Manganese oxide nanorods as a robust Fenton-like catalyst at neutral pH: Crystal phase-dependent behavior

被引:81
作者
Kim, Eun-Ju [1 ,3 ]
Oh, Dasom [1 ]
Lee, Chung-Seop [1 ]
Gong, Jianyu [1 ]
Kim, Jungwon [2 ]
Chang, Yoon-Seok [1 ]
机构
[1] POSTECH, Sch Environm Sci & Engn, Pohang 790784, South Korea
[2] Hallym Univ, Dept Environm Sci & Biotechnol, Chunchon 200702, South Korea
[3] KIST, Ctr Water Resource Cycle Res, Seoul 136791, South Korea
基金
新加坡国家研究基金会;
关键词
Manganese oxides; Fenton-like oxidation; H2O2; activation; Neutral medium; Hydroxyl radicals; HYDROGEN-PEROXIDE DECOMPOSITION; ADVANCED OXIDATION PROCESSES; METHYLENE-BLUE; IRON-OXIDE; AZO DYES; DEGRADATION; KINETICS; DECOLORIZATION; NANOPARTICLES; PHENOL;
D O I
10.1016/j.cattod.2016.03.034
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Manganese oxide nanorods with different crystal phases (alpha-, beta-, and delta-MnO2) were prepared via a mild hydrothermal method, and examined as heterogeneous catalysts for the decomposition of H2O2 into active radicals and concomitant degradation of methylene blue (MB) dye at neutral pH. The catalytic activity of MnO2 nanorods was highly dependent upon their crystal structures, following the order of gamma-MnO2 > beta-MnO2 > alpha-MnO2 > delta-MnO2. Complete degradation of MB was achieved with gamma-MnO2 in a short duration of 20 min. Furthermore, gamma-MnO2 exhibited much higher activity compared to iron-containing nanoparticles (Fe degrees and Fe3O4) and several reported catalysts in the literature. The observed trend in catalyst performance was discussed in terms of surface area, degree of crystallinity, and exposed facets. It was found that gamma-MnO2 showed considerable activity over a broad range of pH and temperature as well as desired reusability for four consecutive cycles. Quenching studies indicated that hydroxyl radicals ((OH)-O-center dot) played a major role in the degradation of MB. These results provide important insight into the design of more efficient manganese oxide catalysts for wastewater treatment. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:71 / 76
页数:6
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