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基于超支化接枝策略的 pulp 纤维素基核壳结构用于增强型大豆胶粘剂的开发。

Pulp cellulose-based core-sheath structure based on hyperbranched grafting strategy for development of reinforced soybean adhesive.

机构信息

College of Chemistry and Materials Engineering, Zhejiang A&F University, Hangzhou 311300, China.

Beijing Key Laboratory of Wood Science and Engineering & MOE Key Laboratory of Wooden Material Science and Application, Beijing Forestry University, Beijing 100083, China.

出版信息

Int J Biol Macromol. 2024 Mar;260(Pt 2):129520. doi: 10.1016/j.ijbiomac.2024.129520. Epub 2024 Jan 18.

Abstract

Formaldehyde adhesive is the primary source of indoor formaldehyde pollution, posing a serious threat to human health. Soybean meal (SM), as an abundant biomacromolecule and co-product of soybean oil industry, emerges as a promising alternative to formaldehyde adhesive. However, the SM adhesive exhibits inferior water resistance and unsatisfactory bonding strength. In this study, a novel core-sheath structure with an inexpensive pulp cellulose core and a hyperbranched polymer sheath is synthesized and introduced into SM to develop a robust bio-based adhesive. Specifically, aldehyde-functionalized pulp cellulose is grafted with hyperbranched polyamide, which is terminated via epoxy groups, to synthesize a core-sheath hybrid (APC@HBPA-EP). The core-sheath APC@HBPA-EP serves as both a crosslinker and an enhancer. The results show that the wet shear strength of the modified SM adhesive exhibits a remarkable 520 % increase to 0.93 MPa, and its dry shear strength reaches 2.10 MPa, meeting the established indoor use standards. The Young's modulus of the modified SM adhesive shows a significant 282 % increase to 19.27 GPa. Additionally, the modified SM adhesive exhibited superior impact toughness (7.48 KJ/m), which increased by 24 times compared with pure SM adhesive. This study provides a versatile strategy for developing robust protein adhesives, hydrogel patch, and composite coatings.

摘要

甲醛胶黏剂是室内甲醛污染的主要来源,严重威胁人类健康。豆粕(SM)作为一种丰富的生物大分子和大豆油工业的副产物,成为替代甲醛胶黏剂的有前途的选择。然而,SM 胶黏剂的耐水性差,胶合强度不理想。本研究合成了一种具有廉价纸浆纤维素核和超支化聚合物鞘的新颖核壳结构,并将其引入 SM 中,开发出一种坚固的生物基胶黏剂。具体而言,醛基化纸浆纤维素接枝超支化聚酰胺,端基为环氧基,合成核壳混合体(APC@HBPA-EP)。核壳 APC@HBPA-EP 既是交联剂又是增强剂。结果表明,改性 SM 胶黏剂的湿剪切强度显著提高 520%,达到 0.93 MPa,干剪切强度达到 2.10 MPa,满足室内使用标准。改性 SM 胶黏剂的杨氏模量显著提高 282%,达到 19.27 GPa。此外,改性 SM 胶黏剂表现出优异的冲击韧性(7.48 KJ/m),比纯 SM 胶黏剂提高了 24 倍。本研究为开发坚固的蛋白质胶黏剂、水凝胶补丁和复合涂层提供了一种通用策略。

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