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101.
关于贝氏体形核和台阶机制的讨论--与徐祖耀院士等商榷 总被引:8,自引:6,他引:8
一些合金固溶化(或淬水)后在预贝氏体(孕育)期内等温淬火(或时效),既保持高温时形成的晶体缺陷,又产生新的晶体缺陷。母相中由于溶质原子扩散而在缺陷处发生偏聚,则形成贫/富溶质微区,即类拐点(spinoclal—like)分解。当贫溶质微区成分作为Ms,其温度等于或高于等温淬火(或时效)温度时,贝氏体将以马氏体样切变形核,故贝氏体是在溶质原子扩散控制下切变形核。在TEM温台试验中未发现台阶生长机制,界面上巨型台阶是贝氏体增宽(厚)速度差异所致。 相似文献
102.
Al-Si-Mg三元合金的溶质分凝及其对凝固过程的影响 总被引:1,自引:0,他引:1
从热力学角度分析了三元合金凝固过程中的溶质分凝行为, 利用耦合热力学计算技术研究了Al-Si-Mg三元合金溶质分凝因数在凝固过程中的变化规律, 获得了其与固相体积分数的定量关系, 进而预测了不同条件下Al-Si-Mg三元合金的凝固过程和相析出规律. 实验发现三元合金中溶质分凝因数在凝固过程变化巨大, 采用二元系中的参数使得对共晶种类和共晶分数的预测均与实验值有较大偏差. 采用耦合热力学计算技术, 获得了分凝因数在凝固过程中的变化规律, 使预测值更好地吻合于实验结果. 相似文献
103.
The macro-homogeneous porous electrode theory is used to develop a model which describes the catalyst layer of the hydrogen electrode formed by catalyst particles that are bonded to the membrane. The water transport in the catalyst layer and polymer electrolyte membrane is considered. The effects of catalyst layer structure parameters such as polymer volume fraction, catalyst layer thickness, platinum loading and reactant gas humidity as well as CO poison on the hydrogen electrode behavior are examined. The results show that the catalyst layer thickness has a significant effect on the electrode performance. A thicker catalyst layer will result in a larger ohmic voltage loss and higher catalyst cost. The optimal polymer volume fraction and catalyst layer thickness are 0.5 and 1.5–4 μm, respectively, for this electrode. An optimal platinum surface coverage on carbon need not exceed 20% (20 wt% Pt/C). Larger platinum coverage will increase the cost, but only slightly enhance the electrode performance. 相似文献
104.
大型露天矿在由山坡型转入深凹型开采后,随着运输条件的恶化,将单一的准轨铁路运输,改变为铁路—汽车联合运输,以延长铁路运输的服务年限,为此,需要解决提高电力机车运输性能、改造运输线路系统等问题。 相似文献
105.
106.
Investigation of transport phenomena in a hybrid ion exchange-electrodialysis system for the removal of copper ions 总被引:2,自引:0,他引:2
A. Mahmoud L. Muhr S. Vasiluk A. Aleynikoff F. Lapicque 《Journal of Applied Electrochemistry》2003,33(10):875-884
Hybrid ion exchange electrodialysis processes allow the removal of metal ions from dilute waste liquids and the recovery of more concentrated solutions. The work reported here was aimed at investigating the two steps in the treatment process, namely, adsorption of metal ions onto the packed bed of resin and electromigration (i.e., the transport of these ions in the complex system under the applied electrical field). The case of copper sulfate was investigated. Dowex resins with a cross-linking degree of 2 and 8% were used. The flux of copper through the resin bed and the current efficiency for ion transfer to the cathode compartment were determined as a function of potential gradient and copper ionic fraction in the bed. Apparent diffusion coefficients of Cu2+ in the overall system were deduced from the experimental data. 相似文献
107.
Vapor pressures were determined for several polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) at 75-275 °C, extending the available literature data to more relevant temperature regions and providing the first experimental data for 2,3,7-trichlorodibenzo-p-dioxin (2,3,7-TriCD). A modification of the effusion technique, based upon controlling the diffusion of the target compound and subsequent high resolution gas chromatography/low resolution mass spectrometry (HRGC/LRMS) analysis, was proven comparable to other accepted methods for determining the vapor pressures of semi-volatile organic compounds (SVOCs). Vapor pressures for octachlorodibenzo-p-dioxin (OCDD) and octachlorodibenzofuran (OCDF) were in excellent agreement with those reported in literature. The application of the current method for the vapor pressure determinations of eight polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDDs/PCDFs) in the extended temperature range (up to 275 °C) is reported. The extension of the vapor pressures to such temperatures, unprecedented for the PCDDs/Fs, is important for vapor-particle partitioning modeling in regions relevant to PCDD/F formation and control. Estimates for the melting temperatures and enthalpies of sublimation and vaporization are also reported, the latter for which no experimentally determined values have been found in the literature. The use of the method to deliver reproducible, trace concentrations (ppt-ppb) of targets was applied to the calibration of the jet-REMPI/TOFMS as an online detector for low chlorinated PCDDs/Fs. 相似文献
108.
福建数座河口水闸发生剧烈淘刷,闸上游和下游的最大冲刷深度达到闸室高度的0.5~1.2倍,且屡修屡毁。有的水闸经多次除险加固后,不得不再花巨资重建。通过数学模型和物理模型揭示了河口水闸下游水位因受东海大潮差海潮影响发生剧烈波动时的变化规律,发现了水闸泄流过程中的间歇性淹没及非常工况甚至出现逆流的独特流动现象,给出了典型日孔流及堰流泄流能力动态变化过程线,分析了消能工变化对闸址水流结构的显著影响,并对水闸水毁修复前后闸下冲刷进行了预测。结果表明:水闸修复前闸下涨急最高水位4.53 m,修复后下降0.67 m,水闸修复后逆流现象减弱。修复后首次水跃位置往上游移动了35 m,平均水跃高度下降47.46%,闸后及二级池末端最大流速2.27 m/s和0.08 m/s,较修复前分别下降了40.58%和96.48%。常遇泄流条件下,水闸的淹没度和泄流能力呈现不断变化的动态过程。当西溪水闸62#先启孔全开,上游保持正常高水位3.2 m,下游为最低潮位-0.72 m时,修复后最大冲刷深度减少64.48%,消能防冲效果十分明显。研究成果对河口水闸安全运行具有一定的参考价值。 相似文献
109.
Selective gas transport in miscible PPO-PS blends 总被引:1,自引:0,他引:1
The permeation rates of He, CO2 and CH4 though miscible blends of polystyrene and poly(phenylene oxide) at 35°C are reported as a function of pressure. Sorption isotherms for CO2 and CH4 are also presented. By using ratios of the permeabilities of the pure gases the separation factors for the gas pairs He---CH4 and CO2---CH4 can be estimated. For both pairs the estimated separation factor goes through a prominent maximum, thus indicating that these blends are more permselective than expected from the behaviour of polystyrene and poly(phenylene oxide). This stems from mobility considerations rather than solubility effects and a qualitative free volume argument is proposed as an explanation. The sorption and transport data have been interpreted and correlated using the dual sorption-mobility models developed previously for glassy polymers. Since the commercial polystyrene used contained a small amount of mineral oil to improve flow behaviour, the effect of this additive on polystyrene properties was explored in some detail. 相似文献
110.