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 - TY - CONF A1 - Vogl, Jochen T1 - IDMS of Low Sulfur in fossil fuels T2 - JEPPIM-Meeting CY - Mechelen, Belgium DA - 2003-12-04 PY - 2003 AN - OPUS4-3802 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Overcoming present limitations in ICP-MS for iron measurements T2 - European Winter Conference on Plasma Spectrochemistry 2003 CY - Garmisch-Partenkirchen, Germany DA - 2003-01-12 PY - 2003 AN - OPUS4-4924 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Bestimmung von Schwefel in Dieselöl mit TIMS T2 - 6. Symposium Massenspektrometrische Verfahren der Elementspurenanalyse / 18. ICP-MS Anwendertreffen CY - Berlin, Germany DA - 2003-10-06 PY - 2003 AN - OPUS4-4927 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Calcium in Serum - Referenzanalysen mit TIMS T2 - 6. Symposium Massenspektrometrische Verfahren der Elementspurenanalyse / 18. ICP-MS Anwendertreffen CY - Berlin, Germany DA - 2003-10-06 PY - 2003 AN - OPUS4-4929 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Steps to a new and improved SI-traceable atomic weight for natural abundance cadmium and certified isotopically enriched materials T2 - 19. ICP-MS-Anwendertreffen CY - Zurich, Switzerland DA - 2004-09-01 PY - 2004 AN - OPUS4-5067 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Ostermann, Markus T1 - On the measurement of the moisture content in different matrix materials N2 - Twelve different samples were analyzed for their water content by the classical oven-drying method and a commercial moisture analyzer. Nominal values have been set by Karl Fischer titration and gravimetry. The decomposition during the drying process of samples containing organic compounds was checked by thermogravimetry coupled with Fourier transform infrared spectrometric and mass spectrometric detection. Summarizing all measurement results, the commercial moisture analyzer demonstrated an average bias for the determination of water contents, which is much smaller than the stated uncertainty and thus is negligible. Compared to the classical oven-drying method, the commercial moisture analyzer shows a smaller bias, more ease in handling and less time consumption per analysis. When validated by a reference procedure like Karl Fischer titration the commercial moisture analyzer is the method of choice for routine analysis. KW - Classical oven-drying KW - Commercial moisture analyzer KW - Karl Fischer titration KW - Moisture KW - Reference materials KW - Thermogravimetry KW - Matrix samples PY - 2006 DO - https://doi.org/10.1007/s00769-006-0159-z SN - 0949-1775 SN - 1432-0517 VL - 11 IS - 7 SP - 356 EP - 362 PB - Springer CY - Berlin AN - OPUS4-12638 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Vogl, Jochen ED - Nelms, S. M. T1 - Calibration strategies and quality assurance PY - 2005 SN - 0-8493-2381-9 SP - 147 EP - 181 PB - Blackwell CY - Oxford AN - OPUS4-11048 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotope ratio measurements with Multi-Collector-ICP-MS using collision cell technology T2 - Seminar on food analysis CY - Beijing, China DA - 2005-10-28 PY - 2005 AN - OPUS4-11652 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotope dilution mass spectrometry - Application to food and related matrices T2 - Seminar on food analysis CY - Beijing, China DA - 2005-10-28 PY - 2005 AN - OPUS4-11653 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Comparative studies between ID-ICP-MS and ID-TIMS T2 - Seminar on food analysis CY - Beijing, China DA - 2005-10-28 PY - 2005 AN - OPUS4-11654 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotope dilution mass spectrometry - Metrological aspects T2 - Seminar on food analysis CY - Beijing, China DA - 2005-10-28 PY - 2005 AN - OPUS4-11655 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotope dilution mass spectrometry - Introduction and basic principles T2 - Seminar on food analysis CY - Beijing, China DA - 2005-10-28 PY - 2005 AN - OPUS4-11656 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - CCQM-P62: purity of nickel with respect to six defined metallic analytes - Final assessment T2 - Meeting of CCQM-Inorganic Analytical Working Group CY - Beijing, China DA - 2006-10-16 PY - 2006 AN - OPUS4-13993 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - CCQM-P76: Analysis of a copper alloy T2 - Meeting of CCQM-Inorganic Analytical Working Group CY - Beijing, China DA - 2006-10-16 PY - 2006 AN - OPUS4-13994 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Establishment of traceability of inorganic chemical measurements to SI unit and application to the environmental analysis T2 - Meeting of CCQM-Inorganic Analytical Working Group CY - Beijing, China DA - 2006-10-16 PY - 2006 AN - OPUS4-13995 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Riebe, Gundel A1 - Pritzkow, Wolfgang A1 - Vogl, Jochen T1 - Schwermetallbestimmung im Boden KW - Königswasserextraktion KW - Bodenanalyse KW - Schwermetallbestimmung KW - Unsicherheitsvergleiche PY - 2006 SN - 0016-3538 IS - 8 SP - 688 EP - 690 PB - GIT-Verlag CY - Darmstadt AN - OPUS4-13725 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Pritzkow, Wolfgang A1 - Wunderli, S. A1 - Vogl, Jochen A1 - Fortunato, G. T1 - The isotope abundances and the atomic weight of cadmium by a metrological approach N2 - Gravimetric synthetic mixtures of seven enriched, purified cadmium isotope materials were used to determine the correction factors for mass fractionation (MC-TIMS) and mass discrimination (MC-ICP-MS). The isotope abundance ratios determined for various natural cadmium materials represents the isotope composition for natural cadmium materials. Correction of the isotope abundance