端视电感耦合等离子体发射光谱测定保温材料中钠和钾的研究

本文利用端视电感耦合等离子体发射光谱建立了一种钠和钾的分析测定方法,优化了分析测试条件,方法对钠和钾氧化物的检出限分别为0.005和0.002μg/mL,将该方法用于保温材料中和钠的分析测定,获得了令人较为满意的结果.     

Analysis of questioned documents: A review

During the last years (2000–2014), many publications concerning the forensic analysis of questioned documents have been published, and new techniques and methodologies are nowadays employed to overcome forensic caseworks. This article reviews a comprehensive collection of the works focused on this issue, including dating studies, the analysis of inks from pens and printers, the analysis of paper, the analysis of other samples related to questioned documents and studies on intersecting lines. These sections highlight the most relevant analytical studies by a wide range of analytical techniques. Separation and spectrometric techniques are critically discussed and compared, emphasizing the advantages and disadvantages of each one. Finally, concluding remarks on the research published are included.     

电感耦合等离子体发射光谱法测定铝合金中痕量锡

本文报道了电感耦合等离子体发射光谱法测定铝合金中痕量锡，通过标准样品分析，加标回收实验以及对铝合金实际样品的不同分析测试手段锡的测定结果的相互对照，分析结果令人满意。该方法简便，快速，灵敏度高，适合于铝合金中低含量锡的分析测定。     

电磁波在非磁化等离子体中衰减效应的实验研究

针对等离子体隐身技术在航空航天领域的良好应用前景, 开展垂直入射到具有金属衬底的非磁化等离子体中电磁波衰减特性的理论与实验研究. 利用WKB方法对电磁波衰减随等离子体参数的变化规律进行了理论分析. 利用射频电感耦合放电方式产生稳定的大面积等离子体层, 搭建了等离子体反射率弓形测试系统, 进行了电磁波在非磁化等离子体中衰减效应的实验研究. 利用微波相位法和光谱诊断法, 得到不同放电功率下的等离子体电子密度, 其范围为8.17×10⁹–7.61× 10¹⁰ cm^-3. 本实验获得的等离子体可以使2.7 GHz 和10.1 GHz电磁波分别得到一定的衰减, 且电磁波衰减的理论与实验结果符合较好. 结果表明, 提高等离子体电子密度和覆盖均匀性有利于增强等离子体对电磁波的衰减效果.     

ICP-OES,AAS和AFS测定肝癌高发区红豆中23种矿质元素含量

收集了6种产自肝癌高发区——江苏省启东市的红豆和6种产自国内其他地区的红豆,经过微波消解或干灰化法处理后,采用电感耦合等离子体发射光谱法(ICP-OES)、原子吸收光谱法(AAS)和原子荧光光谱法(AFS)测定了其中A l、B、Ba、Ca、Cd、Co、Cr、Cu、Fe、Hg、K、Mg、Mn、Mo、Na、N i、P、Pb、Rb、S、Se、Sr和Zn共23种矿质元素的含量,并用生物标准参考物质黄豆评价了分析方法的准确度。结果表明,红豆中人体必需宏量、微量元素含量极为丰富,而传统意义上的有害元素Pb、Cd、Hg含量均较低;与国内其他产地的红豆相比,江苏省启东市产红豆中B、Mg含量显著偏高(P0.05),而大多数矿质元素含量两相比较并不存在显著性差异。产自江苏省启东市的部分红豆样品和产自江苏省海门市的红豆样品中Cd含量极低,预示着自然生态环境中有效态Cd缺乏可能与肝癌的高发病率和高死亡率存在一定程度的相关性。     

Sensitive inductively coupled plasma mass spectrometry assay for the determination of platinum originating from cisplatin, carboplatin, and oxaliplatin in human plasma ultrafiltrate

We present a highly sensitive, rapid method for the determination of platinum originating from the anticancer agents cisplatin, carboplatin, and oxaliplatin in human plasma ultrafiltrate. The method is based on the quantification of platinum by inductively coupled plasma mass spectrometry and allows quantification of 7.50 ng l-1 platinum in only 150 microl of matrix. Sample pretreatment involves dilution of samples with 1% HNO3. Validation fulfilled the most recent FDA guidelines for bioanalytical method validation. Validated ranges of quantification were 7.50 ng l-1 to 1.00x10(5) ng l-1 in plasma ultrafiltrate for all three platinum compounds. The assay is now successfully used to support pharmacokinetic studies in cancer patients treated with cisplatin, carboplatin, or oxaliplatin.     

