Fuseya Go, Takeya Satoshi, Hachikubo Akihiro
Kitami Institute of Technology 165, Koen-cho Kitami 090-8507 Japan
National Institute of Advanced Industrial Science and Technology (AIST) Central 5, 1-1-1, Higashi Tsukuba 305-8565 Japan.
RSC Adv. 2020 May 6;10(30):17473-17478. doi: 10.1039/d0ra02748k. eCollection 2020 May 5.
Large molecules such as 2-methylbutane (CH) or 2,2-dimethylbutane (CH) form structure H (sH) hydrates with methane (CH) as a help gas. In this study, the Raman spectra of the C-H symmetric stretch region of CH enclathrated within various sH hydrates and structure I CH hydrates were analyzed in the temperature range 137.7-205.4 K. Thermal expansions of these sH hydrate samples were also measured using powder X-ray diffraction. Symmetric stretch vibrational frequencies of CH in host-water cages increased because of varying temperature, and the sizes of the host-water cages also increased; variation of CH in small cages was less than in larger cages. Comparing the variations of the C-H symmetric stretching frequencies of CH in gas hydrates with varying pressure and temperature, we suggest that the observed trend is caused by thermal vibrations of the CH molecule in water cages.
诸如2-甲基丁烷(CH)或2,2-二甲基丁烷(CH)等大分子与甲烷(CH)作为辅助气体形成结构H(sH)水合物。在本研究中,分析了在137.7 - 205.4 K温度范围内,包合在各种sH水合物和结构I型CH水合物中的CH的C - H对称伸缩区域的拉曼光谱。还使用粉末X射线衍射测量了这些sH水合物样品的热膨胀。由于温度变化,主体 - 水笼中CH的对称伸缩振动频率增加,并且主体 - 水笼的尺寸也增大;小笼中CH的变化小于大笼中的变化。通过比较不同压力和温度下气体水合物中CH的C - H对称伸缩频率的变化,我们认为观察到的趋势是由CH分子在水笼中的热振动引起的。