Abstract
Vanadium nitride was firstly applied to oxidative desulfurization (ODS) of liquid fuel. Carbon-supported vanadium nitride (VN@C) was prepared from pyrolysis of urea-loaded MOF, MIL-100(V), especially in the absence of external ammonia flow. One catalyst prepared at 1100 °C, VN@C(1100), had the highest turnover frequency of 18.8 h−1 (with a very low activation energy of 29.9 kJmol-1) among the reported vanadium-based catalysts. The ESR and scavenger experiments confirmed •OH radical was the active species for the ODS. Calculations using density functional theory could support the beneficial role of VN (compared with conventional oxides) both in the adsorption of H2O2 and •OH and H2O2 activation to form •OH radical. The VN@C(1100) catalyst could be used for five cycles without any loss in activity. Therefore, supported vanadium nitrides could be suggested as a potential catalyst for oxidations that use H2O2 as an oxidant. Moreover, supported vanadium nitrides could be facilely derived from the pyrolysis of urea-loaded V-based MOFs, without ammonia flow.
Original language | English |
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Article number | 135509 |
Journal | Journal of Cleaner Production |
Volume | 384 |
DOIs | |
State | Published - 15 Jan 2023 |
Keywords
- Metal-organic frameworks
- Oxidative desulfurization
- Pyrolysis
- Vanadium nitride
- •OH radical