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首页> 外文期刊>Topics in Catalysis >Preparation of Phase-Pure M1 MoVTeNb Oxide Catalysts by Hydrothermal Synthesis—Influence of Reaction Parameters on Structure and Morphology
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Preparation of Phase-Pure M1 MoVTeNb Oxide Catalysts by Hydrothermal Synthesis—Influence of Reaction Parameters on Structure and Morphology

机译:水热合成法制备纯相M1 MoVTeNb氧化物催化剂—反应参数对结构形态的影响

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摘要

This work presents a detailed investigation of the preparation of MoVTeNbO x catalysts by hydrothermal synthesis. Phase-pure synthesis of M1 has been achieved applying the metals in a molar ratio Mo/V/Te/Nb = 1/0.25/0.23/0.12. Raman, UV/Vis spectroscopy, and SEM/EDX analysis show that the elements are inhomogeneously distributed in the initial suspension that is formed after mixing the metal salts in an aqueous medium. Iso- and heteropoly anions of molybdenum, free telluric acid as well as supra-molecular polyoxometalate clusters are observed in the solution, whereas all metals have been found in the precipitate. Complete rearrangement of molecular building blocks under hydrothermal conditions is essential for formation of phase-pure materials. Optimized synthesis conditions with respect to temperature and time result in the formation of a precursor consisting of nano-structured M1 characterized by an extended periodic organization in the [001] direction and a fairly homogeneous distribution of the elements. Residual ammonium containing supra-molecular species in the precursor result in the formation of phase mixtures during the subsequent crystallization by heat treatment in inert gas. Phase-pure M1 exhibits a distinct degree of flexibility with respect to the chemical composition that becomes obvious by incorporating Nb not exclusively into pentagonal bi-pyramidal units, but also into octahedral coordinated positions as shown by EXAFS. Anisotropic growth of the needle-like M1 crystals has been observed during the final heat treatment performed at 873–923 K in inert atmosphere disclosing a potential method to control the catalytic properties of MoVTeNbO x catalysts.
机译:这项工作提出了通过水热合成制备MoVTeNbO x 催化剂的详细研究。通过以摩尔比Mo / V / Te / Nb = 1 / 0.25 / 0.23 / 0.12施加金属,实现了M1的纯相合成。拉曼光谱,UV / Vis光谱和SEM / EDX分析表明,元素在金属盐在水性介质中混合后形成的初始悬浮液中分布不均匀。在溶液中观察到钼,游离碲酸以及超分子多金属氧酸盐簇的异多和杂多阴离子,而在沉淀物中发现了所有金属。水热条件下分子结构单元的完全重排对于形成纯相材料至关重要。关于温度和时间的最佳合成条件导致形成由纳米结构的M1组成的前驱体,其特征是在[001]方向上扩展了周期性组织,并且元素的分布相当均匀。前体中含有残留的超分子物质,在随后的惰性气体热处理结晶过程中,会形成相混合物。如EXAFS所示,纯N1不仅将Nb不仅掺入五边形双锥体单元中,而且掺入八面体配位体中,在化学组成方面也表现出明显的灵活性,这很明显。在惰性气氛中于873–923 K进行的最终热处理过程中,观察到了针状M1晶体的各向异性生长,揭示了控制MoVTeNbO x催化剂的潜在方法。

著录项

  • 来源
    《Topics in Catalysis》 |2008年第4期|19-32|共14页
  • 作者单位

    Department of Inorganic Chemistry Fritz Haber Institute of the Max Planck Society Faradayweg 4-6 14195 Berlin Germany;

    Department of Inorganic Chemistry Fritz Haber Institute of the Max Planck Society Faradayweg 4-6 14195 Berlin Germany;

    Department of Inorganic Chemistry Fritz Haber Institute of the Max Planck Society Faradayweg 4-6 14195 Berlin Germany;

    Department of Inorganic Chemistry Fritz Haber Institute of the Max Planck Society Faradayweg 4-6 14195 Berlin Germany;

    Department of Inorganic Chemistry Fritz Haber Institute of the Max Planck Society Faradayweg 4-6 14195 Berlin Germany;

    Institute of Chemistry Technische Universität Berlin Sekr. C 2 Strasse des 17. Juni 135 10623 Berlin Germany;

    Department of Inorganic Chemistry Fritz Haber Institute of the Max Planck Society Faradayweg 4-6 14195 Berlin Germany;

    Department of Inorganic Chemistry Fritz Haber Institute of the Max Planck Society Faradayweg 4-6 14195 Berlin Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Hydrothermal synthesis; MoVTeNbOn xn catalyst; M1 phase; Propane oxidation;

    机译:水热合成MoVTeNbOn xn催化剂M1相丙烷氧化;

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