Department of Chemistry, Faculty of Science, Arak University , Arak 38156-8-8349, Iran.
ACS Appl Mater Interfaces. 2016 Oct 12;8(40):27254-27263. doi: 10.1021/acsami.6b10375. Epub 2016 Sep 30.
Fabrication of hydrogels based on chitosan (CS) with superb self-healing behavior and high mechanical and electrical properties has become a challenging and fascinating topic. Most of the conventional hydrogels lack these properties at the same time. Our objectives in this research were to synthesize, characterize, and evaluate the general properties of chitosan covalently cross-linked with zinc phthalocyanine tetra-aldehyde (ZnPcTa) framework. Our hope was to access an unprecedented self-healable three-dimensional (3D) nanostructure that would harvest the superior mechanical and electrical properties associated with chitosan. The properties of cross-linker such as the structure, steric effect, and rigidity of the molecule played important roles in determining the microstructure and properties of the resulting hydrogels. The tetra-functionalized phthalocyanines favor a dynamic Schiff-base linkage with chitosan to form a 3D porous nanostructure. Based on this strategy, the self-healing ability, as demonstrated by rheological recovery and macroscopic and microscopic observations, is introduced through dynamic covalent Schiff-base linkage between NH groups in CS and benzaldehyde groups at cross-linker ends. The hydrogel was characterized using FT-IR, NMR, UV/vis, and rheological measurements. In addition, cryogenic scanning electron microscopy (cryo-SEM) was employed as a technique to visualize the internal morphology of the hydrogels. Study of the surface morphology of the hydrogel showed a 3D porous nanostructure with uniform morphology. Furthermore, incorporating the conductive nanofillers, such as carbon nanotubes (CNTs), into the structure can modulate the mechanical and electrical properties of the obtained hydrogels. Interestingly, these hydrogel nanocomposites proved to have very good film-forming properties, high modulus and strength, acceptable electrical conductivity, and excellent self-healing properties at neutral pH. Such properties can be finely tuned through variation of the cross-linker and CNT concentration, and as a result these structures are promising candidates for potential applications in various fields of research.
基于壳聚糖(CS)的水凝胶具有出色的自修复性能和较高的机械性能和电学性能,其制备已成为一个具有挑战性和吸引力的课题。然而,大多数传统水凝胶同时缺乏这些特性。本研究的目的是合成、表征和评估壳聚糖与锌酞菁四醛(ZnPcTa)框架共价交联的一般性质。我们希望获得一种前所未有的自修复三维(3D)纳米结构,以利用壳聚糖的优异机械性能和电学性能。交联剂的性质,如分子的结构、空间位阻效应和刚性,在决定所得水凝胶的微观结构和性能方面起着重要作用。四官能化酞菁有利于与壳聚糖形成动态席夫碱键,从而形成 3D 多孔纳米结构。基于这一策略,通过 CS 中的 NH 基团和交联剂末端的苯甲醛基团之间的动态共价席夫碱键,引入了自修复能力,这可以通过流变恢复以及宏观和微观观察来证明。采用傅里叶变换红外光谱(FT-IR)、核磁共振(NMR)、紫外/可见光谱(UV/vis)和流变学测量对水凝胶进行了表征。此外,还采用低温扫描电子显微镜(cryo-SEM)作为一种技术来可视化水凝胶的内部形态。水凝胶表面形态的研究表明其具有均匀形态的 3D 多孔纳米结构。此外,将导电纳米填料,如碳纳米管(CNTs),掺入到结构中,可以调节所得到的水凝胶的机械性能和电学性能。有趣的是,这些水凝胶纳米复合材料表现出非常好的成膜性能、高模量和强度、可接受的电导率以及在中性 pH 下的优异自修复性能。通过改变交联剂和 CNT 浓度,可以精细地调节这些性能,因此这些结构有望成为各个研究领域的潜在应用的候选材料。