中子活化分析在微量元素与肿瘤研究中的应用（摘要）

肿瘤是一种严重威胁人类生命健康的疾病。研究表明，许多微量元素如砷、铬、碘、钼、硒等与肿瘤的发生发展有关。因而研究微量元素在肿瘤发生发展中的作用，对于治疗和预防该类疾病的发生有着极其重要的意义。在微量元素与肿瘤的研究中需要对各种生物材料中的微量元素含量及其赋存状态或化学形态进行分析。然而在人或动物体内大多数微量元素含量极低，化学形态复杂，所以肿瘤与微量元素关系的研究与微量元素的分析技术息息相关。目前用于生物微量元素的分析技术有许多，如原子吸收光谱、原子发射光谱、原子荧光光谱、X一射线荧光光谱和中子…     

人体子宫癌活组织中微量元素的中子活化分析

本文利用样品的低温干燥预处理技术和仪器中子活化分析方法,同时测定了人体子宫癌活组织中的29种微量元素,并分别与宫颈炎组织和正常组织比较,初步研究结果表明,子宫癌组织,宫颈炎组织和正常组织中Au,I,Se等微量元素有显著差异。     

中子活化分析在鄂尔多斯地区元素分析中的应用

利用中子活化对鄂尔多斯盆地油气田上方的地质样品进行了某些元素的检测,通过实验分析,得到了该地区岩石中某些元素的含量,并对该地区的放射性元素作出了评价,绘制了样品的稀土配分模式图和评价了当地的金属矿产资源情况.结果表明,在油气田的上方,放射性元素铀呈现出负异常;钍和钾无明显异常;岩石中的其它元素和中国大陆地壳元素丰度基本...     

痕量铼的同位素稀释中子活化分析

将同位素稀释法的准确性与中子活性分析（ＮＡＡ）的高灵敏度相结合，建立了一种新的痕量铼的测试方法，实验中对Ｒｅ的检出限为０．００４ｎｇ，全流程空白为０．０５ｎｇ，地于Ｒｅ含量为６４ｎｇ／ｇ的样品，在取样量为５０ｍｇ时，单次测定误差（２σ）为３．１％，测定Ｒｅ一为３０ｎｇ／ｇ的样品，本方法的２σ在３％以内，４次分析的ＲＳＤ为４．１％，而采用一般的ＮＡＡ，结果偏低约２０％，并且ＲＳＤ大于５％。     

活化分析

本文是《分析试验室》定期评述中“活化分析”课题的第二篇文章,它对我国活化分析领域在1988年9月～1990年10间的工作进展作了较全面的评述。内容包括活化分析在地球化学、宇宙化学、生命科学、环境科学、工业材料、考古、司法等领域中的应用;活化分析方法学中的化学预处理与放射化学处理;自动化方法;仪器、设备与计算机软件;以及近两年涌现出的一批新课题与新方法。     

石英流体包裹体中液相成分的中子活化分析

研究了应用中子活化分析技术分析石英流休包裹体液相成分中痕量元素的方法，并在超净实验室内完成了样品的清洗，爆裂及提取，蒸干等前处理过程，所建立的方法仅取１５ｇ粒径为０．４～０．８ｍｍ的石英样品，以３％硝酸浸泡清洗后，由真空热爆法打开包裹体，以１％硝酸浸取其液相在分，并且将样品独立地分为两份，分别以１．２×１０＾１３ｎ／ｓ．ｃｍ＾２和３．７×１０＾１３ｎ／ｓ．ｃｍ＾２的中子注量率辐照样品５ｍｉｎ和２４     

低空白镍锍试金预富集中子活化分析测定地球化学标准物质中的铂族元素

研究了镍锍试金预富集中子活化分析测定岩石样品中的铂族元素。纯化捕集剂氧化镍,大大降低了化学分离全流程铂族元素的空白。取样量为50g时,所需溶剂各元素的空白值为(ng/g):Pt<0.05、Pd<0.05、Os<0.01、Ru<0.05、Rh<0.05、Ir=0.002。用平面锗探测器测定Rh使测定下限降低了两个数量级,对几种国标地球化学标准物质的测定结果与推荐值基本符合。     

Determination of Trace Elements in Liquid Fuels by Instrumental Neutron Activation Analysis

Abstract

An instrumental neutron activation analysis with Ge(Li) γ -spectrometry and computer-assisted data reduction, has been developed for the determination of more than 20 elements in different liquid fuels. Organo-metallic standard solutions were mixed to obtain suitable standards. Two neutron irradiations and 4 γ-spectrometric measurements are required for each sample. Corrections were taken into account for a few spectrometric and nuclear interferences. The overall standard deviation for nearly all elements is mainly determined by counting statistics. The following elements can be determined : Na, Al, S, Cl, K, Sc, V, Cr, Fe, Co, Ni, Cu, Zn, As, Se, Br and La whereas the concentration of the following elements are mostly near the limit of detection: Mg, Mo, Sb, Ba, Th and Hg.     

