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

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 dissociat...

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Published inChinese 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
LanguageEnglish
Published Elsevier B.V 01.02.2009
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ISSN1004-9541
2210-321X
DOI10.1016/S1004-9541(09)60043-4

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Abstract 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.
AbstractList The dissociation rates of methane hydrates formed with and without the presence of sodium dodecylsulfate (methane-SDS hydrates), were measured under atmospheric pressure and temperatures below ice point toinvestigate 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 quiescentlywas 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 pressure; the compaction of hydrate after its formation lowered its stability, i.e., increased its dissociation rate. The stability of hydrate could be increased by prolonging the time periodfor which hydrate was held at formation temperature and pressure before it was cooled down, or by prolonging thetime 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.
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.
The dissociation rates of methane hydrates formed with and without the presence of sodium dodecylsulfate (methane-SDS hydrates), were measured under atmospheric pressure and temperatures below ice point toinvestigate 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 quiescentlywas 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 pressure; the compaction of hydrate after its formation lowered its stability, i.e., increased its dissociation rate. The stability of hydrate could be increased by prolonging the time periodfor which hydrate was held at formation temperature and pressure before it was cooled down, or by prolonging thetime 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.
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
AuthorAffiliation State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing 102249, China Development Engineering Institute, China Oilfield Service Limited, Beijing 101149, China
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Keywords hydrate
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Snippet The dissociation rates of methane hydrates formed with and without the presence of sodium dodecyl sulfate (methane-SDS hydrates), were measured under...
The dissociation rates of methane hydrates formed with and without the presence of sodium dodecylsulfate (methane-SDS hydrates), were measured under...
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SubjectTerms 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
Title The Dependence of the Dissociation Rate of Methane-SDS Hydrate below Ice Point on Its Manners of Forming and Processing
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