环氧-PMMA 微胶囊合成参数的建模与优化:响应面方法学

Abdulafeez O. Akorede, Adetutu O Aliyu, A. A. Adebisi
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摘要

自愈合微胶囊修复聚合物或复合材料损伤的效率在很大程度上取决于封装条件的建模,以实现具有所需特性的优化微胶囊。本研究采用响应面方法(RSM)模拟了封装条件(芯壳比、搅拌速率和温度)对环氧-聚甲基丙烯酸甲酯(环氧-PMMA)微胶囊的形态、化学和热特性的影响。采用溶剂蒸发法将环氧树脂封装在聚甲基丙烯酸甲酯(PMMA)中,在不同的封装条件下合成了环氧-PMMA 微胶囊。用光学显微镜(OP)观察合成微胶囊的形态,发现微胶囊有单核和不规则两种类型。模型效应显示,微胶囊的百分收率在 74.96% 到 96.56% 之间变化,受核壳比的影响很大,所研究的封装条件对百分收率的影响用二次方模型进行了最佳描述。微胶囊的核心含量在 54.8% 到 67.2% 之间,受核壳比和搅拌速率的影响较大,符合线性模型。微胶囊的平均直径在 26 至 74 μm 之间,受搅拌速率的影响较大,符合线性模型。合成微胶囊的傅立叶变换红外光谱(FTIR)显示,环氧树脂的特征峰 C-O-C 在 913 cm-1 处,C-O-ph 伸缩在 1032 cm-1 处。在 1386 cm-1 和 1189 cm-1 处观察到 PMMA 的 C-O 双峰。环氧-PMMA 微胶囊的热重分析(TGA)显示了三个分解阶段,分别是水分蒸发、环氧降解和 PMMA 外壳降解。最后,在芯壳比为 1.5:3、搅拌速率为 1000 rpm、搅拌温度为 40 °C 的条件下,对工艺进行了优化,以获得最大产量、最大芯含量和最小胶囊直径。合成的环氧-PMMA 微胶囊具有化学、热和形态稳定性,可通过优化模型获得所需的微胶囊特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modelling and optimization of epoxy-PMMA microcapsule synthesis parameter: A response surface methodology approach
The efficiency of self-healing microcapsule in restoring damages incurred by polymeric or composite materials is heavily dependent on modelling of encapsulation conditions to achieve optimized microcapsule with desired characteristics. This study modelled the effects of encapsulation conditions (core–shell ratio, agitation rate, and temperature) on the morphological, chemical, and thermal characteristics of epoxy-polymethylmethacrylate (epoxy-PMMA) microcapsules using response surface methodology (RSM). Epoxy-PMMA microcapsules were synthesized by encapsulating epoxy resin in polymethylmethacrylate (PMMA) at varied encapsulation conditions using solvent evaporation method. The morphology of the synthesized microcapsule using optical microscope (OP) revealed that the microcapsules are either mononuclear or irregular capsule types. The modelled effect showed that microcapsule percentage yield varied between 74.96 to 96.56%, was highly influenced by core–shell ratio and the effect of studied encapsulation conditions on percentage yield was best described by quadratic model. The core content of the microcapsules varied between 54.8 to 67.2%, observed to be highly influenced by both core–shell ratio and agitation rate which fit into linear model. The microcapsule average diameter was between 26 to 74 μm, highly influenced by agitation rate and fit linear model. Fourier transform infrared (FTIR) spectra of synthesized microcapsules revealed epoxy characteristic peak of C–O–C at 913 cm−1 and C–O-ph stretching at 1032 cm−1. C–O doublet of PMMA was observed at 1386 cm−1 and 1189 cm−1. Thermogravimetric analysis (TGA) of epoxy-PMMA microcapsule showed three stages of decomposition attributed to water evaporation, epoxy degradation, and PMMA shell degradation. Lastly, optimization process to achieve maximum yield, maximum core content and minimum capsule diameter was obtained with core–shell ratio of 1.5:3 and agitation rate of 1000 rpm at 40 °C. The synthesized epoxy-PMMA microcapsules exhibited chemical, thermal, morphological stability and the models can be optimized to achieve microcapsule with desired characteristics.
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