4.7 Article

Electrically regenerated ion-exchange technology: Leveraging faradaic reactions and assessing the effect of co-ion sorption

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 623, 期 -, 页码 985-991

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.05.104

关键词

Capacitive deionization; Brackish groundwater desalination; Ion exchange resin; Electrically regenerative ion exchange

资金

  1. U.S. Department of Energy (DOE) U.S.-China Clean-Energy Research Center-Water Energy Technologies [DE-IA0000018]
  2. Development Impact Lab
  3. USAID Global Development Lab and Higher Education Solutions Network [DEAC02-05CH11231]
  4. Office of Basic Energy Sciences of the U.S. Department of Energy [109-2223-E-002-002-MY3]
  5. Ministry of Science and Technology, Taiwan [106WMRFA0100033]
  6. [AID-OAA-A-13-00002]

向作者/读者索取更多资源

Capacitive deionization (CDI) technologies have the potential to replace reverse osmosis as cost-competitive alternatives for brackish water treatment. This study investigates the impact of co-ion sorption and faradaic side reactions on ion exchange resin functionalized desalination electrodes. The findings show that the electrically regenerated ion exchange (ERI) system effectively captures salt at low applied voltages, and Faradaic side reactions facilitate the functionality of ERI.
Capacitive deionization (CDI) technologies have the potential to become cost-competitive alternatives to reverse osmosis for the treatment of brackish waters. In this study, we report our findings on the effect of co-ion sorption and faradaic side reactions on our ion exchange resin functionalized desalination electrodes which passively capture salt and reject it upon charging. This system, which we previously reported on and refer to as electrically regenerated ion exchange (ERI), avoids the use of expensive ion exchange membranes in an effort to save costs. Surprisingly, we find that, compared to a reference CDI system, ERI electrodes capture salt most effectively at low applied voltages (0.5 mg/cm3 at 0.8 V). Both CDI and ERI systems also seem to suffer from co-ion sorption effects which negatively impact salt adsorption. However, Faradaic side reactions at higher voltages (1 V and 1.2 V) which we track via pH measurements, serve as a detriment to CDI but seem to facilitate the functionality of ERI. (c) 2022 Elsevier Inc. All rights reserved.

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