TY - CONF A1 - Tütken, T. A1 - Tatzel, Michael A1 - Vogl, Jochen A1 - Rosner, M. T1 - Assessing δ26Mg in bioapatite as proxy for faunivory N2 - Knowledge about feeding behavior is essential to determine trophic interactions and reconstruct predator-prey relationships in modern and past foodwebs. Traditionally, nitrogen isotopes (δ15N) of collagen are used to quantify the ingestion of animal protein, however collagen usually does not preserve over geological time scales. To infer the diet of extinct vertebrates from fossil material more resistant dietary proxies such as Ca and Mg isotopes are needed, which are major elements in the bioapatite of bones and teeth. Magnesium is a bio-essential element that replaces calcium in the bioapatite lattice and bone and enamel δ26Mg values of extant mammals increase systematically along the foodchain [1, 2]. The existing δ26Mg data, however, is scarce, in particular with respect to carnivores, thus still limiting the capability of this dietary proxy to reliably determine trophic differences between plant- and animal-feeders. To better constrain trophic-level effects recorded in Mg isotopes, we analyzed δ26Mg of bioapatite from modern mammals with a focus on faunivores, both carnivores and as yet unexplored insectivores. The trophic level effect of δ26Mg is influenced by the geological substrate which causes isotope variability in δ26Mg of faunal remains between different ecosystems [1, 2]. Therefore, as first-order proxy for sample provenance and to assess potential influences of the bedrock substrate of the animals´ habitats on δ26Mg of bones and teeth, we measured the 87Sr/86Sr on the same specimens. This information will enable us to refine trophic level effects and determine whether δ26Mg can be used to distinguish different faunivores isotopically. This will be of paramount importance for dietary reconstructions of trophic niches in fossil foodwebs. [1] Martin et al. (2014) Geochmica Cosmochimica Acta 130, 12-20. [2] Martin et al. (2015) Proceedings of the National Academy of Sciences 112, 430-435. T2 - Goldschmidt CY - Paris, France DA - 13.08.2017 KW - Magnesium stable isotopes KW - Isotope fractionation KW - Trophic level KW - 87Sr/86Sr KW - Provenance PY - 2017 AN - OPUS4-41535 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Biofuels - Background & analytical tools to trace back T2 - EURAMET-Meeting, EMRP Workshop CY - Bucharest, Romania DA - 2009-02-04 PY - 2009 AN - OPUS4-18797 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Development and validation of a single collector ICPMS procedure to determine boron isotopic compositions of water and food samples T2 - European Geosciences Union, General Assembly 2010 CY - Vienna, Austria DA - 2010-05-02 PY - 2010 AN - OPUS4-21565 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Pritzkow, Wolfgang T1 - Isotope reference materials for present and future isotope research N2 - Isotope reference materials are essential to enable reliable and comparable isotope data. This article reviews the work in this field within the past years. The focus is on all stable elements, except for classical stable isotopes (H, C, N, O, S) and for radioactive elements. Currently available isotope reference materials are listed. The limitations of synthetic isotope mixtures being used to characterize these materials are discussed, as well as the limitations of the isotope reference materials, such as uncertainty and homogeneity. The needs for present research on isotope variations are being considered and are compared to the limitations of current isotope reference materials. This disagreement between both can only be solved by providing isotope reference materials defining a δ-scale for each element of interest. Such materials should be provided with additional data on isotope abundances whenever possible. As an outlook a possible outline for a new program on isotope reference materials is discussed. KW - IRM KW - Isotope reference materials KW - Delta-RM KW - ICPMS KW - TIMS KW - Synthetic mixtures PY - 2010 DO - https://doi.org/10.1039/c000509f SN - 0267-9477 SN - 1364-5544 VL - 25 SP - 923 EP - 932 PB - Royal Society of Chemistry CY - London AN - OPUS4-21841 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotope Dilution Mass Spectrometry - A primary method of measurement and its role for RM certification T2 - Workshop on Metrology in Chemistry at NPL CY - New Delhi, India DA - 2009-02-16 PY - 2009 AN - OPUS4-19136 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rosner, Martin A1 - Pritzkow, Wolfgang A1 - Vogl, Jochen A1 - Voerkelius, S. T1 - Boron isotope compositions of crop plants: A new tracer for the origin and authenticity of food T2 - TRACE 5th Annual Meeting and Conference CY - Freising, Germany DA - 2009-04-01 KW - Boron isotopes in food KW - Provenance studies KW - Reference materials KW - Analytical uncertainty PY - 2009 IS - Session A / Part I SP - 1 EP - 2 AN - OPUS4-20293 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Traceability in Environmental Analysis Possible Routes and examples from Germany for elemental analysis T2 - Seminar: Metrology in Chemistry CY - New Delhi, India DA - 2010-03-12 PY - 2010 AN - OPUS4-21030 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Development and validation of a single collector ICPMS procedure for the determination of boron isotopic variations in food and water samples T2 - 9. Symposium Massenspektrometrische Verfahren der Elementspurenanalyse, 22. ICP-MS Anwendertreffen CY - Berlin, Germany DA - 2010-09-06 PY - 2010 AN - OPUS4-22562 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Pritzkow, Wolfgang T1 - Isotope dilution mass spectrometry - a primary method of measurement and its role for RM certification KW - IDMS KW - Reference materials KW - Metrology KW - ICPMS KW - TIMS PY - 2010 SN - 0970-3950 VL - 25 IS - 3 SP - 135 EP - 164 PB - Metrology Society of India CY - New Delhi AN - OPUS4-22603 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Rosner, Martin A1 - Pritzkow, Wolfgang T1 - Development and validation of a single collector SF-ICPMS procedure for the determination of boron isotope ratios in water and food samples N2 - Boron isotope studies on technical materials and geological and environmental samples are one hot topic in nowadays isotope research. Provenance studies of artefacts, food and other products might become another one, as several recent studies demonstrate. Typically boron isotope determinations have been carried out by TIMS. To open up this research field to a broader scientific community we developed two analytical procedures for boron isotope determinations based on single collector SF-ICPMS combined with a sample preparation procedure consisting of dry-ashing and a three step ion chromatographic boron-matrix separation. The developed procedures consist of one low resolution (LR) and one medium resolution (MR) procedure. The repeatability for the δ11B determination in three independently measured aliquots lies between 0.2 and 0.8‰ for the LR procedure and between 0.3 and 1.5‰ for the MR procedure. The expanded uncertainties with a coverage factor of k=2 range between 1.4 and 1.6‰ for the LR procedure and between 2.9 and 3.2‰ for the MR procedure. The accuracy, expressed as average deviation from the reference values, is 0.43‰ for the LR procedure and 0.33‰ for the MR procedure. To test the practicability of the procedures the matrix tolerance has been investigated as well and was found to be up to 2 mg kg-1 of alkaline and alkaline earth elements in the final measurement solution containing 100 µg kg-1 boron. Thus a highly efficient matrix separation for SF-ICPMS boron isotope determinations is required, similar to TIMS. PY - 2011 DO - https://doi.org/10.1039/c0ja00220h SN - 0267-9477 SN - 1364-5544 VL - 26 IS - 4 SP - 861 EP - 869 PB - Royal Society of Chemistry CY - London AN - OPUS4-23419 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rosner, Martin A1 - Pritzkow, Wolfgang A1 - Vogl, Jochen A1 - Voerkelius, S. T1 - Development and validation of a method to determine the boron isotopic composition of crop plants N2 - We present a comprehensive chemical and mass spectrometric method to determine boron isotopic compositions of plant tissue. The method including dry ashing, a three-step ion chromatographic boron–matrix separation, and 11B/10B isotope ratio determinations using the Cs2BO2+ graphite technique has been validated using certified reference and quality control materials. The developed method is capable to determine δ11B values in plant tissue down to boron concentrations of 1 mg/kg with an expanded uncertainty of ≤1.7‰ (k = 2). The determined δ11B values reveal an enormous isotopic range of boron in plant tissues covering three-quarters of the natural terrestrial occurring variation in the boron isotopic composition. As the local environment and anthropogenic activity mainly control the boron intake of plants, the boron isotopic composition of plants can be used for food provenance studies. KW - Boron isotope variations KW - Delta-scale KW - Stable isotopes KW - Isotope reference materials KW - Provenance KW - Authenticity PY - 2011 DO - https://doi.org/10.1021/ac102836h SN - 0003-2700 SN - 1520-6882 VL - 83 IS - 7 SP - 2562 EP - 2568 PB - American Chemical Society CY - Washington, DC AN - OPUS4-23495 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Report from the KCRV working group meeting T2 - CCQM-IAWG-Meeting CY - Paris, France DA - 2008-04-01 PY - 2008 AN - OPUS4-17516 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotope ratio measurements - An Introduction T2 - CCQM IAWG-Meeting, Workshop "Isotope Ratios" CY - Paris, France DA - 2008-04-01 PY - 2008 AN - OPUS4-17517 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Characterization of isotope and