TY - CONF A1 - Tiebe, Carlo A1 - Schütze, A. T1 - Gas sensor characterization and calibration N2 - The lecture about gas sensor characterization and calibration contains the content of 3S: Sensitivity, selectivity and stability, sensor drift, aging and poisoning as well as gas mixing systems for laboratory and field calibration, measurement uncertainty for sensor calibration and traceable calibration of gas sensor systems. T2 - International training course - Low-cost Environmental Monitoring – from sensor principles to novel services CY - Berlin, Germany DA - 09.04.2019 KW - Measurement uncertainty KW - Gas mixing system KW - Sensor drift KW - Sensor aging and poisoning PY - 2019 AN - OPUS4-47850 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Makowski, Maike A1 - Werneburg, M. A1 - Jung, C. A1 - Haase, H. A1 - Koch, Matthias T1 - Hot-spots of non-volatile mycotoxins in cereals: How can we overcome this problem? N2 - Since cereals constitute a staple food worldwide, monitoring of growth, storage and processing represent a perseverative challenge of analytical sciences. Especially during storage infested grains breed fungal clusters (“hot spots”) in which mycotoxins accumulate and can highly exceed allowed maximum levels. Because of their unpredictable presence, analytical procedures – including representative sampling - contain invasive and time intensive steps. To avoid erroneously negative results in mycotoxin analysis in cereals, the samples´ homogeneous headspace might be investigated instead of analyzing subsamples of the grains. So-called microbial volatile organic compounds (MVOC´s) provide information for instance about the fungal status of grains. Previous investigations revealed trichodiene to be a precursor of trichothecene mycotoxins which comprises more than 180 different compounds. Due to its non-functionalised sesquiterpene structure, quantification of trichodiene using Headspace GC-MS methods is possible. Thereby, it could be used as biomarker for trichothecene contamination of cereals. Nevertheless, further investigations are necessary. To be able to draw conclusion about the trichothecene content in cereal samples, a possible correlation between trichodiene concentration in the gas phase and trichothecene concentration in the sample must be examined. Realizing this idea would widely extend the applicability of trichodiene and enormously simplify trichothecene detection. Hence, the first step of an ongoing study aims to develop a laboratory reference method using trichodiene as volatile biomarker to quantify trichothecenes in cereals. Both static headspace and SPME-enrichment coupled to gas chromatography with mass spectrometry (GC-MS) were tested and compared. In a second step, this reference method is intended to validate new approaches for fast on-site screening of trichodiene in cereals. T2 - ANAKON 2019 CY - Münster, Germany DA - 25.03.2019 KW - Trichodiene KW - Gaschromatography-Mass Spectrometry KW - Mycotoxin-Biomarker PY - 2019 AN - OPUS4-47847 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bente, Klaas A1 - Oeff, Julius A1 - Gaal, Mate T1 - Quantitative, zeiteffiziente, winkel- und frequenzaufgelöste Analyse von Elektretwandlern im Hör- und Ultraschallbereich N2 - Die Bildgebung oder Analyse von Materialien mittels luftgekoppelten Ultraschalls profitiert von einer hohen Geschwindigkeit, Flexibilität und Materialschonung des assoziierten Verfahrens. Die Luftankopplung hat jedoch den wesentlichen Nachteil, dass die auftretenden Impedanzsprünge an Grenzflächen zu enormen Verlusten in den Signalamplituden führen. Ultraschallwandler, die laut genug senden und sensitiv genug empfangen, um die geringen Signalamplituden noch auswerten zu können, sind somit zentraler Gegenstand der aktuellen Forschung und Entwicklung. Vielversprechende Wandlertypen sind piezokeramische Wandler, Elektretwandler, aber auch passive, breitbandige Ultraschallempfänger, wie optische Mikrophone. Die quantitative Charakterisierung der Sensitivitäten solcher Wandler wird oft vernachlässigt, da kein simples, universelles Verfahren zur Verfügung steht. In diesem Beitrag geht es um die Methodik der Charakterisierung von Luftultraschallwandlern mittels thermoakustischer Ultraschallsender. Thermoakustische Wandler erzeugen Ultraschall durch das schnelle heizen eines finiten Volumens an Luft vor dem Wandler. Die erhöhte interne Energie führt zu einer Druckänderung, welche sich als akustische Welle fortpflanzen kann. Da keine mechanische Volumenarbeit vom Wandler erbracht wird, funktioniert das Verfahren resonanzfrei. Die Charakterisierung wird am Beispiel von Elektretwandlern durchgeführt. Elektretwandler sind sensitive und immer verschleißresistentere Schallwandler, wodurch sie verbreitet Einsatz im Hör- und Ultraschallbereich finden. Geladene, zelluläre Polypropylen-Folien eignen sich besonders gut als Wandlermaterial aufgrund ihrer, verglichen mit Piezokompositen, hundertfach niedrigeren akustischen Impedanz bei gleichem piezoelektrischem Koeffizienten. Doch das winkel- und