Anisimov Yuriy A, Yang Heng, Kwon Johnny, Cree Duncan E, Wilson Lee D
Department of Chemical Engineering, McMaster University, Hamilton, ON L8S 4M6, Canada.
Department of Chemistry, University of Saskatchewan, 110 Science Place, Saskatoon, SK S7N 5C9, Canada.
Polymers (Basel). 2024 Sep 22;16(18):2663. doi: 10.3390/polym16182663.
Previous research highlights the potential of polyaniline-based biocomposites as unique adsorbents for humidity sensors. This study examines several preparative routes for creating polyaniline (PANI) and chitosan (CHT) composites: Type 1-in situ polymerization of aniline with CHT; Type 2-molecular association in acidic aqueous media; and a control, Type 3-physical mixing of PANI and CHT powders (without solvent). The study aims to differentiate the bonding nature (covalent vs. noncovalent) within these composites, which posits that noncovalent composites should exhibit similar physicochemical properties regardless of the preparative route. The results indicate that Type 1 composites display features consistent with covalent and hydrogen bonding, which result in reduced water swelling versus Type 2 and 3 composites. These findings align with spectral and thermogravimetric data, suggesting more compact structure for Type 1 materials. Dye adsorption studies corroborate the unique properties for Type 1 composites, and H NMR results confirm the role of covalent bonding for the in situ polymerized samples. The structural stability adopts the following trend: Type 1 (covalent and noncovalent) > Type 2 (possible trace covalent and mainly noncovalent) > Type 3 (noncovalent). Types 2 and 3 are anticipated to differ based on solvent-driven complex formation. This study provides greater understanding of structure-function relationships in PANI-biopolymer composites and highlights the role of CHT as a template that involves variable (non)covalent contributions with PANI, according to the mode of preparation. The formation of composites with tailored bonding modalities will contribute to the design of improved adsorbent materials for environmental remediation to versatile humidity sensor systems.
先前的研究突出了聚苯胺基生物复合材料作为湿度传感器独特吸附剂的潜力。本研究考察了制备聚苯胺(PANI)和壳聚糖(CHT)复合材料的几种途径:类型1——苯胺与CHT的原位聚合;类型2——在酸性水介质中的分子缔合;以及一个对照,类型3——PANI和CHT粉末的物理混合(无溶剂)。该研究旨在区分这些复合材料中的键合性质(共价键与非共价键),其假定非共价复合材料无论制备途径如何都应表现出相似的物理化学性质。结果表明,类型1复合材料表现出与共价键和氢键一致的特征,这导致其与类型2和3复合材料相比水膨胀性降低。这些发现与光谱和热重数据一致,表明类型1材料的结构更紧凑。染料吸附研究证实了类型1复合材料的独特性质,并且1H NMR结果证实了原位聚合样品中共价键的作用。结构稳定性呈现以下趋势:类型1(共价键和非共价键)>类型2(可能存在微量共价键且主要为非共价键)>类型3(非共价键)。预计类型2和3会因溶剂驱动的络合物形成而有所不同。本研究加深了对PANI-生物聚合物复合材料结构-功能关系的理解,并突出了CHT作为模板的作用,根据制备方式,CHT与PANI涉及可变的(非)共价贡献。具有定制键合方式的复合材料的形成将有助于设计用于环境修复的改进吸附材料以及多功能湿度传感器系统。