Journal
ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 55, Issue 9, Pages 6042-6051Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.est.0c08018
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Funding
- National Natural Science Foundation P. R. China [22076142, 21677106, 22076140]
- National Key Basic Research Program of China [2017YFA0403402]
- National Natural Science Foundation of China [U1932119]
- Science & Technology Commission of Shanghai Municipality [14DZ2261100]
- Fundamental Research Funds for the Central Universities
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This study successfully accelerated the regeneration of Fe2+ in the electro-Fenton (EF) process by using nitrogen-doped carbon aerogel (NDCA) as a reducing agent, resulting in a higher production of hydroxyl radicals and efficient removal of various pollutants, including organic compounds and ammonia nitrogen.
The regeneration rate of Fe2+ from Fe3+ dictates the performance of the electro-Fenton (EF) process, represented by the amount of produced hydroxyl radicals (center dot OH). Current strategies for the acceleration of Fe2+ regeneration normally require additional chemical reagents, to vary the redox potential of Fe2+/Fe3+. Here, we report an attempt at using the intrinsic property of the electrode to our advantage, i.e., nitrogen-doped carbon aerogel (NDCA), as a reducing agent for the regeneration of Fe2+ without using foreign reagents. Moreover, the pyrrolic N in NDCA provides unpaired electrons through the carbon framework to reduce Fe3+, while the graphitic and pyridinic N coordinate with Fe3+ to form a C-O-Fe-N-2 bond, facilitating electron transfer from both the external circuit and pyrrolic N to Fe3+. Our Fe2+/NDCA-EF system exhibits a 5.8 +/- 0.3 times higher performance, in terms of the amount of generated center dot OH, than a traditional Fenton system using the same Fe2+ concentration. In the subsequent reaction, the Fe2+/NDCA-EF system demonstrates 100.0% removal of dimethyl phthalate, 3-chlorophenol, bisphenol A, and sulfamethoxazole with a low specific energy consumption of 0.17-0.36 kW.h.g(-1). Furthermore, 90.1 +/- 0.6% removal of dissolved organic carbon and 83.3 +/- 0.9% removal of NH3-N are achieved in the treatment of domestic sewage. The purpose of this work is to present a novel strategy for the regeneration of Fe2+ in the EF process and also to elucidate the role of different N species of the carbonaceous electrode in contributing to the redox cycle of Fe2+/Fe3+.
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