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使用动态差示扫描量热法对部分生物基环氧树脂固化过程的动力学分析

Kinetic Analysis of the Curing of a Partially Biobased Epoxy Resin Using Dynamic Differential Scanning Calorimetry.

作者信息

Lascano Diego, Quiles-Carrillo Luis, Balart Rafael, Boronat Teodomiro, Montanes Nestor

机构信息

Escuela Politécnica Nacional, Quito 17-01-2759, Ecuador.

Technological Institute of Materials (ITM), Universitat Politècnica de València (UPV), Plaza Ferrándiz y Carbonell 1, 03801 Alcoy, Spain.

出版信息

Polymers (Basel). 2019 Feb 27;11(3):391. doi: 10.3390/polym11030391.

Abstract

This research presents a cure kinetics study of an epoxy system consisting of a partially bio-sourced resin based on diglycidyl ether of bisphenol A (DGEBA) with amine hardener and a biobased reactive diluent from plants representing 31 wt %. The kinetic study has been carried out using differential scanning calorimetry (DSC) under non-isothermal conditions at different heating rates. Integral and derivative isoconversional methods or model free kinetics (MFK) have been applied to the experimental data in order to evaluate the apparent activation energy, , followed by the application of the appropriate reaction model. The bio-sourced system showed activation energy that is independent of the extent of conversion, with values between 57 and 62 kJ·mol, corresponding to typical activation energies of conventional epoxy resins. The reaction model was studied by comparing the calculated () and () functions with standard master plot curves. A two-parameter autocatalytic kinetic model of Šesták⁻Berggren [SB(,)] was assessed as the most suitable reaction model to describe the curing kinetics of the epoxy resins studied since it showed an excellent agreement with the experimental data.

摘要

本研究对一种环氧体系进行了固化动力学研究,该体系由一种基于双酚A二缩水甘油醚(DGEBA)的部分生物基树脂与胺类固化剂以及一种占31 wt%的植物源生物基反应性稀释剂组成。动力学研究是在不同升温速率的非等温条件下,使用差示扫描量热法(DSC)进行的。为了评估表观活化能,已将积分和导数等转化率方法或无模型动力学(MFK)应用于实验数据,随后应用适当的反应模型。该生物基体系显示出的活化能与转化率程度无关,其值在57至62 kJ·mol之间,对应于传统环氧树脂的典型活化能。通过将计算出的()和()函数与标准主曲线进行比较,对反应模型进行了研究。评估得出Šesták⁻Berggren的双参数自催化动力学模型[SB(,)]是描述所研究环氧树脂固化动力学最合适的反应模型,因为它与实验数据显示出极好的一致性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2933/6473346/52cbc6ee6b2a/polymers-11-00391-sch001.jpg

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