关于贝氏体形核和台阶机制的讨论--与徐祖耀院士等商榷

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。     

高温W/Re流口复合界面上的扩散层

W/Re流口在高温下使用时,复合界面处会发生反应扩散而形成一个由固溶体(W),双相σ,双相x,固溶体(Re)4个相组成的过渡层。并作出了不同反应扩散时间的浓度分布曲线,及浓度突变形成的双相区,从而确定了各相成份组成。对经反应扩散后的复合界面进行微观观察发现x相、σ相内有许多间隔式微裂纹,据此认为高温下W/Re流口失效原因是使用过程中上述两x,σ相内裂纹扩散,熔体渗入所致。     

Diffusion bonding between nickel-base superalloy K24 and heat-resisting steel 1Cr11Ni2W2MoV

IntroductionSLlperalloyandheat-resistingsteelarenowwidelyusedasstructurematerialsinaerospace,a\-lationalldshipbuildingindustries.Nickel-basesuperalloywasfirstlyrevealedasanengineeringmaterialduringtheearly1960swhenitwasrecognizedasbeingsuitableforllledium-temperaturegasturbinel'l.Now.nickel-basesuperalloyhasbeenpracticallyusedinhigheffectiveturbinestosatisfytheincreasingdemandsforhighertemperatureenvironmentsIZI.Insomeaerospaceengines,theimpellersshouldserveattemperatureof1000C~1100C,andala…     

Metallochemical Analysis of the Reaction in a Mixture of Nickel and Aluminum Powders

Phaseformation processes are considered at the level of a mesocell of a mixture with the use of the state diagram for a binary system. Consecutive schemes of metallochemical reactions of formation and decomposition of intermetallide compounds in a mixture of nickel and aluminum powders are suggested. The problem of diffusion annealing of this mixture is numerically solved for two different conditions: at a constant temperature and at a temperature slowly increasing by a linear law.     

Electrocatalysis of oxygen reduction on a carbon supported platinum-vanadium alloy in polymer electrolyte fuel cells

The electrocatalysis of the oxygen reduction reaction (ORR) on carbon supported Pt:V 1:1 catalyst in polymer electrolyte fuel cells (PEFC) was investigated. At an oxygen pressure of 1 atm results indicate a lower electrocatalytic activity for the ORR in the presence of vanadium. However, at an O₂ pressure ≥2 atm an enhanced electrocatalytic property of PtV/C compared with Pt/C is revealed. This result indicates the occurrence of a different electrocatalytic mechanism for the ORR on Pt/C and PtV/C. An increase of mass transport overpotentials is observed for the PtV/C catalyst, and this was related to the presence of vanadium oxide. Indeed, XRD analysis revealed that only about 30% of V present in the catalyst is alloyed with Pt, forming a face centred cubic (fcc) Pt₃V solid solution. A thermal treatment at 850 °C under reducing atmosphere leads to the formation of an ordered fcc Pt₂V phase. After this, the ORR activity of PtV/C at O₂ pressure 1 atm is higher than that of Pt/C.     

非均相固定化酶促反应中“抗激发互交作用”的解析分析与定量计算

通过理论推导证明：在外扩散与化学抑制共存的非均相固定化酶促反应中，总有效系数η为外扩散有效系数ηｄｉｆ和化学抑制有效系数ηｃｈ的乘积，并且分别小于相应的ηｄｉｆ和ηｃｈ；从数学上解释了外扩散抑制和一般性化学抑制间所存在的“抗激发互交作用”。利用所得公式计算表明：底物浓度对外扩散与竞争性、非竞争性和反竞争性等不同化学抑制共存的非均相固定化酶促反应有明显不同的影响；扩散抑制均显著地影响非均相固定化酶促反应，使得反应体系的总有效系数随抑制作用的增加而明显减小，从而对这类反应有了更进一步的认识     

Simulation studies on the fuel electrode of a H2---O2 polymer electrolyte fuel cell

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.     

电化学方法研究碳钢高温水体系中的氢扩散和渗透

本文应用Devanathan渗透装置的原理,设计了一套能用于测量碳钢-高温水体系中氢在碳钢中的扩散和渗透的实验装置,找出了该装置用于测量的最佳工作参数,并用该装置测量了373—473K下氢在碳钢中的扩散系数和扩散速率,讨论了氢在碳钢上还原的机理。     

Internal relative humidity distribution in high-performance cement paste due to moisture diffusion and self-desiccation

This investigation was carried out to study internal relative humidity (IRH) distribution of cement paste made with different water / cement ratios (w / c) and mineral admixtures in isothermal drying conditions. IRH changes in cement paste resulting from self-desiccation and moisture diffusion, respectively, at different ages were studied. The change laws of IRH in cement paste resulting from combining moisture diffusion with self-desiccation were discussed. The results indicate that IRH reduction of cement paste with w / c higher than 0.4 is mainly affected by moisture diffusion. However, IRH reduction of cement paste with w / c no higher than 0.4 is controlled by both moisture diffusion and self-desiccation. With the decrease of w / c, IRH reduction of cement paste resulting from self-desiccation increases, and IRH reduction resulting from moisture diffusion decreases at a given age. IRH decrement of cement paste incorporated with silica fume and ground blast-furnace slag is higher than that of control paste. w / c and the distance to the exposed surface play a significant role in IRH change resulting from moisture diffusion in isothermal drying condition. Change laws of IRH in cement paste with silica fume due to moisture diffusion considering self-desiccation are different from those in cement paste without silica fume.     

极限电流型氧传感器的实验研究

本实验用8mol%Y_2O_3-ZrO_2固体电解质制成了极限电流型氧传感器,并测定了氧在0.23～28.70mol%,温度在550～800℃范围时,传感器的输出特性,观察到该传感器有较好的稳定性和电压电流特性曲线。实验验证了极限电流值与氧摩尔分数和温度的关系。