静电场条件下环戊烷水合物在多孔介质中的相变可视化研究
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TQ 026

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    摘要:

    水合物作为一种新型的清洁能源和碳捕集与埋存(CCS)的重要方式,研究其在多孔介质中的相变机制,对实现相关技术的现场应用至关重要。本文设计制作的微流控芯片模拟了地层中多孔介质,并运用其进行了环戊烷水合物的相变实验。通过显微观察,分析了同一过冷度下外加静电场对水合物形态、生长速率、诱导时间及相平衡温度的影响。结果表明,静电场能够改变环戊烷水合物晶体的生长形态、显著缩短诱导时间,但轻微降低相平衡温度。随着电场强度的增大,水合物诱导时间延长、相平衡温度升高。静电场作用下环戊烷水合物的生长速率明显提高。本研究得到的电场对多孔介质中水合物相变的影响机制,为电场方法在水合物开发和基于水合物的CCS技术中的应用提供了参考。

    Abstract:

    Hydrates, which serve as a novel form of clean energy and a key component in carbon capture and storage (CCS), require a thorough understanding of their phase transition mechanisms within porous media for the effective implementation of related technologies. In this study, a microfluidic chip was developed to emulate subsurface porous media and phase transition experiments were performed on cyclopentane hydrates. By means of microscopic observation, we analyzed the influence of an applied electrostatic field under identical subcooling conditions on hydrate morphology, growth rate, induction time, and equilibrium temperature. The results show that the application of an electrostatic field has the ability to alter the growth morphology of CP hydrate crystals, shortening the induction time, although lowering the phase equilibrium temperature. Furthermore, both the induction time and the phase equilibrium temperature increase with increasing electric field intensity. Under the influence of an electrostatic field, the growth rate of CP hydrates exhibits a noticeable enhancement. This study provides valuable insights into the application of electric fields in hydrate development and hydrate-based CCS technologies.

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  • 收稿日期:2024-03-15
  • 最后修改日期:2024-03-15
  • 录用日期:2024-04-10
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