TY - JOUR A1 - Fabry, Çağtay A1 - Pittner, Andreas A1 - Kaplan, Alexander A1 - Rethmeier, Michael T1 - Digitalisation and Carbon Footprint Evaluation of Gas Metal Arc Welding and Wire-Arc Directed Energy Deposition N2 - This paper showcases how a holistic approach to digitalisation enables data-driven welding applications, exemplarily for a gas metal arc welding (GMAW) laboratory. The workflow integrates advanced process monitoring, synchronised multi-sensor data acquisition and tools for data analytics. A welding domain-specific data exchange format weldx is presented that unifies and aggregates the data sets acquired during process monitoring with final component quality metrics, supporting reuse, traceability, and reproducibility. Two case studies illustrate the approach. First, GMAW parameters are adaptively adjusted according to local seam geometry to compensate joint-preparation deviations from nominal values typical for large-scale steel fabrication. Second, the seamless data aggregation along the welding production chain enables an automatic life-cycle assessment (LCA), quantifying the environmental impacts of additive manufacturing with DED Arc/M and attributing the dominant contributors to the carbon footprint. Collectively, the results indicate that a fully integrated experimental set-up together with standardised data structures and scalable analytics can couple monitoring, control, and sustainability, thereby realising the potential of digitalisation for high-quality and environmentally informed welding production. KW - Digitalisation KW - Arc welding KW - DED-arc KW - Life Cycle Assessment PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-656812 DO - https://doi.org/10.1088/1757-899X/1342/1/012067 SN - 1757-8981 VL - 1342 IS - 1 SP - 1 EP - 15 PB - IOP Publishing AN - OPUS4-65681 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Geburtig, Anja T1 - Messung der effektiven UV-Bestrahlung bei der Bewitterung von Polymeren N2 - Bei der Bestrahlung und Bewitterung von polymeren Werkstoffen wird die Degradation durch eine Absorption von Strahlung initiiert und meistens durch weitere Klimagrößen, wie z.B. Wärme, Feuchte und atmosphärische Gase beeinflusst. Die Messung einer effektiven Bestrahlungsstärke und ihre zeitliche Integration sind deshalb von großer Bedeutung. Photochemische Prozesse werden beim Sehen oder allgemeiner bei Farbstoffen schon durch sichtbare (VIS) Strahlung, dagegen bei der Erythembildung der Haut und der Photodegradation von Polymeren erst durch die energiereicheren Photonen der ultravioletten (UV) Strahlung initiiert. Die spektrale Empfindlichkeit des Auges und die Erythembildung sind im VIS- bzw. UV-Bereich sehr stark wellenlängenabhängig, was durch die Angabe der mit der spektralen Hellempfindlichkeit V() des Auges bewerteten VIS-Strahlung in Lux (lx) bzw. die mit der Erythem-Wirkfunktion bewertete UV Strahlung als dimensionsloser UV-Index berücksichtigt wird. Spektrale Empfindlichkeiten. Die Photodegradation von Polymeren ist im UV-Bereich ebenfalls stark wellenlängenab-hängig, was bisher nicht berücksichtigt wurde. Seit Mitte der 70er Jahre, als die lx- bzw lxh- Messung bei der Strahlungsbeanspruchung langsam durch die Ermittlung der radiometrischen UV-Bestrahlungsstärke bzw. der UV-Bestrahlung im gesamten UV-Bereich abgelöst wurde, gab es hier bei der Bewitterungsprüfung keine weiteren Fortschritte auf dem Gebiet der Charakterisierung der Strahlungsbeanspruchung im UV-Bereich. Seit Jahren liegen zahlreiche Ergebnisse über die spektrale Empfindlichkeit von Photo-degradationsprozessen vor, die zeigen, dass die spektrale Empfindlichkeit im Bereich der Globalstrahlung bei ca. 300 nm, am größten ist und im langwelligen UV-Bereich bei ca. 400 nm gegen Null geht. Die Messungen der radiometrischen Größen UV-Gesamt-bestrahlungsstärke und UV-Gesamtbestrahlung erfasst deshalb über weite Wellen-längenbereiche Strahlungsanteile, die für die Photodegradation bedeutungslos sind und mittelt über potenziell bedeutsame Änderungen im kurzwelligen UV-Bereich hinweg. Es wird das Konzept eines neuen UV-Radiometers vorgestellt, dessen spektrale Empfindlichkeit einer mittleren spektralen Empfindlichkeit der Photodegradation von Polymeren entspricht. Die effektive UV-Bestrahlungsstärke und UV-Bestrahlung kann dadurch wesentlich genauer erfasst werden. T2 - 48. Jahrestagung der