TY - JOUR
T1 - Enhancement effects of reducing agents on the degradation of tetrachloroethene in the Fe(II)/Fe(III) catalyzed percarbonate system
AU - Miao, Zhouwei
AU - Gu, Xiaogang
AU - Lu, Shuguang
AU - Brusseau, Mark L.
AU - Yan, Ni
AU - Qiu, Zhaofu
AU - Sui, Qian
N1 - Funding Information:
This study was financially supported by the grant from the National Natural Science Foundation of China (No. 41373094 and No. 51208199 ), China Postdoctoral Science Foundation (No. 2015M570341 ), and the Fundamental Research Funds for the Central Universities (No. 22A201514057 ). The contributions of Dr. Mark Brusseau were supported by the NIEHS Superfund Research Program ( P42 ES04940 ). We thank the reviewers for their constructive comments.
Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2015/12/1
Y1 - 2015/12/1
N2 - In this study, the effects of reducing agents on the degradation of tetrachloroethene (PCE) were investigated in the Fe(II)/Fe(III) catalyzed sodium percarbonate (SPC) system. The addition of reducing agents, including hydroxylamine hydrochloride, sodium sulfite, ascorbic acid and sodium ascorbate, accelerated the Fe(III)/Fe(II) redox cycle, leading to a relatively steady Fe(II) concentration and higher production of free radicals. This, in turn, resulted in enhanced PCE oxidation by SPC, with almost complete PCE removal obtained for appropriate Fe and SPC concentrations. The chemical probe tests, using nitrobenzene and carbon tetrachloride, demonstrated that HO was the predominant radical in the system and that O2- played a minor role, which was further confirmed by the results of electron spin resonance measurements. PCE degradation decreased significantly with the addition of isopropanol, a HO scavenger, supporting the hypothesis that HO was primarily responsible for PCE degradation. It is noteworthy that Cl- release was slightly delayed in the first 20min, indicating that intermediate products were produced. However, these intermediates were further degraded, resulting in the complete conversion of PCE to CO2. In conclusion, the use of reducing agents to enhance Fe(II)/Fe(III) catalyzed SPC oxidation appears to be a promising approach for the rapid degradation of organic contaminants in groundwater.
AB - In this study, the effects of reducing agents on the degradation of tetrachloroethene (PCE) were investigated in the Fe(II)/Fe(III) catalyzed sodium percarbonate (SPC) system. The addition of reducing agents, including hydroxylamine hydrochloride, sodium sulfite, ascorbic acid and sodium ascorbate, accelerated the Fe(III)/Fe(II) redox cycle, leading to a relatively steady Fe(II) concentration and higher production of free radicals. This, in turn, resulted in enhanced PCE oxidation by SPC, with almost complete PCE removal obtained for appropriate Fe and SPC concentrations. The chemical probe tests, using nitrobenzene and carbon tetrachloride, demonstrated that HO was the predominant radical in the system and that O2- played a minor role, which was further confirmed by the results of electron spin resonance measurements. PCE degradation decreased significantly with the addition of isopropanol, a HO scavenger, supporting the hypothesis that HO was primarily responsible for PCE degradation. It is noteworthy that Cl- release was slightly delayed in the first 20min, indicating that intermediate products were produced. However, these intermediates were further degraded, resulting in the complete conversion of PCE to CO2. In conclusion, the use of reducing agents to enhance Fe(II)/Fe(III) catalyzed SPC oxidation appears to be a promising approach for the rapid degradation of organic contaminants in groundwater.
KW - Hydroxyl radical (HO)
KW - Reducing agents
KW - Sodium percarbonate (SPC)
KW - Tetrachloroethene (PCE)
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U2 - 10.1016/j.jhazmat.2015.07.047
DO - 10.1016/j.jhazmat.2015.07.047
M3 - Article
C2 - 26257094
AN - SCOPUS:84940039289
SN - 0304-3894
VL - 300
SP - 530
EP - 537
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
ER -