混合溶剂对Ru(Ⅳ)萃取的研究

一、前言 在一定浓度盐酸介质中,Ru(Ⅳ)以RuCl_6~(2-)络阴离子状态存在,可被C类溶剂TOA(三辛胺)以离子缔合机制定量地萃入有机相。由实验得到在相同条件下,TOA对Ru(Ⅳ)的萃取率随稀释剂介电常数的增加而下降。     

The Interaction of Glymes with Surfactant Micelles

The critical micelle concentrations (CMC) values and counterion dissociation (α values) have been determined for a number of mixed micellar systems consisting of two typical ionic surfactants and glycol ethers (glymes) as cosurfactants, namely diethylene glycol dimethyl ether, diethylene glycol diethyl ether, triethylene glycol dimethyl ether, and tetraethylene glycol dimethyl ether. Conductance experiments were used to determine the CMC and α values of the mixed micelles as a function of glyme concentration in the aqueous mixed solvent. Favorable interactions between sodium dodecyl sulfate micelles and glyme cosurfactants were deduced from the decreases in the CMC values and the large increase in the α values of these systems as a function of increasing glyme concentration in the mixed solvents. In contrast to the anionic surfactant/glyme systems, in general, there appeared to be little favorable interactions between the surfactant and glymes when micelles of the cationic surfactant dodecyltrimethylammonium bromide were formed in water/glyme solvent systems containing an increasing amount of the glymes. The interaction of glymes with the surfactant micelles was examined closely via ¹³C nuclear magnetic resonance (NMR) chemical shifts for both surfactant and glyme carbons; these chemical shifts changes were interpreted in terms of the distribution and the localization of the glymes in the aggregates. Finally, partition constants, determined from two-dimensional diffusion-oriented spectroscopy (2D-DOSY) experiments, were used to calculate thermodynamic quantities of transfer of the glymes between the bulk phase and the self-assembled aggregates. All these results are interpreted in terms of the key contributions that both the glyme ethoxylated groups and alkyl endgroups make to the hydrophobic interactions.     

大气生物气溶胶的源排放与源解析研究进展

2019年新冠肺炎(COVID-19)的全球爆发引起了公众对生物气溶胶的广泛关注。生物气溶胶是大气气溶胶的重要组成部分。生物气溶胶由于具有普通气溶胶的理化性质和本身特有的生物学特性,在全球生态系统、气候变化、空气质量和公共卫生等领域均扮演十分重要的角色。然而,目前学术界对生物气溶胶的研究主要集中在采样监测、消杀防护以及其环境与健康效应等方面,关于源特性研究相对滞后。基于此,聚焦大气中微生物的来源现状,综述了最近20年来生物气溶胶的自然源和人为源排放特性研究进展,并阐述了影响源排放和输送过程的主要因素(如生物地理区域、土地利用类型和环境因素等),探讨了当前生物气溶胶的各种源解析方法。最后,给出了生物气溶胶来源下一步的研究展望,以期为深入理解生物气溶胶的来源、输送与变化机理,更好地评估大气微生物污染水平与监控病原体的气溶胶传播提供参考。     

锰离子掺杂对PZT-BCW压电陶瓷性能的影响

本文制备了锰离子掺杂的0．9SPZT-0．05Ba(Cu1／2W1／2)O3压电陶瓷，并对该压电陶瓷进行了XRD、SEM和微区成分分析。结果表明材料为钙钛矿结构，掺锰后材料的晶粒变大．但是该压电陶瓷的机械品质因数Qm大幅度提高，由60提高到490。     

基于回归模型的CPU超频仿真软件设计

为了帮助认识CPU超频问题并熟悉超频设置操作,进行CPU超频仿真软件设计的全面研究。分析CPU超频的影响因素,介绍超频的方法和操作流程;讨论软件的功能模块结构、模块的运行流程和样本数据的存储方法;重点研究CPU超频后的性能测试结果估计问题,并为此提出了建立回归模型的解决之道;详细探讨了VB.NET与Matlab混合编程的接口与实现途径,并以此种方式完成了程序代码的编写。试用表明,该软件功能完整、界面直观、使用简便,能够为理解超频理论和熟悉超频操作提供有效帮助。     

基于弹性网格混合特征的脱机手写维文识别

手写体维文识别技术的关键在于特征提取方法的选择。为探求一种可靠性高、可分性强的脱机手写维文特征提取方法,在分析现有方法的基础上,结合维吾尔文字词自身的特点,提出一种在局部特征上基于弹性网格区域笔划密度、方向分解特征,在全局特征上提取交叉点、环、弧形笔划、附加笔划、外围轮廓特征的混合特征提取方法。通过在IFN/ENIT标准数据库及自采样数据集的聚类分析实验,识别正确率分别达到85%、84.3%。结果表明,方法综合统计特征和结构特征提取的优点,具有较强的抗扰能力,可分性优于GSC法。     

提高丙烯和混合碳四产品收率的对策与措施

中国石油化工股份有限公司茂名分公司化工事业部乙烯装置随着运行周期的延长，高低压脱丙烷塔和脱丁烷塔结垢严重，分离效果变差，造成丙烯和混合碳四产品的收率降低。通过分析丙烯和混合碳四产品损失大、收率低的原因，提出对策并采取相应措施，从而有效地提高了丙烯和混合碳四产品的收率。     

Three-dimensional simulation using fixed coarse-grid thermal-fluid scheme and conduction heat transfer scheme in distinct element method

Three-dimensional simulation using particle-thermal-fluid coupling scheme with a mixed Lagrangian-Eulerian approach is presented and the scheme is described by extending author's previous research [Y. Shimizu, 2004. “Fluid Coupling in PFC2D and PFC3D”, numerical modeling in micromechanics via particle methods—2004, Proceeding of 2nd International PFC Conference, Balkema, 2004, pp. 281-287]. The scheme solves the continuity, Navier-Stokes (N-S) and thermal energy equations numerically in Eulerian Cartesian coordinates, then derives pressure, velocity vectors and temperature for each fixed cell by considering particle existence. On the other hand, driving forces and thermal energy from fluid are applied to the particles as external body forces and a source term in the force-displacement law and the heat transfer calculations, respectively. This paper describes the thermal scheme for both fluid and particles. Results of two- and three-dimensional simulations involving forced convective heat transfer by fluid and conduction heat transfer within particles are presented.     

Mechanosynthesis of complex oxides and preparation of mixed conducting nanocomposites for catalytic membrane reactors

Nanopowders of LaGaO₃- and LaMnO₃-based complex perovskites (P) and ceria-based fluorites (F) were prepared by mechanosynthesis. Compatible nanocomposites F + P and P + P with mixed ion and electron conducting (MIEC) properties were prepared and sintered at moderate temperatures up to dense ceramics. The obtained materials were studied by means of XRD, SEM, TEM, electrical conductivity measurements, temperature programmed (TP) reduction/oxidation and preliminary estimations of permeability were obtained. A new strategy based on the advantages of the mechanochemical ceramic approach is proposed to design multilayer ceramic membranes for CMR. Casting technology and one-step sintering were used for the production of thin film membranes with MIEC properties on porous substrates. The coarse fraction of as-milled powders from agglomerates with density 70% was used for the porous substrate, and fine fractions of aggregates with sizes <1 μm were used in preparation of composites for thin dense films. Ceria-based composites prepared by the Pechini route and/or mechanochemical method are proposed as materials for protecting thin films.