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首页> 外文期刊>European Polymer Journal >Redox control of capillary filling speed in poly(ferrocenylsilane)-modified microfluidic channels for switchable delay valves
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Redox control of capillary filling speed in poly(ferrocenylsilane)-modified microfluidic channels for switchable delay valves

机译:聚二茂铁基硅烷改性微流体通道中毛细管填充速度的氧化还原控制,用于可切换延迟阀

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We present a method to reversibly change the wetting of gold-coated microchannel walls, and, as a result, alter the capillary filling speed of water inside such modified microchannels. To this end, we employ the redox-response of surface-anchored poly(ferrocenylsilane) (PFS) films, which allows for a controlled and repeatable switching of the surface energy under low voltages (<1 V). Cyclic voltammetry and chronoamperometry were used to confirm the presence of PFS coatings, to determine surface coverage and to study the redox reaction kinetics of the films inside of microchannels where a 0.1 M sodium perchlorate aqueous solution served as electrolyte. SEM images attested thin, uniform and selective surface modification of the gold electrode by PFS films. Oxidation and reduction of the surface-immobilized PFS were both reached after a characteristic time below 20 s. Capillary filling experiments revealed that the meniscus speed clearly depends on the redox state of the PFS film. The velocity of the meniscus was reversibly switched between 1.8 +/- 0.1 mm/s (reduced state) and 3.4 +/- 0.1 mm/s (oxidized state). Model calculations, based on the Lucas-Washburn equation and adapted to our specific channel setup and partial surface modification, showed a linear dependency of the meniscus position on our observation time interval, in agreement with our experimental results. Meniscus velocities predicted by the model agreed well with the experimentally determined capillary meniscus velocity. (C) 2016 Published by Elsevier Ltd.
机译:我们提出了一种可逆地改变镀金微通道壁的润湿性的方法,结果,改变了这种改性微通道内部水的毛细管填充速度。为此,我们采用了表面锚定的聚二茂铁基硅烷(PFS)膜的氧化还原响应,该膜可在低压(<1 V)下对表面能进行可控和可重复的转换。循环伏安法和计时电流法用于确认PFS涂层的存在,确定表面覆盖率并研究微通道内部薄膜的氧化还原反应动力学,其中0.1M高氯酸钠水溶液用作电解质。 SEM图像证实了PFS膜对金电极的薄,均匀和选择性的表面改性。在低于20 s的特征时间后,均实现了表面固定PFS的氧化和还原。毛细管填充实验表明,弯液面速度明显取决于PFS膜的氧化还原状态。弯月面的速度可逆地在1.8 +/- 0.1 mm / s(还原态)和3.4 +/- 0.1 mm / s(氧化态)之间切换。基于Lucas-Washburn方程并适用于我们特定的通道设置和部分表面修改的模型计算,表明弯月面位置对我们观察时间间隔的线性依赖性,与我们的实验结果一致。该模型预测的弯液面速度与实验确定的毛细管弯液面速度非常吻合。 (C)2016由Elsevier Ltd.出版

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