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Environment-Induced Surface Dynamics of a Biomimetic Ionomer Studied Using in Situ Second Harmonic Generation

机译:使用原位二次谐波研究仿生离聚物的环境诱导表面动力学

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摘要

The environmental-induced surface dynamics of the biomimetic phosphoryl choline (PC)-functionalized poly(trimethylene carbonate) ionomer has been studied and compared to its unfunctionalized counterpart using in situ second harmonic generation measurements. Whereas the nonpolar liquid n-hexane did not induce any surface dynamic processes in the ionomer under study, the presence of water initiated a Debye-type dynamic reaction at the surface of the PC ionomer, which had no equivalent in the unfunctionalized material. This first-order reaction was attributed to a surface enrichment process of the functionalized ionomer in the hydrophilic environment involving movement of the PC endgroups from aggregates in the bulk to the surface. The time constant of the process was found to be about 6 min, and the corresponding activation energy was 0.4 eV. The dehydration process of the PC-functionalized ionomer in nitrogen gas atmosphere could be described by two time constants, one slightly below 1 min and the other one just above 13 min. The results presented in this work show that SHG measurements are well suited for the study of polymer surface restructuring dynamics in response to environmental changes. Such information is very important for the successful design and implementation of biomimetic polymers intended for biomedical applications.
机译:研究了仿生磷酰胆碱(PC)官能化的聚碳酸三亚甲基酯离聚物的环境诱导表面动力学,并使用原位二次谐波生成测量将其与未官能化的对应物进行了比较。非极性液体正己烷在所研究的离聚物中未诱导任何表面动力学过程,而水的存在则在PC离聚物表面引发了德拜型动力学反应,该反应在未官能化的材料中不存在。该一级反应归因于官能化离聚物在亲水环境中的表面富集过程,该过程涉及PC端基从本体中的聚集体向表面移动。发现该过程的时间常数为约6分钟,并且相应的活化能为0.4eV。 PC官能化离聚物在氮气气氛中的脱水过程可以用两个时间常数来描述,一个时间常数略低于1分钟,另一个时间常数略高于13分钟。这项工作提出的结果表明,SHG测量非常适合研究响应于环境变化的聚合物表面重构动力学。此类信息对于成功设计和实施拟用于生物医学应用的仿生聚合物非常重要。

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