TY - JOUR A1 - Jonietz, Florian A1 - Myrach, Philipp A1 - Suwala, H. A1 - Ziegler, Mathias T1 - Examination of Spot Welded Joints with Active Thermography N2 - The method described here allows to determine the size of the thermal contact between two metal sheets joined by spot welding. This size is a measure for the size of the weld nugget, i.e. the zone melted during the welding process, and thus the quality of the welded joint. The method applies active thermography in transmission or reflection setup. Especially the reflection setup offers an attractive possibility for non-destructive testing when components can be accessed from one side only. The spot weld region is optically heated by laser or flash light radiation. The weld nugget provides the mechanical joint, but also constitutes a thermal bridge between the two welded sheets. The latter will be exploited in this method. The better thermal contact at the weld Nugget contrasts with the surrounding material, where the heat transfer between the two sheets is comparatively low. A major advantage of the described method is the applicability on sheets without any surface treatment. This is achieved by a proper normalization of the data, allowing for a correction of the varying surface emissivity. KW - Active thermography KW - Spot weld KW - Automotive industry PY - 2016 UR - http://link.springer.com/article/10.1007/s10921-015-0318-4?wt_mc=internal.event.1.SEM.ArticleAuthorIncrementalIssue DO - https://doi.org/10.1007/s10921-015-0318-4 VL - 35:1 SP - 1 EP - 14 PB - Springer CY - New York AN - OPUS4-35480 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Helmecke, E. A1 - Fleßner, M. A1 - Kaufmann, M. A1 - Staude, Andreas A1 - Hausotte, T. T1 - Numerical measurement uncertainty determination for dimensional measurements of microparts with CT N2 - Up to now, the only standardized method to determine the measurement uncertainty for computed tomography (CT) is to use calibrated workpieces as specified in the Guideline VDI/VDE 2630 Part 2.1. This paper discusses a promising numerical method for uncertainty determination with help of a virtual metrological CT (VMCT). It gives an explanation of the adjustments, the input parameters and the execution of the simulation. Furthermore, it discusses the first results of uncertainty determination compared to the method of using calibrated workpieces with the aid of two example cases. T2 - 6th Conference on Industrial Computed Tomography (iCT) CY - Wels, Austria DA - 09.02.2016 KW - simulation KW - Simulation KW - Computertomographie KW - Dimensionelle Metrologie KW - Normung KW - numerische Messunsicherheitsbestimmung KW - computed tomography KW - dimensional metrology KW - standardization KW - numerical uncertainty determination PY - 2016 UR - http://www.ndt.net/article/ctc2016/papers/ICT2016_paper_id17.pdf SP - Paper ID17, 1 EP - 7 AN - OPUS4-35481 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lehmann, Jens A1 - Burkert, Andreas A1 - Mietz, Jürgen T1 - Investigations proofing the passive layer stability of stainless steels N2 - The presented investigations have proved the principal suitability of the KorroPad method to assess the passive layer stability of stainless steels. The electrochemical mode of action could be described in detail and limitations of the applicability have been demonstrated. The influence of different surface finishes has been investigated and verified by known methods for describing corrosion resistances. As a result, the increased corrosion susceptibility of two ground surfaces has been detected, but also the corrosion resistance of further surface finishes could be confirmed. KW - Stainless steel KW - KorroPad KW - Passive layer PY - 2016 DO - https://doi.org/10.1002/maco.201408202 VL - 1 IS - 67 SP - 84 EP - 91 PB - WILEY-VCH Verlag GmbH & Co. KGaA CY - Weinheim AN - OPUS4-35545 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schmack, R. A1 - Eckhardt, B. A1 - Koch, G. A1 - Ortel, Erik A1 - Kraehnert, R. T1 - ZnO coatings with controlled pore size, crystallinity and electrical conductivity N2 - Zinc oxide is a wide bandgap semiconductor with unique optical, electrical and catalytic properties. Many of its practical applications rely on the materials pore structure, crystallinity and electrical conductivity. We report a synthesis method for ZnO films with ordered mesopore structure and tuneable crystallinity and electrical conductivity. The synthesis relies on dip-coating of solutions containing micelles of an amphiphilic block copolymer and complexes of Zn2+ ions with aliphatic ligands. A subsequent calcination at 400 °C removes the template and induces crystallization of the pore walls. The pore structure is controlled by the template polymer, whereas the aliphatic ligands control the crystallinity of the pore walls. Complexes with a higher thermal stability result in ZnO films with a higher content of residual carbon, smaller ZnO crystals and therefore lower