A novel nano-sized Co3O4@C catalyst derived from Co-MOF template for efficient Hg0 removal at low temperatures with outstanding SO2 resistance

被引:0
作者
Jiacheng Zhou
Qicheng Shen
Jie Yang
Muhammad Tariq
Wei Sun
Limei Cao
Ji Yang
机构
[1] East China University of Science and Technology,School of Resources and Environmental Engineering, State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process
[2] Chinese Academy of Sciences (CAS),Division of Advanced Nanomaterials, Suzhou Institute of Nano
[3] Hainan University,tech and Nano
[4] Shanghai Institute of Pollution Control and Ecological Security,bionics
来源
Environmental Science and Pollution Research | 2021年 / 28卷
关键词
Co; O; @C; Hg; removal; MOFs; Sulfur resistance;
D O I
暂无
中图分类号
学科分类号
摘要
Co3O4 is a promising Hg0 removal catalyst for industrial application. Operating temperature and low sulfur resistance are two of the main problems that hinder its industrial application in Hg0 removal. Herein, a metal-organic framework (Co-BDC) was introduced as a sacrificial template to obtain the catalyst nano-sized Co3O4@C by calcination. Part of the organic ligands is carbonized during the calcination. Carbon wrapped Co3O4 and reduced metal agglomeration. The optimal Hg0 removal temperature of the existing cobalt oxide catalysts was always around 150 °C, but H2-TPR showed that the oxygen atoms on the Co3O4@C were more active than those on Co3O4, causing the Hg0 removal temperature window of Co3O4@C to shift to lower temperatures. The Hg0 removal efficiency of Co3O4@C could reach almost 100% even at 25 °C. In the meanwhile, Co3O4@C also showed a strong SO2 resistance at ambient temperature. Experimental results and characterization proved that SO2 did not compete with Hg0 on the surface of Co3O4 at low temperatures. On the contrary, it participated in the oxidation of Hg0. This is a great improvement for Co3O4 catalyst in Hg0 removal. It reduces the restrictions on the application of Co3O4 in Hg0 removal. Co3O4@C shows considerable potential as an Hg0 removal catalyst.
引用
收藏
页码:65487 / 65498
页数:11
相关论文
共 258 条
[1]  
Bisson TM(2015)Potential hazards of brominated carbon sorbents for mercury emission control Environ Sci Technol 49 2496-2502
[2]  
Xu Z(1998)Chemical and mechanistic aspects of the selective catalytic reduction of NOx by ammonia over oxide catalysts: a review Appl Catal B Environ 18 1-36
[3]  
Busca G(2017)Silica-silver nanocomposites as regenerable sorbents for Hg(0) removal from flue gases Environ Sci Technol 51 11909-11917
[4]  
Lietti L(2019)MOFs-derived ultrathin holey Co3O4 nanosheets for enhanced visible light CO2 reduction Appl Catal B-Environ 244 996-1003
[5]  
Ramis G(2016)Novel effective catalyst for elemental mercury removal from coal-fired flue gas and the mechanism investigation Environ Sci Technol 50 2564-2572
[6]  
Berti F(2020)Transformation and removal of ammonium sulfate aerosols and ammonia slip from selective catalytic reduction in wet flue gas desulfurization system J Environ Sci 88 72-80
[7]  
Cao T(2017)Co@Carbon and Co 3 O4@Carbon nanocomposites derived from a single MOF for supercapacitors Sci Rep 7 12588-296
[8]  
Li Z(2019)Dramatic promotion of visible-light photoreactivity of TiO2 hollow microspheres towards NO oxidation by introduction of oxygen vacancy Appl Catal B Environ 256 117860-1166
[9]  
Xiong Y(2018)Investigation and simulation of the transport of gas containing mercury in microporous silica membranes Chem Eng Sci 190 286-5591
[10]  
Yang Y(2010)Low-temperature selective catalytic reduction of NO with NH(3) over Mn-Ce oxides supported on TiO2 and Al2O3: a comparative study Chemosphere 78 1160-7400