Synthesis of ionic-liquid-functionalized UiO-66 framework by post-synthetic ligand exchange for the ultra-deep desulfurization

被引:50
作者
Qi, Zhaoyang [1 ]
Qiu, Ting [1 ]
Wang, Hongxing [1 ]
Ye, Changshen [1 ]
机构
[1] Fuzhou Univ, Fujian Prov Univ, Coll Chem Engn, Engn Res Ctr React Distillat, Fuzhou 350108, Fujian, Peoples R China
关键词
Ligand exchange; UiO-66; Monocarboxylic functional ionic liquid; Adsorption; Oxidative desulfurization; METAL-ORGANIC FRAMEWORKS; OXIDATIVE DESULFURIZATION; EXTRACTIVE DESULFURIZATION; REMARKABLE ADSORBENTS; CATALYST; FUELS; MIL-100(FE); REMOVAL; MOF;
D O I
10.1016/j.fuel.2020.117336
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Ionic Liquids (IL) has been recently immobilized into the pores of metal-organic framework materials (MOFs) to prepare heterogeneous catalyst. However, the IL@MOFs composites are generally prepared by impregnation method, which is unstable in polar solvents. So, we design a new strategy to immobilize IL, and a novel Fenton-like catalyst [mim(CH2)(3)COO]FeCl4@UiO-66 has been prepared based on the post-synthetic ligand exchange (PSLE) between MOFs and monocarboxylic functional IL. The [mim(CH2)(3)COO]FeCl4@UiO-66 was exploited to act as an efficient heterogeneous catalyst for dibenzothiophene (DBT) oxidation in a biphasic system using H2O2 as the oxidant. Based on optimal conditions, the DBT removal efficiency reached up to 99.1%. Moreover, the heterogeneous catalyst had a good thermal and chemical stability, and the DBT removal efficiency still exhibited over 95% after 6 recycle runs. It is worth noting that the high DBT removal efficiency could be attributed to the synergistic effect between adsorptive and oxidative desulfurization, where [mim(CH2)(3)COO]FeCl4@UiO-66 is both an adsorbent and a catalyst.
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页数:10
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