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Facilitating guest transport in clathrate hydrates by tuning guest-host interactions

机译:通过调整来宾与宿主之间的相互作用,促进包合物水合物中的来宾运输

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The understanding and eventual control of guest molecule transport in gas hydrates is of central importance for the efficient synthesis and processing of these materials for applications in the storage, separation, and sequestration of gases and natural gas production. Previously, some links have been established between dynamics of the host water molecules and guest-host hydrogen bonding interactions, but direct observation of transport in the form of cage-to-cage guest diffusion is still lacking. Recent calculations have suggested that pairs of different guest molecules in neighboring cages can affect guest-host hydrogen bonding and, therefore, defect injection and water lattice motions. We have chosen two sets of hydrate guest pairs, tetrahydrofuran (THF)-CO2 and isobutane-CO2, that are predicted to enhance or to diminish guest-host hydrogen bonding interactions as compared to those in pure CO2 hydrate and we have studied guest dynamics in each using C-13 nuclear magnetic resonance (NMR) methods. In addition, we have obtained the crystal structure of the THF-CO2 sII hydrate using the combined single crystal X-ray diffraction and C-13 NMR powder pattern data and have performed molecular dynamics-simulation of the CO2 dynamics. The NMR powder line shape studies confirm the enhanced and delayed dynamics for the THF and isobutane containing hydrates, respectively, as compared to those in the CO2 hydrate. In addition, from line shape studies and 2D exchange spectroscopy NMR, we observe cage-to-cage exchange of CO2 molecules in the THF-CO2 hydrate, but not in the other hydrates studied. We conclude that the relatively rapid intercage guest dynamics are the result of synergistic guest A-host water-guest B interactions, thus allowing tuning of the guest transport properties in the hydrates by choice of the appropriate guest molecules. Our experimental value for inter-cage hopping is slower by a factor of 10(6) than a published calculated value. (C) 2015 AIP Publishing LLC.
机译:理解和最终控制气体水合物中客体分子的运输对于有效合成和加工这些材料以用于气体,天然气的储存,分离和封存至关重要。以前,在宿主水分子的动力学与客体-主体氢键相互作用之间已经建立了一些联系,但是仍然缺乏以笼对笼客体扩散形式进行运输的直接观察。最近的计算表明,相邻笼子中成对的不同客体分子会影响客体与主体之间的氢键,从而影响缺陷注入和水晶格运动。我们选择了两组水合物客体对,即四氢呋喃(THF)-CO2和异丁烷-CO2,与纯CO2水合物中的那些相比,它们预计会增强或减少客体与主体之间的氢键相互作用,并且我们研究了每个都使用C-13核磁共振(NMR)方法。此外,我们使用组合的单晶X射线衍射和C-13 NMR粉末图案数据获得了THF-CO2 sII水合物的晶体结构,并进行了CO2动力学的分子动力学模拟。 NMR粉末线形研究证实,与CO2水合物相比,分别含有THF和异丁烷的水合物的动力学增强和延迟。此外,通过线形研究和2D交换光谱NMR,我们观察到了THF-CO2水合物中CO2分子的笼对笼交换,但没有观察到其他水合物中的CO2分子。我们得出的结论是,相对快速的笼间客体动力学是客体A-宿主水-客体B协同作用的结果,因此可以通过选择合适的客体分子来调节水合物中的客体转运特性。我们关于笼间跳变的实验值比已发布的计算值慢了10(6)倍。 (C)2015 AIP Publishing LLC。

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