Helmholtz水声换能器弹性壁液腔谐振频率研究

针对传统Helmholtz水声换能器设计中刚性壁假设的局限性,将Helmholtz腔体的弹性计入到液腔谐振频率计算中,实现低频弹性Helmholtz水声换能器液腔谐振频率精确设计.基于细长圆柱壳腔体的低频集中参数模型,导出了腔体弹性引入的附加声阻抗表达式,得到了弹性壁条件下Helmholtz水声换能器等效电路图,给出了考虑了末端修正的弹性壁Helmholtz共振腔液腔谐振频率计算公式.利用ANSYS软件建立了算例模型,仿真分析了不同材质、半径、长度时的Helmholtz共振腔液腔谐振频率.结果对比表明弹性理论值与仿真值符合得很好,相比起传统的刚性壁理论计算结果,本文的弹性壁理论得出的液腔谐振频率值有所降低,与真实情况更加接近.本文的结论可以为精确设计低频弹性Helmholtz水声换能器提供理论支持.     

腔壁弹性对水下小型圆柱形亥姆霍兹共振器共振频率的影响

理论和实验研究了腔壁弹性对水下小型圆柱形亥姆霍兹共振器共振频率的影响.基于电-声类比理论,建立了小型共振器的简化模型,利用电路分析方法得到了便于计算的共振频率一般表达式.分别仿真分析了共振器壁面厚度和材料对共振频率的影响,得到了不同尺寸的小型共振器的近似刚性条件.在充水驻波罐中对不同壁厚、不同材料的小型圆柱形亥姆霍兹共振器的共振频率进行了测量,实验结果较好地验证了理论分析和近似刚性条件的正确性.所得结果对小型圆柱形亥姆霍兹共振器的设计和水下应用具有较好的参考价值. 关键词： 亥姆霍兹共振器 共振频率 传递函数 辐射阻抗     

电子注对谐振腔中TM模式谐振频率和电磁场分布的影响

将电子注视为等离子体柱,从填充等离子体柱的谐振腔的物理模型出发,推导了圆柱腔填充中心电子注时TM0m0模式的特征方程,并重点分析了填充电子注的圆柱腔中TM010模式和TM020模式的谐振频率和电磁场分布随等离子频率的变化情况。研究结果表明,随着电子注的等离子体频率不断增大,谐振频率也不断增大,谐振腔内电场和磁场的分布也随之发生改变。当电子注的等离子体频率超过谐振腔的谐振频率时,谐振腔内的电磁场分布将发生很大的变化,出现了电子注内外电场方向相反和趋肤效应等现象。     

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介绍了开式微波谐振腔测量系统的工作原理及试验结果,获得了Æ10mm钢球模型在6.65kPa干燥空气中以速度5.44km.s-1飞行时的尾迹电子密度测量结果,并且与国外弹道靶试验数据进行了比较。试验结果表明,该系统能够满足模型尾迹电子密度变化对测量系统响应时间的要求,能很好地反映尾迹电子密度变化细节,电子密度测量范围达到109~1011cm-3。     

基于声强测量的圆柱内部全息柱面复声压相位重构

本文把基于声强测量的全息相位重构原理应用到圆柱内部声场中,阐述了圆柱面相位重构原理,推导了相应的有限空间离散算法并计算了圆柱声腔内主要声模态。结果表明,重构相位和理论值有较好的吻合。最后,分析了重构频率、全息孔径及全息柱面与壳体的间距等重构参数对相位重构精度的影响。     

弹道靶开式微波谐振腔测量系统研究

The principle and experimental results of the open microwave resonant cavity measurement system were introduced. The models were steel ball models and the ball models coated with copper. The diameter of the models was 10mm. The models were launched in ballistic range. The model velocity was 5.44 km.s^-1. The wake electron density of the models was obtained. The experimental results presents that the response time of the open microwave resonant cavity measurement system was quicker than 1ms. The results showed the wake electron density ranged from 10⁹cm^-3 to 10¹¹cm^-3 could be achieved.     

