Peng Bao-Zi, Sun Chang-Yu, Liu Peng, Liu Yan-Tao, Chen Jun, Chen Guang-Jin
State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing 102249, People's Republic of China.
J Colloid Interface Sci. 2009 Aug 15;336(2):738-42. doi: 10.1016/j.jcis.2009.04.028. Epub 2009 Apr 14.
The interfacial tensions between methane and aqueous solutions of different contents of VC-713 (a terpolymer of N-vinylpyrrolidone, N-vinylcaprolactam, and dimethylamino-ethyl-methacrylate) were measured at different temperatures and pressures in the hydrate formation region. The surface adsorption free energies of methane were calculated accordingly in order to investigate the effect of this kinetic inhibitor on the nucleation of hydrate. The results show that the presence of VC-713 lowers the interfacial tension, increasing the concentration of methane on the surface of the aqueous phase, and thus promotes nucleation of hydrate at the gas/liquid interface. Additionally, the measured interfacial tension data suggest that VC-713 tends not to form micelles in water. Subsequently, the lateral growth rate of hydrate film on the surface of a methane bubble suspended in the aqueous phase was measured at different pressures to investigate the effect of VC-713 on the growth of hydrate. The results show that the lateral growth rate of hydrate film from aqueous VC-713 solution is much lower than that from pure water, demonstrating that VC-713 significantly inhibits the hydrate growth. The mechanism of the inhibition is also discussed.
在水合物生成区域的不同温度和压力下,测量了甲烷与不同含量VC - 713(N - 乙烯基吡咯烷酮、N - 乙烯基己内酰胺和甲基丙烯酸二甲氨基乙酯的三元共聚物)水溶液之间的界面张力。据此计算了甲烷的表面吸附自由能,以研究这种动力学抑制剂对水合物成核的影响。结果表明,VC - 713的存在降低了界面张力,增加了水相表面甲烷的浓度,从而促进了气/液界面处水合物的成核。此外,测得的界面张力数据表明VC - 713在水中不易形成胶束。随后,在不同压力下测量了悬浮在水相中的甲烷气泡表面水合物膜的横向生长速率,以研究VC - 713对水合物生长的影响。结果表明,来自VC - 713水溶液的水合物膜横向生长速率远低于来自纯水的生长速率,表明VC - 713显著抑制了水合物的生长。还讨论了抑制机理。