Development and characterization of electrospun chitosan-chitin-PVA nanofiber: exploring structural integrity, crystallinity, and thermal stability for advanced applications

IF 2 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Carlos M. Cruz-Segundo, Salomon R. Vasquez-Garcia, Nelly Flores-Ramirez, Raymundo Sanchez-Orozco, Hamdy A. Abdel-Gawwad, Arlette A. Santiago, J. Vargas
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Abstract

Chitosan (CS), a linear polysaccharide derived from chitin (Ch), is known for its excellent biocompatibility, biodegradability, and high chemical resistance, making it suitable for environmental and biomedical applications. However, its relatively low mechanical strength limits its performance in demanding applications. To address this limitation, this study explores the reinforcement of chitosan with chitin via electrospinning, a technique that effectively incorporates chitin as a reinforcing agent. Specifically, electrospun nanofibers were composed of hydrolyzed chitosan (hCS), hydrolyzed chitin (hCh), and polyvinyl alcohol (PVA) as carrier polymer. To evaluate their structural and thermal performance, the nanofibers were characterized using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). SEM images revealed uniform and interconnected fibers, with diameters ranging from 231 to 317 nm, exhibiting a strong correlation between fiber diameter and chitin concentration. FTIR analysis indicated increased hydroxyl and amine group availability in hCS, further enhancing hydrogen bonding, which led to a crystallinity increase from 37.87% to 39.08% after chitosan hydrolysis, as revealed by XRD. Hydrolyzed chitin exhibited a higher crystallinity index of 64.52%. XRD studies showed that increasing hCh content in nanofibers improved crystallinity, with the highest crystallinity index of 51.21% observed in the sample containing 80% hCh. TGA demonstrated that nanofibers with higher chitin content exhibited superior thermal stability, with decomposition temperatures increasing from 317 °C (0% hCh) to 345 °C (100% hCh). This enhancement is attributed to the highly ordered crystalline structure and strong intermolecular hydrogen bonding of hCh. The findings underscore that the integration of chitin into chitosan-based nanofibers significantly improves their structural integrity, thermal resistance, and crystallinity. These optimized nanofibers hold promise for advanced applications in environmental remediation, biomedicine, and sustainable material development.

电纺丝壳聚糖-几丁质-聚乙烯醇纳米纤维的研制与表征:探讨其结构完整性、结晶度和热稳定性
壳聚糖(CS)是一种由几丁质(Ch)衍生而来的线性多糖,具有良好的生物相容性、生物降解性和耐化学性,适合于环境和生物医学应用。然而,其相对较低的机械强度限制了其在苛刻应用中的性能。为了解决这一限制,本研究探索了通过静电纺丝,一种有效地将几丁质作为增强剂的技术,用几丁质增强壳聚糖。具体而言,以水解壳聚糖(hCS)、水解几丁质(hCh)和聚乙烯醇(PVA)为载体聚合物组成电纺纳米纤维。为了评价纳米纤维的结构和热性能,利用扫描电镜(SEM)、傅里叶变换红外光谱(FTIR)、x射线衍射(XRD)和热重分析(TGA)对其进行了表征。扫描电镜图像显示,纤维直径在231 ~ 317 nm之间,纤维直径与甲壳素浓度有很强的相关性。FTIR分析表明,壳聚糖水解后,hCS中羟基和胺基的可用性增加,氢键进一步增强,结晶度从37.87%提高到39.08%。水解甲壳素结晶度较高,为64.52%。XRD研究表明,增加hCh含量可以改善纳米纤维的结晶度,在hCh含量为80%的样品中,结晶度指数最高,达到51.21%。热重分析表明,甲壳素含量高的纳米纤维具有较好的热稳定性,分解温度从317°C (0% hCh)增加到345°C (100% hCh)。这种增强是由于hCh高度有序的晶体结构和强大的分子间氢键。研究结果表明,将甲壳素整合到壳聚糖基纳米纤维中可以显著提高其结构完整性、耐热性和结晶度。这些经过优化的纳米纤维有望在环境修复、生物医学和可持续材料开发方面得到先进应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.60
自引率
0.00%
发文量
1
审稿时长
13 weeks
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