Temperature-insensitive fiber Bragg grating dynamic pressure sensing system

Temperature-insensitive dynamic pressure measurement using a single fiber Bragg grating (FBG) based on reflection spectrum bandwidth modulation and optical power detection is proposed. A specifically designed double-hole cantilever beam is used to provide a pressure-induced axial strain gradient along the sensing FBG and is also used to modulate the reflection bandwidth of the grating. The bandwidth modulation is immune to spatially uniform temperature effects, and the pressure can be unambiguously determined by measuring the reflected optical power, avoiding the complex wavelength interrogation system. The system acquisition time is up to 85 Hz for dynamic pressure measurement, and the thermal fluctuation is kept less than 1.2% full-scale for a temperature range of -10 degrees C to 80 degrees C.     

机载腔增强吸收光谱系统应用于大气NO_2空间高时间分辨率测量

介绍了一套用于机载平台测量的非相干宽带腔增强吸收光谱(IBBCEAS)系统,并应用于实际大气NO_2空间分布的高时间分辨率观测.为满足机载测量中对时间分辨率的需求,系统采用离轴抛物面镜代替消色差透镜提高光学耦合效率;并运用Allan方差,对系统性能进行了分析.通过腔增强吸收光谱系统与长光程吸收光谱系统对实际大气NO_2的对比测试,两者线性相关系数R~2达到0.86.将IBBCEAS系统应用于机载平台,在时间分辨率为2 s的情况下,探测限达到95 ppt(1σ).通过机载观测,获得了华北地区石家庄等地上空对流层大气NO_2的廓线信息.     

蛋白石型光子晶体红外隐身材料的制备

基于光子晶体的红外隐身材料,主要采取一维层层堆叠结构和三维木堆结构等来实现对红外波段电磁波辐射性能的调控.本文报道了一种操作简易、成本低廉的光子晶体红外隐身材料制备方法.通过优化的垂直沉积法,微米级SiO_2胶体微球自组装成高质量的蛋白石型光子晶体结构.对SiO_2胶体微球进行优选,成功制备了禁带位于2.8—3.5μm,8.0—10.0μm的SiO_2胶体晶体蛋白石型光子晶体材料.该材料可改变目标相应波段的红外辐射特征,具有目标红外波段的隐身效果.     

大尺度有效引力的E(2)规范理论模型

微波背景辐射的低l极矩的各向异性可能不能用微波背景辐射静止系boost到本动参考系来解释,我们推断boost对称性在宇宙学尺度上缺失,又由于单纯结合广义相对论和物质结构的标准模型不能解释星系以上尺度的引力现象,需要引入暗物质和暗能量.而迄今为止所有寻找暗物质粒子的实验给出的都是否定结果,暗能量的本质更是一个谜.因此,我们假设洛伦兹对称性是从星系以上尺度开始部分破缺,以非常狭义相对论对称群E(2)为例,用E(2)规范理论来构造大尺度有效引力理论,并分析了此规范理论的自洽性.从这些讨论中发现,当物质源即使为普通标量物质时,contortion也一般非零,非零contortion的存在会贡献一个等效能量动量张量的分布,它可能对暗物质效应给出至少部分的贡献.我们从对称性出发修改引力,有别于其他的修改引力理论.     

Influence of tetraborate anions on manganese electrodeposition in an anion-exchange membrane electrolysis reactor

The influences of tetraborate anions on manganese electrodeposition in an anion-exchange membrane electrolysis reactor were investigated. The experimental results of manganese electrodeposition indicate that a certain amount of tetraborate anions can increase cathode current efficiency and initial pH 7.0–8.0 is suitable for high cathode current efficiency. X-ray diffraction (XRD) and scanning electron microscope (SEM) analysis show the nanocrystalline structure and impact morphology of electrodeposited manganese. The purity of electrodeposited manganese is above 99.88 %. The tests of tetraborate anions on buffer capacity (β) and pH value of the electrolyte near the cathode surface confirm that tetraborate anions facilitate manganese electrodeposition. Tetraborate anions can improve concentration polarization of Mn²⁺ ions and then increase the overpotential of hydrogen evolution reaction. Therefore, ammonium tetraborate can reduce the hydrogen embrittlement, pore, and pitting negative effect on electrodeposit surface, to improve the corrosion resistance of electrodeposited manganese. After tetraborate anions being added in electrolyte, weight loss measurement indicates that the corrosion resistance of electrodeposited manganese is improved. Electrochemical measurements testify that corrosion resistance of electrodeposited manganese containing tetraborate anions in electrolyte is reflected by less negative corrosion potential and higher impedance.     

