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Phase equilibrium of propane and alkanes Part III:Beyond hexacontane

机译:丙烷和烷烃的相平衡第三部分:六烷以外的物质

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Part II of this series showed that at constant temperature and mass fraction a linear relationship exists between the number of carbon atoms and bubble/dew-point pressure of linear alkanes in supercritical propane.This paper investigates the extent to which this linear relationship can be extrapolated.In the crystalline phase linear alkanes undergo molecular folding,yet information on molecular folding in the fluid state is inconclusive.Molecular folding influences the nature of the alkane and it may thus influence the supercritical phase behaviour and thus result in a change in the linear relationship between the number of carbon atoms and the bubble/dew-point pressure of alkanes in supercritical propane.A model is proposed for molecular folding in supercritical solution.Measurements were conducted with a wax mixture containing an average of 102 carbon atoms and results showed that in the low wax mass fraction and mixture critical region the linear relationships hold true and molecular folding most probably does not occur.In the high wax mass fraction region lower pressures than predicted are observed and possible explanations of the lower than expected pressures include the polydisperse nature of the mixture and the possibility that partial molecular folding may have occurred.
机译:该系列的第二部分表明,在恒定温度和质量分数下,超临界丙烷中碳原子数与线性烷烃的气泡/露点压力之间存在线性关系。本文研究了这种线性关系可以外推的程度在结晶相中直链烷烃经历分子折叠,但在流体状态下分子折叠的信息尚无定论。分子折叠会影响烷烃的性质,因此可能会影响超临界相的行为,从而导致线性关系发生变化提出了超临界溶液中分子折叠的模型,用平均含102个碳原子的蜡混合物进行了测量,结果表明,在超临界丙烷中,该混合物的碳原子数与超临界丙烷中烷烃的沸点/露点压力之间的关系。低蜡质量分数和混合物临界区,线性关系成立,分子正确r极有可能不会发生折叠。在高蜡质量分数区域中,观察到的压力低于预期的压力,而比预期的压力更低的可能解释包括混合物的多分散性以及部分分子折叠的可能性。

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