matrix reference materials using multicollector instruments T2 - 8th International Sector Field ICPMS Conference CY - Ghent, Belgium DA - 2009-09-14 PY - 2009 AN - OPUS4-20434 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotope Reference Materials for Future Isotope Research T2 - IUPAC-Meeting, Kommission für die Atomgleichgewichtsbestimmung CY - Vienna, Austria DA - 2009-07-23 PY - 2009 AN - OPUS4-20436 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kipphardt, Heinrich A1 - Matschat, Ralf A1 - Vogl, Jochen A1 - Gusarova, Tamara A1 - Czerwensky, Michael A1 - Heinrich, Hans-Joachim A1 - Hioki, A. A1 - Konopelko, L.A. A1 - Methven, B. A1 - Miura, T. A1 - Petersen, O. A1 - Riebe, Gundel A1 - Sturgeon, R. A1 - Turk, G.C. A1 - Yu, L. L. T1 - Purity determination as needed for the realisation of primary standards for elemental determination: status of international comparability N2 - Within the National Metrology Institutes (NMIs) and designated laboratories, an interlaboratory comparison, CCQM-P107, was conducted to verify the degree of international comparability concerning the results of purity analysis. The mass fractions of Ag, Bi, Cd, Cr, Ni, Tl at the lower mg/kg-level in a high purity zinc material were determined, but the real measurand in metrological sense was the sum of the six mass fractions. Homogeneity was investigated by glow discharge mass spectrometry, reference values were obtained using isotope dilution mass spectrometry. Six NMIs participated, contributing eight independent data sets. The agreement amongst the results of the participants, their median and the agreement with the reference values were usually excellent and in almost all cases below the target uncertainty of 30% relative. In this manner, the accuracy of results and the comparability between the participants was demonstrated to be established. KW - Interlaboratory comparison KW - Purity analysis KW - High purity metals KW - CCQM-P107 KW - Zinc PY - 2010 DO - https://doi.org/10.1007/s00769-009-0557-0 SN - 0949-1775 SN - 1432-0517 VL - 15 IS - 1 SP - 29 EP - 37 PB - Springer CY - Berlin AN - OPUS4-20767 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Semkova, V. A1 - Reimer, P. A1 - Altzitzoglou, T. A1 - Plompen, A.J.M. A1 - Quétel, C. A1 - Sudár, S. A1 - Vogl, Jochen A1 - Koning, A.J. A1 - Qaim, S.M. A1 - Smith, D.L. T1 - Neutron activation cross sections on lead isotopes KW - Cross sections KW - Neutron activation KW - Lead isotopes PY - 2009 DO - https://doi.org/10.1103/PhysRevC.80.024610 SN - 0556-2813 SN - 1089-490X VL - 80 IS - 2 SP - 024610-1 - 024610-12 PB - Inst. CY - Woodbury, NY, USA AN - OPUS4-20698 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rosner, Martin A1 - Pritzkow, Wolfgang A1 - Vogl, Jochen T1 - Boron isotope compositions of food: A potential tool for food authentication T2 - Jahrestagung Deutsche Mineralogische Gesellschaft 2008 CY - Berlin, Deutschland DA - 2008-09-14 KW - Boron isotopes KW - Food KW - Provenance studies PY - 2008 SP - 1 CY - Berlin AN - OPUS4-20785 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ma, L. A1 - Feng, L. A1 - Hioki, A. A1 - Cho, K.H. A1 - Vogl, Jochen A1 - Berger, Achim A1 - Turk, G. A1 - Macleod, S. A1 - Labarraque, G. A1 - Tong, W.F. A1 - Schiel, D. A1 - Yafa, C. A1 - Valiente, L. A1 - Konopelko, L.A. A1 - Quetel, C. A1 - Vermaercke, P. A1 - Manzano, J.V.L. A1 - Linsky, M. A1 - Cortés, E. A1 - Tangpitayakul, S. A1 - Plangsangmas, L. A1 - Bergamaschi, L. A1 - Hearn, R. T1 - International comparison of the determination of the mass fraction of cadmium, chromium, mercury and lead in polypropylene: the Comité Consultatif pour la quantité de matière pilot study CCQM-P106 KW - Cadmium KW - Chromium KW - Mercury KW - Lead KW - Polypropylene KW - CCQM PY - 2010 DO - https://doi.org/10.1007/s00769-009-0574-z SN - 0949-1775 SN - 1432-0517 VL - 15 IS - 1 SP - 39 EP - 44 PB - Springer CY - Berlin AN - OPUS4-20787 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Koenig, Maren A1 - Pritzkow, Wolfgang A1 - Riebe, Gundel T1 - Development of reference procedures for the quantification of toxic metals and S in plastics N2 - The quantitative analysis of toxic metals in plastics is very important for different sectors of industry and daily life. Many routine procedures have been established based on X-ray fluorescence or inductively coupled plasma atomic emission spectrometry. However, all of them require suitable reference materials to calibrate or validate. These reference materials ideally are being certified by reference procedures. The development of such reference procedures for sulfur and the four toxic elements cadmium, chromium, mercury and lead in plastics is described here. The procedures are based on double isotope dilution mass spectrometry including analyte–matrix separation. The applied mass spectrometric techniques are thermal ionization mass spectrometry as well as inductively