Effect of framework Si/Al ratio on the adsorption mechanism of CO2 on small-pore zeolites: II. Merlinoite

吸附 机制(生物学) 化学工程 化学 材料科学 物理化学 物理 工程类 量子力学
作者
Hyun June Choi,Donghui Jo,Suk Bong Hong
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:446: 137100-137100 被引量:13
标识
DOI:10.1016/j.cej.2022.137100
摘要

• Potassium merlinoite with Si/Al = 2.9 is synthesized via a seeding method. • Its CO 2 adsorption behavior is operated by a cooperative cation gating-breathing mechanism. • The adsorption mechanism on small-pore zeolites varies with their framework Al content. • The adsorption mechanism can also differ according to zeolite framework topology. Potassium merlinoite with a framework Si/Al ratio of 2.9 (K-MER-2.9) is synthesized using K-MER with a higher Si/Al ratio of 3.8 (K-MER-3.8) as seed crystals. The CO 2 adsorption properties of K-MER-2.9 are investigated at 25–45 °C and 0–1.0 bar and compared with four other K-MER zeolites with different Si/Al ratios (1.7–4.2) in order to investigate the effect of framework Si/Al ratio (or extraframework cation content) on the CO 2 adsorption mechanism on MER-type zeolites. While the CO 2 uptake (0.8 mmol g −1 ) at 25 °C and 1.0 bar of K-MER-1.7 is negligible, due to a large number of gating cations occupying the 8-membered ring windows, the opposite holds for the uptakes (3.0–3.8 mmol g −1 ) of K-MER-2.3, K-MER-2.9, K-MER-3.8, and K-MER-4.2. In addition, while the former two zeolites show a clear one step adsorption isotherm but at different CO 2 partial pressures, the latter two ones exhibit steep CO 2 adsorption from a low pressure. Structural analysis reveals that the gating cations with high site occupancy in dehydrated K-MER-2.9 relocate upon CO 2 adsorption, which is accompanied by the distinct framework relaxation, i.e., the cooperative cation gating-breathing mechanism like the case of K-MER-2.3, but with the latter effect being more dominant. In contrast, the CO 2 adsorption behavior of K-MER-3.8 and K-MER-4.2 can be explained by the breathing and molecular sieving effects, respectively. These findings extend and confirm our recent report that CO 2 adsorption mechanism on small-pore zeolites can differ notably according to the framework Al content, as well as the framework topology.
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