Determining the resistance of X-pinch plasma

The current and the voltage of an X-pinch were measured. The inductance of the X-pinch was assumed to be a constant and estimated by the calculation of the magnetic field based on the well-known Biot-Savart's Law. The voltage of the inductance was calculated with L · di/dt and subtracted from the measured voltage of the X-pinch. Then, the resistance of the X-pinch was determined and the following results were obtained. At the start of the current flow the resistance of the exploding wires is several tens of Ohms, one order of magnitude, higher than the metallic resistance of the wires at room temperature, and then it falls quickly to about 1 , which reflects the physical processes occurring in the electrically exploding wires, i.e., a current transition from the highly resistive wire core to the highly conductive plasma. It was shown that the inductive contribution to the voltage of the X-pinch is less than the resistive contribution. For the wires we used, the wires' material and diameter have no strong influence on the resistance of the X-pinch, which may be explained by the fact that the current flows through the plasma rather than through the metallic wire itself. As a result, the current is almost equally divided between two parallel X-pinches even though the diameter and material of the wires used for these two X-pinches are significantly different.     

激波冲击R22重气柱所导致的射流与混合研究

基于大涡模拟, 结合五阶加权基本无振荡格式与沉浸边界法对激波自左向右与R22重气柱作用过程进行了数值模拟. 数值结果清晰地显示了激波诱导Richtmyer-Meshkov不稳定性所导致的重气柱变形过程, 并与Haas 和 Sturtevant 的实验结果符合. 另外, 结果还揭示了入射激波在气柱内右侧边界发生聚焦并诱导射流的过程, 以及在Kelvin-Helmhotz 次不稳定性作用下两个主涡滑移层形成次级涡的过程, 并分析了气柱变形过程中与周围空气的混合机理. 最后, 通过改变反射距离对反射激波与不同变形阶段的气柱的再次作用过程进行了研究. 结果表明: 当激波反射距离较长时, 反射激波与充分变形后的气柱作用, 使其在流向方向上进一步被压缩; 而当激波反射距离较短时, 反射激波会在气柱内发生马赫反射, 两个三波点附近产生两个高压区, 当其传播至气柱左侧边界时对气柱边界造成冲击加速, 诱导两道向左传播的反向射流. 关键词： Richtmyer-Meshkov不稳定性 R22重气柱 反射激波 射流     

飞秒激光剥蚀-多接收电感耦合等离子质谱原位微区分析青铜中铅同位素组成-以古铜钱币为例

建立了飞秒激光剥蚀-多接收电感耦合等离子质谱(fLA-MC-ICPMS)铅同位素原位微区分析方法,分别利用溶液法(SN-MC-ICPMS)和激光剥蚀法(fLA-MC-ICPMS)对15个铜(黄铜,青铜)国家标准物质进行了实验分析,测试的结果表明CuPb12(GBW02137)中Pb同位素组成非常均一,可作为以铜为基体的青铜、黄铜及铜矿中Pb同位素原位微区分析的外部参考物质。对CuPb12进行了112次fLA-MC-ICPMS Pb同位素分析测试,其加权平均值与溶液法测定的Pb同位素比值在2σ误差范围内完全一致,208 Pb/204 Pb和207Pb/206Pb比值的内部精度RSE分别小于90和40ppm,外部精度RSD分别小于60和30ppm。利用本实验室建立的fLA-MC-ICPMS分析方法对13个古铜钱币中Pb同位素进行了原位微区无损伤分析,测试结果表明,不同朝代古钱币中Pb同位素组成差异较大,即使同一朝代的古钱币其Pb同位素组成也不尽相同。     

LED毫伏级待测电动势实验仪的设计及其稳定性的研究

为了满足电位差计实验对毫伏级待测电动势需求,设计了LED毫伏级待测电动势实验仪,并对其稳定性进行了研究.待测电动势实验仪是通过光电转换来实现的,输出的毫伏级电动势在电位差计实验仪的各个测量点都能稳定,能够满足箱式电位差计测量范围和精度要求,是比较理想的箱式电位差计实验配套仪器,能够大大提高学生的实验效率和教师对实验设计的选择性,实验效果良好.     

Cu/HMOR催化二甲醚羰基化合成乙酸甲酯: 催化剂制备方法的影响 (cited: 2)

采用氨蒸发法、尿素水解法、离子交换法及浸渍法制备HMOR负载的Cu催化剂, 考察其催化二甲醚(DME)羰基化合成乙酸甲酯(MA)性能. 结果表明离子交换法制得Cu/HMOR催化剂在Cu的金属中心和酸性分子筛载体的共同作用下具有较好催化反应活性. 在210 oC、1.5 MPa、空速4883 h^-1,DME转化率为95.3%,MA选择性为94.9%. 对催化剂进行N2物理吸附、X射线衍射、NH₃程序升温脱附和CO程序升温脱附等表征发现,离子交换法制得Cu/HMOR催化剂具有较高比表面、大量弱酸及一定中强酸、适中的CO吸附强度,提高了CO插入DME羰基化反应活性.