coupled plasma mass spectrometry. Memory effects of mercury and dissolution of chromium(III) oxide have been considered especially. The expanded uncertainties have been improved from the percent range down to the per mill range during the development of the procedure from the early analysis of BCR-680/681 to the recent analysis of CCQM-P106. With the fully developed procedures expanded uncertainties (k = 2) between 0.1 and 0.4% for cadmium, chromium, lead and sulfur and around 1% for mercury can be achieved. The so developed procedures have been successfully applied to the certification of reference materials as well as to intercomparisons organized by CCQM. KW - ICPMS KW - TIMS KW - Reference materials KW - IDMS PY - 2010 DO - https://doi.org/10.1039/c0ja00034e SN - 0267-9477 SN - 1364-5544 VL - 25 IS - 10 SP - 1633 EP - 1642 PB - Royal Society of Chemistry CY - London AN - OPUS4-22044 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ostermann, Markus A1 - Kettisch, P. A1 - Becker, Dorit A1 - Vogl, Jochen T1 - Measurements of sulfur in oil using pressurised wet digestion technique in open vessels and isotope dilution mass spectrometry KW - Wet digestion KW - Open vessel digestion KW - Sulfur in oil KW - Reference materials KW - TIMS KW - IDMS PY - 2003 UR - http://www.springerlink.com/content/b7alk8lgly2v/?p=6237db8a9c28481d87e7b017e6474b73&pi=88 SN - 1618-2642 SN - 1618-2650 VL - 377 IS - 4 SP - 779 EP - 783 PB - Springer CY - Berlin AN - OPUS4-2738 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Klingbeil, Patrick A1 - Pritzkow, Wolfgang A1 - Riebe, Gundel T1 - High accuracy measurements of Fe isotopes using hexapole collision cell MC-ICP-MS and isotope dilution for certification of reference materials N2 - An ICP-MS equipped with collision cell, sector field and multi-collector technology has been applied to developing analytical procedures for Fe in terms of isotope ratio measurements and isotope dilution analysis. Therefore a detailed study on the reduction of molecular interferences by a variety of collision gases (He, Ar, Kr, H2, D2 and N2) was performed. The efficiency of the reduction has been checked by high resolution mass scans. The argon based interferences disturbing the determination of 54Fe and 56Fe could be completely removed when using Faraday detectors. The interferences on mass 57 could be reduced to a level which enables accurate measurements. Also, the 40Ar12C interference, which disturbs the chromium correction, could be completely removed. Reproducibilities of 0.01% could be reached for 54Fe/56Fe isotope ratios and 0.02% for 57Fe/56Fe isotope ratios. Under these measurement conditions a sensitivity of 1.2 V per 50 µg kg–1 Fe is available. This corresponds to 1.5 × 109 cps per mg kg–1. Based on these results highly accurate procedures for Fe isotope ratio determinations were set up, reaching a performance level superior to that of other ICP-MS instruments. Consequently, IDMS procedures were developed on this basis in order to perform certification measurements at the highest metrological level. The first application was the contribution to the Fe reference value by IMEP-12, an interlaboratory comparison with approximately 350 participants worldwide. The analysed Fe mass content is 0.2150 mg kg–1 with its expanded uncertainty (k= 2) of 0.0012 mg kg–1(0.56%), which is ten times less than the uncertainty of the second certification laboratory. Another application was the certification campaign of the two reference materials Tea Leaves and Polish Herbs. The results obtained with the ICP-MS procedure, 542 ± 11 mg kg–1 and 543 ± 12 mg kg–1, were compared with the results analysed by TIMS, 541 ± 12 mg kg–1 and 541 ± 13 mg kg–1, and agree very well within the stated uncertainties (k= 2). The results presented demonstrate quite well the suitability of the developed IDMS procedures for certification or reference measurements. PY - 2003 DO - https://doi.org/10.1039/b301812a SN - 0267-9477 SN - 1364-5544 VL - 18 SP - 1125 EP - 1132 PB - Royal Society of Chemistry CY - London AN - OPUS4-2739 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Einstieg in die massenspektrometrische Isotopenverdünnungsanalyse T2 - 1. Workshop "Isotopenverdünnungsanalyse mit ICP-MS" CY - Berlin, Germany DA - 2002-11-11 PY - 2002 AN - OPUS4-3006 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Fortschritte in der Isotopenverhältnis- und Isotopenverdünnungsanalyse - "Anything elements do, isotopes do better" T2 - Jahrestagung der DGMS 2002 CY - Heidelberg, Germany DA - 2002-03-03 PY - 2002 AN - OPUS4-3007 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Zertifizierung von Referenzmaterialien sowie Referenzanalysen mittels T2 - IDMSBeraterkreis I. Abteilung CY - Berlin, Germany DA - 2002-05-08 PY - 2002 N1 - Geburtsname von Dudek, Gabriele: Wermann, G. - Birth name of Dudek, Gabriele: Wermann, G. AN - OPUS4-3008 