烟气脱硫
微型多孔材料
吸附
沸石
烟气
化学工程
材料科学
多孔性
选择性
多孔介质
动力学
选择性吸附
催化作用
硫黄
精炼(冶金)
无机化学
体积流量
化学动力学
作者
Xiao‐Hong Xiong,Xiang‐Qiong Jiang,Liang Song,Jia‐Pei Qiu,Yu‐Yan Yao,Xiao‐Chun Huang,Jiu‐Xing Jiang,Zhang‐Wen Wei,Cheng‐Yong Su
出处
期刊:Small
[Wiley]
日期:2026-01-27
卷期号:22 (17): e13934-e13934
标识
DOI:10.1002/smll.202513934
摘要
ABSTRACT The development of exceptionally stable porous solid physisorbents is vital for deep flue gas desulfurization (FGD) and SO 2 recovery, as the corrosive and reactive nature of SO 2 restricts the applicability of most porous materials in this demanding scenario. Herein, we report the synthesis of microporous SSZ‐13 zeolite to obtain the exceedingly stable Na‐SSZ‐13 with low‐Si/Al‐ratio (5:1), and systematically evaluate its dynamic SO 2 adsorption performance. Na‐SSZ‐13 exhibits excellent water, thermal, and chemical stability, high SO 2 affinity and adsorption kinetics with extraordinary SO 2 /CO 2 separation selectivity (2673 at zero coverage, 298 K), and exceptional low‐concentration SO 2 adsorption capacity (4.6/2.7 mmol g −1 at 0.1/0.002 bar) with the highest surface‐specific SO 2 uptake among reported zeolites. Column breakthrough experiments demonstrate efficient SO 2 capture capability from a quaternary flue‐gas mixture at high temperature (323 – 423 K). Moreover, it achieves 96.5% purity of the recovered SO 2 during the regeneration process, and shows fully reversible SO 2 uptake and excellent cycling stability. GCMC simulations, DFT calculations, and in situ DRIFT analyses reveal a selective SO 2 adsorption mechanism with the counter‐cations (Na + ) serving as primary SO 2 adsorption sites, elucidating the role of cation···SO 2 interactions that underpin the application of zeolite‐based materials for deep FGD under high‐temperature and low‐concentration working conditions.
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