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视频处理电泳测量在高电场下毫米级油粒子。

Video Processing Electrophoretic Measurements under High Electric Fields for Sub-millimeter Particles in Oil.

机构信息

Research Center for Functional Materials, National Institute for Materials Science.

出版信息

J Oleo Sci. 2022 Mar 2;71(3):445-457. doi: 10.5650/jos.ess21367. Epub 2022 Feb 11.

Abstract

Electrokinetic properties such as the mobility, surface charge, and zeta potential of sub-millimeter particles are vital parameters in various industrial applications. Their measurement and control in aqueous media have been extensively studied. However, despite their growing importance, the electrokinetic properties of organic solvents have not been studied as thoroughly as those of aqueous media. An electrophoresis cell with a microscope monitor was designed for the electrokinetic studies of sub-millimeter particles in cyclohexane, which is a solvent with very low permittivity. The movement of large particles in the range of 4 ~ 478 µm was successfully traced under a strong electric voltage up to 1100 V, even without the addition of surfactants. The particle sizes were at least 300 times larger than those reported previously. By applying electric fields up to 55 kV/m, the electrophoretic mobilities were measured to be of the order of 10 to 10 m/V∙s through image processing of the recorded particle movement. Five organic sub-millimeter particles had charge densities in the range of -3.5 ~ 4.4 e/µm, and polyethersulfone particles showed extremely high mobilities. The surface charge of organic and inorganic particles is mainly generated by the dissociation of hydroxide groups or by the protonation to surface Lewis base oxygen atoms.

摘要

亚毫米颗粒的电动特性,如迁移率、表面电荷和动电位,是各种工业应用中的重要参数。它们在水介质中的测量和控制已经得到了广泛的研究。然而,尽管它们越来越重要,但有机溶剂的电动特性并没有像水介质那样得到彻底的研究。设计了一种带有显微镜监测器的电泳池,用于研究环己烷中亚毫米颗粒的电动特性,环己烷是一种介电常数非常低的溶剂。在高达 1100 V 的强电场下,成功追踪了 4 到 478 µm 范围内的大颗粒的运动,即使没有添加表面活性剂也是如此。颗粒尺寸至少比以前报道的大 300 倍。通过施加高达 55 kV/m 的电场,通过记录的颗粒运动的图像处理,测量到电泳迁移率在 10 到 10 m/V·s 的量级。五种有机亚毫米颗粒的电荷密度范围为-3.5 到 4.4 e/µm,聚醚砜颗粒表现出极高的迁移率。有机和无机颗粒的表面电荷主要是由氢氧化物基团的离解或质子化到表面路易斯碱氧原子产生的。

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