TY - JOUR A1 - Loewer, M. A1 - Guenther, T. A1 - Igel, J. A1 - Kruschwitz, Sabine A1 - Martin, T. A1 - Wagner, N. T1 - Ultra-broad-band electrical spctroscopy of soils and sediments - a combined permittivity and conductivity model N2 - We combined two completely different methods measuring the frequency-dependent electrical properties of moist porous materials in order to receive an extraordinary large frequency spectrum. In the low-frequency (LF) range, complex electrical resistivity between 1 mHz and 45 kHz was measured for three different soils and sandstone, using the spectral induced polarization (SIP) method with a four electrode cell. In the high-frequency (HF) radio to microwave range, complex dielectric permittivity was measured between 1MHz and 10 GHz for the same samples using dielectric spectroscopy by means of the coaxial transmission line technique. The combined data sets cover 13 orders of magnitude and were transferred into their equivalent expressions: the complex effective dielectric permittivity and the complex effective electrical conductivity.We applied the Kramers-Kronig relation in order to justify the validity of the data combination. A new phenomenological model that consists of both dielectric permittivity and electrical conductivity terms in a Debye- and Cole–Cole-type manner was fitted to the spectra. The combined permittivity and conductivity model accounts for the most common representations of the physical quantities with respect to the individual measuring method. A maximum number of four relaxation processes was identified in the analysed frequency range. Among these are the free water and different interfacial relaxation processes, the Maxwell-Wagner effect, the counterion relaxation in the electrical double layer and the direct-current electrical conductivity. There is evidence that free water relaxation does not affect the electrical response in the SIP range. Moreover, direct current conductivity contribution (bulk and interface) dominates the losses in the HF range. Interfacial relaxation processes with relaxations in the HF range are broadly distributed down to the LF range. The slowest observed process in the LF range has a minor contribution to the HF response. KW - Electrical properties KW - Permeability KW - Porosity KW - Hydrogeophysics PY - 2017 DO - https://doi.org/10.1093/gji/ggx242 VL - 210 IS - 3 SP - 1360 EP - 1373 PB - Oxford University Press CY - Oxford AN - OPUS4-42598 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Martin, T. A1 - Zimmermann, E. A1 - Klitzsch, N. A1 - Hördt, A. A1 - Huisman, J. A. A1 - Radic, T. A1 - Kruschwitz, Sabine T1 - Round-robin test of SIP laboratory measurements using electrical test networks N2 - This study presents the results of an interlaboratory test designed to evaluate the accuracy of spectral induced polarization (SIP) measurements using controlled electrical test networks. The study, conducted in Germany since 2006, involved 12 research institutes, six different impedance measurement devices and four types of electrical test networks specifically designed to evaluate phase shift errors in SIP measurements. The test networks, with impedances ranging from 100 to 150 kΩ, represent high-impedance samples with different phase characteristics, and pose the measurement challenges typical of such samples, including high contact impedances and parasitic capacitances. Four key findings emerged from the study: (1) Impedance measurements across all devices showed deviations within 1 per cent over a wide frequency range (0.001–1000 Hz); (2) phase errors remained below 1 mrad up to 100 Hz for most devices, but increased at higher frequencies due to parasitic capacitances and electromagnetic coupling effects; (3) lab-specific instruments have lower phase errors than field instruments when used in a laboratory environment, primarily due to the effects of long cables and too low input impedances of the field instruments; and (4) short cables and