electrical conductivity. The paper discusses the ability of different types of ligands to assist in the synthesis of mesoporous ZnO and relates the structure and thermal stability of the precursor complexes to the crystallinity and electrical conductivity of the zinc oxide. KW - conductivity KW - EISA KW - pore templating KW - pore size control KW - ligands KW - zinc oxide PY - 2016 DO - https://doi.org/10.5755/j01.ms.22.1.8634 SN - 1392–1320 VL - 22 IS - 1 SP - 74 EP - 81 PB - Kaunas University of Technology, Lithuania AN - OPUS4-35550 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Sauer, Andreas A1 - Scharf, Holger A1 - Becker, Roland T1 - Bericht zum 21. BAM-Ringversuch "Altlasten" N2 - Präsentation der Ergebnisse eines Ringversuchs zur Kompetenzbewertung von Prüflaboratorien auf dem Gebiet der anorganischen und organischen Bodenanalytik. KW - Eignungsprüfung KW - Boden KW - PAK KW - MKW KW - Spurenelemente KW - Gesamtcyanid KW - Proficiency testing KW - Soil KW - PAH KW - TPH KW - Trace elements KW - Total cyanide PY - 2015 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-355586 SP - 1 EP - 234 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-35558 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - BOOK A1 - Hübert, Thomas A1 - Boon-Brett, L. A1 - Buttner, W. J. T1 - Sensors for Safety and Process Control in Hydrogen Technologies N2 - This book is on sensors which are regularly deployed in technologies and processes related to hydrogen production, storage, distribution, and use. Not all types of sensors are equally suitable for specific hydrogen applications. The information in this book is intended to help the reader understand the basics of sensors, sensing technologies, sensor applications, and to provide guidelines for choosing the right sensors and the use of them correctly. Correct deployment of appropriate sensors demands knowledge of the sensing principle and of the physical or chemical quantities being measured. Because of the properties of hydrogen, the potential for its vastly increased use in a future low-carbon economy and possible hazards associated with its use, special attention is paid to hydrogen sensors. This book will not focus on the details of the hydrogen technologies nor on the many safety-related aspects of these technologies. Many books are already available on these topics. Instead the detection principle of hydrogen sensors and other sensor types used, in the dynamic and rapidly developing field of hydrogen technologies, are treated in detail in this book. In the first chapter a brief overview is presented on basic hydrogen properties and particularly on those properties which are most relevant for safety and for sensing. To illustrate the extensive field of contemporary applications and the exciting possibilities for near future sensor applications, existing and emerging markets using large quantities of hydrogen are mentioned. The role of sensors as devices for monitoring and control of processes and as safety monitoring devices is outlined. The second chapter gives an introduction to sensing technology and provides the Reader with relevant information pertaining to sensor definitions and classification, sensor metrics, and performance arameters, in addition to background information on sensor preparation technologies and techniques. While there are many books available which provide more exhaustive information on each of these topics, e.g., the level of detail provided in this chapter is sufficient to appreciate the salient features of sensing and sensing Technology which are central to hydrogen safety and monitoring of relevant applications. Chapter 3 provides a comprehensive overview of emerging and commercially available hydrogen sensors, an explanation of their sensing principle, and important aspects of their performance. A comprehensive and up-to-date account of the theory (physical or chemical principles), design, and practical implementations of hydrogen sensors for use in hydrogen related applications is presented. Similar information on chemical sensors for other gases, such as oxygen and trace components, which are also highly important in hydrogen technologies because of potential hazards to human health, process safety or facility performance, is provided in Chapter 4. In Chapter 5 descriptions of physical sensors for temperature, pressure, gas flow, and fire indication, which are also germane for the safe use of hydrogen, are provided. Standards, codes, and regulatory documents, which provide practical advice and legislative requirements regarding sensor deployment and performance, are described in Chapter 6. This chapter also makes reference to the main procedures for sensor testing in gas Standards including precise analytical methods and reference methods. The chapter concludes with a discussion on sensor selection and some installation guidelines are provided. In Chapter 7 traditional and emerging processes and technologies