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MECHANISMS UNDERLYING FOAM-BASED ELECTRONUCLEATION OF HYDRATES

机译:基于泡沫的水合物电化机理

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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 watenTHF 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.
机译:笼形水合物在低温下的成核受到非常长的诱导(等待)时间的限制,诱导时间可能从数小时到数天不等。电核化(在水合物形成溶液中施加电势差)可以显着减少感应时间。这项工作研究了各种材料的多孔开孔泡沫作为电核化电极的用途。用四氢呋喃(THF)水合物进行的实验表明,铝和碳泡沫电极可以实现电压依赖性成核,诱导时间取决于泡沫材料的电离趋势。此外,我们观察到电核化参数(如诱导时间和重新发光温度)对watenTHF摩尔比的非平凡依赖。这项研究进一步证实了先前提出的假说,这些假说将水合物快速成核与金属离子配位化合物的形成联系起来。总的来说,这项工作研究了铝和碳泡沫的电核法的各个方面。

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