Physiochemical performance of electrospun PLA-lignin and PVA-lignin

IF 3.4 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
C C. Odili, O. P. Gbenebour, O A Olanrewaju, T O Badaru, S. O. Adeosun
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Abstract

Polylactic acid (PLA) and polyvinyl alcohol (PVA) are promising biocompatible and biodegradable materials for biomedical uses, yet they have limitations. Similarly, lignin is a precursor for carbon fiber but requires plasticizers to be spun into fibers. This hampers their use in areas like carbon fiber production and tissue engineering, thus the reason for this study. Lignin was extracted from the plantain stem, and a lignin blend with PLA and PVA was made and electrospun into fibers. Thereafter, the physiochemical properties of the composite fibers were analyzed. The XRD spectra revealed increased crystallinity in PLA/Lignin fiber. When 0.75 wt.% of lignin was added to PVA, a new peak and peak shift were formed in the composite fiber, indicating strong interaction. The crystallinity of PVA/lignin decreased from 71.5 to 60.1% when 0.25 wt. % of lignin was added. DSC showed miscibility of polymers and improved melting temperatures from 155 to 228 °C, for PLA/lignin (0.5wt.%) fiber, but a reduction in melting temperatures of PVA, with higher lignin content (149–143 °C). FTIR showed notable functional groups, typical of PLA, PVA, and lignin, such as the OH group between 3800 and 3459 cm−1. The minor peak shift in PLA/lignin showed that the level of molecular interaction is less than that of PVA/lignin. PLA/lignin displayed better fiber morphology compared to PVA/lignin, where fibers became sheet-like with higher lignin content. The addition of lignin improved the tensile strength of PVA (0.7 to 2.7 MPa). Conversely, PLA/lignin’s tensile strength decreased, due to reduced load transfer efficiency. Overall, PVA/lignin and PLA/lignin composites exhibit potential as reinforcement materials for biopolymers and carbon fiber precursors, with PVA showing more promise for carbon fiber production due to robust polymer-lignin interaction.

静电纺pla -木质素和pva -木质素的理化性能
聚乳酸(PLA)和聚乙烯醇(PVA)是很有前途的生物相容性和生物降解材料,但它们也有局限性。同样,木质素是碳纤维的前体,但需要增塑剂纺成纤维。这阻碍了它们在碳纤维生产和组织工程等领域的应用,因此进行了这项研究。从车前草茎中提取木质素,并与聚乳酸和聚乙烯醇共混制成木质素纤维。然后,对复合纤维的理化性能进行了分析。XRD光谱显示PLA/木质素纤维结晶度增加。当木质素的添加量为0.75 wt.%时,复合纤维中出现了一个新的峰和峰移,表明复合纤维相互作用强。当木质素添加量为0.25 wt. %时,PVA/木质素结晶度由71.5%下降到60.1%。DSC显示PLA/木质素(0.5wt.%)纤维的熔融温度从155°C提高到228°C,但PVA的熔融温度降低,木质素含量较高(149°C至143°C)。FTIR显示出明显的官能团,典型的是PLA、PVA和木质素,如3800 ~ 3459 cm−1之间的OH基团。PLA/木质素的峰移较小,表明分子相互作用水平小于PVA/木质素。与PVA/木质素相比,PLA/木质素表现出更好的纤维形态,木质素含量越高,纤维呈片状。木质素的加入提高了PVA的抗拉强度(0.7 ~ 2.7 MPa)。相反,由于载荷传递效率降低,PLA/木质素的抗拉强度下降。总的来说,PVA/木质素和PLA/木质素复合材料显示出作为生物聚合物和碳纤维前体增强材料的潜力,PVA因其强大的聚合物-木质素相互作用而在碳纤维生产中表现出更大的前景。
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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