Bhandari Netra Lal, Bhandari Ganesh, Bist Kabita, Adhikari Deepjyoti, Dhakal Kedar Nath, Adhikari Rameshwar, Lach Ralf, Kim Allison A, Yoo Dong Jin, Poudel Milan Babu
Central Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Department of Chemistry, Tri-Chandra Multiple Campus, Tribhuvan University, Ghantaghar, Kathmandu, Nepal.
Int J Biol Macromol. 2024 Nov;280(Pt 4):136192. doi: 10.1016/j.ijbiomac.2024.136192. Epub 2024 Sep 30.
Polyvinyl alcohol (PVA)-based biocomposites were fabricated by the incorporation of chitosan (Ch), cellulose fibers (CS), and their mixture (1:1 ratio). Fillers with various loading (2, 4, 8, and 10 wt.-%) were incorporated into PVA employing the solution casting method. The fillers and biocomposites were characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), brightfield microscopy, tensile and microindentation tests, contact angle measurement and thermogravimetric analysis (TGA). FTIR spectra revealed the removal of lignin, and intermolecular H-bonding between PVA and fillers promoting their filler-matrix interfacial interactions. Crystallographic results showed varied crystallite sizes and crystallinity of composites. Microscopic techniques revealed a uniform filler distribution, attributed to their compatibility with PVA. Tensile and microindentation tests demonstrated a decreased tensile strength (3.3-8.2 MPa of the composites compared to 15.7 MPa of the matrix) and Martens hardness (HM) of biocomposites. However, their value was increased with higher filler concentration, signifying the mechanical reinforcement. Contact angle analysis confirms the decreased wettability (hydrophilicity) of biocomposites, attributed to higher compatibility of fillers with PVA and intermolecular H-bonding between them. A slightly decreased thermal stability of biocomposites with filler incorporation is implied by TGA results despite their uniform distribution and strong matrix-filler interfacial interactions.
通过掺入壳聚糖(Ch)、纤维素纤维(CS)及其混合物(1:1比例)制备了基于聚乙烯醇(PVA)的生物复合材料。采用溶液浇铸法将各种负载量(2、4、8和10重量%)的填料掺入PVA中。通过傅里叶变换红外(FTIR)光谱、X射线衍射(XRD)、扫描电子显微镜(SEM)、明场显微镜、拉伸和微压痕测试、接触角测量和热重分析(TGA)对填料和生物复合材料进行了表征。FTIR光谱显示木质素的去除,以及PVA与填料之间的分子间氢键促进了它们的填料-基体界面相互作用。晶体学结果表明复合材料的微晶尺寸和结晶度各不相同。微观技术显示填料分布均匀,这归因于它们与PVA的相容性。拉伸和微压痕测试表明生物复合材料的拉伸强度(复合材料为3.3 - 8.2MPa,而基体为15.7MPa)和马氏体硬度(HM)降低。然而,它们的值随着填料浓度的增加而增加,这表明了机械增强作用。接触角分析证实了生物复合材料的润湿性(亲水性)降低,这归因于填料与PVA更高的相容性以及它们之间的分子间氢键。TGA结果表明,尽管填料分布均匀且基体-填料界面相互作用很强,但掺入填料后生物复合材料的热稳定性略有下降。