TY - JOUR A1 - Abere, M. J. A1 - Zhong, M. A1 - Krüger, Jörg A1 - Bonse, Jörn T1 - Ultrafast laser-induced morphological transformations JF - MRS Bulletin N2 - Ultrafast laser processing can be used to realize various morphological surface transformations, ranging from direct contour shaping to large-area-surface functionalization via the generation of “self-ordered” micro- and nanostructures as well as their hierarchical hybrids. Irradiation with high-intensity laser pulses excites materials into extreme conditions, which then return to equilibrium through these unique surface transformations. In combination with suitable top-down or bottom-up manufacturing strategies, such laser-tailored surface morphologies open up new avenues toward the control of optical, chemical, and mechanical surface properties, featuring various technical applications especially in the fields of photovoltaics, tribology, and medicine. This article reviews recent efforts in the fundamental understanding of the formation of laser-induced surface micro- and nanostructures and discusses some of their emerging capabilities. KW - Laser ablation KW - Laser-induced periodic surface structures (LIPSS) KW - Surface morphology KW - Oxidation KW - Tribology PY - 2016 DO - https://doi.org/10.1557/mrs.2016.271 SN - 0883-7694 SN - 1938-1425 VL - 41 IS - 12 SP - 969 EP - 974 PB - Cambride University Press AN - OPUS4-38637 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ammann, Dominic A1 - Becker, Roland A1 - Kohl, Anka A1 - Hänisch, Jessica A1 - Nehls, Irene T1 - Degradation of the ethyl glucuronide content in hair by hydrogen peroxide and a non-destructive assay for oxidative hair treatment using infra-red spectroscopy JF - Forensic science international N2 - The assessment of quantification results of the alcohol abuse marker ethyl glucuronide (EtG) in hair in comparison to the cut-off values for the drinking behavior may be complicated by cosmetic hair bleaching. Thus, the impact of increasing exposure to hydrogen peroxide on the EtG content of hair was investigated. Simultaneously, the change of absorbance in the range of 1000–1100 cm-1 indicative for the oxidation of cystine was investigated non-destructively by attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) using pulverized portions of the respective hair samples. Hair samples treated with hydrogen peroxide consistently displayed a significantly increased absorbance at 1040 cm-1 associated with the formation of cysteic acid. The EtG content decreased significantly if the hair was treated with alkaline hydrogen peroxide as during cosmetic bleaching. It could be shown that ATR-FTIR is capable of detecting an exposure to hydrogen peroxide when still no brightening was visible and already before the EtG content deteriorated significantly. Thus, hair samples suspected of having been exposed to oxidative treatment may be checked non-destructively by a readily available technique. This assay is also possible retrospectively after EtG extraction and using archived samples. KW - Hair testing KW - Oxidation KW - Bleaching KW - Cysteic acid KW - HPLC–MS/MS PY - 2014 DO - https://doi.org/10.1016/j.forsciint.2014.07.029 SN - 0379-0738 SN - 1872-6283 VL - 244 SP - 30 EP - 35 PB - Elsevier CY - Amsterdam [u.a.] AN - OPUS4-31755 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Arlt, Tobias A1 - Manke, I. A1 - Wippermann, K. A1 - Schröder, A. A1 - Mergel, J. A1 - Riesemeier, Heinrich A1 - Banhart, J. T1 - Röntgen-Kanten-Tomografie und -Radiografie zur Untersuchung von Alterungseffekten in Brennstoffzellenmaterialien JF - MP materials testing KW - Resolution neutron-radiography KW - Local current distribution KW - Water transport KW - Carbon-dioxide KW - Methanol KW - Platinum KW - Oxidation PY - 2010 SN - 0025-5300 VL - 52 IS - 10 SP - 692 EP - 697 PB - Hanser CY - München AN - OPUS4-23045 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Baláž, M. A1 - Tešinský, M. A1 - Marquardt, Julien A1 - Škrobian, M. A1 - Daneu, N. A1 - Rajňák, M. A1 - Baláž, P. T1 - Synthesis of copper nanoparticles from refractory sulfides using a semi-industrial mechanochemical approach JF - Advanced Powder Technology N2 - The large-scale mechanochemical reduction of binary sulfides chalcocite (Cu2S) and covellite (CuS) by elemental iron was investigated in this work. The reduction of Cu2S was almost complete after 360 min of milling, whereas in the case of CuS, a significant amount of non-reacted elemental iron could still be identified after 480 min. Upon application of more effective laboratory-scale planetary ball milling, it was possible to reach almost complete reduction of CuS. Longer milling leads to the formation of ternary