Reversibility of the low‐temperature transitions of polytetrafluoroethylene as revealed by temperature‐modulated differential scanning calorimetry

Temperature‐modulated differential scanning calorimetry reveals distinct differences in the kinetics of the low‐temperature phase transitions of polytetrafluoroethylene. The triclinic to trigonal transition at 292 K is partially reversible as long it is not complete. As soon as the total sample is converted, supercooling is required to nucleate the reversal of the helical untwisting involved in the transition. The trigonal phase can be annealed in the early stages after transformation with a relaxtion time of about 5 minutes. The dependence of the reversing heat capacity on the modulation amplitude, after a metastable equilibrium has been reached, is explained by a non‐linear, time‐independent increase of the heat‐flow rate, perhaps caused by an increased true heat capacity. The order‐disorder‐transition at 303 K from the trigonal to a hexagonal condis phase is completely reversible and time‐independent. It extends to temperatures as low as the transition at 292 K or even lower. Qualitatively, the thermal history and crystallization conditions of polytetrafluoroethylene do not affect the transition kinetics, that is, melt‐crystallized film and as‐polymerized powders show similar transition behaviors, despite largely different crystallinities. © 2001 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 750–756, 2001     

Isothermal crystallization of concentrated amorphous starch systems measured by modulated differential scanning calorimetry

The slow isothermal crystallization of concentrated amorphous starch systems is measured by Modulated Differential Scanning Calorimetry (MDSC). It can be followed continuously by the evolution (stepwise decrease) of the MDSC heat capacity signal (Cp), as confirmed with data from X-ray diffractometry, Dynamic Mechanical Analysis, Raman spectroscopy, and conventional Differential Scanning Calorimetry. Isothermal MDSC measurements enable a systematic study of the slow crystallization process of a concentrated starch system, such as a pregelatinized waxy corn starch with 24 wt % water and 76 wt % starch. After isothermal crystallization, a broad melting endotherm with a bimodal distribution is observed, starting about 10°C beyond the crystallization temperature. The bulk glass transition temperature (T_g) decreases about 15°C during crystallization. The isothermal crystallization rate goes through a maximum as a function of crystallization time. The maximum rate is characterized by the time at the local extreme in the derivative of Cp (t_max), or by the time to reach half the decrease in Cp (t_1/2). Both t_max and t_1/2 show a bell-shaped curve as a function of crystallization temperature. The temperature of maximum crystallization rate, for the system studied, lies as high as 75°C. This is approximately 65°C above the initial value of T_g. Normalized Cp curves indicate the temperature dependence of the starch crystallization mechanism. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 2881–2892, 1999     

Method for Finding the Exact Effective Hamiltonian of Time‐Driven Quantum Systems

Time‐driven quantum systems are important in many different fields of physics as cold atoms, solid state, optics, etc. Many of their properties are encoded in the time evolution operator or the effective Hamiltonian. Finding these operators usually requires very complex calculations that often involve some approximations. To perform this task, a systematic scheme that can be cast in the form of a symbolic computational algorithm is presented. It is suitable for periodic and non‐periodic potentials and, for convoluted systems, can also be adapted to yield numerical solutions. The method exploits the structure of the associated Lie group and a decomposition of the evolution operator on each group generator. To illustrate the use of the method, five examples are provided: harmonic oscillator with time‐dependent frequency (Paul trap), modulated optical lattice, time‐driven quantum oscillator, a step‐wise driving of a free particle, and the non‐periodic Caldirola‐Kanai Hamiltonian. To the extent of the authors' knowledge, whereas the exact form of Paul trap's evolution operator is well known, its effective Hamiltonian was until now unknown. The remaining four examples accurately reproduce previous results.     

低栅极电压控制下带有phenyltrimethoxysilane单分子自组装层的有机薄膜晶体管场效应特性研究

制作了底栅极顶接触有机薄膜晶体管器件,60 nm的pentacene被用作有源层,120 nm热生长的SiO₂作为栅极绝缘层.通过采用不同自组装修饰材料对器件的有源层与栅极绝缘层之间的界面进行修饰,如octadecyltrichlorosilane （OTS）,phenyltrimethoxysilane （PhTMS）,来比较界面修饰层对器件性能的影响.同时对带有PhTMS修饰层的OTFTs器件低栅极电压调制下的场效应行为及其载流子的传输机理进行研究.结果得到,当|V 关键词： 有机薄膜晶体管 自组装单分子层 场效应迁移率 低栅极调制电压     

半导体特性的调制自由载流子吸收变距频率扫描方法研究

根据调制自由载流子吸收（modulated free carrier absorption,MFCA）检测技术的三维理论模型,采用变间距频率扫描方式测量单晶硅样品的电子输运参数,进行了仿真与实验,对结果进行了分析;通过多参数拟合,获取了测试样品的载流子扩散系数、少数载流子寿命和前表面复合速度.仿真与实验都表明,变间距频率扫描结合多参数拟合,可以提高输运参数的测量精度. 关键词： 调制自由载流子吸收 电子输运参数 变间距频率扫描 多参数拟合     

激光调制气溶胶红外诱饵对成像制导导弹的干扰分析

概述了气溶胶红外诱饵的工作原理、特点、现状及其发展趋势。介绍了一种新型气溶胶红外诱饵———激光调制气溶胶红外诱饵。仿真实验表明,与传统的红外诱饵相比,激光调制气溶胶红外诱饵有效地增强了保护目标和对抗红外成像制导武器的能力,是气溶胶红外诱饵发展的一个新方向。     

Bipyridine‐Modulated Palladium‐Catalyzed Oxidative Heck‐Type Reactions of Arylboronic Acids with Olefins

We have demonstrated that 4,4′‐dimethyl 2,2′‐bipyridine as ligand for Pd(II) catalysts was very efficient for oxidative Heck‐type coupling reaction of arylboronic acids with olefins in DMA or CH₃CN under atm air at 80 °C. The presence of chelated bipyridine ligand isindispensable to achieve high reaction yields and to suppress the formation of biphenyl as homocoupled byproduct.     

Distribution sensitivity in a highway flow model

We examine a model of traffic flow on a highway segment, where traffic can be impaired by random incidents (usually, collisions). Using analytical and numerical methods, we show the degree of sensitivity that the model exhibits to the distributions of service times (in the queueing model) and incident clearance times. Its sensitivity to the distribution of time until an incident is much less pronounced. Our analytical methods include an M/G_t/∞ analysis (G_t denotes a service process whose distribution changes with time) and a fluid approximation for an M/M/c queue with general distributions for the incident clearance times. Our numerical methods include M/PH₂/c/K models with many servers and with phase‐type distributions for the time until an incident occurs or is cleared. We also investigate different time scalings for the rate of incident occurrence and clearance. Copyright © 2009 John Wiley & Sons, Ltd.     

弹光调制光电转换放大电路设计

弹光调制干涉具调制的干涉光被探测器接收后输出高速变化的微弱电信号,能否将该电信号提取并放大输出对弹光调制-傅里叶变换光谱仪的研制至关重要。通过对调制干涉光进行理论分析,设计一种具有高信噪比和较高带宽的光电转换放大电路,主要由电源电路、光电转换电路、放大电路、理论通频带为100 kHz~3.5 MHz的带通滤波电路组成。实验结果表明:设计的电路能够将探测器输出的最大频率为1.6 MHz的信号放大至670 mV左右,实现了将探测器输出的微弱速变电信号从背景噪声中有效提取与放大,为后续傅里叶变换提供可靠数据。