In-depth analysis of kraft lignin epoxy thermosets.

IF 3.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
Saeid Nikafshar, Kevin Dunne, Sajad Nikafshar, Mojgan Nejad
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引用次数: 0

Abstract

In this study, epoxidized lignins were prepared by reacting softwood (SW) and hardwood (HW) technical (kraft) lignins with a biobased epichlorohydrin. The chemical structures, rheological behaviors, and thermomechanical properties of the epoxidized lignins were measured and compared with those of petroleum-based (DGEBA) epoxy resin. First, the chemical and physical properties of the lignin samples were assessed using Fourier-transform infrared spectroscopy (FTIR), gel permeation chromatography (GPC), quantitative phosphorus nuclear magnetic resonance spectroscopy (31P NMR), and 2D-heteronuclear single quantum coherence (HSQC) NMR analyses. Subsequently, the unmodified lignins were epoxidized over a short period (3 hours), using ethyl lactate as a biobased co-solvent. The 31P NMR and HSQC analysis of the epoxidized lignins confirmed that phenolic hydroxyl and carboxylic acid groups in lignin were selectively epoxidized without any other significant changes to the chemical structure of lignin. Rheological multi-wave curing studies of both lignin-based and bisphenol A-based (DGEBA) resins cured with a biobased curing agent revealed that the lignin-based systems exhibited significantly shorter gelation times and lower activation energies. Further analyses, including gel fraction, swelling ratio, thermal gravimetric analysis (TGA), and dynamic mechanical analysis (DMA) results, demonstrated that lignin-based thermosets had comparable properties to the petroleum-based epoxy system when both were prepared with solvent (40 wt%) inclusion. Notably, the thermoset resin made with kraft hardwood lignin exhibited superior thermomechanical properties compared to the softwood system.

硫酸盐木质素环氧热固性树脂的深入分析。
以软木(SW)和硬木(HW)工艺木质素与生物基环氧氯丙烷反应制备环氧化木质素。测定了环氧化木质素的化学结构、流变行为和热力学性能,并与石油基环氧树脂(DGEBA)进行了比较。首先,利用傅里叶变换红外光谱(FTIR)、凝胶渗透色谱(GPC)、定量磷核磁共振谱(31P NMR)和二维异核单量子相干(HSQC) NMR分析对木质素样品的化学和物理性质进行了评估。随后,未经改性的木质素在短时间内(3小时)环氧化,使用乳酸乙酯作为生物基共溶剂。对环氧化木质素的31P NMR和HSQC分析证实,木质素中的酚羟基和羧酸基团被选择性环氧化,而木质素的化学结构没有发生明显变化。用生物基固化剂固化木质素基和双酚基(DGEBA)树脂的流变多波固化研究表明,木质素基体系的凝胶化时间明显缩短,活化能明显降低。进一步的分析,包括凝胶分数、膨胀比、热重分析(TGA)和动态力学分析(DMA)结果,表明木质素基热固性树脂与石油基环氧树脂具有相当的性能,当两者都加入溶剂(40% wt%)时。值得注意的是,与软木体系相比,由牛皮硬木木质素制成的热固性树脂表现出优越的热机械性能。
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
Faraday Discussions
Faraday Discussions 化学-物理化学
自引率
0.00%
发文量
259
期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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