深亚微米MOSFET衬底电流的模拟与分析

利用器件模拟手段对深亚微米ＭＯＳＦＥＴ的衬底电流进行了研究和分析，给出了有效的道长度，栅氧厚度，源漏结深，衬底掺杂浓度以及电源电压对深亚微米ＭＯＳＦＥＴ衬底电流的影响，发现电源电压对深亚微米ＭＯＳＦＥＴ的衬底电流有着强烈的影响，热载流子效应随电源电压的降低而迅速减小，当电源电压降低到一定程度时，热载流子效应不再成为影响深亚微米ＭＯＳ电路可靠性的主要问题。     

抗洪抢险措施及效果

结合“９８”抗洪抢险实例，对多种险情作了具体分析，通过汛后调查，对抗洪抢险消险措施和效果进行了总结，为今后进一步做好防洪消险工作提供了经验。     

纤维增强铝基复合材料变形损伤过程声发射研究

采用声发射（ＡＥ）技术，通过测定ＡＥ事件数、幅度和持续时间等发射特征参数以及恒载 Ｆｅｌｉｅｉｔｙ效应，对ＳｉＣ／Ａｌ和Ｃ／Ａｌ两类束丝纤维增强铝昨合在拉伸变形过程中的损失失效特征进行了分析探讨。实验结果表明，纤维种类、界面状况对复合材料损伤过程有着显著的影响，声发射技术是表征这类复合材料损伤特征很有潜力的方法。     

MPID─TOF质谱的快速时间分辨微弱信号测试系统

把瞬态记录仪Ｂｉｏｍａｔｉｏｎ８ｌ００与微型计算机ＩＢＭ─ｐＣ／ＸＴ联接建成了一个高速数据采集系统，本文介绍了系统的硬件接口设计及软件设计。在超声分子束条件下，把它应用于环氧乙烷（Ｃ＿２Ｈ＿４Ｏ）的多光子电离与离解飞行时间（ＭＰＩＤ─ＴＯＦ）质谱的实验研究中，并给出了实验结果；本系统在微观基元化学反应动力学实验研究中广泛适用于对时间分辨微弱信号的探测。     

机器人腕力传感器的动态负载效应

本文从时域和频域两方面研究机器人腕力传感器在加载情况下的动态响应，进行动态建模和频谱分析，探讨负载效应的影响。     

运放滞回比较电路在差动式温度控制中的应用研究

从差动式温度控制的角度研究了两种由集成运算放大器构成的滞回比较器（基型和交叉耦合型）的传输特性，发现它们均能用作闭环差动式控温单元，并都具有在温度设置点转换速度快、抗干扰能力强、控制单元设计简单等优点。分析和比较了这两种控温单元的控制参数的调节性能和参数的稳定性，获知后者的预置温度（Ｔｈ或ＴＬ）和差动温度范围（△Ｔ）的设置值均能各自独立地调节，且系统的Ｔｈ，ＴＬ，△Ｔ的实际值几乎仅决定于设置电路本身，因而显得更为优越。文中还讨论了应用中的有关问题，并给出了相关的应用实例。     

A method of identifying latent human errors in work systems

Work system improvements are implemented in various manufacturing processes to prevent problems caused by human errors. However, they are almost always applied to problems which have already occurred. This paper examines a method of identifying latent human errors existing within the work systems beforehand. A procedure for applying failure mode and effect analysis to this identification problem was defined based on over 1000 empirical errors: a work system decomposition criterion and fundamental error modes for listing latent human errors, and then applied to three practical manufacturing processes in order to evaluate its effectiveness.     

Materials modelling: A bridge from atoms to bulk properties

The use of molecular-level materials modelling techniques in the development of advanced performance polymers is discussed, with particular emphasis upon bridging the large difference in the scales of dimensions between atomic structure and fabricated parts. The advantages and disadvantages of bulk quantitative structure-property relations and atomistic modelling are assessed, and the method of group interaction modelling is suggested as a means of bridging the dimensional scales.After a brief introduction to the concept of group interaction modelling, examples of modelling the engineering properties of polymers are presented which are difficult to model quantitatively by any other means. The important phase transitions from the crystal and glassy states of matter to those of rubber- and liquidlike states are shown quantitatively to be due to the same isoenergetic condition. The viscoelastic properties of a polymer are critical for many applications and expressions are derived for the loss and storage components of the complex modulus, with reference to failure initiation conditions. The effect of crosslinking in thermosets upon the glass transition temperature and viscoelastic properties is outlined. Finally, the scaling of time from atomic vibrations to the years involved in creep and ageing effects are discussed.     

分子印迹技术及其应用

分子印迹技术是将高分子科学、材料科学、生物学、化学工程等有机集成。基于分子印迹技术所制备的分子印迹聚合物具有选择性高、稳定性好、应用范围广等特点 ,近年来得到了日益广泛和深入的研究。介绍了分子印迹技术的原理、分子印迹聚合物的制备方法、分子印迹技术的应用场合和实例 ,并简要预测了分子印迹技术领域未来的发展趋势。     

Quantum chemical studies of Li cation binding to polyalkyloxides

A quantum chemical study of the binding of Li⁺ cation to polyalkyloxides has been carried out. The lithium cation interaction with three polyalkyloxides (polyethylene oxide (PEO), polytrimethylene oxide (PTMO), and polypropylene oxide (PPO)) has been investigated using ab initio molecular orbital theory at the HF/6-31G^* level with molecular models for the polymers. Coordination by one to six oxygens was considered. In addition, higher level calculations were carried out using G3(MP2) theory for coordination of Li⁺ by one oxygen. For coordination of lithium by one oxygen, the binding energy ordering is PTMO>PPO>PEO, with PTMO having the largest lithium cation affinity. The same ordering is found for larger coordination numbers with the exception of coordination by six oxygens, where the ordering changes due to the steric interactions.