Abstract:The microstructure of plastic bonded explosives (PBXs) is known to influence behavior during mechanical deformation, but characterizing the microstructure can be challenging. For example, the explosive crystals and binder in formulations such as PBX 9501 do not have sufficient X-ray contrast to obtain three-dimensional data by in situ, absorption contrast imaging. To address this difficulty, we have formulated a series of PBXs using octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) crystals and low-densit… Show more
“…Crystals were paired based on similarly sized flat and parallel faces. The HTPB binder was prepared identically to the low stiffness HTPB binder described in detail in Manner et al [2]. The binder was spread onto the matched face of one crystal while the opposing crystal was placed on top.…”
Section: Experimental Methodsmentioning
confidence: 99%
“…It is known that mesoscale defects such as pores, cracks, and interfacial debonding can alter the mechanical integrity of the composite when subjected to low rate thermo-mechanical loads [1,2]. These defects contribute to heterogeneity in generation of hot spots under dynamic events [3,4].…”
Abstract. The microstructure of plastic bonded explosives (PBXs) significantly affects their macroscale mechanical characteristics. Imaging and modeling of the mesoscale constituents allows for a detailed examination of the deformation of mechanically loaded PBXs. In this study, a pair of explosive HMX crystals were bound with an HTPB based polymer binder and imaged using micro Computed Tomography (µCT). Delamination of the polymer binder from the crystals was induced via macro-scale application of a tensile load. Cohesive parameters for simulation of the crystal/binder interface were determined by comparing numerical and experimental results of the delamination of this bi-crystal system. Simulations showed macro-scale plastic behavior is accommodated through both crystal-binder delamination and plastic deformation of the binder itself. Imaging and simulation of this bi-crystal system demonstrated the complex interplay of material constitutive behavior and grain-scale geometry. Successful parameterization of this relatively simple mechanical system is a step toward a better understanding void nucleation in similarly composed polycrystalline composites.
“…Crystals were paired based on similarly sized flat and parallel faces. The HTPB binder was prepared identically to the low stiffness HTPB binder described in detail in Manner et al [2]. The binder was spread onto the matched face of one crystal while the opposing crystal was placed on top.…”
Section: Experimental Methodsmentioning
confidence: 99%
“…It is known that mesoscale defects such as pores, cracks, and interfacial debonding can alter the mechanical integrity of the composite when subjected to low rate thermo-mechanical loads [1,2]. These defects contribute to heterogeneity in generation of hot spots under dynamic events [3,4].…”
Abstract. The microstructure of plastic bonded explosives (PBXs) significantly affects their macroscale mechanical characteristics. Imaging and modeling of the mesoscale constituents allows for a detailed examination of the deformation of mechanically loaded PBXs. In this study, a pair of explosive HMX crystals were bound with an HTPB based polymer binder and imaged using micro Computed Tomography (µCT). Delamination of the polymer binder from the crystals was induced via macro-scale application of a tensile load. Cohesive parameters for simulation of the crystal/binder interface were determined by comparing numerical and experimental results of the delamination of this bi-crystal system. Simulations showed macro-scale plastic behavior is accommodated through both crystal-binder delamination and plastic deformation of the binder itself. Imaging and simulation of this bi-crystal system demonstrated the complex interplay of material constitutive behavior and grain-scale geometry. Successful parameterization of this relatively simple mechanical system is a step toward a better understanding void nucleation in similarly composed polycrystalline composites.
“…The first is serial sectioning, a destructive characterization tool that involves cropping, polishing, mounting, and optical microscopy [4][5][6][7]. The second is non-destructive X-ray computerized tomography (CT) [8][9][10][11][12][13][14]. Both methods can be costly, time intensive, and limited in resolution.…”
The generation of three-dimensional (3D) microstructures with multiple constituents is an important part of multiscale computational simulation and design for a wide range of materials including heterogeneous polycrystalline metals, ceramics, composites, and energetics. Realistic 3D microstructures for multiphase materials are difficult to obtain experimentally or computationally. Challenges include generation and representation of complex constituent morphologies, topological arrangement and distribution, defect description, and statistical conformity. Here, we present a novel technique for systematically composing complex 3D statistically equivalent microstructure sample sets (SEMSS) with prescribed statistical constituents and morphological attributes. Based on large libraries of varying representations of individual constituents, the technique can be used with experimental micro computerized tomography (CT) scans to establish SEMSS that track the attributes of existing materials as well as to design SEMSS for new materials not yet in existence for computational exploration. Heterogeneous systems involving different combinations of molecular crystallites, metallic particles, oxidizer granules, and a polymeric matrix are designed and generated to track the properties of an existing material. The corresponding SEMSS are used in multiphysics simulations accounting for coupled thermal-mechanical processes or thermal-mechanical-chemically reactive processes. The results are used to quantify microstructure-induced response variations and point out the limitations of two-dimensional (2D) microstructures that are direct sections of the full 3D microstructures. The use of the SEMSS has also enabled uncertainty quantification (UQ) and the development of probabilistic characterizations for variations in macroscopic responses due to intrinsic material microstructural heterogeneities.
“…Besides intrinsic interfacial interactions, the surface structures of the explosive component, e. g. the roughness, also plays an important role in determining the interfacial structures formed within PBXs, as does material processing techniques [6]. These interfacial structures have been studied in multiple scales, from nanometre to centimetre, by utilizing several characterization techniques [5,[14][15][16][17]. Positron annihilation lifetime spectroscopy (PALS), neutron scattering, x-ray computed tomography, and microscopy, have all been employed, though the sensitive nature of explosives and the thin, i. e. nanoscale, nature of the interface means thorough characterization remains challenging.…”
The interface between explosive and binder in plastic‐bonded explosives (PBXs) plays an important role in their properties such as thermal and mechanical stability, and also their performance in detonation processes. However, characterization of their interfacial micro‐structures remains challenging, due to the sensitive nature of the explosive material, and the extremely thin nature of the interface. This work demonstrates a concept of characterizing interfacial structures between explosives and binders by gas permeation. The N2 permeability data of composite films of cyclotetramethylene‐tetranitramine (HMX) particles dispersed in fluororubber binder (copolymers of vinylidene fluoride and chlorotrifluoro‐ethylene, F2311) were tested and fitted by using gas transport mechanism theory, e. g. the Hashemifard‐Ismail‐Matsuura (HIM) model, and the Knudsen diffusion equation. The results indicate the presence of voids of thickness 2.2 nm between HMX and F2311, consistent with the results of neutron reflection and thermal conductivity measurements. These interfacial voids are considered to be related to the surface roughness of HMX particles. This work provides an alternative characterization technique for, as well as a new insight into, the interface between HMX and F2311.
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