托卡马克工程试验混合堆等离子体性能的等值线图分析

本文简要叙述托卡马克工程试验混合堆等离子体概念设计的物理基础,对等离子体性能进行了等值线图(Plasma Operation Contour)分析。根据工程试验混合堆的要求,得出一组等离子体参数。     

SWITRIM��������ƺ�ʹ�øſ�

研制出了用于计算氚投料量在FEB聚变堆各个子系统中的分布及其随时间变化的数值模拟程序包SWITRIM。通过近5年的使用，表明其运行良好、计算结果可靠。用SWITRIM数值模拟研究了聚变堆起动过程中的“氚坑深度和氚坑时间”新现象。简单介绍了SWITRIM程序包的组成和用户使用说明以及最新的运用等。     

Addressing the metabolic activation potential of new leads in drug discovery: a case study using ion trap mass spectrometry and tritium labeling techniques

Metabolic activation of drug candidates to electrophilic reactive metabolites that can covalently modify cellular macromolecules may result in acute and/or idiosyncratic immune system-mediated toxicities in humans. This presents a significant potential liability for the future development of these compounds as safe therapeutic agents. We present here an example of an approach where sites of metabolic activation within a new drug candidate series were rapidly identified using online liquid chromatography/multi-stage mass spectrometry on an ion trap mass spectrometer. This was accomplished by trapping the reactive intermediates formed upon incubation of compounds with rat and human liver microsomes as their corresponding glutathione conjugates and mass spectral characterization of these thiol adducts. Based on the structures of the GSH adducts identified, potential sites and mechanisms of bioactivation within the chemical structure were proposed. These metabolism studies were interfaced with iterative structural modifications of the chemical series in order to block these bioactivation sites within the molecule. This strategy led to a significant reduction in the propensity of the compounds to undergo metabolic activation as evidenced by reductions in the irreversible binding of radioactivity to liver microsomal material upon incubation of tritium-labeled compounds with this in vitro system. With the efficiency and throughput achievable with such an approach, it appears feasible to identify and address the metabolic activation potential of new drug leads during routine metabolite identification studies in an early drug discovery setting.     

紫外线激活氚原子—制备氚标记单磷酸阿糖腺苷的研究

本文采用紫外线激活氚原子的方法,进行氚-氢同位素交换反应,制得氚标记单磷酸阿糖腺苷(9—~3H—mparaA)。产品的纯度是层析纯;放射性比活度16GBq.m mol~(-1);放射化学纯度92.0%。本法的优点是:交换反应温和、反应时间较短、不易破坏生物活性、引起的副产物少、产品分离和纯化较方便。     

A simple polymer electrolyte membrane system for enrichment of low-level tritium (3H) in environmental water samples

Tritium (³H) is an essential tracer of the Earth's water cycle; yet widespread adoption of tritium in hydrologic studies remains a challenge because of analytical barriers to quantification and detection of ³H by electrolytic pre-concentration. Here, we propose a simple tritium electrolytic enrichment system based on the use of solid polymer electrolyte membranes (PEMs) that can be used to enrich ³H in 250–3000?mL environmental water samples to a 10-mL final volume. The IAEA PEM-³H system reported here can produce high enrichment factors (>70-fold) and, importantly, removes some of the deterrents to conventional ³H enrichments methods, including the use of toxic electrolysis and neutralization chemicals, spike standards, a complex electrolysis apparatus that requires extensive cooling and temperature controls, and improves precision by eliminating the need for tracking recovery gravimetrics. Preliminary results with varying operating conditions show ³H enrichments to 70-fold and higher are feasible, spanning a wide range of tritium activities from 5 to 150 TU with a precision of ～4.5?%. Further work is needed to quantify inter-sample memory and to establish lower ³H detection limits. The IAEA PEM-³H system is open source, with 3-D CAD and design files made freely available for adoption and improvement by others.     

