纳米颗粒
分子动力学
聚合物
碳纳米颗粒
碳纤维
曲面(拓扑)
化学工程
材料科学
动力学(音乐)
纳米技术
化学
计算化学
复合材料
复合数
物理
几何学
工程类
数学
声学
作者
Kaixuan Zhang,Dongshuai Hou,Shaochun Li,Muhan Wang
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-03-27
卷期号:41 (13): 8975-8984
被引量:4
标识
DOI:10.1021/acs.langmuir.5c00346
摘要
Polymer concrete (PC) has attracted considerable interest for its excellent deformation resistance and durability. However, the mechanical drawbacks of polymers, particularly their limited compressive strength, constrain the wider application and design flexibility of PC. While experimental techniques such as X-ray diffraction and scanning electron microscopy provide insights into nanoparticle interactions within the polymer matrix, they lack the resolution to fully elucidate nanoscale mechanisms. To bridge this gap, this study utilizes molecular dynamics (MD) simulations to analyze the shearing behavior of carbon nanoparticle (CNP)-reinforced PC composites. MD simulations allow for atomic-level insights into the interactions between CNPs and the polymer matrix, providing a more detailed understanding of how surface-modified CNPs enhance mechanical properties. Our results show that surface-modified CNPs influence the distribution and conformation of epoxy within the PC system. Amino-functionalized CNPs strengthen the epoxy and calcium silicate hydrate (C-S-H) interface by facilitating calcium-oxygen bond formation. These interactions play a crucial role in improving the mechanical properties of PC. This study provides a fundamental understanding of how surface-modified CNPs reinforce PC and offers valuable insights for optimizing the performance of CNP-reinforced cementitious composites.
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