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界面聚合层形成的可视化和特性研究。

Visualization and characterization of interfacial polymerization layer formation.

机构信息

Soft Matter, Fluidics and Interfaces, MESA+ Institute for Nanotechnology, Faculty of Science and Technology, University of Twente, Enschede, The Netherlands.

出版信息

Lab Chip. 2015 Jan 21;15(2):575-80. doi: 10.1039/c4lc01046a.

Abstract

We present a microfluidic platform to visualize the formation of free-standing films by interfacial polymerization. A microfluidic device is fabricated, with an array of micropillars to stabilize an aqueous-organic interface that allows a direct observation of the films formation process via optical microscopy. Three different amines are selected to react with trimesoyl chloride: piperazine, JEFFAMINE(®)D-230, and an ammonium functionalized polyhedral oligomeric silsesquioxane. Tracking the formation of the free-standing films in time reveals strong effects of the characteristics of the amine precursor on the morphological evolution of the films. Piperazine exhibits a rapid reaction with trimesoyl chloride, forming a film up to 20 μm thick within half a minute. JEFFAMINE(®)D-230 displays much slower film formation kinetics. The location of the polymerization reaction was initially in the aqueous phase and then shifted into the organic phase. Our in situ real-time observations provide information on the kinetics and the changing location of the polymerization. This provides insights with important implications for fine-tuning of interfacial polymerizations for various applications.

摘要

我们提出了一种微流控平台,用于通过界面聚合来可视化自由-standing 膜的形成。制造了一种微流控器件,该器件具有阵列状的微柱,以稳定水-有机界面,从而可以通过光学显微镜直接观察膜的形成过程。选择了三种不同的胺与均苯三甲酰氯反应:哌嗪,JEFFAMINE(®)D-230 和铵官能化的多面体低聚倍半硅氧烷。跟踪自由-standing 膜的形成时间揭示了胺前体的特性对膜的形态演化的强烈影响。哌嗪与均苯三甲酰氯迅速反应,在半分钟内形成了厚度达 20μm 的膜。JEFFAMINE(®)D-230 的成膜动力学要慢得多。聚合反应的位置最初在水相,然后转移到有机相。我们的原位实时观察提供了有关动力学和聚合反应位置变化的信息。这为各种应用的界面聚合的精细调整提供了重要的见解。

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