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bohn, T. A1 - Walczyk, Th. A1 - Davidsson, L. A1 - Pritzkow, Wolfgang A1 - Klingbeil, Patrick A1 - Vogl, Jochen A1 - Hurrell, R.F. T1 - Comparison of urinary monitoring, faecal monitoring and erythrocyte analysis of stable isotope labels to determine magnesium absorption in human subjects KW - Magnesium absorption KW - Stable isotopes KW - Faecal monitoring KW - Urinary monitoring KW - Erythrocytes PY - 2004 SN - 0007-1145 SN - 1475-2662 VL - 58 SP - 113 EP - 120 PB - CABI Publ. CY - Wallingford AN - OPUS4-3362 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Diemer, J. A1 - Vogl, Jochen A1 - Quétel, C.R. A1 - Linsinger, T. A1 - Taylor, P.D.P. A1 - Lamberty, A. A1 - Pauwels, J. T1 - SI-traceable certification of the amount content of cadmium below the ng g-1 level in blood samples by isotope dilution ICP-MS applied as a primary method of measurement N2 - The development and implementation of a method for the certification of cadmium in blood samples at low ng g-1 and sub ng g-1 levels is described. The analytical procedure is based on inductively coupled plasma isotope dilution mass spectrometry (ICP-IDMS) applied as a primary method of measurement. Two different sample digestion methods, an optimized microwave digestion procedure using HNO3 and H2O2 as oxidizing agents and a high-pressure asher digestion procedure, were developed and compared. The very high salt content of the digests and the high molybdenum content, which can cause oxide-based interferences with the Cd isotopes, were reduced by a chromatographic matrix separation step using an anion-exchange resin. All isotope ratio measurements were performed by a quadrupole ICP-MS equipped with an ultrasonic nebulizer with membrane desolvator. This sample introduction set-up was used to increase sensitivity and minimize the formation of oxides (less MoO+ interference with the Cd isotopes). Because of the very low Cd concentrations in the samples and the resulting need to minimize the procedural blank as much as possible, all sample-processing steps were performed in a clean room environment. Detection limits of 0.005 ng g-1 Cd were achieved using sample weights of 2.7 g. The method described was used to re-certify the cadmium content of three different blood reference materials from the Community Bureau of Reference (BCR) of the European Commission (BCR-194, BCR-195, BCR-196). Cadmium concentrations ranged between ~0.2 ng g-1 and ~12 ng g-1. For these materials, SI-traceable certified values including total uncertainty budgets according to ISO and Eurachem guidelines were established. PY - 2001 DO - https://doi.org/10.1007/s002160100813 SN - 0937-0633 VL - 370 SP - 492 EP - 498 PB - Springer CY - Berlin AN - OPUS4-3363 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Pritzkow, Wolfgang A1 - Klingbeil, Patrick T1 - The need for new SI-traceable magnesium isotopic reference materials KW - Isotopic Reference Material KW - Multi-collector ICP-MS KW - Isotopic abundance variations KW - Primary Isotopic Reference Material KW - Magnesium PY - 2004 DO - https://doi.org/10.1007/s00216-004-2859-8 SN - 1618-2642 SN - 1618-2650 VL - 380 SP - 876 EP - 879 PB - Springer CY - Berlin AN - OPUS4-6904 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - EUROMET742: Sulfur in fuel - Final report T2 - Metchem-Meeting CY - Madrid, Spain DA - 2005-02-15 PY - 2005 AN - OPUS4-7162 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotopen- und Isotopenverdünnungsanalyse mit ICP-MS T2 - DGMS-Workshop, DGMS- Jahrestagung CY - Rostock, Germany DA - 2005-03-06 PY - 2005 AN - OPUS4-7164 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Quétel, C. A1 - Ostermann, Markus A1 - Papadakis, I. A1 - Van Nevel, L. A1 - Taylor, P.D.P. T1 - Contribution to the certification of B, Cd, Mg, Pb, Rb, Sr, and U in a natural water sample for the International Measurement Evaluation Programme Round 9 (IMEP-9) using ID-ICP-MS N2 - The present paper describes the contribution of the Institute for Reference Materials and Measurements to the certification of B, Cd, Mg, Pb, Rb, Sr, and U amount contents in a natural water sample, in round 9 of the International Measurement Evaluation Programme (IMEP-9). The analytical procedure to establish the reference values for B, Cd, Mg, Pb, Rb, Sr, and U amount contents was based on isotope dilution inductively coupled plasma-mass spectrometry used as a primary method of measurement. Applying this procedure reference values, traceable to the SI, were obtained for the natural water sample of IMEP-9. For each of the certified amount contents presented here a total uncertainty budget was calculated using the method of propagation of uncertainties according to ISO and EURACHEM guidelines. The measurement procedures, as well as the uncertainty calculations are described for all seven elements mentioned above. In order to keep the whole certification