International Institute for Carbon-Neutral Energy Research (WPI-I2CNER), Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
Phys Chem Chem Phys. 2018 Jul 25;20(29):19430-19440. doi: 10.1039/c8cp02521e.
The effect of ambient temperature and relative humidity on the dynamics of ethanol drop evaporation is investigated. Although drop evaporation of mixtures and pure fluids has been extensively studied, very little is known about the transition from a pure fluid to a binary mixture following transfer of a second component present in the atmosphere. This is of importance for industrial, biological and medical applications where the purity of the solvent is paramount. Adsorption-absorption and/or condensation of water into ethanol drops during evaporation is presented through direct quantification of the drop composition in time. In particular, we combine drop profile measurements with Gas Injection Chromatography (GIC) to directly quantify the amount of ethanol evaporated and that of water intake over time. As expected, drops evaporate faster at higher temperatures since both the ethanol saturation concentration and the vapor diffusion coefficient are directly proportional to temperature. On the other hand, increases in the ethanol evaporation rate and in the water intake are observed at higher relative humidity. The increase in ethanol evaporation at higher relative humidity is interpreted by the greater diffusion coefficient of ethanol into humid air when compared to dry air. Moreover, as ethanol evaporates in a high humidity environment, the drop interfacial temperature falls below the dew point due to evaporative cooling and water condenses compared to lower humidity conditions. As a consequence of the heat released by adsorption-absorption and/or condensation, a greater temperature is reported at the liquid-vapor interface as confirmed by IR thermography, inducing a greater ethanol saturation concentration at the surface and hence a greater driving force for evaporation. By coupling the drop profile and the composition of ethanol and water within the drop, we propose a combined evaporation-adsorption/absorption and/or condensation empirical correlation. The proposed correlation accounts for: the decreases in ethanol concentration due to water adsorption-absorption and/or condensation, the diffusion coefficient dependence on relative humidity, and the amount of water intake during evaporation. The proposed empirical correlation agrees remarkably well with experimental observations.
环境温度和相对湿度对乙醇液滴蒸发动力学的影响。虽然混合物和纯流体的液滴蒸发已经得到了广泛的研究,但对于在大气中存在第二种组分转移后从纯流体到二元混合物的转变,人们知之甚少。这对于工业、生物和医疗应用非常重要,因为溶剂的纯度至关重要。在蒸发过程中,通过直接定量测定液滴组成来研究水在乙醇液滴中的吸附-吸收和/或凝结。特别是,我们将液滴轮廓测量与气相色谱注射(Gas Injection Chromatography,GIC)相结合,直接定量测定随时间蒸发的乙醇量和水的吸收量。正如预期的那样,由于乙醇饱和浓度和蒸汽扩散系数都直接与温度成正比,因此温度升高时液滴蒸发得更快。另一方面,在较高的相对湿度下,观察到乙醇蒸发速率和水吸收速率的增加。与干燥空气相比,乙醇在高湿度空气中的扩散系数较大,这解释了相对湿度较高时乙醇蒸发速率的增加。此外,由于乙醇在高湿度环境中蒸发,液滴界面温度由于蒸发冷却而降至露点以下,与较低湿度条件相比,水凝结。由于吸附-吸收和/或凝结释放的热量,通过红外热成像确认,在液-气界面处报告了更高的温度,从而在表面处产生更高的乙醇饱和浓度,从而产生更大的蒸发驱动力。通过耦合液滴轮廓和液滴内乙醇和水的组成,我们提出了一种组合蒸发-吸附/吸收和/或凝结的经验相关性。所提出的相关性考虑了以下因素:由于水的吸附-吸收和/或凝结导致的乙醇浓度降低、扩散系数对相对湿度的依赖性以及蒸发过程中水的吸收量。所提出的经验相关性与实验观察结果非常吻合。