Phase Equilibrium and Dissociation Enthalpies of Trimethylene Sulfide plus Methane Hydrates in Brine Water Systems

In this work, we measured the phase equilibrium data of trimethylene sulfide + methane hydrates in brine water systems with a NaCl mass fraction of 0.035, 0.070, 0.100, and 0.120 by using T-cycle methods. The dissociation enthalpies of trimethylene sulfidemethane hydrates were calculated by the Clau...

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Bibliographic Details
Published in:Journal of Chemical & Engineering Data
Main Authors: Li, Lu, Lv, Qiu-Nan, Li, Xiao-Sen, Feng, Jing-Chun, Chen, Zhao-Yang
Format: Article in Journal/Newspaper
Language:English
Published: 2014
Subjects:
Online Access:http://ir.giec.ac.cn/handle/344007/10623
https://doi.org/10.1021/je500607n
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Summary:In this work, we measured the phase equilibrium data of trimethylene sulfide + methane hydrates in brine water systems with a NaCl mass fraction of 0.035, 0.070, 0.100, and 0.120 by using T-cycle methods. The dissociation enthalpies of trimethylene sulfidemethane hydrates were calculated by the ClausiusClapeyron equation based on the measured phase equilibrium data. The equilibrium pressure of trimethylene sulfide + methane hydrate is much lower than that of the cyclopentane + methane hydrate at the same NaCl concentration in the aqueous solution. Hence, trimethylene sulfide may be a promising water-insoluble chemical promoter. The phase equilibrium pressure of trimethylene sulfide + methane hydrate increases as the temperature rises at the same NaCl concentration. In addition, the concentration of NaCl has more remarkable influence on the equilibrium pressure at a higher temperature. The formation/dissociation enthalpies of trimethylene sulfide + methane hydrate decrease with the increases of the temperature and NaCl concentration, respectively.