敏感工作气体对射流陀螺灵敏度的影响

研究了干燥空气、N2和He等3种常用敏感工作气体对射流陀螺灵敏度的影响。采用有限元法计算了输入角速度ωi=20(°)/s时敏感元件内的流场。计算结果和实验表明,改变敏感元件内敏感工作气体的种类,流场分布也随之变化。ωi=20(°)/s时,两热电阻丝r1、r2处的气流速度差ΔvN2>ΔvAIR>ΔvHe。灵敏度系数KN2>KAIR>KHe,其中KN2=1.05 KAIR,KHe=0.21%KAIR。N2对应的灵敏度最高,热电阻丝抗氧化,稳定性较好,但成本高;干燥空气的灵敏度次之,热电阻丝易氧化,稳定性差;He对应的灵敏度最小,热电阻丝不易氧化,稳定性最好。该文解释了敏感工作气体对射流陀螺灵敏度的影响机理,为提高射流陀螺的实用性,满足不同工程需要开辟了一个新的途径。     

一种新型SAW气体传感器的设计

提出了将纳米线技术与声表面波(SAW)技术相结合,分别利用纳米线气体敏感材料比表面积高,声表面波传感器质量敏感性高的优点,探索研制新一代声表面波气体传感器。该传感器具有响应速度快,灵敏度高,体积小,质量注和易集成等优点。该文主要从SAW专用芯片的研制、专用纳米线研制、专用纳米线的表面修饰与改性研究、检测电路设计等4方面进行了阐述。理论计算表明,相比传统二维结构的SAW气体传感器,三维纳米线结构的SAW气体传感器的在灵敏度和响应速度上都得到提高。     

A市PTN承载LTE网络优化演进策略

本文借中国移动推行TD-LTE网络建设的契机,以A城市为案例,着重介绍了PTN承载LTE网络的演进方案.     

自适应阵列抗干扰性能的解析定量分析

自适应阵列抗干扰性能常用输出信干噪比(Signal-to-Interference and Noise Ratio,SINR)损失、抗干扰改善因子(ECCM Improvement Factor,EIF)等来衡量,但目前尚缺乏解析的定量分析.为此,采用归纳法理论推导了均匀线阵条件下输出SINR损失、EIF等指标的解析表达式,定量获取了自适应阵列抗干扰性能.仿真实验验证了理论分析结果的有效性及快拍数对自适应阵列抗干扰性能的影响.     

Synthesis of Stimuli-responsive Nanoparticles by Solution Polymerization

In this study, stimuli-responsive nanoparticles were prepared by solution polymerization. Two synthesis routes are proposed to synthesize the particles, the monomer route and the polymer/monomer route. For the monomer route, pH and thermal sensitive nanoparticles were synthesized from acrylic acid and N-isopropylacrylamide. For the polymer/monomer route, the pH sensitive nanoparticles were synthesized from chitosan and acrylic acid. The effect of reaction time, initiator concentration and agitation rate on the particle size and the size distribution were investigated. The stimuli-responsive nanoparticles could be directly blended with other polymers to prepare stimuli-responsive functional membranes.     

The Copolymerization of Alkenes with Maleic Anhydride

The investigations presented deal with the experimental results of the copolymerization of maleic anhydride (MAn) with alkenes. The course of the reaction is explained by the overall rate of the copolymerization (v _Br), which correlates with the solution viscosity of the copolymer, and the dependence of the v _Br maximum on the mole ratio of the monomers at constant total monomer concentration. The use of solvents with increasing donor power leads to increased complexing of the free MAn molecules and of the MAn radical chain ends. The results demonstrate that, for low 1-alkenes, the addition of the MAn chain radical is the rate-determining step of the copolymerization. As the substituents on the olefinic double bond become larger or the double bond shifts to the 1,2-position, the addition of MAn to the hydrocarbon radical becomes more and more the rate-determining step. On the other hand, an increase of the CT complexation of the MAn polymer radical by use of donor solvents decreases the alkene addition rate.     

基于3,6-二肼基-1,2,4,5-四嗪的两种高氮含能离子盐

本文通过3,6-二肼基-1,2,4,5-四嗪(DHT)分别与高氯酸和硝酸反应得到2种高氮含能离子盐,并通过X-射线单晶衍射技术对它们的结构进行了表征。(DHT)(NO₃)₂(1)属于单斜晶系,C2/c空间群,晶胞参数:a=1.3000(6)nm,b=0.8349(3)nm,c=1.0187(5)nm,β=118.89(5)°,Z=4;(DHT)(ClO₄)₂(2)属于正交晶系,P2₁2₁2空间群,晶胞参数:a=0.9804(4)nm,b=1.0747(4)nm,c=0.5325(2)nm,Z=2。采用DSC和TG-DTG技术研究了这两种含能离子盐的热分解机理,并对这两种含能离子盐的非等温动力学、爆热及感度进行了测试分析。研究表明这两种含能离子盐在敏感型含能材料领域具有潜在的应用前景。     

基于3,6-二肼基-1,2,4,5-四嗪的两种高氮含能离子盐

本文通过3,6-二肼基-1,2,4,5-四嗪(DHT)分别与高氯酸和硝酸反应得到2种高氮含能离子盐,并通过X-射线单晶衍射技术对它们的结构进行了表征。(DHT)(NO₃)₂(1)属于单斜晶系,C2/c空间群,晶胞参数：a=1.300 0(6) nm,b=0.834 9(3) nm,c=1.018 7(5) nm,β=118.89(5)°,Z=4;(DHT)(ClO₄)₂(2)属于正交晶系,P2₁2₁2空间群,晶胞参数：a=0.980 4(4) nm,b=1.074 7(4) nm,c=0.532 5(2) nm,Z=2。采用DSC和TG-DTG技术研究了这两种含能离子盐的热分解机理,并对这两种含能离子盐的非等温动力学、爆热及感度进行了测试分析。研究表明这两种含能离子盐在敏感型含能材料领域具有潜在的应用前景。     

Preparation,Crystal Structure,and Thermal Decomposition of the Intriguing Five‐coordinated Compound [Cu(IMI)4Cl]Cl (IMI = Imidazole)

The intriguing multi‐ligand compound [Cu(IMI)₄Cl]Cl ( 1 ) with the ligand imidazole (IMI) was synthesized and characterized by elemental analysis and FT‐IR spectroscopy. The crystal structure was determined by X‐ray single crystal diffraction and the crystallographic data showed that the compound belongs to the monoclinic P2₁/n space group [α = 8.847(2) Å, b = 13.210(3) Å, c = 13.870(3) Å, and β = 90.164(3)°]. Furthermore, the Cu^II ion is five‐coordinated by four nitrogen atoms from four imidazole ligands and a chlorine atom. The thermal decomposition mechanism was determined based on differential scanning calorimetry (DSC) and thermogravimetric (TG‐DTG) analysis. The non‐isothermal kinetics parameters were calculated by the Kissinger's method and Ozawa's method, respectively. The energy of combustion, enthalpy of formation, critical temperature of thermal explosion, entropy of activation (ΔS^≠), enthalpy of activation (ΔH^≠), and free energy of activation (ΔG^≠) were measured and calculated.