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工程化爆炸薄膜的微观结构和形态 界面能的控制

Engineering the Microstructure and Morphology of Explosive Films Control of Interfacial Energy.

作者信息

Forrest Eric C, Knepper Robert, Brumbach Michael T, Rodriguez Mark A, Archuleta Kim, Marquez Michael P, Tappan Alexander S

机构信息

Primary Standards Laboratory, Sandia National Laboratories, Albuquerque, New Mexico 87185, United States.

Energetic Materials Dynamic & Reactive Science, Sandia National Laboratories, Albuquerque, New Mexico 87185, United States.

出版信息

ACS Appl Mater Interfaces. 2021 Jan 13;13(1):1670-1681. doi: 10.1021/acsami.0c10193. Epub 2020 Dec 22.

Abstract

Physical vapor deposition of organic explosives enables growth of polycrystalline films with a unique microstructure and morphology compared to the bulk material. This study demonstrates the ability to control crystal orientation and porosity in pentaerythritol tetranitrate films by varying the interfacial energy between the substrate and the vapor-deposited explosive. Variation in density, porosity, surface roughness, and optical properties is achieved in the explosive film, with significant implications for initiation sensitivity and detonation performance of the explosive material. Various surface science techniques, including angle-resolved X-ray photoelectron spectroscopy and multiliquid contact angle analysis, are utilized to characterize interfacial characteristics between the substrate and explosive film. Optical microscopy and scanning electron microscopy of pentaerythritol tetranitrate surfaces and fracture cross sections illustrate the difference in morphology evolution and the microstructure achieved through surface energy modification. X-ray diffraction studies with the Tilt-A-Whirl three-dimensional pole figure rendering and texture analysis software suite reveal that high surface energy substrates result in a preferred (110) out-of-plane orientation of pentaerythritol tetranitrate crystallites and denser films. Low surface energy substrates create more randomly textured pentaerythritol tetranitrate and lead to nanoscale porosity and lower density films. This work furthers the scientific basis for interfacial engineering of polycrystalline organic explosive films through control of surface energy, enabling future study of dynamic and reactive detonative phenomena at the microscale. Results of this study also have potential applications to active pharmaceutical ingredients, stimuli-responsive polymer films, organic thin film transistors, and other areas.

摘要

与块状材料相比,有机炸药的物理气相沉积能够生长出具有独特微观结构和形态的多晶薄膜。本研究表明,通过改变基底与气相沉积炸药之间的界面能,可以控制季戊四醇四硝酸酯薄膜的晶体取向和孔隙率。炸药薄膜在密度、孔隙率、表面粗糙度和光学性质方面实现了变化,这对炸药材料的起爆敏感性和爆轰性能具有重要影响。利用各种表面科学技术,包括角分辨X射线光电子能谱和多液体接触角分析,来表征基底与炸药薄膜之间的界面特性。季戊四醇四硝酸酯表面和断裂横截面的光学显微镜和扫描电子显微镜图像说明了形态演变的差异以及通过表面能改性实现的微观结构。使用Tilt-A-Whirl三维极图绘制和织构分析软件套件进行的X射线衍射研究表明,高表面能基底会导致季戊四醇四硝酸酯微晶形成择优的(110)面外取向以及更致密的薄膜。低表面能基底会产生更随机织构的季戊四醇四硝酸酯,并导致纳米级孔隙率和低密度薄膜。这项工作通过控制表面能进一步拓展了多晶有机炸药薄膜界面工程的科学基础,为未来在微观尺度上研究动态和反应性爆轰现象提供了可能。本研究结果在活性药物成分、刺激响应聚合物薄膜、有机薄膜晶体管及其他领域也具有潜在应用价值。

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