{"title":"Fluoro-polymer Functionalization for Enhanced Interfacial Adhesion and Mechanical Properties in Polymer Bonded Explosives","authors":"Congmei Lin, Chengcheng Zeng, Shijun Liu, Bo Jin, Zhijian Yang, Jiahui Liu, Liping Pan, Chunliang Ji, Lixiao Hao, Yushi Wen, Feiyan Gong, Jiang Li, Shaoyun Guo","doi":"10.1016/j.polymer.2025.128178","DOIUrl":null,"url":null,"abstract":"The poor interfacial adhesion between energetic crystals and polymer matrices results in undesirably low mechanical properties, limiting the application of energetic composites. Surface engineering has been widely implemented in materials science to regulate the mechanical properties. However, to achieve strong interfacial adhesion with precise control of interfacial structure is attractive and highly challenging for polymer bonded explosives. To address this issue, a covalent functionalization strategy were developed via the self-polymerization of dopamine on the surface of the energetic crystals, followed by the covalent grafting of fluoro-polymers using toluene-2,4-diisocyanate (TDI) as a bridging molecule. In-depth characterizations, combined with molecular dynamics simulation, have been systematically adopted to investigate the interfacial interaction and mechanical performance after covalent grafting of fluoro-polymers. Remarkably, both experimental results and numerical simulations revealed that the covalent functionalization and fluorine-containing binder system significantly increased the number of hydrogen bonds and interfacial interactions, thereby enhancing the interfacial adhesion between energetic crystals and the polymer matrix. Energetic composites with fluoro-polymer functionalization exhibited substantial interfacial enhancement effects. The mechanical properties of the composites improved with increasing grafted fluoro-polymer content. The composites based on energetic crystals with 2 wt% grafted fluoro-polymer exhibited optimal performance, with compressive and tensile fracture energies increased by 97.7% and 182.0%, respectively, compared to the unmodified composites. Additionally, computational simulations provided fundamental insights into how the interfacial structure affects the mechanical properties of energetic composites, confirming that the covalent functionalization and fluorine-containing binder system enhance interfacial adhesion by increasing hydrogen bond numbers and interfacial interactions.","PeriodicalId":405,"journal":{"name":"Polymer","volume":"22 1","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.polymer.2025.128178","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
The poor interfacial adhesion between energetic crystals and polymer matrices results in undesirably low mechanical properties, limiting the application of energetic composites. Surface engineering has been widely implemented in materials science to regulate the mechanical properties. However, to achieve strong interfacial adhesion with precise control of interfacial structure is attractive and highly challenging for polymer bonded explosives. To address this issue, a covalent functionalization strategy were developed via the self-polymerization of dopamine on the surface of the energetic crystals, followed by the covalent grafting of fluoro-polymers using toluene-2,4-diisocyanate (TDI) as a bridging molecule. In-depth characterizations, combined with molecular dynamics simulation, have been systematically adopted to investigate the interfacial interaction and mechanical performance after covalent grafting of fluoro-polymers. Remarkably, both experimental results and numerical simulations revealed that the covalent functionalization and fluorine-containing binder system significantly increased the number of hydrogen bonds and interfacial interactions, thereby enhancing the interfacial adhesion between energetic crystals and the polymer matrix. Energetic composites with fluoro-polymer functionalization exhibited substantial interfacial enhancement effects. The mechanical properties of the composites improved with increasing grafted fluoro-polymer content. The composites based on energetic crystals with 2 wt% grafted fluoro-polymer exhibited optimal performance, with compressive and tensile fracture energies increased by 97.7% and 182.0%, respectively, compared to the unmodified composites. Additionally, computational simulations provided fundamental insights into how the interfacial structure affects the mechanical properties of energetic composites, confirming that the covalent functionalization and fluorine-containing binder system enhance interfacial adhesion by increasing hydrogen bond numbers and interfacial interactions.
期刊介绍:
Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics.
The main scope is covered but not limited to the following core areas:
Polymer Materials
Nanocomposites and hybrid nanomaterials
Polymer blends, films, fibres, networks and porous materials
Physical Characterization
Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films
Polymer Engineering
Advanced multiscale processing methods
Polymer Synthesis, Modification and Self-assembly
Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization
Technological Applications
Polymers for energy generation and storage
Polymer membranes for separation technology
Polymers for opto- and microelectronics.