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Latent, Cross-Linkable Triazole Platform on a Carbon Fiber Surface for Enhancing Interfacial Cross-Linking within Carbon Fiber/Epoxy Composites
[Image: see text] A long-running need in carbon fiber composite production is to ameliorate interfacial adhesion between the polymer and carbon fibers. Here, we present a convenient and feasible strategy for controlling the carbon fiber’s surface in a continuous process: syntheses of click-modified...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026132/ https://www.ncbi.nlm.nih.gov/pubmed/35474824 http://dx.doi.org/10.1021/acsomega.2c00045 |
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author | Shin, Jae-Ho Han, Gi-Yeon Kim, Hyun-Joong |
author_facet | Shin, Jae-Ho Han, Gi-Yeon Kim, Hyun-Joong |
author_sort | Shin, Jae-Ho |
collection | PubMed |
description | [Image: see text] A long-running need in carbon fiber composite production is to ameliorate interfacial adhesion between the polymer and carbon fibers. Here, we present a convenient and feasible strategy for controlling the carbon fiber’s surface in a continuous process: syntheses of click-modified silanes via copper(I)-catalyzed azide–alkyne cycloaddition reaction and grafting them onto fiber surfaces which prepare a latent curable platform under mild processes without postmodification. As 1,2,3-triazole moieties from the click reaction were added to the epoxy/dicyandiamide system, they triggered additional reactions in the later conversion stage; approximately, a 20% increase in the total reaction enthalpy compared to the system with no additives was obtained. We expected the enhanced cross-linking between the surface and matrix to expand the interfacial area, leading to reinforcements on interfacial adhesion and stress-transfer abilities within composites. The merit of the approach is well-demonstrated by conductive atomic force microscopy, showing that the interphase can be extended up to 6-fold when the triazole platform acts as curatives and serve as bridges after the epoxy cure. Consequently, the composite’s interfacial shear strength and interlaminar shear strength were increased up to 78 and 72%, respectively. This work affords a reactive platform where a custom-tailored fiber/matrix interface can be designed by virtue of versatility in clickable reactants. |
format | Online Article Text |
id | pubmed-9026132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90261322022-04-25 Latent, Cross-Linkable Triazole Platform on a Carbon Fiber Surface for Enhancing Interfacial Cross-Linking within Carbon Fiber/Epoxy Composites Shin, Jae-Ho Han, Gi-Yeon Kim, Hyun-Joong ACS Omega [Image: see text] A long-running need in carbon fiber composite production is to ameliorate interfacial adhesion between the polymer and carbon fibers. Here, we present a convenient and feasible strategy for controlling the carbon fiber’s surface in a continuous process: syntheses of click-modified silanes via copper(I)-catalyzed azide–alkyne cycloaddition reaction and grafting them onto fiber surfaces which prepare a latent curable platform under mild processes without postmodification. As 1,2,3-triazole moieties from the click reaction were added to the epoxy/dicyandiamide system, they triggered additional reactions in the later conversion stage; approximately, a 20% increase in the total reaction enthalpy compared to the system with no additives was obtained. We expected the enhanced cross-linking between the surface and matrix to expand the interfacial area, leading to reinforcements on interfacial adhesion and stress-transfer abilities within composites. The merit of the approach is well-demonstrated by conductive atomic force microscopy, showing that the interphase can be extended up to 6-fold when the triazole platform acts as curatives and serve as bridges after the epoxy cure. Consequently, the composite’s interfacial shear strength and interlaminar shear strength were increased up to 78 and 72%, respectively. This work affords a reactive platform where a custom-tailored fiber/matrix interface can be designed by virtue of versatility in clickable reactants. American Chemical Society 2022-04-06 /pmc/articles/PMC9026132/ /pubmed/35474824 http://dx.doi.org/10.1021/acsomega.2c00045 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Shin, Jae-Ho Han, Gi-Yeon Kim, Hyun-Joong Latent, Cross-Linkable Triazole Platform on a Carbon Fiber Surface for Enhancing Interfacial Cross-Linking within Carbon Fiber/Epoxy Composites |
title | Latent, Cross-Linkable Triazole Platform on a Carbon
Fiber Surface for Enhancing Interfacial Cross-Linking within Carbon
Fiber/Epoxy Composites |
title_full | Latent, Cross-Linkable Triazole Platform on a Carbon
Fiber Surface for Enhancing Interfacial Cross-Linking within Carbon
Fiber/Epoxy Composites |
title_fullStr | Latent, Cross-Linkable Triazole Platform on a Carbon
Fiber Surface for Enhancing Interfacial Cross-Linking within Carbon
Fiber/Epoxy Composites |
title_full_unstemmed | Latent, Cross-Linkable Triazole Platform on a Carbon
Fiber Surface for Enhancing Interfacial Cross-Linking within Carbon
Fiber/Epoxy Composites |
title_short | Latent, Cross-Linkable Triazole Platform on a Carbon
Fiber Surface for Enhancing Interfacial Cross-Linking within Carbon
Fiber/Epoxy Composites |
title_sort | latent, cross-linkable triazole platform on a carbon
fiber surface for enhancing interfacial cross-linking within carbon
fiber/epoxy composites |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026132/ https://www.ncbi.nlm.nih.gov/pubmed/35474824 http://dx.doi.org/10.1021/acsomega.2c00045 |
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