TY - JOUR
T1 - Benzenesulfonic acid-grafted UIO-66 with improved hydrophobicity as a stable Brønsted acid catalyst
AU - Kou, Zongliang
AU - Sun, Guanlun
AU - Ding, Qiuyan
AU - Li, Hong
AU - Gao, Xin
AU - Fan, Xiaolei
AU - Ou, Xiaoxia
AU - Pan, Qinhe
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/10
Y1 - 2023/10
N2 - 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.]
AB - 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.]
KW - Brønsted acidity
KW - UIO-66
KW - hydrolysis of cyclohexyl acetate
KW - hydrophobicity
KW - metal—organic frameworks (MOFs)
UR - http://www.scopus.com/inward/record.url?scp=85152711728&partnerID=8YFLogxK
U2 - 10.1007/s11705-022-2285-5
DO - 10.1007/s11705-022-2285-5
M3 - Article
AN - SCOPUS:85152711728
SN - 2095-0179
VL - 17
SP - 1389
EP - 1398
JO - Frontiers of Chemical Science and Engineering
JF - Frontiers of Chemical Science and Engineering
IS - 10
ER -