Measurements on thermodiffusion in ternary hydrocarbon mixtures at high pressure

被引:25
|
作者
Srinivasan, S. [1 ]
Saghir, M. Z. [1 ]
机构
[1] Ryerson Univ, Toronto, ON M5B 2K3, Canada
来源
JOURNAL OF CHEMICAL PHYSICS | 2009年 / 131卷 / 12期
关键词
THERMAL-DIFFUSION; SORET COEFFICIENT; OPTICAL MEASUREMENT; LIQUID; POLYSTYRENE; MOTION; MASS;
D O I
10.1063/1.3236745
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Experimental investigations on thermodiffusion have been conducted for five different ternary mixtures of methane, n-butane, and n-dodecane at a high temperature and pressure. While the mole fraction of methane was fixed at 0.2 the mole fraction of n-dodecane was varied from 0.7 to 0.2. The experiments were performed in a microgravity environment on board the satellite FOTON-M3. It was found that in all mixtures, n-dodecane separated to the cold side whereas methane segregated to the hot side. n-butane, the species with an intermediate density, showed a change in sign as its mole fraction was increased. At low concentrations it collected on the cold side but moved in the opposite direction with an increase in its mole fraction. The role of the relative density coupled with the species concentrations has been used to explain the thermodiffusion factor in each mixture. Computational investigations showed a similar behavior. However, the theoretical model was not able to capture the sign change of n-butane accurately. The inadequate representation of the significance of the relative densities and the mole fraction of the species has been found as the reason for this. (C) 2009 American Institute of Physics. [doi:10.1063/1.3236745]
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页数:8
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