Fe颗粒增强Al/PTFE反应材料的力学性能、冲击反应特性及能量释放效应

铝/聚四氟乙烯(Al/PTFE)复合材料是一种非常有前景的反应结构材料。为了提高材料的力学性能和反应性,将Fe颗粒加入Al/PTFE反应材料中。对Al/PTFE/Fe反应材料进行准静态和动态压缩试验,观察到明显的应变和应变率硬化现象,且当Fe含量为30%(质量分数)时,在5000 s^(-1)的应变率下,抗压强度达191.8 MPa,较Al/PTFE提升了39%。定向的PTFE纳米纤维丝能有效地阻碍裂纹的扩展。通过高速摄影对霍普金森杆和落锤冲击下的能量释放进程进行观察,且通过新设计的装置对反应活性进行定量表征。结合TG-DSC和XRD,明确了Al/PTFE和Al/Fe之间的反应。通过霍普金森杆的实验数据建立Johnson-Cook本构模型,模型结果与实验数据吻合较好。在冲击状况下,材料的反应性是多重行为的结果。

Premature thermal decomposition behavior of 3,4-dinitrofurazanfuroxan with certain types of nitrogen-rich compounds

3,4-Dinitrofurazanfuroxan(DNTF),as a high-energy-density material,features good thermal stability and wide applications.This study aimed to elucidate the thermal decomposition mechanism of DNTF combined with nitrogen-rich compounds containing N-H.The thermal stabilities of DNTF and its hybrid systems were investigated using differential thermal analysis/thermogravimetry(TG),vacuum stability test,and accelerating rate calorimetry under isothermal,non-isothermal,and adiabatic conditions,respectively.Results showed that the thermal stability and thermal safety of DNTF significantly decreased after combining with nitrogen-rich compounds containing N-H.Calculation results showed that the activation energy of the DNTF hybrid systems was significantly lower than that of DNTF.The TGIR was used to monitor the generation of fugitive gases during the thermal decomposition of the DNTF/5-aminotetrazole(5-ATZ)hybrid.Moreover,the nitrogen-rich molecules containing N-H interacted extensively with DNTF,and this interaction accelerated the thermal degradation of DNTF.

Synthesis,crystallographic characterization,and potential application of fullerene anisole derivatives as nitrocellulose stabilizer

A series of fullerene anisole derivative stabilizers was synthesized by nucleophilic substitution reaction using hexachlorofullerene and benzyl alcohol as raw materials to extend the service duration of nitrocellulose(NC)-based propellants.Single-crystal X-ray diffraction,nuclear magnetic resonance,highresolution mass spectrometry,Fourier transform infrared(FT-IR)spectroscopy,and UV-Vis spectroscopy were used to characterize the structures of the synthesized fullerene anisole derivative stabilizers.Methyl violet,differential scanning calorimetry test,isothermal weight loss,vacuum stability test,and adiabatic accelerated test were used to study their compatibility with NC and their ability to stabilize NC.The results show that the designed and synthesized novel fullerene anisole derivative stabilizer has good compatibility with NC,and their overall stabilizing effects on NC are better than those of the traditional stabilizers,diphenylamine(DPA),and N,N’-dimethyl-N,N’-diphenylurea(C2).The stabilizing effects was ranked as:3b>2d>2a>2c>C2>2b>DPA>NC.In addition,FT-IR analysis and electron spin resonance spectroscopy were applied to explore the stability mechanism of fullerene-based stabilizers to NC.The results reveal that the new fullerene stabilizer can adsorb and effectively eliminate the nitrogen oxide free radicals generated by NC degradation;therefore,it can forbid the autocatalytic degradation of NC and stabilize NC.

Preparation and characterization of HMX/NH_(2)-GO composite with enhanced thermal safety and desensitization

To improve the safety of HMX,HMX/NH_(2)-GO composite was prepared with aqueous ammonia functionalized graphene oxide(NH_(2)-GO).The composite was characterized by SEM,Zeta potential,XPS,Raman spectrum,XRD,HPLC,DSC and BAM sensitivity test.The results indicated that the functionalization with aqueous ammonia can enhance the interaction between GO and HMX,and more efficiently desensitize the explosive.The optimal impact sensitivity of the HMX/NH_(2)-GO composite can be not less than 40 J,which is also the most insensitivity compared to the previous reports prepared by coating desensitization with non-energetic desensitized material.Moreover,the potential reason for the different impact and friction sensitivity was also discussed,which may bring a novel perspective to achieve the desensitization of energetic material.

Fullerene bisadduct stabilizers:The effect of different addition positions on inhibiting the autocatalytic decomposition of nitrocellulose absorbed nitroglycerin

To explore the effect of different positions and number of pyrrolidine bound to the carbon cage on the stabilization effect of fulleropyrrolidine derivatives to nitrocellulose(NC)/nitroglycerine(NG),we synthesized N-(4-methoxy)phenylpyrrolidine-C_(60) and four different of bis(N-(4-methoxy)phenylpyrrolidine)-C_(60) compounds through Prato reaction.Their structures were characterized by UVevis,^(1)H NMR,^(13)C NMR,high-resolution mass spectroscopy,and single-crystal X-ray diffraction.Their stabilization effect to NC/NG were investigated using differential scanning calorimetry,methyl violet,vacuum stabilization effect,weight loss,and accelerating rate calorimeter tests.The results indicated these compounds had excellent stabilization effect to NC/NG.The stabilization effect of the fulleropyrrolidine bisadducts to NC/NG is significantly better than that of fulleropyrrolidine monoadduct and C_(60).Moreover,the position where pyrrolidine binds to fullerene in fulleropyrrolidine bisadducts is different,and its stabilization effect to NC is also different.The stabilization effect order of different bisadduct isomers to nitrocellulose is as follows:e-edge>trans-2>cis-2>trans-3.Electron paramagnetic resonance(EPR)and FT-IR were used to study the stabilization mechanism of fulleropyrrolidine derivatives to NC/NG.The EPR results also show that fulleropyrrolidine bisadducts with different addition sites have different abilities to absorb nitroxide,and their ability is better than that of the monoadduct and C_(60),which is consistent with the results of stabilization effect performance test.

[0001]-Oriented InN Nanoleaves and Nanowires: Synthesis,Growth Mechanism and Optical Properties

Novel indium nitride （INN） leaf-like nanosheets and nanowires have been grown on Si substrate by chemical vapor deposition method. The characterization results indicate that the samples are single-crystalline, and the growth direction of the nanowires and nanoleaves is [0001]. The growth mechanism of the InN nanoleaves is following the pattern of vapor-liquid-solid process with a three-step growth process. In addition, the room temperature photoluminescence spectra of two nanostructures show band-to-band emissions around 0.706 eV, where the emission from single nanoleaf is stronger than nanowire, showing potential for applications in optoelectronic devices.