driven shielding technology effectively minimized parasitic capacitance and improved measurement accuracy. The study highlights the usefulness of test networks in assessing the accuracy of SIP measurements and raises awareness of the various factors influencing the quality of SIP data. KW - Induced polarization KW - Electrical properties KW - Electrical resistivity tomography (ERT) PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-631522 DO - https://doi.org/10.1093/gji/ggaf153 SN - 0956-540X VL - 242 IS - 1 SP - 1 EP - 13 PB - Oxford University Press (OUP) AN - OPUS4-63152 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Kautek, Wolfgang A1 - Hertwig, Andreas A1 - Martin, Sven A1 - Krüger, Jörg A1 - Lenzner, Matthias A1 - Spielmann, C. A1 - Lenner, M. A1 - Bunte, J. A1 - Puester, T. A1 - Burmester, T. A1 - Fiedler, A. A1 - Heberer, E. A1 - Brose, M. A1 - Stingl, A. A1 - Kiehl, P. A1 - Hönigsmann, H. A1 - Trautinger, F. A1 - Grabner, G. T1 - Safety in Femtosecond Laser Technology - Recent Results of a European Research Project (406) T2 - International Laser Safety Conference 2003 ; ILSC 2003 CY - Jacksonville, FL, USA DA - 2003-03-10 PY - 2003 SN - 0-912035-38-2 SP - 1(?) EP - 10(?) PB - Laser Institute of America CY - Orlando, Fla. AN - OPUS4-2259 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bunte, J. A1 - Barcikowski, S. A1 - Burmester, T. A1 - Püster, T. A1 - Hertwig, Andreas A1 - Kautek, Wolfgang A1 - Krüger, Jörg A1 - Martin, Sven A1 - Spielmann, C. A1 - Lenner, M. A1 - Brose, M. T1 - Sicherer Umgang mit Ultrakurzpuls-Lasern, Teil 1: Primäre Gefährdungen PY - 2005 SN - 0945-8875 IS - 2 SP - 6 EP - 11 PB - Magazin-Verl. CY - Bad Nenndorf AN - OPUS4-11001 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bunte, J. A1 - Barcikowski, S. A1 - Burmester, T. A1 - Püster, T. A1 - Hertwig, Andreas A1 - Kautek, Wolfgang A1 - Krüger, Jörg A1 - Martin, Sven A1 - Spielmann, C. A1 - Lenner, M. A1 - Brose, M. T1 - Sicherer Umgang mit Ultrakurzpuls-Lasern, Teil 2: Sekundäre Gefährdungen PY - 2005 SN - 0945-8875 IS - 4 SP - 13 EP - 18 PB - Magazin-Verl. CY - Bad Nenndorf AN - OPUS4-11002 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - C. Pardo Pérez, L. A1 - Arndt, A. A1 - Stojkovikj, S. A1 - Y. Ahmet, I. A1 - T. Arens,, J. A1 - Dattila, F. A1 - Wendt, R. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Radtke, Martin A1 - Davies, V. A1 - Höflich, K. A1 - Köhnen, E. A1 - Tockhorn, P. A1 - Golnak, R. A1 - Xiao, J. A1 - Schuck, G. A1 - Wollgarten, M. A1 - López, N. A1 - T. Mayer, M. T1 - Determining Structure-Activity Relationships in Oxide Derived CuSn Catalysts During CO2 Electroreduction Using X-Ray Spectroscopy N2 - The development of earth-abundant catalysts for selective electrochemical CO2 conversion is a central challenge. Cu-Sn bimetallic catalysts can yield selective CO2 reduction toward either CO or formate. This study presents oxide-derived Cu-Sn catalysts tunable for either product and seeks to understand the synergetic effects between Cu and Sn causing these selectivity trends. The materials undergo significant transformations under CO2 reduction conditions, and their dynamic bulk and surface structures are revealed by correlating observations from multiple methods—X-ray absorption spectroscopy for in situ study, and quasi in situ X-ray photoelectron spectroscopy for surface sensitivity. For both types of catalysts, Cu transforms to metallic Cu0 under reaction conditions. However, the Sn speciation and content differ significantly between the catalyst types: the CO-selective catalysts exhibit a surface Sn content of 13 at. % predominantly present as oxidized Sn, while the formate-selective catalysts display an Sn content of ≈70 at. % consisting of both metallic Sn0 and Sn oxide species. Density functional theory simulations suggest that Snδ+ sites weaken CO adsorption, thereby enhancing CO selectivity, while Sn0 sites hinder H adsorption and promote formate production. This study reveals the complex