ratios observed yielded isotope abundances of 106Cd 0.012450(8), 108Cd 0.008884(4), 110Cd 0.124846(16), 111Cd 0.127955(14), 112Cd 0.241110(38), 113Cd 0.122254(22), 114Cd 0.287439(60) and 116Cd 0.075183(32). The newly determined atomic weight of natural cadmium based on SI-traceable evaluation of the isotope abundance ratios is 112.41384(18). The cadmium material designated in the paper as Cd-2211 can be used as an isotope reference material with a δ(114Cd/110Cd)-value of 0‰. The results obtained show that the uncertainties for the isotope abundances and the atomic weight given as IUPAC values for cadmium are overestimated. KW - Atomic weight KW - Isotope abundance KW - Isotopic composition KW - Cadmium PY - 2007 SN - 0168-1176 SN - 0020-7381 SN - 1387-3806 SN - 1873-2798 VL - 261 IS - 1 SP - 74 EP - 85 PB - Elsevier CY - Amsterdam AN - OPUS4-14543 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Schwefel, Autofahren und Analytik T2 - 39. Diskussionstagung der Deutschen Gesellschaft für Massenspekrometrie CY - Mainz, Germany DA - 2006-03-05 PY - 2006 AN - OPUS4-14557 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Aktuell in Deutschland verfügbare Rückführungsbasis - Internationale Vergleichs- und Referenzmessungen T2 - Workshop "Rückführung chemischer Messergebnisse in der Umweltanalytik - ein wichtiges Element der Qualitätssicherung" CY - Berlin, Germany DA - 2006-03-14 PY - 2006 AN - OPUS4-14560 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotopenanalytik mit ICP-MS und TIMS in Nahrungsmitteln, Medizin und Umwelt T2 - Jahrestagung der DGMS 2007 CY - Bremen, Germany DA - 2007-03-11 PY - 2007 AN - OPUS4-14696 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotopenanalytik an der BAM T2 - AG "Stoffe in der Landwirtschaft", Expertengremium der DFG CY - Bonn, Germany DA - 2007-05-14 PY - 2007 AN - OPUS4-14866 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen T1 - Characterisation of reference materials by isotope dilution mass spectrometry N2 - This article reviews the application of isotope dilution mass spectrometry (IDMS) to the field of reference material (RM) characterisation within the past 15 years, focusing on elemental and elemental species analysis. Emphasis is placed on liquid and solid RMs and IDMS measurements of the highest analytical quality. Basic principles, as well as the equation system, are being revisited. Different calibration strategies, such as single, double or triple IDMS, are critically reviewed and the achievable uncertainties are discussed. Differences in the application of thermal ionization mass spectrometry (TIMS) and inductively coupled plasma mass spectrometry (ICP-MS) are discussed as well as differences between different types of mass spectrometers, such as single collector versus multi-collector or quadrupole versus magnetic sector instruments. Possible sources of errors and bias are mentioned and correction models introduced and applied within the past years are discussed. Several examples for RM characterisations and inter-laboratory comparisons for elemental as well as elemental species analysis are shown, each demonstrating excellent analytical quality. In general, it can be stated that IDMS is the most important reference method for elemental and elemental species analysis, offering the highest accuracy and precision or smallest measurement uncertainties, when properly applied. Thus, IDMS represents by far the best suited reference method for RM characterisation. Owing to its universal applicability IDMS offers sufficient potential to follow future needs in analytical chemistry as well as in the RM sector. PY - 2007 UR - http://www.rsc.org/Publishing/Journals/JA/article.asp?doi=b614612k SN - 0267-9477 SN - 1364-5544 VL - 22 IS - 5 SP - 475 EP - 492 PB - Royal Society of Chemistry CY - London AN - OPUS4-15724 LA - eng 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 - Jahreskolloquium der Interessengemeinschaft Atomspektroskopie Berlin - IGAS CY - Berlin, Germany DA - 2001-11-07 PY - 2001 AN - OPUS4-16297 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Schwefel in Kraftstoffen - Referenzanalysen am Limit T2 - ANAKON 2005 CY - Regensburg, Germany DA - 2005-03-15 PY - 2005 AN - OPUS4-16302 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Reference material characterization by IDMS applying multi collector instruments T2 - BERM 11 CY - Tsukuba, Japan DA - 2007-10-29 PY - 2007 AN - OPUS4-16306 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Sulfur In Fuel - An ERM collaboration to support sulfur analysis at nowadays sulfur limits T2 - BERM 11 CY - Tsukuba, Japan DA - 2007-10-29 PY - 2007 AN - OPUS4-16308 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - IDMS - a primary method of measurement, its role for RM certification and applications from the food sector T2 - 2nd APMP DEC and TCQM Workshop & Symposium in Metrology in Chemistry CY - Xi'an, China DA - 2007-06-12 PY - 2007 AN - OPUS4-16309 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Linsinger, T. A1 - Andrzejuk, W. A1 - Bau, A. A1 - Charoud-Got, J. A1 - De VOs, P. A1 - Emteborg, H. A1 - Hearn, R. A1 - Lamberty, A. A1 - Oostra, A. A1 - Pritzkow, Wolfgang A1 - Quétel, C. A1 - Roebben, G. A1 - Tresl, I. A1 - Vogl, Jochen A1 - Wood, S. T1 - Production of three certified reference materials for the sulfur content in gasoline (petrol) N2 - Directive 2003/17/EC of the European Parliament and the European Council stipulates that petrol (gasoline) with a total sulfur content below 10 mg kg-1 must be available in all European Union member states by 2009. Three certified reference materials were produced in support of this directive in a joint effort of the members of the