involving hydrogen are described. The application of sensors in processes for the production of hydrogen, hydrogen storage, distribution, and the use of hydrogen in stationary and mobile fuel cells is discussed. Furthermore, the use of hydrogen as a coolant and chemical reagent (medium) in various processes is described. The exploitation of sensors for replacing traditional analytical instrumentation is also discussed. Finally supplementary information is provided on hydrogen properties, measuring quantities, and sensor parameters. KW - Hydrogen Technologies KW - Hydrogen Sensors KW - Gas Sensors, Safety KW - Process Control PY - 2016 SN - 978-1-4665-9654-2 SP - 1 EP - 414 PB - CRC Press Taylor & Francis Group CY - Boca Raton, Florida, USA AN - OPUS4-35507 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Andrzejuk, W. A1 - Bau, A. A1 - Charoud-Got, J. A1 - de Vos, P. A1 - Emteborg, H. A1 - Lamberty, A. A1 - Linsinger, T. A1 - Oostra, A. A1 - Quetel, C. A1 - Roebben, G. A1 - Tresl, I. A1 - Hearn, R. A1 - Wood, S. A1 - Pritzkow, W. A1 - Vogl, Jochen T1 - Certification of the sulfur mass fraction in three commercial petrol materials - Certified reference materials ERM-EF211, ERM-EF212 and ERM-EF213 N2 - Three petrol reference materials were certified for their total sulfur content in support of Directive 2003/17/EC of the European Parliament and of the European Council, which stipulates that petrol with a maximum S content of 10 mg/kg must be available in all member states by 2009. Commercially available petrol was obtained and filled into borosilicate ampoules without further treatment. Homogeneity of the materials was tested and no heterogeneity was detected for two of the materials, whereas minor heterogeneity was observed for the third material. Stability of the materials was tested for 8-12 months at 60 °C and no degradation was observed. Characterisation was based on isotope-dilution mass spectrometry (IDMS) applied as primary method of measurement by three European metrology institutes and certified values were assigned using all results. The certified uncertainties include contributions of (potential) heterogeneity, potential degradation as well as characterisation. The final assigned values are: ERM-EF211: 48.8 ± 1.7 mg/kg ERM-EF212: 20.2 ± 1.1 mg/kg ERM-EF213: 9.1 ± 0.8 mg/kg The materials are available from IRMM (ERM-EF211), LGC (ERM-EF212) and BAM (ERMEF213) KW - Sulfur KW - Petrol KW - IDMS PY - 2007 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-355804 SN - 978-92-79-05370-2 SN - 1018-5593 SP - 1 EP - 37 PB - European Communities CY - Luxembourg AN - OPUS4-35580 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Vogl, Jochen A1 - Becker, Dorit A1 - Koenig, Maren A1 - Rosner, M. T1 - Certification report for the reference materials ERM-AE102a, -AE104a, -AE120, -AE121 and -AE122 N2 - Isotope reference materials are essential to enable reliable and comparable isotope data. Besides the correction of mass fractionation or mass discrimination isotope reference materials are indispensible for validation and quality control of analytical procedures. This article describes the production and certification of a set of five isotope reference materials ERM-AE102a, 104a, AE120, 121 and 122, for boron isotope analysis. The isotopic composition of all materials has been adjusted by mixing boron mother solutions enriched in 10B or 11B with a boron mother solution having natural-like isotopic composition under full gravimetric control. All mother solutions have been analysed for their boron mass fraction as well as their boron isotopic composition by TIMS using IDMS as calibration technique. For all five reference materials the isotopic composition obtained on the basis of the gravimetric data agrees very well with the isotopic composition obtained from different TIMS techniques. Performed stability and homogeneity studies show no significant influence on the isotopic composition as well as on the related uncertainties. The certified isotope abundances for 10B are 0.29995 (27) for ERM-AE102a and 0.31488 (28) for ERM-AE104a. The certified δ11B values are -20.2 (6) ‰ for ERM-AE120, 19.9(6) ‰ for ERM-AE121 and 39.7 (6) ‰ for ERM-AE122. Together with the formerly certified ERM-AE101 and -AE103 a unique set of seven certified reference materials (CRM) for boron isotope analysis is now available from BAM. KW - Boron KW - Delta value KW - Isotope ratio KW - ICPMS KW - TIMS PY - 2010 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-355813 SP - 1 EP - 24 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-35581 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Vogl, Jochen A1 - Becker, Dorit A1 - Koenig, Maren T1 - Certification report for the reference materials ERM-AE123 and ERM-AE124 - Certified for their boron isotope composition N2 - Isotope reference materials are essential to enable reliable and comparable isotope data. Besides the correction of mass fractionation or mass