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壳聚糖吸附介导纤维素的纳观摩擦学性能。

Mediation of the nanotribological properties of cellulose by chitosan adsorption.

机构信息

Department of Chemistry, Surface Chemistry, Royal Institute of Technology, Drottning Kristinas vag 51, Stockholm, Sweden.

出版信息

Biomacromolecules. 2009 Mar 9;10(3):645-50. doi: 10.1021/bm801467w.

Abstract

Cellulosic model surfaces functionalized with chitosan, a naturally occurring cationic biomacromolecule, by in situ adsorption have been studied with an atomic force microscope (AFM) in colloidal probe configuration. The interaction forces on approach and separation, as well as the nanotribological properties, were shown to be highly pH-dependent, and a significant difference in the behavior was seen before and after chitosan adsorption. In general, all forces on approach showed a highly repulsive interaction at shorter distances due to deformation of the probe. At high pH, before chitosan adsorption, a long-range electrostatic repulsion was observed, consistent with DLVO theory. However, at low pH no electrostatic contribution was found before adsorption, probably due to charge neutralization of carboxyl groups. After chitosan adsorption, repulsive forces acting over a much longer distance than predicted by DLVO theory were present at low pH. This effect was ascribed to chain extension of the chitosan species of which the magnitude and the range of the force increased dramatically with higher charge at low pH. In all cases, a typical saw-tooth patterned adhesion was present, with pull-off events occurring at different separations. The frequency of these events after chitosan adsorption was greatly increased at longer distances. Additionally, the adsorbed chitosan markedly reduced the friction, where the largest effect was a 7-fold decrease of the friction coefficient observed at low pH.

摘要

通过胶体探针配置的原子力显微镜(AFM)研究了壳聚糖(一种天然存在的阳离子生物大分子)原位吸附功能化的纤维素模型表面。结果表明,在接近和分离过程中的相互作用力以及纳米摩擦学性质高度依赖于 pH 值,并且在壳聚糖吸附前后观察到明显的行为差异。通常,由于探针的变形,在较短的距离内所有接近时的力都表现出高度的排斥相互作用。在高 pH 值下,在壳聚糖吸附之前,观察到长程静电排斥,与 DLVO 理论一致。然而,在吸附之前,在低 pH 值下没有发现静电贡献,可能是由于羧基的电荷中和。在低 pH 值下,吸附壳聚糖后,存在作用距离比 DLVO 理论预测的长得多的排斥力。这种效应归因于壳聚糖物种的链延伸,其力的大小和范围随着低 pH 值下更高的电荷而显著增加。在所有情况下,都存在典型的锯齿状粘附模式,在不同的分离处发生拉离事件。在更长的距离处,吸附壳聚糖后这些事件的频率大大增加。此外,吸附的壳聚糖显著降低了摩擦,在低 pH 值下观察到摩擦系数降低了 7 倍。

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