Mass transfer analysis of the isochoric-isotherm hydrate-based water desalination from CO2/C3H8 gas mixtures

被引:0
|
作者
Naseh, M. [1 ]
Falamaki, C. [1 ,2 ]
Mohebbi, V. [3 ]
机构
[1] Amirkabir Univ Technol, Chem Engn Dept, Mahshahr Campus, Mahshahr 415, Iran
[2] Amirkabir Univ Technol, Chem Engn Dept, POB 158754413, Tehran, Iran
[3] Petr Univ Technol, Gas Engn Dept, Ahvaz 63431, Iran
关键词
Gas hydrate; Desalination; Mass transfer coefficient ratio; Modeling; Molar content in hydrate phase; Competition in cage hydrate occupancy; CLATHRATE HYDRATE; METHANE HYDRATE; FORMATION TEMPERATURE; MOLECULAR-DYNAMICS; CARBON-DIOXIDE; GROWTH; PREDICTION; REMOVAL; ETHANE; INHIBITION;
D O I
10.1007/s13762-023-05140-z
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The purpose of this study is to investigate the composition of the gas, liquid and hydrate phases during gas hydrate formation. The kinetics of gas hydrate formation from a CO2/C3H8 gas mixture (initial molar ratio 80/20) under isochoric and isothermal (2, 4 and 6 & DEG;C) conditions from pure and saline water has been investigated. Experimental measurement of gas composition was performed by gas chromatography and that of the liquid phase by conductivity analysis. The main and novel finding of the present study is that at early times, the gas hydrate is supersaturated with CO2, following an equilibrium concentration of CO2 and C3H8 molecules at later times. Initially, the occupancy of the 5(12)6(4) cages of the SII structure by the CO2 molecules exceeds the equilibrium plateau. A gradual egress of CO2 to the liquid/gas phase occurs afterward, eventually resulting in the decrease in CO2 and increase in C3H8 apparent mass transfer coefficients.
引用
收藏
页码:11149 / 11164
页数:16
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