Biomass-based adhesives prepared with cellulose and branched polyamines

纤维素 胶粘剂 生物量(生态学) 制浆造纸工业 高分子科学 化学 高分子化学 材料科学 有机化学 农学 生物 工程类 图层(电子)
作者
Heyang Zeng,Wei Bi,Yaohong Yang,Li Liu,Hai‐Yang Guo,Linkun Xie,Xijuan Chai,Kaimeng Xu,Guanben Du,Lianpeng Zhang
出处
期刊:Colloids and Surfaces A: Physicochemical and Engineering Aspects [Elsevier BV]
卷期号:686: 133414-133414 被引量:4
标识
DOI:10.1016/j.colsurfa.2024.133414
摘要

The development of green, sustainable, biomass-based adhesives as alternatives to petroleum-based adhesives has emerged as a critical strategy in addressing environmental pollution and resource depletion. Cellulose represents an abundant and sustainable biomass material. However, the high density of hydroxyl groups along the cellulose molecular chains results in strong hydrophilicity, which limits its application in the adhesive sector. Crafting high water-resistance adhesives from cellulose is a task that is both promising and challenging. In this study, cellulose was modified to generate tosyl cellulose (TC), which was subsequently crosslinked with polyamines of varying degrees of branching. The effects of polyamine branching and the mass ratio of polyamine to tosyl cellulose on the performance of the TC-PA adhesive were investigated. The structure of the TC-PA adhesive was characterized using Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD). The results indicated successful synthesis of the TC-PA adhesive, with the reaction between TC and polyamines leading to the formation of macromolecules. The introduction of TC significantly lowered the curing temperature of the polyamines. Consequently, this novel cellulose-based adhesive demonstrates excellent water resistance and potential for broad applications.
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