论文标题
电荷含量在基于聚(N-异丙基丙烯酰胺)的两步中的两步中的作用
The role of charge content in the two-step deswelling of Poly(N-isopropylacrylamide)-based microgels
论文作者
论文摘要
基于聚(N-异丙基丙烯酰胺)的微凝胶是靠近环境温度的体积相变(VPT)的软胶体。尽管广泛用于基本研究和应用目的,但在VPT处发生的微凝胶内部结构的修改尚未完全了解,尤其是关于静电的作用。在这里,我们在实验和数字上详细研究了丙烯酸(AAC)共同合并者对微凝胶静止过程的影响。通过结合粘度法,光散射和电泳,我们表明AAC的逐步添加会增加微凝胶质量并抑制VPT的发生,从而逐渐将微凝胶倒塌转移到较高的温度上。最重要的是,它还高度增强了这些亚微米尺寸网络的两步,因此内部核心在温度下的倒塌总是低于标志着外电晕过渡的核心。这些结果表明,大体和微凝胶表面之间的电荷密度不匹配的净增加发生。数值模拟充分证实了这种情况,并阐明了电荷分布对两步驱动的两步的影响,移动柜台有效地筛选了内芯内的电荷,同时使更多的单体在表面上电离。我们的工作明确显示了静电相互作用如何影响热敏微凝胶在接近VPT的水性环境中的行为。
Poly(N-isopropylacrylamide)-based microgels are soft colloids undergoing a Volume Phase Transition (VPT) close to ambient temperature. Although widely employed for fundamental research and application purposes, the modifications of the microgel internal structure occurring at the VPT are not yet completely understood, especially concerning the role of electrostatics. Here we study in detail, both experimentally and numerically, the effect of the addition of acrylic acid (AAc) co-monomer on the microgel deswelling process. By combining viscosimetry, light scattering and electrophoresis, we show that the progressive addition of AAc increases the microgel mass and suppresses the occurrence of the VPT, progressively shifting the microgel collapse to higher temperatures. Most importantly, it also highly enhances the two-step deswelling of these submicron-sized networks, so that the inner core collapses at temperatures always lower than those marking the transition of the outer corona. These results indicate that a net increase of the charge density mismatch between the bulk and the surface of the microgels takes place. Numerical simulations fully confirm this scenario and clarify the impact of the charge distribution on the two-step deswelling, with mobile counterions efficiently screening the charges within the inner core, while leaving more monomers ionized on the surface. Our work unambiguously shows how electrostatic interactions influence the behavior of thermosensitive microgels in aqueous environment close to the VPT.