摩擦电喷镀摩擦机理及复合镀层工艺的研究

摩擦电喷镀是一项新发明的金属表面高速电沉积技术,具有高速、优质、低耗等特点.本文利用扫描电镜、X射线衍射、X射线应力测试仪等物理测试手段,首次研究了摩擦对镍镀层组织、结构和力学性能的作用机理.此外,通过对摩擦电喷镀Ni基Al_2O_3复合镀层测试,分析了工艺因素及其对镀层质量的影响,并给出了有参考价值的优化工艺参数.     

不同分散剂对纳米SiO_2水中分散的影响

选取六偏磷酸钠(SHMP)、十二烷基苯磺酸钠(SDBS)及KCl作分散剂,并采用超声分散方法,制备纳米SiO2悬浮液,对纳米SiO2的水中分散性能进行研究。测试分散体系中纳米SiO2粒子的粒径及分布、Zeta电位及透光率,探讨了不同分散剂对纳米SiO2分散性能的影响。结果表明:不同分散剂对纳米SiO2的粒径都有明显影响,但粒径分布宽度差别较大;同在分散粒径较小的条件下,分别添加3种分散剂的悬浮液体系具有不同的稳定性,其中含SDBS的分散体系因静电和空间位阻的作用而表现出良好的分散稳定性。     

多弧离子镀CrNx涂层的工艺与摩擦磨损性能

为了改善发动机活塞环的摩擦学性能和提高其使用寿命,采用多弧离子镀技术在活塞环表面制备了不同N2含量和弧电流的CrNx硬膜,采用X射线衍射技术、扫描电子显微镜、纳米硬度仪和发动机台架试验装置,分别测试了薄膜相结构、表面形貌、纳米硬度和抗高温摩擦磨损性能。研究结果表明：当N2质量分数为45%时,薄膜纳米硬度相对较高,CrNx薄膜中主要以CrN（220）相为主;随着弧电流的增加,薄膜的表面颗粒尺寸增加,当弧电流为60A时,薄膜纳米硬度相对较高。与Cr电镀层活塞环相比,CrNx涂层活塞环具有较强的抗高温粘着磨损性能。     

微乳体系中纳米La2O3的制备

用微乳法在AEO-3、正己烷体系中制备La2O3,纳米粉体,并用X射线粉末衍射(XRD),透射电子显微镜(TEM)及激光粒度仪对制备的La2O3纳米粉体产物结构、形貌和粒径分布进行了表征.结果表明,经热处理后的La2O3产物粒子主要为六方晶形,团聚现象不明显.粉体产物的粒径主要分布于25 nm～35 nm之间,分布区间较窄,且随体系中增溶反应物含量的提高产物粒子粒径呈增大的趋势.     

InSb纳米颗粒的制备与原子力显微镜

为进一步研究半导体纳米材料的物理特性,用真空沉积的方法在SiO2基片上制备了纳米InSb颗粒膜。用原子力显微镜扫描样品表面的分析显示,纳米InSb颗粒均匀地分布在SiO2基片表面。实验结果表明通过改变镀膜时间,可以得到具有不同颗粒尺寸的InSb纳米颗粒。     

TiO_2/ACF复合光催化材料的制备及性能

用适宜载体将粉体材料固定是提高光催化材料稳定性的关键。采用溶胶-凝胶法,以钛酸丁酯为原料,选取活性炭纤维(ACF)为载体,制备了TiO2/ACF复合光催化材料。利用X射线衍射仪(XRD)、热分析仪(DSC-TG)和扫描电子显微镜(SEM)等测试技术对复合光催化材料的结构进行了表征分析。在紫外光照射下,通过对甲醛气体的光催化降解,考察了煅烧温度、煅烧时间、负载次数和负载时间等不同制备条件对复合光催化材料结构和性能的影响,结果表明:当煅烧温度为400℃,煅烧时间为2h,负载3次,负载时间为6min制备的TiO2/ACF光催化性能最佳。     

非均匀形核法制备Cu包覆纳米SiO2复合粉体

采用非均匀形核法制备了Cu包覆纳米SiO2复合颗粒,利用X射线衍射仪、扫描电镜、能谱仪及透射电镜等分析手段对复合颗粒进行了表征,并探讨了包覆结构的形成机制。结果表明:复合颗粒分散均匀,无团聚,单颗粒内包含多个分布均匀的纳米SiO2颗粒,且均被Cu包覆层隔离,纳米SiO2颗粒的分散性得到了显著改善;新制备的复合颗粒不存在氧化,在存放或者制样过程中会部分氧化为Cu2O;纳米SiO2颗粒表面Cu包覆层的形成机制主要是非均匀形核作用,包覆的结构取决于 Cu晶粒在纳米SiO2颗粒表面的沉积以及对复合颗粒的团聚控制。     

