双盘式磁力耦合器振动噪声分析与实验研究

为了在双盘式磁力耦合器设计阶段分析振动噪声特性,优化双盘式磁力耦合器设计,提出了一种利用模态叠加原理来分析其振动噪声的方法。双盘式磁力耦合器具有高转矩密度与高效率等优势,因此逐渐发展成为煤矿机械柔性传动装置。由于双盘式磁力耦合内部的转子磁场非正弦分布以及涡电流谐波等因素影响,双盘式磁力耦合器输出转矩中不可避免的存在波动。若根据计算得出的双盘式磁力耦合器的电磁振动噪声特点,在设计时选取振动噪声小的参数进行优化组合,可在实际中降低其电磁振动及噪声,有利于减少制造成本。本文结合双盘式磁力耦合器的结构特征,提出了一种模态叠加响应法计算电磁振动噪声,建立了其电磁径向力的解析模型,并在多物理场耦合作用下分析主要电磁径向力波在工作频率内的谐波响应,最后在额定功率为55 kW双盘式磁力耦合器实验台上进行试验验证。基于麦克斯韦张量法,建立了双盘式磁力耦合器的径向电磁力解析模型,并得出0阶与10阶电磁径向力波是产生振动噪声的最主要原因;利用多物理场耦合分析法进行谐波响应NVH特性分析,结果显示0阶力波的振动加速度与形变量均大于10阶力波的振动加速度与形变量,因此双盘式磁力耦合器的电磁振动主要来源于0阶力波;在额定功率为55 kW,最高转速为1 500 r/min的双盘式磁力耦合器实验台进行振动测试,试验结果显示在1 500 r/min时,试验得出的最大振动峰值及频率约为35 m/s^2和4 950 Hz,与有限元仿真结果的误差对应为6.3%和1.1%;而当变频电机的输入转速依次增大时,振动加速度的理论值、仿真值与试验值的曲线形态较为接近,误差较小;噪声估计值与实测值的最大误差仅为8.9%,基本验证了本文所提出模态叠加法的正确性。     

Effect of microbial hydrogen consumption on the hydrogen permeation behaviour of AISI 4135 steel under cathodic protection

The feasibility of microbial hydrogen consumption to mitigate the hydrogen embrittlement (HE) under different cathodic potentials was evaluated using the Devanathan-Stachurski electrochemical test and the hydrogen permeation efficiency η. The hydrogen permeation efficiency η in the presence of strain GA-1 was lower than that in sterile medium. The cathodic potential inhibited the adherence of strain GA-1 to AISI 4135 steel surface, thereby reducing the hydrogen consumption of strain GA-1. The adherent GA-1 cells were capable of consuming ‘cathodic hydrogen’ and reducing the proportions of absorbed hydrogen, indicating that it is theoretically possible to control HE by hydrogen-consuming microbes.     

Low-temperature synthesis of pure BiFeO3 phase and variation in its morphology with temperature

Pure BiFeO₃ samples were synthesized at low temperatures using hydrothermal/solvothermal method. The synthesis temperature of pure BiFeO₃ is continuously lowered while maintaining a high yield to lay the foundation for future industrialization. The morphological changes in BiFeO₃ synthesized at different temperatures were analyzed and the growth patterns discovered. The essential factor that affects the morphological changes was analyzed and reasonable explanations for these changes are given. The effect of organic solvent on sample morphology was observed. BiFeO₃ samples with better morphology were prepared by adding a proper surfactant. The synthesized pure BiFeO₃ phase reveals room temperature ferromagnetism, and the magnetism decreases as the particle size decreases.     

