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玻璃纤维增强聚丙烯弯曲板的制备及其在碱性溶液环境中的长期性能

Preparation of Glass Fiber Reinforced Polypropylene Bending Plate and Its Long-Term Performance Exposed in Alkaline Solution Environment.

作者信息

Peng Zhan, Wang Anji, Wang Chen, Li Chenggao

机构信息

Key Lab of Structures Dynamic Behavior and Control, Ministry of Education, Harbin Institute of Technology, Harbin 150090, China.

Key Lab of Smart Prevention and Mitigation of Civil Engineering Disasters, Ministry of Industry and Information Technology, Harbin Institute of Technology, Harbin 150090, China.

出版信息

Polymers (Basel). 2025 Jun 30;17(13):1844. doi: 10.3390/polym17131844.

Abstract

Glass fiber reinforced polypropylene composite plates have gradually attracted more attention because of their repeated molding, higher toughness, higher durability, and fatigue resistance compared to glass fiber reinforced thermosetting composites. In practical engineering applications, composite plates have to undergo bending effect at different angles in corrosive environment of concrete, including bending bars from 0~90°, and stirrups of 90°, which may lead to long-term performance degradation. Therefore, it is important to evaluate the long-term performance of glass fiber reinforced polypropylene composite bending plates in an alkali environment. In the current paper, a new bending device is developed to prepare glass fiber reinforced polypropylene bending plates with the bending angles of 60° and 90°. It should be pointed out that the above two bending angles are simulated typical bending bars and stirrups, respectively. The plate is immersed in the alkali solution environment for up to 90 days for long-term exposure. Mechanical properties (tensile properties and shear properties), thermal properties (dynamic mechanical properties and thermogravimetric analysis) and micro-morphology analysis (surface morphology analysis) were systematically designed to evaluate the influence mechanism of bending angle and alkali solution immersion on the long-term mechanical properties. The results show the bending effect leads to the continuous failure of fibers, and the outer fibers break under tension, and the inner fibers buckle under compression, resulting in debonding of the fiber-matrix interface. Alkali solution (OH ions) corrode the surface of glass fiber to form soluble silicate, which is proved by the mass fraction of glass fiber decreased obviously from 79.9% to 73.65% from thermogravimetric analysis. This contributes to the highest degradation ratio of tensile strength was 71.6% (60° bending) and 65.6% (90° bending), respectively, compared to the plate with bending angles of 0°. A high curvature bending angle (such as 90°) leads to local buckling of fibers and plastic deformation of the matrix, forming microcracks and fiber-resin interface bonding at the bending area, which accelerates the chemical erosion and debonding process in the interface area, bringing about an additional maximum 10.56% degradation rate of the shear strength. In addition, the alkali immersion leads to the obvious degradation of storage modulus and thermal decomposition temperature of composite plate. Compared with the other works on the long-term mechanical properties of glass fiber reinforced polypropylene, it can be found that the long-term performance of glass fiber reinforced polypropylene composites is controlled by the corrosive media type, bending angle and immersion time. The research results will provide durability data for glass fiber reinforced polypropylene composites used in concrete as stirrups.

摘要

玻璃纤维增强聚丙烯复合板由于其可重复模塑、较高的韧性、较高的耐久性以及与玻璃纤维增强热固性复合材料相比具有抗疲劳性,已逐渐引起更多关注。在实际工程应用中,复合板在混凝土的腐蚀环境中要承受不同角度的弯曲作用,包括0°至90°的弯筋以及90°的箍筋,这可能导致其长期性能退化。因此,评估玻璃纤维增强聚丙烯复合弯曲板在碱性环境中的长期性能很重要。在本文中,开发了一种新的弯曲装置来制备弯曲角度为60°和90°的玻璃纤维增强聚丙烯弯曲板。需要指出的是,上述两个弯曲角度分别模拟了典型的弯筋和箍筋。将板材浸泡在碱溶液环境中长达90天进行长期暴露。系统设计了力学性能(拉伸性能和剪切性能)、热性能(动态力学性能和热重分析)以及微观形态分析(表面形态分析),以评估弯曲角度和碱溶液浸泡对长期力学性能的影响机制。结果表明,弯曲作用导致纤维持续破坏,外层纤维在拉伸时断裂,内层纤维在压缩时屈曲,导致纤维 - 基体界面脱粘。碱溶液(OH离子)腐蚀玻璃纤维表面形成可溶性硅酸盐,热重分析表明玻璃纤维的质量分数从79.9%明显降至73.65%,证明了这一点。这使得与弯曲角度为0°的板材相比,拉伸强度的最高降解率分别为71.6%(60°弯曲)和65.6%(

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd23/12252126/903e498149e0/polymers-17-01844-g001.jpg

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