TY - JOUR A1 - You, Yi A1 - Xue, Boyang A1 - Riedel, Jens T1 - Enhancement of LIBS plasma in air with organic solvent vapors N2 - Laser-induced breakdown spectroscopy (LIBS) offers versatile, field-deployable elemental analysis; however, compact, high-repetition-rate nanosecond laser systems typically face constraints in power consumption and size, often compromising emission intensity and thus analytical performance. We demonstrate a significant improvement in LIBS signals through the controlled introduction of common organic solvent vapors into a sheath gas, with a diode-pumped solid-state laser (1064 nm, 2–28 kHz repetition rate, 450–600-μJ pulse energy). Optical and acoustic diagnostics reveal up to ca. 40-fold enhancement of the N II emission line at 567 nm when ambient air serves as the analyte. Maximal enhancement occurs at intermediate repetition rates of ca. 15 kHz, particularly at pulse energies approaching the optical breakdown threshold; this observation suggests a viable strategy for operating LIBS at lower pulse energies and higher repetition rates. Enhancement effects scale jointly with both vapor pressure and ionization energy of the organic species, with acetone and toluene markedly outperforming methanol and isopropanol. These findings provide a rational foundation for significantly improving the analytical performance of portable LIBS instruments without exceeding platform-specific constraints. KW - LIBS PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-653758 DO - https://doi.org/10.1016/j.sab.2025.107309 SN - 0584-8547 VL - 236 SP - 1 EP - 6 PB - Elsevier B.V. AN - OPUS4-65375 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Tuma, Dirk T1 - Trace-level ammonia-water interactions in hydrogen: challenges in purity analysis using Optical-Feedback Cavity-Enhanced Absorption Spectroscopy (OF-CEAS) N2 - ISO 14687 defines a threshold of 100 ppb ammonia for hydrogen to be used in fuel cells. This work presents analysis methods using OF-CEAS and discusses moisture-related surface effects on the results. T2 - Gas Analysis 2026 CY - Paris, France DA - 27.01.2026 KW - OF-CEAS KW - Ammonia KW - Moisture effects PY - 2026 AN - OPUS4-65480 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Spitzer, Stefan A1 - Amyotte, P. A1 - Salzano, E. T1 - Explosion behavior of hybrid mixtures N2 - Flammable mixtures of dusts with gases or liquids occur in the process and energy industries. Most research about these so-called "hybrid mixtures" was, and still is, about coal dust with the admixture of methane because of their occurrence in the mining industry. In the modern industry, hybrid mixture explosions play an increasing role in many existing processes like spray-drying, or in emerging technologies like the direct reduction of iron ore with hydrogen or nuclear/fusion reactors. While some safety characteristics of one of the component substances stay the same or are unaffected by the concentrations that occur in the process, others are severely influenced by only traces of the other substance. This review paper shows in which processes and applications hybrid mixtures pose a risk and gives an overview of the research conducted in the last 150 years. Findings that are reproducible and represent current proven knowledge are stated and compared to each safety characteristic containing only solid particles, gases or liquids as combustible substances. Additionally, fundamental studies on the mechanisms of flame propagation in hybrid mixtures are reviewed. The significance of these studies in enhancing our understanding of explosion behaviors in hybrid mixtures is also discussed. An outlook on what has been missing so far in the literature, is also given comparing the knowledge of single substances with their mixtures, why this might not have been investigated, and where the challenges lie. KW - Hybrid mixtures KW - Safety characteristics KW - Combustion regimes KW - Industrial explosions PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-654013 DO - https://doi.org/10.1016/j.pecs.2025.101276 SN - 0360-1285 VL - 113 SP - 1 EP - 24 PB - Elsevier CY - Amsterdam AN - OPUS4-65401 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rodriguez, Santiago A1 - Kumanski, Sylvain A1 - Ayed, Zeineb A1 - Fournet, Aurélie A1 - Bouanchaud, Charlène A1 - Sagar, Amin A1 - Allemand, Frédéric A1 - Baulin, Vladimir A. A1 - Resch‐Genger, Ute A1 - Cortés, Juan A1 - Sibille, Nathalie A1 - Chirot, Fabien A1 - Wegner, Karl David A1 - Antoine, Rodolphe A1 - Le Guével, Xavier A1 - Bernadó, Pau T1 - Programming the Optoelectronic Properties of Atomically Precise Gold Nanoclusters Using the Conformational Landscape of Intrinsically Disordered Proteins N2 - The rational design of hybrid nanomaterials with precisely controlled properties remains a central challenge in materials science. While atomically precise gold nanoclusters (Au‐NCs) offer molecule‐like control over a metallic core, tuning their optoelectronic behavior via surface engineering is often empirically driven. Here, we establish a design principle by demonstrating that the conformational landscape of intrinsically disordered proteins (IDP) can be used as a programmable scaffold to rationally modulate the photophysical properties of a covalently bound Au‐NC. We synthesized a series of bioconjugates between Au 25 nanoclusters and bioengineered IDPs containing a variable number of cysteine anchoring points. A combination of mass spectrometry, small‐angle X‐ray scattering, and modeling on the conjugates indicates that increasing the number of covalent anchors systematically restricts the conformational ensemble, inducing a progressively more compact protein shell around nanoclusters. This structural rigidification at the interface directly translates into a 15‐fold enhancement of the Au‐NC near‐infrared photoluminescence and a six‐fold increase in its average lifetime. Our findings demonstrate that the conformational plasticity of IDPs and the capacity to engineer them can be harnessed as a molecular tuning knob, moving to a new regime of programmable soft‐matter control over the properties of quantum‐confined nanomaterials for tailored biotechnological applications. KW - Fluorescence KW - Custer KW - Nano KW - Advanced material KW - Characterization KW - Fluorescence quantum yield KW - Integrating sphere spectroscopy KW - Thiol ligands KW - Gold KW - Surface chemistry KW - SWIR KW - Mass spectrometry KW - Protein PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-655086 DO - https://doi.org/10.1002/chem.202502991 SN - 0947-6539 SP - 1 EP - 9 PB - Wiley VHC-Verlag AN - OPUS4-65508 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Holm, O. A1 - Leube, Peter A1 - Vogel, Christian A1 - Kennedy, E. A1 - Stockenhuber, M. A1 - Lucas, J. A1 - Truong, T. A1 - Rappé, A. A1 - Lu, W. A1 - Blotevogel, J. T1 - Thermische Zerstörung von PFAS in der Sondermüllverbrennung: Einfluss von Temperatur und PFAS-Konzentration N2 - Aufgrund ihrer einzigartigen molekularen Beschaffenheit werden per- und polyfluorierte Alkylsubstanzen (PFAS) in vielen unterschiedlichen Produkten und Anwendungsgebieten eingesetzt. Da sie generell eine hohe Persistenz aufweisen und je nach individueller Struktur unterschiedlich mobil sind, sind sie mittlerweile in allen Umweltkompartimenten und ubiquitär nachzuweisen. Ihre potenzielle (ökologische) Toxizität birgt dabei erhebliche Umweltrisiken, weshalb PFAS in den letzten Jahren mehr und mehr in den Fokus von Umweltverbänden und -behörden gelangten. Gleichzeitig beschäftigen sich Forschungseinrichtungen mit der möglichst weitreichenden Entfernung aus der Umwelt sowie mit deren (anschließender) Zerstörung. Im Projekt ER24-4073 „Untersuchung des thermischen Abbaus von PFAS in einer kommerziellen Großanlage zur Verbrennung gefährlicher Abfälle“, welches vom U.S. Department of Defense (DoD ) über das Strategic Environmental Research and Development Program (SERDP) gefördert wird, untersuchen deutsche, australische und amerikanische Partner die Behandlung von PFAS-haltigen Abfallströmen in einer großtechnischen Verbrennungsanlage, um die Einsatzbereitschaft, Machbarkeit und Sicherheit dieser Zerstörungsmethode zu demonstrieren. T2 - Berliner Konferenz Abfallwirtschaft und Energie CY - Berlin, Germany DA - 28.01.2026 KW - Per- and polyfluoroalkyl substances (PFAS) KW - Verbrennung KW - Kontaminierter Boden PY - 2026 SN - 978-3-911006-65-1 SP - 66 EP - 77 PB - TK Verlag AN - OPUS4-65513 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bernardy, Christopher A1 - Habib, Abdel Karim A1 - zur Nedden, Philipp Maximilian A1 - von Saldern, Jakob Georg Raimund A1 - Beuth, Jan Paul A1 - Orchini, Alessandro T1 - Thermal Radiation Of Inclined Large Scale Hydrogen Jet Flames N2 - In order to assess the thermal radiation emanating from hydrogen jet flames, experiments under real scale conditions were carried out at the Test Site Technical Safety of BAM. Herein, the behavior of inclined hydrogen jet flames was investigated. The aim of the work is to determine the Surface Emissive Power (SEP) and radiant heat fraction of these flames and to provide a reliable dataset for model evaluation purposes. Since the aforementioned values are not directly measurable, the incident heat radiation was measured at defined distances from the flame, as well as the flame’s shape and size. The required values were then derived from these measurements. The hydrogen releases ranged from 0.0125 kg/s to 0.175 kg/s with a 30 mm orifice. The mass flows were held constant during the releases, nevertheless a transient behavior of the flame could be observed since the experiments were carried out under open field conditions, with unsteady wind fields. In the literature, the flame lengths are often determined using visible light imaging, either by injecting coloring substances in the low light emitting hydrogen jet flame or by carrying out the measurements in darkness. In this work the jet flames were visualized using infrared (IR) and OH* imaging. The recorded flame shapes and resulting flame lengths are compared. Results from this showed that the flame lengths determined with OH* and IR recordings differ greatly. A flame length ratio lf OH*/lf IR in the range of 0.47–0.62 can be found. In addition, the SEP differ also in the range of 10 kW/m2–16 kW/m2 (IR) and 40 kW/m2–80 kW/m2 (OH*) for hydrogen jet flames due to differences in the determined flame surface. Conclusions regarding the determined xRAD values for IR and OH* result in approximately the same range of 0.031–0.043. T2 - 11th Iinternational conference on hydrogen safety 2025 CY - Seoul, Republic of Korea DA - 22.09.2025 KW - Hydrogen safety KW - Jet flames KW - Thermal radiation KW - Large scale experiment PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-655181 DO - https://doi.org/10.58895/hysafe.27 SN - 2943-5935 VL - 3 IS - 1 SP - 39 EP - 50 PB - Karlsruhe Institute of Technology Library AN - OPUS4-65518 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Blume, Simon T1 - Femtosecond vs. Nanosecond Laser-induced XUV Spectroscopy (LIXS) N2 - In contrast to laser-induced breakdown spectroscopy (LIBS), measuring after a delay as long as a few microseconds, laser-induced XUV spectroscopy (LIXS) takes advantage of emissions from the very first instant of the pristine plasma. This process exhibits stable and intense line and recombination emissions in the XUV-range. Therefore, common challenges for precise measurements (e.g. quantification efforts) in LIBS caused by signal intensity fluctuations due to matrix effects and plasma-flicker noise are improved, as shown for ns-pulses. A femtosecond laser (pulse length ~100 fs) interacts fundamentally different with matter than a nanosecond laser. Of the many photons needed for ionization of the sample, less are absorbed via inverse Bremsstrahlung and more in a Franck-Condon multiphoton absorption (MPA) process. In combination with the higher peak power, and therefore higher initial plasma temperature (> 10 eV), atoms are selectively ionized to a higher degree while at the same time thermal dissipation and equilibration is reduced. This specificity in excitation leads to a reduced background and the highly ionized atoms overwhelmingly emit the desired XUV-radiation. Thus, fs-LIXS promises to lead to “cleaner” spectra with sharper separation of the emission lines. The capabilities of a fs-LIXS setup in comparison to ns-LIXS will be discussed. Samples of pure elements (Al, Si, Ni, Fe, Mg), as well as composite samples (CaF, LiF, PTFE, polypropylene) serve as model systems to demonstrate these capabilities. T2 - EMSLIBS 2025 CY - Senlis, France DA - 26.01.2026 KW - Femtosecond KW - LIXS KW - XUV KW - Elemental analysis PY - 2026 AN - OPUS4-65470 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Völker, Tobias A1 - Blaschke, Jil A1 - Lierenfeld, Matthias A1 - Wilsch, Gerd A1 - Dalichow, Dirk A1 - Truffer, Philipp A1 - Kruschwitz, Sabine T1 - Aktuelle Anwendungsbeispiele der laserinduzierten Plasmaspektroskopie in der Bauwerksdiagnostik N2 - Die Zustandsbewertung und Instandhaltung von Betonbauwerken erfordert zuverlässige und effiziente Analysemethoden, um komplexe Schadensmechanismen frühzeitig erkennen und fundiert bewerten zu können. Klassische chemisch-analytische Verfahren in der Betonanalytik liefern zwar präzise Ergebnisse bezogen auf die Probenmasse, sind jedoch mit erheblichem Laboraufwand verbunden, in ihrer räumlichen Auflösung durch die Probenahme begrenzt und hinsichtlich der Ergebnisinterpretation mit Unsicherheiten behaftet. Die laserinduzierte Plasmaspektroskopie (LIBS) bietet hier ein hohes Potenzial als schnelle, bildgebende und weitgehend zerstörungsarme Alternative. In den vergangenen Jahren hat sich das Verfahren zunehmend in der Bauwerksdiagnostik etabliert und wird heute für ein breites Spektrum an Anwendungen eingesetzt. Der vorliegende Beitrag gibt einen Überblick über den aktuellen Stand der LIBS-Anwendungen und zeigt anhand ausgewählter Praxisbeispiele die Leistungsfähigkeit, den Mehrwert, die Grenzen und die zukünftigen Entwicklungsperspektiven des Verfahrens auf. KW - LIBS KW - Spektroskopie KW - Chemische Analyse KW - Infrastruktur KW - Bauwerksdiagnostik PY - 2026 DO - https://doi.org/10.1002/best.70078 SN - 1437-1006 SP - 1 EP - 13 AN - OPUS4-65445 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Khella, Shady T1 - Integration of Information Models Using Semantic Web Technologies Within the Mixed Reality Data Hub N2 - Engineering information is distributed across heterogeneous data models, ontologies, and reference data libraries (RDLs), which complicates interoperability, hinders workflow automation, and limits the deployment of industrial Mixed Reality (MR) applications. This work uses DEXPI Process semantics and Semantic Web technologies to align and integrate these heterogeneous sources into a single knowledge graph. The resulting graph provides a queryable semantic layer that enables consistent cross-source access to engineering information and supports MR application development. Beyond integration, the semantic graph enables automation of process design workflows. We demonstrate this using a basic engineering use case in which alternative flowsheet design options are generated from a semantically modeled block flow diagram (BFD). T2 - DEXPI Days 1.0 CY - Frankfurt am Main, Germany DA - 20.01.2026 KW - Mixed Reality KW - Data Integration KW - Semantic Web Technologies KW - DEXPI PY - 2026 AN - OPUS4-65489 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Scholl, Juliane A1 - Lisec, Jan A1 - Bagheri, Abbas A1 - Meiers, Emelie A1 - Russo, Francesco Friedrich A1 - Haase, Hajo A1 - Koch, Matthias T1 - Unveiling aging mechanisms of electrolytes in commercial end-of-life lithium-ion batteries N2 - In this study, 77 end-of-life (EOL) commercial lithium-ion batteries (LIBs) of various formats were systematically analyzed to investigate electrolyte degradation and the influence of pristine electrolyte compositions on aging behavior. Comprehensive chemical characterization was conducted using targeted and non-targeted mass spectrometry (MS), employing LC-MS/MS, GC-MS, and high-resolution MS (HRMS). This integrated approach enabled the identification of confirmed pristine components and complex degradation products. The results show that rechargeable pouch and cylindrical cells often deviate from conventional model systems, containing mixed lithium salt anions, ionic liquids (ILs), and high concentrations of triflates, triflimides, and bis(fluorosulfonyl)imide (FSI). These function as solvents, salts, or safety-enhancing additives. Specific IL degradation products were identified, and hypotheses formulated on previously unreported pathways. Furthermore, a novel series of oligomerization products of propylene carbonate (PC) was detected. In contrast, non-rechargeable coin cells revealed widespread use of per- and polyfluoroalkyl substances (PFAS) in their original electrolytes. Based on ex situ analyses, hypothetical PFAS degradation mechanisms are proposed here for the first time. The absence of carbonate oligomers and lithium salt-derived products, alongside the presence of standard carbonates, indicates lithium counterion coordination as a key factor in Lewis acid-catalyzed degradation. This study offers valuable insights into real-world battery aging. KW - Transformation products KW - Lithium-ion batteries KW - Fluorinated Compounds KW - Gas chromatography/ QTOF-MS KW - HILIC-LC-MS/MS KW - PFAS KW - Electrochemistry PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-644991 DO - https://doi.org/10.1016/j.jpowsour.2025.238613 SN - 0378-7753 VL - 661 SP - 1 EP - 10 PB - Elsevier B.V. AN - OPUS4-64499 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Shovo, Redoy Gazi A1 - Thünemann, Andreas A1 - Katcharava, Zviadi A1 - Marinvo, Anja A1 - Hoppe, Richard A1 - Woltersdorf, Georg A1 - Du, Mengxue A1 - Androsch, Rene A1 - de Souza e Silva, Juliana Martins A1 - Busse, Karste A1 - Binder, Wolfgang H. T1 - Generating Tagged Micro- and Nanoparticles of Poly(ethylene furanoate) and Poly(ethylene terephthalate) as Reference Materials N2 - Detecting nanoplastic particles in environmental samples and biological tissues remains a significant challenge, especially in view of newly emerging polymers, not yet commercially exploited. Fluorescent labeling provides a tagging strategy to overcome this limitation by reducing the detection limit of individual particles, especially for small-sized particles. We present a method for producing labeled nanoparticles (NP/MP) of poly(ethylene terephthalate) (PET) and poly(ethylene furanoate) (PEF), tagged with Alexa Fluor 633 or Alexa Fluor 647. Our preparations used mechanical grinding or solvent-based approaches (confined impinging jet mixing, ((CIJ, precipitation), generating particles with hydrodynamic diameters of 200–700 nm, displaying long-term stability in water of up to 57 days. Stable suspensions with concentrations of the particles ranging from 10 µg/mL (surfactant-free, by solvent mixing) to 5.88 mg/mL (precipitation, containing surfactant) were generated with zeta-potentials from −5 to −50 mV. Characterization of the nanoparticles by SEC, DSC, and XRD showed no significant changes in molecular weight, thermal behavior, or crystallinity via the solvent-based methods, compared to the pristine polymer, highlighting their suitability for producing standardized nanoparticle dispersions. Fluorescence spectroscopy of the Alexa-dye-labeled particles confirmed the successful incorporation of the Alexa dyes, so improving monitoring of their biological profiles of the PEF-MP/NPs. s-SNOM (near field imaging) could identify individual PEF-particles sized ∼200 nm by direct imaging. KW - Reference Materials KW - Nanoplastics KW - Microplastics KW - Polymer KW - Fluorescence PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-655531 DO - https://doi.org/10.1002/marc.202500839 SN - 1521-3927 VL - 47 IS - 4 SP - 1 EP - 11 PB - Wiley VHC-Verlag CY - Weinheim AN - OPUS4-65553 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Prakash, Swayam A1 - Bell, Jérémy A1 - Rurack, Knut T1 - Rapid Onsite Detection of Fecal Contamination in Water Using a Portable Fluorometric Assay N2 - Fecal pollution in water poses significant health risks, especially when contaminated sources are used for drinking and food production. Traditional water quality testing methods are expensive, slow, and require skilled personnel, limiting their accessibility. This work addresses these issues by developing a portable fluorometric assay for the detection of the fecal indicator pigment urobilin (UB). The assay uses silane-functionalized glass fiber strips impregnated with zinc chloride, providing a ‘drop-&-detect’ approach with enhanced fluorescence response mediated by the unique complexation properties of ZnCl2 and UB. This approach allows for the detection of UB at sub-nanomolar concentrations in less than 1 min using a 3D-printed setup with miniaturized optical components powered by a smartphone with its camera as a detector. The results validated with a benchtop fluorometer show the effectiveness of this method. The successful application of this userfriendly, rapid, and sensitive assay to real water samples from three rivers and the influx and efflux of a wastewater treatment plant advances field-based water quality monitoring, meets the WHO’s ASSURED criteria, and supports progress toward the global clean water and sanitation goals. KW - Fecal pigment KW - Fluorescence KW - Signal amplification KW - Surface chemistry KW - Water quality testing PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-655543 DO - https://doi.org/10.1021/acssensors.5c03922 SN - 2379-3694 VL - 11 SP - 1 EP - 9 PB - American Chemical Society CY - Washington, D.C. AN - OPUS4-65554 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Holm, O. T1 - Thermische Zerstörung von PFAS in der Sondermüllverbrennung: Einfluss von Temperatur und PFAS-Konzentration N2 - Aufgrund ihrer einzigartigen molekularen Beschaffenheit werden per- und polyfluorierte Alkylsubstanzen (PFAS) in vielen unterschiedlichen Produkten und Anwendungsgebieten eingesetzt. Da sie generell eine hohe Persistenz aufweisen und je nach individueller Struktur unterschiedlich mobil sind, sind sie mittlerweile in allen Umweltkompartimenten und ubiquitär nachzuweisen. Ihre potenzielle (ökologische) Toxizität birgt dabei erhebliche Umweltrisiken, weshalb PFAS in den letzten Jahren mehr und mehr in den Fokus von Umweltverbänden und -behörden gelangten. Gleichzeitig beschäftigen sich Forschungseinrichtungen