Cumulative indices for Spectrochima Acta, Part A and Spectrochimica Acta, Part B

This article is an electronic publication in Spectrochimica Acta Electronica (SAE), a section of Spectrochimica Acta, Part B (SAB). The hardcopy text is accompanied by an electronic archive, stored on the SAE homepage at http://www.elsevier.nl/locate/sabe. The archive contains data, index and program files. The main article discusses the bibliographical purpose of the program and data files. A collective index for Spectrochimica Acta for volumes since it was split into Parts A and B, and continuing through 1991 for SAA and 1997 for SAB, is presented in DBF format, along with rudimentary data entry and access software.     

Free energies of transfer of alkali halides from water to urea-water mixtures at 25°C from EMF measurements

The standard potentials_s E ^o of M/M⁺ (M=Li, Na, K, Rb, and Cs) electrodes in aqueous urea solutions containing 12, 20, 30 and 37% by weight of urea have been determined at 25°C from emf measurements on the cell M(Hg)/MCl (m), solvent/AgCl–Ag, from the activities of metals in amalgams by use of a similar type of cell in water, and from the values of_s E ^o of the Ag/AgCl electrode determined earlier. The standard free energies of transfer of MCl, G _t ^o (MCl), from water to the mixed solvents, computed by use of these values and those for the Ag–AgCl electrode, rise sharply from Li⁺ to Na⁺ but fall from Na⁺ to K⁺ and rather sharply from K⁺ to Cs⁺ with a maximum at Na⁺ in all the solvent compositions. This has been attributed to the superimposition of soft-soft interactions on the electrostatic interactions between the ions and the negative charge centers of the possible hydrogen-bonded solvent complexes in the mixed solvents. Comparison of G _t ^o (i) values for individual ions, obtained by a simultaneous extrapolation procedure, with those in aqueous mixtures of methanol,t-butanol, and dimethyl sulfoxide leads to the conclusion that the solvation of these ions in all these solvents is chiefly dictated by the acid-base type of ion-solvent interactions.     

Refractive index of water-AOT-n-heptane microemulsions

Refractive index measurements on water/AOT/n-heptane microemulsions as a function of the volume fraction of the dispersed phase (water plus AOT) and of the water/AOT molar ratio R have been performed at 25°C. The refractive index was found to vary monotonically with without any change in rate during the crossover of the percolation threshold. Such a behavior suggested that, well above the percolation threshold, the water-AOT-n-heptane microemulsions are still formed by water-containing AOT reversed micelles dispersed in the oil phase. The analysis of the experimental data allowed an evaluation the fraction of the water molecules bonded to the AOT head group as a function of R.     

片状化石燃料的循环流化床燃烧(Ⅰ)--片状颗粒的形貌描述和流态化阻力特征描述

比较了不同球形度概念对片状化石燃料的描述效果,研究了片状化石燃料球形度变化对其流态化特征的影响.分析了Krumbein球形度为0.1～0.4的京西无烟煤在一台50MW循环流化床锅炉上表现出来的特殊现象,如运行床温和炉膛压力大幅度波动、依靠排放冷渣保持稳定运行,揭示了这些现象发生的原因.     

谈谈企业全面业绩指标评价方法——平衡计分卡

分析了传统财务性业绩指标评价方法的缺陷，论述了非财务性业绩指标的几个方面，包括质量评价、交货效率评价、企业应变和创新能力评价、对雇员的评价、对售后服务的评价和对客户的评价等，并阐明了非财务性业绩指标评价方法的特点，进而认为将二者有机结合的平衡计分卡评价方法更具科学性和全面性，因而应是企业生产经营和管理的最优选择。     

基于ASP技术的研究生网上调剂系统的实现

针对五邑大学研究生招生调剂工作的现状,叙述了建立研究生网上调剂系统的必要性,提出了基于ASP技术的调剂系统实现方案.该系统应用于实际,加快了调剂信息的收集和处理速度,节省了大量的人力和财力.     

第指数函数与指数函数之比较

本文给出了第指函数的定义，讨论了第指数函数与指数函数的差异，结合它们的图象，分析了二者的不同特征。     

化学教科书评价指标体系的制定

化学教科书在学校教育中起着重要的作用．客观地、有效地、可操作性地评价化学教科书，对促进化学教科书质量的提高和教科书的多样化有着重要的意义．基于对化学教科书概念的界定、化学教科书的结构以及功能三个方面的分析。提出了构建化学教科书的评价指标体系．     

《内蒙古师范大学学报》(自然科学汉文版)主要文献计量指标评析

对《内蒙古师范大学学报》 （自然科学汉文版）1999-2003年的文献计量指标进行了统计和分析,并选取总被引频次、影响因子、即年指标、他引总引比四项指标与师范类高校学报进行了排序分析.结果表明,学报的各项指标比较稳定,并呈逐年上升趋势,但学报的整体水平不高,与许多同类期刊相比尚有较大差距.学报要改变办刊观念和办刊模式,突出个性和特色,提高学报的学术影响力.     

建立师范生教育技术技能评价和考核标准的若干问题探讨

通过关键要素调查法和问卷法筛选，确定教育技术技能评价的考核指标及权重，从而建立了用以考核师范生教育技术技能水平的指标体系．