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Selective Hydrogenation of Unsaturated Aldehydes into Unsaturated Alcohols: Role of Metal-Support Interactions in Platinum Catalysts

机译:不饱和醛的选择性氢化成不饱和醇:金属支持相互作用在铂催化剂中的作用

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With the aim of finding an environmentally friendly catalytic process leading to selective hydrogenation of α,β unsaturated aldehydes into unsaturated alcohols, the platinum catalysts supported on TiO_2, SnO_2, CeO_2, ZnO have been compared to unsupported platinum and platinum supported on Al_2O_3 and MgO, in gaseous hydrogenation of crotonaldehyde. The first series of catalysts leads to 60-90% selectivity in the formation of crotyl alcohol while it never exceeds 10% for the second series. Using reducible oxides, large effects on the selectivity are shown depending on the metal precursor and the reduction temperature. It is shown that certain catalytic systems are selective up to high conversion, stable in time and, when tested in gaseous and liquid phase, the same selectivity evolution was found in both reaction environments. The catalysts were characterised by Temperature Programmed Reduction, X-Ray Diffraction, High Resolution Transmission Electronic Microscopy and Photoelectron Spectroscopy. It reveals that the particle size does not affect directly the selectivity while the formation of alloy is always present, PtSn, CePt_5 and PtZn, respectively when the catalysts show the highest selectivity. This phenomenon as well as the migration of reducible oxide species and the detrimental or beneficial effects of chlorine are revealed.
机译:目的是寻找环境友好的催化过程,导致α,β不饱和醛的选择性氢化成不饱和醇,将在TiO_2,SnO_2,CeO_2,ZnO上负载的铂催化剂与不支持的铂和铂族,其中Al_2O_3和MgO支持,在克罗特醛的气态氢化中。第一系列催化剂导致曲甘肉形成60-90%的选择性,而第二系列的曲折醇永远不会超过10%。使用可氧化物氧化物,根据金属前体和还原温度显示对选择性的大效果。结果表明,某些催化系统可选择高达高转化率,稳定的时间,并且当在气态和液相中测试时,在两个反应环境中发现相同的选择性进化。通过温度编程,X射线衍射,高分辨率传输电子显微镜和光电子谱表征催化剂的特征。它揭示粒度不影响在催化剂的形成最高选择性时,分别存在于合金的形成,PtSn,Cept_5和PTZN的同时直接影响。这种现象以及可降解氧化物物种的迁移以及氯的有害或有益效果揭示。

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