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Effect of alkali and alkaline earth metal ions on benzyl alcohol oxidation activity of titanate nanotube-supported Au catalysts

机译:碱土金属离子对钛酸盐纳米管支持Au催化剂的苄醇氧化活性的影响

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摘要

Sodium titanate nanotubes (NaTNTs) were prepared by alkali treatment of anatase titania. They were then ion-exchanged with alkali and alkaline earth metal ions to get ATNTs (A = Li+, K+, Cs+, Mg2+, Ca2+, Sr2+ and Ba2+). Gold (1-5 wt%) was supported on these nanotubes by a deposition-precipitation method and investigated as a catalyst for the selective oxidation of benzyl alcohol with air/molecular oxygen (1 atm) under solvent-and alkali-free conditions. Detailed characterization by X-ray powder diffraction, high resolution transmission electron microscopy, N-2-physisorption, diffuse reflectance UV-visible spectroscopy, X-ray photoelectron spectroscopy and CO2-temperature-programmed desorption techniques revealed that the basicity of the catalyst influences the uptake, mean particle size, electronic properties and oxidation activity of the supported gold. Benzaldehyde formed with a selectivity of about 99%. The catalytic activity (turnover frequency) was found to have a direct relationship with the basicity and an inverse relationship with the Au particle size. Among the catalysts investigated, Au/BaTNTs, having higher basicity, smaller Au particles and higher metal dispersion, showed enhanced catalytic activity than the other Au/ATNT catalysts. Pd addition to Au leading to Au-Pd/BaTNTs increased the activity (TOF) but lowered the selectivity for benzaldehyde (80 wt%). Titanate nanotubes donate electron density to Au particles, yielding electron rich Au ions, which are responsible for activating molecular oxygen and oxidizing benzyl alcohol. Au/BaTNTs, having higher basicity and lower size Au nanoparticles than the other Au/ATNT, activates molecular oxygen more easily and thereby enhances the catalytic activity.
机译:钛酸钠纳米管(NaTNTs)由锐钛矿型二氧化钛的碱处理来制备。然后将它们用碱金属和碱土金属离子的离子交换来获得ATNTs(A = Li +的,K +,Cs的+,Mg2 +的,钙离子,锶离子和BA2 +)。金(1-5重量%)是在这些纳米管通过沉积沉淀法,并支持研究作为催化剂为苄基醇与空气/分子氧(1个大气压)溶剂和无碱条件下选择性氧化。通过X-射线粉末衍射,高分辨率透射电子显微镜,N-2-物理吸附,漫反射紫外可见光谱,X射线光电子能谱法和CO 2升温脱附技术详细表征,发现该催化剂的影响的碱度摄取,平均粒度,电子性质和所支持的金的氧化活性。苯甲醛与形成约99%的选择性。催化活性(转换频率)被发现具有与碱度和有Au粒径的反比关系的直接关系。在这些催化剂的调查,金/ BaTNTs,具有较高碱度,更小的Au颗粒和更高的金属分散,表现出比其它的Au / ATNT催化剂增强的催化活性。钯除了金导致金钯/ BaTNTs增加的活性(TOF),但降低了苯甲醛的选择性(80重量%)。纳米管提供电子密度Au颗粒,得到电子富Au离子,其是负责激活分子氧和氧化苄醇。的Au / BaTNTs,具有较高碱度和低尺寸的Au纳米颗粒比其它的Au / ATNT,更容易激活分子氧,并由此增强了催化活性。

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  • 来源
    《RSC Advances》 |2015年第59期|共9页
  • 作者单位

    CSIR Natl Chem Lab Catalysis Div Pune 411008 Maharashtra India;

    CSIR Natl Chem Lab Catalysis Div Pune 411008 Maharashtra India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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