discrimination, isotope reference materials are indispensible for validation and quality control of analytical procedures. This report describes the production and certification of two isotope reference materials, ERM-AE123 and ERM-AE124, for boron isotope analysis. The isotopic composition of ERM-AE123 is the unaltered natural-like isotopic composition of the base material. The isotopic composition of ERM-AE124 has been adjusted by mixing two boron stock solutions enriched in 10B and 11B respectively under full gravimetric control. All stock solutions have been prepared fully under gravimetrical control. The corresponding boron isotopic composition has been analysed by TIMS. For both reference materials the isotopic composition obtained on the basis of the gravimetric data agrees very well with the isotopic composition obtained by TIMS. The certified isotope abundances for 10B are 0.19832 (21) for ERM-AE123 and 0.96006 (6) for ERM-AE124. Together with the formerly certified ERM-AE101, -AE102a, -AE103, -AE104a, -AE120, -AE121 and AE122, a unique set of nine certified reference materials (CRM) for boron isotope analysis is now available from BAM covering a range for the 10B isotope amount fraction from 0.2 to 0.96 and for the δ11B value from -20 ‰ to +40 ‰. KW - boron KW - isotope ratio KW - enriched isotope KW - ICPMS KW - TIMs PY - 2013 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-355826 SP - 1 EP - 17 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-35582 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Vogl, Jochen A1 - Becker, Dorit A1 - Koenig, Maren A1 - Rienitz, O. A1 - Noordmann, J. T1 - Certification report for the reference materials ERM-AE140 and ERM-AE141 - Pd and Pt single spikes certified for their Pd and Pt mass fraction and isotopic composition N2 - Isotope dilution mass spectrometry often is applied for the quantification of platinum group elements in environmental and geological samples. In most cases, however, certified spike solutions offering complete uncertainty statements and SI-traceability are missing. This report describes the production and certification of two isotope reference materials, ERM-AE140 and ERM-AE141, serving as calibrated spike solutions for IDMS based quantification of Pd and Pt, respectively. Both materials were produced by dissolving highly enriched isotopes 106Pd and 194Pt and determining the mass fraction of 106Pd and 194Pt in the final solution by reverse IDMS. Two independent back-spikes were produced for each material from high purity Pd and Pt. Characterization measurements were carried out by MC-ICPMS. For ERM-AE140 the certified mass fractions are w(106Pd) = 20.24(5) mg/kg and w(Pd) = 20.54(5) mg/kg. For ERM-AE141 the certified mass fractions are w(194Pt) = 18.18(11) mg/kg and w(Pt) = 19.90(12) mg/kg. These values are traceable to the International System of Units (SI) in the shortest possible way. KW - Palladium KW - Enriched isotope KW - Platinum KW - Spike KW - IDMS PY - 2015 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-355833 SP - 1 EP - 25 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-35583 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Vogl, Jochen A1 - Pritzkow, W. T1 - Bericht zur Herstellung und Zertifizierung eines Cadmium-Isotopenreferenzmaterials - Zertifiziertes Referenzmaterial BAM-I012 N2 - Dieser Bericht beschreibt die Herstellung und Zertifizierung einer Cadmiumlösung mit natürlicher Isotopenzusammensetzung. Für das Isotopen-Referenzmaterial sind sowohl die Isotopenverhältnisse als auch Isotopenhäufigkeiten und die molare Masse von Cadmium zertifiziert. Die Unsicherheiten sind erweiterte Messunsicherheiten U = k.uc mit k = 2. Der Cadmium-Massenanteil in der Lösung wird als indikativer Wert angegeben mit einer erweiterten Messunsicherheit U = k.uc mit k = 4,5. KW - Absolute Isotopenverhältnisse KW - Primäres Isotopenreferenzmaterial KW - Cadmium PY - 2015 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-355845 SP - 1 EP - 15 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-35584 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Thiel, Erik T1 - Spatial and temporal control of thermal waves by using DMDs for interference based crack detection N2 - Active Thermography is a well-established non-destructive testing method and used to detect cracks, voids or material inhomogeneities. It is based on applying thermal energy to a samples’ surface whereas inner defects alter the non-stationary heat flow. Conventional excitation of a sample is hereby done spatially, either planar (e.g. using a lamp) or local (e.g. using a focused laser) and temporally, either pulsed or periodical. In this work we combine a high power laser with a Digital Micromirror Device (DMD) allowing us to merge all degrees of freedom to a spatially and temporally controlled heat source. This enables us to exploit the possibilities of coherent thermal wave shaping. Exciting periodically while controlling at the same