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以木质素基芳香单酚替代双酚A的生物基环氧胶粘剂

Bio-Based Epoxy Adhesives with Lignin-Based Aromatic Monophenols Replacing Bisphenol A.

作者信息

Van de Velde Nigel, Javornik Saška, Sever Tilen, Štular Danaja, Šobak Matic, Štirn Žiga, Likozar Blaž, Jerman Ivan

机构信息

National Institute of Chemistry, Hajdrihova 19, 1001 Ljubljana, Slovenia.

Steklarna Hrastnik, d. o. o., Cesta 1. maja 14, 1430 Hrastnik, Slovenia.

出版信息

Polymers (Basel). 2021 Nov 10;13(22):3879. doi: 10.3390/polym13223879.

Abstract

A bio-epoxy surface adhesive for adherence of the metal component species to glass substrate with desirable adhesion strength, converted controlled removal upon request, and bio-based resource inclusion was developed. For the development of resin, three different lignin-based aromatic monophenols, guaiacol, cresol, and vanillin, were used in the chemical epoxidation reaction with epichlorohydrin. The forming transformation process was studied by viscoelasticity, in situ FTIR monitoring, and Raman. Unlike other hydroxyl phenyls, guaiacol showed successful epoxide production, and stability at room temperature. Optimization of epoxide synthesis was conducted by varying NaOH concentration or reaction time. The obtained product was characterized by nuclear magnetic resonance and viscosity measurements. For the production of adhesive, environmentally problematic bisphenol A (BPA) epoxy was partially substituted with the environmentally acceptable, optimized guaiacol-based epoxy at 20, 50, and 80 wt.%. Mechanics, rheological properties, and the possibility of adhered phase de-application were assessed on the bio-substitutes and compared to commercially available polyepoxides or polyurethanes. Considering our aim, the sample composed of 80 wt.% bio-based epoxy/20 wt.% BPA thermoset was demonstrated to be the most suitable among those analyzed, as it was characterized by low BPA, desired boundary area and recoverability using a 10 wt.% acetic acid solution under ultrasound.

摘要

开发了一种生物环氧树脂表面粘合剂,用于将金属部件牢固地粘附到玻璃基板上,具有理想的粘附强度,可根据需要进行可控去除,并包含生物基资源。在树脂开发过程中,三种不同的基于木质素的芳香单酚,即愈创木酚、甲酚和香草醛,用于与环氧氯丙烷的化学环氧化反应。通过粘弹性、原位傅里叶变换红外光谱监测和拉曼光谱研究了形成转变过程。与其他羟基苯基不同,愈创木酚成功生成了环氧化物,并在室温下具有稳定性。通过改变氢氧化钠浓度或反应时间对环氧化物合成进行了优化。所得产物通过核磁共振和粘度测量进行了表征。在制备粘合剂时,对环境有问题的双酚A(BPA)环氧树脂被分别用20 wt.%、50 wt.%和80 wt.%的环境可接受的、优化的愈创木酚基环氧树脂部分替代。对这些生物替代品进行了力学性能、流变学性能以及粘附相去除可能性的评估,并与市售的聚环氧化物或聚氨酯进行了比较。考虑到我们的目标,由80 wt.%生物基环氧树脂/20 wt.% BPA热固性材料组成的样品在分析的样品中被证明是最合适的,因为它具有低BPA含量、理想的边界面积,并且在超声作用下使用10 wt.%的乙酸溶液具有可回收性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/217d/8621590/13587ae1d936/polymers-13-03879-g001.jpg

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