Dual hydrogen-bonding network strategy enables fabrication of robust soy protein adhesive capable of excellent bonding at ambient temperature

胶粘剂 环氧树脂 韧性 氢键 材料科学 复合材料 聚乙二醇 大豆蛋白 粘接 共价键 热固性聚合物 部分 高分子化学 化学工程 化学 有机化学 分子 图层(电子) 工程类 生物化学
作者
Sun Yi,Zhi Li,Qian Yan,Shifeng Zhang
出处
期刊:Industrial Crops and Products [Elsevier BV]
卷期号:205: 117477-117477 被引量:9
标识
DOI:10.1016/j.indcrop.2023.117477
摘要

The application of biobased soy protein adhesives is significantly limited by poor initial adhesion during assembly. This deficiency leads to weak interfacial adhesion and cohesion toughness attributed to insufficient intermolecular interactions. In this study, we propose a dual hydrogen bonding system within a waterborne epoxy emulsion (WEU), in which the 2-ureido-4[1 H]-pyrimidinone (UPy) moiety with quadruple hydrogen bonds is grafted onto an epoxy skeleton, and polyethylene glycol (PEG) blocks with regular weak hydrogen bond sites is used to emulsify the WEU by simple mixing. WEU then acts as a crosslinker to improve the mechanical performances of high-temperature soybean meal (HSM) wood adhesives. The introduction of UPy and PEG blocks contributes to the formation of a dense cohesion crosslinking network and an energy dissipation system via multiple hydrogen bonding with peptide chains, enhancing the cold-pressing bond strength of adhesives with a 140% increase, relative to that of a pure HSM adhesive. Thermocuring facilitates interfacial penetration and covalent links via an epoxy ring-opening reaction in the system, creating a secondary crosslinking platform to optimize the water resistance and toughness of the adhesives. Consequently, the cured HSMW-15 adhesive exhibits an improvement in wet bond strength from 0.11 MPa to 0.90 MPa, with optimal toughness at 2.74 MJ/m3. This effective and feasible design provides valuable insights into modification strategies for preparing biobased wood adhesives with superior performance.
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