首页> 外文期刊>The Journal of Chemical Physics >Cross-nucleation between clathrate hydrate polymorphs: Assessing the role of stability, growth rate, and structure matching
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Cross-nucleation between clathrate hydrate polymorphs: Assessing the role of stability, growth rate, and structure matching

机译:笼形水合物多晶型物之间的交叉成核:评估稳定性,生长速率和结构匹配的作用

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Cross-nucleation is a phenomenon where a new crystal nucleates and grows upon the surface of a different polymorph. Previous studies indicate that faster growth rate of the new crystal is a necessary but not sufficient condition for cross-nucleation. The thermodynamic stability of the different polymorphs can also affect cross-nucleation by modulating the rates of crystal growth. The interplay between thermodynamic stability of the polymorphs involved, the growth rate of the crystals, and the need for creation of an interfacial transition layer that seamlessly connects the two structures has not yet been fully elucidated. Predicting cross-nucleation is particularly challenging for clathrate hydrates, for which there are sometimes several polymorphs with similar stability and for which growth rates are not known. In this work, we use molecular dynamics simulations to investigate which factor(stability, growth rate, or formation of interfacial transition layer) controls cross-nucleation between the four known Frank-Kasper clathrate hydrate polymorphs: sI, sII, TS, and HS-I.We investigate the growth and cross-nucleation of these four hydrates filled with a set of guest molecules that produce different order of stabilities for the four crystal structures. We determine that the growth rate of sII clathrate is the fastest, followed by TS, HS-I, and sI. We find that cross-nucleation into or from sII clathrates is preceded by the formation of an interfacial transition layer at the seed crystal/liquid interface because sII does not share a crystal plane with sI, HS-I, or TS. Cross-nucleation between the latter three can occur seamlessly and is determined only by their growth rates. Our results indicate that nucleation of an interfacial transition layer between non-matching polymorphs can control cross-nucleation or lack thereof under conditions of small driving force. Under conditions of sufficient supercooling clathrate hydrate polymorphs cross-nucleate into the fastest growing phase even if that new phase is less stable and does not share a common crystal plane with the initial polymorph.
机译:交叉成核是新晶体成核并在不同多晶型物表面上生长的现象。先前的研究表明,新晶体更快的生长速率是交叉成核的必要条件,但不是充分条件。不同多晶型物的热力学稳定性还可以通过调节晶体生长速率来影响交叉成核。尚未充分阐明所涉及的多晶型物的热力学稳定性,晶体的生长速率以及创建无缝连接两个结构的界面过渡层之间的相互作用。对于包合物水合物而言,预测交叉成核特别具有挑战性,对于包合物水合物而言,有时存在几种具有相似稳定性的多晶型物,并且其生长速率未知。在这项工作中,我们使用分子动力学模拟来研究哪个因素(稳定性,生长速率或界面过渡层的形成)控制着四种已知的Frank-Kasper笼形水合物水合物多晶型物sI,sII,TS和HS- I.我们研究了这四种水合物的生长和交叉成核,这些水合物充满了一组客体分子,这些客体分子对四种晶体结构产生不同的稳定性顺序。我们确定sII包合物的增长率最快,其次是TS,HS-1和sI。我们发现,进入或来自sII笼形物的交叉成核是在晶种/液体界面处形成界面过渡层,因为sII不与sI,HS-1或TS共享晶面。后三个之间的交叉成核可以无缝发生,并且仅由它们的增长率决定。我们的结果表明,在不匹配的多晶型物之间的界面过渡层的成核可以在驱动力较小的情况下控制交叉成核或缺乏交叉成核。在足够的过冷条件下,包合物水合物的多晶型物交叉成核,成为增长最快的相,即使该新相的稳定性较差并且与初始多晶型物不具有相同的晶面。

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