胶粘剂
环氧树脂
纤维素
材料科学
复合材料
傅里叶变换红外光谱
氢键
湿强度
化学工程
高分子化学
化学
有机化学
极限抗拉强度
分子
工程类
图层(电子)
作者
Jie Yuan,Guanben Du,Hongxing Yang,Sichen Liu,Yingchen Wu,Kelu Ni,Xin Ran,Wei Gao,Long Yang,Jun Li
标识
DOI:10.1016/j.ijbiomac.2022.10.053
摘要
Sustainable biomass resources are favored by researchers on account of their biodegradability and biocompatibility, which is a replacement for non-renewable fossil fuels. The development of low-carbon, green, and high-value bio-based adhesives are the inevitable trend of the industry development. However, the main factors limiting their application are poor water resistance and low bonding performance. Herein, the crosslinking network was constructed based on the reaction between the epoxy groups of trimethylolpropane glycidyl ether (TMPEG) and the amino groups of the synthesized aminated cellulose (AC) to form an interlocking bond. Through the synergy of covalent bond, electrostatic interaction, and hydrogen bond, the bonding strength and water resistance of the proposed adhesive can be effectively improved. Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and solid-state nuclear magnetic resonance spectroscopy (13C NMR) demonstrated the formation of epoxy-amine network. The excellent bonding strength and water resistance of the adhesive made with AC and TMPEG (AC-TMPEG) are mainly reflected by the dry lap shear strength of 2.56 MPa and the wet lap shear strength of 1.94/2.09 MPa after soaking in 63 °C/boiling water for 3.0 h. This study reveals an approach for manufacturing wood adhesive with superior bonding performance and exceptional water resistance.
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