mit der möglichst weitreichenden Entfernung aus der Umwelt sowie mit deren (anschließender) Zerstörung. Im Projekt ER24-4073 „Untersuchung des thermischen Abbaus von PFAS in einer kommerziellen Großanlage zur Verbrennung gefährlicher Abfälle“, welches vom U.S. Department of Defense (DoD ) über das Strategic Environmental Research and Development Program (SERDP) gefördert wird, untersuchen deutsche, australische und amerikanische Partner die Behandlung von PFAS-haltigen Abfallströmen in einer großtechnischen Verbrennungsanlage, um die Einsatzbereitschaft, Machbarkeit und Sicherheit dieser Zerstörungsmethode zu demonstrieren. T2 - Berliner Konferenz Abfallwirtschaft und Energie (BKAWE) CY - Berlin, Germany DA - 28.01.2026 KW - Per- and polyfluoroalkyl substances (PFAS) KW - Verbrennung KW - Kontaminierter Boden PY - 2026 AN - OPUS4-65512 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Palásti, Dávid Jenö T1 - Utilizing modern fiber lasers for LIBS N2 - The development of laser sources plays a very important role in the quick advancements in the field of LIBS. However, the development of fiber lasers went mostly unnoticed by the wider LIBS community. These laser sources, traditionally used in industrial cutting and welding processes, despite their high-power output (hundreds of watts) and are very robust nature, were neglected, because they used to work only in continuous mode. Modern fiber lasers however, offer pulsed output with a couple of mJ-s pulse energy, which can be adequate for certain tasks [1,2]. Furthermore, the pulse duration and the pulse repetition rate can be varied in a reasonably wide range, while their price is a fraction of the ones traditionally used in research. In the recent years, our groups made experiences with modern fiber lasers to evaluate the feasibility of their usage in LIBS. The initial experiments proved that they are not just suitable for standard analytical tasks such as quantitative or qualitative analysis, but their unique set of features makes them capable for fundamental research, like no other laser sources currently on the market. The relatively low energy and elongated profile of the pulses are very efficient in ablation and in the generation of low temperature plasmas [3], which means the ionic lines are less numerous, while the emission is mostly free from the background emission typical for the early stages of the plasma lifetime. It can make spectrometer gating and signal integration much simpler and robust. A thorough set of investigations of single pulse, double pulse and even continuous irradiation experiments was performed. The effects of various parameters, such as energy, duration and shape of the pulse as well as inter pulse delay were investigated on the generated signal focusing mainly the signal intensity, the self-absorption and the width of the peaks as well as the plasma properties. T2 - EMSLIBS 2026 CY - Senlis, France DA - 26.01.2026 KW - LIBS KW - Fiber laser PY - 2026 AN - OPUS4-65561 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Resch-Genger, Ute T1 - How to get it right with photoluminescence measurements in the UV/VIS/NIR N2 - Optical measurements of transparent solutions of organic dyes and semiconductor quantum dots and scattering materials such as luminescent nanocomposites and microparticles and phosphors dispersed in liquid and solid matrices play an important role in energy conversion, solid-state lighting, medical diagnostics, and security barcoding. A key performance parameter is the photoluminescence quantum yield QY, i.e., the number of emitted per number of absorbed photons. QY of transparent luminophore solutions can be obtained relative to a fluorescence QY standard of known QY. Such relative QY measurements require a calibrated spectrofluorometer. Here, we address typical sources of uncertainty for luminescence measurements and relative and absolute QY measurements from the instrument and material side and provide recommendations to circumvent or at least minimize them for transparent and scattering samples in the UV/vis/NIR/SWIR. T2 - Workshop "Photoluminescence Spectroscopy and its application in Materials Research" CY - Vienna, Austria DA - 19.02.2026 KW - Quality assurance KW - Reference material KW - Fluorescence KW - Dye KW - Traceability KW - Metrology KW - Calibration KW - Reference data KW - Reference product KW - Digital certificate KW - NIR KW - Instrument performance validation PY - 2026 AN - OPUS4-65575 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogel, Christian A1 - Helfenstein, J. A1 - Massey, M. A1 - Kretzschmar, R. A1 - Schade, U. A1 - Verel, R. A1 - Chadwick, O. A1 - Frossard, E. T1 - Spectroscopic analysis shows crandallite can be a major component of soil phosphorus N2 - Phosphorus (P) bioavailability is crucial for the productivity of natural and agricultural ecosystems, and soil P speciation plays a major role therein. Better understanding of P forms present in soil is thus essential to predict bioavailability. However, P speciation studies are only as powerful as the reference spectra used to interpret them, and most studies rely on a limited set of reference spectra. Most studies on soil P forms differentiate between Ca-bound P (e.g. apatite), organic P, Fe-bound P, and Al-bound P. In our analysis of a Ca, Al, and P rich soil from the Kohala region of Hawaii, we identified the mineral crandallite, CaAl3(PO4)2(OH)5·H2O, a mineral previously not considered to play a significant role in soils. Crandallite was first identified with powder X-ray diffraction. Subsequently reference spectra were collected, and the presence of crandallite was confirmed using micro-focused P K-edge X-ray absorption near edge structure (XANES) spectroscopy, micro-infrared spectroscopy, and solid-state 31P nuclear magnetic resonance (NMR) spectroscopy. Crandallite XANES spectra were distinct from other common XANES spectra due to the presence of features in the post-edge region of the spectrum. Linear combination fitting of bulk P K-edge XANES spectra allowed the determination of the proportion of crandallite to the total P content, indicating that crandallite comprises up to half, possibly even more of the soil P in the samples. Crandallite is therefore an important and potentially overlooked component of soil P, which pedogenically forms in soils with high P, Al, and Ca contents, where it could play an important role in P bioavailability. KW - Phosphorus KW - XANES spectrosocpy KW - Infrared spectroscopy KW - NMR spectrocopy PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-654968 DO - https://doi.org/10.1016/j.geoderma.2026.117712 SN - 0016-7061 VL - 467 SP - 1 EP - 10 PB - Elsevier B.V. AN - OPUS4-65496 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Temgoua, Ranil C. T. A1 - Lisec, Jan A1 - Koch, Matthias T1 - Breaking down phenylurea herbicides: advanced electrochemical approaches for environmental degradation and remediation N2 - Phenylurea herbicides (PUHs) represent one of the most extensively used herbicide families in agriculture worldwide. While effective for weed control, their environmental persistence, bioaccumulation potential, and formation of toxic metabolites raise significant environmental concerns. This review examines current electrochemical strategies for degrading phenylurea herbicides, with special emphasis on electrochemical oxidation (EC), photoelectrochemical processes (PEC), electro-Fenton (ECF) and photo-electro-Fenton (PECF), with particular attention to the various reactor configurations and their operational mechanisms. A critical innovation of this review lies in its systematic parameter assessment framework, which categorizes nine key operational parameters across all electrochemical degradation methods: electrode material, catalyst type, cell configuration, radiation source, operating conditions (pH, current density, temperature), removal efficiency, mineralization rate, degradation kinetics, identified intermediates, and Energy consumption. For each technique, we highlight which parameters are essential, important, critical, or non� applicable, providing a structured framework to guide future experimental design. Selected case studies are presented to illustrate practical applications and performance outcomes. The review concludes with acritical analysis of current knowledge gaps and future research avenues that could enhance the sustainability, efficiency, and scalability of electrochemical remediation technologies. This work is intended as a comprehensive resource for environmental chemists, analytical scientists, and remediation engineers committed to addressing phenylurea herbicide contamination. KW - Mass Spectrometry KW - Phenylurea herbicides KW - Electrochemistry PY - 2026 DO - https://doi.org/10.1039/D5EW00809C SN - 2053-1400 VL - 12 IS - 1 SP - 72 EP - 92 PB - Royal Society of Chemistry (RSC) AN - OPUS4-64822 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Grunewald, Thomas T1 - Nichtelektrischer Explosionsschutz: Zündgefahren durch Funken - Grundlagen und Maßnahmen zum Explosionsschutz N2 - Geräte und Maschinen, die zur bestimmungsgemäßen Verwendung in explosionsgefährdeten Bereichen gemäß 2014/34/EU konstruktiv vorgesehen sind, muss in der europäischen Union eine Zündgefahrenbewertung durchgeführt werden. Dabei müssen alle 13 Zündquellen betrachtet werden. Eine Teilmenge der 13 Zündquellen sind die Gefahren von nichtelektrischen Zündquellen, zu denen auch die mechanischen Schlag-, Schleif- und Reibvorgänge gehören. Bei mechanischen Schlagvorgängen kommt es infolge des Zusammenstoßes zweier Werkstücke bzw. Bauteile zu einer Umwandlung der kinetischen Energie. Dabei erhöht sich die Temperatur der Werkstoffe an der Kontaktstelle und es kommt unter Umständen zu einem Abtrennvorgang kleiner Partikel erhöhter Temperatur. Sowohl die heißen Kontaktstellen (Zündquelle "heiße Oberflächen") als auch die abgetrennten Partikel (Zündquelle "mechanisch erzeugte Funken") können eine wirksame Zündquelle für ein explosionsfähiges Gasgemisch darstellen. Zur Festlegung von Grenzwerten wurden in der Norm DIN EN ISO 80079-36:2016 die Gasgemische anhand ihrer Explosionsgruppe klassifiziert und zu jeder Gruppe die maximale Energie des Schlagvorgangs festgelegt, unter derer die Entstehung einer wirksamen Zündquelle als unwahrscheinlich angenommen werden kann. Weitere Festlegungen von Grenzwerten für die kinetische Schlagenergie und geeignete Werkstoffpaarungen finden sich u.a. in der DIN EN 1755 (ex-geschützte Flurförderzeuge) und in der DIN EN 14986 (ex-geschützte Ventilatoren). T2 - Ausbildung zum Explosionsschutzbeauftragten CY - Essen, Germany DA - 20.01.2026 KW - Schlagfunken KW - Schleiffunken KW - Reibfunken KW - Explosionsschutz KW - Nichtelektrischer Explosionsschutz KW - Mechanischer Explosionsschutz PY - 2026 AN - OPUS4-65398 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Onyenso, Gabriel A1 - AI-Zawity, Jiwar A1 - Farahbakhsh, Nastaran A1 - Schardt, Annika A1 - Yadigarli, Aydan A1 - Vakamulla Raghu, Swathi Naidu A1 - Engelhard, Carsten A1 - Müller, Mareike A1 - Schönherr, Holger A1 - Killian, Manuela S. T1 - Novel Ag-modified zirconia nanomaterials with antibacterial activity N2 - The outcome of an implant procedure largely depends on the implant's surface properties. Biomaterials are now designed to have surfaces with multifunctionality, such as favorable tissue integration and the ability to combat bacterial adhesion and colonization. Herein, we report on a simple approach to improve the antibacterial properties of zirconia nanotubes (ZrNTs) coatings by decorating with silver nanoparticles (AgNP), achieved through electrochemical anodization of a zirconium–silver alloy (Zr–Ag). The AgNPs were shown to partially consist of Ag2O, potentially enhancing the availability of Ag+ ions for antibacterial activity. The modified ZrNTs were characterized using SEM, EDS, ToF-SIMS, and XPS to determine their structural morphology and chemical composition, and were further subjected to antibacterial testing. The silver and zirconium ion release behavior was monitored via ICP-MS. ZrNTs decorated with AgNP exhibit strong antimicrobial activity (>99% bacterial killing) against both S. aureus and E. coli. Antimicrobial tests indicate that the antibacterial activity against the Gram-positive pathogen S. aureus was improved by a factor of 100 compared to unmodified ZrNTs, while unmodified ZrNTs already showed a comparable reduction of viable Gram-negative E. coli. This strategy illustrates a straightforward and effective modification that optimizes the interface between the host environment and the biomaterial surface to meet the very important criteria of biocompatibility and active antibacterial response. KW - Mass Spectrometry KW - Nanoparticles KW - Advanced Materials KW - ICP-MS KW - Antimicrobial material KW - ToF-SIMS PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-653990 DO - https://doi.org/10.1039/d5ra07099f SN - 2046-2069 VL - 16 IS - 3 SP - 2286 EP - 2297 PB - Royal Society of Chemistry (RSC) AN - OPUS4-65399 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schiaroli, Alice A1 - Camplese, Davide A1 - Scarponi, Giordano Emrys A1 - Eberwein, Robert A1 - Ustolin, Federico A1 - Cozzani, Valerio T1 - Modelling the behaviour of cryogenic liquid hydrogen tanks engulfed in fire N2 - The safe use of liquid hydrogen as a clean fuel requires a deep understanding of its behaviour in accident scenarios. Among other scenarios, the possible involvement of cryogenic liquid hydrogen tanks in engulfing fires is of particular concern, due to the potentially severe consequences. This study proposes a computational fluid dynamic model suitable to simulate the behaviour of liquid hydrogen tanks equipped with multi-layer insulation (MLI) engulfed in fire. An original approach has been developed to assess the progressive degradation of the performance of the thermal insulation, that is crucial in determining the tank pressurization and failure. The model is validated against full-scale experimental fire tests. The outcomes of the model reproduce the progressive pressurization and the opening time of the pressure relief valve within 2 % error. The results demonstrate the importance of accounting for the dynamic evolution of the progressive degradation of the insulation when evaluating tank pressurization, and they highlight the limitations of empirical, simplified state-of-the-art approaches. Furthermore, the analysis evidences the key role of the fire temperature in governing tank response, stressing the need for proper fire characterization to support reliable modelling of fire scenarios and the development of emergency planning and mitigation strategies ensuring the structural integrity of liquid hydrogen tanks during fire attacks. KW - LH2 KW - LNG KW - Fire KW - Tank PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-652920 DO - https://doi.org/10.1016/j.psep.2025.108319 SN - 0957-5820 VL - 206 SP - 1 EP - 14 PB - Elsevier Ltd. AN - OPUS4-65292 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kozachynskyi, Volodymyr A1 - Staubach, Dario A1 - Esche, Erik A1 - Biegler, Lorenz T. A1 - Repke, Jens-Uwe T1 - Parameter estimation in dynamic multiphase liquid–liquid equilibrium systems N2 - Modeling dynamic systems with a variable number of liquid phases is a challenging task, especially in scenarios where the model is designed for optimization tasks such as parameter estimation. Although there exist methods to model the appearance and disappearance of liquid phases in dynamic systems, they usually require integer variables. In this work, the smoothed continuous approach (SCA) is developed for use with a large number of solvers, since it relies only on continuous variables. To demonstrate the applicability of the new method, the SCA is then applied to model the batch esterification of acetic acid with 1-propanol to water and propyl acetate, and to estimate the reaction parameters. Since the mixture may separate into two liquid phases during the course of the reaction, the parameters are estimated with information on the liquid compositions of both separated liquid phases, which improves the accuracy of the parameter estimates and opens new possibilities for optimal experimental design. KW - Parameter Estimation KW - Uncertainty KW - Dynamic Modeling PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-650059 DO - https://doi.org/10.1016/j.compchemeng.2025.109485 SN - 0098-1354 VL - 206 SP - 1 EP - 16 PB - Elsevier Ltd. AN - OPUS4-65005 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Hahn, Oliver A1 - Steimer, Hans Gerhard ED - Christen, Felix ED - Vöhler, Martin T1 - Hölderlins Tinten. Röntgenfluoreszenzanalyse an Handschriften des Spätwerks N2 - Erstmalig in der Hölderlin-Forschung wurde mit dem Projekt der geisteswissenschaftlichen Methodik – über die Beachtung der Wasserzeichen hinaus – ein materialwissenschaftlicher Ansatz zur Seite gestellt, um Arbeitsphasen im Werk Friedrich Hölderlins sichtbar zu machen. Wesentlich ist dabei die Verzahnung von philologischer und naturwissenschaftlicher Perspektive. Wesentlicher Bestandteil der Messungen bildet das sogenannte Homburger Folioheft. Weiterhin wurden Briefe und Manuskripte aus den Beständen der Württembergische Landesbibliothek sowie zwei eigenhändige Gehaltsquittungen aus dem Hessischen Hauptstaatsarchiv Wiesbaden untersucht. Zwei in mehreren Manuskripten klar unterscheidbare Tinten lassen sich mit einiger Wahrscheinlichkeit biografisch mit dem Zeitraum zwischen Hölderlins Rückkehr aus der Schweiz im April 1801 und seinem Weggang nach Frankreich im Dezember dieses Jahres in Verbindung bringen. Für den in den untersuchten Handschriften häufigsten Tintentyp liegen datierbare Belege zwischen Januar 1803 und März 1804 vor, anzunehmen ist seine Verwendung zwischen Oktober 1802 und Juni 1804. Er dominiert auch im Homburger Folioheft. Eine vierte mehrfach vertretene Tinte gebraucht Hölderlin nach seiner Übersiedlung von Nürtingen nach Homburg. Sie findet sich im Folioheft und in einigen Einzelhandschriften. Damit können die in der Forschung umstrittenen Fragen geklärt werden, a) ob dem Dichter das Homburger Folioheft bei seinem zweiten Aufenthalt in Homburg zur Verfügung stand und b) ob überhaupt Werkhandschriften aus dieser Zeit erhalten sind. Darüber hinaus lässt sich über die Röntgenfluoreszenzanalyse der Arbeitsstand in den untersuchten Manuskripten zum Zeitpunkt des Ortswechsels im Juni 1804 genau angeben. Auch Einzelbefunde singulärer oder in nur wenigen Stücken belegter Tinten geben gelegentlich Anhaltspunkte zur Datierung. KW - Manuskript KW - Röntgenfluoreszenzanalyse KW - Eisengallustinte PY - 2026 SN - 978-3-7705-7073-7 SN - 0340-6849 VL - 44 SP - 287 EP - 335 PB - Brill CY - Paderborn AN - OPUS4-65600 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wiesner, Yosri A1 - Eisentraut, Paul A1 - Altmann, Korinna T1 - One Year Observation of Microplastic Concentrations in the River Rhine N2 - In recent years, the quantification of microplastics (MP) in aquatic environments has gained increasing attention, particularly regarding their environmental distribution and potential exposure levels. Environmentally relevant exposure data are still essential for a realistic risk assessment of the harmful health potential of microplastics in freshwater systems. This study addresses a large data set of MP concentrations analyzed and processed under statistical aspects and provides mass concentrations as well as associated size fractions of the detected MP. Over a 12 month period, samples were collected at three locations and analyzed across three particle size fractions (100−500 μm, 50−100 μm, and 10−50 μm) using thermalextraction desorption-gas chromatography/mass spectrometry (TED-GC/MS). The most prevalent polymers identified were polyethylene (PE), polypropylene (PP), polystyrene (PS), styrene−butadiene rubber (SBR), and natural rubber (NR). Statistical analyses, including principal component and cluster analysis, revealed size-dependent patterns,minor seasonal variation and spatial variations. These findings are particularly significant for ecotoxicological research and regulatory development, especially regarding tire abrasion a rarely quantified but potentially harmful MP source. The study contributes aluable data for future environmental monitoring and supports EU directives on wastewater and drinking water quality KW - TED-GC/MS KW - Microplastics KW - Environment KW - Monitoring KW - Reference data PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-654669 DO - https://doi.org/10.1021/acsestwater.5c00530 SN - 2690-0637 SP - 1 EP - 10 PB - American Chemical Society (ACS) AN - OPUS4-65466 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Cakir, Cafer Tufan T1 - Algorithm-Assisted Multimodal Synchrotron Experiments: XRD–XES Integration and SpecTwin N2 - Multimodal synchrotron-based techniques are emerging as powerful tools for advanced materials characterization, enabling simultaneous insights into both crystal and electronic structure. We present a combined X-ray diffraction (XRD) and high-resolution X-ray emission spectroscopy (XES) approach implemented in a double-dispersive setup. This configuration enables simultaneous acquisition of structural and spectroscopic information with high precision, allowing us to resolve correlations between lattice arrangements and electronic configurations under in situ conditions. To enhance experimental throughput and reproducibility, we employ digital twin concepts and optimization algorithms for experiment design and parameter control. These methods effectively eliminate trial-and-error procedures when optimizing the setup to achieve the desired resolution for XES analysis. In addition, we introduce SpecTwin, a dedicated software environment that integrates XES data analysis, simulation, and optimization routines. This combined methodology underscores the potential of algorithm-assisted multimodal X-ray experiments to advance the quantitative understanding of structure–property relationships in complex materials. T2 - Joint BAM-HZB Symposium on Multimodal Synchrotron Experiments for Next-Generation Materials Research CY - Berlin, Germany DA - 25.02.2026 KW - XAS KW - Digital Twin KW - Optimization KW - Multimodal PY - 2026 AN - OPUS4-65608 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bartczak, Dorota A1 - Sikora, Aneta A1 - Goenaga-Infante, Heidi A1 - Altmann, Korinna A1 - Drexel, Roland A1 - Meier, Florian A1 - Alasonati, Enrica A1 - Lelong, Marc A1 - Cado, Florence A1 - Chivas-Joly, Carine A1 - Fadda, Marta A1 - Sacco, Alessio A1 - Rossi, Andrea Mario A1 - Pröfrock, Daniel A1 - Wippermann, Dominik A1 - Barbero, Francesco A1 - Fenoglio, Ivana A1 - Booth, Andy M. A1 - Sørensen, Lisbet A1 - Igartua, Amaia A1 - Wouters, Charlotte A1 - Mast, Jan A1 - Barbaresi, Marta A1 - Rossi, Francesca A1 - Piergiovanni, Maurizio A1 - Mattarozzi, Monica A1 - Careri, Maria A1 - Caebergs, Thierry A1 - Piette, Anne-Sophie A1 - Parot, Jeremie A1 - Giovannozzi, Andrea Mario T1 - Multiparameter characterisation of a nano-polypropylene representative test material with fractionation, light scattering, high-resolution microscopy, spectroscopy, and spectrometry methods N2 - Reference and quality control materials with comparable physicochemical properties to nanoplastic contaminants present in environmental and food nanoplastics are currently lacking. Here we report a nanoplastic polypropylene material prepared using a top-down approach involving mechanical fragmentation of larger plastics. The material was found to be homogeneous and stable in suspension and has been characterised for average particle size, size distribution range, particle number concentration, polypropylene mass fraction and inorganic impurity Content using a wide range of analytical methods, including AF4, cFFF, PTA, (MA)DLS, MALS, SEM, AFM, TEM, STEM, EDS,Raman, ICP-MS and pyGC-MS. The material was found to have a broad size distribution, ranging from 50 nm to over 200 nm, with the average particle size value dependent on the technique used to determine it. Particle number concentration ranged from 1.7–2.4 × 1010 g−1 , according to PTA. Spectroscopy techniques confirmed that the material was polypropylene, with evidence of aging due to an increased level of oxidation. The measured mass fraction was found to depend on the marker used and ranged between 3 and 5 μg g−1 . Inorganic impurities such as Si, Al, Mg, K, Na, S, Fe, Cl and Ca were also identified at ng g−1 levels. Comparability and complementarity across the measurement methods and techniques is also discussed. KW - Polypropylene KW - Nanoplastics KW - Analytics KW - Reference material KW - Scattering methods PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-654680 DO - https://doi.org/10.1039/D5EN00917K SN - 2051-8153 SP - 1 EP - 15 PB - Royal Society of Chemistry (RSC) AN - OPUS4-65468 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - Investigating the Thermal Decomposition of PFAS in a Full-Scale Commercial Hazardous Waste Incinerator N2 - Effective and safe treatment of per- and polyfluoroalkyl substances (PFAS)-laden waste in full-scale hazardous waste facilities is currently the only commercial method for large-scale PFAS destruction, but concerns remain about incomplete combustion and harmful byproducts. Therefore, the fate of fluorine during incineration was investigated in a full-scale hazardous waste incinerator to assess the viability and potential risks of this method. The project involves developing advanced analytical tools, including real-time infrared spectroscopy, and conducting trial burns under varied conditions. Conditions that influence incineration performance are identified, analyzing for products of incomplete destruction (PIDs), exploring the role of fly ash and surfaces in PFAS breakdown, and evaluating the potential formation of polyfluorinated dioxins and furans. Collectively, these tasks aim to deliver practical tools and guidance for scientists and engineers, while informing policymakers and the public on the benefits and potential risks of PFAS incineration. T2 - DoW Applied Innovation Workshop CY - Washington, DC, USA DA - 02.03.2026 KW - Per- and polyfluoroalkyl substances (PFAS) KW - Incineration PY - 2026 AN - OPUS4-65638 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - Investigating the Thermal Decomposition of PFAS in a Full-Scale Commercial Hazardous Waste Incinerator (SERDP ER24-4073) N2 - Effective and safe treatment of per- and polyfluoroalkyl substances (PFAS)-laden waste in full-scale hazardous waste facilities is currently the only commercial method for large-scale PFAS destruction, but concerns remain about incomplete combustion and harmful byproducts. Therefore, the fate of fluorine during incineration was investigated in a full-scale hazardous waste incinerator to assess the viability and potential risks of this method. The project involves developing advanced analytical tools, including real-time infrared spectroscopy, and conducting trial burns under varied conditions. Conditions that influence incineration performance are identified, analyzing for products of incomplete destruction (PIDs), exploring the role of fly ash and surfaces in PFAS breakdown, and evaluating the potential formation of polyfluorinated dioxins and furans. Collectively, these tasks aim to deliver practical tools and guidance for scientists and engineers, while informing policymakers and the public on the benefits and potential risks of PFAS incineration. T2 - DoW Applied Innovation Workshop CY - Washington, DC, USA DA - 02.03.2026 KW - Per- and polyfluoroalkyl substances (PFAS) KW - Incineration PY - 2026 AN - OPUS4-65639 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hufgard, Josefin T1 - AIM Forward: Acoustic Ion Manipulation for Efficient Ambient-Pressure Ion Control N2 - In ion-based spectrometry techniques the possibility to manipulate ions is fundamentally important. Currently used ion optics mostly rely on magnetic or electric fields. The electromagnetic forces compete with ion diffusion and are therefore most effective under low-pressure conditions. Therefore, high-pressure ion optics pose challenges related to elevated powers and potentials as well as complex structures and electrode contamination. Acoustic Ion Manipulation (AIM) is a recently discovered phenomenon that relies on the unique interactions between gas-phase ions and acoustic waves. This presentation shows selected patterns of ion manipulation, highlights the flexibility of AIM and discusses its current limitations and potentials. T2 - DGMS Annual Conference 2026 CY - Leipzig, Germany DA - 10.03.2026 KW - Acoustic ion manipulation KW - Mass spectrometry PY - 2026 AN - OPUS4-65680 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - El Abbassi, Abdelouahad A1 - Krenzer, Julius A1 - Petrov, Eugene P. A1 - Biesen, Lukas A1 - Vasylyeva, Vera A1 - Merzenich, Sarah A1 - Resch-Genger, Ute A1 - Müller, Thomas J. J. T1 - Aroyl-S,N-ketene acetal-triarylamine bichromophores – intramolecular energy transfer and dual emission upon induced aggregation and encapsulation N2 - Aroyl-S,N-ketene acetal-based bichromophores are synthesized by a catalytic aryl amination and their photophysics are studied in the solid state, in ethanol–water mixtures inducing aggregation, and after encapsulation in polystyrene nanoparticles. The dye substitution pattern controls aggregation-induced emission and intramolecular energy transfer efficiency, resulting in single-band or dual fluorescence and a strong increase in fluorescence quantum yield upon particle encapsulation. KW - Fluorescence KW - Dye KW - Aggregation KW - Photophysics KW - Enhancement KW - White light emission KW - Energy transfer KW - Quantum yield PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-656700 DO - https://doi.org/10.1039/d5ra09361a SN - 2046-2069 VL - 16 IS - 11 SP - 10255 EP - 10260 PB - Royal Society of Chemistry (RSC) AN - OPUS4-65670 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Tannenberg, Robert A1 - Tscheuschner, Georg A1 - Raab, Christopher A1 - Flemig, Sabine A1 - Döring, Sarah A1 - Ponader, Marco A1 - Thurmann, Melinda A1 - Paul, Martin A1 - Weller, Michael G. T1 - Simplified Sample Preparation and Lateral Flow Immunoassay for the Detection of Plant Viruses N2 - Lateral flow immunoassays (LFAs) are widely used for on-site testing; however, their use for the rapid detection of plant viruses in the field is often limited by inconvenient sample preparation. Here, we present a new sampling method and a simplified dipstick LFA format for the detection and monitoring of cowpea chlorotic mottle virus (CCMV) as a model plant pathogen. The assay employs a monoclonal mouse antibody for capture and a poly-clonal rabbit antibody conjugated to 80 nm gold nanoparticles for detection. Conventional sample and conjugate pads are omitted, allowing the test strips to be dipped directly into wells containing plant extract and antibody–gold conjugate. No plastic casing was required, which could lead to a reduction in waste. It was shown that CCMV concentrations as low as 3.5 µg/L or 350 pg per sample could be reliably detected in 15 min. Specificity tests confirmed that other plant viruses, cowpea mosaic virus (CPMV) and tobacco mosaic virus (TMV), did not produce false-positive results. In addition, we describe a new method for on-site sampling using a manual punch and a syringe equipped with a frit. This step combines grinding the sample, extraction, filtration, and reconstitution and mixing of the antibody-gold conjugate, enabling the analysis of punched leaf disks without laboratory equipment. When applied to CCMV-infected cowpea plants, the assay revealed systemic infection before visual symptoms became apparent. This work demonstrates that simplified LFAs combined with innovative sampling techniques can provide sensitive, specific, and rapid diagnostics for crop monitoring and support early intervention strategies in agriculture. N2 - Lateral-Flow-Immunoassays (LFAs) werden häufig für Vor-Ort-Tests eingesetzt; ihr Einsatz zum schnellen Nachweis von Pflanzenviren im Feld wird jedoch oft durch eine umständliche Probenvorbereitung eingeschränkt. Hier stellen wir eine neue Probenahmemethode und ein vereinfachtes Dipstick-LFA-Format zum Nachweis und zur Überwachung des Cowpea Chlorotic Mottle Virus (CCMV) als Modellpflanzenpathogen vor. Der Test verwendet einen monoklonalen Maus-Antikörper zur Bindung und einen polyklonalen Kaninchen-Antikörper, der an 80-nm-Goldnanopartikel konjugiert ist, zum Nachweis. Herkömmliche Proben- und Konjugatpads entfallen, sodass die Teststreifen direkt in Vertiefungen getaucht werden können, die Pflanzenextrakt und das Antikörper-Gold-Konjugat enthalten. Es ist keine Kunststoffhülle erforderlich, was zu einer Reduzierung des Abfallaufkommens führen könnte. Es zeigte sich, dass CCMV-Konzentrationen von nur 3,5 µg/L oder 350 pg pro Probe innerhalb von 15 Minuten zuverlässig nachgewiesen werden konnten. Spezifitätstests bestätigten, dass andere Pflanzenviren, das Cowpea Mosaic Virus (CPMV) und das Tobacco Mosaic Virus (TMV), keine falsch-positiven Ergebnisse lieferten. Darüber hinaus beschreiben wir eine neue Methode zur Probenahme vor Ort unter Verwendung eines manuellen Lochers und einer mit einer Fritte ausgestatteten Spritze. Dieser Schritt kombiniert das Zerkleinern der Probe, die Extraktion, die Filtration sowie die Rekonstitution und das Mischen des Antikörper-Gold-Konjugats und ermöglicht so die Analyse der ausgestanzten Blattscheiben ohne Laborausrüstung. Bei der Anwendung an mit CCMV infizierten Augenbohnenpflanzen zeigte der Assay eine systemische Infektion, bevor visuelle Symptome erkennbar wurden. Diese Arbeit zeigt, dass vereinfachte LFAs in Kombination mit innovativen Probenahmetechniken eine sensitive, spezifische und schnelle Diagnostik für die Pflanzenüberwachung bieten und Strategien zur frühzeitigen Intervention in der Landwirtschaft unterstützen können. KW - Point-of-care diagnostics KW - Dipstick immunoassay KW - Pre-symptomatic detection KW - Precision agriculture KW - Integrated pest management KW - Crop health monitoring PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-657039 DO - https://doi.org/10.3390/bios16020100 SN - 2079-6374 VL - 16 IS - 2 SP - 1 EP - 16 PB - MDPI AG CY - Basle, Switzerland AN - OPUS4-65703 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Henning, Thorsten A1 - Goerdeler, Cornelius A1 - El-Khatib, Ahmed H. A1 - Meyer, Klas A1 - Bruer, Gustav G. A1 - Abraham, Klaus A1 - Monien, Bernhard T1 - Characterization and quantitation of urinary metabolites of 3-monochloropropane-1,2-diol (3-MCPD) in rats N2 - Fatty acid esters of 3-monochloropropane-1,2-diol (3-MCPD) are heat-induced contaminants formed from fats and sodium chloride. The mode of action for the 3-MCPD mediated induction of renal tubule neoplasms in rats is still unclear, which is in part due to lacking metabolism data. In the current study, urinary metabolites were identified by one- and two-dimensional 13C nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry following oral administration of 3-MCPD or [13C3]3-MCPD in rats. In addition to 3-MCPD itself, nine metabolites were identified. Four of those, N-acetyl-S-(2,3-dihydroxypropyl)cysteine (DHPMA), 3-MCPD sulfate, β-chlorolactic acid (β-ClLA) and oxalic acid have been reported before. Five novel metabolites in rat urine were thiodiglycolic acid (TDGA), thionyldiglycolic acid (TNDGA), 3-MCPD glucuronide (at least three isomers), 3-carboxy-2-hydroxypropyl mercapturic acid (CHPMA), and 3-(S-carboxymethyl)mercaptolactic acid (CMMLA). Only three metabolites were excreted at mean dose ratios > 1% (after treatment with 50 mg 3-MCPD/kg body weight in male and female rats), i.e. 3-MCPD (7.3%, 9.7%), DHPMA (3.5%, 1.7%) and TDGA (1.1%, 4.0%). The overall mean dose excretion in urine samples (males: 12.2%, females: 16.3%) supported hypotheses on formation of conjugates/adducts of reactive metabolites and the possibility that dechlorination leads to suitable building blocks for amino acid and fatty acid synthesis. The identification of TDGA indicated the interim formation 2-chloroacetaldehyde, previously identified to mediate specific nephrotoxic effects of the cytostatic ifosfamide in rats. KW - 3-Monochloropropane-1,2-diol KW - 3-MCPD KW - Metabolism KW - Urine PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-657230 DO - https://doi.org/10.1007/s00204-026-04318-x SP - 1 EP - 17 PB - Springer-Verlag GmbH CY - Heidelberg AN - OPUS4-65723 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Döring, Sarah A1 - Wulfes, Birte S. A1 - Atanasova, Aleksandra A1 - Jaeger, Carsten A1 - Walzel, Leopold A1 - Tscheuschner, Georg A1 - Flemig, Sabine A1 - Gawlitza, Kornelia A1 - Feldmann, Ines A1 - Konthur, Zoltán A1 - Weller, Michael G. T1 - Corundum Particles as Trypsin Carrier for Efficient Protein Digestion N2 - Reusable enzyme carriers are valuable for proteomic workflows, yet many supports are expensive or lack robustness. This study describes the covalent immobilization of recombinant trypsin on micrometer-sized corundum particles and assesses their performance in protein digestion and antibody analysis. The corundum surface was cleaned with potassium hydroxide, silanized with 3-aminopropyltriethoxysilane and activated with glutaraldehyde. Recombinant trypsin was then attached, and the resulting imines were reduced with sodium cyanoborohydride. Aromatic amino acid analysis (AAAA) estimated an enzyme loading of approximately 1 µg/mg. Non-specific adsorption of human plasma proteins was suppressed by blocking residual aldehydes with a Tris-glycine-lysine buffer. Compared with free trypsin, immobilization shifted the temperature optimum from 50 to 60 °C and greatly improved stability in 1 M guanidinium hydrochloride. Activity remained above 80% across several reuse cycles, and storage at 4 °C preserved functionality for weeks. When applied to digesting the NISTmAb, immobilized trypsin provided peptide yields and sequence coverage comparable to soluble enzyme and outperformed it at elevated temperatures. MALDI-TOF MS analysis of Herceptin digests yielded fingerprint spectra that correctly identified the antibody and achieved 60% sequence coverage. The combination of low cost, robustness and analytical performance makes corundum-immobilized trypsin an attractive option for research and routine proteomic workflows. N2 - Wiederverwendbare Enzymcarrier sind für proteomische Arbeitsabläufe von großem Wert, doch viele Trägermaterialien sind teuer oder nicht robust genug. Diese Studie beschreibt die kovalente Immobilisierung von rekombinantem Trypsin auf mikrometergroßen Korundpartikeln und bewertet deren Leistungsfähigkeit beim Proteinverdau und der Antikörperanalyse. Die Korundoberfläche wurde mit Kaliumhydroxid gereinigt, mit 3-Aminopropyltriethoxysilan silanisiert und mit Glutaraldehyd aktiviert. Anschließend wurde rekombinantes Trypsin gebunden, und die entstandenen Imine wurden mit Natriumcyanoborhydrid reduziert. Die aromatische Aminosäureanalyse (AAAA) ergab eine geschätzte Enzymbeladung von etwa 1 µg/mg. Die unspezifische Adsorption von menschlichen Plasmaproteinen wurde durch Blockierung der restlichen Aldehyde mit einem Tris-Glycin-Lysin-Puffer unterdrückt. Im Vergleich zu freiem Trypsin verschob die Immobilisierung das Temperaturoptimum von 50 auf 60 °C und verbesserte die Stabilität in 1 M Guanidiniumhydrochlorid erheblich. Die Aktivität blieb über mehrere Wiederverwendungszyklen hinweg bei über 80 %, und die Lagerung bei 4 °C bewahrte die Funktionalität über Wochen hinweg. Beim Verdau des NISTmAb lieferte das immobilisierte Trypsin Peptidausbeuten und Sequenzabdeckungen, die mit denen des löslichen Enzyms vergleichbar waren, und übertraf dieses bei erhöhten Temperaturen. Die MALDI-TOF-MS-Analyse von Herceptin-Verdauen ergab Fingerabdruck-Spektren, die den Antikörper korrekt identifizierten und eine Sequenzabdeckung von 60 % erreichten. Die Kombination aus niedrigen Kosten, Robustheit und analytischer Leistungsfähigkeit macht auf Korund immobilisiertes Trypsin zu einer attraktiven Option für die Forschung und routinemäßige proteomische Arbeitsabläufe. KW - Bottom-up proteomics KW - Solid-phase digestion KW - Biopharmaceutical analysis KW - Peptide mapping KW - Non-specific binding KW - amino acid analysis PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-657021 DO - https://doi.org/10.3390/biotech15010002 SN - 2673-6284 VL - 15 IS - 1 SP - 1 EP - 23 PB - MDPI CY - Basel AN - OPUS4-65702 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer, Klas T1 - Benchtop NMR-Spektroskopie im industriellen Produktionsumfeld: Herausforderungen auf dem Weg zur Online-Prozessintegration N2 - Benchtop-NMR Spektrometer erobern erfolgreich seit Jahren die Labore und haben sich als ein vielseitiges analytisches Werkzeug etabliert. Zunächst stark fokussiert auf den Forschungs-bereich, sind sie heute zunehmend auch nahe der Produktion auf dem Vormarsch. Die Zielstellung ist nur selten der Ersatz von klassischer „Hochfeld“-NMR-Spektroskopie. Vielmehr erschließen die kompakten Geräte oftmals neue Anwendungsfelder, beispielsweise in der Online-Reaktionsverfolgung im Labor oder der schnellen at-line Qualitätskontrolle in der chemischen Produktion. Hier kommen die Vorteile der geringeren Anschaffungs- und Betriebskosten, die Möglichkeit des prozessnahen Einsatzes, sowie besonders der einfachen Bedienung zum Tragen. Während es zahlreiche Beispiele von Online-Applikationen im Labor gibt, ist die direkte Einbindung in großtechnische Produktionsanlagen bislang selten. Im Vergleich zu etablierten prozessanalytischen Verfahren, wie z.B. der Nahinfrarot- oder Raman-Spektroskopie ist die Benchtop-NMR-Spektroskopie noch Neuland und es existieren kaum prozesstaugliche kommerzielle Lösungen. Im Rahmen eines gemeinsamen Entwicklungsprojekts zwischen BAM und Evonik wurde eine Einhausung für ein handelsübliches Benchtop-NMR-Spektrometer konzipiert und gebaut. Diese dient nicht nur der Erfüllung sicherheitstechnischer Auflagen wie dem Explosionsschutz, sondern auch der Abschirmung rauer Umgebungseinflüsse auf den Betrieb des Laborgeräts. Eine flexible integrierte Automatisierung ermöglicht die skalierbare Anbindung an übergeordnete Prozessleittechnik im Sinne eines PAT-Moduls. Dieser Vortrag gibt einen Überblick über die Herausforderungen auf dem Weg von der Idee, über die Umsetzung bis hin zur tatsächlichen Prozessintegration. T2 - 47. Praktische Probleme der Kernresonanzspektroskopie CY - Göttingen, Germany DA - 17.03.2026 KW - Prozessanalytik KW - NMR Spektroskopie KW - Feldintegration KW - Explosionsschutz PY - 2026 AN - OPUS4-65705 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Pérez-Padilla, Víctor A1 - Burnage, Samual C. A1 - Wittwer, Philipp A1 - Valderrey, Virginia A1 - Bell, Jérémy A1 - Gawlitza, Kornelia A1 - Rurack, Knut T1 - Detection of Perfluoroalkylic Acids From Water Using a Guanidine-Based Fluorescent Probe and Microfluidic Droplet Extraction N2 - Perfluoroalkylic acids (PFAAs), a subclass of per- and polyfluoroalkyl substances (PFAS), are stable, widely used industrial compounds posing environmental concerns due to their persistence and toxicity. Regulatory actions and remediation strategies necessitate effective onsite analytical methods for PFAS management. We developed an optical sensing system using a fluorescent probe with a benzoxadiazole core and guanidine receptor in a droplet-based microfluidic assay to detect PFAAs in water samples with low detection limits. The PFAAs binding enhances the probe's fluorescence in organic media through protonation-mediated hydrogen bond-assisted ion pairing, exploiting two complementary supramolecular forces. Direct detection employs a liquid-liquid extraction protocol in the microfluidic device, achieving detection limits for PFOA and PFOS down to ≥0.5 µm, with a dynamic range up to 200 µm for sample volumes <100 µL. HCl/KCl buffering facilitates analyte desalting and phase transfer for quantitation from surface water. Additionally, we developed a method involving a thin polymer layer of the probe and a crosslinker on submicron silica particles for direct detection of PFAAs in water. Our approaches provide sensitive, direct recognition and indication of PFAAs, advancing the field beyond indirect sensing and offering improved background suppression, rapid assay times, and a modular design for targeting other PFAS subclasses. KW - PFAS KW - Fluorescence KW - Microfluidics KW - Droplet Extraction PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-657330 DO - https://doi.org/10.1002/adsr.70145 VL - 5 IS - 3 SP - 1 EP - 13 PB - Wiley-VCH CY - Weinheim AN - OPUS4-65733 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Devi, Sarita A1 - Goel, S. A1 - Rani, S. A1 - Schneider, Rudolf J. A1 - Rohilla, R. A1 - Kumari, Surbhi A1 - Prabhakar, N. T1 - MOF-metal nanohybrid-assisted charge transfer amplification for electrochemical biosensing of the MUC1 cancer biomarker N2 - Cancer is a severe disease characterized by high mortality and complex pathophysiology; however, its early and accurate diagnosis remains inadequate. Conventional diagnostic approaches often fall short, particularly for dense tissues, and are frequently invasive, costly, and of limited availability. This reinforces the need for a compact, economical, and ultrasensitive assay that is operationally simple and interpretable. We present an efficient electrochemical detection platform for the cancer biomarker mucin 1 (MUC1). A fluorine-doped tin oxide (FTO) surface was modified with an iron-based metal–organic framework (FeMOF) intercalated with palladium nanorods (PdNR). FeMOF was prepared using Fe3+/Fe2+ precursors at a 1.2/1 mmol ratio and dual ligands, i.e. tetrahydroxy-1,4-benzoquinone and 2-aminobenzene-1,4-dicarboxylic acid. AntiMUC1 antibodies were immobilized on a modified electrode via p-phenylenediamine (PDA) (FTO/FeMOF@PdNR/PDA/antiMUC1Ab) and evaluated using electrochemical impedance spectroscopy (EIS) and voltammetry. The designed sensor demonstrated an excellent binding affinity for the MUC1 antigen. Among these techniques, the EIS method stands out for its technical performance, as evidenced by the high sensitivity (detection limit 0.074 fg mL−1), quantification limit 0.24 fg mL−1, and high analytical sensitivity (1.39 × 103 Ω fg−1 mL−1 cm−2). The negligible cross-reactivity with interferent biomolecules, rapid response (10-minute equilibrium), regenerability up to 5 cycles, high reproducibility (RSD ∼1–3%), and long-term stability (up to 35 days) further validate the suitability of the proposed MUC1 immunosensor. This study presents an ultrasensitive biosensor that is compact, cost-effective, and easy for individuals at home to use after further development into a kit-based end product. Moreover, its excellent functionality for spiked serum samples shows promise for next-generation clinical diagnostics. KW - Antibodies KW - Metal-organic framework KW - Immunoassay PY - 2026 DO - https://doi.org/10.1039/D6AN00018E SP - 1 EP - 11 PB - Royal Society of Chemistry CY - London AN - OPUS4-65726 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Werner, Jan A1 - Böttcher, Nils A1 - Soderer, Hannes T1 - Batterieelektrisch betriebene FL/AT-Fzg.