Mustafa Aker Keskin, Yasin Uslugil, Oktay Baykara, Ahmet Avcı
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引用次数: 0
Abstract
Epoxy resins are widely used in structural and functional composite components; however, their inherently brittle fracture behavior and temperature-dependent stiffness degradation limit their reliability under combined mechanical and thermomechanical loading. In this study, L160 epoxy composites were reinforced with electrospun nylon 6.6 (N6.6) nanofiber mats modified with B4C, Gd2O3, or hybrid B4C/Gd2O3 nanoparticles, thereby introducing ceramic functionality through the nanofiber interleaf rather than by direct nanoparticle dispersion into the resin. Five systems were examined: neat epoxy (Epoxy), epoxy with neat N6.6 mats (Epoxy/N6.6), and epoxy with B4C-modified, Gd2O3-modified, or hybrid-modified N6.6 mats (Epoxy/N6.6/B4C, Epoxy/N6.6/Gd2O3, and Epoxy/N6.6/B4C-Gd2O3, respectively). The mats were incorporated by a layer-by-layer hand lay-up route to obtain 16-layer composite plates, and the resulting systems were evaluated by SEM, TEM, XRD, EDX, FTIR, TGA, tensile testing, fracture-surface analysis, and dynamic mechanical analysis. Neat N6.6 mats increased the tensile strength of epoxy from 71.24 to 75.73 MPa, whereas B4C-modified mats produced the highest tensile strength of 88.65 MPa, corresponding to a 24.45% improvement. The hybrid B4C/Gd2O3-modified system exhibited the highest approximate onset temperature of the principal mass-loss stage, 390 \(^{\circ }\text {C}\), and the highest glass transition temperature of 116.8 \(^{\circ }\text {C}\). Fractographic observations showed brittle fracture in epoxy-rich regions and fiber pull-out, fiber breakage, interfacial debonding, and crack bridging in nanofiber-rich regions. Within the tested formulations, B4C modification gave the highest tensile strength, whereas the hybrid-modified system gave the highest reported approximate onset temperature of the principal mass-loss stage and tan-delta peak temperature. Residual voids and incomplete wetting were observed in some laminates and are considered when interpreting the results.
环氧树脂广泛应用于结构和功能复合材料部件;然而,它们固有的脆性断裂行为和温度相关的刚度退化限制了它们在机械和热机械联合载荷下的可靠性。在这项研究中,L160环氧复合材料用B4C、Gd2O3或B4C/Gd2O3混合纳米颗粒改性的静电纺尼龙6.6 (N6.6)纳米纤维垫增强,从而通过纳米纤维交错引入陶瓷功能,而不是直接将纳米颗粒分散到树脂中。研究了五种体系:纯环氧树脂(epoxy),纯N6.6基垫的环氧树脂(epoxy /N6.6), B4C改性、Gd2O3改性或混合改性N6.6基垫的环氧树脂(分别为环氧/N6.6/B4C、环氧/N6.6/Gd2O3和环氧/N6.6/B4C-Gd2O3)。采用逐层手工铺层的方法将垫块掺入,得到了16层复合材料,并通过SEM、TEM、XRD、EDX、FTIR、TGA、拉伸测试、断口分析和动态力学分析对所得体系进行了评价。纯N6.6改性毡的抗拉强度由71.24 MPa提高到75.73 MPa,而b4c改性毡的抗拉强度最高,为88.65 MPa,为24.45 MPa% improvement. The hybrid B4C/Gd2O3-modified system exhibited the highest approximate onset temperature of the principal mass-loss stage, 390 \(^{\circ }\text {C}\), and the highest glass transition temperature of 116.8 \(^{\circ }\text {C}\). Fractographic observations showed brittle fracture in epoxy-rich regions and fiber pull-out, fiber breakage, interfacial debonding, and crack bridging in nanofiber-rich regions. Within the tested formulations, B4C modification gave the highest tensile strength, whereas the hybrid-modified system gave the highest reported approximate onset temperature of the principal mass-loss stage and tan-delta peak temperature. Residual voids and incomplete wetting were observed in some laminates and are considered when interpreting the results.
期刊介绍:
-Chemistry of Fiber Materials, Polymer Reactions and Synthesis-
Physical Properties of Fibers, Polymer Blends and Composites-
Fiber Spinning and Textile Processing, Polymer Physics, Morphology-
Colorants and Dyeing, Polymer Analysis and Characterization-
Chemical Aftertreatment of Textiles, Polymer Processing and Rheology-
Textile and Apparel Science, Functional Polymers