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Fluid dynamic and heat transfer processes between solid surfaces and non-Newtonian liquid droplets

机译:固体表面与非牛顿液滴之间的流体动力学和传热过程

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摘要

This paper addresses the experimental and theoretical description of the fluid dynamic and thermal behaviour of non-Newtonian (shear-thinning) droplets impacting onto smooth and micro-patterned heated surfaces. The shear-thinning liquids are mixtures of water + xanthan gum prepared with different concentrations of the gum, namely 0.05%, 0.10%, 0.15% and 0.35%wt. For droplet impacts over the surfaces heated bellow the boiling temperature of the liquid, the shear-thinning effect is clearly governed by the concentration of the non-Newtonian component, which is associated to the consistency coefficient of the constitutive model describing the viscous behaviour of the flow. In line with this, models predicting the spreading of Newtonian droplets are revisited and an alternative one is proposed, which integrates the non-Newtonian behaviour. The results suggest that heating the surface (and consequently the liquid) alters the rheology of the non-Newtonian mixture and reverses the increase of the zero viscosity, which is observed for impacts onto non-heated surfaces, thus allowing a larger spreading diameter and a significant recoiling phase for droplets with high concentrations of the non-Newtonian component. The heat transferred at droplet surface interaction, during the spreading of the droplet is also evaluated. The analysis evidences the strong coupling between the heat transfer process and the spreading dynamics, for the non-Newtonian droplets. Further heating the surface above the boiling temperature of the liquid, the droplets impact the surfaces within the nucleate boiling regime and thermal induced atomization occurs. In this case, Phase Doppler measurements are taken to characterize the size of the secondary droplets generated within this process. The results show that the thermal induced atomization is mainly triggered by the force balance between surface tension and vapour pressure forces, so the viscosity plays a secondary role. (C) 2014 Elsevier Ltd. All rights reserved.
机译:本文介绍了非牛顿(剪切稀化)液滴撞击到光滑且微图案加热表面上的流体动力学和热行为的实验和理论描述。剪切稀稀液体是水+黄原胶的混合物,其制备有不同浓度的胶,即0.05重量%,0.10重量%,0.15重量%和0.35重量%。对于在液体沸腾温度以下加热的表面上的液滴冲击,剪切稀化效果显然受非牛顿成分浓度的控制,该浓度与描述流体粘性行为的本构模型的一致性系数有关。流。与此相应,重新讨论了预测牛顿液滴扩散的模型,并提出了一种替代方案,该方案整合了非牛顿的行为。结果表明,加热表面(从而加热液体)会改变非牛顿混合物的流变性,并逆转零粘度的增加,这种现象可观察到对非加热表面的影响,从而允许更大的铺展直径和高浓度的非牛顿成分的液滴具有明显的反冲阶段。还评估了在液滴散布期间在液滴表面相互作用下传递的热量。分析证明,对于非牛顿液滴,传热过程与扩散动力学之间存在强耦合。将表面进一步加热到液体的沸腾温度以上,液滴会在成核沸腾范围内撞击表面,并发生热致雾化。在这种情况下,进行相位多普勒测量以表征在此过程中生成的次级液滴的大小。结果表明,热致雾化主要是由表面张力和蒸汽压力之间的力平衡引起的,因此粘度起次要作用。 (C)2014 Elsevier Ltd.保留所有权利。

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