Co3O4-based catalysts derived from natural wood with hierarchical structure for elemental mercury oxidation

被引:12
|
作者
Zhang, Xiaopeng [1 ,2 ]
Zhang, Hang [1 ,2 ]
Song, Xinxin [1 ,2 ]
Han, Xiangkai [1 ,2 ]
Bao, Junjiang [1 ,2 ]
Zhang, Ning [1 ,2 ]
He, Gaohong [1 ,2 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116023, Peoples R China
[2] Dalian Univ Technol, Sch Chem Engn, Panjin 124221, Peoples R China
基金
中国国家自然科学基金;
关键词
Natural wood-derived chars; Vessel structure; 3D porous framework; Elemental mercury; Oxidation; SIMULATED FLUE-GAS; FLY-ASH; SIMULTANEOUS NO; HG-0; OXIDATION; MNOX CATALYSTS; ACTIVATED COKE; REMOVAL; COAL; ADSORPTION; CARBON;
D O I
10.1016/j.joei.2020.09.012
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Wood vessel in natural wood (NW) as the channel for water and inorganic salt transport has a natural aligned microchannel structure and a great hydrophily. In the present work, NW was used as catalyst support which was directly impregnated in Co(NO3)(2) solution and then calcined in N-2 atmosphere to prepare a catalyst (denoted as Co/NWBC-OS), which was called a one-step calcination method. For comparison, NW biochar (NWBC) derived from pyrolytic NW was also impregnated in Co(NO3)(2) solution and calcined in N-2 atmosphere to prepare catalyst (denoted as Co/NWBC-TS), which was called a twostep calcination method. Characterization results reveal that NW possesses a greater hydrophily and wettability than NWBC, which is beneficial to impregnation process resulting in a better active components dispersion. In the meanwhile, Co/NWBC-OS has a higher Co3+/Co2+ ratio and more surface chemisorbed oxygen. The higher Co3+/Co2+ ratio can generate more oxygen vacancies which can capture and activate gaseous oxygen to form more surface chemisorbed oxygen. Surface chemisorbed oxygen as the main active site can greatly promote Hg-0 removal performance. These results lead to an excellent Hg-0 removal efficiency of Co/NWBC-OS which is 99% at 180 degrees C. Additionally, O-2 and NO can promote the Hg-0 removal process whereas H2O, SO2 and NH3 exert an obviously prohibited effect on Hg0 removal performance. (C) 2020 Energy Institute. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:285 / 293
页数:9
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