TY - JOUR
T1 - Insights into boron removal from water using Mg-Al-LDH
T2 - Reaction parameters optimization & 3D-RSM modeling
AU - Eljamal, Osama
AU - Maamoun, Ibrahim
AU - Alkhudhayri, Sami
AU - Eljamal, Ramadan
AU - Falyouna, Omar
AU - Tanaka, Kazuya
AU - Kozai, Naofumi
AU - Sugihara, Yuji
N1 - Funding Information:
We gratefully acknowledge Terumi Dohi and Futoshi Kanno from the Collaborative Laboratories of Advanced Decommissioning Science (CLADS), Sector of Fukushima Research and Development, Japan Atomic Energy Agency (JAEA), Fukushima, Japan, for the great support in conducting TEM-EDS measurements at CLADS, JAEA.
Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/4
Y1 - 2022/4
N2 - In this study, calcined Mg-Al layered double hydroxide (Mg-Al-CLDH) was successfully synthesized for boron (B) removal from aqueous solutions. Batch experiments were conducted considering various reaction conditions, including initial pH, reaction temperature, initial B concentration, Mg-Al-CLDH dosage, ambient condition, and co-existing ions effect, for optimizing B removal efficiency. Results showed that sorption kinetic rate became higher by approaching towards the neutral pH conditions, while it declined at the strong acidic or alkaline conditions. Mg-Al-CLDH was capable of removing high B concentration (80 mg/L) from aqueous solutions at a reasonable dosage of 2 g/L, with a comparable sorption capacity (22.1 mg/g) to other reported studies. Moreover, high B removal rates were observed at high reaction temperatures, reflecting the endothermic nature of the reaction, and reached equilibrium within less than 6 h at temperature of 70 °C. Moreover, results of 3D-RSM modeling confirmed that the middle-high range of Mg-Al-CLDH dosage values was the suitable range to achieve high B removal efficiency, in spite of pH, temperature, and initial concentration effects. Furthermore, isotherm modeling confirmed that B removal by Mg-Al-CLDH occurred via a mono-layer sorption, and thermodynamic modeling revealed the positive value of entropy change, indicating that the randomness of the solid/liquid interaction increased within the adsorption process of B. Spent Mg-Al-CLDH showed great reusability performance by achieving 67%–75% B removal efficiency over three consecutive regeneration cycles, confirming the high potential and applicability of the presented adsorbent in real water treatment applications.
AB - In this study, calcined Mg-Al layered double hydroxide (Mg-Al-CLDH) was successfully synthesized for boron (B) removal from aqueous solutions. Batch experiments were conducted considering various reaction conditions, including initial pH, reaction temperature, initial B concentration, Mg-Al-CLDH dosage, ambient condition, and co-existing ions effect, for optimizing B removal efficiency. Results showed that sorption kinetic rate became higher by approaching towards the neutral pH conditions, while it declined at the strong acidic or alkaline conditions. Mg-Al-CLDH was capable of removing high B concentration (80 mg/L) from aqueous solutions at a reasonable dosage of 2 g/L, with a comparable sorption capacity (22.1 mg/g) to other reported studies. Moreover, high B removal rates were observed at high reaction temperatures, reflecting the endothermic nature of the reaction, and reached equilibrium within less than 6 h at temperature of 70 °C. Moreover, results of 3D-RSM modeling confirmed that the middle-high range of Mg-Al-CLDH dosage values was the suitable range to achieve high B removal efficiency, in spite of pH, temperature, and initial concentration effects. Furthermore, isotherm modeling confirmed that B removal by Mg-Al-CLDH occurred via a mono-layer sorption, and thermodynamic modeling revealed the positive value of entropy change, indicating that the randomness of the solid/liquid interaction increased within the adsorption process of B. Spent Mg-Al-CLDH showed great reusability performance by achieving 67%–75% B removal efficiency over three consecutive regeneration cycles, confirming the high potential and applicability of the presented adsorbent in real water treatment applications.
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U2 - 10.1016/j.jwpe.2022.102608
DO - 10.1016/j.jwpe.2022.102608
M3 - Article
AN - SCOPUS:85123947905
VL - 46
JO - Journal of Water Process Engineering
JF - Journal of Water Process Engineering
SN - 2214-7144
M1 - 102608
ER -