Three-dimensional porous CuO-modified CeO2-Al2O3 catalysts with chlorine resistance for simultaneous catalytic oxidation of chlorobenzene and mercury: Cu-Ce interaction and structure

被引:24
作者
Yan, Xin [1 ,2 ]
Zhao, Lingkui [1 ,2 ]
Huang, Yan [1 ,2 ]
Zhang, Junfeng [1 ,2 ]
Jiang, Su [1 ,2 ]
机构
[1] Xiangtan Univ, Coll Environm & Resources, Xiangtan 411105, Peoples R China
[2] Hunan Prov Environm Protect Engn Technol Ctr Air C, Xiangtan 411105, Peoples R China
基金
中国国家自然科学基金;
关键词
Simultaneous catalytic oxidation; Chlorobenzene and mercury; Three-dimensional porous; Chlorine resistance; SIMULTANEOUS REMOVAL; FLUE-GAS; NO; HG-0; COMBUSTION; REDUCTION; CERIA;
D O I
10.1016/j.jhazmat.2023.131585
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Chlorine poisoning effects are still challenging to develop efficient catalysts for applications in chlorobenzene (CB) and mercury (Hg0) oxidation. Herein, three-dimensional porous CuO-modified CeO2-Al2O3 catalysts with macroporous framework and mesoporous walls prepared via a dual template method were employed to study simultaneous oxidation of CB and Hg0. CuO-modified CeO2-Al2O3 catalysts with three-dimensional porous structure exhibited outstanding activity and stability for simultaneous catalytic oxidation of CB and Hg0. The results demonstrated that the addition of CuO into CeO2-Al2O3 can simultaneously enhance the acid sites and redox properties through the electronic inductive effect between CuO and CeO2 (Cu2+ + Ce3+ <-> Cu+ + Ce4+). Importantly, the synergistic effect between Cu and Ce species can induce abundant oxygen vacancies formation, produce more reactive oxygen species and facilitate oxygen migration, which is beneficial for the deep oxidation of chlorinated intermediates. Moreover, macroporous framework and mesoporous nanostructure dramatically improved the specific surface area for enhancing the contact efficiency between reactants and active sites, leading to a remarkable decrease of byproducts deposition. CB and Hg0 had function of mutual promotion in this reaction system. In tune with the experimental results, the possible mechanistic pathways for simultaneous catalytic oxidation of CB and Hg0 were proposed.
引用
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页数:14
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