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Photoisomerization of n-pentane over nano zno/moo2-zro2

机译:纳米Zno / moo2-zro2上正戊烷的光异构化

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摘要

A series of nano ZnO/MoO3-ZrO2 catalysts with different ZnO loading (1.0, 2.5, 5.0 wt%) were prepared by impregnation method for n-pentane photoisomerization under hydrogen or nitrogen atmosphere. The properties of the catalysts were characterized with X-ray Diffraction (XRD), Brunauer Emmett Teller (BET), Transmission Electron microscope (TEM) and FTIR. The XRD result showed that the fraction of tetragonal phase of ZnO/MoO3-ZrO2 was about 0.67 for all samples. While, the specific BET surface area was about 24 m2 /g. Pyridine adsorbed FTIR results showed that all samples possessed high concentration of strong Lewis acid sites and small concentration of weak Bronsted acid sites. The interaction of hydrogen and surface samples at 298-523 K formed protonic acid sites with the concomitant of the partial elimination of Lewis acid sites. Whereas no changes of the concentration of acid sites were observed in the presence of nitrogen atmosphere. The activity of all samples in the n-pentane photoisomerization was strongly determined by the presence of hydrogen gas. In fact no activity was observed in the absence of hydrogen
机译:通过浸渍法制备了一系列不同的ZnO负载量(1.0、2.5、5.0 wt%)的纳米ZnO / MoO3-ZrO2催化剂,用于在氢或氮气氛下进行正戊烷光异构化。用X射线衍射(XRD),Brunauer Emmett Teller(BET),透射电子显微镜(TEM)和FTIR对催化剂的性能进行了表征。 XRD结果表明,所有样品中ZnO / MoO3-ZrO2的四方相分数约为0.67。而BET比表面积为约24m 2 / g。吡啶吸附的FTIR结果表明,所有样品均具有高浓度的强路易斯酸位点和低浓度的弱布朗斯台德位点。氢和表面样品在298-523 K处的相互作用形成了质子酸位点,并伴有路易斯酸位点的部分消除。而在氮气氛下未观察到酸位浓度的变化。所有样品在正戊烷光异构化中的活性都由氢气的存在强烈地确定。实际上,在没有氢的情况下没有观察到活性

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