NaNO 3 and NaCl solutions very closely resemble stability constant patterns obtained previously in NaClO 4 . For a given YREE, stability constants obtained in NaClO 4 were similar to, but consistently larger than F β 1 (M) values obtained in NaNO 3 which, in turn, were larger than formation constants obtained in NaCl. Stability constants for formation of nitrate and chloride complexes ( NO3β1(M)=[MNO32+][M3+]−1[NO3−]−1">NO3β1(M)=[MNO2+3][M3+]−1[NO−3]−1NO3β1(M)=[MNO32+][M3+]−1[NO3−]−1 and Cl β 1 (M)=[MCl 2+ ][M 3+ ] −1 [Cl − ] −1 ) derived from F β 1 (M) data exhibited ionic strength dependencies generally similar to those of F β 1 (M). However, in contrast to the somewhat complex pattern obtained for F β 1 (M) across the fifteen member YREE series, no patterns were observed for nitrate and chloride complexation constants: neither NO3β1(M)">NO3β1(M)NO3β1(M) nor Cl β 1 (M) showed discernable variations across the suite of YREEs. Nitrate and chloride formation constants at 25 °C and zero ionic strength were estimated as log 10 NO3β1o(M)=0.65±0.06">NO3βo1(M)=0.65±0.06NO3β1o(M)=0.65±0.06 and log 10 Cl β o 1 (M)=0.71±0.05. Although these constants are identical within experimental uncertainty, the distinct ionic strength dependencies of NO3β1(M)">NO3β1(M)NO3β1(M) and Cl β 1 (M) produced larger differences in the two stability constants with increasing ionic strength whereby Cl β 1 (M) was uniformly larger than NO3β1(M)">NO3β1(M)NO3β1(M) .
AB - Stability constants of the form F β 1 (M)=[MF 2+ ][M 3+ ] −1 [F − ] −1 (where [MF 2+ ] represents the concentration of a yttrium or a rare earth element (YREE) complex, [M 3+ ] is the free YREE ion concentration, and [F − ] is the free fluoride ion concentration) were determined by direct potentiometry in NaNO 3 and NaCl solutions. The patterns of log 10 F β 1 (M) in NaNO 3 and NaCl solutions very closely resemble stability constant patterns obtained previously in NaClO 4 . For a given YREE, stability constants obtained in NaClO 4 were similar to, but consistently larger than F β 1 (M) values obtained in NaNO 3 which, in turn, were larger than formation constants obtained in NaCl. Stability constants for formation of nitrate and chloride complexes ( NO3β1(M)=[MNO32+][M3+]−1[NO3−]−1">NO3β1(M)=[MNO2+3][M3+]−1[NO−3]−1NO3β1(M)=[MNO32+][M3+]−1[NO3−]−1 and Cl β 1 (M)=[MCl 2+ ][M 3+ ] −1 [Cl − ] −1 ) derived from F β 1 (M) data exhibited ionic strength dependencies generally similar to those of F β 1 (M). However, in contrast to the somewhat complex pattern obtained for F β 1 (M) across the fifteen member YREE series, no patterns were observed for nitrate and chloride complexation constants: neither NO3β1(M)">NO3β1(M)NO3β1(M) nor Cl β 1 (M) showed discernable variations across the suite of YREEs. Nitrate and chloride formation constants at 25 °C and zero ionic strength were estimated as log 10 NO3β1o(M)=0.65±0.06">NO3βo1(M)=0.65±0.06NO3β1o(M)=0.65±0.06 and log 10 Cl β o 1 (M)=0.71±0.05. Although these constants are identical within experimental uncertainty, the distinct ionic strength dependencies of NO3β1(M)">NO3β1(M)NO3β1(M) and Cl β 1 (M) produced larger differences in the two stability constants with increasing ionic strength whereby Cl β 1 (M) was uniformly larger than NO3β1(M)">NO3β1(M)NO3β1(M) .
KW - Rare earth elements
KW - Fluoride complexation
KW - Nitrate complexation
KW - Chloride complexation
KW - Stability constants
KW - Ionic strength
KW - Lanthanide
KW - Yttrium
UR - https://digitalcommons.usf.edu/msc_facpub/1639
UR - https://doi.org/10.1007/s10953-007-9141-6
U2 - 10.1007/s10953-007-9141-6
DO - 10.1007/s10953-007-9141-6
M3 - Article
VL - 36
JO - Journal of Solution Chemistry
JF - Journal of Solution Chemistry
ER -