环氧树脂
胶粘剂
木质素
双酚A
材料科学
环氧氯丙烷
极限抗拉强度
缩水甘油醚
化学
复合材料
有机化学
高分子化学
图层(电子)
作者
Kanji Ono,Nathalie Minako Ito,Rogério Ramos de Sousa,Francisco Avelino,Diego Lomonaco,Demétrio Jackson dos Santos
标识
DOI:10.1002/slct.202402615
摘要
Abstract Numerous efforts focus on renewable epoxy resin development, with lignin emerging as a viable green alternative to fossil‐derived resources. Being Earth's second‐most abundant organic molecule, lignin, rich in phenolic groups, shows promise as a substitute for bisphenol A in diglycidyl ether of bisphenol A (DGEBA) production. This work successfully modifies Kraft lignin (KL) via one‐step epoxidation (KLE) and phenolation prior to epoxidation (KLPE), significantly increasing oxirane ring content. Characterization via FTIR and 1 H NMR spectroscopy validates the modifications, yielding epoxy equivalent weights of 862.1 and 214.6 g mol −1 for KLE and KLPE, respectively. Incorporating 20 wt% KLE into adhesive maintains tensile and lap shear strength compared to 100 wt% DGEBA adhesives, with an increase in elastic modulus, indicating its potential as a sustainable resin substitute. However, phenolation prior to epoxidation slightly reduces mechanical properties despite higher oxirane ring concentration. These results shed some light on the impact of both modification protocols on the mechanical properties of epoxy adhesives, supporting the development and properties optimization of sustainable epoxy adhesives.
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