time phase and amplitude of the illumination source induces – via absorption at the sample’s surface - a defined thermal wave propagation through a sample. That means thermal waves can be controlled almost like acoustical or optical waves. However, in contrast to optical or acoustical waves, thermal waves are highly damped due to the diffusive character of the thermal heat flow and therefore limited in penetration depth in relation to the achievable resolution. Nevertheless, the coherence length of thermal waves can be chosen in the mm-range for modulation frequencies below 10 Hz which is perfectly met by DMD technology. This approach gives us the opportunity to transfer known technologies from wave shaping techniques to thermography methods. We will present experiments on spatial and temporal wave shaping, demonstrating interference based crack detection. T2 - Photonics West 2016, OPTO, 9761 CY - San Francisco, Cal, USA DA - 15.02.2016 KW - Thermal Waves KW - Laser KW - DMD KW - Active Thermography PY - 2016 AN - OPUS4-35586 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Thiel, Erik A1 - Kreutzbruck, M. A1 - Ziegler, Mathias T1 - Spatial and temporal control of thermal waves by using DMDs for interference based crack detection N2 - Active Thermography is a well-established non-destructive testing method and used to detect cracks, voids or material inhomogeneities. It is based on applying thermal energy to a samples’ surface whereas inner defects alter the nonstationary heat flow. Conventional excitation of a sample is hereby done spatially, either planar (e.g. using a lamp) or local (e.g. using a focused laser) and temporally, either pulsed or periodical. In this work we combine a high power laser with a Digital Micromirror Device (DMD) allowing us to merge all degrees of freedom to a spatially and temporally controlled heat source. This enables us to exploit the possibilities of coherent thermal wave shaping. Exciting periodically while controlling at the same time phase and amplitude of the illumination source induces – via Absorption at the sample’s surface - a defined thermal wave propagation through a sample. That means thermal waves can be controlled almost like acoustical or optical waves. However, in contrast to optical or acoustical waves, thermal waves are highly damped due to the diffusive character of the thermal heat flow and therefore limited in penetration depth in relation to the achievable resolution. Nevertheless, the coherence length of thermal waves can be chosen in the mmrange for modulation frequencies below 10 Hz which is perfectly met by DMD technology. This approach gives us the opportunity to transfer known technologies from wave shaping techniques to thermography methods. We will present experiments on spatial and temporal wave shaping, demonstrating interference based crack detection. T2 - Photonics West 2016, OPTO, 9761 CY - San Francisco, CA, USA DA - 15.02.2016 KW - Active thermography KW - Thermal wave KW - Spatial light modulation KW - Crack detection KW - DMD KW - DMD coupled laser PY - 2016 DO - https://doi.org/10.1117/12.2210918 SN - 0277-786X VL - 9761 SP - 97610N-1 EP - 97610N-13 AN - OPUS4-35587 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Lehmann, Jens T1 - KorroPad - Beurteilung der Korrosionsbeständigkeit von Oberflächen nichtrostender Stähle N2 - Mit dem KorroPad Verfahren ist es dem Anwender möglich den Zustand der Passivschicht nichtrostender Stähle auf sehr einfache und schnelle Weise einschätzen zu können. Das Verfahren eignet sich dazu, den Grad der Passivität in Abhängigkeit der Umgebungsbedingungen und der Zeit nachzuvollziehen. Dies ermöglicht dem Anwender und Verarbeiter von nichtrostenden Stählen, die Lagerungsbedingungen und –zeiten einer frisch bearbeiteten Stahloberfläche zu ermitteln, welche für die Ausbildung einer stabilen Passivschicht notwendig sind, bevor diese risikoarm eingesetzt werden kann. Wie die hier dargestellten Beispiele und auch weitere zahlreiche praktische Anwendungen gezeigt haben, eignet sich das KorroPad ebenfalls für die Identifikation kritischer Prozessparameter bei der Verarbeitung nichtrostender Stähle. Mit dem Verfahren lassen sich viele prozessbedingte Einflussfaktoren auf die Oberflächengüte wie auch auf den Werkstoff charakterisieren. Aufgrund der schnellen und einfachen Auswertung der Prüfergebnisse können positive wie auch negative Veränderungen hinsichtlich der Passivschichtstabilität zügig erkannt werden. Dies ermöglicht es dem Anwender schnell zu reagieren, um kritische Einflüsse zu korrigieren und um eine Optimierung von Inhouse-Prozessen durchzuführen. Weitere Einsatzgebiete sind im Bereich der Wareneingangs- und/oder Warenausgangskontrolle denkbar, überall wo es um die Frage der Passivschichtstabilität einer nichtrostenden Stahloberfläche geht. T2 - Fachtagung Bauwerksdiagnose - Praktische Anwendungen Zerstörungsfreier Prüfungen und Zukunftsaufgaben CY - Berlin, Germany DA - 25.02.2016 