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含叠氮基丙烯酸功能薄膜的分子动力学

Molecular Dynamics of Functional Azide-Containing Acrylic Films.

作者信息

Carsí Marta, Sanchis Maria J, Vallejos Saul, García Félix C, García José Miguel

机构信息

Instituto de Automática e Informática Industrial, Departamento de Termodinámica Aplicada, Universitat Politècnica de Valencia, 46022 Valencia, Spain.

Instituto Tecnológico de la Energía, Departamento de Termodinámica Aplicada, Universitat Politècnica de València, Camí de Vera s/n, 46022 Valencia, Spain.

出版信息

Polymers (Basel). 2018 Aug 2;10(8):859. doi: 10.3390/polym10080859.

DOI:10.3390/polym10080859
PMID:30960784
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6403574/
Abstract

A report on the syntheses, thermal, mechanical and dielectric characterizations of two novel polymeric acrylic materials with azide groups in their pendant structures is presented. Having the same general structure, these polymers differ in length of oxyethylene units in the pendant chain [-CONH-CH₂CH₂-(O-CH₂CH₂)N₃], where n is 1 (poly(-(2-(2-azidoethoxy)ethyl)methacrylamide), PAzMa1) or 2 (poly(-2-(2-(2-azidoethoxy)ethoxy)ethyl)methacrylamide), PAzMa2), leading with changes in their dynamics. As the thermal decomposition of the azide group is observed above 100 °C, dielectric analysis was carried out in the temperature range of -120 °C to 100 °C. Dielectric spectra of both polymers exhibit in the glassy state two relaxations labelled in increasing order of temperature as - and -processes, respectively. At high temperatures and low frequencies, the spectra are dominated by ohmic conductivity and interfacial polarization effects. Both, dipolar and conductive processes were characterized by using different models. Comparison of the dielectric activity obtained for PAzMa1 and PAzMa2 with those reported for crosslinked poly(2-ethoxyethylmethacrylate) (CEOEMA) was performed. The analysis of the length of oxyethylene pendant chain and the effect of the methacrylate or methacrylamide nature on the dynamic mobility was analysed.

摘要

本文报道了两种新型侧链结构含叠氮基的聚合丙烯酸材料的合成、热性能、力学性能和介电性能表征。这些聚合物具有相同的基本结构,但侧链中氧化乙烯单元的长度不同[-CONH-CH₂CH₂-(O-CH₂CH₂)N₃],其中n为1(聚(-(2-(2-叠氮基乙氧基)乙基)甲基丙烯酰胺),PAzMa1)或2(聚(-2-(2-(2-叠氮基乙氧基)乙氧基)乙基)甲基丙烯酰胺),PAzMa2),这导致其动力学发生变化。由于在100℃以上观察到叠氮基的热分解,因此在-120℃至100℃的温度范围内进行了介电分析。两种聚合物的介电谱在玻璃态下均表现出两个弛豫过程,分别按温度升高顺序标记为α-和β-过程。在高温和低频下,谱图主要由欧姆电导率和界面极化效应主导。偶极和导电过程均采用不同模型进行表征。对PAzMa1和PAzMa2获得的介电活性与交联聚(2-乙氧基乙基甲基丙烯酸酯)(CEOEMA)报道的介电活性进行了比较。分析了氧化乙烯侧链长度以及甲基丙烯酸酯或甲基丙烯酰胺性质对动态迁移率的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/99687b51e65f/polymers-10-00859-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/b16050a17c55/polymers-10-00859-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/e5d08aedd4a1/polymers-10-00859-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/a53b067ee763/polymers-10-00859-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/c178d16cc071/polymers-10-00859-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/814f43a933f7/polymers-10-00859-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/03e3b652c108/polymers-10-00859-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/99687b51e65f/polymers-10-00859-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/b16050a17c55/polymers-10-00859-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/e5d08aedd4a1/polymers-10-00859-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/a53b067ee763/polymers-10-00859-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/c178d16cc071/polymers-10-00859-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/814f43a933f7/polymers-10-00859-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/03e3b652c108/polymers-10-00859-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809f/6403574/99687b51e65f/polymers-10-00859-g010.jpg

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本文引用的文献

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Surface-initiated Polymerization of Azidopropyl Methacrylate and its Film Elaboration via Click Chemistry.甲基丙烯酸叠氮丙酯的表面引发聚合及其通过点击化学制备薄膜
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