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首页> 外文期刊>Chemphyschem: A European journal of chemical physics and physical chemistry >Vacuum Surface Science Meets Heterogeneous Catalysis: Dehydrogenation of a Liquid Organic Hydrogen Carrier in the Liquid State
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Vacuum Surface Science Meets Heterogeneous Catalysis: Dehydrogenation of a Liquid Organic Hydrogen Carrier in the Liquid State

机译:真空表面科学与多相催化相遇:液态液态氢载体的脱氢

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摘要

Ultrahigh vacuum (UHV) surface science techniques are used to study the heterogeneous catalytic dehydrogenation of a liquid organic hydrogen carrier in its liquid state close to the conditions of real catalysis. For this purpose, perhydrocarbazole (PH), otherwise volatile under UHV, is covalently linked as functional group to an imidazolium cation, forming a non-volatile ionic liquid (IL). The catalysed dehydrogenation of the PH unit as a function of temperature is investigated for a Pt foil covered by a macroscopically thick PH-IL film and for Pd particles suspended in the PH-IL film, and for PH-IL on Au as inert support. X-ray photoelectron spectroscopy and thermal desorption spectroscopy allows us to follow in situ the catalysed transition of perhydrocarbazole to carbazole at technical reaction temperatures. The data demonstrate the crucial role of the Pt and Pd catalysts in order to shift the dehydrogenation temperature below the critical temperature of thermal decomposition.
机译:超高真空(UHV)表面科学技术用于研究液态有机氢载体在接近真实催化条件的液态下的非均相催化脱氢。为此,在UHV下易挥发的全氢咔唑(PH)作为官能团与咪唑鎓阳离子共价连接,形成不挥发性离子液体(IL)。对于被宏观上厚的PH-IL膜覆盖的Pt箔和悬浮在PH-IL膜中的Pd颗粒,以及作为惰性载体的Au上的PH-IL,都研究了PH单元的催化脱氢随温度的变化。 X射线光电子能谱和热脱附能谱使我们能够在技术反应温度下原位追踪全氢咔唑向咔唑的催化转变。数据证明了Pt和Pd催化剂在使脱氢温度低于热分解的临界温度方面的关键作用。

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