胶粘剂
聚氨酯
异佛尔酮二异氰酸酯
材料科学
耐水性
脲醛
氢键
复合材料
化学工程
高分子化学
化学
图层(电子)
有机化学
分子
工程类
作者
Hao Wang,Hongxing Yang,Miṅ Gu,Guanben Du,Kelu Ni,Sichen Liu,Tongda Liu,Xin Ran,Zhengjun Shi,Wei Gao,Long Yang
标识
DOI:10.1016/j.colsurfa.2023.131860
摘要
Developing formaldehyde-free and excellent water resistance has constantly been at the center of attention of wood adhesives. In addition to enhancing the adhesive itself, the modification of wood interface can also improve its bonding strength and water resistance. In this study, aqueous solutions of NaIO4 and NaClO2 have been sprayed onto the surface of poplar veneer evenly. An activated wood interface equipped with -CHO and -COOH was prepared. Traditional polyurethane adhesives are primarily two-component, with excessive manufacturing cost, complicated production and use procedures. In this study, a single component high branched polyurethane adhesive (GI) was synthesized via a A2 +B3 oligomerization method by using glycerol and isophorone diisocyanate (IPDI). Using branched polyamine (PA4 N) as a modifier, GI was modified to GI-PA4 N, which was used as an adhesive and then hot pressed with the activated wood to make three-layer plywood. The bonding interface was equipped with urethane bonds, urea-based chemical bonds, amide bonds, Schiff bonds and hydrogen bond, which considerably enhanced the stability and water resistance of the bonding interface. FT-IR and XPS confirmed the existence of -CHO and -COOH at the interface of the activated wood, and characterized the synthesis mechanism and bonding mechanism of GI-PA4 N. The results indicated that when the mass ratio of polyurethane to polyamine was 4:1, the overall performance of the adhesive was the best. The dry bonding strength increased from 1.92 MPa to 3.63 MPa, and the wet bonding strength increased from 1.77 MPa to 3.13 MPa, much higher than the minimum requirement of GB/T 17657–2013 (0.7 MPa). A formaldehyde-free, high-performance plywood with excellent water resistance was successfully prepared using wood interfacial activation and branched polyamine modification.
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