Abstract
Ionic clathrate hydrates are promising materials for hydrate-based gas storage and separation processes. Here, we demonstrated that the hydroxide ion in the cubic structure-II (CS-II) and hexagonal structure-III (HS-III) ionic clathrate hydrates can be replaced by fluoride. Me4N+ and Et2Me2N+ cations were selected as guest species for the CS-II and HS-III hydrates, respectively. The crystal structure of each hydrate was identified through Rietveld analysis of the PXRD pattern. The Fd3 ¯ m structure (CS-II) of Me4NF+N2 or O2 hydrates and the P6/mmm structure (HS-III) of Et2Me2NF+CH4 hydrate were confirmed. We also investigated the phase equilibria of hydroxide or fluoride-incorporated CS-II and HS-III hydrate systems, and found that incorporating fluoride destabilizes the hydrate lattice to a greater extent than hydroxide. The present findings will provide better understanding of the guest-host interactions in ionic clathrate hydrates, and suggest their potential for practical applications in gas storage and separation technologies.
| Original language | English |
|---|---|
| Pages (from-to) | 2520-2528 |
| Number of pages | 9 |
| Journal | Korean Journal of Chemical Engineering |
| Volume | 40 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 2023 |
Keywords
- Fluoride
- Gas Storage
- Inclusion Compound
- Ionic Clathrate Hydrate
- Powder X-ray Diffraction
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