process transparent and so traceable, the preparations of various reagents and materials as well as the sample treatment and blending, the measurements themselves, and finally the data treatment are described in detail. Explanations focus on Pb as a representative example. The total uncertainties (relative) obtained were less than 2% for all investigated elements at amount contents in the pmol/kg up to the high 7mol/kg range, corresponding to low 7g/kg and mg/kg levels. KW - IMEP-9 KW - ID-ICP-MS KW - IDMS KW - Uncertainty budget KW - Certification PY - 2000 DO - https://doi.org/10.1007/s007690000145 SN - 0949-1775 SN - 1432-0517 VL - 5 SP - 272 EP - 279 PB - Springer CY - Berlin AN - OPUS4-7216 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Liesegang, D. A1 - Ostermann, Markus A1 - Diemer, J. A1 - Berglund, M. A1 - Quétel, C. A1 - Taylor, P. A1 - Heumann, K. T1 - Producing SI-traceable reference values for Cd, Cr and Pb amount contents in polyethylene samples from the Polymer Elemental Reference Material (PERM) project using isotope dilution mass spectrometry N2 - The present paper describes the certification of the amount content of Cd, Cr and Pb in two different polyethylene materials within the third phase of the Polyethylene Elemental Reference Material (PERM) project. The analytical procedure to establish the reference values for Cd, Cr and Pb amount contents in these materials is based on isotope dilution mass spectrometry used as a primary method of measurement. Cd and Pb were measured with inductively coupled plasma-mass spectrometry and Cr with positive thermal ionization-mass spectrometry. The decomposition of the polymer matrix was carried out using a high pressure asher. Reference values for amount content, traceable to the SI-system, have been obtained for these three elements in both of the polyethylene samples of PERM. For each of the certified amount content values an uncertainty budget was calculated using the method of propagation of uncertainties according to ISO and EURACHEM guidelines. The measurement procedures, as well as the uncertainty calculations, are described for all three elements. In order to keep the whole certification process as transparent as possible, the preparations of various reagents and materials as well as the sample treatment and blending are described in detail. The mass spectrometry measurements and the data treatment are also explained carefully. The various sources of uncertainty present in the procedure are displayed in the uncertainty budgets. The obtained combined uncertainties for the amount content values were less than 2% relative (k=1) for all investigated elements. The amount contents were in the ?mol/kg range, corresponding to mg/kg levels. KW - PERM KW - ICP-MS KW - PTI-MS KW - IDMS KW - Uncertainty budget KW - Certification KW - Polyethylene PY - 2000 DO - https://doi.org/10.1007/s007690000146 SN - 0949-1775 SN - 1432-0517 VL - 5 SP - 314 EP - 324 PB - Springer CY - Berlin AN - OPUS4-7217 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Quétel, C. A1 - Vogl, Jochen A1 - Prohaska, T. A1 - Nelms, S. A1 - Taylor, P.D.P. A1 - De Bièvre, P. T1 - Comparative performance study of ICP mass spectrometers by means of U "isotopic measurements" N2 - The performance of four commercially available ICPMS instruments of three different types was compared by means of uranium "isotopic measurements". Examined were two quadrupole sector (different generation, different manufacturer), one single detector double focusing magnetic sector and one multiple collector double focusing magnetic sector instruments. The same samples of the IRMM-072 series were used under routine conditions to measure the 233U/235U and the 233U/238U ratios which, in these samples, vary over almost three orders of magnitude from ~ 1 to ~ 2 · 10-3. Within expanded (k = 2) uncertainties, good agreement was observed between the certified values and the data internally corrected for mass-discrimination effects. The magnitude of the evaluated uncertainties was different for each type of instrument. With the multiple collector instrument, expanded uncertainties varied from - 0.04% to- 0.24% for the 233U/235U ratio, and from - 0.08% to - 0.27% for the 233U/238U ratio. They were ~ 1 to 5 times larger with the single detector magnetic sector instrument, and ~ 10 to 25 times larger with both quadrupole sector instruments. With the multiple collector instrument, repeatability of the measurements seemed to be limited by the difficulty of correcting properly for instrumental background, whereas with the single detector magnetic sector instrument the counting statistics was the only limitation (on smallest ratios). Apparent mass-discrimination was clearly found to be larger but more reproducible (and hence easier to correct for) in the case of magnetic sector instruments than for both quadrupole sector instruments. If space charge