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首页> 外文期刊>Microporous and mesoporous materials: The offical journal of the International Zeolite Association >Catalytic oxidative desulfurization of model and real diesel over a molybdenum anchored metal-organic framework
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Catalytic oxidative desulfurization of model and real diesel over a molybdenum anchored metal-organic framework

机译:用钼锚定金属有机框架催化氧化脱硫模型和真实柴油

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摘要

In this work, we report the catalytic performance of a MoO2Cl2 anchored metal-organic framework, Mo@COMOC-4, in the oxidative desulfurization (ODS) process on a continuous fixed-bed reactor. Mo@COMOC-4 was examined as a catalyst in the oxidation of model oils containing dibenzothiophene (DBT), benzothiophene (BT) or 4,6-dimethyldibenzothiophene (4,6-DMDBT). In a 50-h ODS reaction of DBT at 70 degrees C, with tert-butyl hydroperoxide (TBHP) as the oxidant, a constant high DBT conversion of nearly 80% was observed along with a high oxidant utility of over 85%, where DBT was converted rapidly into DBT sulfone. XRD and ICP analysis show that the structure of Mo@COMOC-4 was well preserved, with no significant leaching of Mo species. In addition, Mo@COMOC-4 can also oxidize a hydrogenated diesel oil, and 74% sulfur removal efficiency was achieved, with an extraction recovery of 92.5% after acetonitrile extraction. Spectroscopic characterization confirmed the formation of a molybdenum peroxide complex from MoO2Cl2 under TBHP treatment, a plausible catalytic process was proposed based on the experiment evidence as well as FT-IR and FT-FIR characterization results.
机译:在这项工作中,我们报告了在连续固定床反应器上的氧化脱硫(ODS)过程中MOO2Cl2锚定金属 - 有机框架MO @ COMOC-4的催化性能。将Mo @ Comoc-4在含有二苯并噻吩(DBT),苯并噻吩(BT)或4,6-二甲基二苯甲酸噻吩(4,6-DMDBT)的模型油的氧化中被检查为催化剂。在70℃下DBT的50-H ODS反应,用叔丁基氢氧化钠(TBHP)作为氧化剂,观察到近80%的恒定高DBT转化率和高氧化效用超过85%,其中DBT迅速转化为DBT砜。 XRD和ICP分析表明,MO @ Comoc-4的结构保存得很好,Mo物种无明显浸出。此外,Mo @ Comoc-4还可以氧化氢化柴油,实现74%的硫去除效率,乙腈萃取后的提取回收率为92.5%。光谱表征证实,在TBHP处理下,从MOO2Cl2形成过氧化钼​​复合物的形成,基于实验证据以及FT-IR和FT-FIR表征结果提出了一种合理的催化过程。

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