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    刘颖雅

    • 副教授     博士生导师 硕士生导师
    • 性别:女
    • 毕业院校:中科院大连化学物理研究所
    • 学位:博士
    • 所在单位:化工学院
    • 学科:工业催化. 能源化工
    • 办公地点:化工实验楼B325
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    Catalytic oxidative desulfurization of model and real diesel over a molybdenum anchored metal-organic framework

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      发布时间:2020-02-24

      论文类型:期刊论文

      发表时间:2019-03-15

      发表刊物:MICROPOROUS AND MESOPOROUS MATERIALS

      收录刊物:EI、SCIE

      卷号:277

      页面范围:245-252

      ISSN号:1387-1811

      关键字:Molybdenum-bipyridine complex; Metal-organic framework; Oxidative desulfurization; Dibenzothiophene; Diesel

      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.