dependence of catalyst structure, composition, and speciation with electrochemical bias in bimetallic Cu catalysts. KW - Electrochemical CO2 conversion KW - Cu catalysts KW - X-ray absorption spectroscopy PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-547116 DO - https://doi.org/10.1002/aenm.202103328 SN - 1614-6832 VL - 12 IS - 5 SP - 2103328 PB - Wiley-VCH GmbH AN - OPUS4-54711 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kluge, Martin A1 - Kreißig, Michael A1 - Liebner, Christian A1 - Spoormaker, T. T1 - Identifizierung von sicherheitstechnisch gefährlichen Bedingungen für schlagartige Kompressionsvorgänge chemisch instabiler Gase im industriellen Maßstab N2 - Tetrafluorethen wird von der Polymerindustrie seit Jahrzenten als monomeres Ausgangsmaterial sowohl für die Herstellung von Polymeren (PTFE) als auch für Kopolymere (PCTFE) eingesetzt. Aufgrund seiner Eigenschaft als chemisch instabiles Gas kann TFE auch ohne Luftsauerstoff oder einen anderen Oxydator explosionsartig zerfallen. Nach der Initiierung des Zerfalls kann dieser unter bestimmten Bedingungen aufgrund des exothermen Reaktionsverhaltens sich selbstständig in Apparaten und Rohrleitungen ausbreiten. Dies geht aufgrund der freigesetzten Reaktionsenthalpie mit einem schlagartigen Anstieg von Druck und Temperatur einher, was zu erheblichen Belastungen der Materialien bis hin zum Versagen und Bruch und möglichen Folgeschäden einschließlich Personenschäden führen kann und in der Vergangenheit bereits mehrfach geführt hat. Besonders nach Wartungsarbeiten besteht die Gefahr, dass Teilabschnitte im Rohrleitungssystem mit TFE, Stickstoff oder Luft gefüllt sind mit Drücken in einem Bereich zwischen technischem Vakuum und atmosphärischem Druck wohingegen angrenzende Rohrabschnitte oder Behälter immer noch TFE bei Betriebsdrücken bis 32 bar enthalten können. Dabei sind die Abschnitte in der Praxis häufig durch Kugelhähne voneinander getrennt, die aufgrund ihrer Öffnungscharakteristik bereits bei geringen Betätigungswinkeln eine große Querschnittsfreigabe für die Strömung im Rohr ermöglichen. Dadurch können schlagartige Kompressionsvorgänge des Gases im Niederdruckbereich ermöglicht werden, die allein aufgrund der thermodynamischen Zustandsänderung zu einer erheblichen Temperaturerhöhung führen und im schlimmsten Fall zur Initiierung der Zerfallsreaktion führen können. Es wird erstmalig ein Versuchsaufbau im Industriemaßstab, der einer explosionsartigen Zerfallsreaktion von TFE standhalten kann. Zahlreiche Sicherheitskonzepte einschließlich diverser Berstscheibenkonfigurationen als auch zeitgesteuerte Schnellschlussventile wurden eingehend untersucht und bewertet, um die optimale Versuchskonfiguration für bestmögliche Reproduzierbarkeit festzulegen. Es fand eine systematische Untersuchung der schlagartigen Kompression der Systeme Luft/Luft, TFE/Luft, TFE/TFE und TFE/N2 statt. In der Hochdrucksektion wurden Drücke bis 30 bar realisiert und im Niederdrucksektor konnten Anfangsdrücke im Bereich weniger Millibar bis hin zu Atmosphärendruck eingestellt werden. Als Hauptergebnis wurde ein „Hazard diagram" erstellt, mit dessen Hilfe die Zündwahrscheinlichkeit in Abhängigkeit vom Hochdruck und Niederdruck abgeschätzt werden kann. Gefährliche Bedingungen in Rohrleitungen können dadurch auf einfachem Weg identifiziert werden. Als Referenzsystem zur Beurteilung der maximal erreichbaren nicht reaktiven Kompressionstemperaturen wurde Luft/Luft verwendet. Die damit ermittelten Daten dienten zur Bewertung von zusätzlichen exothermen Effekten, wie sie etwa bei Vorreaktion des TFE im Falle einer Dimerisierung auftreten können. Entgegen der ursprünglichen Annahme konnten die Systeme TFE/Stickstoff und TFE/TFE im verwendeten Aufbau nicht durch Kompressionsvorgänge gezündet werden. T2 - 12. Fachtagung Anlagen-, Arbeits- und Umweltsicherheit CY - Köthen, Germany DA - 05.11.2015 KW - Tetrafluoroethen KW - Zerfall KW - Selbstentzündung KW - Adiabate Kompression PY - 2015 SN - 