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材料性能对机械活性动态网络聚合物在涂层应用中的损伤报告及自修复性能的影响

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

作者信息

Son Da Hae, Kim Gi Young, Jeong Ji-Eun, Lee Sang-Ho, Park Young Il, Kong Hoyoul, Cheong In Woo, Kim Jin Chul

机构信息

Center for Advanced Specialty Chemicals, Division of Specialty and Bio-based Chemicals Technology, Korea Research Institute of Chemical Technology (KRICT), Ulsan 44412, Korea.

School of Applied Chemistry, Kyungpook National University, Daegu 41566, Korea.

出版信息

Molecules. 2021 Apr 23;26(9):2468. doi: 10.3390/molecules26092468.

DOI:10.3390/molecules26092468
PMID:33922672
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8122913/
Abstract

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 (3550 °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.

摘要

我们对动态聚合物网络涂层的材料性能对其自修复和损伤报告性能的影响进行了详细研究。合成了一系列含有损伤报告二芳基联苯并呋喃酮单元的可逆聚丙烯酸酯聚氨酯网络,并通过纳米压痕和差示扫描量热法实验测量了它们的材料性能(如压痕模量、硬度模量和玻璃化转变温度)。动态聚合物网络涂层的损伤报告和自修复性能相对于聚合物网络涂层的材料性能呈现出相反的趋势。玻璃化转变温度较低(约10°C)且压痕硬度较低(20 MPa)的软聚合物网络涂层表现出较好的自修复性能(几乎100%),但其损伤报告性能比玻璃化转变温度较高(3550°C)且压痕硬度较高(150200 MPa)的硬聚合物网络涂层差两倍。动态聚合物网络涂层的这些特性是独特的;在聚合物网络与基底表面结合的弹性体、薄膜和水凝胶中未观察到这些特性。有证据表明,控制聚合物的物理性能是设计基于机械响应基团的高性能自修复和损伤报告聚合物涂层的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/59df2c048774/molecules-26-02468-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/539e73c3e28a/molecules-26-02468-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/c350e5dcf329/molecules-26-02468-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/3333ad2c72f0/molecules-26-02468-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/cd3649e6ca2f/molecules-26-02468-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/4378af0f1834/molecules-26-02468-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/c4e9b4b0bea9/molecules-26-02468-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/f2d154bd6a43/molecules-26-02468-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/59df2c048774/molecules-26-02468-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/539e73c3e28a/molecules-26-02468-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/c350e5dcf329/molecules-26-02468-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/3333ad2c72f0/molecules-26-02468-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/cd3649e6ca2f/molecules-26-02468-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/4378af0f1834/molecules-26-02468-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/c4e9b4b0bea9/molecules-26-02468-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/f2d154bd6a43/molecules-26-02468-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa67/8122913/59df2c048774/molecules-26-02468-g007.jpg

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