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Use of diffusion controlled drop evaporation equations for dropwise condensation during dew formation and effect of neighboring droplets

机译:使用扩散控制的液滴蒸发方程式在露水形成过程中逐滴冷凝以及相邻液滴的影响

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摘要

In this study, we determined that the equations derived for the diffusion controlled drop evaporation processes can be successfully applied to the condensation rate of water droplets on polymer surfaces having a surface temperature just below the dew point. The differences between the growth rates of condensed isolated droplets on five different polyolefin surfaces, whose surface free energies were in a close range of 30-37mJ/m ~2, were attributed to the difference in surface roughness which alters the droplet nucleation rate, drop pinning effect and initial contact angles. The condensation rate of isolated droplets decreased with the increase of surface roughness, water contact angle and contact angle hysteresis in the order of ethylene-vinyl acetate copolymer (EVA)>low density polyethylene (LDPE)>high density polyethylene (HDPE)>polypropylene-polyethylene copolymer (PPPE)>polypropylene (PP). The drop radius of the individual isolated droplets was found to grow according a power law with exponent 1/3 except PP similar to previous reports. We also compared the volume increase of an isolated single droplet with the volume increase of another similar sized single droplet which was surrounded by neighboring droplets and found that when neighboring droplets are present in close proximity, the condensation rate was 14-40% lower than that of a single isolated droplet due to blocking of lateral water vapor diffusion. This effect was more pronounced on substrates having high surface roughness
机译:在这项研究中,我们确定为扩散控制的液滴蒸发过程导出的方程式可以成功地应用于水滴在表面温度刚好低于露点的聚合物表面上的凝结率。五个表面表面自由能在30-37mJ / m〜2范围内的聚烯烃表面上的冷凝分离液滴的生长速率之间的差异是由于表面粗糙度的不同而改变了液滴的成核速率,液滴钉扎效应和初始接触角。分离液滴的凝结率随表面粗糙度,水接触角和接触角滞后性的增加而降低,依次为乙烯-醋酸乙烯酯共聚物(EVA)>低密度聚乙烯(LDPE)>高密度聚乙烯(HDPE)>聚丙烯-聚乙烯共聚物(PPPE)>聚丙烯(PP)。发现单个分离液滴的液滴半径按照幂律增长,指数除以PP类似于以前的报道外,指数为1/3。我们还比较了一个孤立的单个液滴的体积增加与另一个被相邻液滴包围的大小相似的单个液滴的体积增加,发现当相邻液滴紧邻时,凝结率比凝结率低14-40%。由于阻塞了水蒸气的横向扩散,导致单个孤立液滴的分离。这种效果在具有高表面粗糙度的基材上更为明显

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