978-3-86011-091-1 SP - 1 EP - 10 AN - OPUS4-34852 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ahlawat, A. A1 - Seeger, Stefan A1 - Gottschalk, Martin A1 - Tuch, T. A1 - Wiedensohler, A. T1 - Observation of systematic deviations between Faraday cup aerosol electrometers for varying particle sizes and flow rates - results of the AEROMET FCAE workshop N2 - Condensation particle counters (CPCs) are widely used for the measurement of aerosol particle number concentrations in the size range from approximately 3 nm to 3 μm. For an SI-traceable calibration of the size-dependent counting efficiency, which is advisable on a regular basis and required in several applications, Faraday cup aerosol electrometers (FCAEs) are considered to be a suitable SI-traceable reference.While the volumetric aerosol inlet flowrate and the electrical current measurement in FCAEs can be related to respective SI references, inter-comparison exercises for FCAEs are still performed on a regular basis to establish reliable uncertainty budgets and to further investigate the influences of designs and operational parameters on comparability. This is strongly demanded in the international community of metrological institutes and aerosol calibration facilities around the world, which provide CPC calibrations. In the present study, the performance of FCAEs was investigated,using Ag test aerosol particles with a 30 nm particle diameter by varying the inlet flowrates from 0.5 l min−1 to 4 l min−1. From our experimental results, significant deviations were observed in FCAE currents at sample flowrates smaller than 1.5 l min−1. It is recommended that these discrepancies should be quantified before an FCAE is used for CPC calibration at low sample flowrates and small particle sizes in the sub-30 nm size range. KW - Faraday cup aerosol electrometer KW - CPC calibration KW - Inter-comparison KW - Aerosol measurement instruments PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-531315 DO - https://doi.org/10.1088/1681-7575/ac0710 SN - 1681-7575 SN - 0026-1394 VL - 58 IS - 5 SP - 1 EP - 8 PB - Institute of Physics (IOP) CY - Bristol, UK AN - OPUS4-53131 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Babutzka, Martin A1 - Grabowski, Sven A1 - Sahrhage, H. A1 - Lampke, T. T1 - Electrochemical corrosion investigations on binary and ternary zinc alloy coatings using gel electrolytes N2 - Novel agar-based test electrolytes are used to perform electrochemical corrosion investigations on ZnFe and ZnNi binary as well as ZnFeMo ternary zinc coatings. The objectives of the electrochemical investigations include the characterization of the corrosion behavior, the description of the protective effect of the coatings as well as the investigation of the layer formation and degradation under artificial aging. ZnFe and ZnFeMo coatings are applied with varying iron content as well as an additional passivation layer, respectively, to study the effect on corrosion resistance. The results show that the protective effect of the coatings is not negatively influenced by different iron contents or the addition of molybdenum. Additional passivation of the ZnFe-containing coatings by means of a passivating agent leads to a significant improvement in the protective effect. Artificial aging leads to slight degradation of the additional passivation layer whereas coatings without post-treatment enhance their protective effect by the formation of corrosion product layers. KW - Binary zinc alloys KW - Ternary zinc alloys KW - Corrosion testing KW - Gel electrolytes KW - Corrosion PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-543013 DO - https://doi.org/10.1002/adem.202101336 SN - 1438-1656 SP - 1 EP - 14 PB - Wiley-VCH CY - Weinheim AN - OPUS4-54301 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rosemann, P. A1 - Babutzka, Martin A1 - Heyn, Andreas A1 - Halle, T. T1 - Influence of heat treatment on corrosion resistance of martensitic stainless steels 1.4034 and 1.4021 N2 - In the last years, new approaches for the evaluation of the corrosion resistance of stainless steels were developed which allow short term corrosion testing with increased information content. This work analyses the extensive influence of heat treatment on microstructure and the resulting corrosion resistance of the martensitic stainless steels 1.4034 and 1.4021 with advanced methods. Different heat treatments at various austenitization temperatures up to 1100°C and the effect of different cooling rates were evaluated; the last has not yet been studied in literature at all. The resulting corrosion behaviour in relation to the different carbon content in the two used alloys and the applied heat treatment will be presented and discussed. The applied methods of investigation were conventional evaluation of the critical pitting corrosion potential (PP), modified electrochemical potentiodynamic reactivation (mEPR) and the "KorroPad" (KP) technique. The performance of modified EPR and its interpretation were optimized to provide additional information about the general passivation ability and the extent of chromium depletion as result of applied heat treatment. The aim using PP and KP was the correlation between the Parameters of the mEPR with the changes in the pitting corrosion resistance. Furthermore the results will demonstrate the functionality and usability of the short term corrosion test methods mEPR and KP in order to increase their acceptance within the scientific community. The results indicate a surprisingly large influence of both austenitization temperature and cooling rate on the corrosion resistance within all three used test methods, which can explain the different corrosion behaviour of martensitic stainless steels in earlier investigations. T2 - EUROCORR 2014 - European corrosion congress CY - Pisa, Italy DA - 08.09.2014 KW - Martensitic stainless steel KW - KorroPad KW - Pitting corrosion KW - Polarisation PY - 2014 SN - 978-3-89746-159-8 SP - O EP - 7455, 146 AN - OPUS4-31481 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Seewald, J.S. A1 - Reeves, E.P. A1 - Bach, W. A1 - Saccocia, P.J. A1 - Craddock, P.R. A1 - Shanks III, W.C. A1 - Sylva, S.P. A1 - Pichler, T. A1 - Rosner, Martin A1 - Walsh, E. T1 - Submarine venting of magmatic volatiles in the Eastern Manus Basin, Papua New Guinea N2 - The SuSu Knolls and DESMOS hydrothermal fields are located in the back-arc extensional transform zone of the Eastern Manus Basin. In 2006, highly acidic and ΣSO4-rich vent fluids were collected at both sites and analyzed for the chemical and isotopic composition of major and trace species. Fluids exiting the seafloor have measured temperatures from 48 to 215 °C and are milky white in appearance due to precipitation of elemental S0. Vent fluid concentrations of Na, K, and Mg are depleted by as much as 30% relative to seawater, but have the same relative abundance. In contrast, the fluids are highly enriched in dissolved ΣCO2, Cl, SiO2(aq), Fe, and Al relative to seawater. Measured pH (25 °C) ranged from 0.95 to 1.87 and aqueous ΣSO4 ranged from 35 to 135 mmol/kg. The chemical and isotopic composition points to formation via subsurface mixing of seawater with a Na-, K-, Mg-, and Ca-free, volatile-rich magmatic fluid exsolved from subsurface magma bodies during a process analogous to subaerial fumarole discharge. Estimates of the magmatic end-member composition indicate a fluid phase where H2O > SO2 > CO2 ≈ Cl > F. The hydrogen and oxygen isotopic composition of H2O and carbon isotopic composition of ΣCO2 in the vent fluids strongly suggest a contribution of slab-derived H2O and CO2 to melts generated in the mantle beneath the Eastern Manus volcanic zone. Abundant magmatically-derived SO2 undergoes disproportionation during cooling in upflow zones and contributes abundant acidity, SO42-, and S0 to the venting fluids. Interaction of these highly acidic fluids with highly altered mineral assemblages in the upflow zone are