Tailoring Interphase Architecture for Toughened Epoxy Systems Using Multilayer Poly(ether imide) Films

IF 5.2 2区 化学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
ACS Applied Polymer Materials Pub Date : 2026-10-09 Epub Date: 2026-09-29 DOI:10.1021/acsapm.6c01098
Ujala Farooq, Dong Quan, Julie Teuwen, Clemens Dransfeld
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引用次数: 0

Abstract

This study presents a systematic investigation into tailoring interphase architecture in hierarchically toughened epoxy systems using multilayer poly(ether imide) (PEI) films as ductile interlayers. Processing parameters, including PEI film thickness (60 and 120 μm), volume fraction (20–50%), and cure cycle (first dwell temperatures of 120–180 °C), were varied to optimize fracture toughness. Single-edge notched bending (SENB) tests, coupled with microscopic analyses, revealed that fracture toughness is governed by the interplay between interphase morphology and the relative thickness of the PEI layer compared to the plastic zone size. Microscopic analysis showed that low cure temperatures reduce gradient interphase formation, leading to weak interfaces, enabling high energy dissipation, while higher temperatures yield strong interfaces with reduced crack tortuosity and hence brittle fracture. A critical crack tortuosity threshold (∼1.8) was identified, beyond which crack deflection and delamination dominate over microstructural mechanisms. Interphase thickness and particle size distribution were governed by diffusion-driven phase separation. In thinner epoxy cavities, PEI saturation occurred quickly, reducing the diffusion gradient and limiting interphase growth, in agreement with predictions from Fick’s law. These findings demonstrate that fracture toughness in PEI–epoxy systems is controlled by the interplay of intrinsic mechanisms (plastic deformation, particle debonding) and geometric mechanisms (crack deflection, tortuosity). Controlling both through process design enables toughness improvements beyond that of pure PEI, providing a framework for developing next-generation damage-tolerant materials.

使用多层聚醚亚胺薄膜的增韧环氧体系的界面结构
本研究采用多层聚醚亚胺(PEI)薄膜作为延展性夹层,对分层增韧环氧体系的界面结构进行了系统的研究。通过改变PEI膜厚度(60 μm和120 μm)、体积分数(20-50%)和固化周期(120 - 180℃)等工艺参数,优化断裂韧性。Single-edgenotched弯曲(SENB)测试,加上微观分析,revealedthat断裂韧性之间的相互作用是由interphasemorphology和裴层的相对厚度对塑性区大小。微观分析表明,低固化温度减少了梯度界面相的形成,导致弱界面,使能量耗散高,而高固化温度产生强界面,裂纹弯曲度降低,从而导致脆性断裂。确定了临界裂纹弯曲阈值(~ 1.8),超过该阈值,裂纹挠曲和分层在微观结构机制中占主导地位。相间厚度和颗粒分布受扩散驱动相分离的控制。在较薄的环氧树脂腔中,PEI饱和发生得很快,降低了扩散梯度并限制了间相的生长,这与菲克定律的预测一致。这些发现表明,pei -环氧树脂体系的断裂韧性是由内在机制(塑性变形、颗粒脱粘)和几何机制(裂纹挠度、弯曲度)的相互作用控制的。通过工艺设计控制两者,使韧性的提高超越了纯PEI,为开发下一代耐损伤材料提供了框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
6.00%
发文量
810
期刊介绍: ACS Applied Polymer Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics, and biology relevant to applications of polymers. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates fundamental knowledge in the areas of materials, engineering, physics, bioscience, polymer science and chemistry into important polymer applications. The journal is specifically interested in work that addresses relationships among structure, processing, morphology, chemistry, properties, and function as well as work that provide insights into mechanisms critical to the performance of the polymer for applications.
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