Characterization of the Insoluble Sludge from the Dissolution of Irradiated Fast Breeder Reactor Fuel

Insoluble sludge is generated in the reprocessing of spent fuel. The sludge obtained from the dissolution of irradiated fuel from the “Joyo” experimental fast reactor was analyzed to evaluate its chemical form. The sludge was collected by the filtration of the dissolved fuel solution, and then washed in nitric acid. The yields of the sludge weight were less than 1% of the total fuel weight. The chemical composition of the sludge was analyzed after decomposition by alkaline fusion. Molybdenum, technetium, ruthenium, rhodium, and palladium were found to be the main constituent elements of the sludge. X-ray diffraction patterns of the sludge were attributable to Mo₄Ru₄RhPd, regardless of the experimental conditions. The concentrations of molybdenum and zirconium in the dissolved fast reactor fuel solutions were low, indicating that zirconium molybdate hydrate is produced in negligible amounts in the process.     

Radioimmunologische Bestimmung von Pflanzenhormonen

In vorliegender Arbeit wird eine kurze Darstellung der Grundlagen, Erfordernisse, Vor- und Nachteile des Radioimmunoassay für Pflanzenhormone gegeben.

The purpose of this paper is to discuss briefly the basis, requirements, advantages, and disadvantages of radioimmunoassay with respect to plant hormones.     

Zur hydrogeologischen Interpretation von Isotopendaten im Zusammenhang mit Stofftransportprozessen

The migration of radionuclides and other tracers in porous layers is determined by substance transport. The physical and hydraulic basis of retardation is investigated. A definition of a factor of retardation is given, describing the ratio between the pore velocity of the water and the velocity of tracer migration. Consequences to the groundwater protection are discussed.     

Hydrogen Isotope Exchange Catalyzed by Ru Nanocatalysts: Labelling of Complex Molecules Containing N-Heterocycles and Reaction Mechanism Insights

Ruthenium nanocatalysis can provide effective deuteration and tritiation of oxazole, imidazole, triazole and carbazole substructures in complex molecules using D₂ or T₂ gas as isotopic sources. Depending on the substructure considered, this approach does not only represent a significant step forward in practice, with notably higher isotope uptakes, a broader substrate scope and a higher solvent applicability compared to existing procedures, but also the unique way to label important heterocycles using hydrogen isotope exchange. In terms of applications, the high incorporation of deuterium atoms, allows the synthesis of internal standards for LC-MS quantification. Moreover, the efficacy of the catalyst permits, even under subatmospheric pressure of T₂ gas, the preparation of complex radiolabeled drugs owning high molar activities. From a fundamental point of view, a detailed DFT-based mechanistic study identifying undisclosed key intermediates, allowed a deeper understanding of C−H (and N−H) activation processes occurring at the surface of metallic nanoclusters.     

MnCl_2改性γ-Al_2O_3毛细管填充柱气相色谱分析氢同位素

针对常规气相色谱填充柱分析稳定氢同位素的柱效低、峰宽大、保留时间长等问题,采用MnCl_2改性γ-Al_2O_3填充的石英毛细管柱开展了系统性柱效分析及氢同位素分析技术研究。研究结果表明,使用MnCl_2对γ-Al_2O_3进行改性后,可大大改善单纯的γ-Al_2O_3表面有序度、孔结构和吸附性质,并将正氢(o-H_2)和仲氢(p-H_2)峰洗脱在单一谱峰区域内。制备的长1.0 m、内径0.53 mm的石英毛细填充柱与热导检测器(TCD)级联测试,在体积浓度1至10 m L/L范围内有较好的线性关系,对于低浓度样品检测的相对误差不大于5%。H_2、HD和D_2的保留时间可分别缩短至39、46和60 s,检出限可分别降低至0.046、0.067和0.072 m L/L。毛细管填充柱较常规填充柱具有峰形尖锐、相邻组分分离度高、保留时间短、检出限低等优点,可用于低浓度氢同位素快速测量及氢同位素在线分析。