TY - JOUR
T1 - Investigation of the mechanism of Cu(II) removal using Mg-Al layered double hydroxide intercalated with carbonate
T2 - Equilibrium and pH studies and solid-state analyses
AU - Yang, Xinyi
AU - Kameda, Tomohito
AU - Saito, Yuko
AU - Kumagai, Shogo
AU - Yoshioka, Toshiaki
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/10
Y1 - 2021/10
N2 - Layered double hydroxides (LDHs) are effective in removing metal cations from aqueous solutions, but the mechanism of the process has not been thoroughly investigated. In this study, we conduct the removal of Cu(II) from aqueous solutions using the CO3·Mg-Al LDH and investigate the mechanism of the process based on equilibrium and pH studies and solid-state analyses. Adsorption isotherms show that the equilibrium removal of Cu follows the Freundlich and Halsey models (R2 = 0.973), inducing a multilayer adsorption process. pH studies show that Cu is removed at pH < pHPZC(=12.1), consistent with chemical binding, rather than electrostatic attraction, as the predominant mechanism of removal. XRD reveals the formation of CuCl2·3[Cu(OH)2] and retention of the LDH structure, and SEM images show a thick-layer morphology. Solid-state analyses confirm the formation of CuCl2·3[Cu(OH)2] and its multilayer accumulation on the LDH surface, in accordance with the equilibrium and pH studies.
AB - Layered double hydroxides (LDHs) are effective in removing metal cations from aqueous solutions, but the mechanism of the process has not been thoroughly investigated. In this study, we conduct the removal of Cu(II) from aqueous solutions using the CO3·Mg-Al LDH and investigate the mechanism of the process based on equilibrium and pH studies and solid-state analyses. Adsorption isotherms show that the equilibrium removal of Cu follows the Freundlich and Halsey models (R2 = 0.973), inducing a multilayer adsorption process. pH studies show that Cu is removed at pH < pHPZC(=12.1), consistent with chemical binding, rather than electrostatic attraction, as the predominant mechanism of removal. XRD reveals the formation of CuCl2·3[Cu(OH)2] and retention of the LDH structure, and SEM images show a thick-layer morphology. Solid-state analyses confirm the formation of CuCl2·3[Cu(OH)2] and its multilayer accumulation on the LDH surface, in accordance with the equilibrium and pH studies.
KW - Equilibrium
KW - Layered double hydroxide
KW - Removal mechanism
KW - Solid-state analyses
KW - Sorption
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U2 - 10.1016/j.inoche.2021.108839
DO - 10.1016/j.inoche.2021.108839
M3 - Article
AN - SCOPUS:85113349013
SN - 1387-7003
VL - 132
JO - Inorganic Chemistry Communication
JF - Inorganic Chemistry Communication
M1 - 108839
ER -