frequenzabhängige Verhalten der Wandler ist kaum untersucht und wenig quantifiziert. Es wird gezeigt, dass diese Folien eine schichtdickenabhängige Sensitivität in Größenordnungen zwischen 0.1 mV/Pa und 10 mV/Pa aufwiesen. Ein Maximum in der Sensitivität fand sich nahe ihrer mechanischen Resonanzfrequenz im Ultraschallbereich, aber auch im niederfrequenten Hörschallbereich. Darüber hinaus konnte die Winkelabhängigkeit der Sensitivität charakterisiert werden. Die Analyse konnte dabei zeiteffizient gestaltet werden, da pro Winkel eine Messung für die Berechnung der Übertragungsfunktion des Wandlers genügte. Quantifiziert wurden die Ergebnisse durch das einmalige Vermessen des Emitters mittels Laser-Doppler-Vibrometrie (LDV). Mit den erzielten Ergebnissen wurde zum einen das komplexe Sensitivitätsverhalten der Wandler untersucht, aber auch eine grundlegende Methodik aufgezeigt, wie Wandler quantitativ, multivariat charakterisiert werden können. Winkel- und frequenzaufgelöste Sensitivitäten erlauben zum einen die Analyse der Anwendbarkeit der Wandler für sämtliche Einsatzgebiete, zum anderen stehen so Rückschlüsse über die mechanische Dynamik von Elektretfolien in Aussicht, da deren Sensitivität direkt mit ihrem Elastizitätsmodul skaliert. T2 - DAGA 2019 CY - Rostock, Germany DA - 18.03.2019 KW - Luftultraschall KW - Ultraschall KW - Elektretwandler KW - Thermoakustik KW - Wandlercharakterisierung PY - 2019 SP - 748 AN - OPUS4-47712 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Roethke, A. A1 - Görlitz, V. A1 - Jährling, R. A1 - Kipphardt, Heinrich A1 - Matschat, Ralf A1 - Richter, Silke A1 - Rienitz, O. A1 - Schiel, D. T1 - SI-traceable monoelemental solutions on the highest level of accuracy: From the foundation of CCQM to recent advances N2 - Shortly after founding the CCQM in 1993, the first key comparison (CCQM-K2) about the determination of Cd and Pb content in river water was hosted by IRMM. It has been clear from the beginning that for the determination of an element mass fraction in a matrix, accurate reference solutions would be the key point for a metrologically sound analysis. Triggered by the not entirely satisfactory results it was decided to investigate the basis of all measurements: the reference solutions. Thus in 1999, CCQM-K8, hosted by EMPA/LNE, started the tedious but indispensable work on elemental solutions standards. Additionally, PTB, BAM and Merck KGaA initiated a project to establish a traceability system for inorganic analysis based on accurate monoelemental solutions. Within this unique approach ten high purity reference materials were fully characterized, and solutions were prepared gravimetrically thereof. These materials (forming the primary standards of elemental analysis) are available for NMIs/DIs from BAM. CCQM-P46 (Cu, Mg, Rh) demonstrated the actuality of the topic and the challenges to prepare elemental solutions for every element. The accurate preparation and use of monoelemental solutions is consequently reflected in the recurrent conduct of (key) comparisons: CCQM-P149 (purity of zinc), CCQM-K87 (Co, Cr, Pb), and the current CCQM-K143/P181 (Cu solutions), to name only a few in a long series. Is it necessary to put so much effort into the preparation of reference solutions? It clearly is! An example outside the world of academia: Recently, EDQM*, PTB, BAM and JRC have developed monoelemental reference standards traceable to the SI for toxic elements in support of the chapters of the European Pharmacopoeia, related to the analysis of elemental impurities in medicinal products. A new ICP OES method has been established allowing the comparison of two 1 g/kg mercury solutions with an outstandingly small uncertainty of Urel(w(Hg)) = 0.16 %. However, this technical progress would not have been possible without the ongoing effort of the metrological community within 25 years of research in the field of high accuracy monoelemental solutions. * EDQM: European Directorate for the Quality of Medicines and HealthCare T2 - CCQM Workshop on Advances in Metrology in Chemistry and Biology CY - Sevre DA - 10.04.2019 KW - CCQM KW - SI-traceable KW - Monoelemental solutions PY - 2019 UR - https://youtu.be/iVLk8CFnJTI AN - OPUS4-47846 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Richter, Silke T1 - Plasmaspectrochemistry in material sciences N2 - Plasmas as atomization and ionization/excitation sources have been used for more than 50 years. The term plasma spectrochemistry was introduced in the 1980s and is nowadays a topic of annual reviews and different conferences such as the Winter Conference on Plasma Spectrochemistry (held in USA), the European Winter Conference on Plasma Spectrochemistry, and The Nordic conference on Plasma Spectrochemistry. The development of advanced materials is inherently connected with improvements in analytical chemistry, and often is the driving force for method development in plasma-based spectrometry. Besides the determination of physical characteristics such as tensile strength, density, and conductivity, the investigation of their chemical constituents down to the trace and ultra-trace levels becomes more and more important and, therefore, the demand of sensitive and precise analytical methods is growing. In some cases, the determination of the average content is a sufficient result, for instance for the characterisation of raw material or waste management. However, lately laterally resolved analysis, depth profiling of layered materials and characterization of high purity materials are of growing importance. The aim of this article is to give an introduction into plasma spectrometry and its application in materials science. A theoretical overview of the used plasma techniques and a review on applications with a special focus on direct solid sampling will be presented. KW - Material Science KW - Plasma KW - Plasmaspectrochemistry PY - 2019 DO - https://doi.org/10.1002/9780470027318.a9341.pub2 SP - 1 PB - John Wiley & Sons CY - Hoboken, New Jersey AN - OPUS4-47840 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Weber, M. A1 - Lodi, A. A1 - Charoud-Got, J. A1 - Rienitz, O. A1 - Röthke, A. A1 - Richter, Silke T1 - Pharmacopoeial Reference Standards for Elemental Impurities N2 - Elemental impurities (EI) in medicinal products for human use are limited according to ICH guideline Q3D, which is in force since December 2017 in Europe and US. As a consequenceconsequence, the relevant texts of the European Pharmacopoeia (Ph. Eur.) and the United States Pharmacopeia (USP) have been modified to reflect and complement ICH Q3D, providing details on the analytical methods to be used. In those chapters (Ph. Eur. 2.4.20., USP <233>), it is stated that for the quantification of elemental impurities, certified reference materials (CRM) from a national metrology institute (NMI) or reference materials that are traceable to the CRM of an NMI should be used. The Ph. Eur. has so far implemented elemental impurity standards of this type for the four most important elemental impurities i.e. those corresponding to ICH Q3D Class 1: lead, cadmium, mercury and arsenic. The poster provides details on the development of those four reference standards, which was undertaken in partnership with a major institute accredited CRM producer (JRC, European Commission), and a national metrology institute (BAM and PTB, Germany), and a Designated Institute and accredited CRM producer (BAM, Germany). The reference standards were established and characterised according to rigorous metrological principles and are supplied with extended supporting information as required for the intended use. After successful completion of the project, the four reference standards have been added to the Ph.Eur. catalogue and are in distribution. It is expected that another three elemental impurity standards will be implemented and made available to users within the next three years. T2 - Joint EDQM-USP 13th International Symposium on Pharmaceutical Reference Standards CY - Strasbourg, France DA - 13.03.2019 KW - ICH guideline Q3D KW - Elemental Impurities KW - Pharmacopoeial Reference Standards PY - 2019 AN - OPUS4-47845 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Richter, Silke A1 - Pfeifer, Jens A1 - Hoffmann, V. A1 - Recknagel, Sebastian T1 - Der Einsatz der Glimmentladungsmassenspektroskopie für die Charakterisierung von Renststoffen als primäre Kalibriersubstanzen N2 - Messergebnisse in der chemischen Analyse müssen vergleichbar sein. Dies wird durch die metrologische Rückführbarkeit (traceability) auf SI realisiert. In der Chemie dienen Reinststoffe als Primärnormale, deren Reinheit mit einer Unsicherheit von < 0.01% ermittelt werden soll. Ein eleganter Weg, die Reinheit eines realen Materials mit hoher Präzision zu bestimmen, ist, alle Verunreinigungen zu messen, diese aufzusummieren und von der idealen Reinheit von 100 Prozent abzuziehen. Die metallischen Verunreinigungen in Metallen lassen sich mittels hochauflösender Massenspektrometer ermitteln. Eine weit größere Herausforderung ist die Bestimmung von Nichtmetallen wie Sauerstoff, Wasserstoff und Stickstoff im Metall, zumal diese auch oft die Hauptverunreinigung darstellen. Für die quantitative Bestimmung von Verunreinigungen wurden mit Standards dotierte Pulverpresslinge und mit H, O und N dotierte, gesinterte Materialien auf ihre Eignung als Kalibrierstandards für die GD-OES und GD-MS untersucht. Dabei kamen unterschiedliche Plasmabedingungen (pulsed/ continuous mode; verschiedene Plasmagase) zum Einsatz. Ein Überblick über analytische Kenngrößen und Grenzen der verwendeten Kalibrierstrategien wird gegeben. T2 - ANAKON 2019 CY - Münster, Germany DA - 25.03.2019 KW - GDMS KW - Primäre Kalibriersubstanzen KW - Reinststoffe PY - 2019 AN - OPUS4-47843 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Weltschev, Margit A1 - Pötzsch, Sina A1 - Bäßler, Ralph T1 - Entwicklung einer Prüfmethode zur Bewertung der Materialbeständigkeit von Bauteilen in Mitteldestillatanwendungen N2 - Für Bauteile (Komponenten) von Versorgungsanlagen für flüssige Brenn- und Kraftstoffe muss die Beständigkeit der metallenen Werkstoffe und Polymere nachgewiesen werden. Im Anwendungsfall von Heizöl mit 20 % biogenen Anteilen in Form von Rapsölfettsäuremethylester (FAME, Biodiesel) ist es für eine konservative Beurteilung des Korrosionssystems Werkstoff/Medium/Umgebung wichtig, die Alterungs­effekte des Mediums einzubeziehen. Entwicklung eines Prüfverfahrens für die Untersuchung der Beständigkeit von metallenen Werkstoffen und Polymeren in Heizöl und Heizöl-FAME-Blends, das für eine Vorauswahl der Werkstoffe und zum Nachweis der Beständigkeit im Hinblick auf die bauaufsichtlichen Zulassungsverfahren geeignet ist. Ein Schwerpunkt wird bei den metallenen Werkstoffen auf der Erprobung von Messmethoden liegen, mit denen sich in kurzer Versuchszeit ein Korrosionsangriff detektieren lässt. Metallene Werkstoffe: Weder örtliche Korrosion noch erhöhte Flächenkorrosion (Korrosionsrate:< 0,1 m/Jahr) sind bei den bisher geprüften Werkstoffen: Aluminium, C-Stahl 1.0037, austenitischer CrNi-Stahl 1.4301, Kupfer und Messing in Heizöl und B20 (Heizöl mit 20% Biodiesel) aufgetreten. Diese Werkstoffe sind in den Prüfmedien Heizöl und B20 als beständig zu bewerten. Es wurde keine signifikante Veränderung des pH-Wertes der Prüfmedien gemessen. Polymere: Massebestimmung: Die Prüfkörper der Elastomere ACM, HNBR und PUR sowie in geringerem Maße PE neigten zur Quellung in Heizöl und B20 nach 42 d und 84 d Auslagerung; für PA 6, POM und PVC wurde keine Masseänderung gemessen. Die Masseänderung der Prüfkörper in Heizöl und B20 ist mit Ausnahme von PUR vergleichbar. Bei PE traten Verfärbungen durch die Brennstoffe auf. Zugeigenschaften: ACM, HNBR, PE und PVC sind in Heizöl und B20 beständig, da die Änderung der Zugfestigkeit und der Reißdehnung < 15 % beträgt. PA und POM sind bedingt beständig, da die Änderung der Zugfestigkeit und der Reißdehnung < 30% beträgt. T2 - DGMK-Projekttreffen CY - Rostock, Germany DA - 28.03.2019 KW - Beständigkeitsbewertung KW - Metallene Werkstoffe KW - Polymere KW - Heizöl KW - Heizöl-FAME-Blends PY - 2019 AN - OPUS4-47841 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Akhmetova, Irina A1 - Haferkamp, Sebastian A1 - Emmerling, Franziska T1 - New transition metal phosphonates obtained by mechanochemistry N2 - Metal phosphonates are metal-organic compounds consisting of a metal core and a phosphonate ligand. Depending on the nature of the ligand, metal phosphonates appear in different structures covering the range from molecular compounds to three-dimensional networks. Due to their structural diversity, the chemistry of metal phosphonates has gained great interest during the last decades. Metal phosphonates can be used for various applications as gas storage and separation, magnetism, and energy conversion. Especially transition metal phosphonates are promising candidates as electrocatalysts. Mechanochemistry is a versatile approach for green and fast synthesis of pure substances. By milling the reactants, various organic, inorganic, and metal-organic compounds can be obtained in high yields. Here, we present the synthesis of different new metal phosphonates obtained by grinding of metal acetates with respective phosphonic acids. By varying the ratio of the reactants, we are able to determine the composition of the final products. The addition of small amounts of liquid to the grinding process tends to increase the product’s crystallinity. The crystal structures of the new compounds were determined from powder X-ray data. T2 - 27th Annual Meeting of the German Crystallographic Society CY - Leipzig, Germany DA - 25.03.2019 KW - Metal phosphonates KW - Mechanochemistry KW - PXRD KW - Structure solution PY - 2019 AN - OPUS4-47837 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Epping, Ruben T1 - View into the depths of copolymer microstructure by a special approach of LC-MS data evaluation N2 - It is a well-known story that copolymers beside their molar mass distribution (MMD) can exhibit a functionality type distribution (FTD), a copolymer composition distribution (CCD), a monomer sequence distribution (MSD) and additionally different topologies within one sample. This is and will remain a challenge for analysts. First a very short overview will be given concerning the common liquid separation techniques for polymers (SEC, LAC, LCCC, GELC) coupled to soft ionization mass spectrometric methods like MALDI and ESI-MS with focus on their limitations. For very broadly distributed samples or chemical very similar species the superposition of different separation mechanisms in chromatography is unavoidable or the separation efficiency cannot be optimized. Different ionization probabilities and species of the same nominal mass with completely different structures are just two problems of mass spec of complex polymer mixtures. Subsequently, different examples will be shown how these limitations in some cases could be outsmarted. First example will be the separation of statistical EO-PO copolymers of different chemical compositions by end group functionality and the quantification of end group fractions over the whole CCD. Here an UP-LCCC / ESI-TOF-MS coupling is applied. Further for different kinds of polymers it will be shown how it could be realized to obtain information on small isobaric/isomeric topological heterogeneities by coupling UP-SEC / ESI-TOF-MS. All results are based on the data processing of reconstructed ion chromatograms of single mass traces of complex ESI-MS spectra. T2 - SCM-9 CY - Amsterdam, The Netherlands DA - 29.01.2019 KW - Reconstructed ion chromatograms KW - Copolymer KW - Microstructure KW - LC x ESI-TOF-MS PY - 2019 AN - OPUS4-47836 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Günther, Martin A1 - Lorenzetti, Alessandra A1 - Schartel, Bernhard T1 - Investigating the fire phenomena of rigid polyurethane foams N2 - This work investigates the fire phenomena of rigid polyurethane foams (RPUF) in detail. Rigid polyurethane foams (RPUF) are widely used in industry and daily life because of their outstanding mechanical and thermal insulating properties. In case of fire, cellular polymers like RPUF behave differently from bulk materials, the reason for this is their low thermal inertia. The aim of this study is to investigate the fire phenomena of RPUF in detail. Characterized by simultaneous physical and chemical processes which interact, depend, and compete with each other, the combustion of RPUF is a highly complex occurrence. Therefore it is necessary to study all aspects in detail. The fire phenomena that were examined are gasification, liquefaction, charring and structural integrity as well as collapse. The comprehensive understanding of the processes taking place during combustion is the foundation of customized development of successful flame retardant approaches. Advanced cone calorimeter investigations provide insight into the fire behavior under forced flaming conditions. Thermocouples in the inside of specimens give information about the temperature gradient and temperature of the pyrolysis zone during combustion. Changes in the morphology and thickness of the pyrolysis zone were examined using a hot-stage microscope, as well as SEM images of cross-sections of quenched foam specimens. Furthermore, fire phenomena were characterized using LOI and thermal analysis. By using a multimethodological approach and systematically varied sets of Polyurethane and Polyisocyanurate foams, new insights into the burning of RPUF were won. The detailed knowledge of fire phenomena is essential for future development of tailored flame retardant strategies for RPUF. T2 - AMI Fire Retardants in Plastics 2019 CY - Pittsburgh, PA, USA DA - 02.04.2019 KW - Fire behavior KW - Rigid polyurethane foam PY - 2019 AN - OPUS4-47835 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Léonard, Fabien A1 - Bruno, Giovanni T1 - On nominal-actual comparisons for additive manufacturing applications N2 - Nominal-actual comparisons are routinely performed to compare a manufactured specimen to a reference specimen. X-ray Computed Tomography (CT) has brought a profound change in the way that tolerance verifications are performed in industry, by allowing the inner and outer geometries of an object to be measured, without the need for external access or destructive testing. As a results, CT is increasingly used in additive manufacturing applications, where a nominal-actual comparison performed between the digital model (CAD file), used as an input for the 3D printer, and the CT volume from the printed part, can provide invaluable information as to the accuracy of the printing process. However, the nominal-actual comparison process is somewhat different when applied to additively manufactured specimens by comparison to conventionally manufactured specimens. T2 - 9th Conference on Industrial Computed Tomography CY - Padova, Italy DA - 14.02.2019 KW - Computed tomography KW - X-ray computed tomography PY - 2019 AN - OPUS4-47833 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Léonard, Fabien A1 - Bruno, Giovanni T1 - On nominal-actual comparisons for additive manufacturing applications N2 - Nominal-actual comparisons are routinely performed to compare a manufactured specimen to a reference specimen. X-ray Computed Tomography (CT) has brought a profound change in the way that tolerance verifications are performed in industry, by allowing the inner and outer geometries of an object to be measured, without the need for external access or destructive testing. As a results, CT is increasingly used in additive manufacturing applications, where a nominal-actual comparison performed between the digital model (CAD file), used as an input for the 3D printer, and the CT volume from the printed part, can provide invaluable information as to the accuracy of the printing process. However, the nominal-actual comparison process is somewhat different when applied to additively manufactured specimens by comparison to conventionally manufactured specimens. T2 - 9th Conference on Industrial Computed Tomography CY - Padova, Italy DA - 14.02.2019 KW - Computed tomography KW - X-ray computed tomography KW - Implants PY - 2019 AN - OPUS4-47832 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Léonard, Fabien T1 - Distance transforms and correlation maps: advanced impact damage characterisation in composite panels N2 - One of the great strengths of X-ray computed tomography over conventional inspection methods (ultrasound, thermography, radiography) is that it can image damage in 3D. However for curved or deformed composite panels, it can be difficult to automatically ascribe the damage to specific plies or inter-ply interfaces. An X-ray computed tomography (CT) data processing methodology is developed to extract the through-thickness distribution of damage in curved or deformed composite panels. The method is applied to [(0°/90°)2]s carbon fibre reinforced polymer (CFRP) panels subjected low velocity impact damage (5 J up to 20 J) providing 3D ply-by-ply damage visualisation and analysis. Our distance transform approach allows slices to be taken that approximately follow the composite curvature allowing the impact damage to be separated, visualised and quantified in 3D on a ply-by-ply basis. In this way the interply delaminations have been mapped, showing characteristic peanut shaped delaminations with the major axis oriented with the fibres in the ply below the interface. This registry to the profile of the panel constitutes a significant improvement in our ability to characterise impact damage in composite laminates and extract relevant measurements from X-ray CT datasets. T2 - Dagstuhl Seminar 19151 Quantitative data visualisation challenge CY - Dagstuhl, Germany DA - 11.04.2019 KW - Computed tomography KW - X-ray computed tomography KW - Data processing PY - 2019 AN - OPUS4-47830 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hassanein, Yosri-Kamal A1 - Eisentraut, Paul A1 - Goedecke, Caroline A1 - Müller, Axel A1 - Kittner, Maria A1 - Bannick, C.G. A1 - Barthel, A.K. A1 - Braun, Ulrike T1 - Detection of microplastics in compost samples using a thermal decomposition method N2 - The ubiquitous presence of unwanted plastics in the environment, especially microscale particles, has been an issue in scientific studies and public debate in the last years. It is well known that oxidative degradation and subsequent fragmentation, caused by UV-radiation, oxidative aging and abrasion lead to the decomposition of larger plastic products into microplastics (MP). Possible effects of these MP on ecosystems are still unclear. Recent studies on MP findings are focused mainly on aquatic systems, while little is known about MP in terrestrial ecosystems. A possible source of MP input into the soil is compost from domestic bio-waste. Inappropriate waste separation causes plastic fragments in the bio-waste, some of which end up in the compost. In Germany compost is used as fertilizer in agriculture, hence MP could enter the soil by this pathway. So far, there have been only a few studies on this object. For this reason, analysis of compost as a sink and source of MP in ecosystems is of high interest. To estimate and monitor the MP content in compost and soil, fast and harmonised analytical methods are essential, which not only measure the polymer type and number of particles, but also the mass content. The most common spectroscopic methods are very time-consuming, often require complex sample preparation steps and cannot determine mass contents. Therefore, we used ThermoExtractionDesorption-GasChromatography-MassSpectrometry (TED-GC-MS) as a fast, integral analytical technique. The sample is pyrolyzed to 600°C in a nitrogen atmosphere and an excerpt of the pyrolysis gases is collected on a solid phase adsorber. Afterwards, the decomposition gases are desorbed and measured in a GC-MS system. Characteristic pyrolysis products can be used to identify the polymer type and determine the mass contents. This method is well established for the analysis of MP in water filtrate samples. In the present work we optimized the TED-GC-MS method for compost and compost/soil matrix and very common polymers, such as polyethylene, polypropylene, polyethylene-terephthalate and polystyrene (sample mass, detection limits, interfering signals, etc.). Additionally, specific pyrolysis products of polymers used for bio-waste bags, such as polylactide (PLA) and polybutylenadipat-terephthalat (PBAT) had to be identified and evaluated. First measurements were carried out on model and real samples from prepared mixtures and composting plant. The samples were sterilized, fractionated, filtered and dried. In addition, half of the sample material was treated with hydrogen peroxide to investigate a possible effect on detection. T2 - European Geosciences Union (EGU) General Assembly 2019 CY - Vienna, Austria DA - 07.04.2019 KW - Microplastics KW - Compost KW - Detection PY - 2019 AN - OPUS4-47829 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Yildirim, Arda A1 - Bühlmeyer, A. A1 - Hayashi, S. A1 - Haenle, J. C. A1 - Sentker, K. A1 - Huber, P. A1 - Laschat, S. A1 - Schönhals, Andreas T1 - Molecular Dynamics of Dipole Functionalized Triphenylene-based Discotics N2 - In this study, the molecular dynamics of a series of dipole functionalized triphenylene-based discotics, forming a columnar mesophase, were investigated by broadband dielectric spectroscopy (BDS). In addition to conductivity and localized dynamics, glassy dynamics were also observed. At higher temperatures an α1-processes and at low temperatures an α2 processes were detected having a completely different temperature dependence of its relaxation times. Different molecular assignments of α1- and α2-processes are suggested. The phase behavior of the material was explored under helium purge down to 100 K by differential scanning calorimetry (DSC). Besides the phase transition temperatures and enthalpies, one or two thermal glass transitions were found for all the materials. Moreover, the glassy dynamics were further investigated by Flash DSC, which is a chip-based calorimetry technique allowing for fast heating and cooling rates as high as 10000K/s. T2 - Spring Meeting of German Physical Society CY - Regensburg, Germany DA - 01.04.2019 KW - Liquid Crystals PY - 2019 AN - OPUS4-47827 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogler, M. A1 - Müller, Axel A1 - Braun, Ulrike A1 - Grathwohl, P. T1 - Sampling and Sample Preparation for Analysis of Microplastics in Soils N2 - Despite abundant evidence of the occurrence of microplastics (MP) – these are particles smaller 5 mm – in aquatic environments, little is known about the accumulation of plastic in terrestrial environments, especially in soils. Possible major input pathways could be the use of plastic mulching, the use of compost, sewage sludge or residues from biogas facilities as fertilizers, as well as littering in urban areas. To estimate the MP pollution, the development of reliable, fast methods for sampling, sample preparation, and detection is needed. The obtained data must be representative of the sampled environmental compartment and measurements from different environmental compartments must be comparable. A first breakthrough is an application of ThermoExtractionDesorption-Gas Chromatography-MassSpectrometry (TED-GC-MS) for the detection of MP, including tire abrasives. This method allows the determination of mass content within a few hours and only a minimum of sample preparation for samples from aquatic environments is needed. However, in contrast to filtrate samples from aquatic environments, sediment or soil samples need an enrichment of MP. Whereas MP concentration from marine sediments can be obtained by floatation and density Separation techniques using NaCl solutions, the extraction or separation from soils proves to be more difficult, as plastic particles are often part of organo-mineral aggregates within the soil matrix. The aim of this study is the development of a practicable processing guideline for representatively taken soil samples in order to concentrate microplastics, without complex and time-consuming treatment steps. Dispersants or detergents can be applied to decompose the soil matrix, but each preparation step carries the risk of crosscontamination of the sample and prolongs the preparation procedure. For this reason, we choose ZnCl2-solution with a density of 1.7 g/cm3, which include the densities of relevant MP types (0.9-1.7 g/cm3). It was tested to achieve both, disaggregation and separation as it decomposes organic material and dissolves carbonates. Also, ZnCl2 is inert to the precipitation of undesirable salts and Carbonates during the process of density separation, as polytungstate solution does. ZnCl2 can be reused after stepwise filtering (7 µm, 1.5 µm, 0.7 µm). Thus, disposal costs can be reduced. Efficiency and reproducibility of the sample preparation as well as the degradation behavior of MP under the present conditions were demonstrated with model samples. Real sampling campaigns were conducted at several agricultural sites and floodplains in south-west Germany. The sampling was performed according to practice for soil sampling, using adequate sampling strategies (pattern of sampling, number of field samples, homogenization, etc). The lab sample was fractioned into three size classes (5-100 µm, 100-1000 µm, and 1-5 mm). The identification and determination of mass fraction were done using TED-GC-MS. T2 - EGU 2019 - European Geoscience Union General Assembly 2019 CY - Wien, Austria DA - 07.04.2019 KW - Microplastics KW - Density separation KW - Sample preparation KW - Soil PY - 2019 AN - OPUS4-47824 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Müller, Axel A1 - Vogler, M. A1 - Grathwohl, P. A1 - Hollert, H. A1 - Braun, Ulrike T1 - Analysis of microplastics in soil samples by using a thermal decomposition method N2 - While plastics have become indispensable in our daily lives over the last decades, the input into the environment has been increasing concurrently. Plastics often end up in the environment because of intensive use and poor waste