Pastorino Claudio, Urrutia Ignacio, Fiora María, Condado Federico
Departamento de Física de la Materia Condensada, Centro Atómico Constituyentes, CNEA, Av. Gral. Paz 1499, San Martín, Buenos Aires, 1650, Argentina.
Instituto de Nanociencia y Nanotecnología, CONICET-CNEA, CAC.
J Phys Condens Matter. 2022 Jun 24;34(34). doi: 10.1088/1361-648X/ac77ce.
Heat transfer through a liquid-vapor interface is a complex phenomenon and crucially relevant in heat-removal and cryogenic applications. The physical coupling among confining walls, liquid and vapor phases is very important for controlling or improving cooling rates or condensation efficiency. Surface modification is a promising route, which has been explored to taylor the heat transfer through confined two-phase systems. We use coarse-grained molecular-dynamics simulations to study the heat transfer through a nano-confined liquid-vapor interface as a function of fluid filling. We set up a stationary heat flow through a liquid-vapor interface, stabilized with the liquid in contact with a colder wall and a vapor in contact with a hotter wall. For these physical conditions, we perform extensive simulations by progressively increasing the number of fluid particles, i.e. the channel filling, and measure the fluid distribution in the channel, density, pressure and temperature profiles We also compare the heat flux behavior between a bare-surfaces nano-channel and others where the hot surface was coated with end-grafted polymers, with different wetting affinities and bending properties. We take extreme cases of polymer properties to obtain a general picture of the polymer effect on the heat transfer, as compared with the bare surfaces. We find that walls covered by end-grafted solvophylic polymers change the heat flux by a factor of 6, as compared with bare walls, if the liquid phase is in contact with the polymers. Once the liquid wets the coated wall, the improve on heat flux is smaller and dominated by the grafting density. We also find that for a wall coated with stiff polymers, the jump in heat flux takes place at a significantly lower channel filling, when the polymers' free ends interact with the liquid surface. Interestingly, the morphology of the polymers induces a 'liquid bridge' between the liquid phase and the hot wall, through which heat is transported with high (liquid-like) thermal conductivity.
通过液-气界面的热传递是一个复杂的现象,在散热和低温应用中至关重要。受限壁、液相和气相之间的物理耦合对于控制或提高冷却速率或冷凝效率非常重要。表面改性是一条很有前景的途径,已被用于研究如何通过受限两相系统来调节热传递。我们使用粗粒度分子动力学模拟来研究通过纳米受限液-气界面的热传递与流体填充量之间的关系。我们建立了一个通过液-气界面的稳定热流,液相与较冷的壁接触,气相与较热的壁接触。在这些物理条件下,我们通过逐步增加流体粒子的数量(即通道填充量)进行了广泛的模拟,并测量了通道内的流体分布、密度、压力和温度分布。我们还比较了裸表面纳米通道与热表面涂有端接枝聚合物的其他通道之间的热通量行为,这些聚合物具有不同的润湿性亲和力和弯曲特性。我们选取聚合物特性的极端情况,以获得与裸表面相比聚合物对热传递影响的总体情况。我们发现,如果液相与端接枝亲溶剂聚合物覆盖的壁接触,与裸壁相比,热通量会改变6倍。一旦液体润湿了涂层壁,热通量的改善就较小,且主要由接枝密度决定。我们还发现,对于涂有刚性聚合物的壁,当聚合物的自由端与液体表面相互作用时,热通量的跃升发生在显著更低的通道填充量下。有趣的是,聚合物的形态在液相和热壁之间形成了一个“液桥”,热量通过该液桥以高(类似液体)的热导率进行传输。