Synthesis of polyoxometalate encapsulated in UiO-66(Zr) with hierarchical porosity and double active sites for oxidation desulfurization of fuel oil at room temperature

被引:99
|
作者
Ye, Gan [1 ]
Hu, Liangliang [1 ,2 ]
Gu, Yulong [1 ]
Lancelot, Christine [2 ]
Rives, Alain [2 ]
Lamonier, Carole [2 ]
Nuns, Nicolas [3 ]
Marinova, Maya [3 ]
Xu, Wei [4 ]
Sun, Yinyong [1 ]
机构
[1] Harbin Inst Technol, MIIT Key Lab Crit Mat Technol New Energy Convers, Sch Chem & Chem Engn, Harbin 150001, Peoples R China
[2] Univ Artois, UCCS Unite Catalyse & Chim Solide, UMR 8181, Univ Lille,CNRS,Cent Lille,ENSCL, F-59000 Lille, France
[3] Univ Artois, IMEC Inst Michel Eugene Chevreul, FR 2638, Univ Lille,CNRS,INRA,Cent Lille, F-59000 Lille, France
[4] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
关键词
METAL-ORGANIC FRAMEWORK; LIGHT PHOTOCATALYTIC ACTIVITY; N-DOPED CARBON; PHOSPHOTUNGSTIC ACID; CATALYTIC PERFORMANCE; HIGHLY EFFICIENT; LIQUID FUEL; HYDRODESULFURIZATION; NANOPARTICLES; MIL-101;
D O I
10.1039/d0ta04337k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Catalytic oxidative desulfurization (ODS) of fuel oil has received much attention. For this, the synthesis of a highly efficient ODS catalyst has been strongly pursued. Polyoxometalates (POMs) as active centers have been studied for ODS reactions. However, generally the obtained POM catalysts exhibited ordinary catalytic ODS performance mainly due to the role of single active sites. Moreover, the synthesis needs to be completed with the addition of solvent. In this work, we report a new approach to prepare highly efficient ODS catalysts with POM sites. This process can be simply realized by the combination of a common POM (H3PW12O40) and a stable metal-organic framework (MOF) material UiO-66(Zr) without the addition of solvent. More importantly, it is found that polyoxometalate encapsulated in UiO-66(Zr) possesses hierarchical porosity and double active sites. As a result, the catalyst exhibited extraordinary catalytic activity by using H(2)O(2)as an oxidant in the ODS reactions of benzothiophene, dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene. The turnover frequency (TOF) for the removal of DBT reached 293 h(-1)at room temperature, which is much higher than that of the reported catalysts. Such outstanding catalytic performance could be mainly attributed to easy accessibility of active sites and the existence of two types of active centers in polyoxometalate species and defective UiO-66(Zr).
引用
收藏
页码:19396 / 19404
页数:9
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