Fluorido-bridged iron-based metal-organic frameworks for carbon dioxide capture in humid flue gas

被引:0
|
作者
Wang, Xin-Yue [1 ]
Gu, Yi-Ming [2 ]
Zong, Xu-Peng [2 ]
Zhao, Sheng-Sheng [2 ]
Wang, Shu-Dong [2 ]
机构
[1] Univ Sci & Technol China, Hefei 230026, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
关键词
Metal-organic frameworks; Carbon capture; CO2; /N2; separation; Moisture; Adsorbent; INITIO MOLECULAR-DYNAMICS; TOTAL-ENERGY CALCULATIONS; CO2; CAPTURE; ADSORPTION; SEPARATION; ENHANCEMENT; TRANSITION; N-2; MOF; CH4;
D O I
10.1016/j.fuel.2024.131669
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
The inevitable combustion of fossil fuels in human industrial activities results in significant greenhouse gas emissions, leading to the pressing challenge of CO2/N2 separation in humid flue gas. Iron-based Metal-organic frameworks (MOFs) have proven to be cheap, robust against water vapor attack due to the enhanced coordination bonds. In this study, we present two distinct MOFs i.e., DNL-9(Fe) and PCN-233(FeMII), constructed by Fe clusters and 2,5-furandicarboxylic acid ligands. Static adsorption experiments revealed that DNL-9(Fe), featuring an exclusive Fe-F-Fe spiral packing structure, exhibited higher surface areas and enhanced CO2 adsorption performance that outcompeted PCN-233 candidates. DNL-9(Fe) demonstrated a high IAST selectivity of CO2/N2 at 247 (15/85, v/v, P/P0 = 0.01), superior to the most of state-of-the-art Fe-MOFs reported up to date. The further theoretical calculations elucidated the binding sites of the framework with CO2 molecules. Importantly, DNL-9(Fe) showed sufficient water stability and cyclic separation, as confirmed by dynamic breakthrough tests, indicating it as a promising candidate for practical CO2 capture from humid flue gas.
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页数:9
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