The surface modification effect on the interfacial properties of glass fiber-reinforced epoxy: A molecular dynamics study

In this work, the effect of common functional groups, namely hydroxyl, formyl, carboxyl, and amine groups on the interfacial behavior of surface-modified glass fiber-reinforced epoxy is investigated at molecular scale. The interfacial properties of the epoxy/silica coated with different functional g...

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Main Authors: Deng Jiangang, Song You, Lan Zhenbo, Xu Zhuolin, Chen Yanming, Yang Bing, Hao Huali
Format: Article
Language:English
Published: De Gruyter 2022-03-01
Series:Nanotechnology Reviews
Subjects:
Online Access:https://doi.org/10.1515/ntrev-2022-0068
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author Deng Jiangang
Song You
Lan Zhenbo
Xu Zhuolin
Chen Yanming
Yang Bing
Hao Huali
author_facet Deng Jiangang
Song You
Lan Zhenbo
Xu Zhuolin
Chen Yanming
Yang Bing
Hao Huali
author_sort Deng Jiangang
collection DOAJ
description In this work, the effect of common functional groups, namely hydroxyl, formyl, carboxyl, and amine groups on the interfacial behavior of surface-modified glass fiber-reinforced epoxy is investigated at molecular scale. The interfacial properties of the epoxy/silica coated with different functional group systems are quantified by performing pulling test using the steered molecular dynamics simulations. It is found that the system with hydroxyl groups has a relatively lower interfacial interaction, exhibiting an adhesive failure mode. When partial hydroxyl groups are replaced by carboxyl, amine, and formyl groups, respectively, the interfacial interactions are increased and these systems exhibit a cohesive failure mode where failure happens in the epoxy close to interface. A relatively higher force is required for the adhesive debonding, while more energy can be dissipated for the cohesive debonding. Because the increased interfacial interactions can prevent the mobility of polymer chains, and delay the propagation of micropores in the matrix, leading to the epoxy matrix with a high ability of energy absorption. Our work provides an insight into how functional groups affect the interface debonding behavior of glass fiber-reinforced epoxy, offering a guideline for control of the interfacial properties of such composites through surface modification techniques.
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spelling doaj.art-ff6891ca5de94e519cbaa9da1ee39e5a2022-12-22T03:33:58ZengDe GruyterNanotechnology Reviews2191-90972022-03-011111143115710.1515/ntrev-2022-0068The surface modification effect on the interfacial properties of glass fiber-reinforced epoxy: A molecular dynamics studyDeng Jiangang0Song You1Lan Zhenbo2Xu Zhuolin3Chen Yanming4Yang Bing5Hao Huali6Wuhan Nari Limited Liability Company of State Grid Electric Power Research Institute, Wuhan, Hubei Province, 430074, ChinaWuhan Nari Limited Liability Company of State Grid Electric Power Research Institute, Wuhan, Hubei Province, 430074, ChinaWuhan Nari Limited Liability Company of State Grid Electric Power Research Institute, Wuhan, Hubei Province, 430074, ChinaWuhan Nari Limited Liability Company of State Grid Electric Power Research Institute, Wuhan, Hubei Province, 430074, ChinaSchool of Power and Mechanical Engineering, Wuhan University, Wuhan, Hubei Province, 430072, ChinaSchool of Power and Mechanical Engineering, Wuhan University, Wuhan, Hubei Province, 430072, ChinaSchool of Power and Mechanical Engineering, Wuhan University, Wuhan, Hubei Province, 430072, ChinaIn this work, the effect of common functional groups, namely hydroxyl, formyl, carboxyl, and amine groups on the interfacial behavior of surface-modified glass fiber-reinforced epoxy is investigated at molecular scale. The interfacial properties of the epoxy/silica coated with different functional group systems are quantified by performing pulling test using the steered molecular dynamics simulations. It is found that the system with hydroxyl groups has a relatively lower interfacial interaction, exhibiting an adhesive failure mode. When partial hydroxyl groups are replaced by carboxyl, amine, and formyl groups, respectively, the interfacial interactions are increased and these systems exhibit a cohesive failure mode where failure happens in the epoxy close to interface. A relatively higher force is required for the adhesive debonding, while more energy can be dissipated for the cohesive debonding. Because the increased interfacial interactions can prevent the mobility of polymer chains, and delay the propagation of micropores in the matrix, leading to the epoxy matrix with a high ability of energy absorption. Our work provides an insight into how functional groups affect the interface debonding behavior of glass fiber-reinforced epoxy, offering a guideline for control of the interfacial properties of such composites through surface modification techniques.https://doi.org/10.1515/ntrev-2022-0068functional groupsinterfacial failureconformational changesteered molecular dynamicsatomistic scale
spellingShingle Deng Jiangang
Song You
Lan Zhenbo
Xu Zhuolin
Chen Yanming
Yang Bing
Hao Huali
The surface modification effect on the interfacial properties of glass fiber-reinforced epoxy: A molecular dynamics study
Nanotechnology Reviews
functional groups
interfacial failure
conformational change
steered molecular dynamics
atomistic scale
title The surface modification effect on the interfacial properties of glass fiber-reinforced epoxy: A molecular dynamics study
title_full The surface modification effect on the interfacial properties of glass fiber-reinforced epoxy: A molecular dynamics study
title_fullStr The surface modification effect on the interfacial properties of glass fiber-reinforced epoxy: A molecular dynamics study
title_full_unstemmed The surface modification effect on the interfacial properties of glass fiber-reinforced epoxy: A molecular dynamics study
title_short The surface modification effect on the interfacial properties of glass fiber-reinforced epoxy: A molecular dynamics study
title_sort surface modification effect on the interfacial properties of glass fiber reinforced epoxy a molecular dynamics study
topic functional groups
interfacial failure
conformational change
steered molecular dynamics
atomistic scale
url https://doi.org/10.1515/ntrev-2022-0068
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