Aladko E Ya, Ancharov A I, Goryainov S V, Kurnosov A V, Larionov E G, Likhacheva A Yu, Manakov A Yu, Potemkin V A, Sheromov M A, Teplykh A E, Voronin V I, Zhurko F V
Nikolaev Institute of Inorganic Chemistry, SD RAS, Ac. Lavrentiev ave. 3, Novosibirsk 630090, Russian Federation.
J Phys Chem B. 2006 Oct 26;110(42):21371-6. doi: 10.1021/jp061698r.
In this work, we present a new, previously unknown type of structure transformation in the high-pressure gas hydrates, which is related to the existence of two different isostructural phases of the sulfur hexafluoride clathrate hydrates. Each of these phases has its own stability field on the phase diagram. The difference between these hydrates consists of partial filling of small D cages by SF(6) molecules in the high-pressure phase; at 900 MPa, about half of small cages are occupied. Our calculations indicate that the increase of population of small cavities is improbable, therefore, at any pressure value, a part of the cavities remains vacant and the packing density is relatively low. This fact allowed us to suppose the existence of the upper pressure limit of hydrate formation in this system; the experimental results obtained confirm this assumption.
在这项工作中,我们展示了高压气体水合物中一种新的、此前未知的结构转变类型,它与六氟化硫笼形水合物的两种不同等结构相的存在有关。这些相中的每一个在相图上都有其自己的稳定域。这些水合物之间的差异在于高压相中SF(6)分子对小D笼的部分填充;在900兆帕时,约一半的小笼被占据。我们的计算表明,小笼占有率增加是不太可能的,因此,在任何压力值下,一部分笼仍然是空的,堆积密度相对较低。这一事实使我们推测该体系中水合物形成存在压力上限;所获得的实验结果证实了这一假设。