Thermal aqueous liquid chromatography—the TALC technique

Thermal Aqueous Liquid Chromatography (TALC) using pure water as a mobile phase should be a very attractive technique promoting the use of liquid chromatography in routine analysis, either in the laboratory or in future on-line process control. This simple form of chromatography, the selectivity of which depends on the fixed phase only, would allow the use of flame ionization as an almost universal, low-cost detector in liquid chromatography. The potential of the TALC technique is illustrated by selected examples.     

Partial molar volumes of organic compounds in water. VI. α,ω-diaminoalkane hydrochlorides

Measurements of the partial molar volumes in water at 25°C of the mono-and dihydrochlorides of the ,-diaminoalkanes, up to a chain length of 10 carbon atoms, are reported. Volumes of ionization have been determined and the electrostriction of the solvent calculated. Effects of the substituents are felt up to the -carbon atom, but thereafter are only very weak or nonexistent.     

Radiative heat transfer analysis in pure water heater used for semiconductor processing

A simplified one-dimensional model is presented to analyze the non-gray radiative transfer in pure water heater used in the rinsing processes within semiconductor production lines, and the ray-tracing method is extended to simulate the radiative heat transfer. To examine the accuracy of the simplified model, the distribution of radiation absorption is determined by the ray-tracing method based the simplified model and compared with the data obtained by three-dimensional non-gray model in combination with Monte Carlo method in reference, and the effects of the water thickness on the radiation absorption are analyzed. The results show that the simplified model has a good accuracy in solving the radiation absorption in the pure water heater. The radiation absorption increases with the water thickness, but when the water thickness is greater than , the radiation absorption increases very slowly with the water thickness.     

Fluorimetric determination of aluminium in water by sequential injection through column extraction

A fluorimetric procedure for the determination of aluminium with matrix removal in drinking water is proposed. The system is based both on the solid phase extraction of aluminium on a new chelating resin (XAD-4 modified by grafting salicylic acid) and the fluorimetric detection of a complex formed between 8-hydroxyquinoline-5-sulfonic acid (HQS) and Al(III), after elution of the resin by hydrochloric acid. The sorption and elution of aluminium were studied in both competitive and non-competitive conditions, varying pH, flow-rates, volume and concentration of reagents, as well as time contact. The optimised procedure allows determination of Al³⁺ at the sub-ppb level (LOD: 0.2 g L^–1 for 1 ml of sample) within a working range of 0.2–500 g L^–1. The analytical procedure was successfully employed for the determination of aluminium in drinking water during and after flocculation/coagulation treatment processes.     

中国理论物理学家与生物学家结合的典范——回顾汤佩松和王竹溪先生对植物细胞水分关系研究的历史性贡献(上)

文章介绍了我国生物学家汤佩松先生和理论物理学家王竹溪先生42年前在植物生理学方面作出的一项具有重要历史意义的贡献．他们于1941年先于西方科学家二十多年提出解释植物细胞水分关系的热力学理论,首先引入了水势概念．然而这项贡献一直被埋没四十多年才得到承认．文章分析了汤佩松和王竹溪先生工作的内容、历史地位及其产生的背景,讨论了其在国内外的遭遇的原因及今日应当从中记取的教训．     

Nuclear Physics in Norway, 1933–1955

In the late 1940s and the 1950s, Norwegian nuclear scientists, engineers, and administrators were deeply split over their nation’s goals, organization, politics, and tools for research in nuclear physics. One faction was determined to build a nuclear reactor in Norway, while another fiercely opposed the reactor plans and focused on particle accelerators. The first faction comprised scientific entrepreneurs and research technologists, the second academic scientists, most of whom began their research careers in nuclear physics in the 1930s. To understand this conflict, I trace the development of nuclear research in Norway from the early 1930s to the mid-1950s, placing it within an international context. Roland Wittje is working on his habilitation thesis in the History of Science Unit at the University of Regensburg, Germany.     

Stability of low levels of perchlorate in drinking water and natural water samples

Perchlorate ion (ClO₄⁻) is an environmental contaminant of growing concern due to its potential human health effects, impact on aquatic and land animals, and widespread occurrence throughout the United States. The determination of perchlorate cannot normally be carried out in the field. As such, water samples for perchlorate analysis are often shipped to a central laboratory, where they may be stored for a significant period before analysis. The stability of perchlorate ion in various types of commonly encountered water samples has not been generally examined—the effect of such storage is thus not known. In the present study, the long-term stability of perchlorate ion in deionized water, tap water, ground water, and surface water was examined. Sample sets containing approximately 1000, 100, 1.0, and 0.5 μg l⁻¹ perchlorate ion in deionized water and also in local tap water were formulated. These samples were analyzed by ion chromatography for perchlorate ion concentration against freshly prepared standards every 24 h for the first 7 days, biweekly for the next 4 weeks, and periodically after that for a total of 400 or 610 days for the two lowest concentrations and a total of 428 or 638 days for the high concentrations. Ground and surface water samples containing perchlorate were collected, held and analyzed for perchlorate concentration periodically over at least 360 days. All samples except for the surface water samples were found to be stable for the duration of the study, allowing for holding times of at least 300 days for ground water samples and at least 90 days for surface water samples.     

Ultrasound-assisted dispersive liquid–liquid microextraction for the determination of six pyrethroids in river water

A simple ultrasound-assisted dispersive liquid–liquid microextraction method combined with liquid chromatography was developed for the preconcentration and determination of six pyrethroids in river water samples. The procedure was based on a ternary solvent system to formatting tiny droplets of extractant in sample solution by dissolving appropriate amounts of water-immiscible extractant (tetrachloromethane) in watermiscible dispersive solvent (acetone). Various parameters that affected the extraction efficiency (such as type and volume of extraction and dispersive solvent, extraction time, ultrasonic time, and centrifuging time) were evaluated. Under the optimum condition, good linearity was obtained in a range of 0.00059–1.52 mg L⁻¹ for all analytes with the correlation coefficient (r²) > 0.999. Intra-assay and inter-assay precision evaluated as the relative standard deviation (RSD) were less than 3.4 and 8.9%. The recoveries of six pyrethroids at three spiked levels were in the range of 86.2–109.3% with RSD of less than 8.7%. The enrichment factors for the six pyrethroids were ranged from 767 to 1033 folds.     

感应电压叠加器中水介质开关脉冲自击穿特性

设计了应用于感应电压叠加器中的水介质主开关与峰化开关,主开关的电极结构为“平板 环型”,峰化开关的电极结构为“环型”。研究了开关在300 ns脉冲电压下的自击穿特性,给出了不同工作电压下开关的间隙距离。实验结果表明,主开关与峰化开关的结构合理、击穿特性稳定、相互配合良好,峰化开关可以有效地峰化主脉冲,降低预脉冲的幅值。主开关的实验结果同时验证了Martin经验公式的适用性。