Separation and preconcentration procedures for the determination of lead using spectrometric techniques: a review

Lead is recognized worldwide as a poisonous metal. Thus, the determination of this element is often required in environmental, biological, food and geological samples. However, these analyses are difficult because such samples contain relatively low concentrations of lead, which fall below the detection limit of conventional analytical techniques such as flame atomic absorption spectrometry and inductively coupled plasma optical emission spectrometry. Several preconcentration procedures to determine lead have therefore been devised, involving separation techniques such as liquid-liquid extraction, solid phase extraction, coprecipitation and cloud point extraction. Citing 160 references, this paper offers a critical review of preconcentration procedures for determining lead using spectroanalytical techniques.     

High-precision measurement of mercury isotope ratios in sediments using cold-vapor generation multi-collector inductively coupled plasma mass spectrometry

An on-line Hg reduction technique using stannous chloride as the reductant was applied for accurate and precise mercury isotope ratio determinations by multi-collector (MC)-ICP/MS. Special attention has been paid to ensure optimal conditions (such as acquisition time and mercury concentration) allowing precision measurements good enough to be able to significantly detect the anticipated small differences in Hg isotope ratios in nature. Typically, internal precision was better than 0.002% (1 RSE) on all Hg ratios investigated as long as approximately 20 ng of Hg was measured with a 10-min acquisition time. Introducing higher amounts of mercury (50 ng Hg) improved the internal precision to <0.001%. Instrumental mass bias was corrected using ²⁰⁵Tl/²⁰³Tl correction coupled to a standard-sample bracketing approach. The large number of data acquired allowed us to validate the consistency of our measurements over a one-year period. On average, the short-term uncertainty determined by repeated runs of NIST SRM 1641d Hg standard during a single day was <0.006% (1 RSD) for all isotope pairs investigated (²⁰²Hg/¹⁹⁸Hg, ²⁰²Hg/¹⁹⁹Hg, ²⁰²Hg/²⁰⁰Hg, and ²⁰²Hg/²⁰¹Hg). The precision fell to <0.01% if the long-term reproducibility, taken over 11 months (over 100 measurements), was considered. The extent of fractionation has been investigated in a series of sediments subject to various Hg sources from different locations worldwide. The ratio ²⁰²Hg/¹⁹⁸Hg expressed as δ values (per mil deviations relative to NIST SRM 1641d Hg standard solution) displayed differences from +0.74 to −4.00‰. The magnitude of the Hg fractionation per amu was constant within one type of sample and did not exceed 1.00‰. Considering all results (the reproducibility of Hg standard solutions, reference sediment samples, and the examination of natural samples), the analytical error of our δ values for the overall method was within ±0.28‰ (1 SD), which was an order of magnitude lower than the extent of fractionation (4.74‰) observed in sediments. This study confirmed that analytical techniques have reached a level of long-term precision and accuracy that is sufficiently sensitive to detect even small differences in Hg isotope ratios that occur within one type of samples (e.g., between different sediments) and so far have unequivocally shown that Hg isotope ratios in sediments vary within approximately 5‰.     

Schwermetalle in der Umwelt. Auf Ultra‐Spurensuche

The reliable determination of (ultra‐)trace elements is not a trivial task at all. Trace analyses of extremely clean environmental samples (ground water, snow, ice) require the cleanest sample collection and pre‐treatment procedures currently available, the most sensitive analysis techniques as well as highly motivated and well experienced lab personnel. It is only through the perfect interaction of all mentioned components that modern analysis strategies allow to answer succesfully questions of sociopolitical relevance. As such, looking back to ancient periods – through the analysis of ice cores – allows to put the current heavy metal pollution into perspective and to better predict future trends. Tap water or mineral water? What is better? Here too, modern ultra trace analysis opens news perspectives.     

鸡蛋和乌鸡蛋中12种金属元素含量的研究

本文利用原子荧光光度计(AFS)和电感耦合等离子体发射光谱仪(ICP)测定普通鸡蛋和乌鸡蛋中的12种金属元素的含量,方法操作简单、数据准确可靠,且具有良好的精密度,样品的回收率为88.0%～116.5%.从样品检测的结果来看,从金属元素的角度来讲乌鸡蛋的营养价值比鸡蛋的营养价值要高.