纳米铜润滑油添加剂的制备及其性能研究

采用KBH4液相还原法制备了具有面心立方结构,粒径约为40nm的纳米铜颗粒。利用环块摩擦磨损试验机考察了其作为添加剂在不同润滑油中的摩擦学性能,利用SEM、EDS等对摩擦表面进行了形貌、成分分析,探讨了纳米铜颗粒作为添加剂的作用机理。     

纳米氧化镁的合成及抗菌活性研究

以氯化镁和碳酸钠为原料,采用液相直接沉淀法制备了纳米氧化镁粉体,并研究了粉体的抗菌活性。采用X-射线衍射和透射电子显微镜对制备的纳米氧化镁粉体进行了表征。以金黄色葡萄球菌为试验菌株,对制备的纳米氧化镁粉体的杀菌性能进行了评价,结果表明:纳米氧化镁具有良好的杀菌能力,粉体质量浓度越高,粒径越小,杀菌效果越好;杀菌率随着作用时间的延长而增大,长效杀菌率可达到100%。     

氧化铝气凝胶复合材料的制备与隔热性能

以仲丁醇铝为先驱体,采用溶胶一凝胶工艺制备氧化铝溶胶,并将其与无机陶瓷纤维毡复合经超临界流体干燥得到氧化铝气凝胶隔热复合材料.利用扫描电子显微镜(SEM)和氮气吸附等方法对样品微观结构进行分析,利用热平板法对材料的隔热性能进行测试,并分析了氧化铝气凝胶隔热复合材料隔热机理.研究表明:与氧化硅气凝胶相比,氧化铝气凝胶具有更好的耐高温性能,经1000℃热处理后仍然能够较好地保持其纳米多孔结构;将气凝胶与纤维复合后,充分发挥了氧化铝气凝胶优良的隔热特性,使得复合材料的隔热性能较纯纤维毡有了明显的改善,其热面温度1000℃时导热系数为0.0685 W/m·K.     

边界润滑膜的微观分析

利用X—射线光电子能谱、扫描电镜等手段对新研制的含S、O、Mo油溶性化合物作为极压剂所形成的边界润滑膜进行了微观分析。结果表明:该极压剂的极压抗磨作用除了与极压剂在摩擦表面上分解,生成具有良好润滑性能的MoS_2、MoO_3、MoO_2等化合物有关外,还与极压剂对摩擦表面有化学抛光作用有关。     

Thermodynamics and performance of Al/CuO nanothermite with different storage time

The storage stability of energetic materials is important for its application. Here, the storage stability of Al/CuO nanothermite, which was prepared by electrospray method and stored with different storage time, was systematically researched. The activation energy of Al/CuO nanothermite was calculated by differential scanning calorimetry (DSC). The ignition temperature and the curve pressure history of Al/CuO nanothermite was measured using ignition temperature measuring device and constant-volume pressurization tests, respectively. Further, the thermites were characterized by X-ray Diffractometer (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM) and Transmission electron microscopy (TEM). The results show that the morphology of the thermites did not change significantly. The activation energy was decreased from 254.1 kJ/mol to 181.8 kJ/mol after storage for 13 months. When stored for 0, 7 and 13 months, the peak pressures of Al/CuO nanothermite were 685.8 kPa, 626.3 kPa and 625.5 kPa, respectively. In addition to the ignition temperature, it was 775 ℃, 739 ℃ and 754 ℃, respectively. This result indicated that the ignition and combustion properties of Al/CuO nano-thermite are obviously reduced when stored for a long time, at room temperature.     

