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41.
Xinyu Huang Roham Solasi Yue Zou Matthew Feshler Kenneth Reifsnider David Condit Sergei Burlatsky Thomas Madden 《Journal of Polymer Science.Polymer Physics》2006,44(16):2346-2357
The life of proton exchange membrane fuel cells (PEMFC) is currently limited by the mechanical endurance of polymer electrolyte membranes and membrane electrode assemblies (MEAs). In this paper, the authors report recent experimental and modeling work toward understanding the mechanisms of delayed mechanical failures of polymer electrolyte membranes and MEAs under relevant PEMFC operating conditions. Mechanical breach of membranes/MEAs in the form of pinholes and tears has been frequently observed after long‐term or accelerated testing of PEMFC cells/stacks. Catastrophic failure of cell/stack due to rapid gas crossover shortly follows the mechanical breach. Ex situ mechanical characterizations were performed on MEAs after being subjected to the accelerated chemical aging and relative humidity (RH) cycling tests. The results showed significant reduction of MEA ductility manifested as drastically reduced strain‐to‐failure of the chemically aged and RH‐cycled MEAs. Postmortem analysis revealed the formation and growth of mechanical defects such as cracks and crazing in the membranes and MEAs. A finite element model was used to estimate stress/strain states of an edge‐constrained MEA under rapid RH variations. Damage metrics for accelerated testing and life prediction of PEMFCs are discussed. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 2346–2357, 2006 相似文献
42.
Juray De Wilde Denis Constales Geraldine J. Heynderickx Guy B. Marin 《International Journal of Multiphase Flow》2007
The propagation speeds of linear waves in gas–solid suspensions depend strongly on the solids volume fraction and the wave frequency. The latter is due to gas–solid momentum transfer and allows a simple test on filtered gas–solid momentum transfer models. Such models may predict linear wave propagation speeds different from those obtained with the non-filtered model at wave frequencies higher than the filter frequency, but not at wave frequencies lower than the filter frequency. 相似文献
43.
利用变温X射线衍射技术,在预烧过程中分析了Nd掺杂Bi4Ti3O12后生成Bi3.15Nd0.85Ti3O12(BNT)相的形成过程以及微结构的变化.实验观察到以30℃/min的升温速率,BNT相在700℃时开始形成,其衍射峰强度随温度的继续升高而增强,衍射峰半高宽随烧结时间延长而减小.X射线衍射分析结果表明,在900℃恒温条件下,烧结约2h,可形成单一的BNT相. 相似文献
44.
Solid state laser (SSL) powers can be realistically scaled when pumped by a real, efficient and multimode pulse. In this work,
a fourth-order super-Gaussian pulse was assumed as a pump for SSL’s and a complete analytical expression for the thermal phase
shift is given. Moreover, the focal length of thermal lens in paraxial ray approximation regime was studied. The results when
applied to a Ti: sapphire crystal show an appreciable correction for abberation compared to a top-hat pulse. 相似文献
45.
Chi-So Lee 《中国化学会会志》1987,34(3):207-210
A differential pulse polarographic method for the determination of nitrate ion has been developed. With 0.5 M CaCl2 as supporting electrolyte, NO?3 is reduced to give a peak with E1/2=–1.836 Volt vs. the Ag/AgCl electrode. The differential pulse polarographic peak height is proportional to the nitrate concentration from 20 to 60 ppm. The detection limit for nitrate is 2 ppm in pure aqueous solution. In the determination of 40 ppm nitrate a relative precision (relative standard deviation) of less than 2% was achieved. Nitrite interferes seriously and should be absent if accurate results are required. The method has been applied to the determination of nitrate in Ammonium Uranyl Tricarbonate (AUT) Solution, results obtained by this method are compared to those obtained by ion chromatography. The agreement between the two sets of results suggests that the DPP method can be used with a fair degree of confidence. 相似文献
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The solid diffusion coefficient of lithium-ion in LiCoO2 cathode material has been investigated by the capacity intermittent titration technique (CITT) at different voltages and at different charge/discharge cycles. By SEM, XRD and FTIR techniques, the structure of LiCoO2 was studied before and after charge-discharge cycles, and the relationship between solid diffusion coefficient and crystal structure was further discussed. CITT results show that the value of Li+ solid diffusion coefficient of LiCoO2 is about 10-12 cm2·s-1. During the whole charge-discharge cycles, the Li+ solid diffusion coefficient decreased within the voltage of 4.0~4.3 V, which is attributed to the change of the structure of LiCoO2. 相似文献
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