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Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditions

机译:粉状SiC和其他商用载体上的Pt浸渍催化剂,用于在氧化剂条件下燃烧氢气

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摘要

We report the study of the catalytic hydrogen combustion over Pt-impregnated powdery silicon carbide (SiC) using H2PtCl6 as precursor. The reaction was conducted in excess of oxygen. β-SiC was selected for the study because of its thermal conductivity, mechanical properties, chemical inertness and surface area. The obtained Pt particles over SiC were medium size (average particle diameter of 5 nm for 0.5 wt% Pt). The activity of the Pt-impregnated catalyst over SiC was compared to those obtained in oxidized form over TiO2 and Al2O3 commercial supports (Pt particles very small in size, average particle diameter of 1 nm for 0.5 wt% Pt in both cases). The case of a SiO2 support was also discussed. Those Pt/SiC particles were the most active because of their higher contribution of surface Pt0, indicating that partially oxidized surfaces have better activity than those totally oxidized in these conditions. SiC was modified with an acid treatment and thus bigger (average particle diameter of 7 nm for 0.5 wt% Pt) and more active Pt particles were obtained. Durability of the SiC and TiO2 supported catalysts was tested upon 5 cycles and both have shown to be durable and even more active than initially. Exposure to the oxidative reaction mixture activates the catalysts and the effect is more pronounced for the completely oxidized particles. This is due to the surface oxygen chemisorption which activates catalystś surface.
机译:我们报告了使用H2PtCl6作为前驱体,在Pt浸渍的粉末状碳化硅(SiC)上催化氢燃烧的研究。反应在过量的氧气下进行。选择β-SiC是因为其导热性,机械性能,化学惰性和表面积。在SiC上获得的Pt颗粒为中等尺寸(0.5wt%的Pt的平均粒径为5nm)。将Pt浸渍的催化剂在SiC上的活性与以氧化形式在TiO2和Al2O3商业载体上获得的活性进行了比较(Pt颗粒尺寸很小,两种情况下0.5 wt%Pt的平均粒径为1 nm)。还讨论了SiO2载体的情况。那些Pt / SiC颗粒具有最高的活性,因为它们对表面Pt0的贡献更大,这表明在这些条件下,部分氧化的表面比完全氧化的表面具有更好的活性。通过酸处理对SiC进行了改性,从而获得了更大的粒径(对于0.5 wt%的Pt,平均粒径为7 nm),并且具有更高的活性Pt颗粒。经过5个循环测试了SiC和TiO2负载型催化剂的耐用性,两者均显示出比最初更耐久甚至更具活性的特性。暴露于氧化反应混合物中会激活催化剂,并且对于完全氧化的颗粒,其效果更为明显。这是由于表面氧化学吸附作用激活了催化剂的表面。

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