| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 201738 | Fluid Phase Equilibria | 2015 | 6 Pages |
•The effects of large molecular alcohols on N2 hydrates are examined.•PCA and tAA form sH hydrates in the presence of N2 as a help gas.•The N2 + PCA hydrate exhibits a more significant equilibrium curve shift than the N2 + tAA hydrate.
The influences of large molecular alcohols (LMAs) (pinacolyl alcohol (PCA) and tert-amyl alcohol (tAA)) on N2 hydrate were examined with a primary focus on the hydrate phase equilibria and structural transition. The four-phase (H–Lw–LLMA–V) equilibria of the N2 + PCA + water and N2 + tAA + water systems were experimentally measured in order to determine the thermodynamic stability conditions of the N2 hydrates with LMAs. The H–Lw–LLMA–V curves of both N2 + PCA and N2 + tAA hydrates were significantly shifted to more thermodynamically stable regions. Powder X-ray diffraction (PXRD) and Raman analyses verified that the structure of N2 hydrates with LMAs was transformed from the original structure of sII to sH (P6/mmm) as a result of the inclusion of LMAs. In addition, the formation of sH hydrate from the N2 + PCA + water system was further verified using an endothermic dissociation thermogram from a high pressure micro-differential scanning calorimeter (HP μ-DSC) by confirming the appearance of three distinct peaks that correspond to ice, sII hydrate, and sH hydrate. Therefore, the experimental results that were obtained in this study are expected to be informative for understanding the roles of LMAs in affecting the macroscopic hydrate phase behavior and microscopic hydrate structure.