新的固相反应法合成钼青铜化合物 NaxMo6O17的研究

本文介绍了一种以MoO_3和NaI 为原料,在高温、惰性气氛中通过氧化还原反应合成Na_xMo_6O_(17)化合物的新方法。进而研究了Na_xMo_6O_(17)化合物的组成分析和热分析方法。     

Scale-up synthesis and characterization of 2,6-diamino-3,5-dinitropyrazine-1-oxide

2,6-diamino-3,5-dinitropyrazine-1-oxide (ANPZO), as an insensitive high explosive, with a high yield and excellent purity has been prepared at pilot plant scale by an improved method. The synthesized ANPZO is characterized by IR, laser granularity measurement, SEM and HPLC. The particle analysis revealed that the improved method could offer desired product with average particle size of 40 μm and high purity (>98.45%). The experimental parameters exhibited that the detonation velocity of the formulation based on ANPZO was higher than that of the corresponding TATB formulation. The DSC curve showed that the exothermic decomposition of the product occurred at the temperature between 300.5 °C and 360.4 °C. Furthermore, the sensitivity test suggests its safe nature towards mechanical stimulus.     

Combustion of B4C/KNO3 binary pyrotechnic system

Presented herein is an experimental study on the combustion of B4C/KNO3 binary pyrotechnic system.Combustion products were tested using X-ray diffraction(XRD),scanning electron microscopy(SEM),and energy dispersive spectrometer(EDS).According to the results of tests and CEA calculation,the combustion reaction equation was established.The flames and burning rates were recorded by a high speed camera and a spectrophotometer.The effect of B4C particle size on the thermal sensitivity of B4C/KNO3 was investigated by differential scanning calorimetry(DSC)techniques.In addition,a reliable method for calculating the flame temperature was proposed.Based on the results of experiments,the combustion reaction mechanism was briefly analyzed.The burning rate,flame temperature and thermal sensitivity of B4C/KNC3 increase with the decrease of B4C particle size.The mass ratio of B4C/KNO3 has a great effect on combustion properties.Oxidizer-rich compositions have low flame temperatures,low burning rates,and provide green light emission.The combustion reactions of fuel-rich compositions are vigorous,and the B4C/KNO3 with mass ratio of 25:75 has the highest burning rate and the highest flame temperature.     

Effect of particle gradation of aluminum on the explosion field pressure and temperature of RDX-based explosives in vacuum and air atmosphere

To optimize the energy output and improve the energy utilization efficiency of an aluminized explosive, an explosion device was developed and used to investigate the detonation pressure and temperature of R1 (Al6) aluminum powder and the aluminum powder particle gradation of R2 (Al6+Al13), R3 (Al6+Al24) and R4 (Al6+Al flake) in a confined space. By using gas chromatography, quantitative analysis and calculations were carried out to analyze the gaseous detonation products. Finally, the reaction ratios of the aluminum powder and the explosion reaction equations were calculated. The results show that in a confined space, the quasi-static pressures and equilibrium temperature of the aluminum powder in air are higher than in vacuum. In vacuum, the quasi-static pressures and equilibrium temperatures of the samples in descending order are R1>R3>R4>R2 and R3>R4>R1>R2, respectively. In air, the quasi-static pressures and equilibrium temperatures of the samples in descending order are R1>R2>R4>R3 and R1>R4>R2>R3, respectively. R4 (Al6+Al flake) and R3 (Al6+Al24) have relatively higher temperatures after detonation, which shows that the particle gradation method can enhance the reaction energy output of aluminum during the initial reaction stage of the explosion and increase the reaction ratio by 10.6% and 8.0%, respectively. In air, the reaction ratio of Al6 aluminum powder can reach as high as 78.16%, and the reaction ratio is slightly reduced after particle gradation. Finally, the reaction equations of the explosives in vacuum and in air were calculated by quantitative analysis of the explosion products, which provides a powerful basis for the study of RDX-based explosive reactions.     

利用镁金属化学还原法制备多孔Si/Si-O-C负极材料机理研究

以二乙烯基苯和聚硅氧烷为原料经先驱体转化法制备了Si-O-C材料，利用镁金属在惰性气氛保护下高温还原制备了多孔的Si/Si-O-C负极材料。Si/Si-O-C负极材料的首次放电与充电容量分别为547.2和450.7mAh?g-1，第二次放电与充电容量分别为487.4和422.9mAh?g-1，库伦效率分别为82.3%、86.8%，材料具有较好的循环性能。利用X射线衍射(XRD)、能谱分析(EDX)、元素分析和场发射扫描电镜(FE-SEM)分析了多孔Si/Si-O-C负极材料的组成、结构、形貌，从而研究利用镁金属化学还原法制备多孔Si/Si-O-C负极材料的机理。结果表明，镁金属在还原过程中生成MgO和Mg2SiO4等产物，经HCl洗涤后可形成多孔的Si/Si-O-C负极材料。Si/Si-O-C材料中的单质硅分布于多孔的Si-O-C相中，一定程度上可缓解Si在循环过程中产生的体积效应。利用镁金属还原Si-O-C材料制备多孔Si/Si-O-C材料是一种可行的制备方法。     