European Reference Materials Initiative (ERM). Two of the materials were made from commercial petrol, while the third one was prepared from a blend of commercial petrols. Relative between-ampule heterogeneity of the materials was quantified and found to be below 2.5%. Potential degradation during storage and dispatch was quantified, and shelf lives based on these values were set. The three materials were characterized by three institutes using different variants of isotope-dilution mass spectrometry. The results from the three institutes were combined, and the final uncertainties of the respective sulfur mass fractions were estimated including contributions from heterogeneity, stability, and characterization. The following mass fractions were derived: ERM-EF211, 48.8 ± 1.7 mg kg-1; ERM-EF212, 20.2 ± 1.1 mg kg-1; and ERM-EF213, 9.1 ± 0.8 mg kg-1. KW - CRM KW - IDMS KW - ERM PY - 2007 DO - https://doi.org/10.1021/ef070155t SN - 0887-0624 SN - 1520-5029 VL - 21 IS - 4 SP - 2240 EP - 2244 PB - ACS Publ. CY - Washington, DC AN - OPUS4-16371 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - IDMS with multi collector mass spectrometers - What do we again? T2 - Workshop Multi-collector Mass Spectrometry CY - Charleston, SC, USA DA - 2007-10-01 PY - 2007 AN - OPUS4-16403 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Vogl, Jochen T1 - Book review: Diane Beauchemin and Dwight E. Matthews (Eds.): The encyclopedia of mass spectrometry, Volume 5: Elemental and isotope ratio mass spectrometry N2 - The encyclopedia of mass spectrometry, Volume 5: Elemental and isotope ratio mass spectrometry covers the subject almost entirely and serves as a reference work with links to specialist literature if more details are required. Therefore, this book can be recommended to all beginners, students, and experts working in this broad field. KW - Elemental mass spectrometry KW - Isotope ratio mass spectrometry PY - 2011 DO - https://doi.org/10.1007/s00216-011-5106-0 SN - 1618-2642 SN - 1618-2650 VL - 401 IS - 2 SP - 573 EP - 574 PB - Springer CY - Berlin AN - OPUS4-24089 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotope reference materials for present and future isotope research T2 - Goldschmidt 2011 CY - Prague, Czech Republic DA - 2011-08-14 PY - 2011 AN - OPUS4-24109 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - An alternative lead-matrix-separation procedure exemplarily shown for lead isotope analysis in the Trojan silver artefacts T2 - Technart 2011 CY - Berlin, Germany DA - 2011-04-26 PY - 2011 AN - OPUS4-23818 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rigo, E. A1 - Rosner, Martin A1 - Vogl, Jochen T1 - Herkunftsbestimmung von Kalken N2 - Analytische Methoden zur Feststellung der Herkunft eines Baustoffes sind bislang kaum entwickelt worden. In Deutschland gibt es eine Reihe von Kalkiagerstätten, die in unterschiedlichen geologischen Formationen Kalk oder Dolomit enthalten. Das unterschiedliche geologische Alter von Kalken sowie die ursprüngliche mineralische Zusammensetzung und die geologische Historie spiegeln sich im 87Sr/88Sr-lsotopenverhältnis weder. Mittels der Thermionen-Massenspektrometrie kann dieses Verhältnis ermittelt und somit zur Herkunftsbestimmung eines Kalkes herangezogen werden. T2 - GDCh-Fachtagung Bauchemie 2011 CY - Hamburg-Harburg, Deutschland DA - 06.10.2011 KW - Isotopenverhältnisse KW - Kalke KW - Herkunft KW - TIMS PY - 2011 SN - 978-3-936028-69-0 N1 - Serientitel: GDCh-Monographien – Series title: GDCh-Monographien VL - 44 SP - 282 EP - 284 CY - Frankfurt/M. AN - OPUS4-25576 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Key Comparison on isotope ratio determinations - K98/P134 Pb isotope ratios T2 - CCQM, IAWG Meeting CY - Paris, France DA - 2012-04-16 PY - 2012 AN - OPUS4-25947 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 ICP-MS instruments T2 - 50-Jarig Jubileum Werkgroep Atoomspectrometrie CY - Tilburg, Netherlands DA - 2012-06-07 PY - 2012 AN - OPUS4-25948 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Herkunftsbestimmung von Kalken T2 - GDCh Tagung Bauchemie 2011 CY - Hamburg, Germany DA - 2011-10-06 PY - 2011 AN - OPUS4-25952 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Reference materials for isotope research T2 - 13th International Symposium on Biological and Environmental Reference Materials, BERM 13 CY - Vienna, Austria DA - 2012-06-25 PY - 2012 AN - OPUS4-26134 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Isotopenanalytik mit ICP-MS und TIMS in Nahrungsmitteln, Medizin und Umwelt T2 - DGMS 2013, Workshop Einführung in die anorganische Massenspektrometrie CY - Berlin, Germany DA - 2013-03-10 PY - 2013 AN - OPUS4-27894 LA - deu 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 - DGMS 2013, Workshop Einführung in die anorganische Massenspektrometrie CY - Berlin, Germany DA - 2013-03-10 PY - 2013 AN - OPUS4-27895 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Metrology for boron isotope analysis T2 - Boron Isotope Workshop, Goldschmidt Conference 2013 CY - Florence, Italy DA - 2013-08-24 PY - 2013 AN - OPUS4-29083 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Production and certification of Pd and Pt single spikes T2 - Goldschmidt Conference 2013 CY - Florence, Italy DA - 2013-08-25 PY - 2013 AN - OPUS4-29084 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Rosner, Martin A1 - Pritzkow, Wolfgang T1 - The need for new isotope reference materials N2 - Isotope reference materials are needed to calibrate and validate analytical procedures used for the determination of isotope amount ratios, procedurally defined isotope ratios or so-called δ values. In contrast to the huge analytical progress in isotope ratio