McElligott Adam, Whalen Alex, Du Chong Yang, Näveke Lukas, Meunier Jean-Luc, Servio Phillip
Department of Chemical Engineering, McGill University, Montreal, Quebec H3A 0C5, Canada.
Nanotechnology. 2020 Nov 6;31(45):455703. doi: 10.1088/1361-6528/abaae0. Epub 2020 Jul 30.
Emerging nanofluid-based technologies for cooling, transport, and storage applications have previously been enhanced through the use of graphene nanoflake (GNF) nanofluids. Many of the beneficial effects of GNFs have now been documented, though little work has yet been completed to characterize the morphological behaviour of GNF nanofluids both during and after the phase change process. In this study, the crystallization behaviour of sessile water droplets was evaluated for two plasma-functionalized, hydrophilic GNF concentrations (20 and 100 ppm) at three driving force temperatures (-5 °C, -10 °C, and -20 °C). At low driving forces, the GNFs were wholly expelled from the solid matrix due to low crystallization velocities. At high driving forces, more rapid crystallization rates resulted in the entrapment of GNFs within the air bubbles and inter-dendritic spaces of the solid droplet. However, individual particle dispersion was not achieved within the solid matrix at any driving force. Furthermore, for all experimental conditions, the functionalized GNF clusters which formed during freezing did not disperse spontaneously upon melting as drying-like effects may have altered the attraction properties of their surfaces and destabilized the suspension. Compared to previous studies using multi-walled carbon nanotubes, the GNFs were found to have higher liquid mobility at the solid front, provide less resistance to that front as it ascended, and be better dispersed after melting. These effects may have been geometrical; the square nanoflake geometry does not result in any physical particle entanglement.
新兴的基于纳米流体的冷却、传输和存储应用技术,此前通过使用石墨烯纳米片(GNF)纳米流体得到了改进。现在,GNF的许多有益效果已有文献记载,但在表征GNF纳米流体在相变过程中及之后的形态行为方面,尚未完成多少工作。在本研究中,评估了在三种驱动力温度(-5°C、-10°C和-20°C)下,两种等离子体功能化的亲水性GNF浓度(20 ppm和100 ppm)下静置水滴的结晶行为。在低驱动力下,由于结晶速度低,GNF完全从固体基质中排出。在高驱动力下,更快的结晶速度导致GNF被困在固体液滴的气泡和枝晶间空间内。然而,在任何驱动力下,固体基质内均未实现单个颗粒的分散。此外,在所有实验条件下,冷冻过程中形成的功能化GNF团簇在融化时不会自发分散,因为类似干燥的效应可能改变了其表面的吸引力特性并使悬浮液不稳定。与先前使用多壁碳纳米管的研究相比,发现GNF在固体前沿具有更高的液体流动性,在前沿上升时对其提供的阻力更小,并且在融化后分散性更好。这些效应可能是几何形状造成的;方形纳米片几何形状不会导致任何物理颗粒缠结。