management practice. They are subjected to aging and fragmentation and finally be deposited as microplastic particles or in short microplastics (MP). MP are defined as particles originating from synthetic polymers between 1 µm and 5 mm. Although the pervasive abundance of MP in aquatic environments has been demonstrated comprehensively, less is known about the occurrence and fate of MP in terrestrial ecosystems. It is still unclear if soil functions as a MP source or a sink for aquatic environments. MP can either be transported into water bodies by soil erosion or be retained in soils. The few studies published are not comparable because of non-existent harmonized and standardized methods for sampling, sample preparation, and analysis. For an assessment of a potential exposure situation of MP, the determination of a mass content in the soil is crucial. Consequently, spectroscopic methods like Raman or FTIR are not suitable, as they deliver information about the shape and size of individual particles. Therefore, we show the application of ThermoExtractionDesorption-GasChromatography-MassSpectrometry (TED-GC-MS) for MP analysis in the soil. In this method, the soil sample is heated up to 600 °C in a nitrogen atmosphere. The decomposition gases are sorbed on a solid phase, then transferred to a GS-MS system where they are desorbed, separated and identified. The method allows the rapid identification of individual polymers through the detection of specific decomposition products, but also the quantitative determination of the MP mass. Besides thermoplastics, elastomers originated from tire abrasion, can be detected. In the present study, several terrestrial ecosystems in south-west Germany were systematically sampled. Subsequent sample preparation included sieving in fractions of 5-100 µm, 100-1000 µm, and 1-5 mm. MP were extracted by density separation using ZnCl2 solutions. The detection was done by TED-GC-MS measurements. Data of agricultural areas and floodplains are presented exemplarily. A quantitative assessment of highly occurring MP from littering as well as tire abrasion is conducted. T2 - EGU 2019 - European Geoscience Union General Assembly 2019 CY - Wien, Austria DA - 07.04.2019 KW - TED-GC-MS KW - Soil KW - Microplastics KW - Analysis PY - 2019 AN - OPUS4-47822 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Seeger, Stefan T1 - Overview on the EMPIR Project "AEROMET" N2 - Overview on the ongoing EU EMPIR Project "AEROMET" Aerosol Metrology for Atmospheric Science and Air Quality, Overview on preliminary resuilts in Workpackages 3 "Calibration of MPSS and CPCs" and 4 "Quantifying airborne particle compositions in the field" T2 - Meeting des ISO TC24/SC4, Joint session of Working Groups 9 "Single particle light interaction methods" and 12 "Electrical mobility and number concentration analysis for aerosol particles" CY - Graz, Austria DA - 11.04.2019 KW - Ambient air pollution KW - EU EMPIR KW - Chemical analysis KW - Total reflection X-ray spectroscopy KW - Airborne Particles PY - 2019 AN - OPUS4-47820 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hahn, Marc Benjamin T1 - Geant4: A universal Monte-Carlo toolkit for Particle scattering simulations N2 - Particle scattering simulations are an useful tool to plan experiments, design detectors, estimate doses in irradiated materials and medical treatment planning. Geant4 is a Monte-Carlo toolkit for the simulation of of particles scattering in matter. Photons, electrons, ions etc can be simulated with energies in the eV to GeV range. Their interactions with matter in arbitrary scattering geometries be studied. Scattering models, cross sections and material parameters can be set to cover interactions in gas, liquid and solid state. The import of geometries from computer aided design files or the protein data base is possible. It is currently being applied in high energy and nuclear physics, accelerator and detector design, space application, dosimetry and medical sciences. In this first part of the talk a brief overview over the structure, functionality and possible applications of Geant4 will be given. In the second part an example application will be presented: The determination of the microscopic dose-damage relations in aqueous environment for electron irradiated plasmid DNA will be explained. Therefore, we combine electron scattering simulations in water with calculations concerning the movement of biomolecules to obtain the energy deposit in the biologically relevant nanoscopic volume. We present, how to combine these simulational results and experimental data via a generalized damage model to determine the microscopic dose-damage relation at a molecular level. T2 - Department 6 Seminar CY - Berlin, Germany DA - 04.04.2019 KW - Geant4 KW - Dosimetry KW - Microdosimetry KW - Radiation damage KW - Electron irradiation KW - Monte-Carlo Simulation KW - Monte-Carlo Simulations KW - DNA KW - Computer simulation KW - Geant4-DNA PY - 2019 AN - OPUS4-47819 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -