材料科学
玻璃化转变
流变学
动力学
复合数
复合材料
粘度
扩散
反向
热力学
片状模塑料
热固性聚合物
自催化
玻璃纤维
聚合物
指数函数
曲率
学位(音乐)
化学动力学
作者
Festus Ifeanyi Anagwu,Daniel J. Preston,Alexandros A. Skordos
出处
期刊:Polymer
[Elsevier BV]
日期:2025-11-09
卷期号:342: 129319-129319
被引量:2
标识
DOI:10.1016/j.polymer.2025.129319
摘要
This study reports the matrix material models for the manufacturing of reinforced fibre composites using a disulphide-enabled aerospace-grade benzoxazine vitrimer. Cure kinetics and chemoviscosity models, crucial for fibrous composite manufacturing optimisation, were developed using calorimetric and rheometric data, respectively. An autocatalytic model with a logistic term accounting for diffusion represents accurately the resin cure kinetics, with 4 % average relative error in degree of cure prediction. The glass transition ( T g ) evolution follows the DiBenedetto equation, with a curvature parameter (λ) of 1.84. A chemorheological model based on the kinetics of viscosity at a reference temperature and an inverse temperature exponential dependence—appropriate for low degrees of cure prevailing during the filling/consolidation step of fibrous composite manufacturing—simulates rheological behaviour with an average error of 8.3 %. The initial viscosity ranges from 144.7 mPa·s at 130°C to 1119 mPa·s at 100°C, with fast evolution which limits impregnation, meaning that composites processing using a resin film infusion or pre-impregnation route is applicable to this vitrimeric matrix. • Cure kinetics of an aerospace-grade benzoxazine vitrimer is modelled accurately. • T g evolution in a benzoxazine vitrimer follows concave dependence on degree of cure. • Chemoviscosity is successfully modelled using the kinetics of reference viscosity. • Dynamic bond exchange supresses gelation, enabling lower temperature processing.
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