scholarly journals Efficient Preparation and Performance Characterization of the HMX/F2602 Microspheres by One-Step Granulation Process

2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Conghua Hou ◽  
Xinlei Jia ◽  
Jingyu Wang ◽  
Yingxin Tan ◽  
Yuanping Zhang ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Thermal Stability ◽  
Particle Size ◽  
Particle Morphology ◽  
Xrd Analysis ◽  
Impact Sensitivity ◽  
Scanning Calorimetry ◽  
Granulation Process ◽  
One Step ◽  
The Impact

A new one-step granulation process for preparing high melting explosive- (HMX-) based PBX was developed. HMX/F2602 microspheres were successfully prepared by using HMX and F2602 as the main explosive and binder, respectively. The particle morphology, particle size, crystal structure, thermal stability, and impact sensitivity of the as-prepared HMX/F2602 microspheres were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), laser particle size analyzer, differential scanning calorimetry (DSC), and impact sensitivity test, respectively. The SEM analysis indicated successful coating of F2602 on the surface of HMX, and the resulting particles are ellipsoidal or spherical with a median particle size of 940 nm; the XRD analysis did not show any change in the crystal structure after the coating and still has β-HNX crystal structure; according to the DSC analysis, HMX/F2602 prepared by the new method has better thermal stability compared to that prepared by the water suspension process. The impact sensitivity of HMX/F2602 prepared by this one-step granulation process decreased, and its characteristic height H50 increased from 37.62 to 40.13 cm, thus significantly improving the safety performance. More importantly, this method does not need the freeze-drying process after recrystallization, thus increasing the efficiency by 2 to 3 times.

Analysis of the Samples of Fe-Cu-Nb-Si-B Amorphous Alloys Obtained by Dynamic Compacting Method

2005 ◽  
Vol 903 ◽  
Author(s):  
Victor A. Golubev ◽  
Andrey V. Strikanov ◽  
Grigory A. Potemkin ◽  
Ludmila V. Zueva ◽  
Aleksey V. Golubev ◽  
...  
Keyword(s):  
Shock Wave ◽  
Amorphous Alloys ◽  
Analysis Data ◽  
Xrd Analysis ◽  
Soft Magnetic ◽  
Scanning Calorimetry ◽  
Soft Magnetic Alloys ◽  
Nano Crystalline ◽  
The Impact ◽  
Magnetic Conductivity

AbstractThe Dynamic Compacting (DC) method is promising method to produce considerable-size nonporous wares. The phenomenon is based on the impact of shock wave on the initial powders of amorphous alloys. Every time when the shock wave propagates through the bulk of substance then the temperature rises substantially. Therefore there is a need of study of the DC’s effect on the structure and properties of the amorphous alloys. The results of the thermal analysis (in particular, Differential Scanning Calorimetry) of the samples of the soft magnetic alloys are presented in the report. These results concern with amorphous alloys of 5BDSR, GM414, 10NSR trademarks before DC and after DC, respectively. It is shown there is single low-temperature endothermic peak (near 300C) and there are several high temperature exothermic peaks (near 540C, 650C, and 700C). The first peak is related to glass-transition, the following peaks are related to formation of nano-crystalline phases. It was proved by XRD analysis data. The optimal regimes of the thermal processing of final wares were chosen on the base of thermal- and XRD-analysis. The study of the effects of these regimes on the properties (magnetic conductivity, specific losses etc.) of the circular magnetic conductors was executed. In particular, thermal- as well as thermo-magnetic processing of magnetic conductors based on 5BDSR amorphous alloy (after DC) essentially improves their magnetic properties. For example, magnetic conductivity fÝ increases approximately by factor 17 with respect to the magnitude before DC.

scholarly journals Green Preparation, Spheroidal, and Superior Property of Nano-1,3,5,7-Tetranittro-1,3,5,7-Tetrazocane

2018 ◽  
Vol 2018 ◽  
pp. 1-8 ◽  
Author(s):  
Xinlei Jia ◽  
Jingyu Wang ◽  
Conghua Hou ◽  
Yingxin Tan
Keyword(s):  
Activation Energy ◽  
Particle Size ◽  
Fractal Dimension ◽  
Particle Size Distribution ◽  
Size Distribution ◽  
Fractal Theory ◽  
Crystal Form ◽  
Decomposition Temperature ◽  
Scanning Calorimetry ◽  
The Impact

