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Measuring the Transition Rates of Coalescence Events during Double Phase Separation in Microgravity

机译:测量微重力双相分离过程中聚结事件的转变速率

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Phase transition is a ubiquitous phenomenon in nature, science and technology. In general, the phase separation from a homogeneous phase depends on the depth of the temperature quench into the two-phase region. Earth’s gravity masks the details of phase separation phenomena, which is why experiments were performed under weightlessness. Under such conditions, the pure fluid sulphur hexafluoride (SF 6 ) near its critical point also benefits from the universality of phase separation behavior and critical slowing down of dynamics. Initially, the fluid was slightly below its critical temperature with the liquid matrix separated from the vapor phase. A 0.2 mK temperature quench further cooled down the fluid and produced a double phase separation with liquid droplets inside the vapor phase and vapor bubbles inside the liquid matrix, respectively. The liquid droplets and the vapor bubbles respective distributions were well fitted by a lognormal function. The evolution of discrete bins of different radii allowed the derivation of the transition rates for coalescence processes. Based on the largest transition rates, two main coalescence mechanisms were identified: (1) asymmetric coalescences between one small droplet of about 20 μ m and a wide range of larger droplets; and (2) symmetric coalescences between droplets of large and similar radii. Both mechanisms lead to a continuous decline of the fraction of small radii droplets and an increase in the fraction of the large radii droplets. Similar coalescence mechanisms were observed for vapor bubbles. However, the mean radii of liquid droplets exhibits a t 1 / 3 evolution, whereas the mean radii of the vapor bubbles exhibit a t 1 / 2 evolution. View Full-Text
机译:相变是自然,科学和技术中普遍存在的现象。通常,从均相的相分离取决于温度骤冷进入两相区域的深度。地球的重力掩盖了相分离现象的细节,这就是为什么在失重条件下进行实验的原因。在这种条件下,接近其临界点的纯流体六氟化硫(SF 6)也得益于相分离行为的普遍性和动力学的严重减慢。最初,流体略低于其临界温度,液体基质与气相分离。 0.2 mK温度骤冷进一步冷却了流体,并产生了两相分离,分别在气相内部的液滴和液相基质内部的蒸汽泡。通过对数正态函数很好地拟合了液滴和蒸气泡的各自分布。不同半径的离散区间的演变允许推导合并过程的跃迁速率。基于最大的过渡速率,确定了两个主要的聚结机制:(1)一个约20μm的小液滴与较大的大液滴之间的不对称聚结; (2)大半径和相似半径的小滴之间的对称合并。两种机制都导致小半径小滴的分数连续下降,而大半径小滴的分数不断增加。对于蒸气气泡观察到类似的聚结机理。然而,液滴的平均半径呈现出t 1/3的演变,而气泡的平均半径呈现出t 1/2的演变。查看全文

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