Carbon-supported vanadium nitride catalyst, prepared from urea-loaded MIL-100(V) in the absence of external ammonia flow, having good performance in oxidative desulfurization

被引:16
作者
Ahmed, Imteaz [1 ,2 ]
Kim, Chul-Ung [3 ]
Jhung, Sung Hwa [1 ,2 ]
机构
[1] Kyungpook Natl Univ, Dept Chem, Daegu 41566, South Korea
[2] Kyungpook Natl Univ, Green Nano Mat Res Ctr, Daegu 41566, South Korea
[3] Korea Res Inst Chem Technol KRICT, Chem & Proc Technol Div, POB 107,141 Gajeong Ro, Daejeon 34114, South Korea
基金
新加坡国家研究基金会;
关键词
Metal-organic frameworks; OH radical; Oxidative desulfurization; Pyrolysis; Vanadium nitride; METAL-ORGANIC FRAMEWORK; HIGHLY-ACTIVE CATALYST; DOPED CARBON; DIESEL FUEL; OXIDE; DENITROGENATION; TEMPERATURE; GRAPHENE; OIL;
D O I
10.1016/j.jclepro.2022.135509
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Vanadium nitride was firstly applied to oxidative desulfurization (ODS) of liquid fuel. Carbon-supported vana-dium 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 degrees 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 center dot 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 center dot OH and H2O2 activation to form center dot 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.
引用
收藏
页数:11
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