Design criteria for tetradentate phenanthroline-derived heterocyclic ligands to separate Am(Ⅲ) from Eu(Ⅲ)

To design novel phenanthroline-derived soft ligands for selectively separating minor actinides from lanthanides, four tetradentate phenanthroline-derived heterocyclic ligands(BTPhen, BPyPhen, BPzPhen, and BBizPhen) were constructed and their complexation behaviors with Am(ⅡI) and Eu(ⅡI) were systematically investigated by density functional theory(DFT) coupled with relativistic small-core pseudopotential. In all the 1:1-type species, the metal ion is in the center of the cavity and coordinates with two nitrogen atoms(N1 and N1′) of the phenanthroline skeleton and the other two nitrogen atoms(N2 and N2′) of the auxiliary groups. The bond lengths of Am–N are comparable to or even shorter than those of Eu–N bonds because the ionic radii of Am(ⅡI) are larger than those of Eu(ⅡI). Additionally, the negative ΔΔGAm/Eu value for the reaction of [M(H2O)4-(NO3)3] + L → ML(NO3)3 + 4H2 O indicates that the complexation reaction of Am(ⅡI) is more energetically favorable than that of Eu(ⅡI); this can be considered as an important design criterion to screen phenanthroline-derived ligands for MA(ⅡI) extraction. According to this criterion, the selectivity of tetradentate phenanthroline-derived ligands for separating Am(ⅡI) over Eu(ⅡI) follows the order of BTPhen BBizPhen BPyPhen BPzPhen.     

磁致伸缩-压电联合激励凹筒型发射换能器

设计制作了一种新型磁致伸缩-压电联合激励凹筒型发射换能器,采用稀土超磁致伸缩材料Terfenol-D与PZT压电陶瓷作为联合激励元件,模拟计算与实测结果均表明,与采用单一振子激励的凹筒型发射换能器相比,此种新型换能器在保持尺寸小、频率低等优点的同时,显著拓宽了工作频带并提高了辐射声功率.换能器外型尺寸为φ88 mm×316 mm,水中谐振频率1.30 kHz,-3 dB带通Q值1.43,谐振频率下发射电压响应级135.1 dB.     

Robust tracking for MIMO nonlinear time-dependent mismatched uncertain systems: non-adaptive versus adaptive control

This paper considers the problem of robust output-tracking controlfor multi-input multi-output (MIMO) nonlinear systems in thepresence of mismatched time-dependent uncertainties. It firstgeneralizes the stable combined-variable perturbation method(SCVPM) which was proposed by Li et al. (1996) to derive a newrobust controller and its adaptive version for MIMO systemsto track a desired trajectory. It is shown that both controllersnot only stabilize the closed-loop systems but also guaranteethat the tracking errors remain in an O() neighbourhood of theorgin, where is a small design parameter of the controller.Moreover, the adaptive robust controller is only based on thenominal system, and no a priori data on the uncertainties areneeded. Therefore, it is more feasibly implemented than thenon-adaptive controller.     

现代数字物理教学连载⑩——在数字技术平台上的研究式学习

介绍了大学物理教学中,如何利用数字技术平台引导学生进行自主的研究式学习.首先是知识的拓展与转移,接着是教师指导下的研究与探索,最后是学生自主独立的研究与创新.实践证明,我们创造的这一教学方法对于培养学生的科学素质与能力十分奏效.     

Solvent extraction of uranium(VI) by p-tert-butylcalix[n]-arene acetate

The solvent extraction of U(VI) by p-tert-butylcalix[n]-arene acetate (H _n L) (n=4, 6, 8) has been studied. The effects of acidity in aqueous phase and concentration of extractant in organic phase on the distribution ratio were examined. It has been found that the distribution ratio is proportional to [H⁺]⁻² and [H _n L]_(O) and the extracted complex species is UO₂H _n ⁻²L. The equilibrium constants of the extraction reactions have been determined. The reaction mechanism is discussed.     

圆形工件正次品检验及再加工模型

针对圆形工件合格性检验问题建立了两个优化模型,运用Matlab软件进行编程求解,确定了圆心的位置,据此判断出工件一为正品,工件二为次品.接下来为判断能否将次品经过再加工使其成为正品,建立了模型三,并指出了对工件二的简单再加工方法.     

AVS-P3音频解码器的算法优化

基于嵌入式系统应用中实时解码对速度和存储空间的要求，通过分析AVS—P3解码器原理及其技术特点，以AV3 release version1为蓝本对AVS音频解码器进行结构和算法上的优化．其中时频变换模块对intIMDCT算法进行分析与处理，量化模块定点化处理和AVS解码器熵解码模块的实现算法提出了新的方法．经过ARM9平台测试，在音乐质量没有受到损害的前提下，解码速度比原来提高10倍以上，存储空间也减少了一半以上．     

多维随机变量的线性相关性

本文研究了n维随机变量分量间的线性相关性,给出了衡量线性相关性程度的量以及具有(在概率1意义下)严格线性关系的充分必要条件.     

一类带输入时滞的线性时滞系统的新型自适应控制

针对一类带输入时滞且状态时滞常数未知的线性时滞系统,基于LMI方法,采用一种Lyapunov-Krasovskii函数和新型带记忆的状态反馈控制,突破以往自适应控制对估计值的大小限制,研究了一种新型的对该类系统未知状态时滞常数进行自适应控制的控制器设计问题,并且通过带记忆控制器中的常数的适当选取使得带记忆控制始终能反映未知时滞,仿真例子显示了该种方法的有效性.     

荧光光谱结合表面增强拉曼光谱法研究紫檀芪与人血清白蛋白相互作用

在模拟人体生理条件下,应用荧光光谱和表面增强拉曼光谱法研究了紫檀芪(PTE)与人血清白蛋白(HSA)之间相互作用机制.结果表明,HSA的荧光能被PTE静态猝灭,并伴随有非辐射能量转移作用,两者形成了1:1复合物,结合距离r=1.495 nm,结合常数KA=1.12×104(298 K)、4.07×104(304 K)和2.45×105 L/mol(310 K).表面增强拉曼光谱研究揭示,PTE分子通过甲氧基与HSA进行结合;热力学数据表明,二者间的作用主要为疏水作用;标记竞争实验指出PTE优先结合HSA的位点Ⅲ.三维荧光光谱、同步荧光光谱和表面增强拉曼光谱结果显示,与PTE作用后,HSA构象发生变化,导致色氨酸残基周围环境疏水性降低,但对PTE分子构象影响不大.