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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
    • 联系方式:email:yingya.liu@dlut.edu.cn 0411-84986124
    • 电子邮箱:yingya.liu@dlut.edu.cn

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    Gas phase adsorption of alkanes, alkenes and aromatics on the sulfone-DUT-5 Metal Organic Framework

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    论文类型:期刊论文

    发表时间:2015-04-01

    发表刊物:MICROPOROUS AND MESOPOROUS MATERIALS

    卷号:206

    期号:C

    页面范围:217-225

    ISSN号:1387-1811

    关键字:Metal-Organic Frameworks; Shape selectivity; Inverse gas chromatography; Breakthrough experiments; Hydrocarbons

    摘要:A sulfone functionalized DUT-5 Metal Organic Framework 'SO2-DUT-5' was synthesized using 4,4'-bibenzoic acid-2,2'-sulfone linkers. Its adsorption properties were studied and compared to those of the pristine DUT-5 material. The inverse gas chromatographic method was used to study the adsorption of C-5-C-7 linear, branched and cyclic alkanes, alkenes and aromatic molecules. SO2-DUT-5 shows shape-selective behaviour in the adsorption of linear, branched and iso-alkanes, whereas DUT-5 is non-selective. The presence of sulfone groups results in both a reduced pore size and more specific interaction sites, leading to the shape-selective behaviour towards linear alkanes and the slightly elevated preference for aromatic compounds in the low coverage area.
       The separation of n-hexane/benzene and 1-hexene/benzene mixtures at higher coverage was studied by performing breakthrough experiments at different temperatures and pressures. A remarkable change in selectivity is observed when the loading of the adsorbing molecules increases. At low degree of pore filling, no significant separation between n-hexane/benzene or 1-hexene/benzene occurs, while at higher loading separation becomes apparent with a preferential adsorption of benzene. This separation at high loading is a result of the more favourable packing of benzene in this unidimensional pore system. (C) 2014 Elsevier Inc. All rights reserved.