responsible for extensive aqueous mobilization of SiO2(aq), Fe, and Al. Temporal variability in the speciation and abundance of aqueous S species between 1995 and 2006 at the DESMOS vent field suggests an increase in the relative abundance of SO2 in the magmatic end-member that has mixed with seawater in the subsurface. Results of this study constrain processes responsible for the formation of hot-spring fluids in magmatically active back-arc environments and the resulting chemical exchange between the lithosphere and water column. PY - 2015 DO - https://doi.org/10.1016/j.gca.2015.04.023 SN - 0016-7037 SN - 1872-9533 VL - 163 SP - 178 EP - 199 PB - Elsevier Science CY - New York, NY AN - OPUS4-33433 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rosner, Martin A1 - Wiedenbeck, M. A1 - Ludwig, T. T1 - Composition-induced variations in SIMS instrumental mass fractionation during boron isotope ratio measurements of silicate glasses N2 - An analytical artefact is reported here related to differences in instrumental mass fractionation between NIST SRM glasses and natural geological glasses during SIMS boron isotope determinations. The data presented demonstrated an average 3.4‰ difference between the NIST glasses and natural basaltic to rhyolitic glasses mainly in terms of their sputtering-induced fractionation of boron isotopes. As no matrix effect was found among basaltic to rhyolitic glasses, instrumental mass fractionation of most natural glass samples can be corrected by using appropriate glass reference materials. In order to confirm the existence of the compositionally induced variations in boron SIMS instrumental mass bias, the observed offset in SIMS instrumental mass bias has been independently reproduced in two laboratories and the phenomenon has been found to be stable over a period of more than one year. This study highlights the need for a close match between the chemical composition of the reference material and the samples being investigated. Nous montrons l'existence d'un artefact analytique reliéà différents fractionnements de masse instrumentaux, observés sur les verres NIST SRM et des verres naturels durant des mesures des isotopes de bore par SIMS. Les données montrent une différence d'environ 3.4‰ entre les verres NIST et les verres naturels, de composition variant de basaltique à rhyolitique, en termes de fractionnement des isotopes du bore principalement induit par le phénomène de dispersion. Comme aucun effet de matrice n'a été observé entre les verres basaltiques et les verres rhyolitiques, le fractionnement de masse instrumental de la plupart des verres naturels peut être corrigé en utilisant des verres de références appropriés. Dans le but de confirmer l'existence de biais de masse liéà la composition lors de mesure du bore par SIMS, nous avons reproduit indépendamment le décalage observé entre deux laboratoires et ce phénomène s'est révélé stable sur une période de plus d'un an. Cette étude met en lumière le besoin d'ajuster précisément les compositions chimiques des matériaux de référence et des échantillons à analyser. KW - Boron isotopes KW - SIMS KW - Matrix effect KW - Glass reference materials KW - Instrumental mass fractionation KW - Isotope du bore KW - Effet de matrice KW - Matériaux vitreux de référence KW - Fractionnement de masse instrumental PY - 2008 DO - https://doi.org/10.1111/j.1751-908X.2008.00875.x SN - 1639-4488 SN - 1751-908X VL - 32 IS - 1 SP - 27 EP - 38 PB - Blackwell CY - Oxford AN - OPUS4-17783 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rosner, Martin A1 - Wiedenbeck, M. A1 - Ludwig, T. T1 - Determination of true boron isotope compositions of silicate glasses by SIMS: NIST SRM glasses and composition-induced variations in SIMS instrumental mass fractionation T2 - Jahrestagung Deutsche Mineralogische Gesellschaft 2008 CY - Berlin, Deutschland DA - 2008-09-14 KW - SIMS KW - Boron isotopes KW - Instrumental mass bias PY - 2008 SP - 1 CY - Berlin AN - OPUS4-20786 