sulfides and oxidation product, namely cuprospinel CuFe2O4. The rate constant calculated from the magnetometry measurements using a diffusion model for Cu2S and CuS reduction by iron in a large-scale mill is 0.056 min−0.5 and 0.037 min−0.5, respectively, whereas for the CuS reduction in a laboratory-scale mill, it is 0.1477 min−1. The nanocrystalline character of the samples was confirmed by TEM and XRD, as the produced Cu exhibited sizes up to 16 nm in all cases. The process can be easily scaled up and thus copper can be obtained much easier from refractory minerals than in traditional metallurgical approaches. KW - Mechanochemistry KW - Copper sulfides KW - Copper nanoparticles KW - Magnetometry KW - Oxidation PY - 2020 DO - https://doi.org/10.1016/j.apt.2019.11.032 VL - 31 IS - 2 SP - 782 EP - 791 PB - Elsevier B.V. AN - OPUS4-50665 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Brandes, E. A1 - Hieronymus, Hartmut T1 - Sicherheit bei mikrostrukturierten Reaktoren - Ergebnisse und Schlussfolgerungen aus Untersuchungen am Beispiel von Ethan/Sauerstoff-, Ethen/Sauerstoff- und Ethen/Lachgas-Gemischen JF - PTB-Mitteilungen N2 - Die Mikroverfahrenstechnik (typische innere Abmessungen der Apparaturen < 1000 pin) erfährt zunehmend Interesse für industrielle Anwendungen. Grund hierfür sind verschiedene Vorteile gegenüber konventionellen chemischen. Reaktoren wie ein erhöhter Wärme- und Stofftransport und größere spezifische Phasengrenzen. Hierdurch können im Zuge einer Prozessintensivierung höhere Raum-Zeil-Ausbeuten und Selektivitäten und darüber hinaus eine sicherere Prozessführung erreicht werden. Dies trifft vor allem dann zu, wenn als Oxidationsmittel reiner Sauerstoff, Distickstoffmonoxid (Lachgas) oder ähnliche Substanzen mit hohem Oxidationspotential eingesetzt werden. Vielfach wird angenommen, dass Mikroreaktoren inhärent sicher gegenüber Deflagrations- und Detonationsvorgängen sind. Durchmesser der Reaktionskanäle von 0,5 nun und kleiner lassen Flammendurchschläge zumindest bei Stoffen der Explosionsgruppen I1A und TIB für Gemische mit Luft als Oxidationsmittel und Umgebungsbedingungen (ca. 20 °C, ca. 1.013 mbar) als ausgeschlossen erscheinen. Für die in der Mikroverfahrenstechnik bevorzugten Reaktionsbedingungen wie erhöhter Druck, erhöhte Temperatur und vor allem Oxidationsmittel mit erhöhtem Oxidalionspotential gilt dies jedoch nicht. KW - Mikroreaktor KW - Explosion KW - Detonation KW - Oxidation PY - 2011 SN - 0030-834X VL - 121 IS - 1 SP - 55 EP - 58 PB - Wirtschaftsverl. NW CY - Bremerhaven AN - OPUS4-23515 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Chandra, K. A1 - Dörfel, Ilona A1 - Wollschläger, N. A1 - Kranzmann, Axel T1 - Microstructural investigation using advanced TEM techniques of inner ocide layers formed on T92 steel in oxyfuel environment JF - Corrosion Science N2 - T92 steel was oxidized at 650 °C for 1000 h in dry and wet oxyfuel gases. The microstructure of inner oxide layer was investigated using scanning transmission electron microscopy and energy dispersive spectroscopy on thin lamellas of oxide cross-sections. The oxides were composed of fine equiaxed grains and separated into Fe-rich and Cr-rich regions. Fe-rich regions were wustite and iron sulphide while Cr-rich regions consisted of Fe-Cr spinel with different stoichiometries. Precipitates of (W,Mo)-rich oxides were formed within the oxide scale and beneath the oxide/alloy interface. Often iron sulphide and (W,Mo)-rich oxide were surrounded by Cr-rich spinel. KW - Steel KW - STEM KW - High temperature corrosion KW - Oxidation KW - Internal oxidation PY - 2019 DO - https://doi.org/10.1016/j.corsci.2018.12.008 SN - 0010-938X SN - 1879-0496 VL - 148 SP - 94 EP - 109 PB - Elsevier AN - OPUS4-47423 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Chandra, K. A1 - Kranzmann, Axel T1 - High temperature oxidation of 9–12% Cr ferritic/martensitic steels under dual-environment conditions JF - Corrosion engineering, science and technology N2 - In normal operations, the opposite surfaces of the power plant components are exposed to two different environments, i.e. air/flue gas on the one side and steam on the other side. Exposure under such dual-environment can lead to accelerated corrosion of the components on the air side. The oxidation behaviour of ferritic/martensitic steel T92 was investigated under dual-environment in a specially designed test equipment. The samples were exposed to dry oxyfuel flue gas (CO2–27%N2–2%O2–1%SO2) on one side and to steam on the other side up to 1000 h at 650°C. The formation of oxide scales was characterised by optical microscopy and scanning electron microscopy with attached energy-dispersive spectroscopy. Oxidation