首页> 外文期刊>Journal of the Taiwan Institute of Chemical Engineers >Fabrication of mesoporous SiO2/Au/Co3O4 hollow spheres catalysts with core-shell structure for liquid phase oxidation of benzyl alcohol to benzaldehyde
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Fabrication of mesoporous SiO2/Au/Co3O4 hollow spheres catalysts with core-shell structure for liquid phase oxidation of benzyl alcohol to benzaldehyde

机译:介孔SiO2 / Au / Co3O4中空球体催化剂的制备,其具有核 - 壳结构的液相氧化苄醇与苯甲醛

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摘要

A core-shell structure Au-based catalysts mSiO(2)/Au/Co3O4-HS were successfully derived from in-situ growth ZIF-67 hollow spheres, which were synthesized by a one-step soft template method. The samples were characterized by SEM, TEM, EDX, XPS, XRD and BET to confirm its successful preparation and structural features. The catalytic performance of the catalysts were evaluated by liquid phase oxidation of benzyl alcohol to benzaldehyde with O-2 as the oxidant under alkaline conditions. The experimental results illustrated that reaction conditions, including effect of catalyst amount, oxygen flow rate, reaction temperature and reaction time, were optimized to be 40 mg, 50 ml/min, 140 degrees C and 5 h, respectively. Meanwhile, 55% conversion of benzyl alcohol and 84% selectivitiy to benzaldehyde together with the excellent reusability and stability were achieved under optimal reaction conditions, which was attributed to the core-shell structure leading to the encapsulation of Au NPs and provision of multiple active reaction interface. Based on the intermediates formed from the de-protonation of substrate, a plausible oxidation reaction mechanism with mSiO(2)/Au/Co3O4 -HS catalysts was tentatively proposed to study the relationship between structure and catalytic performance. (C) 2019 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
机译:核 - 壳结构Au的催化剂MSIO(2)/ AU / CO3O4-HS源自原位生长ZIF-67中空球体,其通过一步软模板方法合成。通过SEM,TEM,EDX,XPS,XRD和BET表征样品,以确认其成功的制备和结构特征。通过将苄醇的液相氧化在碱性条件下作为氧化剂,通过苄醇的液相氧化对苯甲醛的液相氧化来评价催化剂的催化性能。实验结果表明,反应条件,包括催化剂量,氧气流速,反应温度和反应时间的影响,分别优化为40mg,50ml / min,140℃和5h。同时,在最佳反应条件下,在最佳反应条件下实现了55%苄醇转化为苯甲醇和84%选择与苯甲醛的优异可重用性和稳定性,这归因于核心 - 壳结构,导致Au NPS的包封和多重活性反应的提供界面。基于由底物的去脱模形成的中间体,暂时提出了一种具有MSIO(2)/ Au / CO 3 O 4 -HS催化剂的可粘附氧化反应机理,以研究结构与催化性能之间的关系。 (c)2019年台湾化工工程师研究所。 elsevier b.v出版。保留所有权利。

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  • 作者单位

    Southeast Univ Sch Chem &

    Chem Engn Jiangsu Optoelect Funct Mat &

    Engn Lab Nanjing 211189 Jiangsu Peoples R China;

    Southeast Univ Sch Chem &

    Chem Engn Jiangsu Optoelect Funct Mat &

    Engn Lab Nanjing 211189 Jiangsu Peoples R China;

    Southeast Univ Sch Chem &

    Chem Engn Jiangsu Optoelect Funct Mat &

    Engn Lab Nanjing 211189 Jiangsu Peoples R China;

    Southeast Univ Sch Chem &

    Chem Engn Jiangsu Optoelect Funct Mat &

    Engn Lab Nanjing 211189 Jiangsu Peoples R China;

    Southeast Univ Sch Chem &

    Chem Engn Jiangsu Optoelect Funct Mat &

    Engn Lab Nanjing 211189 Jiangsu Peoples R China;

    Southeast Univ Sch Chem &

    Chem Engn Jiangsu Optoelect Funct Mat &

    Engn Lab Nanjing 211189 Jiangsu Peoples R China;

    Southeast Univ Sch Chem &

    Chem Engn Jiangsu Optoelect Funct Mat &

    Engn Lab Nanjing 211189 Jiangsu Peoples R China;

    Southeast Univ Sch Chem &

    Chem Engn Jiangsu Optoelect Funct Mat &

    Engn Lab Nanjing 211189 Jiangsu Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学工业;
  • 关键词

    Core-shell; Au NPs; MOFs; Liquid phase oxidation; Benzaldehyde;

    机译:核心壳;au nps;mofs;液相氧化;苯甲醛;

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