-Vorschriften und Sicherheit N2 - Überblick über Vorschriftenlage, Technik der Batterien und aktuelle Forschung. Aufzeigen bestehender Unschärfen in der Rechtslage, Sicherheitsfragestellungen zu Batterietechnik sowie Interaktion mit Gefahrgut. T2 - E-Mobilität in der Chemielogistik CY - Duisburg, Germany DA - 04.03.2026 KW - Batterieelektrische Antriebe KW - Gefahrgut KW - ADR KW - Unfallfeuer KW - Wärmeübertragung KW - Lithium Ionen Batterien PY - 2026 AN - OPUS4-65663 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Recknagel, Sebastian T1 - The digital reference material document - how to get standards into instruments N2 - Activities of BAm on the transfer of paper-based RM-certificates into machine readable XML-documents, based on the digital calibration certificate are described and highlighted with examples T2 - 2026 European Chemistry Meeting - Jernkontoret TO 45 CY - Stockholm, Sweden DA - 18.03.2026 KW - Reference material KW - Digital reference material document PY - 2026 AN - OPUS4-65737 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dalgic, Mete‐Sungur A1 - Kumar, Sourabh A1 - Weidner, Steffen T1 - Quantitative Analysis of Polymers by MALDI‐TOF Mass Spectrometry: Correlation Between Signal Intensity and Arm Number N2 - The signal intensities of linear and star‐shaped poly(L‐lactides) (PLA) and poly (ethylene oxides) (PEO) were compared to determine the influence of the number of arms on the ionization in matrix‐assisted laser desorption/ionization time‐of‐flight (MALDI‐TOF) mass spectrometry. In this study, a variety of blends were prepared and investigated, including binary and ternary combinations of linear and star‐shaped polymers with similar molecular masses. The focus was on examining their intensity ratios. In equimolar binary PLA blends, polymer stars were observed to exhibit higher intensities than their linear counterparts. This result was supported by experiments with equimolar ternary PLA blends, which clearly demonstrated an intensity dependence on the number of polymer arms. It was observed that four‐arm PLA exhibited higher intensities than three‐arm PLA. A similar trend was observed in investigations involving acetylated polymer end groups, suggesting that differences in ionization are primarily influenced by polymer architecture rather than end groups. In order to validate this assumption, the binding energies for [polymer‐K] + adduct ions utilizing the most stable geometry obtained from GOAT (Global Optimizer Algorithm) were calculated, revealing that star‐shaped lower mass oligomers have slightly higher binding energies. KW - MALDI-TOF MS KW - Starlike polymers KW - Quantification KW - Topology PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-653401 DO - https://doi.org/10.1002/jms.70023 SN - 1076-5174 VL - 61 IS - 1 SP - 1 EP - 12 PB - John Wiley & Sons Ltd. AN - OPUS4-65340 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Weidner, Steffen A1 - Meyer, Andreas A1 - Falkenhagen, Jana A1 - Kricheldorf, Hans R. T1 - Cyclic polyglycolide by means of metal acetylacetonates N2 - Glycolide was polymerized in bulk at 160 °C using various metal acetylacetonates as catalysts. Zirconium acetylacetonate was particularly efficient, enabling rapid polymerization even at 130 °C. The formation of cyclic poly(glycolic acid) (PGA), most likely via a ring-expansion polymerization (REP) mechanism, was proven by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. Depending on the polymerization conditions, the formation of even-numbered cycles was favored to varying degrees. Number-average molecular weights (Mn) in the range of 2000–3500 g mol−1 were achieved with dispersities below 2.0. Wide-angle X-ray scattering (WAXS) powder patterns showed that the crystal lattice was the same as that of known linear PGAs, regardless of the Mn values. These patterns enabled a comparison of crystallinities with values derived from DSC measurements. KW - MALDI-TOF MS KW - Polyglycolide KW - Crystallization KW - Small-angle X-ray scattering KW - Cyclization PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-653731 DO - https://doi.org/10.1039/d5ra07961f SN - 2046-2069 VL - 16 IS - 2 SP - 1757 EP - 1764 PB - Royal Society of Chemistry (RSC) AN - OPUS4-65373 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Duch, Karsten T1 - Sauerstoffsicherheit in Elektrolyseanlagen N2 - Nichtmetallische Materialien müssen für den Einsatz in Sauerstoff unter Druck geprüft werden. Im S3dEL Projekt wird die O2-Sicherheit für Elektrolyseanlagen untersucht und ein Prüfverfahren entwickelt das reale EL-bedingungen abbildet, als Erweiterung zur standardisierten Prüfung mit reinem O2. T2 - 1. Berliner Fachtagung für Prozess- und Anlagensicherheit CY - Berlin, Germany DA - 24.03.2026 KW - Sauerstoffsicherheit KW - Sauerstoff KW - Elektrolyse PY - 2026 AN - OPUS4-65762 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kaminski, Katja A1 - Kluge, Stephanie A1 - Frenzel, Olivia A1 - Bücker, Michael A1 - Westphalen, Tanja ED - Ziegahn, Karl-Friedrich T1 - Entwicklung, Validierung und Anwendung eines beschleunigten Bewitterungsprotokolls zur Bewertung der Freisetzung von Bisphenol A (BPA) aus Polycarbonat (PC)-Materialien in die Umwelt N2 - BPA unterliegt einer kontinuierlichen behördlichen Kontrolle und ist als besonders besorgniserregender Stoff (SVHC) gelistet. Besondere Besorgnis besteht hinsichtlich seines häufigen Nachweises in Oberflächengewässern, obwohl es leicht biologisch abbaubar ist. In mehreren Studien wurden die Quellen und Wege von BPA in die Umwelt untersucht, wobei festgestellt wurde, dass seine Hauptverwendung als Monomer in PC nur marginal zu den BPA-Freisetzungen in die Umwelt über seinen Lebenszyklus beiträgt. Um die tatsächlichen Freisetzungen von BPA aus PC unter umweltrelevanten Bedingungen besser zu verstehen, wurde eine neu entwickelte Methodik (Bundesanstalt für Materialforschung und -prüfung, BAM) angewendet, die ein neuartiges beschleunigtes Bewitterungsprotokoll für Polycarbonat-Materialien in Kombination mit einem sensitiven Analysenverfahren umfasst, welches eine Bestimmung von BPA im Ultraspurenbereich ermöglicht. Das Bewitterungsprotokoll erreicht eine 13,6-fache Beschleunigung im Vergleich zu mitteleuropäischen Wetterbedingungen und simuliert Umweltstressoren (globale Strahlung, Regen, Temperaturschwankungen) in einer Bewitterungskammer, wobei gleichzeitig die BPA-Freisetzung mit einem validierten LC-MS/MS-Verfahren unter Verwendung einer organischen Isotopenverdünnungskalibrierung bestimmt wird. In parallelen Freilandversuchen wurden die Trübung und die Vergilbung („Yellowness-Index“) der zu untersuchenden Proben als Referenzparameter untersucht. T2 - 54. Jahrestagung der GUS 2026 CY - Blankenloch-Stutensee, Germany DA - 25.03.2026 KW - Polycarbonat KW - Bisphenol A KW - Bewitterung PY - 2026 SN - 978-3-9826129-3-5 VL - 54 SP - 139 EP - 153 AN - OPUS4-65793 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Piechotta, Christian T1 - Entwicklung, Validierung und Anwendung eines beschleunigten Bewitterungsprotokolls zur Bewertung der Freisetzung von Bisphenol A (BPA) aus Polycarbonat (PC)-Materialien in die Umwelt N2 - BPA unterliegt einer kontinuierlichen behördlichen Kontrolle und ist als besonders besorgniserregender Stoff (SVHC) gelistet. Besondere Besorgnis besteht hinsichtlich seines häufigen Nachweises in Oberflächengewässern, obwohl es leicht biologisch abbaubar ist. In mehreren Studien wurden die Quellen und Wege von BPA in die Umwelt untersucht, wobei festgestellt wurde, dass seine Hauptverwendung als Monomer in PC nur marginal zu den BPA-Freisetzungen in die Umwelt über seinen Lebenszyklus beiträgt. Um die tatsächlichen Freisetzungen von BPA aus PC unter umweltrelevanten Bedingungen besser zu verstehen, wurde eine neu entwickelte Methodik (Bundesanstalt für Materialforschung und -prüfung, BAM) angewendet, die ein neuartiges beschleunigtes Bewitterungsprotokoll für Polycarbonat-Materialien in Kombination mit einem sensitiven Analysenverfahren umfasst, welches eine Bestimmung von BPA im Ultraspurenbereich ermöglicht. Das Bewitterungsprotokoll erreicht eine 13,6-fache Beschleunigung im Vergleich zu mitteleuropäischen Wetterbedingungen und simuliert Umweltstressoren (globale Strahlung, Regen, Temperaturschwankungen) in einer Bewitterungskammer, wobei gleichzeitig die BPA-Freisetzung mit einem validierten LC-MS/MS-Verfahren unter Verwendung einer organischen Isotopenverdünnungskalibrierung bestimmt wird. In parallelen Freilandversuchen wurden die Trübung und die Vergilbung („Yellowness-Index“) der zu untersuchenden Proben als Referenzparameter untersucht. T2 - 54. Jahrestagung der GUS 2026 CY - Blankenloch-Stutensee, Germany DA - 25.03.2026 KW - Bewitterung KW - Bisphenol A KW - Polycarbonat PY - 2026 AN - OPUS4-65794 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gerbeit, Marco T1 - Experimentelle und numerische Charakterisierung von Druckwellen im offenen Stoßwellenrohr zur Auslegung von Entlastungssystemen N2 - In industriellen Prozessanlagen können Druckwellen bei unfallbedingten Ereignissen (z. B. Detonation oder Bersten von Druckbehältern) schwere Schäden verursachen. Die Norm EN ISO 4126 beschreibt daher Druckentlastungseinrichtungen, die in solchen Fällen wirksam eingreifen. Dabei entweicht das Gas nach dem Öffnen der Berstscheibe und belastet das Umfeld, wie zum Beispiel benachbarte Module oder Personal (Burgess et al 2013). Daher soll in dieser Arbeit das Strömungsfeld hinter solch einer Einrichtung betrachtet werden, um exemplarisch Daten zur Einschätzung der Gefährdung im Nahbereich hinter einer Berstscheibe zu geben. Zu diesem Zweck wurde auf dem BAM TTS ein Versuchskonzept entwickelt, bei dem ein druckfester Autoklav (Stoßwellengenerator, SWG) als zu entlastende Anlage dient. Damit lassen sich die Ausbreitung und die Impulsübertragung von Gasen und Druckwellen sowie deren Phänomenologie am offenen Ende mit verschiedenen Gasen untersuchen. In diesem Beitrag werden die Ergebnisse eines Gemischs aus Acetylen und Sauerstoff vorgestellt. Dieses Gemisch wurde gewählt, da es hohe Explosionsdrücke und Flammentemperaturen erreicht, die mit anderen Gasgemischen kaum möglich sind und somit ein Worst-Case-Szenario darstellt. Eine solche Untersuchung wurde bereits mit Wasserstoff durchgeführt (Kuang et al. 2024). Es wurden verschiedene Auslassgeometrien von Schutzarmaturen – etwa Entlastungsöffnungen, wie bereits von Heinrich publiziert (Heinrich et al. 1966) – untersucht, um eine fundierte Nahfeldbewertung zu ermöglichen. Die experimentellen Daten können beispielsweise zur Validierung von CFD- Simulationen dienen und erlauben, den Einfluss von Geometrie und Umgebungsbedingungen systematisch abzubilden, und liefern praxisrelevante Daten als Basis für Leitlinien für den Explosionsschutz und die Bewertung von Störfallauswirkungen in modularen Anlagen und tragen somit zur Steigerung der Anlagensicherheit bei. T2 - 1. Berliner Fachtagung Prozess- und Anlagensicherheit CY - Berlin, Germany DA - 24.03.2026 KW - Blast KW - Druckstoß KW - Messtechnik PY - 2026 AN - OPUS4-65761 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Bayat, Mehmet Emin A1 - Nandayapa, Edgar R. A1 - Tiebe, Carlo A1 - Unger, Eva L. A1 - List-Kratochvil, Emil J. W. T1 - Raw data from: "An operando spectroscopic examination of the influence of trace humidity on interdigital back contact metal halide perovskite solar cells" N2 - Controlling trace humidity is vital for both the fabrication and long-term stability of metal halide perovskite (MHP) solar cells. Relevant humidity levels are typically below 10 ppmV, especially in glovebox-based processing and in well-encapsulated devices. Even minute amounts during fabrication can influence crystallization, introducing defects and lowering efficiency. Over time, humidity accelerates degradation of the perovskite layer and internal interfaces, ultimately reducing operational lifetime. Probing these effects at low concentrations under operando conditions is therefore essential for advancing device performance and durability. In this work, we employed a high-precision transfer standard dew point hygrometer to investigate humidity levels between 5 and 35 ppmV in non-encapsulated MHP solar cells. To permit unobstructed water migration during operation, we fabricated interdigital back contact devices. Operando measurements revealed water transport through the perovskite layer and enabled quantification of outgassing. Under trace-humidified conditions, devices exhibited initial charge-carrier quenching, followed by gradual recovery. Notably, the photocurrent response to humidified nitrogen demonstrated that the MHP layer behaves fully reversibly within the explored timescale and across the investigated humidity levels and conditions. These findings establish a systematic operando framework for examining extrinsic stressors in perovskites and highlight opportunities for assessing passivation strategies. KW - Metal halide perovskite PY - 2026 DO - https://doi.org/10.5281/zenodo.18600851 PB - Zenodo CY - Geneva AN - OPUS4-65757 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meier, F. A1 - Drexel, R. A1 - Wiesner, Yosri A1 - Altmann, Korinna A1 - Bartczak, D. A1 - Alasonati, E. T1 - Nano-sized Polypropylene as a Promising Candidate Reference Material: Preparation, Characterization and Stability in Complex Matrices N2 - The lack of nanoplastic (NPs) reference materials capable of mimicking real-world scenarios is currently hampering the development of validated extraction techniques from complex matrices, the development of analytical approaches for robust identification and quantification, and the ability to use environmentally relevant test materials in (eco)toxicity testing and hazard assessment. Here, we present a strategy towards the development of a potential NP reference material based on nano-sized polyproplyene particles (nanoPP) developed within the EURAMET-funded PlasticTrace project (https://plastictrace.eu/). The strategy includes the preparation, the physicochemical characterization and the stability assessment of nanoPP in suspension both in its pristine state, but also when spiked into complex matrices like mineral water and milk. NanoPP was produced reproducibly in a top-down approach by crushing in acetone with an UltraTurrax, filtering and change of solvent to MilliQ water. The prepared nanoPP material was subjected to a comprehensive physicochemical characterization including e.g., DLS, PTA and AF4-MALS for particle size distribution assessment, PTA and SEM for particle number concentration determination, SEM and AFM for shape analysis and pyrolysis GC-MS for chemical identification. Performed studies showed that the prepared nanoPP material is irregularly shaped and highly polydisperse with a particle size of around 180 nm (e.g., Dh,z-ave from DLS) and a particle size distribution from around 15 nm up to 135 nm (radius of gyration Rg from AF4-MALS). Storage stability studies using DLS, PTA and AF4-MALS revealed nanoPP in aqueous suspension to be stable for at least 22 months with respect to particle size distribution and number concentration rendering it a promising NP candidate reference material. However, conducted spiking experiments in mineral water and milk showed a time-dependent agglomeration of nanoPP that needs further investigation. T2 - MICROPLASTICdays CY - Ljubliana, Slovenia DA - 03.02.2026 KW - Nanoplastics KW - Reference materials PY - 2026 AN - OPUS4-65769 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Grunewald, Thomas T1 - Experimentelle Untersuchung der Zündwirksamkeit von mechanischen Schlagvorgängen mit nicht-metallischen Materialien in Wasserstoffatmosphäre - HICON-Projekt N2 - Bei der sicherheitstechnischen Beurteilung einer möglichen Wasserstofffreisetzung muss die Wirksamkeit verschiedener potenzieller Zündquellen beurteilt werden. In den einschlägigen internationalen Regelwerken des Explosionsschutzes werden insgesamt 13 verschiedene Arten von Zündquellen definiert, die zu beurteilen sind. Der mechanische Schlagvorgang ist einer dieser Zündquellen. Die Wirksamkeit dieser Zündquelle hängt vor allem von der kinetischen Schlagenergie, der Materialpaarung und der Zusammensetzung des Brenngas-Luft-Gemisches ab. Aufgrund des stochastischen Charakters der mechanisch erzeugten Funken gibt es keine geeigneten Berechnungsmethoden, um die Wirksamkeit des mechanischen Schlags als Zündquelle in Abhängigkeit dieser Parameter vorherzusagen. Anhand von geeigneten experimentellen Daten ist eine Einschätzung jedoch empirisch möglich. In früheren Arbeiten wurden vor allem homogene metallische Materialpaarungen untersucht. Damit werden einige Szenarien nicht abgedeckt, die bei der vermehrten Installation von Wasserstoffanlagen vor allem im nicht-industriellen Raum relevant sind. Dazu gehört z.B. die Beurteilung der Zündwirksamkeit von Steinschlägen im Zusammenhang mit Anlagen, die auf Untergrund oder Bodenabdeckungen aus Kiesgestein installiert werden, der aufgewirbelt werden kann oder die Beurteilung der Zündwirksamkeit bei Schlägen auf verunreinigte Oberflächen. In dieser Arbeit wurde die Zündwirksamkeit von mechanischen Schlagvorgängen mit Gesteinen und verunreinigten Oberflächen in wasserstoffhaltiger Atmosphäre systematisch untersucht. Dazu wurden Versuche in einer Schlagfunkenapparatur durchgeführt. Die Schlagfunkenapparatur erzeugt reproduzierbare streifende Schläge zwischen Schlagbolzen und Schlagplatten aus beliebigem festem Material mit stufenweise verstellbarer kinetischer Schlagenergie in einer beliebigen Gasatmosphäre. Um Steinschläge zu erzeugen, wurden spezielle Schlagplatten aus Beton mit ausgesuchten, eingebetteten Gesteinen sowie Schlagbolzenhalter mit eingeklebten Gesteinen konstruiert. Grundsätzlich konnte festgestellt werden, dass die Zündwirksamkeit bei Schlagvorgängen mit Quarzgestein in wasserstoffhaltigen Atmosphären gegenüber Schlagvorgängen mit metallischen Werkstoffen deutlich erhöht ist. Im Vergleich dazu waren dieselben Schläge in erdgas- bzw. methanhaltiger Atmosphäre nicht zündwirksam. Das ist vor allem bei der Umstellung von Erdgasanlagen bzw. bei der Übertragung von Risikomodellen für Erdgasanlagen auf Wasserstoffanlagen relevant, da neue Zündquellen berücksichtigt werden müssen. Es konnte darüber hinaus festgestellt werden, dass die Art des Gesteins einen großen Einfluss auf die Zündwirksamkeit hat. Weiterhin konnte eine deutlich erhöhte Zündwahrscheinlichkeit bei Schlagvorgängen mit homogenen Metallpaarungen bei ölbenetzten und sandgestrahlten Oberflächen beobachtet werden. Die Ergebnisse dieser Arbeit liefern Erkenntnisse, die relevant sind für die Risikoanalyse von Wasserstoffanlagen, für die Beurteilung von nicht-elektrischen Zündquellen in explosionsgefährdeten Bereichen und für die Weiterentwicklung der Regelsetzung im Explosionsschutz. T2 - 1. Berliner Fachtagung Prozess- und Anlagensicherheit CY - Berlin, Germany DA - 24.03.2026 KW - Schlagfunken KW - Schleiffunken KW - Reibfunken KW - Mechanisch erzeugte Funken KW - Nichtelektrischer Explosionsschutz KW - Mechanischer Explosionsschutz KW - Gesteinsfunken KW - sandgestrahlte Oberflächen KW - Ölbenetzte Oberflächen KW - Benzinbenetzte Oberflächen KW - Sandbenetzte Oberflächen PY - 2026 AN - OPUS4-65763 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Holtappels, Kai T1 - Ammoniak als Energieträger in Deutschland: Zwischen Sicherheitsanforderungen, Infrastruktur und Akzeptanz N2 - Die Gewährleistung einer sicheren, zuverlässigen und klimaneutralen Energieversorgung stellt eine der zentralen Herausforderungen der kommenden Jahrzehnte dar. Als zentraler Baustein für die Energiewende wird Grüner Wasserstoff gesehen. Allerdings müssen bis zum Hochlauf einer flächendeckenden Wasserstoffinfrastruktur effektive Speicher- und Transportlösungen bereitgestellt werden. Verschiedene Wasserstoff-derivate, insbesondere Ammoniak, Methanol, synthetisches Methan und flüssige organische Wasserstoffträger (LOHCs), können dabei eine tragende Rolle spielen. Aufgrund seiner etablierten globalen Infrastruktur und der vorhandenen industriellen Produktions- und Handelsketten (weltweit über 170 Mio. Tonnen jährlich) stellt Ammoniak, besonders kurzfristig, eine vielversprechende Option für die energetische Nutzung dar. Zusätzlich zeichnet sich Ammoniak durch seine hohe Energiedichte und, im Vergleich zu Wasserstoff, einfache Lager- und Transportfähigkeit aus. Auch langfristig bietet Grüner Ammoniak, insbesondere der in sonnen- und windreichen Regionen aus