共 50 条
Elemental Mercury Removal by MnO2 Nanoparticle-Decorated Carbon Nitride Nanosheet
被引:60
作者:

Liu, Dongjing
论文数: 0 引用数: 0
h-index: 0
机构:
Jiangsu Univ, Sch Energy & Power Engn, Zhenjiang 212013, Jiangsu, Peoples R China Jiangsu Univ, Sch Energy & Power Engn, Zhenjiang 212013, Jiangsu, Peoples R China

Zhang, Zhen
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h-index: 0
机构:
Shanghai Univ Elect Power, Coll Energy & Mech Engn, Shanghai 200090, Peoples R China Jiangsu Univ, Sch Energy & Power Engn, Zhenjiang 212013, Jiangsu, Peoples R China

Wu, Jiang
论文数: 0 引用数: 0
h-index: 0
机构:
Shanghai Univ Elect Power, Coll Energy & Mech Engn, Shanghai 200090, Peoples R China Jiangsu Univ, Sch Energy & Power Engn, Zhenjiang 212013, Jiangsu, Peoples R China
机构:
[1] Jiangsu Univ, Sch Energy & Power Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Shanghai Univ Elect Power, Coll Energy & Mech Engn, Shanghai 200090, Peoples R China
基金:
中国国家自然科学基金;
关键词:
CATALYTIC-OXIDATION;
VISIBLE-LIGHT;
ADSORPTION;
G-C3N4;
REDUCTION;
CAPTURE;
CHARS;
OXIDE;
HG-0;
COMPOSITE;
D O I:
10.1021/acs.energyfuels.9b00149
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:
Carbon nitride nanosheet (CNNS) is facilely synthesized via a two-step thermal oxidative etching approach and then decorated with MnO2 nanoparticles via incipient wetness impregnation method for Hg-0 removal at low temperature. Pristine CNNS exhibits a good Hg-0 adsorption performance associated with the optimal He removal efficiency of similar to 65.8% at 150 degrees C due to its two-dimensional planar structure and big surface area. MnO2 decoration can greatly enhance the Hg-0 removal performance of CNNS, presumably ascribed to the improved electron transfer at the interface of MnO2 and g-C3N4. 10MnO(2)/CNNS presents a superior Hg-0 oxidation ability with He removal efficiencies all above 91% within the temperature range of 90-240 degrees C. The long-term test and XPS analysis disclose that 10MnO(2)/CNNS is a cost-effective catalyst/sorbent for oxidation removal of elemental mercury. The gaseous He is oxidized into Hg-0 by the lattice oxygen of MnO2, which is the dominant active site for Hg-0 oxidation via redox couple of Mn4+/Mn3+.
引用
收藏
页码:3089 / 3097
页数:9
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