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天然聚电解质多层膜水合作用的奇偶效应:一项原位同步辐射傅里叶变换红外光谱显微研究。

Odd-even effects on hydration of natural polyelectrolyte multilayers: An in situ synchrotron FTIR microspectroscopy study.

作者信息

Benbow Natalie L, Webber Jessie L, Pawliszak Piotr, Sebben Damien A, Karpiniec Sam, Stringer Damien, Tobin Mark J, Vongsvivut Jitraporn, Krasowska Marta, Beattie David A

机构信息

Future Industries Institute, University of South Australia, Mawson Lakes, South Australia 5095, Australia; School of Information Technology and Mathematical Sciences, University of South Australia, Mawson Lakes, South Australia 5095, Australia.

Future Industries Institute, University of South Australia, Mawson Lakes, South Australia 5095, Australia.

出版信息

J Colloid Interface Sci. 2019 Oct 1;553:720-733. doi: 10.1016/j.jcis.2019.06.036. Epub 2019 Jun 12.

Abstract

HYPOTHESIS

Odd-even effects in polysaccharide polyelectrolyte multilayers influence their hydration content and the chemical environment of the water within them.

EXPERIMENTS

Polysaccharide polyelectrolyte multilayers (PEMs) composed of pharmaceutical grade fucoidan and chitosan were studied under confinement using synchrotron FTIR microspectroscopy at increasing pressure, in order to isolate and measure infrared spectra of water within the PEM, without interference from bulk water. Complementary studies of the PEMs were carried out using lab-based in situ attenuated total reflectance Fourier transform spectroscopy (ATR FTIR) and quartz crystal microbalance with dissipation monitoring (QCM-D), as well as zeta potential measurements, to determine the quantity of adsorbed polymer, hydration content, film thickness, viscoelastic properties and surface charge during layer-by-layer deposition.

FINDINGS

The hydration of the PEM followed a saw-tooth profile, known as the odd-even effect, where the film increased hydration with fucoidan adsorption and dehydrated/densified with chitosan adsorption. The water structure within the film showed a lower degree of hydrogen bonding than water in the bulk electrolyte. However, the water structure/environment was independent of the terminating layer of the PEM, in spite of the alteration in percentage hydration water, indicating only a partial proof of the initial hypothesis for this multilayer system (hydration amount changes, hydration water environment does not).

摘要

假设

多糖聚电解质多层膜中的奇偶效应会影响其水合含量以及其中水的化学环境。

实验

使用同步加速器傅里叶变换红外光谱仪(FTIR),在压力增加的情况下对由药用级岩藻依聚糖和壳聚糖组成的多糖聚电解质多层膜(PEMs)进行受限条件下的研究,以便分离并测量PEMs内部水的红外光谱,不受大量水的干扰。使用基于实验室的原位衰减全反射傅里叶变换光谱仪(ATR FTIR)、带耗散监测的石英晶体微天平(QCM-D)以及zeta电位测量对PEMs进行补充研究,以确定逐层沉积过程中吸附聚合物的量、水合含量、膜厚度、粘弹性性质和表面电荷。

发现

PEMs的水合作用呈现出锯齿状分布,即奇偶效应,其中膜在吸附岩藻依聚糖时水合作用增强,而在吸附壳聚糖时脱水/致密化。膜内的水结构显示出比本体电解质中的水更低程度的氢键。然而,尽管水合水的百分比发生了变化,但水结构/环境与PEMs的终止层无关,这仅部分证明了该多层系统的初始假设(水合量变化,水合水环境不变)。

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