注射模分型面设计中靠破孔的研究

针对应用Pro／E软件进行注射模分型面设计中出现的靠破孔问题，以阿尔卡特的OT535手机为例，归纳总结了设计分型面时填补破孔的基本思路和主要方法，解决了分型面设计中的关键问题。     

Kinetics of synthesis of Li4Ti5O12 through solid-solid reaction

1. Introduction The solid-solid reaction used in synthesizing various kinds of electrochemical materials has many advantages, such as simple process, without using solvent, saving energy, friendly to the environment and easy to obtain good quality materials like nano-size materials. Recently, the manufacturing of electrochemistry materials has been paid more atten- tion due to its increasing needs. Therefore it is a natural interest to study the synthesis of electro- chemical materials by usin…     

EPS模陶瓷型精密铸造失模工艺研究

针对EPS陶瓷壳型精铸失模时容易裂壳的现象,对EPS消失模精密铸造工艺进行了研究。利用自制的膨胀率检测设备对不同密度的EPS模试样在不同加热温度下的最大膨胀率进行了测试,研究了壳型膨胀与失模温度之间的关系;对陶瓷壳型中EPS模失模时的温度场分布进行测量,发现EPS模试样的密度大小对失模时温度场有着很重要的影响。在试验和分析的基础上,对EPS模失模机制进行了探讨,提出了高温失模机制。高温失模有利于降低失模时对壳型的膨胀作用力,为获得洁净而健全的陶瓷型壳提供了可靠保证。     

Airslip结晶器内凝固壳形成特性分析

根据Airslip结晶器的传热特性,建立了凝固壳厚度和临界凝固壳厚度的数学模型.理论分析和实验结果表明,凝固壳厚度与铸造速度的乘积为常数,铸造速度增大,凝固壳厚度减小,铸锭表面质量提高;铸造速度的波动引起凝固壳厚度的波动,降低了铸锭的表面质量;铸锭直径和铸造速度的乘积也为常数,铸锭直径增大,铸造速度相应减小.     

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.     

锂电极表面膜的组成和阻抗行为

介绍了锂电池中锂电极的表面膜的组成和阻抗行为，并根据其表面膜的阻抗行为提出了电化学模型。     

注射充模过程的压力求解方法及其比较

提出了一个LU局部分解方法来求解注射充模过程的压力方程,并与其他迭代方法进行了比较。LU局部分解法是当矩阵在逐渐变大时,保留已经分解的部分,只对新增加的部分进行分解,因此相当于只对最后的稀疏矩阵进行了分解。计算表明,LU局部分解法比预条件共轭梯度法快大约1个量级,而预条件共轭梯度方法又比超松弛迭代法快大约1个量级。     

注塑流动与传热分析的自适应隐式控制体积法

在注塑流动与传热分析中采用自适应隐式控制体积法,利用自动控制的参数识别方法来自动调节时间步长,在每个时间步长流动将向前推进大约半个单元大小的距离,厚度方向的温度采用契比雪夫配点法进行计算,压力方程的求解方法是预条件共轭梯度法。计算结果表明,自适应隐式控制体积法的时间复杂度是结点数目的平方,而且1h之内可以求解10000结点规模的问题。     

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.     

Nile blue adsorbed onto silica gel modified with niobium oxide for electrocatalytic oxidation of NADH

A study of modified carbon paste electrode employing Nile blue (NB) adsorbed on silica gel modified with niobium oxide (SN) for electrocatalytic oxidation of reduced nicotinamide adenine dinucleotide (NADH) is described. The adsorbed organic dye on SN was used to prepare a modified carbon paste electrode to investigate its electrochemical properties. The formal potential (E°′) of the adsorbed NB (−230 mV vs. saturated calomel electrode, SCE) showed a shift of 70 mV towards a more positive potential value, compared to NB dissolved in aqueous solution. In solutions with pH between 6.0 and 8.0 did stability and E°′ remained almost constant. However, for a solution pH lower than 6.0 the E°′ was affected by the acidity of the contacting solution, shifting the E°′ towards more positive values. For the solution pHs between 6.0 and 8.0 the electrocatalytic activity remained almost constant. A linear response range for NADH between 1.0×10⁻⁵ and 5.2×10⁻⁴ mol l⁻¹, at pH 7.0, was observed for the electrode, with an applied potential of −200 mV versus SCE. The formation of an intermediate charge transfer (CT) complex was proposed to the CT reaction between NADH and adsorbed NB. The heterogeneous electron transfer rate, k_obs, was 1400 M⁻¹ s⁻¹ and the apparent Michaelis-Menten constant, was 0.21 mM at pH 7.0 evaluated from rotating disk electrode (RDE) experiments with an electrode coverage of about 5.2×10⁻⁹ mol cm⁻². The increase in the reaction rate between NADH and the immobilized NB compared to those obtained with dissolved NB was assigned to the shift of the E°′ towards more positive values.