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首页> 外文期刊>The Journal of Chemical Physics >CONDENSATION OF SUPERSATURATED VAPORS OF HYDROGEN BONDING MOLECULES - ETHYLENE GLYCOL, PROPYLENE GLYCOL, TRIMETHYLENE GLYCOL, AND GLYCEROL
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CONDENSATION OF SUPERSATURATED VAPORS OF HYDROGEN BONDING MOLECULES - ETHYLENE GLYCOL, PROPYLENE GLYCOL, TRIMETHYLENE GLYCOL, AND GLYCEROL

机译:氢键合分子超饱和蒸汽的缩合-乙二醇,丙二醇,三甲基乙二醇和甘油

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摘要

The critical supersaturations required for the homogeneous nucleation (rate of 1 drop cm(-3) s(-1)) of ethylene glycol, propylene glycol, trimethylene glycol and glycerol vapors have been measured over wide temperature ranges (e.g., 280-400 K) using an upward thermal diffusion cloud chamber. At lower temperatures the experimental nucleation rates are much higher than the predictions of the classical nucleation theory. Glycerol shows the best agreement between experiment and theory in the temperature range of 340-370 K. An apparent increase in the critical supersaturation of glycerol is observed with increasing carrier gas (helium) pressure and this effect is more pronounced at lower temperatures. The results from corresponding states and scaled nucleation models indicate that the nucleation behavior of glycerol is quite different from other glycols. Glycerol requires higher critical supersaturations compared to the other glycols at the same reduced temperatures. This implies quite small critical clusters for glycerol (20-50 molecules) in the temperature range 300-380 K. The discrepancy between experiment and theory at lower temperatures may be explained by considering that the surface tension of the critical clusters is lower than the bulk surface tension. It is, however, surprising that a Tolman type correction for the curvature dependent surface tension could be applicable for such small critical clusters. Further theoretical work is required in order to fully understand the observed higher nucleation rates at lower temperatures of glycols and glycerol. (C) 1996 American Institute of Physics. [References: 83]
机译:乙二醇,丙二醇,三亚甲基二醇和甘油蒸气的均匀成核(速率为1滴cm(-3)s(-1)的成核所需的临界过饱和度)已在较宽的温度范围内(例如280-400 K )使用向上的热扩散云室。在较低温度下,实验成核速率比经典成核理论的预测值高得多。甘油在340-370 K的温度范围内显示出实验和理论之间的最佳一致性。随着载气(氦气)压力的升高,甘油的临界过饱和度明显增加,并且在较低温度下这种影响更为明显。相应状态和成比例的成核模型的结果表明,甘油的成核行为与其他二醇完全不同。在相同的降低温度下,甘油比其他二醇需要更高的临界过饱和度。这意味着在300-380 K的温度范围内,甘油的临界簇非常小(20-50分子)。在较低温度下,实验和理论之间的差异可以通过考虑临界簇的表面张力低于整体张力来解释。表面张力。然而,令人惊讶的是,针对曲率相关的表面张力的托尔曼类型校正可适用于如此小的临界簇。为了充分理解在较低的乙二醇和甘油温度下观察到的较高的成核速率,需要进行进一步的理论工作。 (C)1996年美国物理研究所。 [参考:83]

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