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Langenberg, K. J. A1 - Marklein, R. A1 - Mayer, K. A1 - Krylow, T. A1 - Ampha, P. A1 - Streicher, Doreen A1 - Krause, Martin ED - Pinto, I. M. T1 - Wavefield inversion in nondestructive testing T2 - Workshop/Minisymposium on "Electromagnetics in a Complex World: Challenges and Perspectives" CY - Benevento, Italy DA - 2003-02-20 PY - 2003 SN - 3-540-20235-8 SN - 0930-8989 N1 - Serientitel: Springer proceedings in physics – Series title: Springer proceedings in physics IS - 96 SP - 1 EP - 10(?) PB - Springer CY - Berlin AN - OPUS4-2357 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wondraczek, L. A1 - Reinsch, Stefan A1 - Gaber, Martin A1 - Deubener, J. A1 - Müller, Ralf A1 - Komatsu, T. T1 - Nano-crystalline germanate glass-ceramics T2 - 78. Glastechnische Tagung CY - Nürnberg, Deutschland DA - 2004-06-07 PY - 2004 SP - 37 EP - 40 PB - Deutsche Glastechnische Gesellschaft CY - Offenbach AN - OPUS4-6953 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Jörg A1 - Martin, Sven A1 - Mädebach, Heinrich A1 - Urech, L. A1 - Lippert, T. A1 - Wokaun, A. A1 - Kautek, Wolfgang T1 - Femto- and nanosecond laser treatment of doped polymethylmethacrylate N2 - Femto- and nanosecond laser ablation of polymethylmethacrylate (PMMA) and PMMA doped with a linear absorber was investigated in the infrared spectral region. Ablation thresholds were determined and incubation phenomena were identified. The ‘degree’ of incubation was calculated employing a phenomenological model. The influence of the pulse duration on the machining quality of the polymers was examined. The presence of an absorbing chromophore is not a prerequisite for a controllable fs-laser structuring in contrast to the ns-treatment. Surface swelling always accompanied ablation. KW - Laser ablation KW - Laser beam machining KW - Doping thin films KW - Polymers-radiation effects PY - 2005 DO - https://doi.org/10.1016/j.apsusc.2005.01.078 SN - 0169-4332 SN - 1873-5584 VL - 247 SP - 406 EP - 411 PB - North-Holland CY - Amsterdam AN - OPUS4-7470 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Starke, K. A1 - Ristau, D. A1 - Martin, Sven A1 - Hertwig, Andreas A1 - Krüger, Jörg A1 - Allenspacher, P. A1 - Riede, W. A1 - Meister, S. A1 - Theiss, C. A1 - Sabbah, A. A1 - Rudolph, W. A1 - Raab, V. A1 - Grigonis, R. A1 - Rakickas, T. A1 - Sirutkaitis, V. ED - Exarhos, G. J. T1 - Results of a round-robin experiment in multiple-pulse LIDT measurement with ultrashort pulses T2 - 35th Annual Boulder Damage Symposium ; 35th Annual Symposium on Optical Materials for High-Power Lasers CY - Boulder, CO, USA DA - 2003-09-22 KW - Multiple-pulse damage KW - ISO 11254-2 KW - S on 1-LIDT KW - Round-robin experiment KW - CHOCLAB PY - 2004 SN - 0-8194-5163-0 DO - https://doi.org/10.1117/12.525135 SN - 0038-7355 N1 - Serientitel: Proceedings of SPIE – Series title: Proceedings of SPIE IS - 5273 SP - 388 EP - 395 PB - SPIE, the International Society for Optical Engineering CY - Bellingham, Wash. AN - OPUS4-4948 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Urech, L. A1 - Lippert, T. A1 - Wokaun, A. A1 - Martin, Sven A1 - Mädebach, Heinrich A1 - Krüger, Jörg T1 - Removal of doped poly(methylmetacrylate) from tungsten and titanium substrates by femto- and nanosecond laser cleaning N2 - The influence of different laser pulse lengths on the removal of a polymer layer from metal substrates was investigated. As model systems, doped poly(methylmetacrylate) (PMMA) on titanium and tungsten substrates were selected. The ablation threshold and irradiation spot morphology of titanium and tungsten were compared for femtosecond (fs) and nanosecond (ns) laser irradiation and different pulse numbers. Nanosecond laser treatment resulted in a non-homogeneous surface morphology for both titanium and tungsten substrates. Femtosecond irradiation of tungsten revealed a homogeneous ablation spot with little changes in the surface morphology. For titanium, the