KW - Korrosionsschnelltest KW - nichtrostender Stahl KW - Passivschicht KW - KorroPad PY - 2016 AN - OPUS4-35570 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Platin- und Palladium-Analytik mit ID-ICPMS N2 - Zertifizierung von Pt und Pd-Spikes und deren Anwendung auf die Quantifizierung von Pd und Pt in Kfz-Emissionen T2 - 15. Edelmetallforum CY - Freising, Germany DA - 14.03.2016 KW - PGE KW - Emissionen KW - IDMS KW - ICPMS PY - 2016 AN - OPUS4-35572 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogl, Jochen T1 - Real-world examples of how to calculate a KCRV N2 - In this presentation the different ways are presented, which are used to calculate in practice the key comparison reference value. T2 - EURAMET TC Metrology in Chemistry Meeting CY - Geel, Belgium DA - 03.02.2016 KW - key comparison KW - CCQM KW - Degree of equivalence PY - 2016 AN - OPUS4-35573 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Vogl, Jochen A1 - Becker, Dorit A1 - Janisch, N. A1 - Klingbeil, P. A1 - Ludwig, H. P. A1 - Riebe, G. A1 - Pritzkow, W. A1 - Wermann, G. T1 - Zertifizierungsbericht für ERM-AE101 (auch BAM-I001), ERM-AE102 (auch BAM-I002) und ERM-AE103 (auch BAM-I003) N2 - Dieser Bericht beschreibt die Zertifizierung von 3 synthetischen Isotopenmischungen aus natürlicher und angereicherter Borsäure. Diese Isotopen-ZRM liegen als konzentrierte, wäs-serige Borsäure-Lösungen vor und sind bezüglich ihrer Isotopenzusammensetzung zertifi¬ziert. Der Bor-Gesamtgehalt ist als Richtwert angegeben. Die Unsicherheiten sind erweiterte Messunsicherheiten mit k=2. Sie sind in Klammern angegeben und beziehen sich auf die letzten beiden Stellen. Die vorliegenden Isotopen-ZRM sind bezüglich ihrer Isotopenzu¬sam-mensetzung mit erweiterten relativen Messunsicherheiten kleiner 0,12% zertifiziert. Die ab-solute, kombinierte Standardunsicherheit des prozentualen Stoffmengenanteils der Isotope (Isotopenhäufigkeit) liegt zwischen 0.012 und 0.017. KW - Isotope KW - Bor KW - Kernkraftwerke PY - 2009 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-355777 SP - 1 EP - 21 CY - Berlin AN - OPUS4-35577 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Vogl, Jochen A1 - Ostermann, Markus A1 - Becker, Dorit A1 - Janisch, N. T1 - Zertifiziertes Referenzmaterial ERM-AE104 bzw. BAM-I004 N2 - Dieser Bericht beschreibt die Zertifizierung einer synthetischen Isotopenmischung aus natürlicher und angereicherter Borsäure. Dieses Isotopen-ZRM liegt als konzentrierte, wässerige Borsäure-Lösung vor und ist bezüglich ihrer Isotopenzusammensetzung zertifiziert. Der Bor-Gesamtgehalt ist als Richtwert angegeben. Die Unsicherheiten sind erweiterte Messunsicherheiten mit k=2. Sie sind in Klammern angegeben und beziehen sich auf die letzten beiden Stellen. Das vorliegende Isotopen-ZRM ist bezüglich der Isotopenzusammensetzung mit erweiterten relativen Messunsicherheiten kleiner 0,08% zertifiziert. Die absolute, kombinierte Standardmessunsicherheit des prozentualen Stoffmengenanteils der Isotope (Isotopenhäufigkeit) liegt bei 0,014. In diesem Zertifizierungsbericht wird nur auf die Kapitel eingegangen, die abweichend vom bestehenden Zertifizierungsreport für die Referenzmaterialien BAM I001 bis BAM I003 sind und Einfluss auf die Endergebnisse haben. Dabei handelt es sich um die Kapitel 3.3, 3.4, 4, 6, 7 und 8, Die Kapitel 1, 2, 3, 3.1, 3.2, 5, 9 und 10 des alten Zertifizierungsberichts für die Referenzmaterialien BAM I001 bis BAM I003 behalten unverändert ihre Gültigkeit und sind nicht noch einmal aufgeführt worden. KW - Isotope KW - Kernkraftwerk KW - Bor PY - 2009 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-355786 SP - 1 EP - 9 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-35578 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Vogl, Jochen A1 - Klingbeil, P. A1 - Pritzkow, W. A1 - Riebe, Gundel A1 - Wermann, G. A1 - Turner, P. A1 - Wortel, N. A1 - Woittiez, J. T1 - HIIRM final report N2 - Accurate analytical results have become more and more an absolute essential tool for further progresses in technology and science. Precision however, often used in this context as a quality criterion for analytical methods, is not a replacement for accuracy in any way. Therefore, analytical procedures are necessary, which will generate reliable and accurate results and can be used for evaluation of other analytical procedures and certification of reference materials (RM). Especially the certification of reference materials for the amount content of trace elements requires highly accurate results with a small combined uncertainty. The best example for an analytical procedure having this capability is undoubtedly Isotope Dilution Mass Spectrometry, for inorganic as well as for organic applications. Applied on Thermal Ionization Mass Spectrometry (TIMS) isotope dilution provides results of highest quality and proven high accuracy especially in the field of RM certifications for more than 30 years. The major drawback of this approach often is the necessity for a complex chemical separation step. A major advantage of Inductively Coupled Plasma Mass Spectrometry (ICP-MS) is the potential to cope with a simplified or an on-line-carried-out sample preparation. A key requirement of isotope dilution analysis however is the accurate and precise determination of isotope ratios, because of its limiting factor for the accuracy and the total uncertainty of the result. Very precise isotope ratios can be determined in combination with a detection system that is capable of simultaneous detection of different isotopes, a so-called multi-collector system. The objective of the presented project is to evaluate the advantages of such a multi-collector ICP-MS for the application of IDMS in the field of trace elemental analysis in reference materials. The focus is on the development of simple and fast procedures for isotope ratio measurements in general and IDMS analysis in particular. Furthermore, it is an objective to develop and evaluate on-line spiking procedures. One of the first conclusions, which had a severe impact on the HIIRM project, arose during the early days of the project. Currently most certification experiments are accomplished by certification campaign based on a variety of participants’ results. The sample preparation, sending, analyzing and data evaluation however require lot of resources and the process may take a long time. An alternative way is given by using fewer participants with methods of higher metrological quality. For elemental amount contents such a method undoubtedly is isotope dilution analysis and multi-collector ICP-MS offers the necessary precision and matrix robustness and ruggedness as said above. Therefore, a multiple collector ICP-MS was manufactured as part of the project instead of the originally planned high-resolution instrument. Due to the novelty of the multicollector ICP-MS instrument, a lot of additional fundamental research became necessary. Especially interferences needed further attention. Fortunately, the IsoProbe is additionally equipped with a high-resolution option and with a brand new collison cell. The high-resolution option however can only be used to identify interferences but cannot be used to quantify them. On the other hand, the use of the collision cell proved to be a vital tool to overcome interferences. This is especially true because high resolution would have reduced the available sensitivity by a factor of ~100. Applying the collision cell technology the high sensitivity was maintained whilst most interferences were eliminated. However finding the right parameters of operation for the collision cell became a huge part of the method development process. A variety of gases like argon, helium, hydrogen, deuterium, nitrogen, krypton and xenon were tested for their suitability. Especially the tests accomplished for iron determinations revealed that carefully selected parameters have an incredible influence on the quality of the final results. Nonetheless collision cell technology will undoubtedly be widely used for newer ICP-MS instrumentation and contribute to eliminate wrong analytical values caused by interferences. The enhanced sensitivity of the instrument revealed also problems not detectable by other means. The control of contaminations seems to be one of the major analytical challenges in the future. Sector field based ICP-MS will give the user an opportunity to trace sources of contamination back to their origin and eliminate them. Even lower limits of detection will be the result as well as an enhanced reliability for analysts dealing with higher amount contents. The analyst will also benefit in controlling blank levels when the method of isotopically spiked procedure blanks is used as demonstrated in this project. Another main part of the project was the validation of the developed procedures. The first validation step was successfully accomplished by applying these procedures on the standard solutions provided by NRG. The main part of this validation however consisted of the evaluation of the fundamental parameters of the isotope dilution process and related measurements. This approach turned out to be superior compaired to the first step as a highly reliable uncertainty calculation can be easily performed. The best reputation and acceptance of the methods can however only be accomplished by participating in certification campaigns or in interlaboratory comparisons on highest metrological level. The results of the participations in general were brilliant. Not only the results but also the obtained realistic uncertainties were of superior quality. Direct comparisons at BAM with the results obtained by a multicollector TIMS applying the same calculation schemes showed the benefits of using multicollector ICP-MS. The main benefits of ICP-MS were identified, of which the first one is the enhanced precision of the isotope ratio measurement. For a variety of elements