erneuerbaren Energiequellen erzeugte, das Potenzial für eine wirtschaftliche Produktion und eine vielversprechende Option für künftige Energieimporte. Aufgrund der toxischen Eigenschaften und potenziellen Umweltrisiken sind allerdings umfassende sicherheitstechnische Maßnahmen sowie eindeutige regulatorische Rahmenbedingungen erforderlich. Darüber hinaus gilt es, technologische Herausforderungen zu lösen, die sich in Abhängigkeit von der Nutzung von Ammoniak ergeben. Hierzu zählen unter anderem die Emissionskontrolle bei der direkten Verbrennung von Ammoniak sowie die Verbesserung der Effizienz bei der Rückumwandlung von Ammoniak in Wasserstoff (Ammoniak-Cracking). Vor diesem Hintergrund hat die Bundesanstalt für Materialforschung und -prüfung (BAM) im Rahmen zweier Workshops in Kooperation mit relevanten Stakeholdern aus Behörden, Wirtschaft und aus der Wissenschaft zentrale Handlungsempfehlungen für die Politik abgeleitet, mit dem Ziel, den Einsatz von Ammoniak als Energieträger in Deutschland voranzubringen. Diese Handlungsempfehlungen werden im Beitrag päsentiert und anschließend zur Diskussion gestellt. Zusammenfassend lässt sich festhalten, dass Ammoniak ein vielversprechendes Wasserstoffderivat für die Dekarbonisierung darstellt, sofern politischer Wille und eine klare Strategie den zielgerichteten Ausbau der notwendigen Infrastruktur, die Schaffung regulatorischer Rahmenbedingungen sowie die Förderung technologischer Innovationen vorantreiben. T2 - 1. Berliner Fachtagung Prozess- und Anlagensicherheit CY - Berlin, Germany DA - 24.03.2026 KW - Ammoniak KW - Wasserstoffderivate KW - Energieträger KW - Herausforderungen PY - 2026 AN - OPUS4-65766 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer, Klas T1 - Benchtop-NMR Spectroscopy as a PAT tool in industrial environments – Field integration of a laboratory instrument N2 - Chemical industry is currently in a rapidly changing environment, e.g., due to variability of raw material quality, high energy costs and demand for improving efficiency. Process optimization and new process concepts become more and more important. Flexible chemical plants can produce various high-quality products using multi-purpose equipment with short downtimes between campaigns and reduce time to market for new products. Intensified continuous production plants allow for difficult to produce compounds like exothermic reactions with high heat dissipation. Highly automated chemical process monitoring along with real-time quality control are prerequisites to such concepts and, thus, should be based on “real-time” chemical information. A commercially available benchtop NMR spectrometer was integrated to the full requirements of an automated chemical production environment such as explosion safety, field communication, and robust evaluation of sensor data. Field studies in modular and conventional production plant setups show promising results gaining process knowledge for further optimization. NMR spectroscopy appeared as powerful online analytical method and allows using a modular data analysis approach, which can even serve as reliable reference method for further calibration-dependent PAT applications (e.g., NIR or Raman spectroscopy). Based on experiences from earlier field studies an enhanced field enclosure setup was developed and built, including the option of a secondary analytical method (e.g., optical spectroscopy). Integrated control systems allow for a flexible implementation based on the available automation infrastructure at the chemical plant or pilot plant setup. In the future, modular interconnecting “smart” PAT systems and process equipment have the potential speed up the setup of production equipment for chemicals and pharma-ceuticals and therefore help to reduce the time-to-market. T2 - Analytica Conference 2026 CY - Munich, Germany DA - 24.03.2026 KW - Benchtop NMR spectroscopy KW - Process Analytical Technology KW - Field integration KW - Explosion safety PY - 2026 AN - OPUS4-65771 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meier, F. A1 - Altmann, Korinna T1 - Challenges in nanoplastic analysis: Reference materials, complex matrices, and limits of detection N2 - The growing concern over nanoplastic particles (< 1 µm) in food and the environment has intensified the need for robust analytical approaches to detect, quantify, and characterize these particles. But the lack is high of standardized and well-characterized reference materials that reflect environmentally relevant nanoplastics according to: • Size distribution • Low abundance • Chemical diversity • Surface properties • Behavior in complex matrices. This poster shows different methods like FFF and AF4-MALS and their results when measuring a nanoPP reference materials candidate. T2 - Analytica Conference 2026 CY - Munich, Germany DA - 24.03.2026 KW - Nanoplastics KW - Reference materials KW - AF4-MALS KW - FFF PY - 2026 AN - OPUS4-65770 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hartwig, Peter T1 - Sichere Wasserstoffnetze ModuH2Pipe N2 - Der Wasserstofftransport durch Pipelines in Deutschland und Europa ist von zentraler Bedeutung für die zukünftige Energieversorgungssicherheit. Neben dem Neubau einer Wasserstoff-Transportinfrastruktur wird vor allem die kosteneffiziente Umwidmung bestehender Erdgasnetze für den Wasserstofftransport vorangetrieben. Dabei ergeben sich zahlreiche sicherheitstechnische Fragestellungen, insbesondere zur Materialeignung und -kompatibilität, der Zustandsanalyse und -überwachung von Pipelines sowie der Gewährleistung der Gasqualitäten. Die Validierung der wissenschaftlich-technischen Tragfähigkeit der Antworten zu diesen Fragen unter realen Bedingungen ist erforderlich für die erfolgreiche Transformation des Energietransports. Hierzu stellt die BAM eine neue, einzigartige Prüfinfrastruktur vor, die ab Juli 2026 zur Verfügung stehen wird. T2 - 1. Fachtagung für Anlagen- und Prozesstechnik CY - Berlin, Germany DA - 24.03.2026 KW - Wasserstoff KW - ModuH2Pipe KW - Modulare-Testplattform KW - Realmaßstab KW - Wasserstoffkernnetz PY - 2026 AN - OPUS4-65767 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Askar, Enis T1 - Sicherheitstechnische Eigenschaften von Wasserstoff-Sauerstoff-Gemischen unter Prozessbedingungen der Elektrolyse N2 - Die Bildung von Wasserstoff-Sauerstoff-Gemischen, beispielsweise aufgrund von Cross-Over, Fehlfunktionen oder An- und Abschaltvorgängen, stellt eine für Elektrolyseprozesse ganz spezifische Gefahr dar, die angemessen berücksichtigt werden muss. In dieser Arbeit wurden die Explosionsgrenzen von Wasserstoff-Sauerstoff-Gemischen bei Prozessbedingungen von bis zu 30 bar und 300 °C experimentell bestimmt. Es zeigte sich, dass die vorhandenen experimentellen Daten mithilfe empirischer Ansätze mit guter Genauigkeit interpoliert werden können. Darüber hinaus wurden auch die Explosionsgrenzen unter atmosphärischen Bedingungen mit reduzierter Zündenergie bis hinunter zu 1 mJ bestimmt. Obwohl in der Literatur zu finden ist, dass die Zündenergie von brennbaren Gasen stark ansteigt, wenn die Konzentration von stöchiometrisch in den Bereich nahe den Explosionsgrenzen wechselt, wurde innerhalb des getesteten Zündenergiebereichs für H₂/O₂-Gemische kein signifikanter Einfluss der Gemischkonzentration festgestellt. Schließlich wurde die Zündung an heißen Oberflächen für Gemische mit 6 Mol-% Wasserstoff in Sauerstoff, also leicht oberhalb der Explosionsgrenze, experimentell bei verschiedenen Drücken bis zu 30 bara untersucht. Auch hier wurden nur geringe Abweichungen von den für stöchiometrische Gemische ermittelten Zündtemperaturen festgestellt. Zur Berechnung der Zündtemperaturen wurde ein 0D-Reaktormodell mit adiabatischem, konstantem Volumen verwendet. Das Modell wurde hinsichtlich seiner Vorhersage der Zündtemperaturen von Wasserstoffgemischen bei verschiedenen Drücken getestet. T2 - 1. Berliner Fachtagung Prozess- und Anlagensicherheit CY - Berlin, Germany DA - 24.03.2026 KW - Elektrolyse KW - Explosionsgrenzen KW - Zündenergie KW - Zündtemperatur PY - 2026 AN - OPUS4-65782 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Funnemann, Patrick T1 - Nachhaltige TiFe‑basierte H2-Speicher: Sicherheit entlang des Lebenszyklus - Ex-Kenngrößen eines hybriden Staub/H2 (2 %)/Luft‑Gemischs N2 - Der sichere Umgang mit Legierungen auf TiFe-Basis ist für deren Einsatz als reversible Wasserstoffspeichermaterialien von entscheidender Bedeutung. Während der Herstellung, des Betriebs und des Recyclings werden diese Legierungen häufig in Form feiner Pulver verarbeitet, die zündfähige Staubwolken und hybride Gemische mit Wasserstoff bilden können. In diesem Vortrag werden die Explosionscharakteristika einer pulverförmigen TiFe–Mn-Legierung unter zwei verschiedenen Atmosphären systematisch untersucht: Luft und Luft mit 2 % Wasserstoff, was 50 % der unteren Explosionsgrenze entspricht. Schlüsselparameter, darunter der maximale Explosionsdruck (pmax), die maximale Druckanstiegsrate ((dp/dt)max) und der Kst-Wert, wurden mittels standardisierter Versuche in einem 20-Liter-Kugel-Apparat bestimmt. Die Ergebnisse zeigen, dass Wasserstoff in Konzentrationen unterhalb der unteren Explosionsgrenze (UEG) in Kombination mit Staub die Druckanstiegsrate und den Kst-Wert tendenziell erhöht, während der maximale Explosionsdruck aufgrund der verringerten Sauerstoffverfügbarkeit leicht absinkt. Diese Ergebnisse unterstreichen, dass bereits geringe Wasserstoffzugaben die Flammenausbreitung beschleunigen und die Explosionsschwere erhöhen können, was für die Risikobewertung und die Auslegung von Explosionsschutzmaßnahmen in Wasserstoffspeichersystemen von entscheidender Bedeutung ist. Darüber hinaus liefert die durchgeführte umfassende chemische Charakterisierung eine solide Grundlage für zukünftige Untersuchung der sicherheitstechnischen Eigenschaften und unterstützt damit die Entwicklung sicherer und nachhaltiger Wasserstoffspeicher-Technologien. T2 - 1. Berliner Fachtagung Prozess- und Anlagen-sicherheit CY - Berlin, Germany DA - 24.03.2026 KW - Staubexplosionen KW - Hybride Gemische KW - Wasserstoffspeicherung KW - Wasserstoffsicherheit PY - 2026 AN - OPUS4-65781 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Askar, Enis T1 - HICON Experimental Campaign 3 - Ignition of Hydrogen due to Single Impact N2 - The experimental campaigns within HICON aim to obtain quantitative and qualitative data through experiments for statistics and understanding of ignition probabilities. Based on that hydrogen ignition models are developed transfering the risk-based models from the natural gas applications. Within the presented experimental campaign the focus was on impacts with gravel and with contaminated surfaces. It was found that the ignition probabilty of hydrogen atmospheres by mechanical impacts can be highly increased when gravel is involved and when surfaces are contaminated with oil or with fine sand (sandblasted surfaces), while natural gas atmospheres cannot be ignited under similar conditions. T2 - FABIG Fire and Blast Information Group 111th UK Technical Meeting CY - London, United Kingdom of Great Britain and Northern Ireland DA - 24.03.2026 KW - Explosion protection KW - Ignition sources KW - Mechanical sparks KW - Natural gas KW - Safety KW - Risk assessment PY - 2026 AN - OPUS4-65783 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hartwig, Peter T1 - Sichere Wasserstoffnetze ModuH2Pipe N2 - Modulare Testplattform für den sicheren Transport von Wasserstoff in neuen und vorhandenen Gasverteilnetzen Die BAM schafft mit der modularen Testplattform ModuH2Pipe erstmals in Europa eine Testinfrastruktur, welche die Betrachtung sicherheitstechnischer Fragestellungen im Realmaßstab und zugleich unter kritischen Bedingungen erlaubt, die sich im Zusammenhang mit Wasserstoff-und Wasserstoff-Erdgas-Pipelines stellen. Ziel ist, Gasnetzbetreibern u. a. ein Dienstleistungsangebot zur Verfügung zu stellen, welches die umfassende Beantwortung dieser und weiterer sicherheitstechnischer Fragestellungen ermöglicht. Die Testplattform ModuH2Pipe wird auf dem BAM Testgelände Technische Sicherheit (BAM TTS) stehen und integriert zwei Module, die für die experimentelle Untersuchung von Pipelinesegmenten, -komponenten (Dichtungen, Ventile etc.) und Polymerkomponenten im Originalmaßstab ausgelegt sind. Aber auch digitale Aspekte für Wasserstoffnetze können betrachtet werden. T2 - 1. Fachtagung für Anlagen- und Prozesstechnik CY - Berlin, Germany DA - 24.03.2026 KW - Wasserstoff KW - ModuH2Pipe KW - Testplattform KW - Realmaßstab KW - Wasserstoffkernnetz PY - 2026 AN - OPUS4-65765 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Falkenhagen, Jana A1 - Beskers, Timo. F. A1 - Myxa, Anett A1 - Pursch, Matthias T1 - Round-robin test for size exclusion chromatography – Data summary N2 - Size exclusion chromatography (SEC or GPC) is one critical component of polymer analysis to meet the increasing requirements in regulatory context – namely, determination of Mn, as well as oligomers of less than 500 g mol-1 and 1000 g mol-1. The underlying test methods (OECD 118/119 and DIN EN ISO 13885 1 to 3) provide a framework for SEC measurements; however, they lack sufficient specificity to obtain accurate results. Previous SEC round robin tests were mostly performed on homopolymers and did not collect data on oligomer contents. A new round robin test was initiated and conceptualized within the Task force “Method Evaluation for Polymer REACh (MeEP)”, an initiative of “Industrieforum Analytik” within the German Chemical Society (GDCh). Samples for this study were selected to represent both easy benchmark polymers as well as real-life, industry-relevant polymer materials. Data collection focused on the regulatory requirements. Distribution of samples, gathering of individual results and evaluation were carried out by BAM. A data summary as initial result is reported here. Further evaluation and interpretation are a part of ongoing research. KW - Size exclusion chromatography KW - Polymers KW - Oligomer content KW - Round-robin test PY - 2026 DO - https://doi.org/10.26272/opus4-65587 SP - 1 EP - 84 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-65587 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bayat, Mehmet Emin A1 - Nandayapa, Edgar R. A1 - Tiebe, Carlo A1 - Unger, Eva L. A1 - List-Kratochvil, Emil J. W. T1 - An operando spectroscopic examination of the influence of trace humidity on interdigital back contact metal halide perovskite solar cells N2 - Controlling trace humidity is vital for both the fabrication and long-term stability of metal halide perovskite (MHP) solar cells. Relevant humidity levels are typically below 10 ppmV, especially in glovebox-based processing and in well-encapsulated devices. Even minute amounts during fabrication can influence crystallization, introducing defects and lowering efficiency. Over time, humidity accelerates degradation of the perovskite layer and internal interfaces, ultimately reducing operational lifetime. Probing these effects at low concentrations under operando conditions is therefore essential for advancing device performance and durability. In this work, we employed a high-precision transfer standard dew point hygrometer to investigate humidity levels between 5 and 35 ppmV in non-encapsulated MHP solar cells. To permit unobstructed water migration during operation, we fabricated interdigital back contact devices. Operando measurements revealed water transport through the perovskite layer and enabled quantification of outgassing. Under trace-humidified conditions, devices exhibited initial charge-carrier quenching, followed by gradual recovery. Notably, the photocurrent response to humidified nitrogen demonstrated that the MHP layer behaves fully reversibly within the explored timescale and across the investigated humidity levels and conditions. These findings establish a systematic operando framework for examining extrinsic stressors in perovskites and highlight opportunities for assessing passivation strategies. KW - Metal halide perovskite KW - IBC solar cells KW - In operando KW - Extrinsic stressors KW - Fabrication and encapsulation KW - Trace humidity KW - Two-site Stern-Volmer KW - Charge-carrier quenching PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-657560 DO - https://doi.org/10.1039/D6TA01295G SP - 1 EP - 16 PB - The Royal Society of Chemistry CY - London AN - OPUS4-65756 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kasch, Thomas T1 - Sicherheit von Sauerstoffanlagen - aus Unfällen und Erfahrungen lernen N2 - Der Vortrag zeigt Beispiele auf, wie einerseits durch Untersuchungen von Unfällen sowie andererseits durch die zahlreichen Prüfungen an der BAM Erkenntnisse gewonnen wurden. Diese sind in die Überarbeitung von Normen und Standards sowie in die Modifikation von Prüfverfahren und von Bewertungskriterien eingeflossen. So wird zum Beispiel bei der Untersuchung nichtmetallischer Materialien versucht, den tatsächlichen, praktischen Anwendungsfall zu berücksichtigen und diesen durch die Prüfungen möglichst abzubilden. Änderungen beim Herstellungsprozess, bei der Materialzusammensetzung und bei Weiterverarbeitungsprozessen nichtmetallischer Materialien haben in der Vergangenheit immer wieder zu deutlich unterschiedlichen Prüfergebnissen geführt. Dem wurde nunmehr durch die Einführung chargenbezogener Prüfungen Rechnung getragen. Für Ventile mit integriertem Druckregler (Valves with Integrated Pressure Regulator - VIPR) wurden neue und überarbeitete Prüfanforderungen für die Lebensdauer und für die Ausbrennsicherheit festgeschrieben, um den gestiegenen sicherheitstechnischen Anforderungen für Anwendungen mit medizinischem Sauerstoff Rechnung zu tragen. Ziel ist es, auch zukünftig die Sicherheit von Sauerstoffanlagen durch die Betrachtung von Unfällen und die Erfahrungen aus Prüfungen zu verbessern. T2 - 1. Berliner Fachtagung für Prozess- und Anlagensicherheit CY - Berlin, Germany DA - 24.03.2026 KW - Sauerstoff KW - Unfälle KW - Chargenprüfung KW - Prüfanforderungen KW - Sicherheit PY - 2026 AN - OPUS4-65813 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Simon, Fabian A1 - von der Au, Marcus A1 - Gehrenkemper, Lennart A1 - Meermann, Björn T1 - An optimized method for PFAS analysis using HR–CS–GFMAS via GaF detection N2 - The analysis of per- and polyfluoroalkyl substances (PFAS) via sum parameters like extractable organic fluorine (EOF) in combination with high resolution-continuum source-graphite furnace molecular absorption spectrometry (HR–CS–GFMAS) is highly promising regarding fluorine sensitivity and selectivity. However, the HR–CS–GFMAS method includes several drying and heating steps which can lead to losses of volatile PFAS before the molecular formation step using e.g., GaF formation. Hence, the method leads to a strong discrimination of PFAS within the EOF depending on their physical/chemical properties and is therefore associated with reduced accuracy. To reduce this discrepancy and to indicate realistic PFAS pollution values, an optimization of the HR–CS–GFMAS method for PFAS analysis is needed. Hence, we determined fluorine response factors of several PFAS with different physical/chemical properties upon application of systematic optimization steps. We could therefore improve the method's sensitivity for PFAS analysis using a modifier drying pre-treatment step followed by a sequential injection of sample solutions. The highest improvement in sensitivity of volatile PFAS was shown upon addition of a Mg modifier during drying pre-treatment. Thereby, during optimization the relative standard deviation of fluorine response factors could be reduced from 55 % (initial method) to 27 % (optimized method) leading to a more accurate determination of organofluorine sum parameters. The method provides an instrumental LOD and LOQ of β(F) 1.71 μg/L and 5.13 μg/L, respectively. Further validation aimed to investigate several matrix effects with respect to water matrices. Here, substance-specific behavior was observed. For example, perfluorooctanoic acid (PFOA) which was used as calibrator, showed signal suppressions upon high chloride concentrations (>50 mg/L). Hence, a thorough separation of Cl from analytes during sample preparation is needed for accurate sum parameter analysis. KW - PFAS KW - GF-AAS KW - Method optimization PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-610522 DO - https://doi.org/10.1016/j.talanta.2024.126811 VL - 281 SP - 1 EP - 11 PB - Elsevier B.V. AN - OPUS4-61052 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krone, David A1 - Esche, Erik A1 - Skiborowski, Mirko A1 - Repke, Jens-Uwe T1 - Optimization-based process synthesis by phenomena-based building blocks and an MINLP framework featuring structural screening N2 - An existing approach for optimization-based process synthesis with abstracted phenomena-based building blocks (PBB) is extended by implementing it into a novel MINLP framework with structural screening. Consistency across the multilayer MINLP framework is guaranteed by creating a MathML/XML data model and subsequently exporting the code to the different program parts. The novel framework focuses both on fidelity by implementing thermodynamically sound models and on generality by employing a state-space superstructure that spans a large search space. In order to retain tractability, we insert a structural screening layer which prescreens based on binary decision variables of the superstructure by graph- and rule-based analyses, penalizing non-physical instances without solution of the underlying MINLP. The MINLP framework is successfully applied on two challenging synthesis tasks to determine the separation of the feed streams of benzene and toluene, as well as of n-pentane, n-hexane, and n-heptane utilizing superstructures with two, respectively four PBB. KW - Process synthesis KW - Superstructure optimization KW - Distillation KW - Mathematical programming KW - Structural screening PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-621955 DO - https://doi.org/10.1016/j.compchemeng.2024.108955 VL - 194 SP - 1 EP - 19 PB - Elsevier Ltd. AN - OPUS4-62195 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wilrich, Cordula A1 - Wilrich, Thomas T1 - Explosion bei Tankinstandhaltung N2 - Bei Instandhaltungsarbeiten an einem Tank kam es – ohne Personenschaden – zu einer Explosion. Da als Ursache nur solche aus dem Obhuts- und Gefahrenbereich des mit der Instandhaltung beauftragten Dienstleisters und seines Subunternehmers in Frage kamen, mussten diese sich im Zuge einer Beweislastumkehr entlasten, d.h. sie mussten aufzeigen, dass sie nicht pflichtwidrig gehandelt haben. Das gelang ihnen nicht und das Gericht ging zur Begründung auch detailliert auf Technische Regeln zur Betriebssicherheit ein (was in Urteilsbegründungen eher selten vorkommt). Die Gefährdungsbeurteilung spielte dahingegen in der Urteilsbegründung keine Rolle. Dies zeigt wie unterschiedlich Juristen und Arbeitsschützer denken: Zur Klärung einer möglichen Haftung sind die Pflichtverletzung und der Kausalzusammenhang relevant, während für den Arbeitsschutz die Prävention im Vordergrund steht – vor allem die Gefährdungsbeurteilung und die daraus abgeleiteten Schutzmaßnahmen. KW - Arbeitsschutz KW - Technische Regeln für Betriebssicherheit KW - TRBS KW - Instandhaltung KW - Explosion KW - Tank PY - 2025 DO - https://doi.org/10.37307/j.2199-7349.2025.01.09 IS - 1 SP - 32 EP - 37 PB - Erich Schmidt Verlag (ESV) CY - Berlin AN - OPUS4-62380 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Grunewald, Thomas T1 - Explosionsschutz - Grundlagen und Maßnahmen zum nichtelektrischen Explosionsschutz N2 - Bei Geräten und Maschinen zur bestimmungsgemäßen Verwendung in explosionsgefährdeten Bereichen gemäß 2014/34/EU muss in der europäischen Union eine Zündgefahrenbewertung durchgeführt werden. Dabei müssen unter anderem die Gefahren von nichtelektrischen Zündquellen betrachtet werden, zu denen auch die mechanischen Schlagvorgänge gehören. Bei mechanischen Schlagvorgängen kommt es infolge des Zusammenstoßes zweier Werkstücke bzw. Bauteile zu einer Umwandlung der kinetischen Energie. Dabei erhöht sich die Temperatur der Werkstoffe an der Kontaktstelle und es kommt unter Umständen zu einem Abtrennvorgang kleiner Partikel erhöhter Temperatur. Sowohl die heißen Kontaktstellen (Zündquelle "heiße Oberflächen") als auch die abgetrennten Partikel (Zündquelle "mechanisch erzeugte Funken") können eine wirksame Zündquelle für ein explosionsfähiges Gasgemisch darstellen. Zur Festlegung von Grenzwerten wurden in der Norm DIN EN ISO 80079-36:2016 die Gasgemische anhand ihrer Explosionsgruppe klassifiziert und zu jeder Gruppe die maximale Energie des Schlagvorgangs festgelegt, unter derer die Entstehung einer wirksamen Zündquelle als unwahrscheinlich angenommen werden kann. Aufgrund neuerer Erkenntnisse der BAM zum Verhalten von Schlagvorgängen in Wasserstoff/Luft-Gemischen bei bestimmten Werkstoffpaarungen werden Änderungen der relevanten Regelwerke des nichtelektrischen Explosionsschutzes angestrebt. Weitere Festlegungen von Grenzwerten für die kinetische Schlagenergie und geeignete Werkstoffpaarungen finden sich u.a. in der DIN EN 1755 (ex-geschützte Flurförderzeuge) und in der DIN EN 14986 (ex-geschützte Ventilatoren) T2 - Ausbildung zum Explosionsschutzbeauftragten (Veranst.-Nr. VA25-00302-050-E) CY - Essen, Germany DA - 28.01.2025 KW - Schlagfunken KW - Schleiffunken KW - Reibfunken KW - Mechanisch erzeugte Funken KW - Nichtelektrische Funken KW - Nichtelektrischer Explosionsschutz KW - Mechanischer Explosionsschutz PY - 2025 AN - OPUS4-62469 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Casperson, Ralf A1 - Leinenbach, F. A1 - Martin, J. ED - Meyendorf, N. ED - Ida, N. ED - Singh, R. ED - Vrana, J. T1 - DICONDE: Enabling FAIR Data and Communication in NDE 4.0 N2 - For the digital transformation and the integration of NDE into the Industry 4.0, standardized data formats and communication interfaces are mandatory. The Standard Practice for Digital Imaging and Communication in Nondestructive Evaluation (DICONDE), based on Digital Imaging and Communication in Medicine (DICOM), offers both a standardized data format and standardized communication interfaces. Furthermore, DICONDE meets the requirements of the EU Data Act by supporting the FAIR data principle (findable, accessible, interoperable, and reusable data). DICONDE standards are available for radiography including computed tomography, ultrasonic, and eddy current testing. Standards for thermography and secondary capture are under development. The basic concept of DICONDE, storage of eddy current and ultrasonic raw data, and the use case of railway rail inspection at the AIFRI project are discussed in detail. KW - Data format KW - Data communication KW - FAIR data KW - NDE 4.0 KW - Industry 4.0 KW - EU Data Act KW - DICONDE PY - 2025 SN - 978-3-030-48200-8 DO - https://doi.org/10.1007/978-3-030-48200-8 SP - 1 EP - 20 PB - Springer Nature CY - Heidelberg ET - 2 AN - OPUS4-62657 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kozachynskyi, Volodymyr A1 - Hoffmann, Christian A1 - Esche, Erik T1 - Why fixing alpha in the NRTL model might be a bad idea – Identifiability analysis of binary vapor-liquid equilibria N2 - New vapor-liquid equilibrium (VLE) data are continuously being measured and new parameter values, e.g., for the nonrandom two-liquid (NRTL) model are estimated and published. The parameter α, the nonrandomness parameter of NRTL, is often not estimated but is heuristically fixed to a constant value based on the involved components. This can be seen as a manual application of a (subset selection) regularization method. In this work, the practical parameter identifiability of the NRTL model for describing the VLE is analyzed. It is shown that fixing α is not always a good decision and sometimes leads to worse prediction properties of the final parameter estimates. Popular regularization techniques are compared and Generalized Orthogonalization is proposed as an alternative to this heuristic. In addition, the sequential Optimal Experimental Design and Parameter Estimation (sOED-PE) method is applied to study the influence of the regularization methods on the performance of the sOED-PE loop. KW - NRTL KW - VLE KW - Nonlinear programming KW - Model-based optimal experimental design PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-623605 DO - https://doi.org/10.1016/j.ces.2024.121122 VL - 305 SP - 1 EP - 18 PB - Elsevier Ltd. AN - OPUS4-62360 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hauschildt, Charlotte T1 - New Approaches to PFAS Quali- and Quantification using GC-MS N2 - Known as “forever chemicals”, per- and polyfluoroalkyl substances (PFAS) are a class of synthetically produced chemicals that includes an estimated 10.000 compounds. Due to the persistence, toxicity and ubiquitous occurrence, research has focused on the qualification and quantification of the most important compounds as well as on the investigation of toxicity and possible routes of entry over the last 10 years. Liquid chromatography - mass spectrometry (LC-MS) is the analytical standard to test for PFAS, as the spectrum of detectable compounds is significantly more comprehensive than it is currently the case with gas chromatography - mass spectrometry (GC-MS). However, to be able to test for PFAS contamination in a more process-independent manner and to make the analysis more widely accessible, methods based on GC-MS are currently being developed. Since GC-MS methods only cover a fraction of the compounds belonging to the PFAS group so far, further development of the corresponding measurement methods is inevitable [1, 2]. The here described work is part of the EU project 23IND13 ScreenFood [3]. The aim is to develop sensitive analytical GC-MS methods that contribute to an improved identification and quantification of various PFAS (both currently regulated and emerging PFAS) in selected food and food packaging matrices. Of particular interest as a food contact material are native and recycled polymers such as PET. Besides, various techniques, including solvent-free variants such as thermal desorption GC-MS, will be tested for a quick and easy analysis. Multiple derivatization approaches, which cover different PFAS subgroups, will also be tested and evaluated. This poster will present the overall project objectives and first results. T2 - ANAKON 2025 CY - Leipzig, Germany DA - 10.03.2025 KW - Per- and Polyfluoroalkyl Substances (PFAS) KW - Gas chromatography - mass spectrometry (GC-MS) KW - EU Project KW - Derivatization methods PY - 2025 AN - OPUS4-62709 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Vogel, Christian A1 - Slee, D. ED - Naidu, R. T1 - Chapter 5 Analytical techniques for Per- and Polyfluoroalkyl substances (PFAS) N2 - Per- and polyfluoroalkyl substances (PFAS) are a group of various anthropogenic organic products, in which the hydrogen atoms on the carbon skeleton of at least one carbon atom have been completely replaced by fluorine atoms. Because this group contains more than 7 million compounds, they can have very different properties. PFAS analysis in environmental samples is currently mainly utilized by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and related techniques as well as gas chromatography-mass spectrometry (GC-MS) to conduct target analysis. However, to get a better overview of the amount of “total” amount of PFAS, sum parameter methods like total oxidizable precursor assay (TOPA), absorbable organic fluorine (AOF), and extractable organic fluorine (EOF) are in development. Additionally, for research purposes, several spectroscopical methods like X-ray photoelectron spectroscopy (XPS), fluorine K-edge X-ray absorption near-edge structure (XANES) spectroscopy, particular induced gamma-ray emission (PIGE) spectroscopy as well as19 F nuclear magnetic resonance (NMR), infrared, and Raman spectroscopy are available. Therefore, an overview is given on currently available analytical techniques for PFAS in environmental samples and their application possibilities discussed for different kinds of PFAS subgroups. KW - Per- and polyfluoroalkyl substances (PFAS) KW - Analytics KW - Liquid chromatography - mass spectrometry (GC-MS) KW - Sum parameter PY - 2025 DO - https://doi.org/10.1515/9783110796797-005 SP - 143 EP - 168 PB - De Gruyter AN - OPUS4-62662 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Kozachynskyi, Volodymyr A1 - Staubach, Dario T1 - Monte Carlo analysis of esterification reaction model with disappearing second liquid phase N2 - This research item is associated with the publication: Parameter estimation in dynamic multiphase liquid-liquid equilibrium systems (submitted after 2025-02-15) The software used to generate and analyze the experimental data is stored with the research data. KW - Parameter Estimation KW - NRTL KW - LLE KW - Phase Detection PY - 2025 DO - https://doi.org/10.14279/depositonce-21232 PB - Technische Universität Berlin CY - Berlin AN - OPUS4-62670 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schwarz, Silke T1 - Roughness of selected friction plates and its influence on friction sensitivity measurements of explosives N2 - Roughness of selected friction plates from different sources and their influence on the measurement of the friction sensitivity of explosives were investigated. This test plays a decisive role for the work of notified bodies in the context of conformity assessment of explosives and pyrotechnics as well as transport classification, and differences were observed that should be taken into account in the work. T2 - 34th Meeting of the forum of the notified bodies for explosives CY - Online meeting DA - 06.03.2025 KW - Friction test KW - Porcelain plates KW - Explosives PY - 2025 AN - OPUS4-62677 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Zöllner, Moritz T1 - Raman spectroscopy as a thermometric tool for the analysis of mortar binders N2 - The reconstruction of the thermal history of anthropogenic materials is crucial for understanding historical manufacturing techniques. Preparatory parameters such as firing temperature, heating and cooling rates, soaking time, and kiln atmosphere significantly affect the chemical and structural properties of the final product. Comparing historical materials with replicas produced under well-defined laboratory conditions helps identify indicators for these parameters. This comparative approach is greatly enhanced by spectroscopic analyses. Raman spectroscopy has proven to be a powerful tool in this field due to its high sensitivity to crystal-chemical alterations and high spatial resolution. The results of thermal experiments with gypsum and carbonate raw materials at burning temperatures up to 1000 °C are presented. Precise measurements of Raman peak positions and Raman band widths enable the differentiation of chemically similar phases. Changes in the Raman band parameters are evident even after the subsequent hydration-hardening process of the fired samples, allowing the spectral discrimination of samples treated at different temperatures steps. These findings from the thermal experiments are further applied to Raman micro-spectroscopic mappings of medieval and reenacted mortars. The extracted Raman band parameters show comparable values between the experimental and real-life samples, proving Raman spectroscopy as a suitable tool for estimating the burning temperature and thus elucidating the manufacturing procedures of anthropogenic materials. T2 - Jahrestagung Archäometrie und Denkmalpflege 2025 CY - Dresden, Germany DA - 18.03.2025 KW - Raman spectroscopy KW - Mineral thermometry PY - 2025 AN - OPUS4-62778 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer, Klas T1 - NMR Spectroscopy as a PAT tool: Field integration of a laboratory instrument N2 - Companies of chemical industry find themselves more often in a rapidly changing environment, e.g., due to variability of raw material quality or energy costs and efficiency. Process optimization and new process concepts become more and more important. Flexible and modular chemical plants can produce various high-quality products using multi-purpose equipment with short downtimes between campaigns and reduce time to market for new products. Intensified continuous production plants allow for difficult to produce compounds like exothermic reactions with high heat dissipation. Highly automated chemical process monitoring along with real-time quality control are prerequisites to such concepts and, thus, should be based on chemical information. A commercially available benchtop NMR spectrometer was integrated to the full requirements of an automated chemical production environment such as explosion safety, field communication, and robust evaluation of sensor data. Field studies in modular and conventional production plant setups show promising results gaining process knowledge for further optimization. NMR spectroscopy appeared as preeminent online analytical method and allows using a modular data analysis approach, which can even serve as reliable reference method for further calibration-dependent PAT applications (e.g., NIR or Raman spectroscopy). Based on experiences from earlier field studies an improved field enclosure setup was developed and built, including the option of a secondary analytical method (e.g., optical spectroscopy). Integrated control systems allow for a flexible implementation based on the available automation infrastructure at the chemical plant or pilot plant setup. In the future, modular interconnecting “smart” PAT systems and process equipment have the potential speed up the setup of production equipment for chemicals and pharmaceuticals and therefore help to reduce the time-to-market. T2 - ANAKON 2025 CY - Leipzig, Germany DA - 10.03.2025 KW - NMR Spectroscopy KW - Process Analytical Technology KW - Field Integration KW - Benchtop-NMR PY - 2025 AN - OPUS4-62744 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Lohrer, Christian T1 - Jahresbericht der Konformitätsbewertungsstelle Explosivstoffe / Pyrotechnik N2 - Der Bericht gibt einen Überblick über die Aufgaben des Fachbereichs im Zusammenhang mit der Konformitätsbewertung ziviler Explosivstoffe und pyrotechnischer Gegenstände. Diese umfassen maßgeblich die Prüfung und Bewertung dieser Produkte, Gremientätigkeiten (Normung, Group of Experts und Forum der benannten Stellen), Beratung von Behörden und Organisationen mit Sicherheitsaufgaben und Ministerien und Entwicklung modernen Prüfverfahren. Weiterhin werden die Einnahmen und Anzahl der Anträge aus den letzten Jahren vorgestellt. T2 - 27. Sitzung des Beirat der BZS CY - Berlin, Germany DA - 20.03.2025 KW - Konformitätsbewertung KW - CE KW - Pyrotechnik KW - Explosivstoffe KW - UKCA PY - 2025 AN - OPUS4-62750 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Völker, Tobias T1 - Laser-Induced Breakdown Spectroscopy for Concrete Analysis: Applications and Practical Benefits N2 - Reinforced concrete structures are exposed not only to mechanical loads but also to chemical degradation, which can significantly impact their longevity and performance. Effective assessment and maintenance require a detailed understanding of the ingress of harmful species, such as chlorides or sulfates. Traditional analysis methods, like wet chemical analysis of drill dust or ground core samples, often require homogenization leading to the loss of crucial spatial information in sub-millimeter regions such as localized high concentrations of elements, e.g. in cracks. Laser-induced breakdown spectroscopy (LIBS) offers a cutting-edge solution, providing rapid, multi-element analysis with high spatial resolution from micrometer to millimeter scales. LIBS is capable of detecting both light and heavy elements, making it a powerful tool for detailed concrete analysis. Despite its clear advantages, LIBS is not commonly used in civil engineering. This presentation will showcase practical examples demonstrating the effectiveness and advantages of LIBS in concrete analysis, highlighting real-world applications provided by members of the “LIBS” subcommittee of the technical committee “Civil-Engineering” of the German Society for Non-Destructive Testing (DGZfP). Key examples will be discussed, including measurements from car parks or bridges, alongside an introduction to the newly released DGZfP leaflet B14 providing guidelines for the quantitative determination of chlorine content in concrete by LIBS. Furthermore, prospective applications of LIBS including material identification and classification for concrete recycling, and other emerging uses in civil engineering, will also be presented, showcasing the versatility and future potential of this technology. T2 - Conference on durability of building materials and systems in the transportation infrastructure CY - Mendrisio, Switzerland DA - 22.03.2025 KW - LIBS KW - Spectroscopy KW - Concrete KW - Structural Diagnostics PY - 2025 AN - OPUS4-62822 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hauschildt, Charlotte T1 - New Approaches to PFAS Quali- and Quantification using GC-MS N2 - Known as “forever chemicals”, per- and polyfluoroalkyl substances (PFAS) are a class of synthetically produced chemicals that includes an estimated 10.000 compounds. Due to the persistence, toxicity and ubiquitous occurrence, research has focused on the qualification and quantification of the most important compounds as well as on the investigation of toxicity and possible routes of entry over the last 10 years. Liquid chromatography - mass spectrometry (LC-MS) is the analytical standard to test for PFAS, as the spectrum of detectable compounds is significantly more comprehensive than it is currently the case with gas chromatography - mass spectrometry (GC-MS). However, to be able to test for PFAS contamination in a more process-independent manner and to make the analysis more widely accessible, methods based on GC-MS are currently being developed. Since GC-MS methods only cover a fraction of the compounds belonging to the PFAS group so far, further development of the corresponding measurement methods is inevitable [1, 2]. The here described work is part of the EU project 23IND13 ScreenFood [3]. The aim is to develop sensitive analytical GC-MS methods that contribute to an improved identification and quantification of various PFAS (both currently regulated and emerging PFAS) in selected food and food packaging matrices. Of particular interest as a food contact material are native and recycled polymers such as PET. Besides, various techniques, including solvent-free variants such as thermal desorption GC-MS, will be tested for a quick and easy analysis. Multiple derivatization approaches, which cover different PFAS subgroups, will also be tested and evaluated. This poster will present the overall project objectives and first results. Acknowledgment: The project (23IND13, ScreenFood) has received funding from the European Partnership on Metrology, co-financed from the European Union’s Horizon Europe Research and Innovation Programme and by the Participating States. T2 - PFAS - Vermeidbar, Ersetzbar, Unverzichtbar?! (FU Berlin) CY - Berlin, Germany DA - 07.04.2025 KW - Per- and Polyfluoroalkyl Substances (PFAS) KW - Gas Chromatography - Mass Spectrometry (GC-MS) KW - EU Project KW - Derivatization Methods KW - Food Contact Material (FCM) PY - 2025 AN - OPUS4-62970 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zöllner, Moritz T. A1 - Dariz, Petra A1 - Riedel, Jens A1 - Schmid, Thomas T1 - Dolomite and Mg Calcite as Mineral Thermometers in Mortar Binders. A High Resolution Raman Spectroscopic Study N2 - This paper suggests the use of high‐resolution Raman scattering bands of MgCa carbonates as posteriori thermometer minerals in archaeometric studies. Therefore, the thermal behavior of two dolomite samples and the hydration and carbonation reaction in air of the decomposition products were investigated by Raman microspectroscopy. The increase in the calcination temperature resulted in the formation of – Raman silent MgO and – inert Mg calcite at 700°C–750°C. In contrast, the decarbonation, hydration, and recarbonation of sample material exposed to 750°C–900°C in a muffle furnace led to the appearance of Mg‐free calcite. High spectral resolution Raman spectroscopy enabled a spectral distinction between these two groups due to differences in the band parameters (peak position, bandwidth) of the vibrational (v1, v4, L) modes of calcite. In combination with Raman microspectroscopic mapping, this spectral information represents a new approach for the estimation of burning temperatures of medieval high‐fired gypsum mortars via natural dolomite impurities. Thus, the results of this work highlight the importance and potential of Raman microspectroscopy as a thermometric tool for elucidating the thermal history of anthropogenic fired materials, with potential applications for archaeometry and art technology, as well as for quality controls in the frame of the production of mineral mortar binders and ceramics or bricks, respectively. KW - Mineral thermometry KW - Raman spectroscopy KW - Dolomite KW - High-fired gypsum mortar PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-630270 DO - https://doi.org/10.1002/jrs.6810 SN - 1097-4555 SP - 1 EP - 13 PB - Wiley AN - OPUS4-63027 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schragen, Christian A1 - Lohrer, Christian T1 - A brief journey through the world of standardization of fireworks of the last decade and into the future N2 - This paper aims at giving an overview about this entire standardization process, explaining the main differences of the EN versions from 2015 and 2022, outlining the practical implications for the stakeholders applying these ENs and giving a cautious look into the future requirements for fireworks in Europe. T2 - 19th International Symposium on Fireworks CY - Liling, P.R. China DA - 21.04.2025 KW - Fireworks KW - Standardization PY - 2025 SP - 1 EP - 17 AN - OPUS4-63077 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schragen, Christian A1 - Lohrer, Christian T1 - A brief journey through the world of standardization of fireworks of the last decade and into the future N2 - This presentation aims at giving an overview about this entire standardization process, explaining the main differences of the EN versions from 2015 and 2022, outlining the practical implications for the stakeholders applying these ENs and giving a cautious look into the future requirements for fireworks in Europe. T2 - 19th International Symposium on Fireworks CY - Liling, China DA - 21.04.2025 KW - Fireworks KW - Standardization PY - 2025 AN - OPUS4-63076 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - Quantification of Perfluorocarboxylic Acids in Water Samples via Static Headspace Gas Chromatography Coupled to Mass Spectrometry N2 - Perfluorocarboxylic acids (PFCAs) are one of the most prominent and studied subgroups of per- and polyfluoroalkyl substances (PFASs), which have attracted great interest in environmental and toxicology research due to their intensive use in combination with their persistence, mobility and potential threat to ecosystems and human health. The standard method to quantify PFCAs in water samples is liquid chromatography or, for additional quantification of ultrashort-chain PFCAs (carbon chain length of two or three carbon atoms) too, hydrophilic interaction liquid chromatography, in each case coupled with mass spectrometry. However, there are a lot of laboratories using MS coupled to headspace gas chromatography systems (HS-GC-MS), usually to quantify a wide range of volatile organic compounds. While PFCAs themselves are difficult to measure with HS-GC-MS in water samples, this challenge can be solved by derivatizing the acids to more volatile compounds, like esters. This approach could enable laboratories using HS-GC-MS to analyse and monitor PFCAs in environmental water samples. By following this idea, we successfully developed a HS-GC-MS method to quantify PFCAs in ultrapure water. Trifluoric acid (TFA), perfluoropropionic acid (PFPrA), perfluorobutanoic acid (PFBA) and perfluorooctanoic acid (PFOS) served as exemplary analytes of PFCAs, which were derivatized with methanol and concentrated sulfuric acid to form methyl esters. The method was optimized by varying different preparation and measurement parameters, leading to limits of detection and quantification in the two-digit ppt-range for all four analytes. The method was than tested on various real water samples, including tap and bottled water, groundwater, landfill leachate, treated wastewater and impinger water from a sewage sludge incineration experiment. Furthermore, snow samples from a ski slope were analysed too. TFA was the most frequently detected PFAA, with concentrations in the ppt and low ppb range. The detection and quantification of the remaining three PFCAs vary with the sample types and sampling location.Our results show that HS-GC-MS is suitable, and enables laboratories with this technique, to quantify PFCAs water samples. T2 - SETAC Europe CY - Vienna, Austria DA - 11.05.2025 KW - Per- and polyfluoroalkyl substances (PFAS) KW - Groundwater KW - GC-MS PY - 2025 AN - OPUS4-63094 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - Detection, quantification, and treatment of per- and polyfluoroalkyl substances (PFAS) in groundwater (DFEAT-PFAS) N2 - Per- and polyfluoroalkyl substances (PFAS) are a large group of chemicals used in the formulations of thousands of consumer goods. Because of the recent regulations and restrictions on the use of long chain (≥C8) PFAS a significant shift in the industry towards short (C4-C7) and ultrashort (C1-C3) chain alternatives has been recognized the last years. Due to the high polarity and water solubility of ultrashort PFAS, the potential for bioaccumulation is low. However, the high persistence of ultrashort-chain PFAS will result in environmental accumulation, especially in aquatic environments, leading to potential risks for aquatic organisms and increased human external exposure through drinking water. Ultrashort PFAS like trifluoroacetic acid (TFA) are low to moderately toxic to a range of organisms. In the project we are focusing on detecting and removing PFAS, especially ultrashort-chain PFAS from contaminated groundwater. Therefore, we suggest developing and optimizing short- and ultrashort-chain PFAS detection, quantification, and removal. We will design passive sampling devices, which can collect and monitor the temporal profile of PFAS species in groundwater. This will allow us to analyze PFAS contaminations in German and Israeli groundwater using state-of-the-art novel analytical techniques. In addition, contaminated groundwater will be treated via a two-stage process, designed to concentrate the relatively low PFAS concentrations by novel membrane processes including closed-circuit reverse osmosis (CCRO) and mixed matrix composite nanofiltration membranes (MMCM). Afterwards the rejected streams, containing higher concentrations of PFAS will be treated by coagulation and the remaining PFAS adsorbed onto carbonaceous nanomaterials (CNMs). T2 - SETAC Europe CY - Vienna, Austria DA - 11.05.2025 KW - Per- and polyfluoroalkyl substances (PFAS) KW - Groundwater KW - Remediation PY - 2025 AN - OPUS4-63095 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Grunewald, Thomas T1 - Explosionsschutz - Grundlagen und Maßnahmen zum nichtelektrischen Explosionsschutz N2 - Bei Geräten und Maschinen zur bestimmungsgemäßen Verwendung in explosionsgefährdeten Bereichen gemäß 2014/34/EU muss in der europäischen Union eine Zündgefahrenbewertung durchgeführt werden. Dabei müssen unter anderem die Gefahren von nichtelektrischen Zündquellen betrachtet werden, zu denen auch die mechanischen Schlagvorgänge gehören. Dies erfordert umfangreiche Kenntnisse über die insgesamt 13 relevanten Zündquellen u.a. gemäß DIN EN ISO 80079-36 und EN 1127-1. Bei nichtelektrischen Zündquellen bzw. mechanischen Schlag- und Schleifvorgängen kommt es infolge des Zusammenstoßes zweier Werkstücke bzw. Bauteile zu einer Umwandlung der kinetischen Energie. Dabei erhöht sich die Temperatur der Werkstoffe an der Kontaktstelle und es kommt unter Umständen zu einem Abtrennvorgang kleiner Partikel erhöhter Temperatur. Sowohl die heißen Kontaktstellen (Zündquelle "heiße Oberflächen") als auch die abgetrennten Partikel (Zündquelle "mechanisch erzeugte Funken") können eine wirksame Zündquelle für ein explosionsfähiges Gasgemisch darstellen. Zur Festlegung von Grenzwerten wurden in der Norm DIN EN ISO 80079-36:2016 die Gasgemische anhand ihrer Explosionsgruppe klassifiziert und zu jeder Gruppe die maximale Energie des Schlagvorgangs festgelegt, unter derer die Entstehung einer wirksamen Zündquelle als unwahrscheinlich angenommen werden kann. Aufgrund neuerer Erkenntnisse der BAM zum Verhalten von Schlagvorgängen in Wasserstoff/Luft-Gemischen bei bestimmten Werkstoffpaarungen sind Änderungen der relevanten internationalen Regelwerke des nichtelektrischen Explosionsschutzes bereits erfolgt bzw. werden für weitere Regelwerke angestrebt. Weitere Festlegungen von Grenzwerten für die kinetische Schlagenergie und geeignete Werkstoffpaarungen finden sich u.a. in der DIN EN 1755 (ex-geschützte Flurförderzeuge) und in der DIN EN 14986 (ex-geschützte Ventilatoren) T2 - Ausbildung zum Explosionsschutzbeauftragten (Veranst.-Nr. VA25-00303-050-E) CY - Essen, Germany DA - 13.05.2025 KW - Schlagfunken KW - Schleiffunken KW - Reibfunken KW - Mechanisch erzeugte Funken KW - Nichtelektrischer Explosionsschutz PY - 2025 AN - OPUS4-63101 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Capitain, C. A1 - Schüßler, M. A1 - Bugsel, B. A1 - Zweigle, J. A1 - Vogel, Christian A1 - Leube, Peter A1 - Zwiener, C. T1 - Implementation of matrix-matched semiquantification of PFAS in AFFF-contaminated soil N2 - This study presents a novel semiquantification approach for nontarget screening (NTS), combining matrix-matched calibration and ionization class-specific average calibration curves (ACCs) to address the lack of analytical reference standards for most per- and polyfluoroalkyl substances (PFAS). Ionization class-specific ACCs for carboxylic and sulfonic acids, sulfonamides, and cationic PFAS result in high accuracy, with median absolute accuracy quotients below 2.27×. The approach was applied to soil impacted by aqueous film-forming foam (AFFF) contamination. A total of 96 tentatively identified PFAS were semiquantified in addition to 28 quantified compounds based on available standards. Semiquantified concentrations exceeded those of target analytes, demonstrating the critical role of this method in capturing broader PFAS contamination. In this case, validation against extractable organofluorine (EOF) showed a 102% closed mass balance. The innovative approach not only enables comprehensive PFAS contamination assessment in complex matrices but also expands the scope of the NTS for environmental monitoring, remediation, and risk assessment of AFFF-contaminated sites. KW - Per- and polyfluoroalkyl substances (PFAS) KW - Contaminated soil KW - Non-targeted analysis KW - Combustion ion chromatography PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-629445 DO - https://doi.org/10.1021/acs.est.4c14255 SN - 1520-5851 VL - 59 IS - 14 SP - 7338 EP - 7347 PB - American Chemical Society (ACS) CY - Columbus, Ohio AN - OPUS4-62944 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Grunert, Wiebke T1 - Green primary explosives – a step towards more sustainable mining N2 - This project aims at breaking down barriers that hinder the wide application of green primary explosives. In a joint effort of several organisational units at BAM we connect chemistry, process engineering and plant and process safety to investigate how green primary explosives can be produced in an economical and safe process. T2 - 46. Informationstagung Sprengtechnik CY - Siegen, Germany DA - 25.04.2025 KW - Green explosives KW - Lead-free KW - Detonators KW - Process technics PY - 2025 AN - OPUS4-62996 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Michael-Schulz, Heike T1 - Classification of Hydrogen peroxide emulsions (HPE) N2 - Hydrogen peroxide emulsion (HPE) explosives are a type of emulsion explosive that uses hydrogen peroxide as the oxidizing agent, offering advantages over traditional ammonium nitrate-based explosives. HPEs are gaining popularity as a more environmentally friendly and safer alternative. Nevertheless investigations show a low thermal stability which is discussed in the context of classification. This presentation contains confidential data and can therefore not be published in full lenght here. T2 - IGUS EOS meeting 2025 CY - Verneuil-en-Halatte, France DA - 02.04.2025 KW - Green explosives KW - Hydrogen peroxide emulsion KW - Thermal stability KW - Classification KW - Environmental friendly PY - 2025 AN - OPUS4-63207 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Willms, Thomas A1 - Kryk, Holger A1 - Hampel, Uwe T1 - An improved method for the analysis of the reaction products of the partial isobutane oxidation by gas chromatography using a green solvent N2 - In the present work, an improved GC/MS method for the analysis of the reaction products of the non-catalytic partial oxidation of isobutane at a starting temperature of 25°C has been developed and compared to a previously published method. Two green GC-solvents (dimethyl carbonate (DMC), diethyl carbonate (DEC)) and several internal standards (hexane, benzene, toluene, DEC) have been tested. The separation of the products at low retention times (methanol, isobutane, isobutene) could be significantly improved. For the liquid main products t-butyl hydroperoxide (TBHP), di-t-butyl peroxide (DTBP), t-butanol (TBA), propanone and most trace products (isopropanol, isobutanal, methyl formate, isopropyl formate, t-butyl formate and some acetates – 24 compounds in total), a coefficient of determination CoD > 0.999 has been achieved. For all weighing and GC/MS measurements uncertainties have been calculated. The peaks of the peak pair t-butyl formate (CoD >0.999) and isobutanol (CoD >0.99), have been simulated and used for calibrations. DEC gave a decomposition of TBHP on the column. With DMC, a problem of peak purity of TBHP appeared but could be resolved. The use of the green solvent DMC, compared to also studied traditional solvents like heptane and toluene, proved to be very beneficial, since it also permitted to determine polar compounds, e. g. carbon dioxide and formic acid. KW - GC/MS KW - Green solvent KW - Method development KW - Peroxide KW - Measurement uncertainties KW - Oxidation products KW - Simulation PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-632026 DO - https://doi.org/10.1016/j.chroma.2025.465892 SN - 0021-9673 VL - 1753 SP - 1 EP - 16 PB - Elsevier CY - Amsterdam AN - OPUS4-63202 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gödde, Markus T1 - Screening Procedures for Self-Reactive Substances, Differential Scanning Calorimetry-Onset and Heat-Flux Criteria (paper) N2 - We present a new screening procedure for the determination of the thermal stability of potential candidates for the class of self-reactive substances. For the classification of self-reactive substances, elaborate testing is necessary to determine the applicable type, according to the regulations. Annex 6 of the UN Manual of Tests and Criteria permits that the classification procedure for self-reactive substances may be omitted, if the estimated self accelerating decomposition temperature (SADT) is greater than 75 °C for a 50 kg package using an appropriate calorimetric technique, but no technique is described. Based on stationary theories of thermal explosion, we developed a screening approach using differential scanning calorimetry (DSC) onset and heat-flux criteria, respectively, at relevant temperatures. The proposed approach is validated with experimental data. T2 - IGUS EOS meeting 2025 CY - Verneuil-en-Halatte, France DA - 02.04.2025 KW - Classification KW - Differential scanning calorimetry KW - Self-reactive substances KW - Self accelerating decomposition temperature KW - Screening-procedures PY - 2025 AN - OPUS4-63204 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Malow, Marcus T1 - CEQAT-DGHS Interlaboratory test programme for chemical safety - status and activities - New RR UN Test N.5 with verification apparatus - N2 - The UN Test N.5 "Test method for substances which in contact with water with flammable gases", according to the Chapter 33.5.4 of the UN Manual of Tests and Criteria is one of the tests performed at BAM and was already investigated in detail. As a conclusion from these investigations a new verification method for the verification of this gas flow measuring test apparatus for the method UN Test N.5 was developed at BAM and is presented in this presentation as well as general aspects in the development of verification procedures will be explained. The planned interlaboratory test to validate the new verification method is discussed in this presentation. T2 - IGUS EOS meeting 2025 CY - Verneuil-en-Halatte, France DA - 02.04.2025 KW - CEQAT-DGHS KW - Gas flow rate KW - Verification of test apparatuses KW - Interlaboratory tests KW - UN Test N.5 PY - 2025 AN - OPUS4-63205 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Michael-Schulz, Heike T1 - Classification of thermites N2 - In this presentation the classification of thermites is discussed. Even though these products are used in industry, e.g. for rail welding since the 19th century, new discussions arose questioning wether these kind of products should be classified in the class of explosives. The presentation reviews the screening procedures for explosives as well as test series 2 for explosives testing. Based on this evaluation it is questioned that the class of explosives adequaltey describes the hazards of these substances. T2 - IGUS EOS meeting 2025 CY - Verneuil-en-Halatte, France DA - 02.04.2025 KW - Thermites KW - Thermite reaction KW - Classification KW - Transport regulations KW - Screnning procedures for explosives testing PY - 2025 AN - OPUS4-63206 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Malow, Marcus T1 - Update on the revision of test method for oxidizing solids N2 - The results of the round robin test on the solid oxidiser test have already been presented at IGUS EOS. In this presentation, we will show how the findings from the round robin test can be transferred into the regulations as easily as possible. This proposal serves as a basis for a proposal that can be discussed in the ECOSOC Sub-Committee of Experts on TDG (30 June - 04 July 2025). T2 - IGUS_EOS meeting 2025 CY - Verneuil-en-Halatte, France DA - 20.04.2025 KW - Classification KW - Test method KW - Oxidizer KW - Solids PY - 2025 AN - OPUS4-63203 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Chazeau, E. A1 - Pipier, A. A1 - Wegner, Karl David A1 - Ghiringhelli, F. A1 - Sancey, L. A1 - Paul, C. A1 - Goze, C. T1 - NIR-II aza-BODIPY Platform for the Development of a Fluorescent Antibody Drug Conjugate N2 - Real-time imaging of antibody-drug conjugates (ADCs) offers valuable insights for assessing tumor targeting specificity, monitoring therapeutic efficacy, and detecting off-target accumulation that may cause adverse effects. To enable precise tracking, we developed a versatile fluorescent platform based on an NIR-II emitting aza-BODIPY dye, which can be site-specifically grafted onto an IgG1 antibody to generate well-defined fluorescent ADCs. As a proof of concept, we synthesized an HER2-targeting trastuzumab immunoconjugate bearing a NIR-II aza-BODIPY fluorophore. The cytotoxic monomethyl auristatin E (MMAE) payload was introduced in the final step, resulting in a trackable and homogeneous ADC suitable for both in vitro and in vivo investigations. The resulting Trastu-azaNIRII-MMAE selectively accumulated in HER2-positive subcutaneous tumors, significantly reducing the tumor growth. Using NIR-II optical imaging, a single injection of the NIR-II-ADC allowed for the detection of the conjugate over a period of more than one month, highlighting its potential for long-term tracking and therapeutic applications. KW - NIR-II KW - Fluorescence KW - Quality assurance KW - Antibody drug conjugate KW - In vivo imaging PY - 2025 DO - https://doi.org/10.1021/acs.jmedchem.4c02777 VL - 68 IS - 7 SP - 7232 EP - 7242 PB - ACS Publications AN - OPUS4-63025 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Burkert, Andreas T1 - Qualitätsüberwachung durch das KorroPad®-Verfahren N2 - Am Beispiel des KorroPad®-Verfahrens wird ein Ergebnis des H2Mare Teilprojektes "TransferWind" vorgestellt. Im Rahmen des Vorhabens konnte für das Verfahren die DIN 50024:2025-07 erstellt und verabschiedet werden. Das Prüfverfahren ermöglicht es, die Barrierefunktion der Passivschicht auf nichtrostenden Stählen einfach und schnell, direkt durch die Verarbeiter zu prüfen und somit die werkstoffgerechte Verarbeitung sicherzustellen. Das Verfahren liefert ein optisches Prüfergebnis, ist zerstörungsfrei und ermöglicht eine direkte Intervention durch den Verarbeiter bei einer unvollständigen Ausbildung der Passivschicht. Damit kann es helfen spätere Korrosionserscheinungen an Bauteilen und Komponenten aus nichtrostenden Stählen zu vermeiden. Erforderliche Nacharbeiten wären insbesondere bei Offshore -Prozessanlagen mit erheblichen Kosten verbunden. T2 - Verbundtreffen PtX-Wind / Transferwind CY - Bremerhaven, Germany DA - 09.07.2025 KW - Nichtrostender Stahl KW - Passivität KW - KorroPad KW - Normung PY - 2025 AN - OPUS4-63745 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gerbeit, Marco A1 - Seeber, Henrik A1 - Grasse, Dennis A1 - Donner, Marcel A1 - Grobert, Steffen A1 - Krentel, Daniel T1 - Test set-up for reproducible shock wave generation N2 - A test setup was developed at the BAM test site to generate and record reproducible, adjustable shock waves resulting from gas detonations. The setup is used to study the impact of blasts on humans and structures with short setup times. To further develop this innovative test bench and improve reproducibility, the ignition source and gas composition is analysed in more detail. The experimental setup consists of a cylindrical pressure vessel (autoclave) that is operated with acetylene and oxygen at ambient pressure. The elevated pressure resulting from the combustion process is released through an orifice by the instantaneous rupture of a diaphragm. The shock propagates symmetrically into the free field, where it interacts with the models and sensors to be analysed. With this design, shock waves with a typical ideal Friedlander waveform characteristic, except for a reflection and a muzzle blast-like behavior that deviates from the ideal characteristics, can be generated. This setup enables an average peak overpressure of 88 kPa. By using exploding wires as an ignition source in comparison to a fusehead, the reproducibility was significantly increased during the test to σ=2.8 kPa from σ=9.5 kPa previously. The presented data confirms the quality and reliability of this setup in generating realistic, reproducible shocks. KW - Overpressure KW - Shock wave KW - Blast KW - Ignition source KW - Autoclave PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-637859 DO - https://doi.org/10.1016/j.jlp.2025.105736 SN - 0950-4230 VL - 98 SP - 1 EP - 6 PB - Elsevier Ltd. AN - OPUS4-63785 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schiaroli, Alice A1 - Mata, Christian A1 - Scarponi, Giordano Emrys A1 - Habib, Abdel Karim A1 - Kluge, Martin A1 - Ustolin, Federico A1 - Cozzani, Valerio T1 - Digital image processing for the advanced characterization and simulation of experimental fire tests N2 - The fire engulfment of storage tanks of hazardous materials is among the most critical scenarios in hazard assessment of industrial value chains. Laboratory and full-scale experimental trials are used to test the tank performance and integrity in such scenarios. However, strong uncertainties usually affect the actual fire load experienced by the tank, in particular when large-scale experiments are carried out in open test fields. Such uncertainties arise from several factors difficult to control during experimental tests, such as the atmospheric conditions as there is the influence of wind drifts influencing the actual fire engulfment, the flame temperature and the flame dynamic distribution around the target. Consequently, verifying the concordance of an experimental test with standard test criteria and defining accurate boundary conditions in correlated model simulations is challenging. In this study, the development of a novel method for the analysis of fire conditions based on image processing is presented. The approach allows identifying the flame coverage on the target surface during the test and provides an accurate map of the flame distribution on the equipment over time. The approach is tested using experimental data from a full-scale fire test campaign carried out on liquid hydrogen cryogenic tanks. The results prove to be accurate in replicating the experimental temperatures measured on the outer tank shell during the test. The proposed methodology can be used to better understand the results of experimental fire tests and to characterize realistic fire scenarios, also supporting the definition of fire test requirements. Moreover, the approach produces results that can be implemented as advanced space-time-varying boundary conditions in simulation models, improving their accuracy in reproducing real cases. KW - Fire test KW - Digital image processing KW - Flame coverage KW - Storage tank KW - Boundary conditions KW - Fire engulfment PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-636956 DO - https://doi.org/10.1016/j.psep.2025.107571 SN - 0957-5820 VL - 201 IS - B SP - 1 EP - 15 PB - Elsevier Ltd. AN - OPUS4-63695 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Abad Andrade, Carlos Enrique T1 - Data-Driven Spectrochemical Methods for Elemental and Isotopic Analysis N2 - High-resolution optical spectrometers generate spectra containing tens of thousands of data points per sample. Picometre-scale isotope shifts, matrix-induced line broadening, and strong inter-feature correlations render classical peak fitting unreliable. Current analytical challenges, therefore, require rigorous algorithms able to expose latent structure, quantify uncertainty, and remain chemically interpretable. The research program presented in this lecture integrates state-of-the-art spectrochemical instrumentation with mathematically disciplined data models. Principal Component Analysis and Partial Least Squares provide chemically meaningful latent variables, while gradient-boosted decision trees or deep neural networks (ANNDL) capture residual non-linearity without sacrificing traceability. All models are trained on isotope-enriched or synthetically generated spectra and distributed with full validation workflows. T2 - Chemisches Institutskolloquium, Humboldt-Universität zu Berlin CY - Berlin, Germany DA - 21.05.2025 KW - Spectrochemistry KW - Isotopes KW - Machine learning KW - Battery KW - Data fusion PY - 2025 AN - OPUS4-63488 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wilke, Olaf A1 - Poelke, Birte A1 - Klein, Luise A1 - Rohloff, Alexander A1 - Hoffmann, Holger T1 - Initial VOC Emissions from Consumer Products Determined in Micro-Scale Test Chambers: Results of a Round Robin Test N2 - Emissions of volatile organic compounds (VOCs) from consumer products may have a negative impact on indoor air quality, potentially also affecting human wellbeing. Since consumers may be exposed to these VOCs immediately after e.g. unwrapping of newly purchased products, reliable analytical methods are needed to determine air concentration profiles in the early phase of VOC emissions. Concerning typical sample sizes of consumer products, micro-scale test chambers (μ-chambers) were considered suitable for this purpose. In addition, compared to medium- or large-scale test chambers, μ-chambers require lower initial investment and operational costs, and offer options for emissions screenings where higher sample throughput is essential. For these reasons, a μ-chamber-based method to determine initial concentrations of VOCs emitting within the first hours of simulated product use was developed. The chamber air was frequently sampled on desorption tubes loaded with Tenax® TA, followed by quantification of emitted VOCs via thermal desorption gas chromatography mass spectrometry (TD-GC-MS). The method was assessed in a round robin test involving eight participating laboratories from 2 countries. Pieces of a rain poncho (sample area A: 2.01·10-4 m2) emitting cyclohexanone, phenol, 2-ethylhexanol, naphthalene and isophorone in significant concentrations were distributed as sample material. Each laboratory conducted triplicate emission tests over a period of 48 h in μ-chambers with volumes of 44 or 114 mL. The loading factors L of 4.57 m2·m-3 (44 mL) or 1.76 m2·m-3 (114 mL) and air flow rates of 24 mL·min-1 resulted in area-specific air flow rates q of 7.17 m3·m-2·h-1 in both chamber types. The temperature was set to 23°C and, if possible, relative humidity was set to approx. 50%. The chamber air was sampled after 0.5, 1, 2, 4, 24 and 48 hours. In addition, to assess the analytical performance, each participating laboratory received two analyte-spiked Tenax® TA-loaded desorption tubes for quality control (QC). Very low relative standard deviations (11–17%) were obtained for the QC test. The results of the emissions tests in the early phase (0.5–4 h) were also adequate, with acceptable z scores (|z|≤2.00) received by six to seven participating laboratories. All eight laboratories obtained acceptable z scores after the longer sampling periods (24 and 48 h). Hence, the inter-laboratory comparability of the results obtained with the developed μ-chamber method was successfully confirmed. T2 - Healthy Buildings Europe 2025 CY - Reykjavik, Iceland DA - 08.06.2025 KW - VOC Emissions KW - Consumer Product KW - Test Chamber KW - Round Robin Test PY - 2025 AN - OPUS4-63706 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Abad Andrade, Carlos Enrique T1 - Lithium isotope fractionation as a diagnostic tool for aging lithium-ion batteries N2 - Lithium-ion batteries (LIBs) are central to modern energy storage technologies, powering applications from portable electronics to electric vehicles and grid storage systems. Their popularity comes from their high energy density, efficiency, and extended cycle life. However, over time, various aging mechanisms lead to capacity loss, increased internal resistance, and, ultimately, battery failure. Understanding and predicting these aging processes is crucial for enhancing the reliability and longevity of LIBs. This necessity makes the development of advanced diagnostic tools essential. This study uses plasma-based spectrometry techniques to explore lithium isotope fractionation (LIF) as a predictive tool for monitoring LIB aging and degradation. Mass spectrometric techniques —including MC-ICP-MS, LA-ICP-MS, and MICAP-MS— were employed to analyze lithium isotopic composition in both new and aged lithium cobalt oxide (LCO) cells, including lab-made coin cells and commercial batteries. An isotopic fractionation was identified during electrochemical cycling: 6Li migrates towards the anode, while 7Li accumulates in the cathode. These isotopic patterns correlate with structural degradation, including solid electrolyte interphase (SEI) growth and crack formation, as confirmed by FIB-SEM, XANES, and EXAFS analyses. This correlation demonstrates that LIF aligns with key aging mechanisms in model coin cells and commercial batteries, such as capacity fade and impedance growth. LIF provides a powerful diagnostic tool for battery health monitoring and aging prediction by linking isotopic fractionation to structural degradation. This approach offers significant potential to extend battery lifespan and improve the reliability of energy storage systems. T2 - ANAKON 2025 CY - Leipzig, Germany DA - 10.03.2025 KW - Isotope KW - Lithium KW - Battery aging KW - Degradation KW - Fractionation KW - Battery PY - 2025 AN - OPUS4-63487 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bruno, Francesco A1 - Fiorucci, Letizia A1 - Vignoli, Alessia A1 - Meyer, Klas A1 - Maiwald, Michael A1 - Ravera, Enrico T1 - pyIHM: Indirect Hard Modeling, in Python N2 - NMR is a powerful analytical technique that combines an exquisite qualitative power, related to the unicity of the spectra of each molecule in a mixture, with an intrinsic quantitativeness, related to the fact that the integral of each peak only depends on the number of nuclei (i.e., the amount of substance times the number of equivalent nuclei in the signal), regardless of the molecule. Signal integration is the most common approach in quantitative NMR but has several drawbacks (vide infra). An alternative is to use hard modeling of the peaks. In this paper, we present pyIHM, a Python package for the quantification of the components of NMR spectra through indirect hard modeling, and we discuss some numerical details of the implementation that make this approach robust and reliable. KW - Algorithms KW - Chemical Structure KW - Deconvolution KW - Mixtures KW - NMR spectroscopy PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-626793 DO - https://doi.org/10.1021/acs.analchem.4c06484 SN - 1520-6882 VL - 97 IS - 8 SP - 4598 EP - 4605 PB - ACS Publications CY - Washington D.C. AN - OPUS4-62679 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Blotevogel, J. T1 - Thermal PFAS Destruction in a Full-Scale Hazardous Waste Incinerator N2 - Incineration is currently the only commercial full-scale technology available to destroy per- and polyfluoroalkyl substances (PFAS) in large solid and liquid waste streams. Given previous experience of dioxin formation during halogenated waste incineration, concerns about the emission of products of incomplete destruction (PIDs) from PFAS incineration exist. The overarching objective of this project is to track the fate of fluorine during full-scale hazardous waste incineration in order to demonstrate the readiness, viability, and level of safety for thermal PFAS destruction in various waste streams. The specific objectives of this project are (1) to enhance our understanding of key variables and conditions on PFAS incineration performance, (2) to identify major PIDs under insufficient treatment conditions, (3) to explore the catalytic role of fly ash and other process-relevant surfaces in thermal PFAS decomposition, and (4) to determine the potential formation of polyfluorinated dibenzodioxins and dibenzofurans. T2 - 2025 SERDP & ESTCP PFAS Project Meeting CY - Long Beach, CA, USA DA - 04.08.2025 KW - PFAS KW - Hazardous waste incineration PY - 2025 AN - OPUS4-64189 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Avci, Fatma T1 - Characterization of black mass by X-Ray fluorescence spectroscopy N2 - X-ray fluorescence analysis (XRF) is a method of elemental analysis that is used either as wavelength dispersive XRF (WDXRF) or energy dispersive XRF (EDXRF). Using EDXRF, it is possible to analyze samples within a few minutes without time-consuming sample preparation. This makes the method potentially suitable for analyzing larger sample quantities under industrial conditions. However, the XRF method is matrix-dependent. Depending on the cathode material of the recycled batteries, there are significant differences in the composition of the resulting black mass. This means that specific calibration models must be developed for different types of black mass. The aim of our work is to use the EDXRF method to reliably analyze black mass of different origins with regard to the elements that are particularly interesting for recycling: nickel (Ni), manganese (Mn), cobalt (Co), aluminum (Al), iron (Fe), zinc (Zn), silicon (Si), copper (Cu), and phosphorus (P). Based on the different mass fractions of the elements mentioned, black masses from used lithium-ion batteries can be divided into three groups according to the cathode chemistry: lithium nickel manganese cobalt oxide (NMC), lithium cobalt oxide (LCO), and mixed chemistries (MC), the latter of which may contain lithium iron phosphate (LFP). The division into groups is necessary to determine the matrices and thus select the appropriate calibration model for the analysis of the EDXRF data in order to achieve the most accurate determination of the elemental content possible. Reference analyses are performed using WDXRF. The score plots obtained by PLS-DA of the specific elemental composition of the black masses examined to date by both WDXRF and EDXRF reveal a correct separation of the BM matrix types LCO, NMC, and MC. Our preliminary results with test samples yielded 100 % correct predictions with both data sets. However, only two matrix types, NMC and LCO, have been tested with the EDXRF data so far. Data for MC is pending as work progresses. T2 - Doctoral seminar 2025 - Working Group Chemometrics and Quality Assurance (GDCh) CY - Hamburg, Germany DA - 11.09.2025 KW - Black Mass KW - XRF Spectroscopy KW - Chemometric Modeling KW - PLS-DA PY - 2025 AN - OPUS4-64095 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - Current status of monitoring of PFAS release from industrial facilities N2 - Increasing studies report per- and polyfluoroalkyl substances (PFAS) in the ambient air and emissions from diverse industrial sources. Therefore, a comprehensive framework for characterizing PFAS emissions by identifying source-specific chemical fingerprints, evaluating emission pathways and assessing the impact of remediation technologies is needed. Depending on the type of PFAS, dedicated sampling and analytical procedures are required. Here, also the detection of possible PFAS transformation products, so-called products of incomplete combustion (PICs) are more mobile or toxic, is also of great interest to evaluate these technologies in terms of mineralisation potential and fluorine mass balance. T2 - PFAS study and technical exchange tour of MEE-FECO in Germany CY - Online meeting DA - 12.09.2025 KW - Per- and polyfluoroalkyl substances (PFAS) KW - Incineration PY - 2025 AN - OPUS4-64081 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Eiben, Mario T1 - Die Aufgaben der BAM im Gefahrgutbereich - ein Überblick N2 - Die BAM ist eine der zuständigen Behörden im Gefahrgutbereich in Deutschland und nach der Gefahrgutverordnung Straße, Eisenbahn und Binnenschifffahrt (GGVSEB) und der Gefahrgutverordnung See (GGVSee) für diverse Aufgaben zuständig, wie z. B. große Teile der Klassifizierung gefährlicher Güter, die Verwendung, Prüfung, und Zulassung von Gefahrgutverpackungen oder auch die Verwendung, den Bau und die Prüfung von Gefahrguttanks. Sie berät die Bundesregierung bei der Ausrichtung der Gefahrgutpolitik durch Mitarbeit im Ständigen Ausschuss Gefahrgutbeförderung (AGGB) des Gefahrgut-Verkehrs-Beirates beim BMV und wirkt nach dem Erlass über die BAM im Einvernehmen mit dem BMWK in nationalen und internationalen Regel setzenden Gremien und Normungsgremien mit. Damit leistet sie einen wertvollen Beitrag zur Sicherheit im Gefahrgutbereich. T2 - 35. Münchner Gefahrgut-Tage CY - Munich, Germany DA - 25.05.2025 KW - Gefahrgut KW - Zuständige Behörde KW - GGVSEB KW - GGVSee KW - AGGB KW - Normung PY - 2025 AN - OPUS4-64051 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Paul, Andrea T1 - Classification of mineral wool by spectroscopic methods N2 - Mineral wools from demolition projects are currently disposed of in landfills. To reintroduce them into the material cycle, it is essential (i) to distinguish between glass wool (GW) and rock wool (RW), (ii) to detect foreign substances, and (iii) to assess the period of production (before/after 2000) to identify “old”, potentially carcinogenic wool. Both X-ray and NIR spectroscopic methods are being developed for this purpose and handheld (portable) devices are being tested for field application. To this end, more than 160 mineral wool samples were collected and examined. Since no reference information on the “material” or “age” was available for many samples, we characterized the elemental composition of the mineral wool using wavelength dispersive X-ray fluorescence spectroscopy (WDXRF). For this purpose, pellets and melt tablets were evaluated using a spectrometer-integrated semi-quantitative approach (Omnian). The resulting mass fractions of SiO2, Al2O3, CaO, MgO, K2O, Na2O, Fe2O3, and TiO2 could be used to distinguish between GW and RW and, in the case of RW, also whether it was “old” or “new” wool according to VDI guideline 3492. In some cases, however, ambiguous results were obtained in the material classification. Therefore, a principal component analysis (PCA) was performed enabling the identification of possible outliers and subgroups. Since the classification of “old” and “new” rock wool based on VDI 3492 yielded many unclear results, with the help of partial least squares discriminant analysis (PLS-DA), the classification was significantly improved [1]. WDXRF spectroscopy delivers accurate results, however, the spectrometers are not mobile and require time demanding sample preparation (pellets, melt tablets). Therefore, it was examined whether useful results could be achieved with portable energy dispersive (EDXRF) spectrometers. For this purpose, a portable EDXRF spectrometer (pXRF) was calibrated based on the WDXRF results. In general, oxides of the lighter elements (MgO and Na2O) could not be analyzed with EDXRF. Although prediction of oxide contents in melt tablets was successful by this approach, no reliable results could be obtained when predicting the oxide content of natural mineral wools. Attempts to perform calibration based on natural wools also failed. However, PCA of EDXRF spectra in the “Light” range was able to distinguish between GW and RW, even with “real-world” samples from so-called Bigbags [2], in which mineral wool in Germany is collected in recycling centers. In addition to XRF, a previous study has already demonstrated that at least the distinction between GW and RW can be performed using near-infrared spectroscopy (NIR) [3]. For this reason, measurements were also carried out with a handheld NIR device (pNIR) in parallel with the pXRF investigations. Using PLS-DA, it was possible to classify RW and GW using the handheld device with a sensitivity and specificity of 95% for 38 test samples, including wool from big bags. pNIR also remains sensitive when it comes to determining non-metallic “foreign materials.” For example, materials such as brick, plaster, concrete, and organic fibers could be detected by SIMCA as “non-mineral” wool with a specificity of 92% for 19 tested interferents [2]. Questions regarding the detection of metallic impurities based on EDXRF measurements are the subject of ongoing investigations. T2 - Doctoral Seminar of the Working Group Chemometrics & Quality Assurance CY - Hamburg, Germany DA - 10.09.2025 KW - Mineral wool KW - X-ray fluorescence KW - Data analyis PY - 2025 AN - OPUS4-64077 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bernardy, Christopher A1 - Habib, Abdel Karim A1 - Kluge, Martin A1 - Schalau, Bernd A1 - Kant, Hanjo A1 - Schulze, Marcel A1 - Orchini, Alessandro T1 - Large-scale investigations of the thermal radiation of hydrogen jet flames N2 - For industrial applications dealing with hydrogen, the definition of safety distances and the assessment of possible hazards emanating from releases is mandatory. Since hydrogen is usually stored and transported under pressure, one scenario to be considered is the momentum driven release of hydrogen from a leakage with subsequent ignition. In this scenario, the emitted heat radiation from the resulting jet flame to the surroundings has to be determined to define adequate safety distances. For hydrocarbon flames, different jet flame models are available to assess the hazards resulting from an ignited jet release. Since hydrogen flames differ from hydrocarbon flames in their combustion behavior, it has to be checked if these models are also applicable for hydrogen. To evaluate the accuracy of these models for hydrogen jet flames, tests with a horizontal outlet at large-scale are carried out at the BAM Test Site for Technical Safety (BAM-TTS). Herein, the flame geometry and the heat radiation at defined locations in the surroundings are recorded for varying release parameters such as release pressure (currently up to max. 250 bar), mass flow (up to max. 0.175 kg/s) at an outlet diameter of 30 mm (with an upstream nozzle of 7.7 mm). The challenge here is the characterization of the flame geometry in an open environment and its impact on the thermal radiation. Existing heat radiation data from the literature are mostly based on unsteady outflow conditions. For a better comparability with the steady state jet flame models, the experiments presented here are focused on ensuring a constant mass flow over the release duration (currently 120 s) to obtain a stationary jet flame. In addition, stationary outflow tests with hydrocarbons (methane) were also carried out, which are intended to serve as reference tests for checking flame models based on hydrocarbon data. The comparison of the flame geometry shows that hydrogen jet flames with the same outlet mass flow have a greater flame length (average deviation of 15 %) but a smaller flame diameter than methane jet flames (average deviation of 17 %). Conclusions regarding thermal radiation show that the proportion of total combustion energy emitted as thermal radiation is lower for hydrogen (x_rad= 0.04–0.09) than for methane (x_rad = 0.06–0.1). A comparison of the surface emissive power (SEP) of the jet flame shows a SEP range of 7 kW/m2-15 kW/m2 for hydrogen and 3 kW/m2 - 9,5 kW/m2 for methane. KW - Hydrogen KW - Release KW - Thermal radiation KW - Jet flame KW - Radiant heat fraction PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-622891 DO - https://doi.org/10.1016/j.jlp.2024.105491 SN - 1873-3352 VL - 94 SP - 1 EP - 6 PB - Elsevier B.V. AN - OPUS4-62289 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -