Adsorption kinetics of polyacrylamide-based polyelectrolyte onto a single silica particle studied using microfluidics and optical tweezers
Adsorption kinetics of polyacrylamide-based polyelectrolyte onto a single silica particle studied using microfluidics and optical tweezers
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使用微流体和光镊研究聚丙烯酰胺基聚电解质在单个二氧化硅颗粒上的吸附动力学
DOI:
10.1016/j.jcis.2022.10.067
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发表时间:
2023
影响因子:
9.9
通讯作者:
Adachi Yasuhisa
中科院分区:
文献类型:
--
作者:
Geonzon Lester C.;Kobayashi Motoyoshi;Sugimoto Takuya;Adachi Yasuhisa
HypothesisPolyelectrolyte adsorption is considered important in tuning the surface property and the fate of particles; however, often studied on macroscopic surfaces. To gain insights into how polyelectrolytes are adsorbed onto a single particle, it is imperative to utilize techniques capable of elucidating adsorption kinetics on a single-particle level in a controlled flow field.ExperimentsThe polyelectrolyte adsorption kinetics was investigated by electrophoretic mobility measurements combined with the kinetics study onto a single-particle viewpoint using microfluidics and optical tweezers. We directly evaluated the thickness,δH, of adsorbed polyelectrolyte onto a negatively-charged silica particle to deduce the adsorbed polyelectrolyte’s conformation. The effect of charge density and salt concentrations were studied.FindingsAll polyelectrolytes exhibited dependence ofδHon salt concentration. The attractive interactions control the cationic polyelectrolytes adsorption process. TheδHdepends on charge density indicating more loops and tail confirmation for the weakly-charged polyelectrolytes. The anionic polyelectrolytes showed a dependence of the initial rate and saturation value ofδHon salt concentrations, attributed to the repulsion between charged segments and the silica surfaces. Here, we present new insights into the polyelectrolyte adsorption kinetics, particularly the influence of electrostatic interaction from the single-particle perspective, inaccessible to conventional bulk measurements.