Abstract
Microporous SpectraCarb carbon cloth was treated using nitric acid to enhance negative surface charges of COO- in a neutral solution. This acid-treated carbon was further modified by ethylenediamine to attach -NH2 surface functional groups, resulting in positive surface charges of -NH3+ via pronation in a neutral solution. Through multiple characterizations, in comparison to pristine SpectraCarb carbon, amine-treated SpectraCarb carbon displays a decreased potential of zero charge but an increased point of zero charge, which is opposed to the effect obtained for acid-treated SpectraCarb carbon. An inverted capacitive deionization cell was constructed using amine-treated cathodes and acid-treated anodes, where the cathode is the negatively polarized electrode and the anode is the positively polarized electrode. Constant-voltage switching operation using NaCl solution showed that the salt removal capacity was approximately 5.3 mg g-1 at a maximum working voltage of 1.1/0 V, which is an expansion in both the salt capacity and potential window from previous i-CDI results demonstrated for carbon xerogel materials. This improved performance is accounted for by the enlarged cathodic working voltage window through ethylenediamine-derived functional groups, and the enhanced microporosity of the SpectraCarb electrodes for salt adsorption. These results expand the use of i-CDI for efficient desalination applications.
Original language | English |
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Pages (from-to) | 10920-10926 |
Number of pages | 7 |
Journal | Environmental Science and Technology |
Volume | 49 |
Issue number | 18 |
DOIs | |
State | Published - Sep 15 2015 |
Bibliographical note
Publisher Copyright:© 2015 American Chemical Society.
Funding
Funders | Funder number |
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U.S. Department of Energy Oak Ridge National Laboratory U.S. Department of Energy National Science Foundation National Energy Research Scientific Computing Center | DE-PI0000017 |
ASJC Scopus subject areas
- General Chemistry
- Environmental Chemistry