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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Dynamics of Coalescence of Plugs with a Hydrophilic Wetting Layer Induced by Flow in a Microfluidic Chemistrode
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Dynamics of Coalescence of Plugs with a Hydrophilic Wetting Layer Induced by Flow in a Microfluidic Chemistrode

机译:微流控化学流中流动引起的带有亲水性润湿层的塞子的聚结动力学

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摘要

This manuscript analyzes the dynamics of coalescence of an incoming aqueous plug with a wetting layer above a hydrophilic surface in the chemistrode. The chemistrode is a recently described (Chen, D.; Du, W.; Liu, Y.; Liu, W.; Kuznetsov, A.; Mendez, F. E.; Philipson, L. H.; Ismagilov, R. F. Proc. Natl. Acad. Sci. U.S.A. 2008, 105, 16843-16848) microfluidic analogue of an electrode, but operating at the chemical rather than electrical level, developed with the aim of capturing local stimulus-response processes in chemistry and biology. The chemistrode consists of open-ended V-shaped microfluidic channels that can be brought into contact with a chemical or biological hydrophilic substrate. The chemistrode relies on multiphase aqueous/fluorous flow and uses plugs to achieve high temporal resolution of stimulation and sampling. Coalescence of the incoming plugs, containing the stimuli, with the liquid in the wetting layer is required for chemical exchange to take place in the chemistrode. Here, we investigate the system with triethyleneglycol mono[1H, 1H-perfluorooctyl] ether RfOEG as the surfactant. This surfactant was necessary to prevent nonspecific absorption of proteins to the aqueous fluorous interface and to ensure biocompatibility of the system, but too much surfactant increased the barrier for coalescence. In this system, coalescence was controlled by the capillary number. At a higher value of the capillary number, coalescence took more time, and deformation of the interface of the incoming plug and the wetting layer was more significant. Above a critical capillary number, coalescence did not occur between the incoming plug and the wetting layer. The critical capillary number was an increasing function of surface tension but was independent of viscosity ratio. Coalescence was surprisingly reproducible, presumably because film rupture during coalescence was reliably initiated at the hydrophilic substrate. These results are useful in rational operation of the chemistrode and also provide an experimental description of deformation, film drainage, and coalescence of surfactant-coated droplets in an external flow field.
机译:该手稿分析了在化学溶极中亲水表面上方带有润湿层的进水栓塞的聚结动力学。最近已经描述了该化学电极(Chen,D .; Du,W .; Liu,Y .; Liu,W .; Kuznetsov,A .; Mendez,FE; Philipson,LH; Ismagilov,RF Proc.Natl.Acad.Sci (US 2008,105,16843-16848)电极的微流体类似物,但是在化学而不是电水平上操作,其开发旨在捕获化学和生物学中的局部刺激响应过程。该化学电极由可与化学或生物亲水性底物接触的开放式V形微流体通道组成。该化学电极依赖于多相水/氟流,并使用塞子来实现刺激和采样的高时间分辨率。包含刺激物的进入的塞子与润湿层中的液体的聚结需要化学交换在化学溶极中进行。在这里,我们研究了以三乙二醇单[1H,1H-全氟辛基]醚RfOEG作为表面活性剂的体系。该表面活性剂对于防止蛋白质非特异性地吸收到氟离子水溶液界面并确保系统的生物相容性是必需的,但是过多的表面活性剂会增加聚结的障碍。在该系统中,聚结由毛细管数控制。在较高的毛细管数下,聚结需要更多的时间,并且进入的堵塞物和润湿层的界面变形更明显。高于临界毛细管数,在进入的堵塞物和润湿层之间未发生聚结。临界毛细管数是表面张力的增加函数,但与粘度比无关。聚结令人惊讶地可重现,大概是因为聚结期间的膜破裂是在亲水性基材上可靠地引发的。这些结果可用于化学电极的合理操作,并且还提供了在外部流场中表面活性剂涂覆的液滴变形,膜排水和聚结的实验描述。

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