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氢气和氘气在多孔碳材料上吸附/脱附过程中量子分子筛分的动力学同位素效应。

Kinetic isotope effect for H2 and D2 quantum molecular sieving in adsorption/desorption on porous carbon materials.

作者信息

Zhao Xuebo, Villar-Rodil Silvia, Fletcher Ashleigh J, Thomas K Mark

机构信息

Northern Carbon Research Laboratories, School of Natural Sciences, University of Newcastle upon Tyne, Newcastle upon Tyne, UK.

出版信息

J Phys Chem B. 2006 May 25;110(20):9947-55. doi: 10.1021/jp060748p.

Abstract

Adsorption and desorption of H(2) and D(2) from porous carbon materials, such as activated carbon at 77 K, are usually fully reversible with very rapid adsorption/desorption kinetics. The adsorption and desorption of H(2) and D(2) at 77 K on a carbon molecular sieve (Takeda 3A), where the kinetic selectivity was incorporated by carbon deposition, and a carbon, where the pore structure was modified by thermal annealing to give similar pore structure characteristics to the carbon molecular sieve substrate, were studied. The D(2) adsorption and desorption kinetics were significantly faster (up to x1.9) than the corresponding H(2) kinetics for specific pressure increments/decrements. This represents the first experimental observation of kinetic isotope quantum molecular sieving in porous materials due to the larger zero-point energy for the lighter H(2), resulting in slower adsorption/desorption kinetics compared with the heavier D(2). The results are discussed in terms of the adsorption mechanism.

摘要

在77K下,氢气(H₂)和氘气(D₂)在多孔碳材料(如活性炭)上的吸附和解吸通常是完全可逆的,且吸附/解吸动力学非常迅速。研究了77K下H₂和D₂在碳分子筛(武田3A,通过碳沉积引入动力学选择性)以及通过热退火改变孔结构以使其具有与碳分子筛基质相似孔结构特征的一种碳材料上的吸附和解吸情况。对于特定的压力增加/减少,D₂的吸附和解吸动力学明显比相应的H₂动力学快(高达1.9倍)。这是多孔材料中动力学同位素量子分子筛分的首次实验观察,原因是较轻的H₂具有较大的零点能,与较重的D₂相比,导致吸附/解吸动力学较慢。根据吸附机理对结果进行了讨论。

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