The Molecular & Crystal Structures of Polycyclic Energetic Materials

1992 ◽  
Vol 296 ◽  
Author(s):  
Richard Gilardi

AbstractEven before the ‘Buckey-ball’ (or fullerene) era, organic chemists were interested in, and attracted to, the synthesis of compounds containing many rings fused together - especially the symmetric ones. By virtue of their balanced linkages, such compounds may be kinetically stable despite inclusion of massive deviations from normal bond distances and angles. These distortions, in compounds such as cubanes, tetrahedranes, dodecahedranes and prismanes, comprise a storehouse of chemical potential energy known to the chemist as ‘strain energy’ (unrelated to overall crystal strain discussed in many materials studies).Besides the obvious benefit of including more potential energy in an energetic material, the arrangement of atoms in ring assemblies (rather than chains) leads to a material with a high intrinsic crystal density - a sine qua non for an explosive or propellant. It has long been recognized that the next generation of energetics - better in performance and/or safety - will contain many polycyclic compounds. Hundreds of model compounds were synthesized in the last decade, and their molecular structures identified or verified at the Naval Research Lab. Some of the most promising, beautiful, and unusual ones, including many energetic cubanes, will be discussed.

2021 ◽  
Vol 45 (38) ◽  
pp. 18059-18064
Author(s):  
Dongxu Chen ◽  
Jiangshan Zhao ◽  
Hongwei Yang ◽  
Hao Gu ◽  
Guangbin Cheng

Introduction of the acylamino group into energetic material compounds will contribute to balancing the sensitivity and the energy.


2017 ◽  
Vol 5 (28) ◽  
pp. 14604-14610 ◽  
Author(s):  
Yaqian Zhang ◽  
Haoyang Jiang ◽  
Feibo Li ◽  
Yanhong Xia ◽  
Yu Lei ◽  
...  

Hygroresponsive biomimetic actuators that convert chemical potential energy contained within the humidity gradient into mechanical deformation are of particular significance for realizing a sustainable society.


Author(s):  
Lothar Schäfer ◽  
John D. Ewbank

The tacit assumption underlying all science is that, of two competing theories, the one in closer agreement with experiment is the better one. In structural chemistry the same principle applies but, when calculated and experimental structures are compared, closer is not necessarily better. Structures from ab initio calculations, specifically, must not be the same as the experimental counterparts the way they are observed. This is so because ab initio geometries refer to nonexistent, vibrationless states at the minimum of potential energy, whereas structural observables represent specifically defined averages over distributions of vibrational states. In general, if one wants to make meaningful comparisons between calculated and experimental molecular structures, one must take recourse of statistical formalisms to describe the effects of vibration on the observed parameters. Among the parameters of interest to structural chemists, internuclear distances are especially important because other variables, such as bond angles, dihedral angles, and even crystal spacings, can be readily derived from them. However, how a rigid torsional angle derived from an ab initio calculation compares with the corresponding experimental value in a molecule subject to vibrational anharmonicity, is not so easy to determine. The same holds for the lattice parameters of a molecule in a dynamical crystal, and their temperature dependence as a function of the molecular potential energy surface. In contrast, vibrational effects are readily defined and best described for internuclear distances, bonded and non-bonded ones. In general, all observed internuclear distances are vibrationally averaged parameters. Due to anharmonicity, the average values will change from one vibrational state to the next and, in a molecular ensemble distributed over several states, they are temperature dependent. All these aspects dictate the need to make statistical definitions of various conceivable, different averages, or structure types. In addition, since the two main tools for quantitative structure determination in the vapor phase—gas electron diffraction and microwave spectroscopy—interact with molecular ensembles in different ways, certain operational definitions are also needed for a precise understanding of experimental structures. To illustrate how the operations of an experimental technique affect the nature of its observables, gas electron diffraction shall be used as an example.


2020 ◽  
Vol 22 (43) ◽  
pp. 25284-25296
Author(s):  
Maija M. Kuklja ◽  
Roman Tsyshevsky ◽  
Anton S. Zverev ◽  
Anatoly Mitrofanov ◽  
Natalya Ilyakova ◽  
...  

Photo-stimulated chemical reactions in energetic materials can be highly controlled by selectively designing energetic material – metal oxide interfaces with tailored properties.


Author(s):  
Dawei Sun ◽  
S. Ravi Annapragada ◽  
Suresh V. Garimella ◽  
Sanjeev Sing

This paper investigates the problem of base separation in the casting of energetic materials in a projectile. Special challenges that arise in casting high Prandtl number energetic materials in projectiles of complex geometries are addressed. A comprehensive numerical model is developed by integrating finite volume and finite element methods to analyze the thermal and flow fields as well as the residual stresses. The predictions, which are confirmed by experimental measurements, suggest that sustenance of a linear temperature profile along the projectile axis can eliminate base separation, and also reduce residual stresses in the final casting.


2003 ◽  
Vol 800 ◽  
Author(s):  
Alexander E. Gash ◽  
Joe H. Satcher ◽  
Randall L. Simpson ◽  
Brady J. Clapsaddle

AbstractThe utilization of sol-gel chemical methodology to prepare nanostructured energetic materials as well as the concepts of nanoenergetics is described. The preparation and characterization of two totally different compositions is detailed. In one example, nanostructured aerogel and xerogel composites of sol-gel iron (III) oxide and ultra fine grained aluminum (UFG Al) are prepared, characterized, and compared to a conventional micron-sized Fe2O3/Al thermite. The exquisite degree of mixing and intimate nanostructuring of this material is illustrated using transmission and scanning electron microscopies (TEM and SEM). The nanocomposite material has markedly different energy release (burn rate) and thermal properties compared to the conventional composite, results of which will be discussed. Small-scale safety characterization was performed on the nanostructured thermite. The second nanostructured energetic material consists of a nanostructured hydrocarbon resin fuel network with fine ammonium perchlorate (NH4ClO4) oxidizer present.


2012 ◽  
Vol 184-185 ◽  
pp. 1408-1417
Author(s):  
Ying Hui Shao ◽  
Zi Ru Liu ◽  
Xiao Ning Ren ◽  
Shu Yun Heng ◽  
Pu Yue ◽  
...  

The kinetic parameters of thermal explosion tests with five-second delay for 273 energetic materials were analyzed. The compensation effect exists between the two thermal explosion kinetic parameters of these energetic materials, e.g. lnA and Eb. The kinetic parameters of these energetic materials can be expressed by a single linear regression equation for the single compound or mixture under all conditions. The slopes of the regression equation for various systems are in the range from 0.1952 to 0.2413 (mol•kJ-1). The regression equation for single compound or mixture with one type of energetic material as main component has better linearity. Therefore, their “iso-kinetic temperature” Tik is close to their thermal explosion temperature Tb and the “iso-kinetic delay period”τik is also close to the 5 seconds.


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