Complementary surface charge for enhanced capacitive deionization

被引:188
作者
Gao, X. [1 ]
Porada, S. [2 ]
Omosebi, A. [1 ]
Liu, K. -L. [1 ,3 ]
Biesheuvel, P. M. [2 ,4 ]
Landon, J. [1 ]
机构
[1] Univ Kentucky, Ctr Appl Energy Res, 3572 Iron Works Pike, Lexington, KY 40511 USA
[2] European Ctr Excellence Sustainable Water Technol, Wetsus, Oostergoweg 9, NL-8911 MA Leeuwarden, Netherlands
[3] Univ Kentucky, Dept Mech Engn, Lexington, KY 40506 USA
[4] Wageningen Univ, Lab Phys Chem & Soft Matter, Dreijenpl 6, NL-6703 HB Wageningen, Netherlands
基金
美国国家科学基金会;
关键词
Capacitive deionization; Enhanced salt removal; Extended working voltage window; Amphoteric Donnan model; DESALINATION PERFORMANCE; ACTIVATED CARBON; ZERO CHARGE; WATER DESALINATION; BATCH-MODE; ELECTRODES; REMOVAL; ENERGY; TECHNOLOGY; DEPENDENCE;
D O I
10.1016/j.watres.2016.01.048
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Commercially available activated carbon cloth electrodes are treated using nitric acid and ethylenediamine solutions, resulting in chemical surface charge enhanced carbon electrodes for capacitive deionization (CDI) applications. Surface charge enhanced electrodes are then configured in a CDI cell to examine their salt removal at a fixed charging voltage and both reduced and opposite polarity discharge voltages, and subsequently compared to the salt removal of untreated electrodes. Substantially improved salt removal due to chemical surface charge and the use of a discharge voltage of opposite sign to the charging voltage is clearly demonstrated in these CDI cycling tests, an observation which for the first time validates both enhanced CDI and extended-voltage CDI effects predicted by the Donnan model [Biesheuvel et al., Colloids Interf. Sci. Comm., 10.1016/j.colcom.2015.12.001 (2016)]. Our experimental and theoretical results demonstrate that the use of carbon electrodes with optimized chemical surface charge can extend the CDI working voltage window through discharge voltages of opposite sign to the charging voltage, which can significantly enhance the salt adsorption capacity of CDI electrodes. Thus, in addition to carbon pore size distribution, chemical surface charge in carbon micropores is considered foundational for salt removal in CDI cells. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:275 / 282
页数:8
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