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71.
新的拓扑结构,新的调制方法和未来的宽能带隙的半导体器件技术将会满足电力电子系统更高效率,更高功率密度和更低成本的要求。但是,在设计过程中通过使用多范畴/多目标优化,亦即对设计变量都用最优值,也能显著地提高目前技术系统的性能。为了实现这些优化,首先需要对主电路建立一个综合的数学模型,包括热模型,DM和CM EMI滤波器模型。基于这些模型,可以得到诸如效率,功率密度等的多目标优化。这样,可以充分地使用设计自由度的所有等级,也允许确定根据诸如功率半导体器件的品质因数或磁芯材料的性质等基本技术决定的系统性能的敏感度。而且,能够容易地比较不同拓扑结构和识别固有性能的限制。本文首先描述设计一个电力电子变换器的主要功能要素的分析途径和一个线性设计过程。接着连接诸如电、磁、热和热-机设计范畴的元件模型,讨论基于这些连接模型的各个设计变量的优化。最后,研究不同范畴的耦合和实施这些耦合的等效电路的利用实例。  相似文献   
72.
This paper introduces a high-performance voltage-scalable SRAM design in a 32 nm strain-enhanced high-k + metal-gate logic CMOS technology. The 291 Mb SRAM design features a 0.171 ?m2 six-transistor bitcell that supports a broad range of operating voltages for low-power and high-frequency embedded applications. The tileable 128 kb SRAM subarray achieves 72% array efficiency with 4.2 Mb/mm2 bit density, and consumes 5 mW of leakage power at the supply voltage of 1 V. The design provides 4 GHz and 2 GHz of operating frequencies at the supply voltages of 1.0 V and 0.8 V, respectively. The integrated power management scheme features close-loop memory array leakage control, floating bitline, and wordline driver sleep transistor, resulting in a 58% reduction in subarray leakage power consumption.  相似文献   
73.
74.
The demand for decreasing cost and volume and also for increasing efficiency leads to a constantly increasing power density of converter systems. For maximizing the power density of a 5 kW telecom supply, an optimization procedure that automatically balances the switching frequency, semiconductor and passive losses, and thermal performance has been developed. This procedure and the belonging analytical converter and transformer models are presented in this paper. Moreover, the resulting optimized design, which has a power density of 10 kW/dm 3 and an efficiency of 94.5% at a height of 1 U, is presented.  相似文献   
75.
Perturbation of the Bray? Liebhafsky non‐oscillating subsystem (mixture of KIO3 and H2SO4), i.e., Dushman reaction (DR), by piroxicam (PX), was observed in an open reactor, i.e., in the continuously fed well‐stirred tank reactor (CSTR). Monitoring the response of DR to perturbations by different concentrations of PX allows developing a simple procedure for quantitative determination of this analyte in both bulk drug and pharmaceutical preparation (injection). A tentative perturbation mechanism of PX action on the DR matrix, based on a kinetic scheme that was suggested by Agreda et al., is proposed. The PX reactivity in DR has been generally related to the reaction of PX with hypoiodous acid (HIO) present in the matrix.  相似文献   
76.
ABSTRACT

Syntheses of 4-O-methyl-β-rhodomycins are described. Glycosylation (trimethylsilyl triflate, dichloromethane-acetone 10:1, -30 °C) of 4-O-methyl-10-O-p-nitrobenzoyl-β-rhodomycinone, obtained from β-rhodomycinone (βRMN) in a 6-step synthesis, with 1-O-tert-butyl(dimethyl)silylated derivatives of 4-O-acetyl- or 4-O-p-nitrobenzoyl-2,3,6-tri-deoxy-3-trifluoroacetylamino-β-L-arabino- and lyxo-hexopyranoses or 2,6-di-O-acetyl-2,6-dideoxy-β-L-lyxo-hexopyranose afforded 7-O-α-L-glycosyl-β-rhodomycinones. Removal of the O- and N-acyl groups with 0.1M and 1M NaOH gave the 7-O-(3-amino-2,3,6-trideoxy-α-L-arabino- and lyxo-hexopyranosyl)-4-O-methyl-β-rhodomycinones and 7-O-(2,6-dideoxy-α-L-lyxo-hexopyranosyl)-4-O-methyl-β-rhodomycinone.  相似文献   
77.
78.
Based on the combination of a three-phase diode bridge and a DC/DC boost converter, a new three-phase three-switch three-level pulsewidth modulated (PWM) rectifier system is developed. It can be characterized by sinusoidal mains current consumption, controlled output voltage, and low-blocking voltage stress on the power transistors. The application could be, e.g., for feeding the DC link of a telecommunications power supply module. The stationary operational behavior, the control of the mains currents, and the control of the output voltage are analyzed. Finally, the stresses on the system components are determined by digital simulation and compared to the stresses in a conventional six-switch two-level PWM rectifier system  相似文献   
79.
80.
Effect of hydrolysis time on molar mass, glass transition temperature, crystallinity, and resistance to thermooxidation at elevated temperatures was analyzed for Estanes 54600, 54610, and 54650. Kinetics of the hydrolysis can be plausibly described in terms of the first-order reaction with an average induction period of about 7 days. Reduction of molar mass induced by hydrolysis brings about an appreciable decrease in glass transition temperature, fraction of crystalline domains of soft segments, and thermooxidative stability. The latter effect is manifested by shortening of the lifetimes (related to 5% mass loss) the temperature dependence of which obeys the Arrhenius plot. The observed differences in hydrolysis resistance of Estanes can be related to their chemical composition.  相似文献   
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