analytics, the production of isotope reference materials has not kept pace with the increasing needs of isotope analysts. Three representative isotope systems are used to explain the technical and non-technical difficulties and drawbacks, on one hand, and to demonstrate what can be achieved at its best, on the other hand. A clear statement is given that new isotope reference materials are needed to obtain traceable and thus comparable data, which is essential for all kinds of isotope research. The range of available isotope reference materials and δ reference materials should be increased and matrix reference materials certified for isotope compositions or δ values, which do not exist yet, should be provided. KW - Isotope reference materials KW - Delta reference materials KW - Synthetic isotope mixtures KW - Mass spectrometry KW - Comparability KW - Traceability KW - Measurement uncertainty PY - 2013 DO - https://doi.org/10.1007/s00216-012-6605-3 SN - 1618-2642 SN - 1618-2650 VL - 405 IS - 9 SP - 2763 EP - 2770 PB - Springer CY - Berlin AN - OPUS4-28169 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Paz, B. A1 - Koenig, Maren A1 - Pritzkow, Wolfgang T1 - A modified lead-matrix separation procedure shown for lead isotope analysis in Trojan silver artefacts as an example N2 - A modified Pb–matrix separation procedure using NH4HCO3 solution as eluent has been developed and validated for determination of Pb isotope amount ratios by thermal ionization mass spectrometry. The procedure is based on chromatographic separation using the Pb·Spec resin and an in-house-prepared NH4HCO3 solution serving as eluent. The advantages of this eluent are low Pb blanks (<40 pgmL-1) and the property that NH4HCO3 can be easily removed by use of a heating step (>60 °C). Pb recovery is >95 % for water samples. For archaeological silver samples, however, the Pb recovery is reduced to approximately 50 %, but causes no bias in the determination of Pb isotope amount ratios. The validated procedure was used to determine lead isotope amount ratios in Trojan silver artefacts with expanded uncertainties (k=2) <0.09 %. KW - Analyte-matrix separation KW - Mass spectrometry KW - Pb isotope ratio thermal ionization mass spectrometry KW - Archaeometry PY - 2013 DO - https://doi.org/10.1007/s00216-012-6323-x SN - 1618-2642 SN - 1618-2650 VL - 405 IS - 9 SP - 2995 EP - 3000 PB - Springer CY - Berlin AN - OPUS4-28170 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen T1 - Advances in isotope ratio mass spectrometry and required isotope reference materials N2 - The article gives a condensed version of the keynote lecture held at the International Mass Spectrometry Conference 2012 in Kyoto. Starting with some examples for isotope research the key requirements for metrologically valid procedures enabling traceable and comparable isotope data are discussed. Of course multi-collector mass spectrometers are required which offer sufficiently high isotope ratio precision for the intended research work. Following this, corrections for mass fractionation/discrimination, validation of the analytical procedure including chemical sample preparation and complete uncertainty budgets are the most important issues for obtaining a metrologically valid procedure for isotope ratio determination. Only the application of such metrologically valid procedures enables the generation of traceable and comparable isotope data. To realize this suitable isotope and/or δ-reference materials are required, which currently are not sufficiently available for most isotope systems. Boron is given as an example, for which the situation regarding isotope and δ-reference materials is excellent. Boron may therefore serve as prototype for other isotope systems. KW - Isotope reference materials KW - Delta reference materials KW - Traceability KW - Comparability KW - Measurement uncertainty KW - Synthetic isotope mixtures KW - Mass fractionation KW - Mass discrimination PY - 2013 DO - https://doi.org/10.5702/massspectrometry.S0020 SN - 2187-137X SN - 2186-5116 VL - 2 IS - 50020 SP - 1 EP - 7 AN - OPUS4-28562 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Reference Materials and Metrological Principles for Isotope Research T2 - 15th Beijing Conference and Exhibition on Instrumental Analysis (BCEIA 2013) CY - Beijing, China DA - 2013-10-23 PY - 2013 AN - OPUS4-29295 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - CCQM-K98/P134 - Pb isotope amount ratios in bronze T2 - CCQM IAWG Meeting CY - Pretoria, South Africa DA - 2013-11-05 PY - 2013 AN - OPUS4-29296 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Riebe, Gundel A1 - Klingbeil, Patrick A1 - Pritzkow, Wolfgang A1 - Vogl, Jochen T1 - Erfahrungen mit mikrowelleninduzierten Aufschluss-Verfahren für die Elementspurenanalytik T2 - MLS-Tagesseminar CY - Berlin, Deutschland DA - 2001-03-19 PY - 2001 AN - OPUS4-1111 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Riebe, Gundel A1 - Ostermann, Markus A1 - Pritzkow, Wolfgang A1 - Vogl, Jochen T1 - Combination of sophisticated sample digestion methods and highly accurate determination procedures shown for Sulphur in oil and Cadmium and Lead in sediment T2 - Internationale Konferenz "Trends in Sample Preparation 2002" CY - Seggau, Austria DA - 2002-06-30 PY - 2002 AN - OPUS4-1398 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ostermann, Markus A1 - Janisch, Nadine A1 - Vogl, Jochen T1 - On the determination of the moisture content in different matrix materials T2 - Internationale Konferenz "Trends in Sample Preparation 2002" CY - Seggau, Austria DA - 2002-06-30 PY - 2002 AN - OPUS4-1399 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Paz, B. A1 - Meyer, H.