Promoting mechanism of SO2 and NO adsorption on activated carbon at sub-zero temperature

被引:0
|
作者
Zhang, Zhichao [1 ]
Liu, Yuan [1 ]
Xiao, Yi [1 ]
Wang, Jiawei [1 ]
Wang, Tao [1 ]
Zhang, Yongsheng [1 ]
Xiao, Ping [2 ]
Wang, Shiqing [3 ]
Wang, Yutong [2 ]
Min, Fanfei [4 ]
Pan, Weiping [1 ]
机构
[1] North China Elect Power Univ, Key Lab Power Stn Energy Transfer Convers & Syst, Minist Educ, Beijing 102206, Peoples R China
[2] Huaneng Clean Energy Res Inst, Beijing 102209, Peoples R China
[3] Natl Key Lab High Efficiency Flexible Coal Power G, Beijing 102209, Peoples R China
[4] Anhui Univ Sci & Technol, Sch Mat Sci & Engn, Anhui 232001, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Low-temperature adsorption; Pore structure; Molecular dynamics simulations; POROUS CARBONS; SPECTROSCOPY;
D O I
10.1016/j.jece.2024.114907
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The adsorption of SOS and NO on activated carbon (AC) was studied between -40 degrees C and 20 degrees C. The results showed that the adsorption capacity of AC-2-750 (AC reacted with a 2:1 ratio of KOH at 750 degrees C) for SO2 and NO were 374.2 mg/g and 83.1 mg/g at -40 degrees C, respectively. As the temperature decreased, the van der Waals and electrostatic forces strengthened while molecular movements weakened, favouring low-temperature adsorption. During co-adsorption, SO2 was preferentially adsorbed in ultramicropores, whereas NO was primarily adsorbed in supermicropores. When NO was oxidised to NO2, it occupied the original adsorption sites of SO2, leading to a reduction in SO2 adsorption. The presence of NO2 favoured the adsorption of the entire system. This study provided directions for the design of activated carbon for LAS (low-temperature adsorption) technology and illustrated its mechanism at the microscopic level.
引用
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页数:15
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