Herein, a green process for preparing nano-HMX, mechanical demulsification shearing (MDS) technology, was developed. Nano-HMX was successfully fabricated via MDS technology without using any chemical reagents, and the fabrication mechanism was proposed. Based on the “fractal theory,” the optimal shearing time for mechanical emulsification was deduced by calculating the fractal dimension of the particle size distribution. The as-prepared nano-HMX was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). And the impact sensitivities of HMX particles were contrastively investigated. The raw HMX had a lower fractal dimension of 1.9273. The ideal shearing time was 7 h. The resultant nano-HMX possessed a particle size distribution ranging from 203.3 nm to 509.1 nm as compared to raw HMX. Nano-HMX particles were dense spherical, maintaining β-HMX crystal form. In addition, they had much lower impact sensitivity. However, the apparent activation energy as well as thermal decomposition temperature of nano-HMX particles was decreased, attributing to the reduced probability for hotspot generation. Especially when the shearing time was 7 h, the activation energy was markedly decreased.

scholarly journals Preparation and Characterization of Spherical Submicron CL-20 by Siphon Spray Refinement

2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
Author(s):  
Jiangtao Xing ◽  
Weili Wang ◽  
Wenzheng Xu ◽  
Tianle Yao ◽  
Jun Dong ◽  
...  
Keyword(s):  
Impact Sensitivity ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Crystal Forms ◽  
Refined Method ◽  
Diffraction Angle ◽  
Ultrasonic Assisted ◽  
The Impact ◽  
Thermal Stability Of

In order to improve the safety of hexanitrohexaazaisowurtzitane (CL-20), submicron CL-20 particles were prepared by a siphon ultrasonic-assisted spray refining experimental device. The samples were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and differential scanning calorimetry (DSC), and the impact sensitivity of the samples was tested. The results show that the particle size of siphon-refined CL-20 is about 800 nm~1 μm, which is more smooth, mellow, and dense than that of CL-20 prepared by a traditional pressure-refined method. The peak diffraction angle of pressure- and siphon-refined CL-20 is basically the same as that of raw CL-20, and their crystal forms are ε type. The peak strength of pressure- and siphon-refined CL-20 decreased obviously. The apparent activation energy of pressure-refined CL-20 and siphon-refined CL-20 is 13.3 kJ/mol and 11.95 kJ/mol higher than that of raw CL-20, respectively. The thermal stability of CL-20 is improved. The activation enthalpy (ΔH#) is significantly higher than that of raw CL-20, and the characteristic drop is 70.4% and 82.7% higher than that of raw CL-20. The impact sensitivity of siphon-refined CL-20 is lower than that of pressure-refined CL-20, so the safety performance of an explosive is improved obviously.

scholarly journals One-Step Synthesis of Spherical γ-Fe2O3 Nanopowders and the Evaluation of Their Photocatalytic Activity for Orange I Degradation

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Chunhua Liang ◽  
Hui Liu ◽  
Jianmin Zhou ◽  
Xiaochun Peng ◽  
Haizhou Zhang
Keyword(s):  
Particle Size ◽  
Reaction Time ◽  
Synthesis Method ◽  
Total Pore Volume ◽  
Xrd Analysis ◽  
Bet Surface Area ◽  
Particle Sizes ◽  
Aqueous Synthesis ◽  
One Step ◽  
The One

Maghemite (γ-Fe2O3) nanopowders were synthesized under aeration (oxidizing) conditions by aqueous synthesis in this study. The microstructures of the prepared powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and BET-BJH. The XRD analysis and the chemical experiments showed that well-crystallized γ-Fe2O3 nanoparticles were successfully obtained with a mean particle size of approximately 17 nm. The prepared γ-Fe2O3 was spherical with a BET surface area of 14.357 m2/g and a total pore volume of 0.050 cm3/g. Varying the reaction conditions, such as pH, temperature, and reaction time, we obtained crystallized γ-Fe2O3 powders with different crystallization extent and different particle sizes. When the pH of the reaction suspension was increased, the reaction time was prolonged, and the reaction temperature was increased, the γ-Fe2O3 powders underwent superior crystallization and had larger particle sizes. All the obtained γ-Fe2O3 powders had significant photocatalytic activities under both UV and visible light irradiation for Orange I degradation, and the powders with better crystallization and larger particle size had relatively lower activities for Orange I photocatalytic degradation. The one-step aqueous synthesis method presented in this paper may provide an advantageous pathway to synthesize large quantities of this important iron oxide.

scholarly journals Continuous-Flow Synthesis of Thermochromic M-Phase VO2 Particles via Rapid One-Step Hydrothermal Reaction: Effect of Mixers

