Abstract

The robust cucurbituril-MOF composite CB6@MIL-101-Cl was synthesized by a wet impregnation method and a concomitant OH-to-Cl ligand exchange {CB6 = cucurbit[6]uril, 31 wt% content in the composite, MIL-101-Cl = [Cr3(O)Cl(H2O)2(BDC)3], BDC = benzene-1,4-dicarboxylate}. MIL-101-Cl was formed postsynthetically from standard fluorine-free MIL-101 where Cr-OH ligands were substituted by Cl during treatment with HCl. CB6@MIL-101-Cl combines the strong SO2 affinity of the rigid CB6 macrocycles and the high SO2 uptake capacity of MIL-101, and shows a high SO2 uptake of 438 cm3 g-1 (19.5 mmol g-1) at 1 bar and 293 K (380 cm3 g-1, 17.0 mmol g-1 at 1 bar and 298 K). The captured SO2 amount is 2.2 mmol g-1 for CB6@MIL-101-Cl at 0.01 bar and 293 K (2.0 mmol g-1 at 298 K), which is three times higher than that of the parent MIL-101 (0.7 mmol g-1) under the same conditions. The near zero-coverage SO2 adsorption enthalpies of MIL-101 and CB6@MIL-101-Cl are -35 kJ mol-1 and -50 kJ mol-1, respectively, reflecting the impact of the incorporated CB6 macrocycles, having higher affinity towards SO2. FT-IR spectroscopy confirms the interactions of the SO2 with the cucurbit[6]uril moieties of the CB6@MIL-101-Cl composite and SO2 retention for a few minutes under ambient air. Comparative experiments demonstrated loss of crystallinity and porosity after dry SO2 adsorption for MIL-101, while CB6@MIL-101-Cl exhibits nearly complete retention of crystallinity and porosity under the exposure to both dry and wet SO2. Thus, CB6@MIL-101-Cl can be an attractive adsorbent for SO2 capture because of its excellent recycling stability, high capacity and strong affinity toward SO2 at low pressure.

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