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Hollow γ-Al_2O_3 microspheres as highly “active” supports for Au nanoparticle catalysts in CO oxidation

机译:空心γ-Al_2O_3微球作为CO氧化中的金纳米颗粒催化剂的高度“活性”载体

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Consisted of closely packed nanoflakes, γ-Al_2O_3 hollow microspheres with ca. 4–6 μm in diameter, and 500–700 nm in shell thickness have been hydrothermally synthesized through utilizing Al(NO_3)_3·9H_2O as precursor, urea as precipitant agent and sulfate K_2SO_4, (NH_4)_2SO_4, or KAl(SO_4)_2·12H_2O as additive, followed by a calcination step. The samples were further characterized by thermogravimetric analysis, scanning electron microscope, x-ray powder diffraction, nitrogen adsorption, and in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) of adsorbed CO etc. The morphology of alumina products was strongly dependent on the presence of SO_4~(2-). Then via a deposition–precipitation method, 3 wt.% Au nanoparticles supported on γ-Al_2O_3 hollow microspheres exhibit excellent performance with a complete CO conversion at 0 °C (T_(100%)=0 °C) and 50 % conversion at 125 °C (T_(50%)=-25 °C). The good catalytic activity is associated with the special hollow microsphere structures assembled by nanoflakes of γ-Al_2O_3 support. The DRIFTS confirms the presence of Auδ+ and Au0 on the surface of γ-Al2_O_3 hollow microspheres. As a contrast, Au catalyst prepared using alumina support with undefined morphology shows low activity under the same catalytic test conditions (T_(100%)=190 °C, T_(50%)=80 °C).
机译:γ-Al_2O_3空心微球由紧密堆积的纳米薄片组成,约以Al(NO_3)_3·9H_2O为前驱体,尿素为沉淀剂和硫酸盐K_2SO_4,(NH_4)_2SO_4或KAl(SO_4)_2为水热合成了直径4–6μm,壳厚500-700 nm的水。 ·添加12H_2O作为添加剂,然后进行煅烧步骤。通过热重分析,扫描电子显微镜,X射线粉末衍射,氮气吸附以及吸附的CO等原位漫反射红外傅里叶变换光谱(DRIFTS)等对样品进行进一步表征。氧化铝产物的形态强烈依赖于其存在。 SO_4〜(2-)的然后通过沉积-沉淀方法,负载在γ-Al_2O_3中空微球上的3 wt。%Au纳米颗粒表现出优异的性能,在0°C(T_(100%)= 0°C)时具有完全的CO转化率,在125°C时具有50%的转化率°C(T_(50%)=-25°C)。良好的催化活性与由γ-Al_2O_3载体的纳米薄片组装而成的特殊空心微球结构有关。 DRIFTS证实了γ-Al2_O_3中空微球表面上存在Auδ+和Au0。相比之下,使用具有不确定形态的氧化铝载体制备的Au催化剂在相同的催化测试条件下(T_(100%)= 190°C,T_(50%)= 80°C)表现出较低的活性。

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