增强拉伸强度的聚酰亚胺/二氧化硅纳米复合材料:尺寸效应和共价键合界面

IF 1.8 4区 工程技术 Q3 POLYMER SCIENCE
Yu Wang, Wenlong Yang, Jiaqi Lin, Xinmei Liu, Yuhang Zuo, Hongguo Sun, Ying Yang
{"title":"增强拉伸强度的聚酰亚胺/二氧化硅纳米复合材料:尺寸效应和共价键合界面","authors":"Yu Wang,&nbsp;Wenlong Yang,&nbsp;Jiaqi Lin,&nbsp;Xinmei Liu,&nbsp;Yuhang Zuo,&nbsp;Hongguo Sun,&nbsp;Ying Yang","doi":"10.1002/mats.202200066","DOIUrl":null,"url":null,"abstract":"<p>In this work, the tensile strength of polyimide/silica composites with the covalently bonded interface (bonded PI/SiO<sub>2</sub>) is investigated by molecular dynamic simulation. It is found that the nanofiller with smaller size can bring out a larger number of hydrogen bonds and interfacial non-bond energy in the composites, resulting in higher tensile strength. As the immobilization of the PI chains in the vicinity of SiO<sub>2</sub>, the covalently bonded interface is found to offer a greater reinforcing effect than the unbonded interface that is confirmed by the self-diffusion coefficient. The tensile strength of 9 wt.% bonded PI/SiO<sub>2</sub> composites is 11.34% higher than that of the unbounded composites. The tensile strength of PI/SiO<sub>2</sub> composites is enhanced with the increase of SiO<sub>2</sub> concentration up to critical mass percent (<i>X<sub>c</sub></i>), beyond which it will be decreased. To quantitatively predict <i>X<sub>c</sub></i> of PI/SiO<sub>2</sub> composites, an empirical equation based on the non-bond energy of the composites is proposed. The empirical equation showed that the <i>X<sub>c</sub></i> of PI/SiO<sub>2</sub> composites ranged from 8.03 to 10.36 wt.%, which is consistent with experimental values. These results provided the understanding of size-dependent covalently bonded interface structure, which would be beneficial to the design of nanocomposites with excellent mechanical performances.</p>","PeriodicalId":18157,"journal":{"name":"Macromolecular Theory and Simulations","volume":null,"pages":null},"PeriodicalIF":1.8000,"publicationDate":"2022-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Polyimide/Silica Nanocomposites with Enhanced Tensile Strength: Size Effects and Covalently Bonded Interface\",\"authors\":\"Yu Wang,&nbsp;Wenlong Yang,&nbsp;Jiaqi Lin,&nbsp;Xinmei Liu,&nbsp;Yuhang Zuo,&nbsp;Hongguo Sun,&nbsp;Ying Yang\",\"doi\":\"10.1002/mats.202200066\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In this work, the tensile strength of polyimide/silica composites with the covalently bonded interface (bonded PI/SiO<sub>2</sub>) is investigated by molecular dynamic simulation. It is found that the nanofiller with smaller size can bring out a larger number of hydrogen bonds and interfacial non-bond energy in the composites, resulting in higher tensile strength. As the immobilization of the PI chains in the vicinity of SiO<sub>2</sub>, the covalently bonded interface is found to offer a greater reinforcing effect than the unbonded interface that is confirmed by the self-diffusion coefficient. The tensile strength of 9 wt.% bonded PI/SiO<sub>2</sub> composites is 11.34% higher than that of the unbounded composites. The tensile strength of PI/SiO<sub>2</sub> composites is enhanced with the increase of SiO<sub>2</sub> concentration up to critical mass percent (<i>X<sub>c</sub></i>), beyond which it will be decreased. To quantitatively predict <i>X<sub>c</sub></i> of PI/SiO<sub>2</sub> composites, an empirical equation based on the non-bond energy of the composites is proposed. The empirical equation showed that the <i>X<sub>c</sub></i> of PI/SiO<sub>2</sub> composites ranged from 8.03 to 10.36 wt.%, which is consistent with experimental values. These results provided the understanding of size-dependent covalently bonded interface structure, which would be beneficial to the design of nanocomposites with excellent mechanical performances.</p>\",\"PeriodicalId\":18157,\"journal\":{\"name\":\"Macromolecular Theory and Simulations\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2022-12-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecular Theory and Simulations\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/mats.202200066\",\"RegionNum\":4,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecular Theory and Simulations","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/mats.202200066","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 1

摘要

本文采用分子动力学模拟的方法研究了具有共价键界面(键合PI/SiO2)的聚酰亚胺/二氧化硅复合材料的抗拉强度。研究发现,粒径越小,复合材料中产生的氢键和界面非键能越多,抗拉强度越高。作为PI链在SiO2附近的固定,发现共价键合界面比非键合界面具有更大的增强作用,这一点由自扩散系数证实。9 wt.%粘结的PI/SiO2复合材料的抗拉强度比未粘结的复合材料高11.34%。当SiO2浓度达到临界质量百分数(Xc)时,PI/SiO2复合材料的抗拉强度随SiO2浓度的增加而增强,超过临界质量百分数则降低。为了定量预测PI/SiO2复合材料的Xc,提出了基于复合材料非键能的经验方程。经验方程表明,PI/SiO2复合材料的Xc范围为8.03 ~ 10.36 wt.%,与实验值一致。这些结果为纳米复合材料的尺寸依赖共价键界面结构的理解提供了依据,这将有助于设计具有优异力学性能的纳米复合材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Polyimide/Silica Nanocomposites with Enhanced Tensile Strength: Size Effects and Covalently Bonded Interface

Polyimide/Silica Nanocomposites with Enhanced Tensile Strength: Size Effects and Covalently Bonded Interface

In this work, the tensile strength of polyimide/silica composites with the covalently bonded interface (bonded PI/SiO2) is investigated by molecular dynamic simulation. It is found that the nanofiller with smaller size can bring out a larger number of hydrogen bonds and interfacial non-bond energy in the composites, resulting in higher tensile strength. As the immobilization of the PI chains in the vicinity of SiO2, the covalently bonded interface is found to offer a greater reinforcing effect than the unbonded interface that is confirmed by the self-diffusion coefficient. The tensile strength of 9 wt.% bonded PI/SiO2 composites is 11.34% higher than that of the unbounded composites. The tensile strength of PI/SiO2 composites is enhanced with the increase of SiO2 concentration up to critical mass percent (Xc), beyond which it will be decreased. To quantitatively predict Xc of PI/SiO2 composites, an empirical equation based on the non-bond energy of the composites is proposed. The empirical equation showed that the Xc of PI/SiO2 composites ranged from 8.03 to 10.36 wt.%, which is consistent with experimental values. These results provided the understanding of size-dependent covalently bonded interface structure, which would be beneficial to the design of nanocomposites with excellent mechanical performances.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Macromolecular Theory and Simulations
Macromolecular Theory and Simulations 工程技术-高分子科学
CiteScore
3.00
自引率
14.30%
发文量
45
审稿时长
2 months
期刊介绍: Macromolecular Theory and Simulations is the only high-quality polymer science journal dedicated exclusively to theory and simulations, covering all aspects from macromolecular theory to advanced computer simulation techniques.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信