Perovskite SrFe1-xTixO3-δ (x < = 0.1) cathode for low temperature solid oxide fuel cell

Stable and compatible cathode materials are a key factor for realizing the low-temperature (LT, ≤600?°C) operation and practical implementations of solid oxide fuel cells (SOFCs). In this study, perovskite oxides SrFe_1-xTi_xO_3-δ (x?< = 0.1), with various ratios of Ti doping, are prepared by a sol-gel method for cathode material for LT-SOFCs. The structure, morphology and thermo-gravimetric characteristics of the resultant SFT powders are investigated. It is found that the Ti is successfully doped into SrFeO_3-δ to form a single phase cubic perovskite structure and crystal structure of SFT shows better stability than SrFeO_3-δ. The dc electrical conductivity and electrochemical properties of SFT are measured and analysed by four-probe and electrochemical impedance spectra (EIS) measurements, respectively. The obtained SFT exhibits a very low polarization resistance (R_p), .01 Ωcm² at 600?C. The SFT powders using as cathode in fuel cell devices, exhibit maximum power density of 551?mW?cm^?2 with open circuit voltage (OCV) of 1.15?V at 600?C. The good performance of the SFT cathode indicates a high rate of oxygen diffusion through the material at cathode. By enabling operation at low temperatures, SFT cathodes may result in a practical implementation of SOFCs.     

Structures and electrical conductivities of Gd3+ and Fe3+ co-doped cerium oxide electrolytes sintered at low temperature for ILT-SOFCs

Gd³⁺ and Fe³⁺ co-doped cerium oxide electrolytes, Ce_0.9Gd_0.1‐xFe_xO_2-δ (x?=?0.00, 0.01, 0.03, 0.05, 0.07, 0.10), were prepared by co-precipitation for ultrafine precursor powders and sintering for densified ceramic pellets. The crystal and microscopic structures were characterized by XRD, FESEM and Raman spectroscopy and their electrical properties were studied by AC impedance spectroscopy and the measurement of single cell's outputs. In comparison with Ce_0.9Gd_0.1O_1.95, the ceramic pellets of Ce_0.9Gd_0.1‐xFe_xO_2-δ with a relative density of 95% can be obtained after sintered at 1000?°C for 5?h, showing a remarkably enhanced sintering performance with a sintering temperature reduction of 500?°C, which might be ascribed to the highly activated migration of constituent species in the cerium oxide lattice doped with Gd³⁺ and Fe³⁺ions. Moreover, the electrical conductivity of Ce_0.9Gd_0.1‐xFe_xO_2-δ can be significantly enhanced depending on the mole fraction x, with Ce_0.9Gd_0.07Fe_0.03O_1.95 exhibiting the highest electrical conductivity of 38 mS/cm at 800?°C, about 36% higher than that of Ce_0.9Gd_0.1O_1.95 electrolyte sintered at 1500?°C for 5?h. So, The Gd³⁺ and Fe³⁺ co-doped cerium oxide would be an excellent candidate electrolyte for ILT SOFCs due to its prominent sintering performance and enhanced electrical conductivity.     

Highly porous nano-SiC with very low thermal conductivity and excellent high temperature behavior

Highly porous nano-SiC is fabricated by partial sintering and decarburizing process using SiC nano-powders as starting materials and graphite flakes as pore forming agents. The prepared porous nano-SiC ceramics possess multiple pore structures, including well-distributed meso-pores in the skeleton and interconnected flakelike micro-pores. The samples prepared at 1800 °C have relatively low thermal conductivities of 5.61 ～ 0.25 W m^?1 K^?1 with porosities of 55.5–76.1%. While the samples sintered at 1500 °C with porosities between 54.0% to 76.3% show very low thermal conductivities of 0.74 ～ 0.14 W m^?1 K^?1, which is attributed to the integrated nano-scale phonon-scattering mechanisms and duplex pore structures. Porous nano-SiC ceramics also show good retention of elastic stiffness up to 1350 °C and low thermal conductivity at 1400 °C. Our results shed light on porous nano-SiC as a promising thermal insulator used in extreme thermal and chemical environments.     

