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非带电聚合物和胶体溶液中聚丙烯酸的电荷调节

Charge Regulation of Poly(acrylic acid) in Solutions of Non-Charged Polymer and Colloids.

作者信息

Yekymov Evgenee, Attia David, Levi-Kalisman Yael, Bitton Ronit, Yerushalmi-Rozen Rachel

机构信息

Department of Chemical Engineering, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.

The Center for Nanoscience and Nanotechnology, The Institute of Life Sciences, The Hebrew University, Jerusalem 91904, Israel.

出版信息

Polymers (Basel). 2023 Feb 23;15(5):1121. doi: 10.3390/polym15051121.

Abstract

Weak polyelectrolytes (WPEs) are responsive materials used as active charge regulators in a variety of applications, including controlled release and drug delivery in crowded bio-related and synthetic environments. In these environments, high concentrations of solvated molecules, nanostructures, and molecular assemblies are ubiquitous. Here, we investigated the effect of high concentrations of non-adsorbing, short chains of poly(vinyl alcohol), PVA, and colloids dispersed by the very same polymers on charge regulation (CR) of poly(acrylic acid), PAA. PVA does not interact with PAA (throughout the full pH range) and thus can be used to examine the role of non-specific (entropic) interactions in polymer-rich environments. Titration experiments of PAA (mainly 100 kDa in dilute solutions, no added salt) were carried out in high concentrations of PVA (13-23 kDa, 5-15 wt%) and dispersions of carbon black (CB) decorated by the same PVA (CB-PVA, 0.2-1 wt%). The calculated equilibrium constant (and pKa) was up-shifted in PVA solutions by up to ~0.9 units and down-shifted in CB-PVA dispersions by ~0.4 units. Thus, while solvated PVA chains increase the charging of the PAA chains, as compared to PAA in water, CB-PVA particles reduce PAA charging. To investigate the origins of the effect, we analyzed the mixtures using small-angle X-ray scattering (SAXS) and cryo-TEM imaging. The scattering experiments revealed re-organization of the PAA chains in the presence of the solvated PVA but not in the CB-PVA dispersions. These observations clearly indicate that the acid-base equilibrium and the degree of ionization of PAA in crowded liquid environments is affected by the concentration, size, and geometry of seemingly non-interacting additives, probably due to depletion and excluded volume interactions. Thus, entropic effects that do not depend on specific interactions should be taken into consideration when designing functional materials in complex fluid environments.

摘要

弱聚电解质(WPEs)是一类响应性材料,在包括拥挤的生物相关和合成环境中的控释和药物递送等各种应用中用作活性电荷调节剂。在这些环境中,高浓度的溶剂化分子、纳米结构和分子聚集体无处不在。在此,我们研究了高浓度的非吸附性聚乙烯醇(PVA)短链以及由相同聚合物分散的胶体对聚丙烯酸(PAA)电荷调节(CR)的影响。PVA在整个pH范围内都不与PAA相互作用,因此可用于研究富含聚合物的环境中非特异性(熵)相互作用的作用。在高浓度的PVA(13 - 23 kDa,5 - 15 wt%)和由相同PVA修饰的炭黑(CB)分散体(CB - PVA,0.2 - 1 wt%)中进行了PAA(稀溶液中主要为100 kDa,无添加盐)的滴定实验。计算得到的平衡常数(和pKa)在PVA溶液中最多上移约0.9个单位,在CB - PVA分散体中下移约0.4个单位。因此,与水中的PAA相比,溶剂化的PVA链增加了PAA链的带电性,而CB - PVA颗粒则降低了PAA的带电性。为了研究这种效应的起源,我们使用小角X射线散射(SAXS)和低温透射电子显微镜(cryo - TEM)成像对混合物进行了分析。散射实验表明,在溶剂化PVA存在的情况下PAA链发生了重排,但在CB - PVA分散体中没有。这些观察结果清楚地表明,在拥挤的液体环境中,PAA的酸碱平衡和电离程度受到看似非相互作用的添加剂的浓度、尺寸和几何形状的影响,这可能是由于耗尽和排除体积相互作用所致。因此,在复杂流体环境中设计功能材料时,应考虑不依赖于特定相互作用的熵效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/357e/10007678/48fd07429432/polymers-15-01121-ske001.jpg

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