H. S. Peiser
United States Geological Survey
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Featured researches published by H. S. Peiser.
Journal of Physical and Chemical Reference Data | 1991
John Karl Böhlke; J. R. De Laeter; P. De Bièvre; H. Hidaka; H. S. Peiser; K.J.R. Rosman; Philip D. P. Taylor
The Commission on Atomic Weights and Isotopic Abundances of the International Union of Pure and Applied Chemistry completed its last review of the isotopic compositions of the elements as determined by isotope-ratio mass spectrometry in 2001. That review involved a critical evaluation of the published literature, element by element, and forms the basis of the table of the isotopic compositions of the elements (TICE) presented here. For each element, TICE includes evaluated data from the “best measurement” of the isotope abundances in a single sample, along with a set of representative isotope abundances and uncertainties that accommodate known variations in normal terrestrial materials. The representative isotope abundances and uncertainties generally are consistent with the standard atomic weight of the element Ar(E) and its uncertainty U[Ar(E)] recommended by CAWIA in 2001.
Pure and Applied Chemistry | 2002
Tyler B. Coplen; John Karl Böhlke; P. De Bièvre; T. Ding; Norman E. Holden; Jessica Hopple; H. R. Krouse; A. Lamberty; H. S. Peiser; Kinga Revesz; S.E. Rieder; K.J.R. Rosman; E. Roth; Philip D. P. Taylor; R. D. Vocke; Y. K. Xiao
Documented variations in the isotopic compositions of some chemical elements are responsible for expanded uncertainties in the standard atomic weights published by the Commission on Atomic Weights and Isotopic Abundances of the International Union of Pure and Applied Chemistry. This report summarizes reported variations in the isotopic compositions of 20 elements that are due to physical and chemical fractionation processes (not due to radioactive decay) and their effects on the standard atomic-weight uncertainties. For 11 of those elements (hydrogen, lithium, boron, carbon, nitrogen, oxygen, silicon, sulfur, chlorine, copper, and selenium), standard atomic-weight uncertainties have been assigned values that are substantially larger than analytical uncertainties because of common isotope-abundance variations in materials of natural terrestrial origin. For 2 elements (chromium and thallium), recently reported isotope-abundance variations potentially are large enough to result in future expansion of their atomic-weight uncertainties. For 7 elements (magnesium, calcium, iron, zinc, molybdenum, palladium, and tellurium), documented isotope variations in materials of natural ter- restrial origin are too small to have a significant effect on their standard atomic-weight uncertainties. This compilation indicates the extent to which the atomic weight of an element in a given material may differ from the standard atomic weight of the element. For most elements given above, data are graphically illustrated by a diagram in which the materials are specified in the ordinate and the compositional ranges are plotted along the abscissa in scales of (1) atomic weight, (2) mole fraction of a selected isotope, and (3) delta value of a selected isotope ratio.
Journal of Physical and Chemical Reference Data | 1994
P. De Bièvre; H. H. Ku; H. S. Peiser
The reliability of the (standard) atomic‐weight (mean atomic mass) values is quantified based on the analysis of changes made from published improved measurements as they become available for each periodic evaluation. This numerical analysis tests the evaluation procedures and the current reliability of the tables published by the International Union of Pure and Applied Chemistry. One instance of faulty evaluation is highlighted. The post facto test of past performance of evaluations might under appropriate conditions also serve for other data sets such as the fundamental constants of physics or property data for pure elements. §
Journal of Research of the National Institute of Standards and Technology | 1991
S. Valkiers; P. De Bievre; G. Lenaers; H. S. Peiser
In a series of gas mass-spectrometric measurements performed near the highest attainable accuracy, samples from two highly homogeneous batches of silicon crystals and silica powder were compared directly with a synthetic mixture of the three stable isotopes of silicon. Thereby, this work not only established the “absolute” atomic weight of these batches, but also makes portions of these batches available as an Isotopie Reference Material for accurate isotopic abundance measurements in geochemical and other isotope-abundance studies of silicon.
Pure and Applied Chemistry | 2009
John R. de Laeter; John Karl Böhlke; P. De Bièvre; H. Hidaka; H. S. Peiser; K.J.R. Rosman; Philip D. P. Taylor
Water-Resources Investigations Report | 2002
Tyler B. Coplen; Jessica Hopple; John Karl Böhlke; H. S. Peiser; S.E. Rieder; H. R. Krouse; K.J.R. Rosman; T. Ding; R. D. Vocke; Kinga Revesz; A. Lamberty; Philip Taylor; P. De Bievre
Archive | 2003
Isotopic Abundances; J. R. De Laeter; John Karl Böhlke; P. De Bièvre; H. Hidaka; H. S. Peiser; K.J.R. Rosman; Philip D. P. Taylor
Pure and Applied Chemistry | 1984
H. S. Peiser; Norman E. Holden; P. De Bièvre; I.L. Barnes; R. Hagemann; John R. de Laeter; T. J. Murphy; E. Roth; M. Shima; H. G. Thode
Fresenius Journal of Analytical Chemistry | 1997
P. De Bièvre; H. S. Peiser
Mass Spectrometry Reviews | 1992
John R. de Laeter; Paul De Bièvre; H. S. Peiser