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The catalytic oxidation of toluene at low temperature over palladium nanoparticles supported on Alumina sphere catalysts: effects of Palladium precursors and preparation method

机译:低温低温催化氧化在氧化铝球催化剂上的钯纳米颗粒:钯前体的影响及制备方法

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In this study, 1 wt.% Pd/Al_(2)O_(3)sphere catalysts were prepared using the wet-impregnation (WI) and deposition-precipitation (DP) method using palladium chloride and tetraamminepalladium (II) nitrate as salt precursors. All catalysts were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM) and Fourier-transform infrared (FTIR) spectroscopy. The catalytic activity in toluene oxidation under gas-phase conditions was measured. The obtained results showed that metal dispersion and catalytic activity were strongly dependent on the salt precursor and method of catalyst preparation. The use of tetraamminepalladium (II) nitrate as the precursor presented smaller particle size, an enhanced dispersion and higher specific surface area. Moreover, the catalyst prepared with this precursor also showed higher catalytic activity than that prepared with palladium chloride. At 1 wt.% Pd loading, complete oxidation of toluene was achieved at 250°C. However, there was only approximately 80–90% efficient at the same temperature when the catalyst was prepared with palladium chloride as the precursor.
机译:在该研究中,使用氯化钯和四氨基钯(II)硝酸盐前体使用湿浸渍(Wi)和沉淀沉淀(DP)方法制备1wt.%Pd / Al_(2)O_(3)球催化剂。 。使用X射线衍射(XRD),透射电子显微镜(TEM)和傅里叶变换红外(FTIR)光谱来表征所有催化剂。测量甲苯氧化在气相条件下的催化活性。得到的结果表明,金属分散和催化活性强烈依赖于盐前体和催化剂制剂的方法。使用四氨基钯(II)硝酸盐作为前体呈现较小的粒度,增强的分散体和更高的比表面积。此外,用该前体制备的催化剂也显示出比用氯化钯制备的催化活性更高。在1重量%。%PD负载,在250℃下实现完全氧化甲苯。然而,当用氯化钯作为前体制备催化剂时,在相同的温度下,在相同的温度下只有大约80-90%。

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