The Dependence of the Dissociation Rate of Methane-SDS Hydrate below Ice Point on Its Manners of Forming and Processing

• Published in: Chinese journal of chemical engineering Vol. 17; no. 1; pp. 128 - 135
• Main Author: 王秀林 陈光进 孙长宇 杨兰英 马庆兰 陈俊 刘鹏 唐绪龙 赵焕伟 陈卫东
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.02.2009
• Subjects: Atmospheric pressure; Barometric pressure; Chemical engineering; dissociation; hydrate; Hydrates; kinetics; Methane hydrates; SDS; Sodium; Stability; storage; surfactant; Surfactants; 分解速率; 生成方式; 甲烷水合物; 表面活性剂; hydrate; storage; kinetics; dissociation; surfactant
• ISSN: 1004-9541; 2210-321X
• DOI: 10.1016/S1004-9541(09)60043-4

The dissociation rates of methane hydrates formed with and without the presence of sodium dodecyl sulfate （methane-SDS hydrates）, were measured under atmospheric pressure and temperatures below ice point to investigate the influence of the hydrate production conditions and manners upon its dissociation kinetic behavior. The experimental results demonstrated that the dissociation rate of methane hydrate below ice point is strongly dependent on the manners of hydrate formation and processing. The dissociation rate of hydrate formed quiescently was lower than that of hydrate formed with stirring; the dissociation rate of hydrate formed at lower pressure was higher than that of hydrate formed at higher oressure; the comoaction of hydrate after its formation lowered its stability, i.e., increased＇its dissociation rate.The stability of hydrate could beincreased by prolonging the time period for which hydrate was held at formation temperature and pressure before it was cooled down, or by prolonging the time period for which hydrate was held at dissociation temperature and formation pressure before it was depressurized to atmospheric pressure. It was found that the dissociation rate of methane hydrate varied with the temperature （ranging from 245.2 to 272.2 K） anomalously as reported on the dissociation of methane hydrate without the presence of surfactant as kinetic promoter. The dissociation rate at 268 K was found to be the lowest when the manners and conditions at which hydrates were formed and processed were fixed.