Molecular dynamics study of methane hydrate formation at a water/methane interface

• Published in: The Journal of Physical Chemistry B
• Main Authors: Zhang, Junfang, Hawtin, R. W., Yang, Ye, Nakagava, Edson, Rivero, M., Choi, S. K., Rodger, P. Mark
• Format: Article in Journal/Newspaper
• Language: unknown
• Published: American Chemical Society 2008
• Subjects: QD Chemistry; QP Physiology; Methane hydrate
• Online Access: http://wrap.warwick.ac.uk/29504/; https://doi.org/10.1021/jp076904p

We present molecular dynamics simulation results of a liquid water/methane interface, with and without an oligomer of poly(methylaminoethylmethacrylate), PMAEMA. PMAEMA is an active component of a commercial low dosage hydrate inhibitor (LDHI). Simulations were performed in the constant NPT ensemble at temperatures of 220, 235, 240, 245, and 250 K and a pressure of 300 bar. The simulations show the onset of methane hydrate growth within 30 ns for temperatures below 245 K in the methane/water systems; at 240 K there is an induction period of ca. 20 ns, but at lower temperatures growth commences immediately. The simulations were analyzed to calculate hydrate content, the propensity for hydrogen bond formation, and how these were affected by both temperature and the presence of the LDHI. As expected, both the hydrogen bond number and hydrate content decreased with increasing temperature, though little difference was observed between the lowest two temperatures considered. In the presence of PMAEMA, the temperature below which sustained hydrate growth occurred was observed to decrease. Some of the implications for the role of PMAEMA in LDHIs are discussed.