TI C28X系列MCU电源管理设计TI C28X系列MCU电源管理设计

A brief summary of TI C28X MCU is presented in this paper. The key points of power management design for all C28X MCU based on different requirements on power management are proposed. Two different solutions of power management design with specific examples can help C28X MCU developers with technical advice and have positive impact on application of C28X MCU in the field of industrial control.中文摘要：本文对 TI C28X 系列 MCU 作了简要归纳和介绍 针对各款 MCU 对电源管理的不同要求,提出了全系列 MCU 的电源管理部分设计要点,总结了两类不同的电源管理设计方案,对每类方案均给出了具体的设计案例 为 C28X 系列 MCU 的电源管理设计提供了技术指导,对促进 C28X 系列 MCU 在工业控制领域内的应用有积极的意义.

Flat currents and solutions of the green-schwarz superstring on AdS(5)xS(5)

IEECAS SKLLQG

New vortex solutions of Jackiw-Pi model

Based on current phi-mapping topological theory, a kind of self-dual equations in Jackiw-Pi model are studied. We first obtain explicit, self-dual solutions that satisfy Liouville equation which contains delta-function. Then we get perfect vortex solutions which reflect the system's internal topological structure, and consequently the quantization of flux.

Pd/C-catalyzed hydrodehalogenation of aromatic halides in aqueous solutions at room temperature under normal pressure

The hydrodehalogenation of aromatic halides, catalyzed by Pd/C in aqueous solutions, yields arenes in short reaction times at room temperature under normal pressure. The nature of the solvents has an important influence on the reaction rates and the activity of the catalyst. The catalyst shows the highest activity in water. In the hydrodechlorination of 4-chlorohypnone, it was in water that C-Cl bond was easier to be hydrogenated, and in isopropanol that C=O was easier to be hydrogenated. (C) 2004 Elsevier B.V. All rights reserved.

Ultrafast vibrational and thermal relaxation of dye molecules in solutions

Intra- and intermolecular relaxations of dye molecules are studied after the excitation to the high-lying excited states by a femtosecond laser pulse, using femtosecond time-resolved stimulated emission pumping fluorescence depletion spectroscopy (FS TR SEP FD). The biexponential decays indicate a rapid intramolecular vibrational redistribution (IVR) depopulation followed by a slower process, which was contributed by the energy transfer to the solvents and the solvation of the excited solutes. The time constants of IVR in both oxazine 750 and rhodamine 700 are at the 290-360 fs range, which are insensitive to the characters of solvents. The solvation of the excited solutes and the cooling of the hot solute molecules by collisional energy transfer to the surrounding takes place in the several picoseconds that strongly depend on the properties of solvents. The difference of Lewis basicity and states density of solvents is a possible reason to explain this solvent dependence. The more basic the solvent is, which means the more interaction between the solute and the neighboring solvent shell, the more rapid the intermolecular vibrational excess energy transfer from the solute to the surroundings and the solvation of the solutes are. The higher the states density of the solvent is, the more favorable the energy transfer between the solute and solvent molecules is.