Post modification of Oxo-clusters in robust Zirconium-Based metal organic framework for durable SO2 capture from flue gas

被引:38
|
作者
Zhang, Zhonghui [1 ]
Yang, Bolun [1 ]
Wu, Yue [1 ]
Zhang, Wenxiang [1 ]
Ma, Heping [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Chem Engn & Technol, 28 Xianning West Rd, Xian 710049, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic framework; Post modification; Sulfur dioxide sorption; Flue gas desulfurization; ADSORPTION; CO2;
D O I
10.1016/j.seppur.2021.119349
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The efficient capture of SO2 after the combustion of fossil fuels is of great challenge as the low SO2 concentration (<500 ppm) and coexisting with CO2, water, O-2 in flue gas. Robust zirconium-based MOFs possessing accessible polar sites usually have high SO2 adsorption capacity but poor durably in adsorption desulfurization due to the acidic sulfate deposition on the Zr-O cluster. Herein, a Zr-O cluster post-modification method was introduced in a Zr-MOF (MOF-808) to form EDTA-MOF-808 (EDTA, ethylene diaminetetraacetic acid) for selective and durable removal of SO2. The introduction of EDTA not only improve their SO2 adsorption capacity, but also sharply increase their SO2/CO2 selectivity (57.2 vs 8.9) and SO2/N-2 selectivity (1915.8 vs 292.7) at low SO2 partial pressure. Moreover, the synergistic effects of dipole and hydrogen bonding interaction between SO2 and EDTA in EDTA-MOF-808 make the capture of SO2 in a reversible manner, which can prevent the formation of S(VI) species in Zr-MOF. DFT calculation confirmed that SO2 was interacted with EDTA through moderate dipole-dipole interaction (S(SO2) with N(EDTA)) and hydrogen bonds (H(-COOH) with O(SO2)). Systematic investigations including thermodynamic SO2 adsorption, dynamic breakthrough experiments, stability tests and DFT-calculations in both MOF-808 and EDTA-MOF-808 confirmed the efficient performance of post modification of Zr-O clusters with EDTA in Zr-MOFs for durable SO2 capture.
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页数:10
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