Giant permittivity and low dielectric loss of Fe doped BaTiO3 ceramics: Experimental and first-principles calculations

Fe doped BaTiO₃ ceramics with giant permittivity and low dielectric loss were synthesized in N₂/H₂ atmosphere started with BaTiO₃ powders and iron powders. XRD analysis exhibited the tetragonal-pseudocubic phase transition when the Fe content is 3 mol%. XPS spectra confirmed the iron oxides with mixed-valence structure of Fe²⁺/Fe³⁺, while Ti-ions maintain Ti⁴⁺3d⁰ states without any oxidization-reduction. For the case of ceramics with 5 mol% Fe, the dielectric constant was 66,650 at 1000 Hz at room temperature, 19 times higher than that of pure BaTiO₃ ceramics, while the dielectric loss tangent was 0.13. Comparison with other giant-permittivity materials demonstrated the superior potential of present ceramics. First-principles calculations investigated the interfacial interaction of Fe-[TiO₂] interface and Fe-[BaO] interface. Giant dielectric constant was induced by the interfacial polarization between insulating ferroelectrics and semiconducting iron oxides with mixed-valence states, as well as the contribution from the generated electron hopping conduction.     

Li2AGeO4 (A = Zn,Mg): Two novel low-permittivity microwave dielectric ceramics with olivine structure

Two low-permittivity dielectric materials Li₂AGeO₄ (A?=?Zn, Mg) were prepared via the solid-state reaction method. X-ray diffraction analysis and Rietveld refinement indicated that both ceramics crystallize in an orthorhombic olivine structure with a space group Pmn2₁. Dense ceramics with high relative density and homogeneous microstructure were obtained. Li₂ZnGeO₄ densified at 1200?°C possessed a relative permittivity ε_r?=?6.5, a quality factor Q?×?f?=?35,400?GHz, and a temperature coefficient of resonant frequency. Li₂MgGeO₄ exhibited ε_r?=?6.1, Q?×?f?=?28,500?GHz, and τ_f?=?–74.7?ppm/°C when sintered at 1220?°C. Additionally, the large negative τ_f values of Li₂AGeO₄ (A?=?Zn, Mg) ceramics were successfully adjusted compensated by forming composite ceramics with CaTiO₃ and near-zero τ_f values of +2.9?ppm/°C and +5.8?ppm/°C were achieved in 0.92Li₂ZnGeO₄-0.08CaTiO₃ and 0.90Li₂MgGeO₄-0.10CaTiO₃, respectively.     

Elevated temperature impact on performance of Low Temperature Co-fired Ceramic dielectrics

The need for electronics to operate at temperatures of 200°C and above continues to grow. These applications include avionics, aerospace, automotive, downhole drilling, mining, and many others. To satisfy this demand, a significant amount of research and development has been conducted. Despite the efforts, the number of new electronic components designed specifically for high-temperature operation is still relatively limited. In Low Temperature Co-fired Ceramic (LTCC) packages, LTCC materials are generally used as the host media for a number of pre-fabricated semiconductor components. As a result, reliability of the entire LTCC package largely depends on the performance of the least robust component. Ferro A6M-E and Ferro L8 are the two well-established and recognized LTCC dielectrics widely used for mid and high frequency LTCC applications, including several high reliability aerospace and defense applications that require demanding Mil-Spec qualifications. This study is our first attempt to characterize and understand basic high-temperature dielectric properties of these two commercial LTCC materials. The secondary objective is to initiate a dialogue in attempt to establish reliability requirements for LTCC packages dedicated for high-temperature operation.     

非高斯噪声激励下非线性漂移Fokker-Planck方程的非稳态解及其应用

非高斯噪声广泛存在于各种非线性系统，对非高斯噪声所驱动系统的非稳态演化行为进行研究可以更为深入的了解其内在的演化机理．本文对非高斯噪声和高斯白噪声共同驱动的非线性动力学系统的非稳态演化问题进行研究．首先应用格林函数的 $\Omega$ 展开理论在初始区域对非线性动力学系统进行线性化，然后结合本征值和本征矢理论推导出了该系统 Fokker-Planck 方程的近似非稳态解的表达式，最后以 Logistic 系统模型为例分析了非高斯噪声强度，关联时间及非高斯噪声偏离参数对非稳态解以及一阶矩的影响．研究结果表明，用 Logistic 模型描述产品产量增长时，其非稳态解可更好地反映产品产量在不稳定点附近的演化行为．