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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Dynamic Electrophoretic Mobility of Spherical Colloidal Particles in Realistic Aqueous Salt-Free Concentrated Suspensions
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Dynamic Electrophoretic Mobility of Spherical Colloidal Particles in Realistic Aqueous Salt-Free Concentrated Suspensions

机译:实际无盐浓缩悬浮液中球形胶体颗粒的动态电泳迁移率

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摘要

In this contribution, the dynamic (or alternating current (AC)) electrophoretic mobility of spherical colloidal particles in a realistic salt-free concentrated suspension subjected to an oscillating electric field is studied theoretically using a cell model approach. Such a suspension is a concentrated one (in charged solid particles) in an aqueous solution without any electrolyte added during the preparation. The ionic species in solution can solely be: (i) the "added counterions" stemming from the particles (for example, by ionization of particle surface ionizable groups), (ii) the H~+ and OH~- ions from water dissociation, and (iii) the ions produced by the atmospheric CO2 contamination. The corrections related to water dissociation and CO2 contamination in suspensions open to the atmosphere have turned out to be tremendous in many of the experimental situations of interest in direct current (DC) electric fields. Thus, it is mandatory to explore their influence in the more complex situation of AC electrophoresis. The results confirm the importance of ions produced by water dissociation and those originated by the acidification of the aqueous solution in suspensions contaminated with atmospheric CO2, for low to moderate particle volume fractions, where the role of the added counterions is screened by the other ionic species. It is worth mentioning that, for high particle charges, two Maxwells-Wagner processes develop in the mobility frequency spectrum, respectively linked to the diffuse layer relaxation and to the relaxation of a condensed layer of counterions located very close to the particle surface. This is the so-called ionic condensation effect for highly charged particles, already described in the literature, and which for the first time will be studied in detail in realistic salt-free systems. The dynamic electrophoretic mobility will be numerically computed throughout a wide frequency range and compared with the cases of pure and realistic salt-free conditions. In addition, the competition between different relaxation processes associated to the complex electric dipole moment induced on the particles by the field, the particle inertia, as well as their influence on the dynamic response, will be explored for pure and realistic cases.
机译:在这一贡献中,理论上使用细胞模型方法研究了球形胶体颗粒在现实的无盐浓缩悬浮液中经受振荡电场的动态(或交流(AC))电泳迁移率。这种悬浮液是在水溶液中的浓缩悬浮液(在带电的固体颗粒中),在制备过程中未添加任何电解质。溶液中的离子种类可以单独为:(i)源自粒子的“添加抗衡离子”(例如,通过粒子表面可电离基团的电离),(ii)水离解的H〜+和OH〜-离子, (iii)大气CO2污染产生的离子。在对直流(DC)电场感兴趣的许多实验情况下,与水离解和向大气开放的悬浮液中的CO2污染有关的校正已被证明是巨大的。因此,必须探索它们在更复杂的交流电泳条件下的影响。该结果证实了水解离产生的离子和水溶液中被大气CO2污染的酸化产生的离子对于中低颗粒体积分数的重要性,其中添加的抗衡离子的作用由其他离子物质筛选。值得一提的是,对于高粒子电荷,在迁移谱中出现了两种麦克斯韦-瓦格纳过程,分别与扩散层弛豫和与非常靠近粒子表面的抗衡离子凝聚层的弛豫有关。这就是所谓的高电荷粒子的离子缩合效应,已经在文献中进行了描述,并且将首次在现实的无盐系统中进行详细研究。动态电泳迁移率将在很宽的频率范围内进行数值计算,并与纯净和现实的无盐条件进行比较。此外,在纯净和现实的情况下,将探索与磁场引起的粒子上的复杂电偶极矩相关的不同弛豫过程之间的竞争,粒子惯性及其对动态响应的影响。

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