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Enhanced Catalytic Performance of UiO-67 Supported Pd Catalyst for Toluene Degradation
Owing to the intrinsic nature of the uniformed topologies and ultrasmall Zr 6 nodes of Zr-MOFs, herein, we employed Zr-MOFs (UiO-66 and UiO-67), as opposed to the support of traditional ZrO 2 , to prepare the Pd catalysts for toluene degradation. Compared with the catalysts of Pd/UiO-66 and Pd/ZrO 2...
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Published in: | Catalysis letters 2024-09, Vol.154 (9), p.5223-5235 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Owing to the intrinsic nature of the uniformed topologies and ultrasmall Zr
6
nodes of Zr-MOFs, herein, we employed Zr-MOFs (UiO-66 and UiO-67), as opposed to the support of traditional ZrO
2
, to prepare the Pd catalysts for toluene degradation. Compared with the catalysts of Pd/UiO-66 and Pd/ZrO
2
, Pd/UiO-67 catalyst boosted an excellence catalytic performance for toluene degradation, giving the lowest T
90%
value of 235 °C with long-term stability. With the assisting of the cavity confinement of Zr-MOFs, Pd nanoparticles are prone to be encapsulated in the 3D frameworks of Zr-MOFs, and the bigger micropores of UiO-67 are more conducive to the formation of larger Pd nanoparticles. The
in situ
FT-IR results further declared that although the active sites are partly sacrificed due to the larger Pd nanoparticles formed in UiO-67, the stable adsorbed toluene on Pd/UiO-67 boosted the quick degradation of toluene in the reaction interval even without undergoing intermediate processes of benzoate and benzaldehyde.
Graphical Abstract
UiO-66, UiO-67 and ZrO
2
were employed to prepare the Pd catalysts for toluene degradation, Pd/UiO-67 catalyst boosted an excellence catalytic performance with long-term stability. |
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ISSN: | 1011-372X 1572-879X |
DOI: | 10.1007/s10562-024-04712-z |