-P. A1 - Varychev, A. A1 - Rosner, M. A1 - Vogl, Jochen A1 - Behrendt, S. ED - Treister, M. ED - Yablonsky, L. T1 - Археометрические исследования стеклянных сосудов из погребений ранних кочевников Южного Приуралья T1 - Archäometrische Untersuchungen an achaimenidischen Glasgefäßen aus den Gräbern der frühen Nomaden des südlichen Urals N2 - Die untersuchten Gläser lassen sich in drei Gruppen einteilen. Die beiden Fragmente aus der Nekropole von Pjatimary deuten auf eine frühe Herstellungszeit hin und lassen sich mit eisenzeitlichen Fragmenten iranischer Herkunft vergleichen. Die Glasfunde aus der Nekropole Filippovka bestehen aus völlig unterschiedlichen Glasmaterialien und müssen einer späteren Herstellungszeit zugeordnet werden. Sowohl die unterschiedlichen Rezepturen als auch der definitive Hinweis auf verschiedene Rohstoffquellen zur Herstellung der untersuchten Gläser, lassen ein breitgefächertes Netz von weitreichenden Handelsbeziehungen erkennen. KW - Archäometrie KW - Isotopenverhältnisse Strontium und Blei KW - Elementanalyse KW - Massenspektrometrie KW - Herkunft PY - 2012 SN - 978-5-903011-85-8 VL - 1 SP - 262 EP - 267 PB - TAUS CY - Moskau AN - OPUS4-26899 LA - rus AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rienitz, O. A1 - Schiel, D. A1 - Görlitz, V. A1 - Jährling, R. A1 - Vogl, Jochen A1 - Lara-Manzano, J.V. A1 - Zon, A. A1 - Fung, W.-H. A1 - Buzoianu, M. A1 - De Sena, R.C. A1 - Dos Reis, L.A. A1 - Valiente, L. A1 - Yim, Y.-H. A1 - Hill, S. A1 - Champion, R. A1 - Fisicaro, P. A1 - Bing, W. A1 - Turk, G.C. A1 - Winchester, M. R. A1 - Saxby, D. A1 - Merrick, J. A1 - Hioki, A. A1 - Miura, T. A1 - Suzuki, T. A1 - Linsky, M. A1 - Barzev, A. A1 - Máriássy, M. A1 - Cankur, O. A1 - Ari, B. A1 - Tunc, M. A1 - Konopelko, L.A. A1 - Kustikov, Y.A. A1 - Bezruchko, M. T1 - Final report on CCQM-K87: Mono-elemental calibration solutions N2 - The aim of this comparison was to demonstrate the capability of national metrology institutes to measure elemental mass fractions at a level of w(E) ≈ 1 g/kg as found in almost all mono-elemental calibration solutions. These calibration solutions represent an important link in traceability systems in inorganic analysis. Virtually all traceable routine measurements are linked to the SI through these calibration solutions. Every participant was provided with three solutions of each of the three selected elements chromium, cobalt and lead. This comparison was a joint activity of the Inorganic Analysis Working Group (IAWG) and the Electrochemical Analysis Working Group (EAWG) of the CCQM and was piloted by the Physikalisch-Technische Bundesanstalt (PTB, Braunschweig, Germany) with the help of the Bundesanstalt für Materialforschung und -prüfung (BAM, Berlin, Germany), the Centro Nacional de Metrología (CENAM, Querétaro, Mexico) and the National Institute of Standards and Technology (NIST, Gaithersburg, USA). A small majority of participants applied inductively coupled plasma optical emission spectrometry (ICP OES) in combination with a variety of calibration strategies (one-point-calibration, bracketing, calibration curve, each with and without an internal standard). But also IDMS techniques were carried out on quadrupole, high resolution and multicollector ICP-MS machines as well as a TIMS machine. Several participants applied titrimetry. FAAS as well as ICP-MS combined with non-IDMS calibration strategies were used by at least one participant. The key comparison reference values (KCRV) were agreed upon during the IAWG/EAWG meeting in November 2011 held in Sydney as the added element content calculated from the gravimetric sample preparation. Accordingly the degrees of equivalence were calculated. Despite the large variety of methods applied no superior method could be identified. The relative deviation of the median of the participants' results from the gravimetric reference value was equal or smaller than 0.1% (with an average of 0.05%) in the case of all three elements. KW - CCQM KW - Metrology KW - IDMS PY - 2012 DO - https://doi.org/10.1088/0026-1394/49/1A/08010 SN - 0026-1394 SN - 1681-7575 VL - 49 IS - 08010, 1A (Technical Supplement 2012) SP - 1 EP - 104 PB - Inst. of Physics Publ. CY - Bristol AN - OPUS4-30458 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Rosner, Martin T1 - Production and certification of a unique set of isotope and delta reference materials for Boron isotope determination in geochemical, environmental and industrial materials N2 - Isotopic reference materials are essential to enable reliable and comparable isotope data. In the case of boron only a very limited number of such materials is available, thus preventing adequate quality control of measurement results and validation of analytical procedures. To address this situation a unique set of two boron isotope reference materials (ERM-AE102a and -AE104a) and three offset δ11B reference materials (ERM-AE120, -AE121 and -AE122) were produced and certified. The present article describes the production and certification procedure in detail. The isotopic composition of all the materials was adjusted by mixing boron parent solutions enriched in 10B or 11B with a boron parent solution having a natural isotopic composition under full gravimetric control. All parent solutions were analysed for their boron concentration as well as their boron isotopic composition by thermal ionisation mass spectrometry (TIMS) using isotope dilution as the calibration technique. For all five reference materials the isotopic composition obtained on the basis of the gravimetric data agreed very well with the isotopic composition obtained from different TIMS techniques. Stability and homogeneity studies that were