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在稳定性极限附近增强水合物成核

Enhanced Hydrate Nucleation Near the Limit of Stability.

作者信息

Jimenez-Angeles Felipe, Firoozabadi Abbas

出版信息

J Phys Chem C Nanomater Interfaces. 2015;119(16):8798-8804. doi: 10.1021/acs.jpcc.5b01869. Epub 2015 Mar 30.

Abstract

Clathrate hydrates are crystalline structures composed of small guest molecules trapped into cages formed by hydrogen-bonded water molecules. In hydrate nucleation, water and the guest molecules may stay in a metastable fluid mixture for a long period. Metastability is broken if the concentration of the guest is above certain limit. We perform molecular dynamics (MD) simulations of supersaturated water-propane solutions close to the limit of stability. We show that hydrate nucleation can be very fast in a very narrow range of composition at moderate temperatures. Propane density fluctuations near the fluid-fluid demixing are coupled with crystallization producing en- hanced nucleation rates. This is the first report of propane-hydrate nucleation by MD simulations. We observe motifs of the crystalline structure II in line with experiments and new hydrate cages not reported in the literature. Our study relates nucleation to the fluid-fluid spinodal decomposition and demonstration that the enhanced nucleation phenomenon is more general than short range attractive interactions as suggested in nucleation of proteins.

摘要

笼形水合物是由被困在氢键结合的水分子形成的笼中的小分子客体分子组成的晶体结构。在水合物成核过程中,水和客体分子可能会在亚稳态流体混合物中长时间停留。如果客体的浓度高于一定限度,亚稳态就会被打破。我们对接近稳定性极限的过饱和水 - 丙烷溶液进行了分子动力学(MD)模拟。我们表明,在中等温度下,水合物成核在非常窄的组成范围内可能非常快。流体 - 流体 demixing 附近的丙烷密度波动与结晶耦合,产生增强的成核速率。这是通过 MD 模拟首次报道丙烷 - 水合物成核。我们观察到符合实验的晶体结构 II 的图案以及文献中未报道的新水合物笼。我们的研究将成核与流体 - 流体旋节线分解联系起来,并证明增强的成核现象比蛋白质成核中所暗示的短程吸引相互作用更普遍。

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