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Lee, Changha
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Activation of Persulfates by Graphitized Nanodiamonds for Removal of Organic Compounds

Author(s)
Lee, HongshinKim, Hyoung-ilWeon, SeunghyunChoi, WonyoungHwang, Yu SikSeo, JiwonLee, ChanghaKim, Jae-Hong
Issued Date
2016-09
DOI
10.1021/acs.est.6b02079
URI
https://scholarworks.unist.ac.kr/handle/201301/20564
Fulltext
http://pubs.acs.org/doi/abs/10.1021/acs.est.6b02079
Citation
ENVIRONMENTAL SCIENCE & TECHNOLOGY, v.50, no.18, pp.10134 - 10142
Abstract
This study introduces graphited nanodiamond (G-ND) as an environmentally friendly, easy-to-regenerate, and cost-effective alternative catalyst to activate persulfate (i.e., peroxymonosulfate (PMS) and peroxydisulfate (PDS)) and oxidize organic compounds in water. The G-ND was found to be superior for persulfate activation to other benchmark carbon materials such as graphite, graphene, fullerene, and carbon nanotubes. The G-ND/persulfate showed selective reactivity toward phenolic compounds and some pharmaceuticals, and the degradation kinetics were not inhibited by the presence of oxidant scavengers and natural organic matter. These results indicate that radical intermediates such as sulfate radical anion and hydroxyl radical are not majorly responsible for this persulfate-driven oxidation of organic compounds. The findings from linear sweep voltammetry, thermogravimetric analysis, Fourier transform infrared spectroscopy, and electron paramagnetic resonance spectroscopy analyses suggest that the both persulfate and phenol effectively bind to G-ND surface and are likely to form charge transfer complex, in which G-ND plays a critical role in mediating facile electron transfer from phenol to persulfate. © 2016 American Chemical Society
Publisher
AMER CHEMICAL SOC
ISSN
0013-936X
Keyword
ZERO-VALENT IRONHYDROXYL RADICALSCARBON NANOTUBESRATE CONSTANTSSULFATE RADICALSMOLECULAR-OXYGENAQUEOUS-SOLUTIONWALLED CARBONOXIDATIONDEGRADATION

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