Synergistic catalysis of Co3O4 and graphene oxide on Co3O4/GO catalysts for degradation of Orange II in water by advanced oxidation technology based on sulfate radicals

被引:200
|
作者
Shi, Penghui [1 ,3 ]
Dai, Xianfeng [2 ]
Zheng, Hongai [1 ,3 ]
Li, Dengxin [3 ]
Yao, Weifeng [1 ]
Hu, Chenyan [1 ]
机构
[1] Shanghai Univ Elect Power, Coll Environm & Chem Engn, Shanghai 200090, Peoples R China
[2] Shanghai Maple Automobile Co Ltd, Shanghai 201501, Peoples R China
[3] Donghua Univ, Coll Environm Sci & Engn, Shanghai 201620, Peoples R China
基金
中国国家自然科学基金;
关键词
Synergistic catalysis; Graphene oxide; Co3O4; Co-OH complexes; OXYGEN REDUCTION REACTION; COBALT OXIDE; HETEROGENEOUS ACTIVATION; THIN-FILMS; NANOPARTICLES; CARBON; PERFORMANCE; COMPOSITE; ACID; NANOCOMPOSITES;
D O I
10.1016/j.cej.2013.11.089
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, the synergistic catalytic mechanism of Co3O4 and graphene oxide (GO) nanocomposite in the heterogeneous activation of peroxymonosulfate (PMS) to generate sulfate radicals was studied. The activation of Co3O4/GO with different Co3O4 loadings in the catalyst [bare graphene oxide (GO), 20% Co3O4/GO, 30% Co3O4/GO, 50% Co3O4/GO, 70% Co3O4/GO, 90% Co3O4/GO, 95% Co3O4/GO, and pure Co3O4] were tested though the degradation of Orange II in water. The results show that the highest performance achieved using the Co3O4/GO catalyst was based on a synergistic catalysis between Co3O4 and GO. Furthermore, a proportional relation exists between Co3O4 and the catalyst. The highest catalytic activity is observed when the Co3O4 loading was about 50% in the catalyst. Co-OH complexes form on the surface of the GO sheet through the direct interaction of Co species with nearby hydroxyl groups or through the dissociation of H2O with Co2+. The formation is proposed to facilitate the heterogeneous activation of PMS. However, a high Co3O4 loading on the GO surface prevents the formation of Co-OH complexes, which is important in the catalytic reaction. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:264 / 270
页数:7
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