Multiple Function Hyperbranched Polysiloxane Nanoclusters for Controlling a Cross-Linking Structure to Convert Soy Meal into a Strong, Tough, and Multifunctional Adhesive

IF 7.3 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jiawei Shao, Xinyi Li, Tao Liu, Shiqing Chen, Shanshan Gong, Jinfeng Cao, Wenrui Zhou*, Cheng Li* and Jianzhang Li*, 
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Abstract

From an environmentally sustainable perspective, soybean meal (SM) adhesive presents an ideal alternative to petrochemical-based adhesives. Generally, strength and toughness are mutually exclusive for an adhesive. Hence, the creation of protein-based adhesives with high water-resistant strength of bonding, remarkable toughness, and multifunctionality remains a notable challenge. This study reports a dual hyperbranched siloxane nanocluster cross-linking strategy for creating SM-based adhesives with superior performance. In detail, synthesized hyperbranched epoxy siloxane nanocluster (ESN) and hyperbranched phenylboronic acid siloxane nanocluster (BPA@SN) were introduced into the SM matrix to establish a targeted cross-linking network between epoxy groups and protein chains as well as phenylboronic acid and polysaccharides. Meanwhile, the flexible Si–O segments within the hyperbranched siloxane facilitated energy dissipation, significantly boosting the adhesive toughness. After cross-linking modification, SM/ESN/BPA@SN-1 adhesive demonstrated outstanding dry bonding strength (2.04 ± 0.18 MPa), water-resistant bonding strength (1.12 ± 0.06 MPa), and toughness (18.5 ± 4.02 kJ/m3). Moreover, the adhesive exhibited distinctly improved resistance to mold, thermal stability, and flame retardancy. Therefore, this new strategy of using functional hyperbranched siloxane nanoclusters and SM to design strong, tough, and multifunctional green and sustainable wood-based biomass adhesives provides new ideas for achieving green development.

Abstract Image

Abstract Image

控制交联结构的多功能超支化聚硅氧烷纳米团簇,将豆粕转化为强韧的多功能粘合剂
从环境可持续发展的角度来看,豆粕(SM)粘合剂是石化基粘合剂的理想替代品。一般来说,粘合剂的强度和韧性是相互排斥的。因此,创造具有高防水粘合强度、显著韧性和多功能性的蛋白质基粘合剂仍然是一个值得注意的挑战。本研究报告了一种双重超支化硅氧烷纳米团簇交联策略,用于制造具有优异性能的 SM 基粘合剂。具体而言,将合成的超支化环氧硅氧烷纳米团簇(ESN)和超支化苯硼酸硅氧烷纳米团簇(BPA@SN)引入 SM 基体,在环氧基团与蛋白质链以及苯硼酸与多糖之间建立起定向交联网络。同时,超支化硅氧烷中的柔性 Si-O 段有利于能量耗散,显著提高了粘合韧性。经过交联改性后,SM/ESN/BPA@SN-1 粘合剂表现出出色的干粘接强度(2.04 ± 0.18 兆帕)、耐水粘接强度(1.12 ± 0.06 兆帕)和韧性(18.5 ± 4.02 kJ/m3)。此外,粘合剂的抗霉性、热稳定性和阻燃性也有明显提高。因此,利用功能性超支化硅氧烷纳米团簇和 SM 来设计高强度、韧性和多功能的绿色可持续木基生物质粘合剂的新策略为实现绿色发展提供了新思路。
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来源期刊
ACS Sustainable Chemistry & Engineering
ACS Sustainable Chemistry & Engineering CHEMISTRY, MULTIDISCIPLINARY-ENGINEERING, CHEMICAL
CiteScore
13.80
自引率
4.80%
发文量
1470
审稿时长
1.7 months
期刊介绍: ACS Sustainable Chemistry & Engineering is a prestigious weekly peer-reviewed scientific journal published by the American Chemical Society. Dedicated to advancing the principles of green chemistry and green engineering, it covers a wide array of research topics including green chemistry, green engineering, biomass, alternative energy, and life cycle assessment. The journal welcomes submissions in various formats, including Letters, Articles, Features, and Perspectives (Reviews), that address the challenges of sustainability in the chemical enterprise and contribute to the advancement of sustainable practices. Join us in shaping the future of sustainable chemistry and engineering.
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