2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Xiaojie Yan ◽  
William Trevillyan ◽  
Ioannina Castano ◽  
Yugang Sun ◽  
Ralph Muehleisen ◽  
...  
Keyword(s):  
Continuous Flow ◽  
Hydrothermal Reaction ◽  
Xrd Analysis ◽  
Single Step ◽  
Hot Water ◽  
Scanning Calorimetry ◽  
Smart Windows ◽  
M Phase ◽  
One Step ◽  
Resident Time

VO2 particles are promising materials for thermochromic smart windows that reduce building energy loss. Continuous-flow hydrothermal processes showcase advantages for synthesizing VO2 particles compared with traditional batch reaction systems. Mixers play a crucial role in particle fabrication in continuous-flow systems. In this study, a Center T-Mixer and a Collision Cross-Mixer are developed and implemented in a hot water fluidized suspension reaction (HWFSR) system. The influence of the resident time on the particle phase and size was evaluated, and properties of particles derived from systems equipped with differing mixers were compared. The resulting particles were characterized using techniques of X-ray powder diffraction (XRD) analysis, scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). When compared with the Center T-Mixer, results indicate that the Collision Cross-Mixer has better control regarding the morphology and size distribution of resulting particles while improving the transition temperatures of the as-synthesized materials. HWFSR systems containing novel mixer designs are capable of producing pure M-phase VO2 particles in a single step contrary to the current reactor design that use a second postheat treatment step, and they are capable of synthesizing many other nanoparticle species, especially those requiring high temperature and pressure reaction conditions.

Solidification and Boride Characteristics of Boron-Containing Austenitic Stainless Steel

2011 ◽  
Vol 704-705 ◽  
pp. 563-568 ◽  
Author(s):  
Ming Jia Wang ◽  
Er Bao ◽  
Zi Xi Wang ◽  
Shang Yi Zhang ◽  
Chu Chen ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Differential Scanning Calorimetry ◽  
Stainless Steel ◽  
Austenitic Stainless Steel ◽  
Elemental Composition ◽  
Stainless Steels ◽  
Boron Content ◽  
Austenitic Stainless Steels ◽  
Xrd Analysis ◽  
Scanning Calorimetry

Differential scanning calorimetry was used to study melt and solidification and microstructure of austenitic stainless steels containing boron. The liquidus and solidus temperatures decreased because of the boron content, and boron inhibited the formation of δ-Fe. A large content of eutectic boride structure was detected when the boron content was higher. The boride was M2B, and the crystal structure was orthorhombic. The crystal structure and elemental composition of M2B were investigated in detail by SEM-EDS and XRD analysis.

Comparative theoretical studies of dinitromethyl- or trinitromethyl-modified derivatives of CL-20

2013 ◽  
Vol 91 (12) ◽  
pp. 1243-1251 ◽  
Author(s):  
Yong Pan ◽  
Weihua Zhu ◽  
Heming Xiao
Keyword(s):  
Thermal Stability ◽  
Density Functional ◽  
Parent Compound ◽  
Initial Step ◽  
Impact Sensitivity ◽  
Detonation Properties ◽  
Energetic Properties ◽  
The Stability ◽  
The Impact ◽  
Trinitromethyl Group

The heats of formation (HOFs), energetic properties, strain energies, thermal stability, and impact sensitivity for a series of trinitromethyl- or dinitromethyl-modified CL-20 derivatives were studied by using density functional theory. It is found that the trinitromethyl group is an effective structural unit for improving the gas-phase HOFs and energetic properties of the derivatives. However, incorporating the dinitromethyl group into the parent compound is not favorable for increasing its HOFs and detonation properties. The effects of the dinitromethyl or trinitromethyl groups on the stability of the parent compound are discussed. The studies on strain energies show that the introduction of the trinitromethyl group intensifies the strain of the cage skeleton for the title compounds, whereas for the dinitromethyl groups, the case is quite the contrary. An analysis of the bond dissociation energies for several relatively weak bonds suggests that the substitution of the dinitromethyl or trinitromethyl group decreases the thermal stability of the derivatives. The C−NO2 bond in the dinitromethyl or trinitromethyl group is the weakest one and the homolysis of the C−NO2 bond may be the initial step in thermal decomposition. In addition, according to the calculated free space per molecule, the introduction of the dinitromethyl or trinitromethyl group increases the impact sensitivities of the derivatives. Considering the detonation performance, thermal stability, and impact sensitivity, six compounds can be regarded as the target high-energetic compounds.

scholarly journals Preparation and Characterization of TATB/VitonA Nanocomposites

2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Wenzheng Xu ◽  
Zhaoying Pang ◽  
Jingyu Wang ◽  
Chao Ping ◽  
Jie Wang ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Particle Size ◽  
Energetic Materials ◽  
Raw Materials ◽  
Sustainable Use ◽  
Impact Sensitivity ◽  
Dynamics Simulation ◽  
Spray Method ◽  
Particle Size Analyzer ◽  
Ultrasonic Assisted

