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Characterization of Gationic Polyelectrolytes Adsorption to an Anionic Emulsion via Zeta-Potential and Microcalorimetry

机译:Zeta-电位和微量量热法测定阳离子聚电解质对阴离子乳液的吸附特性

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摘要

The adsorption of cationic polyelectrolytes (PEs) onto anionic silicone emulsion droplets, suspended in a sodium chloride solution is studied via electrophoretic mobility measurements and isothermal titration calorime-try. These model systems are studied to better understand the interactions governing PE adsorption-induced emulsion flocculation, which is relevant to many industrial applications. Electrophoretic mobility measurements provide critical information for rationalizing the effect of the PE charge density on the loss of stability of silicone emulsions. The interaction strength is calculated from a Langmuir adsorption isotherm determined by a ζ-potential titration measurement. Microcalorimetry measurements independently validate the adsorption free energy. Emulsion flocculation and coacervation are observed in the visual phase behavior as well as the (-potential titration measurements. The effect of PE charge density shows that PE-surfactant coacervation is the driving force in these PE-emulsion systems.
机译:通过电泳迁移率测量和等温滴定热法研究了悬浮在氯化钠溶液中的阳离子聚电解质(PEs)在阴离子有机硅乳液小滴上的吸附。对这些模型系统进行了研究,以更好地理解控制PE吸附引起的乳液絮凝的相互作用,这与许多工业应用有关。电泳迁移率测量为合理化PE电荷密度对有机硅乳液稳定性损失的影响提供了关键信息。相互作用强度由通过ζ电位滴定法测定的Langmuir吸附等温线计算得出。微量热法测量独立地验证了吸附自由能。在可见相行为和(电位滴定法)测量中观察到乳液的絮凝和凝聚。PE电荷密度的影响表明,PE表面活性剂的凝聚是这些PE乳液体系的驱动力。

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