共查询到18条相似文献,搜索用时 31 毫秒
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锂化学试剂中锂同位素丰度及原子量的异常刘卫国,肖应凯,周引民(中国科学院青海盐湖研究所,西宁810008)在1993年第37届国际纯粹与应用化学联会(IUPAC)上,原子量与同位素丰度委员会(CAWIA)根据世界上对锂化学试剂中锂同位素丰度异常的报道... 相似文献
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1 引言 化学元素的原子量是自然科学中的重要常数 ,它在科学技术领域中有广泛的应用 ,尤其在化学领域中是不可缺少的基本数据。如果没有原子量 ,物质的质量将不可能与摩尔量联系起来。在化学发展的进程中 ,原子分子学说与元素周期律均以原子量为基础。 早在 1 894年 ,美国化学会就发表了F .W .Clarke的极具准确性的原子量标准表 ,几年后德国化学会也开始发表原子量表。鉴于原子量的重要性 ,原子量应有国际一致的公认值 ,并应有一个国际性的机构统一负责定期公布原子量表 ,因此成立了由 3人 (美F .W .Clarke ,英T .… 相似文献
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张青莲教授是中国科学院院士,我国同位素化学的奠基人.本文介绍他在90高龄之际在原子量新值测定方面所取得的杰出成就.从1990年代初以来,他主持一个科研小组采用质谱法,实施了测定10项原子量新值的长期计划.至2001年7月已经有In、Ir、Sb、Eu、Ce、Er、Ge、Dy和Zn等9个原子量新值被国际纯粹与应用化学联合会(IUPAC)的原子量与同位素丰度委员会(CAWIA)正式确定为原子量的国际新标准;另外一个Sm原子量新值也于2005年被国际组织确认. 相似文献
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张青莲先生的原子量新值测定 总被引:1,自引:0,他引:1
1 九旬豪情再创辉煌 2 0 0 0年 3月 ,人民教育出版社发行的全日制普通高级中学教科书《化学》(第一册 )向全国高中生介绍了我国两位杰出化学家以及他们建树的足以使国人自豪的科学成就。其中之一是我国同位素化学的奠基人、中国科学院资深院士、北京大学化学学院教授张青莲先生。展示的业绩是张青莲先生于 90高龄之际在原子量新值测定方面所取得的举世瞩目的成果。 2 0世纪 90年代初以来 ,张青莲先生主持了一个科研小组 ,实施了测定 1 0项原子量新值的长期计划。现在这项在张先生 82岁高龄时正式启动的研究课题经过历时 1 2年的研… 相似文献
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介绍了IUPAC元素原子量2007-2017年版的变化情况及我国科学家在原子量测定方面所做的贡献,并指出了现行化学教材中的元素周期表和原子量表存在的问题,以期引起化学教材编写者及出版者的注意. 相似文献
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With enriched antimony isotopes of 99.224 atom% ~(121)Sb and 99.528 atom% ~(123)Sb, twotracer solutions were prepared, whose antimony content was ascertained by the isotopicdilution analysis utilizing an accurately assayed laboratory standard. Mass spectrometricmeasurements were made on a Finnigan MAT- 261 instrument to find the ratio of masses121 and 123. Five synthetic mixtures formed from the tracers served to determine thecorrection factor of mass discrimination. The isotopic abundances thus found for the anti-mony in the mineral stibnite together with the known nuclidic masses yield an accurateatomic weight of antimony as 121 .7575± 0 .0009. 相似文献
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通过用高浓缩同位素142Ce和140Ce配制9种混合样品,精确测定质谱计的系统误差校正系数,来校正用该仪器测定的天然铈的同位素丰度比,从而建立了准确测定铈同位素丰度的质谱分析方法,用这种绝对质谱法测定的铈相对原子质量是1401157±00008。该数值已于1995年为国际理论与应用化学联合会(IUPAC)的原子量与同位素丰度委员会所采纳 相似文献
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Oto Mestek Kateřina Mališová Richard Koplík Jan Polák Miloslav Suchánek 《Accreditation and quality assurance》2008,13(6):305-310
The postulated uncertainty of many commercially available standard solutions is estimated on the basis of uncertainties of individual preparation steps. The declared concentration of Cu standard solution (1000 ± 2) mg/L was verified by gravimetric analysis (found (1000.7 ± 0.4) mg/L), isotope dilution with commercial and laboratory-prepared isotope-enriched solutions (found (1000.6 ± 16.8) mg/L and (1002.4 ± 3.6) mg/L, respectively), and by atomic absorption spectrometry (found (1001.4 ± 5.3) mg/L). Uncertainty budgets of all used methods are given and the procedures of uncertainty estimation are fully documented. 相似文献
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Meyer VR 《Analytical and bioanalytical chemistry》2003,377(4):775-778
The mass fraction of a certain atom species in a molecule is needed for the calculation of the result of some chemical analyses. Common examples are gravimetric determinations (e.g., the sulfur concentration in a sample that can be obtained from the mass of precipitated barium sulfate). A similar problem is encountered when a reference solution of an ion is prepared by dissolution of a salt. This paper presents how the uncertainty of the mass fraction is calculated from the uncertainties of the atomic weights as published by IUPAC. The value is needed for the determination of the combined standard uncertainty of the analysis. Some calculated examples illustrate the mathematical considerations presented in the paper. 相似文献
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E. Robens P. Klobes D. Balköse S. Amarasiri A. Jayaweera 《Journal of Thermal Analysis and Calorimetry》2008,94(3):619-622
A short survey is given on mass units and recommendations on the proper use of the notations mass and weight.Whereas mass
is an inertial physical quantity in classical mechanics, weight is a force due to the gravitational field and depending on
the geographic situation. 相似文献
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Ángel Castillo Emma Gracia-Lor Antoni Francesc Roig-Navarro Juan Vicente Sancho Pablo Rodríguez-González J. Ignacio García Alonso 《Analytica chimica acta》2013
Isotope dilution mass spectrometry (IDMS) based on isotope pattern deconvolution (IPD) has been applied here to MS/MS (QqQ) in order to carry out the quantification and confirmation of organic compounds in complex matrix water samples without the use of a methodological IDMS calibration graph. In this alternative approach, the isotope composition of the spiked sample is measured after fragmentation by SRM and deconvoluted into its constituting components (molar fractions of natural abundance and labeled compound) by multiple linear regression (IPD). The procedure has been evaluated for the determination of the pharmaceutical diclofenac in effluent and influent urban wastewaters and fortified surface waters by UHPLC (ESI) MS/MS using diclofenac-d4 as labeled compound. Calculations were performed acquiring a part and the whole fragment cluster ion, achieving in all cases recoveries within 90–110% and coefficients of variation below 5% for all water samples tested. In addition, potential false negatives arising from the presence of diclofenac-d2 impurities in the labeled compound were avoided when the proposed approach was used instead of the most usual IDMS calibration procedure. The number of SRM transitions measured was minimized to three to make possible the application of this alternative technique in routine multi-residue analysis. 相似文献