formation of columnar structures within the irradiation spot was observed. Two different dopant concentrations were used for PMMA to achieve an equal linear absorption coefficient for the femto- and nanosecond laser wavelengths of 790 and 1064 nm. The best results were achieved for the removal of doped PMMA by femtosecond laser irradiation, where only a minimal modification of the metal surface was detected. In the case of nanosecond laser exposure, a pronounced change of the structure was observed, suggesting that damage-free cleaning of the selected metal may only be possible using femtosecond laser pulses. Different experimental parameters, such as laser fluence, pulse repetition rate and sample speed were also investigated to optimize the cleaning quality of doped PMMA from tungsten substrates with femtosecond laser pulses. KW - Poly(methylmetacrylate) KW - Laser treatment KW - Tungsten KW - Titanium KW - Femtosecond PY - 2006 DO - https://doi.org/10.1016/j.apsusc.2005.07.109 SN - 0169-4332 SN - 1873-5584 VL - 252 IS - 13 SP - 4754 EP - 4758 PB - North-Holland CY - Amsterdam AN - OPUS4-12368 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ritter, Martin A1 - Dziomba, T. A1 - Hemmleb, M. A1 - Koenders, L. A1 - Kranzmann, Axel T1 - A 3D-Calibration Method for the Quantitative SPM Measurement of Hardness Indenters KW - 3D Calibration KW - SPM KW - Hardness Indenter PY - 2007 SN - 0970-3950 VL - 22 IS - 3 SP - 167 EP - 175 PB - Metrology Society of India CY - New Delhi AN - OPUS4-16357 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ritter, Martin A1 - Dziomba, T. A1 - Kranzmann, Axel A1 - Koenders, L. T1 - A landmark-based 3D calibration strategy for SPM N2 - We present a new method for the complete three-dimensional (3D) calibration of scanning probe microscopes (SPM) and other high-resolution microscopes, e.g., scanning electron microscopes (SEM) and confocal laser scanning microscopes (CLSM), by applying a 3D micrometre-sized reference structure with the shape of a cascade slope-step pyramid. The 3D reference structure was produced by focused ion beam induced metal deposition. In contrast to pitch featured calibration procedures that require separate lateral and vertical reference standards such as gratings and step height structures, the new method includes the use of landmarks, which are well established in calibration and measurement tasks on a larger scale. However, the landmarks applied to the new 3D reference structures are of sub-micrometre size, the so-called 'nanomarkers'. The nanomarker coordinates are used for a geometrical calibration of the scanning process of SPM as well as of other instrument types such as SEM and CLSM. For that purpose, a parameter estimation routine involving three scale factors and three coupling factors has been developed that allows lateral and vertical calibration in only one sampling step. With this new calibration strategy, we are able to detect deviations of SPM lateral scaling errors as well as coupling effects causing, e.g., a lateral coordinate shift depending on the measured height position of the probe. KW - Scanning probe microscopy KW - Focused ion beam KW - Calibration KW - 3D standards KW - Parameter estimation KW - Spatial coupling KW - Distortions KW - SPM KW - Landmarks KW - Nanomarker KW - Coupling KW - 3D calibration PY - 2007 DO - https://doi.org/10.1088/0957-0233/18/2/S12 SN - 0957-0233 SN - 1361-6501 VL - 18 SP - 404 EP - 414 PB - IOP Publ. Ltd. CY - Bristol AN - OPUS4-16358 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Ritter, Martin A1 - Dziomba, T. A1 - Xu, M. A1 - Koenders, L. A1 - Kranzmann, Axel T1 - Eine neue 3D Kalibrierstrategie für Mikro- und Nanomessverfahren T2 - Tagung "Messtechnik für Mikro- und Nano-Engineering" CY - Erlangen, Deutschland DA - 29.11.2006 KW - 3D Kalibrierung KW - Rastermikroskopie KW - Nanomarker PY - 2006 SN - 3-18-091950-7 IS - 1950 SP - 15 EP - 24 AN - OPUS4-16359 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -