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Supported ionic liquid phase catalysis on functionalized carbon nanotubes

机译:功能化碳纳米管上的负载型离子液体催化

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Highly active rhodium catalysts have been prepared by immobilization of an ionic liquid film on carbon nanotubes functionalized with imidazolium-based ionic moieties.rnOne of the main drawbacks in homogeneous catalysis concerns the difficulty in separating the reaction products from the soluble catalyst and any solvent. This problem becomes even more crucial when expensive noble metal based catalysts are involved. Furthermore, the use of distillation columns increases the energy consumption and often leads to catalyst degradation, increasing the overall cost of the process. Many alternative approaches have been attempted using supported homogeneous catalysts or bipha-sic systems. One very attractive concept combines these approaches by immobilising the catalyst in a thin film of either water or an ionic liquid, absorbed within the pores of a high surface area solid. When ionic liquids (ILs), green, non volatile solvents, are used as a supported phase (supported ionic liquid phase catalysts, SILPCs), long-term reactions have shown promising results. Indeed, the ionic character of ILs confers to these media a spatial organization over several nanometres that induces peculiar solvation phenomena and specific reactivity, which can be linked either to confinement effects in these organized structures or to molecular interactions.
机译:通过将离子液体薄膜固定在以咪唑基离子部分官能化的碳纳米管上,可以制备高活性铑催化剂。均相催化的主要缺点之一是难以将反应产物与可溶性催化剂和任何溶剂分离。当涉及昂贵的贵金属基催化剂时,这个问题变得更加关键。此外,使用蒸馏塔会增加能量消耗并经常导致催化剂降解,从而增加了该方法的总成本。已经尝试使用负载的均相催化剂或双相体系的许多替代方法。一个非常吸引人的概念是通过将催化剂固定在吸收在高表面积固体的孔中的水或离子液体的薄膜中来结合这些方法。当将离子液体(ILs),绿色的非挥发性溶剂用作载体相(载体离子液体催化剂,SILPC)时,长期反应已显示出令人鼓舞的结果。的确,IL的离子特性赋予这些介质数纳米的空间组织,从而引起特殊的溶剂化现象和比反应,这可以与这些组织结构中的限制作用或分子相互作用联系在一起。

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