Enhanced electrochemical performance and boron removal capacity of Mg-Al layered double hydroxide composite for membrane-free capacitive deionization applications

• A membrane-free CDI system was developed using Mg–Al LDH/carbon paper electrodes. • Achieved >94% boron removal efficiency within 20 minutes at 1.2 V and pH 11. • Demonstrated high mean deionization capacity (MDC = 2.58 mg/g) and charge efficiency (CE = 79%). • Energy consumption remained low (∼0.82 kWh/m³) with excellent cycling stability. • The system shows strong pH- and voltage-dependent performance, making it suitable for practical boron remediation Water purification is significantly inhibited by the ineffective removal of boron from aqueous solutions, particularly because traditional membrane-based purification exhibits poor removal of neutral boric acid. This study investigates the efficiency of a Mg-Al layered double hydroxide electrode supported on carbon paper for boron removal by capacitive deionization (CDI). Cyclic voltammetry was used to confirm the capacitive properties of the electrode, which displayed quasi-rectangular profiles with notable reversibility and rate capability. Chronoamperometric observations revealed a voltage-dependent electrosorption activity; 1.2 V showed optimal charge storage and boron removal performance. At this voltage, the system achieved a mean deionization capacity of 2.58 mg/g, over 94% boron removal within 20 min, and a peak charge efficiency of 79%, accompanied by a moderate energy consumption of 0.82 kWh/m3. The system exhibited a notable pH dependence and the optimal performance at pH 11 correlated with the dominance of the negatively charged borate ion (B(OH)⁻). Increasing the pH increased the capacity and rate in the Ragone plot (mean deionization capacity vs. mean deionization rate). Although system efficiency dropped slightly to 88% after 120 min of operation, the electrode showed remarkable cyclic stability across several charge-discharge cycles. Dynamic variations in real-time pH monitoring during CDI were observed, with an initial increase during charging, followed by a slow decline during discharging. The results demonstrate the effectiveness of Mg-Al layered double hydroxide-based CDI systems as flexible and chemically strong platforms for boron removal in water treatment applications.

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Publication Details

Journal
Chemical Engineering Journal Advances
Published
2025-06-27
DOI
https://doi.org/10.1016/j.ceja.2025.100798
Citations
3
Primary Topic
Membrane-based Ion Separation Techniques
Type
article
Field-Weighted Citation Impact
2.02
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article

Enhanced electrochemical performance and boron removal capacity of Mg-Al layered double hydroxide composite for membrane-free capacitive deionization applications

Ismail Abdulazeez, Isam H. Aljundi, Mohammed Benaafi, Niaz Ali Khan et al.
3 citations
Chemical Engineering Journal Advances
Membrane-based Ion Separation Techniques
2.02
article

Enhanced electrochemical performance and boron removal capacity of Mg-Al layered double hydroxide composite for membrane-free capacitive deionization applications

Ismail Abdulazeez, Isam H. Aljundi, Mohammed Benaafi, Niaz Ali Khan, Jamilu Usman, Nadeem Baig, Billel Salhi, Juliana Alabdrabalreda
article en
3 citations

Abstract

• A membrane-free CDI system was developed using Mg–Al LDH/carbon paper electrodes. • Achieved >94% boron removal efficiency within 20 minutes at 1.2 V and pH 11. • Demonstrated high mean deionization capacity (MDC = 2.58 mg/g) and charge efficiency (CE = 79%). • Energy consumption remained low (∼0.82 kWh/m³) with excellent cycling stability. • The system shows strong pH- and voltage-dependent performance, making it suitable for practical boron remediation Water purification is significantly inhibited by the ineffective removal of boron from aqueous solutions, particularly because traditional membrane-based purification exhibits poor removal of neutral boric acid. This study investigates the efficiency of a Mg-Al layered double hydroxide electrode supported on carbon paper for boron removal by capacitive deionization (CDI). Cyclic voltammetry was used to confirm the capacitive properties of the electrode, which displayed quasi-rectangular profiles with notable reversibility and rate capability. Chronoamperometric observations revealed a voltage-dependent electrosorption activity; 1.2 V showed optimal charge storage and boron removal performance. At this voltage, the system achieved a mean deionization capacity of 2.58 mg/g, over 94% boron removal within 20 min, and a peak charge efficiency of 79%, accompanied by a moderate energy consumption of 0.82 kWh/m3. The system exhibited a notable pH dependence and the optimal performance at pH 11 correlated with the dominance of the negatively charged borate ion (B(OH)⁻). Increasing the pH increased the capacity and rate in the Ragone plot (mean deionization capacity vs. mean deionization rate). Although system efficiency dropped slightly to 88% after 120 min of operation, the electrode showed remarkable cyclic stability across several charge-discharge cycles. Dynamic variations in real-time pH monitoring during CDI were observed, with an initial increase during charging, followed by a slow decline during discharging. The results demonstrate the effectiveness of Mg-Al layered double hydroxide-based CDI systems as flexible and chemically strong platforms for boron removal in water treatment applications.

Chemical Engineering Journal AdvancesVol. 23
King Fahd University of Petroleum and Minerals (SA)
Openalex Percentile: Top 13%
Membrane-based Ion Separation Techniques
2.02
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