首页> 美国卫生研究院文献>Materials >CO Preferential Photo-Oxidation in Excess of Hydrogen in Dark and Simulated Solar Light Irradiation over AuCu-Based Catalysts on SBA-15 Mesoporous Silica-Titania
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CO Preferential Photo-Oxidation in Excess of Hydrogen in Dark and Simulated Solar Light Irradiation over AuCu-Based Catalysts on SBA-15 Mesoporous Silica-Titania

机译:在SBA-15介孔二氧化硅-二氧化钛上的AuCu基催化剂上在黑暗和模拟的太阳光照射下氢气中CO优先发生光氧化。

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摘要

In this work, SBA-15 silica and silica-titania have been used as supports for photocatalysts based on AuCu alloy (Au:Cu = 1) to be used in the preferential oxidation of CO (CO-PROX) in excess of hydrogen at room temperature and atmospheric pressure both in the dark and under simulated solar light irradiation. To study their textural, structural, chemical and optical properties, the samples were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HR-TEM), adsorption-desorption of N2 at −196 °C, 13C and 29Si solid state nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS) and diffuse reflectance ultraviolet-visible (DRUV-vis) spectroscopy. Titanium was present mainly in the form of titania aggregates, but also as small particles interacting with the SBA support. In both catalysts, the metal alloy nanoparticles displayed an average size of 4 nm as demonstrated by TEM measurements. AuCu/Ti-SBA turned out to be photoactive and selective in the photo-CO-PROX reaction showing the highest activity, with conversion and selectivity towards CO2 of 80%, due both to the presence of titania incorporated in SBA-15 and to the synergistic effect of Cu when alloyed with Au.
机译:在这项工作中,SBA-15二氧化硅和二氧化硅-二氧化钛已用作基于AuCu合金(Au:Cu = 1)的光催化剂的载体,可用于在室温下过量氢气中的CO(CO-PROX)优先氧化在黑暗和模拟太阳光照射下的温度和大气压。为了研究其结构,结构,化学和光学性质,通过X射线衍射(XRD),高分辨率透射电子显微镜(HR-TEM),-196°C下N2的吸附-脱附对样品进行了表征> 13 C和 29 Si固态核磁共振(NMR),X射线光电子能谱(XPS)和漫反射紫外可见光谱(DRUV-vis)。钛主要以二氧化钛聚集体的形式存在,但也以与SBA载体相互作用的小颗粒形式存在。在两种催化剂中,金属合金纳米颗粒均显示出4 nm的平均粒径,这是通过TEM测量证明的。事实证明,由于在SBA-15中掺入了二氧化钛,并且由于SBA-15中存在二氧化钛,AuCu / Ti-SBA在光CO-PROX反应中具有光活性和选择性,显示出最高的活性,对CO2的转化率和选择性为80%。 Cu与Au合金化时的协同作用。

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