Zr-Metal-Organic Framework Catalysts for Oxidative Desulfurization and Their Improvement by Postsynthetic Ligand Exchange

被引:53
|
作者
Fu, Guangxia [1 ]
Bueken, Bart [1 ]
De Vos, Dirk [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, Celestijnenlaan 200F, B-3001 Leuven, Belgium
来源
SMALL METHODS | 2018年 / 2卷 / 12期
基金
比利时弗兰德研究基金会;
关键词
accessible open sites; catalysts; ligand exchange; metal-organic frameworks; oxidative desulfurization; DEEP DESULFURIZATION; POLYOXOMETALATE; DIESEL; EFFICIENT; DIBENZOTHIOPHENE; PERFORMANCE; REACTIVITY; CRYSTALS; SYSTEM; MODEL;
D O I
10.1002/smtd.201800203
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
Two types of Zr-6-based metal-organic frameworks (MOF), {Zr6O4(OH)(4)(C6H3(COO)(3))(2)(HCOO)(6)} (MOF-808) and {Zr6O4(OH)(4)(C24H15(COO)(3))(2)(HCOO)(6)} (UMCM-309) are investigated as heterogeneous catalysts in oxidative desulfurization reactions. Postsynthetic approaches targeting the removal of the coordinating formate ligands are applied to further improve the MOFs' catalytic activity, resulting in the formation of additional Zr-IV open sites. Thus, three modified MOFs, namely MOF-808-M, UMCM-309-M1, and UMCM-309-M2, are synthesized with larger numbers of open sites, as shown by CD3CN chemisorption monitored by Fourier-transform infrared spectroscopy (FTIR), leading to higher catalytic activity. Even at low catalyst loading, MOF-808-M exhibits high catalytic activity in the oxidation of sulfur compounds as well as high selectivity and reusability.
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页数:8
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