performed showed no significant influence on the isotopic composition or on the related uncertainties. The three reference materials ERM-AE120, ERM-AE121 and ERM-AE122 are the first reference materials with natural δ11B values not equal to 0‰. The certified δ11B values are -20.2‰ for ERM-AE120, 19.9‰ for ERM-AE121 and 39.7‰ for ERM-AE122, each with an expanded uncertainty (k = 2) of 0.6‰. These materials were produced to cover about three-quarters of the known natural boron isotope variation. The 10B enriched isotope reference materials ERM-AE102a and ERM-AE104a were produced for industrial applications utilising 10B for neutron shielding purposes. The certified 10B isotope abundances are 0.29995 for ERM-AE102a and 0.31488 for ERM-AE104a with expanded uncertainties (k = 2) of 0.00027 and 0.00028, respectively. Together with the formerly certified ERM-AE101 and ERM-AE103 a unique set of four isotope reference materials and three offset δ11B reference materials for boron isotope determination are now available from European Reference Materials. KW - Boron isotope variations KW - Delta-scale KW - Stable isotopes KW - Isotope reference materials KW - Delta reference materials KW - Metrology in chemistry KW - Absolute isotope abundance PY - 2012 DO - https://doi.org/10.1111/j.1751-908X.2011.00136.x SN - 1639-4488 SN - 1751-908X VL - 36 IS - 2 SP - 161 EP - 175 PB - Blackwell CY - Oxford AN - OPUS4-26260 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Völling, E. A1 - Reifarth, N. A1 - Vogl, Jochen ED - Nosch, M.-L. ED - Laffineur, R. T1 - The intercultural context of treasure A in Troy - Jewellery and textiles N2 - At the end of May 1873, Heinrich Schliemann recovered Treasure A in Troy. He brought all the metal artifacts illegally to Athens and published his iscoveries one year later. Then he bequeathed the Trojan finds to Berlin where from 1881 onwards, Treasure A was exhibited in the Museum of Arts and Crafts (later Gropius Bau). Hubert. Schmidt inventoried and catalogued the Trojan remains in 1902 without the so-called “Dubletten” (duplicates). The transfer of the Treasure trove in 1945 to former Leningrad (St. Petersburg) and Moscow is well known, but there was a partial restoration of the looted art from the former Soviet Union back to the former GDR: eight out of eleven silver vessels of Treasure A came via Leipzig in 1979 finally back to Berlin’s Museum für Vor- und Frühgeschichte, Stiftung Preussischer Kulturbesitz in 1994. During its safe keeping in Leningrad and Leipzig, these silver jars remained ignored in the boxes in which they were transported, a Situation, which today permits them to be investigated almost in their condition of discovery. The study of the Originals allowed Information to be gleaned about their manufacture and offered opportunities for various analyses. After the gold jewellery came to light, technical data and an archaeological appraisal of the Trojan gold kept in the Pushkin Museum of Fine Arts in Moscow could be published in 1996. The considerable quantity of the outstanding gold artifacts of Treasure A was deposited inside the great silver vessel Sch 5873 and listed by Heinrich Schliemann. T2 - 13th International Aegean Conference CY - Copenhagen, Denmark DA - 21.04.2010 PY - 2012 SN - 978-90-429-2665-3 SP - 531 EP - 538 PB - Peeters Publishers CY - Liège, Belgium AN - OPUS4-26408 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen T1 - Measurement uncertainty in single, double and triple isotope dilution mass spectrometry N2 - Triple IDMS has been applied for the first time to the quantification of element concentrations. It has been compared with single and double IDMS obtained on the same sample set in order to evaluate the advantages and disadvantages of triple IDMS over single and double IDMS as an analytical reference procedure. The measurement results of single, double and triple IDMS are indistinguishable, considering rounding due to the individual measurement uncertainties. As expected, the relative expanded uncertainties (k = 2) achieved with double IDMS (0.08 %) are dramatically smaller than those obtained with single IDMS (1.4 %). Triple IDMS yields the smallest relative expanded uncertainties (k = 2, 0.077 %) unfortunately at the expense of a much higher workload. Nevertheless triple IDMS has the huge advantage that the isotope ratio of the spike does not need to be determined. Elements with high memory effects, highly enriched spikes or highest metrological requirements may be typical applications for triple IDMS. KW - Single IDMS KW - Double IDMS KW - Triple IDMS KW - Measurement uncertainty KW - Cd mass fraction PY - 2012 DO - https://doi.org/10.1002/rcm.5306 SN - 0951-4198 SN - 1097-0231 VL - 26 IS - 3 SP - 275 EP - 281 PB - Wiley CY - Chichester AN - OPUS4-25292 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Klingbeil, Patrick A1 - Vogl, Jochen A1 - Pritzkow, Wolfgang A1 - Riebe, Gundel A1 - Müller, J. T1 - Comparative studies on the certification of reference materials by ICPMS and TIMS using isotope dilution procedures N2 - A comparison of different isotope dilution mass spectrometric (IDMS) procedures using inductively coupled plasma mass spectrometry (ICPMS) and thermal ionization mass spectrometry (TIMS) was carried out to examine the degree of equivalence between the used procedures in terms of requirements for reference material certification. The comparison was based on the measurement results and their uncertainties. The sample used in this study is a pure zinc metal to be certified by the Bureau Communie de Référence (BCR) for amount contents of different trace elements. This study focuses on cadmium and thallium. The TIMS values contributed to the certified values. To guarantee identical conditions as far as possible for the procedures under investigation, the samples were split into subsamples after spiking and digestion took place. Thus, every IDMS procedure started with an identical set of samples. In total, four different IDMS procedures and one external calibration procedure using internal standardization as an example of routine analysis were applied. The IDMS procedures divide in a group with and a group without trace/matrix separation. Multicollector TIMS (TI-MC-MS) and multicollector ICPMS (ICP-MC-MS) were used in combination with trace/matrix separation, whereas quadrupole ICPMS (ICP-QMS) and ICP-MC-MS were also applied to nonseparated samples. All IDMS results agree well within their combined uncertainties, while some results from the external calibration procedure do not. IDMS results obtained by ICPMS without separation are comparable to those obtained by TI-MC-MS with separation regarding precision and accuracy. The smallest uncertainties were achieved using ICP-MC-MS in combination with trace/matrix separation. KW - ICP-MS KW - TIMS KW - IDMS KW - multi-collector KW - uncertainty budget KW - Certification KW - reference material PY - 2001 DO - https://doi.org/10.1021/ac001278c SN - 0003-2700 SN - 1520-6882 VL - 73 IS - 8 SP - 1881 EP - 1888 PB - American Chemical Society CY - Washington, DC AN - OPUS4-909 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - You, Zengchao A1 - Winckelmann, Alexander A1 - Vogl, Jochen A1 - Recknagel, Sebastian A1 - Abad Andrade, Carlos Enrique T1 - Determination of calcium, iron, and selenium in human serum by isotope dilution analysis using nitrogen microwave inductively coupled atmospheric pressure plasma mass spectrometry (MICAP-MS) N2 - In this study, we demonstrate the applicability of nitrogen microwave inductively coupled atmospheric pressure mass spectrometry (MICAP-MS) for Ca, Fe, and Se quantification in human serum using isotope dilution (ID) analysis. The matrix tolerance of MICAP-MS in Na matrix was investigated, uncovering that high Na levels can suppress the signal intensity. This suppression is likely due to the plasma loading and the space charge effect. Moreover, 40Ca and 44Ca isotopic fractionation was noted at elevated Na concentration. Nine certified serum samples were analyzed using both external calibration and ID analysis. Overestimation of Cr, Zn, As, and Se was found in the results of external calibration, which might be resulted from C-induced polyatomic interference and signal enhancement, respectively. Further investigations performed with methanol showed a similar enhancement effect for Zn, As, and Se, potentially supporting this assumption. The mass concentrations determined with ID analysis show metrological compatibility with the reference values, indicating that MICAP-MS combined with ID analysis can be a promising method for precise Ca, Fe, and Se determination. Moreover, this combination reduces the influences of matrix effects, broadening the applicability of MICAP-MS for samples with complex matrix. KW - Selenium KW - Nitrogen microwave inductively coupled atmospheric pressure mass spectrometry KW - Isotope dilution KW - Human serum KW - Calcium KW - Iron PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-598664 DO - https://doi.org/10.1007/s00216-024-05274-0 SN - 1618-2642 SP - 3117 EP - 3125 PB - Springer CY - Berlin AN - OPUS4-59866 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Knobbe, N. A1 - Vogl, Jochen A1 - Pritzkow, Wolfgang A1 - Panne, Ulrich A1 - Fry, H. A1 - Lochotzke, H.M. A1 - Preiss-Weigert, A. T1 - C and N stable isotope variation in urine and milk of cattle depending on the diet N2 - The stable carbon and nitrogen isotopic composition of urine and milk samples from cattle under different feeding regimes were analysed over a period of six months. The isotope ratios were measured with isotope ratio mass spectrometry (IRMS). The δ13C values of milk and urine were dependent on different feeding regimes based on C3 or C4 plants. The δ13C values are more negative under grass feeding than under maize feeding. The δ13C values of milk are more negative compared to urine and independent of the feeding regime. Under grass feeding the analysed milk and urine samples are enriched in 13C relative to the feed, whereas under maize feeding the 13C/12C ratio of urine is in the same range and milk is depleted in 13C relative to the diet. The difference between the 15N/14N ratios for the two feeding regimes is less pronounced than the 13C/12C ratios. The δ15N values in urine require more time to reach the new equilibrium, whereas the milk samples show no significant differences between the two feeding regimes. KW - Cattle KW - Urine KW - Milk KW - Feeding regime KW - Stable isotope PY - 2006 DO - https://doi.org/10.1007/s00216-006-0644-6 SN - 1618-2642 SN - 1618-2650 VL - 386 IS - 1 SP - 104 EP - 108 PB - Springer CY - Berlin AN - OPUS4-12746 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Abad Andrade, Carlos Enrique A1 - Florek, S. A1 - Becker-Ross, H. A1 - Huang, M.