SVPWM教学研究之重点解析

SVPWM是电力电子技术教学中的重要内容,本文对空间矢量调制的教学重点做了一个较为全面系统的梳理。重点阐述SVPWM的核心思想,特别是三相正弦交流电SVPWM的基本原理,严格证明了三相电压的空间矢量相等与线电压相等等价。同时,证明在SVPWM下,逆变器输出的最大圆为基本空间矢量构成的正六边形的内接圆、直流母线电压利用率提高了约15.4%。     

Voltammetry in Undiluted Acetic Acid. In Situ Determination of Water

Water present in undiluted acetic acid can be monitored in situ with Pt and Au microelectrodes using differential pulse and square‐wave voltammetries. Both reduction and oxidation peaks can be obtained. The best quantitative analytical results were obtained for the anodic peak, the Pt microelectrode, and differential pulse voltammetry. The anodic water peak is located at +1.55 V vs. the quasi reference Pt electrode. The voltammetric peak obtained at Pt electrode is apparently not a diffusional one, however, the calibration plot obtained by employing this peak is linear over a wide concentration range, up to 4 mol dm^?3. The detection limit has been estimated as 2.3 mM or 0.0043 v/v%. The developed method may be particularly useful, since the Karl Fischer method can not be used to determine water in glacial acetic acid due to the estrification reaction of acetic acid with methanol. A voltammetric wave of undiluted acetic acid could not be obtained in the positive and negative ranges of potential.     

OH-Induced shift from carbon to oxygen acidity in the side-chain deprotonation of 2-, 3- and 4-methoxybenzyl alcohol radical cations in aqueous solution: results from pulse radiolysis and DFT calculations

DFT calculations have been carried out for 2-, 3- and 4-methoxybenzyl alcohol radical cations (1⁺, 3⁺ and 4⁺, respectively) and the α-methyl derivatives 2⁺ and 5⁺ using the UB3LYP/6-31G(d) method. The theoretical results have been compared with the experimental rate constants for deprotonation of 1⁺-5⁺ under acidic and basic conditions. In acidic solution, the decay of 1⁺-5⁺ proceeds by cleavage of the C-H bond, while in the presence of ⁻OH all the radical cations undergo deprotonation from the α-OH group. This pH-dependent change in mechanism has been interpreted qualitatively in terms of simple frontier molecular orbital theory. The ⁻OH induced α-O-H deprotonation is consistent with a charge controlled reaction, whereas the C-H deprotonation, observed when the base is H₂O, appears to be affected by frontier orbital interactions.     

Study of a Catalytic Mechanism in Additive Differential Pulse Techniques

The new electrochemical double pulse technique, known as additive differential normal pulse voltammetry (ADNPV) when there is no restriction on the duration of both pulses, and additive differential pulse voltammetry (ADPV) when t₂?t₁, has been applied to a pseudo‐first‐order catalytic mechanism. The expressions obtained here are applicable to planar and spherical electrodes, of any radius. This is of great interest since the size of the electrode plays an important role in the preponderating of diffusive and kinetics processes. The signal obtained with this technique presents the same morphological characteristics as the triple pulse technique, double differential pulse voltammetry (DDPV) and is more advantageous than DDPV and than the double pulse one, differential pulse voltammetry (DPV).     

Voltammetric studies on the interactions between camazepam metabolic series and human serum albumin. Determination of oxazepam using adsorptive stripping voltammetry

The behaviour of oxazepam in adsorptive stripping voltammetry was studied taking into account those conditions which have an influence on the accumulation step (electrolyte, pH, time, potential, drop size and stirring rate), rest time and stripping step (pulse amplitude and scan rate). Oxazepam can be determined at a hanging mercury drop electrode by differential-pulse voltammetry in 0.008 M Britton-Robinson buffer at pH 2.0 with a ?0.50 V accumulation potential. Its detection limit was found to be 3.6 × 10^?10 M (30-s accumulation) and the relative standard deviation for oxazepam concentrations in the range 2.8 × 10^?8?4.0 × 10^?7 M is lower than 2.8% (80-s accumulation). In addition, a procedure using adsorptive stripping voltammetry was developed to study the interactions occurring between human albumin and the camazepam metabolic series (camazepam, temazepam and oxazepam). The interactions decreased in the order temazepam ? oxazepam ? camazepam and the groups and structural modifications favouring interaction were determined.     

非跟踪体制炮位侦察雷达目标自动识别技术的实现

非跟踪体制炮位侦察雷达要实现目标的自动识别,其关键技术是背景杂波的处理和对目标信号的识别。文中提出了采用脉冲积累技术,对非相参脉冲串信号处理进行视频积累,由门限判决器判断有无目标回波、抑制噪声和杂乱脉冲干扰,降低系统的虚警率;采用杂波存储技术存储全画面杂波,建立静态杂波图,有效地抑制地物杂波的影响;采用单片机主-从系统双机速度识别技术,对回波信号进行速度识别和相关处理,实现非跟踪体制炮位侦察雷达目标自动识别。     

基于SOA和NOLM的光脉冲放大与压缩的设计模型

设计了一种基于半导体光放大器(SOA)和非线性光学环镜(NOLM)的光脉冲放大与压缩的模型。数值研究结果表明:在NOLM中,当调节合适的控制脉冲的输入和初始时延时,具有较低峰值功率、宽度为几十皮秒的高斯信号脉冲经此模型放大压缩后,可以得到脉冲峰值增益高、脉冲宽度窄以及基本无基座的高质量超短信号光脉冲。     

微流控光脉冲调制器

为了解决常见光调制器偏振依赖或结构复杂的问题,本文基于微流控光学提出一种可控光脉冲调制器。利用基于T形结产生的离散液滴和全反射原理的微流控光开关,将连续光变换成数字脉冲信号,并通过调节液滴的长度和生成速率调制光脉冲的宽度和频率。所提微流控光脉冲调制器具有结构简单、插入损耗低、消光比高、易集成的优点。微流控光脉冲调制器的流场与光场特性被分析,结构被优化。研究结果显示：该光脉冲调制器的消光比为17.74 dB,插入损耗为0.49 dB。     

Cr∶LiSAF再生放大系统

设计了灯抽运Cr∶LiSAF(Cr∶LiSrAlF6)飞秒再生放大系统 ,对 80fs光脉冲 (展宽后约 10 3ps)进行了再生放大研究 ,获得了再生放大的输出能量与输入能量和放大倍率与放大往返次数间的关系 ,得到了 8× 10 5的放大倍率和 0 4mJ的单脉冲再生放大输出     

五阶非线性作用下光纤中类明孤子的演化特性

根据含五阶非线性微扰修正项的非线性薛定谔方程,采用变分法,导出了光纤中类明孤子各参数随传输距离演化的方程组,研究了脉宽与距离、啁啾与脉宽之间的关系,并对描述相位和频率的方程组用龙格-库塔算法进行了数值求解.结果表明:五阶非线性使类明孤子的脉宽压缩,可在一定程度上抵消初始啁啾和三阶色散对脉宽的展宽作用;五阶非线性对类明孤子的相位和频率演化特性的影响不明显,因而适度的五阶非线性(γ在0.0001到0.1之间)有利于类明孤子的稳定传输.