effects were the main source of mass-discrimination for all instruments, these results are in contradiction with the hypothesis of the size of mass-discrimination decreasing with the acceleration voltage. With the single detector magnetic sector instrument in particular (when operated by changing the ion energy only), our results pointed at more than only one major source of mass-discrimination, with variable size depending on the ratios measured. KW - ICP-MS KW - Isotope ratio KW - Uranium PY - 2000 DO - https://doi.org/10.1007/s002160000499 SN - 0937-0633 VL - 368 SP - 148 EP - 155 PB - Springer CY - Berlin AN - OPUS4-7218 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nelms, S. A1 - Quétel, C. A1 - Prohaska, T. A1 - Vogl, Jochen A1 - Taylor, P.D.P. T1 - Evaluation of detector dead time calculation models for ICP-MS KW - ICP-MS KW - Dead time KW - Uncertainty PY - 2001 DO - https://doi.org/10.1039/b007913h SN - 0267-9477 SN - 1364-5544 VL - 16 IS - 4 SP - 333 EP - 338 PB - Royal Society of Chemistry CY - London AN - OPUS4-7219 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Pritzkow, Wolfgang A1 - Vogl, Jochen A1 - Berger, Achim A1 - Ecker, Klaus A1 - Grötzschel, R. A1 - Klingbeil, Patrick A1 - Persson, L. A1 - Riebe, Gundel A1 - Wätjen, U. T1 - Contribution of ICP-IDMS to the certification of antimony implanted in a silicon wafer - comparison with RBS and INAA results N2 - A thin-layer reference material for surface and near-surface analytical methods was produced and certified. The surface density of the implanted Sb layer was determined by Rutherford backscattering spectrometry (RBS), instrumental neutron activation analysis (INAA), and inductively coupled plasma isotope dilution mass spectrometry (ICP-IDMS) equipped with a multi-collector. The isotopic abundances of Sb (121Sb and 123Sb) were determined by multi-collector ICP-MS and INAA. ICP-IDMS measurements are discussed in detail in this paper. All methods produced values traceable to the SI and are accompanied by a complete uncertainty budget. The homogeneity of the material was measured with RBS. From these measurements the standard uncertainty due to possible inhomogeneities was estimated to be less than 0.78% for fractions of the area increments down to 0.75 mm2 in size. Excellent agreement between the results of the three different methods was found. For the surface density of implanted Sb atoms the unweighted mean value of the means of four data sets is 4.8121016 cm-2 with an expanded uncertainty (coverage factor k=2) of 0.0921016 cm-2. For the isotope amount ratio R (121Sb/123Sb) the unweighted mean value of the means of two data sets is 1.435 with an expanded uncertainty (coverage factor k=2) of 0.006. KW - ICP-MS KW - IDMS KW - Reference material KW - Surface analysis PY - 2001 DO - https://doi.org/10.1007/s002160100987 SN - 0937-0633 VL - 371 SP - 867 EP - 873 PB - Springer CY - Berlin AN - OPUS4-7220 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dudek, Gabriele A1 - Alber, D. A1 - Pritzkow, Wolfgang A1 - Riebe, Gundel A1 - Vogl, Jochen A1 - Görner, Wolf T1 - Determination of the beta- branching ratio of 64Cu by mass spectrometric investigations of the decay products in neutron transmuted copper N2 - The ?- branching ratio of 64Cu was determined by investigating the resulting decay products in copper doped by neutron transmutation. The numbers of 64Zn and 64Ni atoms were analyzed using isotope dilution analysis combined with thermal ionization mass spectrometry. A ?- branching ratio of (38.06±0.30)% was obtained, which agrees with the study of Kawada (Appl. Radiat. Isot. 37 (1) (1986) 7) to a higher accuracy. However, our result differs from the value cited in the NUDAT database of (39.0±0.3)%. KW - NTD KW - Copper KW - Zinc KW - Nickel KW - Branching ratio KW - Cu-64 KW - TIMS KW - IDMS KW - Isotope dilution KW - Thermal ionization mass spectrometry KW - Neutron transmutation doping PY - 2002 DO - https://doi.org/10.1016/S0969-8043(01)00180-4 SN - 0883-2889 SN - 0969-8043 N1 - Geburtsname von Dudek, Gabriele: Wermann, G. - Birth name of Dudek, Gabriele: Wermann, G. VL - 56 SP - 145 EP - 151 PB - Elsevier CY - Amsterdam AN - OPUS4-7221 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Pritzkow, Wolfgang A1 - Vogl, Jochen A1 - Köppen, Robert A1 - Ostermann, Markus T1 - Determination of sulfur isotope abundance ratios for SI-traceable low sulfur concentration measurements in fossil fuels by ID-TIMS N2 - The present work describes the development of an existing TIMS procedure to a reference procedure for low sulfur concentration measurements in fossil fuels. With this enhanced procedure SI-traceable sulfur mass fractions below 10 mg kg-1 can be obtained. The achieved detection limit is approximately 0.2 mg kg-1. The procedure was validated by certified reference materials. The procedure was already applied to candidate reference materials and to samples analysed within projects of the “Comité Consultatif pour la Quantité de Matière – CCQM”. Additionally the influence of the isotopic composition on the results and its corresponding uncertainty was studied. Reference data published in the literature on the isotopic composition of sulfur were assessed. KW - TIMS KW - IDMS KW - Low sulfur KW - Fossil fuel KW - Reference procedure PY - 2005 DO - https://doi.org/10.1016/j.ijms.2004.10.024 SN - 0168-1176 SN - 0020-7381 SN - 1387-3806 SN - 1873-2798 VL - 242 SP - 309 EP - 318 PB - Elsevier CY - Amsterdam AN - OPUS4-7222 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Heumann, K. G. A1 - Marx, G. A1 - Rädlinger, G. A1 - Vogl, Jochen ED - Frimmel, F. H. T1 - Heavy Metal and Halogen Interactions with Fractions of Refractory Organic Substances Separated by Size-exclusion Chromatography PY - 2002 SN - 3-527-30173-9 SP - 55 EP - 72 PB - Wiley-VCH CY - Weinheim AN - OPUS4-7223 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Heumann, K. G. A1 - Abbt-Braun, G. A1 - Behrens, K. A1 - Burba, P. A1 - Frimmel, F. H. A1 - Jakubowski, B. A1 - Knöchel, A. A1 - Mielcke, J. A1 - Rädlinger, G. A1 - Marx, G. A1 - Vogl, Jochen ED - Frimmel, F. H. T1 - Element determination and its quality control in fractions of refractory organic substances and the corresponding original water samples PY - 2002 SN - 3-527-30173-9 DO - https://doi.org/10.1002/9783527611195.ch1b SP - 39 EP - 53 PB - Wiley-VCH CY - Weinheim AN - OPUS4-7224 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Verbesserung bei der Zertifizierung von Referenzmaterialien durch Anwendung der Multikollektor ICP-MS T2 - 5. Symposium Massenspektrometrische Verfahren der Elementspurenanalyse und 16. ICP-MS Anwendertreffen CY - Jülich, Germany DA - 2000-09-18 PY - 2000 AN - OPUS4-7467 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Pb in Red Wine-Reference Measurements by Multi-Collector ICP-IDMS 17 T2 - ICP-MS Anwendertreffen und 2 nd International Conference on High-resolution Sector Field ICP-MS CY - Vienna, Austria DA - 2001-09-10 PY - 2001 N1 - Geburtsname von Dudek, Gabriele: Wermann, G. - Birth name of Dudek, Gabriele: Wermann, G. AN - OPUS4-7469 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Schwefel in Kraftstoffen - Referenzanalysen am Limit T2 - Tag der Chemie CY - Berlin, Germany DA - 2005-06-08 PY - 2005 AN - OPUS4-7457 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Validierung in der Elementaranalytik mittels Referenzmaterialien und -verfahren T2 - 11. Jahreskolloquium der Interessengemeinschaft Atomspektrometrie Berlin CY - Berlin, Germany DA - 2004-11-17 PY - 2004 N1 - Geburtsname von Dudek, Gabriele: Wermann, G. - Birth name of Dudek, Gabriele: Wermann, G. AN - OPUS4-7702 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - JEPPIM Project 014: Sulfur in fuel - Improvement of existing IDMS procedures T2 - EUROMET-METHEM Meeting CY - Ghent, Belgium DA - 2004-06-17 PY - 2004 AN - OPUS4-7704 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Preparation of Cd synthetic isotope mixtures for the determination of the atomic weight of natural Cd T2 - JEEPIM-Meeting CY - Brussels, Belgium DA - 2004-12-02 PY - 2004 AN - OPUS4-7705 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Final comment on JEPPIM-014: Sulfur in fuel T2 - JEPPIM-Meeting CY - Brussels, Belgium DA - 2004-12-02 PY - 2004 AN - OPUS4-7706 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Zertifizierte Isotopenstandards für die Isotopenverdünnungsanalyse T2 - Analytica Messe 2000 CY - Munich, Germany DA - 2000-04-11 PY - 2000 AN - OPUS4-7707 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Reduzierung von Molekülinterferenzen mit Hexapol-Kollisionszelle für die Bestimmung von Isotopenverhältnissen mit Multikollektor ICP-MS T2 - 5. Symposium Massenspektrometrische Verfahren der Elementspurenanalyse und 16. ICP-MS Anwendertreffen CY - Jülich, Germany DA - 2000-09-18 PY - 2000 AN - OPUS4-7712 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Zertifizierung einer in Silizium implantierten Antimon-Schicht mit ICP-IDMS T2 - INAA und RBS ANAKON 2001 CY - Konstanz, Germany DA - 2001-04-04 PY - 2001 AN - OPUS4-7713 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen T1 - MS Verfahren der Elementspurenanalyse PY - 2004 SN - 0939-0065 VL - 1 SP - 30 EP - 31 PB - Gesellschaft Deutscher Chemiker CY - Frankfurt, M. AN - OPUS4-3724 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Reference Measurements by Multi-Collector ICP-IDMS T2 - 10th Beijing Conference and Exhibition on Instrumental Analysis CY - Beijing, China DA - 2003-10-13 PY - 2003 AN - OPUS4-3799 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Preparation of Cd synthetic isotope mixtures for the determination of the atomic weight of natural Cd T2 - JEPPIM-Meeting CY - Mechelen, Belgium DA - 2003-12-04 PY - 2003 AN - OPUS4-3801 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -