Dehydrogenation Catalyst for Organic Hydride on the Basis of Superheated Liquid-Film Concept

A. Shono, K. Otake, D. Kobayashi, S. Kobayashi, Y. Saito
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Abstract

Reversible reaction couples of hydrogenation and dehydrogenation of organic compounds e.g. methylcyclohexane and toluene, or 2-propanol and acetone, are described in terms of hydrogen supplier to fuel cells, which will satisfy our demands of combined heat and power at various compact sizes. Carbon supported nano-sized metal particles, wetted with the liquid substrate in a reactor, was used for conversion of organic hydrides into hydrogen and organic compounds, being separable by distillation. Vigorous nucleate boiling is important for heat transfer as well as for irreversible bubble evolution, leading hydrogen to the vapor phase. Once the bubble is broken at the interface, catalytic hydrogenation will be prohibited, because gaseous hydrogen is unable to dissolve into the boiling liquid. Catalytic dehydrogenation under superheated liquid-film conditions can thus convert low-quality heats into hydrogen energy.
基于过热液膜概念的有机氢化物脱氢催化剂
从燃料电池供氢的角度描述了甲基环己烷和甲苯、2-丙醇和丙酮等有机化合物加氢和脱氢的可逆反应对,这将满足我们在各种紧凑尺寸下的热电联产需求。碳负载的纳米金属颗粒在反应器中被液体衬底润湿,用于将有机氢化物转化为氢和有机化合物,并通过蒸馏可分离。剧烈的核沸腾对于传热和不可逆的气泡演化是重要的,导致氢进入蒸汽相。一旦气泡在界面处破裂,催化加氢将被禁止,因为气态氢无法溶解到沸腾的液体中。因此,在过热液膜条件下的催化脱氢可以将低质量的热量转化为氢能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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