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首页> 外文期刊>Petroleum Science and Technology >Kinetics for Oxidation of Dibenzothiophene Catalyzed by Keggin-based Heteropoly Acids/H_2O_2 in bmimBF_4
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Kinetics for Oxidation of Dibenzothiophene Catalyzed by Keggin-based Heteropoly Acids/H_2O_2 in bmimBF_4

机译:bmim中基于Keggin的杂多酸/H_2O_2催化二苯并噻吩氧化动力学BF_4

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摘要

Extraction and catalytic oxidative desulfurization (ECODS) could success-fully integrate phosphomolybdic acid (H_3PM0_(12)O_(40)26H_2O, PM0_(12)), hydrogen peroxide (H_2O_2), and 1 -butyl-3-methylimidazolium tetrafluoroborate (bmimBF4) into a single efficient system that was manipulated to facilitate the separation and oxidation of sulfur compounds. The peroxometal complex was formed rapidly as PM0_(12) was oxidized by H_2O_2 and it could be solubilized in hydrophilic ionic liquid. The experimental results showed high sulfur removal up to 99.4 under the optimized desulfurization system. Kinetics of the ECODS system of dibenzothiophene was pseudo first order with the apparent activation energy of 53.8 kJ-mol~(-1). The catalytic reaction system could be recycled eight times without a significant decrease in reaction activity.
机译:萃取催化氧化脱硫(ECODS)可以成功地将磷钼酸(H_3PM0_(12)O_(40)26H_2O,PM0_(12))、过氧化氢(H_2O_2)和1-丁基-3-甲基咪唑鎓四氟硼酸盐([bmim]BF4)完全整合到一个高效的体系中,该体系纵以促进硫化合物的分离和氧化。当PM0_(12)被H_2O_2氧化时,过氧金属络合物迅速形成,并能溶解在亲水性离子液体中。实验结果表明,优化后的脱硫系统脱硫率高达99.4%。二苯并噻吩ECODS体系的动力学为准一级,表观活化能为53.8 kJ-mol~(-1)。催化反应体系可循环8次,反应活性无明显下降。

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