Isothermal curing of an epoxy resin by alternating differential scanning calorimetry

The quasi-isothermal curing of a diepoxide resin with a triamine of polyoxypropylene was studied by alternating differential scanning calorimetry (ADSC), which is a temperature modulated DSC technique. The complex heat capacity measurements allows to analyse the vitrification process at curing temperatures (T_c) below the maximum glass transition of the fully cured epoxy (T_g∞=85.8°C). Initially, the modulus of the complex heat capacity, |C^*_p|, increases until a maximum (conversion between 0.42 and 0.56) and then decreases. This step is followed by an abrupt decay of |C^*_p|, due to the vitrification of the system, which allows the determination of the vitrification time. This value agrees well with that determined by the partial curing method. The phase angle and out-of-phase heat capacity show an asymmetric wide peak during the vitrification process. The change in |C^*_p| at vitrification decreases with the increase of T_c becoming zero at temperature T_g∞. This epoxy-triamine system shows a delay of the vitrification process respect to other model epoxy systems probably due to the presence of polyoxypropylene chains in the network.

The decay of |C^*_p| during vitrification may be normalised between unity and zero by defining a mobility factor. This mobility factor has been used to simulate the reaction rate during the stage where the reaction is controlled by diffusion. The observed reaction rate is simulated by the product of the kinetic reaction rate, determined by the autocatalytic model, and the mobility factor.     

A Theoretical Approach to Temperature Modulated Power Compensation DSC

The steady state of temperature modulated power compensation DSC has been theoretically investigated for measurements of complex heat capacity, taking accounts of heat capacities of heat paths, heat loss to the environment, and mutual heat exchange between the sample and the reference material. Thermal contact between the sample cell and the cell holder is also taken into accounts. Rigorous and general solutions are obtained. From these solutions application of the technique to heat capacity measurements is discussed. This revised version was published online in August 2006 with corrections to the Cover Date.     

实用化双折射式光纤温度传感器系统最佳设计

利用双折射效应和偏振调制原理,设计了一种实用化的反射式光纤温度传感器,分析了精度、灵敏度等的主要指标与光源、双折射晶体及传输光纤之间的相互关系,并进行了相应的实验,给出了系统参数选择的最佳设计方案。     

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。