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微流控法制备用于电泳显示微胶囊的微液珠研究
引用本文:朱云飞,水玲玲,周国富,金名亮.微流控法制备用于电泳显示微胶囊的微液珠研究[J].华南师范大学学报(自然科学版),2015,47(3):19-0.
作者姓名:朱云飞  水玲玲  周国富  金名亮
作者单位:1.1.华南师范大学华南先进光电子研究院
基金项目:国家自然科学基金项目(21303060);教育部“长江学者和创新团队发展计划”项目(IRT13064);广东省引进创新科研团队计划资助项目(2011D039);广东省高等学校人才引进专项资金项目(2050205);华南师范大学研究生科研创新基金项目(2013KYJJ043)
摘    要:本文基于微流控技术,提出一种制备电泳显示液微胶囊的新方法,解决了传统电泳微胶囊制备方法中颗粒粒径不均匀、影响显示器件的显示性能及其驱动波形设计等问题。实验中使用了两种玻璃汇聚流通道(小型和大型),外相溶液为1.5%明胶阿拉伯胶混合溶液,内相为四氯乙烯溶液。当小型通道和大型通道外相溶液流速与内相溶液体积流速比分别为2:1和10:6时,可以得到液滴平均直径分别为47 m和315 m的均匀的微液珠。同时,该方法可以精确控制微胶囊粒径大小,通过调节内外相流速,可以得到粒径在40 m至375 m范围内的大小均匀的微胶囊。与传统机械搅拌法制备的微液珠(52 18.81 m)相比,微流控法制备的微液珠(450.28 m)粒径分布得到了很大改善。该方法为电泳显示器显示效果的改善提供了可行方法。

关 键 词:粒径分布
收稿时间:2015-03-27

Microfluidic Fabrication of Monodisperse Microdroplets for Electrophoretic Display Applications
Zhu Yunfei , Shui Lingling , Zhou Guofu , Jin Mingliang.Microfluidic Fabrication of Monodisperse Microdroplets for Electrophoretic Display Applications[J].Journal of South China Normal University(Natural Science Edition),2015,47(3):19-0.
Authors:Zhu Yunfei  Shui Lingling  Zhou Guofu  Jin Mingliang
Institution:Zhu Yunfei;Shui Lingling;Zhou Guofu;Jin Mingliang;Institute of Electronic Paper Displays,South China Academy of Advanced Optoelectronics,South China Normal University;Shenzhen Guohua Optoelectronics Tech. Co. Ltd.;
Abstract:In this paper, a novel method of creating monodisperse microdroplets for electrophoretic display microcapsules application is introduced. The microcapsules fabricated by common agitation are lack of uniformity, which result in difficulty in driving waveform design. In this report, we fabricated the narrow distributed microdroplets of EPD materials using two types of microchannel with the outer phase of 15% gelatin and Arabic gum solution and the inner phase of tetrachloroethylene. Controlling the flow rate ratio of the inner to outer phase at 2:1 (small channel) and 10:6 (big channel), we could obtain monodisperse microdroplets with diameter of 47 ?m and 315 ?m, respectively. At the same, the size of the microdroplet could be precisely controlled by the fluidic flow rates. The size distribution of the microdroplets fabricated by microfluidic channels was (450.28) m which was highly improved comparing to the droplets created by agitation with the size of (5218.81) m. This implies that the microfluidics is a reliable technology which would be a feasible way to improve the quality and performance of the electrophoretic displays.
Keywords:electrophoretic displays  microcapsules  microfluidics  size distribution
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