Electrogeneration of hydrogen peroxide for electro-Fenton system by oxygen reduction using chemically modified graphite felt cathode
Electrogeneration of hydrogen peroxide for electro-Fenton system by oxygen reduction using chemically modified graphite felt cathode
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化学改性石墨毡阴极氧还原电 Fenton 系统电产生过氧化氢
DOI:
10.1016/j.seppur.2013.03.038
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发表时间:
2013-06
影响因子:
8.6
通讯作者:
Zhou M.H.
中科院分区:
文献类型:
--
作者:
Zhang C.;Bi Z.H.;Jin T.;Zhou M.H.
A simple chemical method using hydrazine hydrate as the main reagent was firstly used to modify graphite felt as cathode for efficient electro-Fenton process. The influences of the different concentration of hydrazine hydrate were comparatively studied on the yield and current efficiency of H2O2production, confirming that the modified cathode had much higher electrocatalytic activity. The optimum concentration of the hydrazine hydrate was 10%, and the yield of H2O2was as 2.6 times as that without modification under the same conditions. The cyclic voltammetry analysis indicated that the modified cathodes exhibited stronger current responses and more negative hydrogen evolution potentials than the unmodified one. The operational parameters such as cathodic potential, pH and O2flow rate were optimized for the efficient H2O2electrogeneration. The maximum accumulation of H2O2, up to 247.2mg/L, was obtained at −0.75V (vs. SCE) and O2flow rate of 0.4L/min. The influence of pH on the yield of H2O2was slight, but it was obvious on current efficiency. The modified cathode was confirmed to be more efficient in degradation of p-nitrophenol by electro-Fenton process at both acidic and neutral pH, indicating the positive effect of chemical modification onto the performance.
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影响因子:
12.8
作者:
Qiang, ZM;Chang, JH;Huang, CP
通讯作者:
Huang, CP
影响因子:
6.6
作者:
M. Zarei;D. Salari;Aligoli Niaei;A. Khataee
通讯作者:
M. Zarei;D. Salari;Aligoli Niaei;A. Khataee
影响因子:
6.6
作者:
Panizza, Marco;Oturan, Mehmet A.
通讯作者:
Oturan, Mehmet A.
影响因子:
13.6
作者:
Chu, Y. Y.;Qian, Y.;Deng, X. L.
通讯作者:
Deng, X. L.
影响因子:
13.6
作者:
Ming-hua Zhou;Qin-Bo Tan;Qian Wang;Yongli Jiao;N. Oturan;M. Oturan
通讯作者:
Ming-hua Zhou;Qin-Bo Tan;Qian Wang;Yongli Jiao;N. Oturan;M. Oturan