Cation selectivity during flow electrode capacitive deionization

被引:2
|
作者
Ren, Panyu [1 ,2 ]
Wang, Bin [1 ]
Ruthes, Jean Gustavo de Andrade [1 ,2 ]
Torkamanzadeh, Mohammad [1 ]
Presser, Volker [1 ,2 ,3 ]
机构
[1] INM Leibniz Inst New Mat, Campus D2 2, D-66123 Saarbrucken, Germany
[2] Saarland Univ, Dept Mat Sci & Engn, Campus D2 2, D-66123 Saarbrucken, Germany
[3] Saarene Saarland Ctr Energy Mat & Sustainabil, Campus C4 2, D-66123 Saarbrucken, Germany
关键词
Activated carbon; Cation separation; Flowable electrode capacitive deionization; CARBON-BLACK SUSPENSIONS; WATER DESALINATION; ELECTROSORPTION; METAL; IONS; HYDRATION; MOBILITY;
D O I
10.1016/j.desal.2024.118161
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Efficient separation of specific ions from aqueous media is crucial for advanced water treatment and resource recovery. Flow electrode capacitive deionization (FCDI) offers potential for selective ion removal through continuous operation. This study evaluates the performance of selective cation separation using a commercial activated carbon slurry in a multi-ion solution of monovalent (Li+, Na+, K+) and bivalent (Ca2+, Mg2+) cations. We assess ion removal and cation selectivity under different operational parameters, such as applied potential, slurry flow rate, and feed water flow rate. Our data show that bivalent cations, namely Ca2+ and Mg2+, are preferentially removal due to their higher charge-to-size ratio, aligning with hydrated ion sizes. The highest separation rate was observed for Ca2+ (5.7 mu g cm(-2) min(-1)), and the lowest for Li+ (0.2 mu g cm(-2) min(-1)). At the highest applied voltage (1.2 V), charge efficiencies reached 70 %, with an energy consumption of 41 Wh mol(-1) for nearly complete cation removal. Optimal conditions were identified with a slurry flow rate of 6 mL min(-1), feed water flow rate of 2 mL min(-1), activated carbon content of 10 mass%, 1 mass% carbon black, and a cell voltage of 1.2 V. These findings highlight the importance of optimizing operational parameters to enhance ion removal.
引用
收藏
页数:12
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