TY - JOUR
T1 - Affinity of potassium-form cation exchange resin for alkaline earth and transition metals
AU - Foster, Jerrine T T
AU - Hu, Yue
AU - Boyer, Treavor
N1 - Funding Information:
This publication was made possible by U.S. Environmental Protection Agency grant R835334 to THB. Its contents are solely the responsibility of the grantee and do not necessarily represent the official views of the USEPA. Further, USEPA does not endorse the purchase of any commercial products or services mentioned in the publication. The authors thank Judith Labrada for her assistance with laboratory experiments.
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2017/3/24
Y1 - 2017/3/24
N2 - This research conducted bench-scale batch equilibrium tests to generate new selectivity data for the alkaline earth metals Ca2+, Sr2+, and Ba2+ and the transition metals Cd2+ and Co2+ for binary cation exchange involving sulfonic acid, polystyrene, gel and macroporous resins using the potassium (K+) mobile counterion. Calculations for separation factor, and Langmuir and Freundlich isotherm models were used to investigate the sorption behavior of metals onto the cation exchangers. The separation factor and Langmuir isotherm were used to determine the selectivity sequence of cations for the resins. It was determined that the K-form cation exchangers were more selective for alkaline earth metals than the corresponding sodium (Na+) form resin, and the gel resin was more selective than the macroporous resin for all metals. Using the separation factor to determine the selectivity sequence for K-form cation exchange resin showed similar order as published selectivity sequences for Li- and Na-form resins. The hydrated radius and ionic radius of the metals had a strong influence on the selectivity sequence for both types of cation exchange resins. Smaller hydrated radius resulted in an increase in the affinity of the resin for contaminants. Overall, K-form cation exchange resin has the potential to replace Na-form resin, as indicated by higher selectivity and comparable selectivity sequence for common metal contaminants.
AB - This research conducted bench-scale batch equilibrium tests to generate new selectivity data for the alkaline earth metals Ca2+, Sr2+, and Ba2+ and the transition metals Cd2+ and Co2+ for binary cation exchange involving sulfonic acid, polystyrene, gel and macroporous resins using the potassium (K+) mobile counterion. Calculations for separation factor, and Langmuir and Freundlich isotherm models were used to investigate the sorption behavior of metals onto the cation exchangers. The separation factor and Langmuir isotherm were used to determine the selectivity sequence of cations for the resins. It was determined that the K-form cation exchangers were more selective for alkaline earth metals than the corresponding sodium (Na+) form resin, and the gel resin was more selective than the macroporous resin for all metals. Using the separation factor to determine the selectivity sequence for K-form cation exchange resin showed similar order as published selectivity sequences for Li- and Na-form resins. The hydrated radius and ionic radius of the metals had a strong influence on the selectivity sequence for both types of cation exchange resins. Smaller hydrated radius resulted in an increase in the affinity of the resin for contaminants. Overall, K-form cation exchange resin has the potential to replace Na-form resin, as indicated by higher selectivity and comparable selectivity sequence for common metal contaminants.
KW - Adsorption isotherm
KW - Metals
KW - Selectivity sequence
KW - Separation factor
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U2 - 10.1016/j.seppur.2016.11.034
DO - 10.1016/j.seppur.2016.11.034
M3 - Article
AN - SCOPUS:84998817176
SN - 1383-5866
VL - 175
SP - 229
EP - 237
JO - Gas Separation and Purification
JF - Gas Separation and Purification
ER -