Abstract
Hydrothermal and catalytic stability of UIO-66 MOFs with defective structures are critical aspects to be considered in their catalytic applications, especially under the conditions involving water, moisture and/or heat. Here, we report a facile strategy to introduce the macromolecular acid group to UIO-66 to improve the stability of the resulting UIO-66—PhSO3H MOF in aqueous phase catalysis. In detail, UIO-66—PhSO3H was obtained by grafting benzenesulfonic acid on the surface of the pristine UIO-66 to introduce the hydrophobicity, as well as the Brønsted acidity, then assessed using catalytic hydrolysis of cyclohexyl acetate (to cyclohexanol) in water. The introduction of hydrophobic molecules to UIO-66 could prevent the material from being attacked by hydroxyl polar molecules effectively, explaining its good structural stability during catalysis. UIO-66—PhSO3H promoted the conversion of cyclohexyl acetate at ca. 87%, and its activity and textural properties were basically intact after the cyclic stability tests. The facile modification strategy can improve the hydrothermal stability of UIO-66 significantly, which can expand its catalytic applications in aqueous systems.[Figure not available: see fulltext.]
| Original language | English |
|---|---|
| Pages (from-to) | 1389-1398 |
| Number of pages | 10 |
| Journal | Frontiers of Chemical Science and Engineering |
| Volume | 17 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - Oct 2023 |
Free Keywords
- Brønsted acidity
- UIO-66
- hydrolysis of cyclohexyl acetate
- hydrophobicity
- metal—organic frameworks (MOFs)
ASJC Scopus subject areas
- General Chemical Engineering