Determination of Trace Elements in Tea and Coffee by Neutron Activation Analysis

Thermal neutron activation analysis, a high-resolution Ge(Li) gamma-ray spectrometer, and an IBM 360/67 digital computer were used to determine the concentration of Na, K, Sc, Cr, Mn, Fe, Co, Cu, Zn, Se, Br, Rb, Sb, Cs, and Hg in ground coffee and tea. This nondestructive multielement technique requires neither pre- nor postirradiation chemistry and eliminates problems of reagent contamination. The method is simple, precise and sensitive to 15 elements. Interferences from fast neutron (n, p) and (n, α) reactions are small and, if necessary, corrections may be applied easily. This technique can be applied to percolated tea and coffee.     

Determination of Trace Molybdenum in Biological Matrices by Neutron Activation Analysis

Based on consecutive extractions using bismuth diethyldithiocarbamate and thallium diethyldithiocarbamate as reagents, molybdenum was selectively and highly enriched from biological matrices, and then subjected to neutron activation analysis. Most of interfering elements, e.g., Na, K, Br, P, Fe, U, etc. were simultaneouly removed and the preconcentrated samples always showed only the r rays from molybdenum after neutron bombardment. Thus, molybdenum in the biological matrices could be accurately determined.     

The Determination by Neutron Activation Analysis of Selected Elements in Cigarettes

Abstract

Neutron activation analysis was used for the determination of Na, Al, CI, K, Ca, Sc, Mn, Cu, Br, and La in the tobacco, mainstream smoke condensate, paper, and dropped ash of the Kentucky Reference Cigarette (IRI). The procedure requires no sample transfers prior to activation and no radiochemical separations before counting.     

Determination of Trace Amount of Mercury in Human Hair by Neutron Activation Analysis

Trace amount of mercury in human hair has been determined by destructive neutron activation analysis. It was found that the contents of mercury in the hair of normal people in Taiwan area is the order of 6 ppm. It is of interest to point out that very little fluctuation is observed in the contents of mercury in human hair regardless of sex and age of the normal people under investigation. On the other hand for those people who are working in the caustic soda manufacturing plant in which mercury is used as cathode in the electrolysis process of saline water, the mercury contents in their hair are definitely much higher (ca. 30 times) than the average values of normal people.     

Determination of Elements in Japanese Standard Soil Materials by Means of Insturmental Neutron Activation Analysis

Instrumental neutron activation analysis (INAA), and inductively coupled plasma mass spectroscopy (ICP-MS) were applied to the determination of major elements and rare earth elements in Japanese Standard Soil Materials (NDG-1 to -8). Eight major elements, Al, Fe, Ti, Ca, Mg, Mn, K, and Na were determined by INAA. A comparison of the data for rare earth elements obtained by INAA and ICP-MS shows that the data of the contents determined by the two different analytical methods are in fairly good agreement with each other.     

Instrumental Neutron Activation Analysis of Trace Elements in Organs and Tissues of Zinc Deficient Mice

Eleven elements in ten organs and tissues of mice fed with Zn-deficient diet (Zn-def. mice) and those fed with control diet (control mice) were determined by INAA. Zinc concentrations in the organs of Zn-def. mice were not distinctly lower than those of control mice except for bone and pancreas, as similar to the predecessors' reported results. However, the Co content increased significantly in all the organs and tissues of Zn-def. mice compared with control mice. The organs and tissues observed were histologicaly normal and no typical symptoms of Zn deficiency disease were recognised. The results suggest that the change of Co-concentration may be regarded as a mark of the prestage for a Zn deficiency disease.     

An Internal-Standard Method for Determination of Trace Impurities in Semiconductor Grade Silicon by Neutron Activation Analysis

An internal-standard method^1–4) has been applied for the determination of La, Sb, Au, Cr and Ag in silicon single-crystal by neutron activation analysis using cobalt as an internal-standard element. No chemical separation is required in this case and the precision obtained with the present method is satisfactory.