rate of specimens under dual-Environment condition was almost three times higher than that in single-environment condition. This is explained based on hydrogen transport through the bulk alloy from the steam side to the flue gas side. KW - Oxidation KW - Dual-environment KW - Oxyfuel KW - Ferritic/martensitic steel KW - Steam PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-457101 DO - https://doi.org/10.1080/1478422X.2017.1374049 VL - 53 IS - 31 SP - 27 EP - 33 PB - Taylor & Francis AN - OPUS4-45710 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Chandra, Kamlesh A1 - Kranzmann, Axel A1 - Saliwan Neumann, Romeo A1 - Oder, Gabriele A1 - Rizzo, F. T1 - High temperature oxidation behavior of 9-12 % Cr ferritic/martensitic steels in a simulated dry oxyfuel environment JF - Oxidation of metals N2 - The materials in oxyfuel power plant will be subjected to CO2– and SO2–rich gases on the fireside. The oxidation behaviour of two 9–12 % Cr steels T92 and VM12 was studied under dry oxyfuel environment in the temperature range of 580–650 °C for up to 1,000 h. The oxide structure and morphology were analyzed using various experimental techniques. A complex temperature dependence of oxidation rate is observed for both T92 and VM12 whereby the oxidation rate decreased with increasing temperature. This is attributed to increased Cr-enrichment in the inner scale with increasing temperature. T92 and VM12 alloys are also susceptible to carburization in an oxyfuel environment. KW - Oxyfuel environment KW - Ferritic/martensitic steel KW - Oxidation KW - High temperature corrosion KW - Carburization KW - Steel KW - EPMA KW - SEM PY - 2015 DO - https://doi.org/10.1007/s11085-014-9521-4 SN - 0030-770X SN - 1573-4889 VL - 83 IS - 3-4 SP - 291 EP - 316 PB - Springer CY - New York, NY AN - OPUS4-32737 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Chandra, Kamlesh A1 - Kranzmann, Axel A1 - Saliwan Neumann, Romeo A1 - Rizzo, F. T1 - Comparative study on high temperature oxidation of T92 steel in dry and wet oxyfuel environments JF - Oxidation of metals N2 - Fireside oxidation of T92 steel was studied after exposure times up to 1000 h in the temperature range of 580–650 °C in simulated dry (CO2–27 % N2–2 % O2–1 % SO2) and wet (CO2–20 % H2O–7 % N2–2 % O2–1 % SO2) oxyfuel environments. Water vapour addition to the oxyfuel gas substantially increased the oxidation rate. The oxide scales developed under wet environment contained more defects, resulting in higher access of oxidants to the substrate material and enhanced oxidation. In addition, the oxide scales had lower chromium enrichment in the inner layer as compared to that in the dry condition. The oxide scales consisted of hematite and magnetite in the outer layer and a mixture of (Fe, Cr)-spinel, sulphides and wustite in the inner layer. The sulphur distribution differed between the oxide scales developed in dry and wet oxyfuel environments. Sulphur was mainly concentrated in the inner layer and at the oxide/alloy interface. In contrast to the wet oxyfuel gas, very high sulphur concentration was measured in the inner oxide scale formed in the dry oxyfuel gas. Additionally, Fe-sulphide was formed at the interface of inner and outer oxide layer in the wet condition. KW - Oxyfuel environment KW - Oxidation KW - High temperature corrosion KW - Water vapour KW - Sulphur PY - 2015 DO - https://doi.org/10.1007/s11085-015-9565-0 SN - 0030-770X SN - 1573-4889 VL - 84 IS - 3-4 SP - 463 EP - 490 PB - Springer CY - New York, NY AN - OPUS4-34585 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Falk, Florian A1 - Sobol, Oded A1 - Stephan-Scherb, Christiane T1 - The impact of the microstructure of Fe-16Cr-0.2C on high-temperature oxidation – sulphidation in SO2 JF - Corrosion Science N2 - This study elucidates the impact of the microstructure of Fe-16Cr-0.2C on oxide layer formation at 650 ◦C in Ar-0.5 % SO2. A cold-rolled and two heat-treated states of the alloy were exposed for up to 1000 h. The samples were characterised in detail from microstructural and chemical perspectives using scanning electron microscopy (SEM), X-ray diffraction (XRD) and time-of-flight secondary ion mass spectrometry (ToF-SIMS). The microstructural modification of the alloy by heat-treatment was advantageous. It was found that Cr-carbides support chromia formation and reduce sulphidation when their area fraction is low and diameter is small. KW - Steel KW - Iron KW - SIMS KW - SEM KW - High temperature corrosion KW - Oxidation KW - Sulphidation PY - 2021 DO - https://doi.org/10.1016/j.corsci.2021.109618 VL - 190 SP - 109618 PB - Elsevier Ltd. AN - OPUS4-53001 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -