Jinghua Wang , Zhishen Yin , Jie Sun , Yeqing Liu , Ruoxi Fan , Jialiang Li , Duo Chen , Jia Yan , Shichao Li , Zhanjun Wu
{"title":"端羟基PES/纳米sio2对环氧树脂超低温力学性能协同作用机理的研究","authors":"Jinghua Wang , Zhishen Yin , Jie Sun , Yeqing Liu , Ruoxi Fan , Jialiang Li , Duo Chen , Jia Yan , Shichao Li , Zhanjun Wu","doi":"10.1016/j.coco.2025.102401","DOIUrl":null,"url":null,"abstract":"<div><div>The mechanical properties of resin matrixes are predominant factors influencing the overall performance of fiber-reinforced composites. In this study, the high brittleness and low toughness of epoxy resin (EP) are addressed by incorporating hydroxyl-terminated polyether-sulfone (PES-OH) and nano-silica (Nano-SiO<sub>2</sub>) into the EP. The incorporation of PES-OH into EP led to a 22.6 % increase in tensile strength and a 27.8 % improvement in elongation at break at ultra-low temperatures. These enhancements are attributed to the formation of a semi-interpenetrating polymer network (SIPN) during the curing process, which strengthens the molecular network of the epoxy resin matrix through physical entanglement, interfacial reinforcement, and stress dispersion, enhancing crack resistance. The simultaneous introduction of PES-OH and Nano-SiO<sub>2</sub> synergistically improves the mechanical properties of EP at ultra-low temperatures (90 K). Specifically, the tensile strength, elongation at break, and modulus of elasticity of the modified EP were increased by 30.63 %, 19.6 %, 20.9 % and a 65.61 % improvement in fracture toughness (K<sub>IC</sub>), respectively, compared to the pure EP. The synergistic effect arises from the covalent bonding between the hydroxyl groups on Nano-SiO<sub>2</sub> and those in PES-OH and EP, thereby toughening and strengthening the epoxy molecular structure. Additionally, microdroplet debonding tests of carbon fiber with EP showed a 25.22 % increase in interfacial shear strength after introducing PES-OH and Nano-SiO<sub>2</sub>. Dynamic thermo-mechanical analysis confirmed that the incorporation of PES-OH and Nano-SiO<sub>2</sub> does not compromise the thermal stability of EP.</div></div>","PeriodicalId":10533,"journal":{"name":"Composites Communications","volume":"56 ","pages":"Article 102401"},"PeriodicalIF":6.5000,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Investigation on the synergistic effect mechanism of hydroxyl-terminated PES/Nano-SiO2 on the mechanical properties of epoxy resin at ultra-low temperatures\",\"authors\":\"Jinghua Wang , Zhishen Yin , Jie Sun , Yeqing Liu , Ruoxi Fan , Jialiang Li , Duo Chen , Jia Yan , Shichao Li , Zhanjun Wu\",\"doi\":\"10.1016/j.coco.2025.102401\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The mechanical properties of resin matrixes are predominant factors influencing the overall performance of fiber-reinforced composites. 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引用次数: 0
摘要
树脂基体的机械性能是影响纤维增强复合材料整体性能的主要因素。本研究通过在环氧树脂(EP)中加入羟基封端聚醚砜(PES-OH)和纳米二氧化硅(Nano-SiO2),解决了环氧树脂(EP)脆性大、韧性低的问题。在 EP 中加入 PES-OH 后,超低温下的拉伸强度提高了 22.6%,断裂伸长率提高了 27.8%。这些提高归功于在固化过程中形成的半互穿聚合物网络(SIPN),该网络通过物理缠结、界面强化和应力分散加强了环氧树脂基体的分子网络,从而提高了抗裂性。同时引入 PES-OH 和纳米二氧化硅可协同改善 EP 在超低温(90 K)下的机械性能。与纯 EP 相比,改性 EP 的拉伸强度、断裂伸长率和弹性模量分别提高了 30.63%、19.6% 和 20.9%,断裂韧性(KIC)提高了 65.61%。这种协同效应源于纳米二氧化硅上的羟基与 PES-OH 和 EP 中的羟基之间的共价键,从而韧化和加强了环氧分子结构。此外,碳纤维与 EP 的微滴脱粘测试表明,引入 PES-OH 和 Nano-SiO2 后,界面剪切强度提高了 25.22%。动态热机械分析证实,加入 PES-OH 和 Nano-SiO2 不会影响 EP 的热稳定性。
Investigation on the synergistic effect mechanism of hydroxyl-terminated PES/Nano-SiO2 on the mechanical properties of epoxy resin at ultra-low temperatures
The mechanical properties of resin matrixes are predominant factors influencing the overall performance of fiber-reinforced composites. In this study, the high brittleness and low toughness of epoxy resin (EP) are addressed by incorporating hydroxyl-terminated polyether-sulfone (PES-OH) and nano-silica (Nano-SiO2) into the EP. The incorporation of PES-OH into EP led to a 22.6 % increase in tensile strength and a 27.8 % improvement in elongation at break at ultra-low temperatures. These enhancements are attributed to the formation of a semi-interpenetrating polymer network (SIPN) during the curing process, which strengthens the molecular network of the epoxy resin matrix through physical entanglement, interfacial reinforcement, and stress dispersion, enhancing crack resistance. The simultaneous introduction of PES-OH and Nano-SiO2 synergistically improves the mechanical properties of EP at ultra-low temperatures (90 K). Specifically, the tensile strength, elongation at break, and modulus of elasticity of the modified EP were increased by 30.63 %, 19.6 %, 20.9 % and a 65.61 % improvement in fracture toughness (KIC), respectively, compared to the pure EP. The synergistic effect arises from the covalent bonding between the hydroxyl groups on Nano-SiO2 and those in PES-OH and EP, thereby toughening and strengthening the epoxy molecular structure. Additionally, microdroplet debonding tests of carbon fiber with EP showed a 25.22 % increase in interfacial shear strength after introducing PES-OH and Nano-SiO2. Dynamic thermo-mechanical analysis confirmed that the incorporation of PES-OH and Nano-SiO2 does not compromise the thermal stability of EP.
期刊介绍:
Composites Communications (Compos. Commun.) is a peer-reviewed journal publishing short communications and letters on the latest advances in composites science and technology. With a rapid review and publication process, its goal is to disseminate new knowledge promptly within the composites community. The journal welcomes manuscripts presenting creative concepts and new findings in design, state-of-the-art approaches in processing, synthesis, characterization, and mechanics modeling. In addition to traditional fiber-/particulate-reinforced engineering composites, it encourages submissions on composites with exceptional physical, mechanical, and fracture properties, as well as those with unique functions and significant application potential. This includes biomimetic and bio-inspired composites for biomedical applications, functional nano-composites for thermal management and energy applications, and composites designed for extreme service environments.