烟雾干扰光学制导武器中Mie散射系数快速算法

烟雾干扰光学制导武器中烟雾中的颗粒物的浓度、平均粒径的精确测量是评价武器隐蔽效果的关键指标。Mie散射中的消光系数计算是烟雾中颗粒物的平均粒径和浓度测量中的关键步骤。在传统Mie散射计算的基础上提出一种适用不同颗粒大小和复折射率的Mie散射系数算法。推导了散射系数计算公式,分析了不同折射率和粒径的递推公式。计算表明,该方法的计算精度高、范围广、时间短,适用于干扰烟雾中生成颗粒物的平均粒径和浓度在线测量。     

Preparation of ammonium nitrate-based solid composite propellants supplemented with polyurethane/nitrocellulose blends binder and their thermal decomposition behavior

To improve the performance of solid composite propellants (SCPs) supplemented with ammonium nitrate (AN) as an oxidizer, the incorporation of energetic ingredients such as explosives, energetic binders or catalysts is a common effective approach. For this purpose, polyurethane (PU), a typical inert binder, was mixed with nitrocellulose (NC) as an energetic polymer. Numerous composite solid propellant compositions based on AN and NC-modified polyurethane binder with different NC ratios were prepared. The prepared formulations were characterized using Fourier transform infrared spectroscopy (FTIR), RAMAN spectroscopy, X-ray diffraction (XRD), electron densimetry, thermogravimetric (TG) analysis, and differential scanning calorimetry (DSC). A kinetic study was then performed using the iterative Kissinger-Akahira-Sunose (It-KAS), Flynn-Wall-Ozawa (It-FWO), and non-linear Vyazovkin integral with compensation effect (VYA/CE) methods. The theoretical performances, such as theoretical specific impulse, adiabatic flame temperature, and ideal exhaust gaseous species, were also determined using the NASA Lewis Code, Chemical Equilibrium with Application (CEA). Spectroscopic examinations revealed the existence of NC and full polymerization of PU in the prepared propellants. According to density tests, the density of the propellant increases as the nitrocellulose component increases. According to the thermal analysis and kinetics study, the increase in NC content catalyzed the thermal decomposition of the AN-based composite solid propellants. Based on the theoretical study, increasing the amount of NC in the propellant increased the specific impulse and, as a result, the overall performance.     

Liquid phase in-situ synthesis of LiF coated boron powder composite and performance study

Among practical metal additives, boron (B) has a high volumetric heating value, making it a promising choice as a fuel additive. Although B can theoretically yield a large amount of energy upon complete combustion, its combustion is retarded by the initial presence of B oxide, which coats the surfaces of B particle. To improve the ignition and combustion properties of B powder, LiOH and NH₄F were used as precursors to synthesize uniformly LiF-coated B composites (LiF-B) in situ. The LiF-B mixture was also prepared for comparison using a physical method. X-ray diffraction (XRD), Fourier-transform infrared (FTIR), scanning electron microscope (SEM), and energy-dispersive X-ray spectroscopy (EDS) were used to characterize the morphologies and compositions of the products. The thermal and combustion properties of the samples were characterized by thermal gravity-differential thermal gravity (TG-DTG), differential scanning calorimetry (DSC) and closed bomb experiment. The XRD, FTIR, SEM and EDS results demonstrated the successful preparation of the coated LiF-B sample. The TG-DTG and closed bomb experiment results indicated that the addition of LiF decreased the ignition temperature of B powder, and increasing its reaction efficiency. DSC results show that when LiF-B was added, the released heat of underwater explosive increased by 6727.2, 7280.4 and 3109.6 J/g at heating rates of 5, 10, and 15 °C/min, respectively. Moreover, LiF-B decreased the activation energy of secondary combustion reaction of explosive system as calculated through Kissinger's method by 28.9%, which indicated an excellent catalytic effect for the thermal decomposition of underwater explosive. The results reveal that LiF can improve the combustion efficiency of B powder, thereby increasing the total energy of explosives. The mechanical sensitivity increased slightly after adding LiF-B to the underwater explosive. Compared to the underwater explosive with added B, the mechanical sensitivity of the explosive with added LiF-B was significantly lower.