-D. A1 - Heinrich, Hans-Joachim A1 - Recknagel, Sebastian A1 - Vogl, Jochen A1 - Jakubowski, Norbert A1 - Panne, Ulrich T1 - Determination of boron isotope ratios by high-resolution continuum source molecular absorption spectrometry using graphite furnace vaporizers N2 - Boron isotope amount ratios n(10B)/n(11B) have been determined by monitoring the absorption spectrum of boron monohydride (BH) in a graphite furnace using high-resolution continuum source molecular absorption spectrometry (HR-CS-MAS). Bands (0→0) and (1→1) for the electronic transition X1Σ+ → A1Π were evaluated around wavelengths 433.1 nm and 437.1 nm respectively. Clean and free of memory effect molecular spectra of BH were recorded. In order to eliminate the memory effect of boron, a combination of 2% (v/v) hydrogen gas in argon and 1% trifluoromethane in argon, an acid solution of calcium chloride and mannitol as chemical modifiers was used. Partial least square regression (PLS) for analysis of samples and reference materials were applied. For this, a spectral library with different isotopes ratios for PLS regression was built. Results obtained around the 433.1 nm and 437.1 nm spectral regions are metrologically compatible with those reported by mass spectrometric methods. Moreover, for the evaluated region of 437 nm, an accuracy of 0.15‰ is obtained as the average deviation from the isotope reference materials. Expanded uncertainties with a coverage factor of k = 2 range between 0.15 and 0.44‰. This accuracy and precision are compatible with those obtained by mass spectrometry for boron isotope ratio measurements. KW - Boron isotopes KW - Isotope ratios KW - Boron monohydride KW - Molecular absorption KW - High-resolution continuum source absorption spectrometry KW - Graphite furnace KW - Memory effect KW - HR-CS-MAS PY - 2017 UR - http://www.sciencedirect.com/science/article/pii/S0584854717302537 DO - https://doi.org/10.1016/j.sab.2017.08.012 SN - 0584-8547 VL - 136 SP - 116 EP - 122 PB - Elsevier CY - Amsterdam, The Netherlands AN - OPUS4-42071 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Phukphatthanachai, Pranee A1 - Panne, Ulrich A1 - Jakubowski, Norbert A1 - Vogl, Jochen T1 - SI-traceable quantification of sulphur in copper metal and its alloys by ICP-IDMS N2 - Previously applied methods for the quantification of sulphur in copper and other pure metals revealed a lack of SI-traceability and additionally showed inconsistent results, when different methods were compared. Therefore, a reference procedure is required which allows SI-traceable values accompanied by a Sound uncertainty budget. In this study a procedure was developed for the quantification of total sulphur in copper at low concentration levels using inductively coupled plasma-isotope dilution mass spectrometry (ICP-IDMS). The major part of the copper matrix was separated by adding ammonia which forms a complex with the copper while releasing the sulphur followed by chromatographic separation using a weak cation resin. After that the sulphur fraction was further purified by chromatographic means using first an anion exchange method and second a chelating resin. The developed procedure shows high performance, especially concerning high efficiency in matrix removal (>99.999%) while keeping the recovery of sulphur above 80%. Procedure blanks are in the order of 3–53 ng resulting in LOD and LOQ values of 0.2 mg g1 and 0.54 mg g1, respectively. The procedure is sufficient to facilitate value assignment of the total sulphur mass fraction in reference materials. Additionally, relative measurement uncertainties were calculated to be below 1% and the measurement results were traceable to the SI. The procedure reported in this study is a new reference procedure for sulphur measurement in copper, being fit for two major purposes, certification of reference materials and assignment of reference values for inter-laboratory comparison. KW - Traceability KW - Measuremment uncertainty KW - Isotope dilution mass spectrometry KW - Reference measurements PY - 2018 DO - https://doi.org/10.1039/c7ja00338b SN - 0267-9477 SN - 1364-5544 VL - 33 IS - 1 SP - 90 EP - 101 PB - Royal Society of Chemistry CY - Cambridge, UK AN - OPUS4-43614 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Scharek, Vera M. A1 - Pfeifer, Jens A1 - Vogl, Jochen A1 - Traub, Heike A1 - Meermann, Björn T1 - Tin fractionation analysis in sediment samples via on-line ID ETV/ICP-MS N2 - We report a quantification approach for directly determining total tin and tin-based pollutants/species in sediments via electrothermal vaporization/inductively coupled plasma-mass spectrometry (ETV/ICP-MS) utilizing an on-line isotope dilution mass spectrometry (IDMS) approach. The method was developed and validated using an estuarine sediment reference material (BCR-277R), yielding a recovery of 106%. A relative standard deviation (RSD) of 14%, comparable to published data using a similar method, was obtained. A limit of quantification (LOQ) was estimated at 0.008 mg Sn kg−1 and sufficient for quantifying the total tin mass fraction of surface sediments along the tidal River Elbe course. Hereby, a decrease towards the river mouth, presumably due to dilution effects by less polluted marine sediment, was observed. Besides total tin, monitoring of organotin compounds (OTCs)/species is of interest in sediments due to their toxic effects on aquatic life. The method’s capability was extended by separating an OTC fraction in a sediment certified reference material (CRM) through the ETV temperature program. While spiking experiments with OTC standards confirmed the assignment, only a small fraction of the total certified OTC amount (3%), likely due to matrix effects, was recovered. However, applying the method to real-world samples, OTCs were detectable along the River Elbe course. By this, we demonstrated the potential of our method as a complementary fast-screening approach to species-specific analysis procedures. KW - ETV KW - Sn-Speciation KW - Sediment PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-640137 DO - https://doi.org/10.1007/s00216-025-06064-y SN - 1618-2642 SP - 1 EP - 10 PB - Springer Science and Business Media LLC AN - OPUS4-64013 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -