基于泡沫的水合物电子成核机制

Palash V. Acharya, Denise Lin, V. Bahadur
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引用次数: 0

摘要

笼形物水合物在低温下的成核受到很长的诱导(等待)时间的限制,这可以从几个小时到几天不等。电气化(在水合物形成溶液中施加电位差)可以显著缩短诱导时间。本工作研究了不同材料的多孔开孔泡沫作为电子核电极的使用。四氢呋喃(THF)水合物实验表明,铝和碳泡沫电极可以实现电压依赖的成核,诱导时间取决于泡沫材料的电离倾向。此外,我们还观察到电致核参数(如感应时间和再发光温度)与水:THF摩尔比的关系不容小视。这项研究进一步证实了先前提出的假设,即快速水合物成核与金属离子配位化合物的形成有关。总的来说,这项工作研究了铝和碳泡沫的电子化的各个方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanisms Underlying Foam-Based Electronucleation of Hydrates
Nucleation of clathrate hydrates at low temperatures is constrained by very long induction (wait) times, which can range from hours to days. Electronucleation (application of an electrical potential difference across the hydrate forming solution) can significantly reduce the induction time. This work studies the use of porous open-cell foams of various materials as electronucleation electrodes. Experiments with tetrahydrofuran (THF) hydrates reveal that aluminum and carbon foam electrodes can enable voltage-dependent nucleation, with induction times dependent on the ionization tendency of the foam material. Furthermore, we observe a non-trivial dependence of the electronucleation parameters such as induction time and the recalescence temperature on the water:THF molar ratio. This study further corroborates previously developed hypotheses which associated rapid hydrate nucleation with the formation of metal-ion coordination compounds. Overall, this work studies various aspects of electronucleation with aluminum and carbon foams.
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