Abstract

Epoxy resins are widely applicable in the aircraft, automobile, coating, and adhesive industries because of their good chemical resistance and excellent mechanical and thermal properties. However, upon external impact, the crack propagation of epoxy polymers weakens the overall impact resistance of these materials. Therefore, many impact modifiers have been developed to reduce the brittleness of epoxy polymers. Polyurethanes, as impact modifiers, can improve the toughness of polymers. Although it is well known that polyurethanes (PUs) are phase-separated in the polymer matrix after curing, connecting PUs to the polymer matrix for enhancing the mechanical properties of polymers has proven to be challenging. In this study, we introduced epoxy functional groups into polyol backbones, which is different from other studies that focused on modifying capping agents to achieve a network structure between the polymer matrix and PU. We confirmed the molecular weight of the prepared PU via gel permeation chromatography. Moreover, the prepared material was added to the epoxies and the resulting mechanical and thermal properties of the materials were evaluated. Furthermore, we conducted tensile, flexural strength, and impact resistance measurements. The addition of PU to the epoxy compositions enhanced their impact strength and maintained their mechanical strength up to 10 phr of PU. Furthermore, the morphologies observed with field emission scanning electron microscopy and transmission electron microscopy proved that the PU was phase separated in the epoxy matrix.

Highlights

  • Epoxy resins are thermosetting polymers that form 3D network structures after exothermic reactions with amine or acidic anhydride hardeners [1,2]

  • The results show that the synthesized fatty-acid-modified hydrogenated epoxy polyol (FMEP)-PU increased the impact strength, while the well-known agent CTBNagent enhanced tensile strength

  • A bisphenol A epoxy resin was modified with a dimeric fatty acid, both of which contained polyol and diglycidyl groups

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Summary

Introduction

Epoxy resins are thermosetting polymers that form 3D network structures after exothermic reactions with amine or acidic anhydride hardeners [1,2]. Epoxy resins are interesting materials due to their excellent mechanical and thermal properties as well as chemical resistance [3,4,5,6]. Many studies have been conducted to overcome this weakness by adding toughening agents that enhance impact resistance. Rubbery resins, such as carboxyl-terminated butadiene (CTBN) [7] and amine-terminated butadiene (ATBN) [8] have been used as toughening agents, whereas thermoplastic polyethersulfone [9] and polyetherimide [10] have been applied. Elastomeric polyurethanes (PUs) are representative tougheners for thermosetting polymers. PUs are composed of a soft segment of polyol and a hard segment of diisocyanate [11], which are not compatible with each other and lead to phase separation

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