Oxabicyclic Guest Compounds as sII Promoters: Spectroscopic Investigation and Equilibrium Measurements.

In this study, we investigate three oxabicyclic compounds, 3,6-dioxabicyclo[3. 1.0]hexane (CHO, ETHF), 7-oxabicyclo[2.2.1]heptane (CHO, 14ECH), and 7-oxabicyclo[4.1.0]heptane (CHO, 12ECH) as novel promoters for gas hydrates. According to the outcomes of powder X-ray diffraction (PXRD) and synchrotron high-resolution powder diffraction (HRPD), all CH hydrates formed with ETHF, 14ECH, and 12ECH were identified to be sII (Fd-3m) hydrates with corresponding lattice parameters of 17.195, 17.330, and 17.382 Å, respectively. It was also clearly demonstrated that CH molecules are accommodated in the sII-S cages through solid-state C NMR and Raman spectra. Consequently, we clarified that the three compounds observed are large guest molecules (LGMs) that occupy the sII-L cages. Moreover, the thermodynamic stability of each LGM + CH (and N) hydrate system was remarkably improved compared to that of the simple CH (and N) hydrate. In particular, 14ECH manifested several unique features compared to the other two promoters. First, the 14ECH + CH hydrate did not dissociate up to room temperature (298 K), even at a moderate pressure of approximately 60 bar. At a given pressure, 14ECH increased the dissociation temperature of the CH hydrate by 18 K, indicating that its promotion capability is as strong as that of tetrahydrofuran (THF), currently considered to be the most powerful promoter. Second, more interestingly, it was revealed by further PXRD, NMR, and Raman analyses that 14ECH forms a simple sII hydrate in the absence of help gases. According to differential scanning calorimetry (DSC) outcomes, we revealed that the simple 14ECH hydrate dissociates at 270278 K under ambient pressure. In addition to the thermodynamic stability, we also note that the 14ECH + CH hydrate presented a sufficiently high temperature of formation, requiring little additional cooling. Given these promising features, we expect that the 14ECH hydrate system can be adopted to realize hydrate-based technologies. We also believe that the LGMs introduced here have considerable potential to serve as alternates to conventional promoters and that they can be widely utilized in both engineering and scientific research fields.