the values obtained by multicollector ICP-MS are even more precise than the ones obtainable by multicollector TIMS. The second important advantage identified was the simplified sample preparation. The laborious and time consuming analyte-matrix-separation step as necessary for TIMS measurements can either be omitted or at least be drastically reduced. Therefore, the advantages regarding time and enhanced sample throughput will result in further spread of ICP-MS in general and multicollector ICP-MS in particular. The third major part in terms of the method development process was mainly focused on developing an online isotope dilution system. The volumetric instead of the gravimetric IDMS approach proved difficult, if the high demands necessary for RM definition measurements are to be fulfilled. The major obstacle in this case is the missing stability and precision in terms of mass flow. Consequently, the initial development failed as the system made up of two piezoelectric droplet injectors was unable to reach the required stability as well as precision. The thereupon-created system consisting of two HPLC pumps proved to be far more valuable regarding automation and particularly the quantification of transient signals. Nevertheless, such a system will probably be rarely used in certification campaigns, as the gain of time is too small compared to the loss of reliability. However, this system proved most valuable in terms of species-specific elemental analysis as preliminary investigations showed. In this context this system will be suitable for certification measurements, as the major uncertainty contributions derive from sampling, sample treatment and species distribution and as moreover all availabel methods demonstrate far beyond. During the whole project, one of the main concerns regarding the multicollector ICP-MS instrument were software issues caused by the early development state of the original control programs. A lot of effort was necessary to accomplish the necessary data manipulations externally. The development of a new software suite by Micromass for the HIIRM project has solved this issue almost completely. With the new software suite and the validated parameters of measurement a step forward for institutes dealing with reference material certifications was achieved. Future certifications campaigns for minor elemental contents in different matrices should be performed by a small number of participants from highly qualified institutes. These institutes should apply very reliable methods of measurement like the ones developed in the HIIRM project. Many resources may be saved that way while the outcome of the certifications may easily be improved. ICP-MC-MS has the potential to be an important method in this context. Stable isotope dilution analysis in combination with a multi-detector ICP-MS, equipped with a hexapole collision cell for the suppression of important spectral interferences and for enhanced sensitivity, proved to be an advanced method of elemental analysis with a high potential for matrix independent measurements. Since ICP mass spectrometers of this type have only recently been introduced, no systematic evaluation of the capabilities of this specific application of the ICP-IDMS method has yet been made. KW - interferences KW - collision cell KW - ICPMS KW - IDMS PY - 2002 SP - 1 EP - 166 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-35579 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Abali, B. E. A1 - Wu, Cheng-Chieh A1 - Müller, W.H. T1 - An energy-based method to determine material constants in nonlinear rheology with applications N2 - Many polymer-type materials show a rate-dependent and nonlinear rheological behavior. Such a response may be modeled by using a series of spring-dashpot systems. However, in order to cover different time scales the number of systems may become unreasonably large. A more appropriate treatment based on continuum mechanics will be presented herein. This approach uses representation theorems for deriving material equations and allows for a systematic increase in modeling complexity. Moreover, we propose an approach based on energy to determine thematerial parameters.This method results in a simple linear regression problemeven for highly nonlinearmaterial equations. Therefore, the inverse problem leads to a unique solution. The significance of the proposed method is that the stored and dissipated energies necessary for the procedure are measurable quantities. We apply the proposed method to a 'semi-solid' material and measure its material parameters by using a simple-shear rheometer. KW - Material equations KW - Constitutive relations KW - Nonlinear rheology KW - Simple-shear rheometer KW - Inverse analysis PY - 2016 DO - https://doi.org/10.1007/s00161-015-0472-z SN - 0935-1175 SN - 1432-0959 VL - 28 IS - 5 SP - 1221 EP - 1246 PB - Springer CY - Berlin AN - OPUS4-34333 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -