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后固化对混杂纤维增强聚合物拉伸性能的影响:实验与数值洞察

Post-Curing Effects on the Tensile Properties of Hybrid Fiber-Reinforced Polymers: Experimental and Numerical Insights.

作者信息

Zaini Mohammed, Hamlaoui Oumayma, Chafiq Jalal, El Fqih Mohamed Ait, Idiri Mohamed, Aqil Said, Hajji Mohamed Karim, Bal Alperen, Tozan Hakan, Harnicárová Marta, Valicek Jan

机构信息

Laboratory of Artificial Intelligence & Complex Systems Engineering (AICSE), National Graduate School of Arts and Crafts, Hassan II University, Casablanca 20360, Morocco.

College of Engineering and Technology, American University of the Middle East, Egaila 54200, Kuwait.

出版信息

Polymers (Basel). 2025 May 6;17(9):1261. doi: 10.3390/polym17091261.

DOI:10.3390/polym17091261
PMID:40363046
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12073501/
Abstract

This study investigates the effects of post-curing temperatures on the tensile properties of hybrid basalt-jute-glass-carbon fiber-reinforced polymers (FRPs). Composite specimens were post-cured at 60 °C and 100 °C for 60 min, and their tensile behavior was assessed using a servo-hydraulic testing machine. Numerical simulations using the Abaqus software V6.14 were also conducted to compare experimental and computational results. The findings indicate that post-curing heat treatment enhances ductility due to increased polymer cross-linking, but excessive heat treatment at 100 °C negatively impacts elongation at fracture. The results revealed that specimens post-cured at 60 °C exhibited the optimal balance between strength and ductility, with increased elongation and moderate tensile strength. However, at 100 °C, while tensile strength improved in some cases, a significant decrease in elasticity and an increased risk of brittleness were observed, suggesting that extreme heat treatment may degrade polymer integrity. Natural fiber composites, particularly jute-based samples, outperformed synthetic composites in terms of elongation and overall mechanical stability. The numerical simulations provided further insights but showed discrepancies with experimental results, mainly due to fiber property variations and fabric waviness, underscoring the challenges of accurately modeling woven composites. The study highlights the importance of controlled post-curing temperatures in optimizing the mechanical performance of FRP composites, with 60 °C identified as the most effective condition for achieving a favorable balance between tensile strength, flexibility, and material durability. These findings offer valuable insights for material scientists and engineers working on the development of high-performance composite materials for structural and industrial applications.

摘要

本研究调查了后固化温度对混杂玄武岩-黄麻-玻璃-碳纤维增强聚合物(FRP)拉伸性能的影响。将复合材料试样在60℃和100℃下后固化60分钟,并使用伺服液压试验机评估其拉伸行为。还使用Abaqus软件V6.14进行了数值模拟,以比较实验结果和计算结果。研究结果表明,后固化热处理由于聚合物交联增加而提高了延展性,但在100℃下进行过度热处理会对断裂伸长率产生负面影响。结果显示,在60℃下后固化的试样在强度和延展性之间表现出最佳平衡,伸长率增加且拉伸强度适中。然而,在100℃时,虽然在某些情况下拉伸强度有所提高,但观察到弹性显著下降且脆性风险增加,这表明极端热处理可能会降低聚合物的完整性。天然纤维复合材料,特别是黄麻基样品,在伸长率和整体机械稳定性方面优于合成复合材料。数值模拟提供了进一步的见解,但与实验结果存在差异,主要是由于纤维性能变化和织物波纹,这突出了精确模拟编织复合材料的挑战。该研究强调了控制后固化温度对优化FRP复合材料机械性能的重要性,60℃被确定为在拉伸强度、柔韧性和材料耐久性之间实现良好平衡的最有效条件。这些发现为致力于开发用于结构和工业应用的高性能复合材料的材料科学家和工程师提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/071d37695111/polymers-17-01261-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/ad2845dcb2c3/polymers-17-01261-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/8303f5ea0c47/polymers-17-01261-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/8411d8d9012f/polymers-17-01261-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/ae87b3f67c70/polymers-17-01261-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/2779f62ee355/polymers-17-01261-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/d301924bbb51/polymers-17-01261-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/071d37695111/polymers-17-01261-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/ad2845dcb2c3/polymers-17-01261-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/8303f5ea0c47/polymers-17-01261-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/8411d8d9012f/polymers-17-01261-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/ae87b3f67c70/polymers-17-01261-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/2779f62ee355/polymers-17-01261-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/d301924bbb51/polymers-17-01261-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5af/12073501/071d37695111/polymers-17-01261-g007.jpg

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