Nano-TATB particles were prepared by an ultrasonic-assisted spray method. Molecular dynamics simulation was used to select the best binder—VitonA. Then, using VitonA as a binder, TATB/VitonA nanocomposites were prepared by a compressed air spray evaporation method and the formation mechanism of TATB/VitonA nanocomposites was proposed. Meanwhile, the crystal morphology, particle size, crystal structure, thermal decomposition properties, and impact sensitivity properties of the raw materials of TATB, the prepared nano-TATB particles, and the TATB/VitonA nanocomposites were characterized by a scanning electron microscope (SEM), laser particle size analyzer (LPSA), X-ray diffractometer (XRD), differential scanning calorimeter (DSC), and impact sensitivity instrument. The detonation performances of TATB/VitonA were calculated by the EXPLO5 program. The results indicated that the size of TATB/VitonA nanocomposites was 0.5–1 μm. The results also indicated that TATB/VitonA nanocomposites were composed of many nano-TATB particles (40–60 nm). The crystal structure of TATB/VitonA nanoparticles was not changed. The activation energy of TATB/VitonA nanocomposites was higher than nano-TATB particles by 42.62 kJ·mol−1, and the characteristic drop of the proportion of TATB/VitonA nanocomposites was higher than nano-TATB particles by 13.8 cm. The thermal stability of TATB/VitonA nanocomposites was higher, while their mechanical sensitivities were lower, which showed potential for sustainable use in the field of energetic materials.

scholarly journals Organic Salts of p-Coumaric Acid and Trans-Ferulic Acid with Aminopicolines

Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 751
Author(s):  
Sosthene Nyomba Kamanda ◽  
Ayesha Jacobs
Keyword(s):  
Crystal Structure ◽  
Thermal Stability ◽  
Differential Scanning Calorimetry ◽  
Fourier Transform ◽  
Ferulic Acid ◽  
Hirshfeld Surface ◽  
Coumaric Acid ◽  
Scanning Calorimetry ◽  
Organic Salts ◽  
Thermal Stability Of

p-Coumaric acid (pCA) and trans-ferulic acid (TFA) were co-crystallised with 2-amino-4-picoline (2A4MP) and 2-amino-6-picoline (2A6MP) producing organic salts of (pCA−)(2A4MP+) (1), (pCA̶ )(2A6MP+) (2) and (TFA̶ )(2A4MP+)·( 3 2 H2O) (3). For salt 3, water was included in the crystal structure fulfilling a bridging role. pCA formed a 1:1 salt with 2A4MP (Z’ = 1) and a 4:4 salt with 2A6MP (Z’ = 4). The thermal stability of the salts was determined using differential scanning calorimetry (DSC). Salt 2 had the highest thermal stability followed by salt 1 and salt 3. The salts were also characterised using Fourier transform infrared (FTIR) spectroscopy. Hirshfeld surface analysis was used to study the different intermolecular interactions in the three salts. Solvent-assisted grinding was also investigated in attempts to reproduce the salts.

scholarly journals Effect of polyaniline content and protonating dopants on electroconductive composites

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Katarzyna Bednarczyk ◽  
Wiktor Matysiak ◽  
Tomasz Tański ◽  
Henryk Janeczek ◽  
Ewa Schab-Balcerzak ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Morphological Properties ◽  
Electrospun Fibers ◽  
Thermal And Mechanical Properties ◽  
Visible Spectroscopy ◽  
Scanning Calorimetry ◽  
Good Thermal Stability ◽  
Uv Visible ◽  
The Impact ◽  
Scanning Electron

AbstractElastic constructive elements prepared by electrospinning using polyacrylonitrile/polyaniline (PAN/PANI) electroconductive composites were prepared and investigated in terms of their thermal and mechanical properties. This study was focused on the impact of the type of counterion of polyaniline and the PANI content in composites on the thermal, conductive and morphological properties of electrospun fibers. In this study, composites obtained from PANI doped with sulfuric acid showed the highest conductivity, and composites obtained from PANI doped with hydrochloric acid showed the highest thermal stability. All obtained composites exhibited good thermal stability, with T5 values in the range of 230–268 °C that increased with increasing PANI content. The prepared composites exhibited comparable PAN Tg values, which indicates their suitability for processing. Instrumental analysis of polymers and composites was carried out using UV–visible spectroscopy, thermogravimetric analysis, differential scanning calorimetry, dynamic mechanical thermal analysis and scanning electron microscopy.

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