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Influence of Material Properties on the Damage-Reporting and Self-Healing Performance of a Mechanically Active Dynamic Network Polymer in Coating Applications

We conducted a detailed investigation of the influence of the material properties of dynamic polymer network coatings on their self-healing and damage-reporting performance. A series of reversible polyacrylate urethane networks containing the damage-reporting diarylbibenzofuranone unit were synthesi...

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Autores principales: Son, Da Hae, Kim, Gi Young, Jeong, Ji-Eun, Lee, Sang-Ho, Park, Young Il, Kong, Hoyoul, Cheong, In Woo, Kim, Jin Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122913/
https://www.ncbi.nlm.nih.gov/pubmed/33922672
http://dx.doi.org/10.3390/molecules26092468
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author Son, Da Hae
Kim, Gi Young
Jeong, Ji-Eun
Lee, Sang-Ho
Park, Young Il
Kong, Hoyoul
Cheong, In Woo
Kim, Jin Chul
author_facet Son, Da Hae
Kim, Gi Young
Jeong, Ji-Eun
Lee, Sang-Ho
Park, Young Il
Kong, Hoyoul
Cheong, In Woo
Kim, Jin Chul
author_sort Son, Da Hae
collection PubMed
description We conducted a detailed investigation of the influence of the material properties of dynamic polymer network coatings on their self-healing and damage-reporting performance. A series of reversible polyacrylate urethane networks containing the damage-reporting diarylbibenzofuranone unit were synthesized, and their material properties (e.g., indentation modulus, hardness modulus, and glass-transition temperature) were measured conducting nanoindentation and differential scanning calorimetry experiments. The damage-reporting and self-healing performances of the dynamic polymer network coatings exhibited opposite tendencies with respect to the material properties of the polymer network coatings. Soft polymer network coatings with low glass-transition temperature (~10 °C) and indentation hardness (20 MPa) exhibited better self-healing performance (almost 100%) but two times worse damage-reporting properties than hard polymer network coatings with high glass-transition temperature (35~50 °C) and indentation hardness (150~200 MPa). These features of the dynamic polymer network coatings are unique; they are not observed in elastomers, films, and hydrogels, whereby the polymer networks are bound to the substrate surface. Evidence indicates that controlling the polymer’s physical properties is a key factor in designing high-performance self-healing and damage-reporting polymer coatings based on mechanophores.
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spelling pubmed-81229132021-05-16 Influence of Material Properties on the Damage-Reporting and Self-Healing Performance of a Mechanically Active Dynamic Network Polymer in Coating Applications Son, Da Hae Kim, Gi Young Jeong, Ji-Eun Lee, Sang-Ho Park, Young Il Kong, Hoyoul Cheong, In Woo Kim, Jin Chul Molecules Article We conducted a detailed investigation of the influence of the material properties of dynamic polymer network coatings on their self-healing and damage-reporting performance. A series of reversible polyacrylate urethane networks containing the damage-reporting diarylbibenzofuranone unit were synthesized, and their material properties (e.g., indentation modulus, hardness modulus, and glass-transition temperature) were measured conducting nanoindentation and differential scanning calorimetry experiments. The damage-reporting and self-healing performances of the dynamic polymer network coatings exhibited opposite tendencies with respect to the material properties of the polymer network coatings. Soft polymer network coatings with low glass-transition temperature (~10 °C) and indentation hardness (20 MPa) exhibited better self-healing performance (almost 100%) but two times worse damage-reporting properties than hard polymer network coatings with high glass-transition temperature (35~50 °C) and indentation hardness (150~200 MPa). These features of the dynamic polymer network coatings are unique; they are not observed in elastomers, films, and hydrogels, whereby the polymer networks are bound to the substrate surface. Evidence indicates that controlling the polymer’s physical properties is a key factor in designing high-performance self-healing and damage-reporting polymer coatings based on mechanophores. MDPI 2021-04-23 /pmc/articles/PMC8122913/ /pubmed/33922672 http://dx.doi.org/10.3390/molecules26092468 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Son, Da Hae
Kim, Gi Young
Jeong, Ji-Eun
Lee, Sang-Ho
Park, Young Il
Kong, Hoyoul
Cheong, In Woo
Kim, Jin Chul
Influence of Material Properties on the Damage-Reporting and Self-Healing Performance of a Mechanically Active Dynamic Network Polymer in Coating Applications
title Influence of Material Properties on the Damage-Reporting and Self-Healing Performance of a Mechanically Active Dynamic Network Polymer in Coating Applications
title_full Influence of Material Properties on the Damage-Reporting and Self-Healing Performance of a Mechanically Active Dynamic Network Polymer in Coating Applications
title_fullStr Influence of Material Properties on the Damage-Reporting and Self-Healing Performance of a Mechanically Active Dynamic Network Polymer in Coating Applications
title_full_unstemmed Influence of Material Properties on the Damage-Reporting and Self-Healing Performance of a Mechanically Active Dynamic Network Polymer in Coating Applications
title_short Influence of Material Properties on the Damage-Reporting and Self-Healing Performance of a Mechanically Active Dynamic Network Polymer in Coating Applications
title_sort influence of material properties on the damage-reporting and self-healing performance of a mechanically active dynamic network polymer in coating applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122913/
https://www.ncbi.nlm.nih.gov/pubmed/33922672
http://dx.doi.org/10.3390/molecules26092468
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