基于混合气体分子复合弛豫模型的一氧化碳浓度检测算法

研究了声波通过混合气体时,复合弛豫声吸收和声速与气体各成分浓度和声频率之间的依赖关系.以一氧化碳气体、水蒸气、氮气和氧气的混合气体为例,分别建立了弛豫声吸收和声速与气体浓度的三维模型,以及弛豫声吸收与声频率的二维模型.完成了通过测量弛豫声吸收和声速计算一氧化碳气体浓度的算法推导,提出了一种依据弛豫声吸收和声速检测气体浓度的简化算法.仿真实验结果不仅证明了算法的理论可行性,还给出了算法的最佳适用声频率范围,并估计了将算法应用于实验的误差原因,证明了算法具有实际可行性. 关键词： 气体浓度声学检测 一氧化碳浓度检测 复合弛豫声吸收 声速     

Effect of viscosity on stability and accuracy of the two-component lattice Boltzmann method with a multiple-relaxation-time collision operator investigated by the acoustic attenuation model

A two-component lattice Boltzmann method (LBM) with a multiple-relaxation-time (MRT) collision operator is presented to improve the numerical stability of the single relaxation time (SRT) model. The macroscopic and the momentum conservation equations can be retrieved through the Chapman—Enskog (C-E) expansion analysis. The equilibrium moment with the diffusion term is calculated, a diffusion phenomenon is simulated by utilizing the developed model, and the numerical stability is verified. Furthermore, the binary mixture channel model is designed to simulate the sound attenuation phenomenon, and the obtained simulation results are found to be consistent with the analytical solutions. The sound attenuation model is used to study the numerical stability and calculation accuracy of the LBM model. The simulation results show the stability and accuracy of the MRT model and the SRT model under different viscosity conditions. Finally, we study the influence of the error between the macroscopic equation of the MRT model and the standard incompressible Navier—Stokes equation on the calculation accuracy of the model to demonstrate the general applicability of the conclusions drawn by the sound attenuation model in the present study.     

电子注对谐振腔中TM模式谐振频率和电磁场分布的影响

将电子注视为等离子体柱,从填充等离子体柱的谐振腔的物理模型出发,推导了圆柱腔填充中心电子注时TM0m0模式的特征方程,并重点分析了填充电子注的圆柱腔中TM010模式和TM020模式的谐振频率和电磁场分布随等离子频率的变化情况。研究结果表明,随着电子注的等离子体频率不断增大,谐振频率也不断增大,谐振腔内电场和磁场的分布也随之发生改变。当电子注的等离子体频率超过谐振腔的谐振频率时,谐振腔内的电磁场分布将发生很大的变化,出现了电子注内外电场方向相反和趋肤效应等现象。     

Energy calibration issues in nuclear resonant vibrational spectroscopy: observing small spectral shifts and making fast calibrations

The conventional energy calibration for nuclear resonant vibrational spectroscopy (NRVS) is usually long. Meanwhile, taking NRVS samples out of the cryostat increases the chance of sample damage, which makes it impossible to carry out an energy calibration during one NRVS measurement. In this study, by manipulating the 14.4 keV beam through the main measurement chamber without moving out the NRVS sample, two alternative calibration procedures have been proposed and established: (i) an in situ calibration procedure, which measures the main NRVS sample at stage A and the calibration sample at stage B simultaneously, and calibrates the energies for observing extremely small spectral shifts; for example, the 0.3 meV energy shift between the 100%‐⁵⁷Fe‐enriched [Fe₄S₄Cl₄]⁼ and 10%‐⁵⁷Fe and 90%‐⁵⁴Fe labeled [Fe₄S₄Cl₄]⁼ has been well resolved; (ii) a quick‐switching energy calibration procedure, which reduces each calibration time from 3–4 h to about 30 min. Although the quick‐switching calibration is not in situ, it is suitable for normal NRVS measurements.