GUS 2019 CY - Stutensee, Germany DA - 27.03.2019 KW - UV-Bestrahlungsstärke PY - 2019 AN - OPUS4-49712 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Geburtig, Anja T1 - Evaluation of Outdoor Exposures by means of Exposure Response Functions N2 - Outdoor exposure tests are a common tool to evaluate the weathering resistance of a polymeric material or component. However, they have only a limited validity, mainly due to the limited reproducibility of the weather as well as of the bad adaptability to other exposure sites. Typically, an outdoor exposure is characterized by the measured radiant exposure; sometimes averaged temperature data are added. These can be – separately – related to long-term annual means, to get an idea on the severity of the exposure. However, as for polymeric ageing, irradiance and temperature act simultaneously, such severity of an outdoor exposure could be better described by a computed property change of a similar material, which is calculated from the hourly irradiance and temperature values on the base of established exposure response functions. In this way, various outdoor exposures are evaluated. For several exposure sites, annual deviations of the ageing amount are related to annual mean values, to evaluate the weathering reproducibility at the exposure site. Additionally, correlations to relevant weather parameters are illuminated. Also some specific exposure conditions, such as tilt angle, are tested. Compared to the use of weathering reference materials, this procedure unfavourably depends on the availability of a suited control as well as on the quality of the established exposure response function. In contrast, it enables a later exposure evaluation, on the base of documented weather data, if for instance no reference material was exposed. T2 - 8th European Weathering Symposium CY - Vienna, Austria DA - 20.09.2017 KW - Photodegradation KW - Weathering KW - Service life prediction PY - 2017 AN - OPUS4-42576 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wachtendorf, Volker A1 - Barthel, Anne-Kathrin A1 - Geburtig, Anja A1 - Trubiroha, P. ED - Reichert, T. T1 - Low-Temperature Irradiation Experiments for PE, PA, and PC Matrices N2 - In this paper, we demonstrate the effects of radiation exposures of polymeric materials with UV-A 340 nm lamps (ISO 4892-3, Type 1A) at -10 °C in comparison to an irradiation at +50 °C using a Global UV Test 200 fluorescent lamp device from Weiss Umwelttechnik GmbH, which incorporates an active cooling appliance. While the effects at -10 °C actually are lower than at + 50°C their extent was clearly beyond expectations. T2 - 8th European Weathering Symposium CY - Vienna, Austria DA - 20.09.2017 KW - Artificial weathering KW - Irradiation KW - Low-temperature KW - Photo-oxidation KW - Polyamide KW - Polycarbonate KW - Polyethylene PY - 2017 SN - 978-3-9818507-1-0 VL - 18 SP - Paper 22, 319 EP - 329 PB - Thomas Würtz Grafik Design CY - Karlsruhe AN - OPUS4-42130 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kalbe, Ute A1 - Krüger, Oliver A1 - Bandow, Nicole A1 - Geburtig, Anja ED - Reichert, Thomas T1 - Laboratory Weathering Test for Simulating the Leaching from Artificial Sporting Grounds N2 - In order to estimating the amount and kind of emissions from polymeric sporting tracks a laboratory test was developed in BAM that combines artificial weathering and subsequent batch and column tests [1, 2, 3]. The goal consisted in nvestigating a possible change of emissions into soil and groundwater of a new sporting ground as a function of ageing and egradation of the system. At various stages of the weathering, the samples were removed and subjected to especially designed column extraction tests for the solid samples. Both these extracts and the accumulated rainwater run-off of the weathering device were subjected to analytical tests of their ingredients. The overall aim of the test consisted in developing ontrollable, reproducible, and standardisable conditions and methods of investigation that would allow an estimation of the emissions in the course of outdoor application of about five years. T2 - 7th European Weathering Symposium. Natural and Artificial Ageing of Polymers CY - Naples, Italy DA - 16.09.2015 KW - artificial weathering KW - emission KW - leaching KW - sporting track KW - degradation KW - ageing KW - rubber KW - extraction PY - 2015 SN - 978-3-9816286-6-1 VL - CEES 17 SP - 195 EP - 208 PB - Thomas Würtz CY - Karlsruhe, Germany AN - OPUS4-35401 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Geburtig, Anja T1 - Testing of HDPE containers for dangerous goods after outdoor exposure N2 - Focus areas of BAM as well as testing results of HDPE containers for dangerous goods after outdoor exposure of were presented. T2 - 70th CEEES Meeting CY - Hørsholm, Danmark DA - 13.11.2018 KW - HDPE KW - Dangerous goods KW - Chemical resistance PY - 2018 AN - OPUS4-47032 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Geburtig, Anja A1 - Wachtendorf, Volker A1 - Trubiroha, P. T1 - Quantitative Auswertemöglichkeiten bei der spektralen Bestrahlung – Berechnung des Wirkungsspektrums N2 - Für die Bewertung des Wellenlängeneinflusses auf die Alterungsvorgänge bei der Bestrahlung UV- oder lichtempfindlicher Materialien kann die Methode der spektralen Bestrahlung angewendet werden. Im Prinzip wird dabei das linear dispergierte Spektrum einer Strahlenquelle mit kontinuierlichem Spektrum (z.B. Xe-Lampe) auf eine Probenoberfläche abgebildet, so dass Ort einer Materialänderung und Wellenlänge der Bestrahlung einander zugeordnet werden können. Nachfolgende lokal-auflösende Analysemethoden ermitteln eine Eigenschaftsänderung an einem spezifischen Ort der Probe, aus dem sich dann die Bestrahlungswellenlänge ergibt. Der verwendete Aufbau wird beschrieben. Es wird an einem ausgewählten Beispiel gezeigt, wie durch geeignete Anbindung eines Messsystems zur Bestimmung der spektralen Bestrahlungsstärke und ortsaufgelöste Messungen der Eigenschaftsänderungen eine quantitative Auswertung realisiert werden kann. Der Einfluss nichtlinearer Alterungsverläufe wird diskutiert. Grenzen der Methode werden aufgezeigt und Erweiterungsmöglichkeiten dargestellt. T2 - 46. Jahrestagung der GUS CY - Stutensee-Blankenloch, Germany DA - 22.03.2017 KW - Bewitterung KW - Spektrale Bestrahlung KW - Kunststoffe PY - 2017 SN - 978-3-9816286-9-2 SP - 91 EP - 99 AN - OPUS4-39595 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Oliveira Menezes, Letícia Gonçalves A1 - Trajano Silveira, Beatriz Aiub A1 - de Castro Raucci, Larissa Moreira Spinola A1 - Martorano, Antônio Secco A1 - de Oliveira, Paulo Tambasco A1 - Arai, Marylyn Setsuko A1 - de Camargo, Andréa Simone Stucchi A1 - Hannig, Christian A1 - Sterzenbach, Torsten A1 - Brighenti, Fernanda Lourenção A1 - de Oliveira, Analú Barros A1 - Moraes, João Carlos Silos A1 - Danelon, Marcelle T1 - Functional glass ionomer cement modified with phosphate and zinc oxide nanoparticles: in vitro insights into physicomechanical behavior, cytotoxicity and antimicrobial activity N2 - Objectives: To evaluate the effect of incorporating zinc oxide nanoparticles (ZnONPs) and sodium trimetaphosphate microparticles (TMP) into resin-modified glass ionomer cement (RMGIC) on its physicomechanical, microbiological, and cytotoxic properties. Methods: Six groups were prepared: 1) RMGIC (Fuji II LC); 2) RMGIC-1.0 %ZnONPs; 3) RMGIC-2.0 %ZnONPs; 4) RMGIC-14.0 %TMP; 5) RMGIC-1.0 %ZnONPs-14.0 %TMP; and 6) RMGIC-2.0 %ZnONPs-14.0 %TMP. Tensile/diametral compressive strengths (TS, DCS), surface hardness (SH) and degree of monomer conversion (%DC) were evaluated in 24 h and 7 days. Fluoride (F) release was assessed over 15 days using alternating demineralizing/remineralizing solutions. Antimicrobial/antibiofilm activity against S. mutans (UA159) was assessed through adhesion, biofilm growth measurements, and XTT assays. Cytotoxicity was tested on MDPC23 odontoblasts using the resazurin assay. Results: The DCS for the RMGIC-2.0 %ZnONPs group was 22.5 % higher when compared to RMGIC after 24 h (p <0.05); after 7 days, RMGIC-2.0 %ZnONPS-14.0 %TMP group was 23.4 % higher than RMGIC (p < 0.05). For TS after 7 days, the RMGIC-2.0 %ZnONPs-14.0 % TMP group showed the highest values (37 % and 55.4 %) than RMGIC and RMGIC-14.0 % TMP, respectively (p < 0.05). At 24 h, the RMGIC-2.0 %ZnONPs-14.0 %TMP Group showed the highest SH among all groups (p < 0.05). The greatest effect on reducing bacterial viability was observed for the RMGIC-2.0 %ZnONPs-14.0 %TMP group (p < 0.05). For cytotoxicity analysis, at 24 h, the RMGIC-1.0 %ZnONPs-14.0 %TMP group showed the highest cytocompatibility (p < 0.05). At 48 and 72 h, RMGIC-1.0 %ZnONPs, RMGIC-2.0 %ZnONPs, RMGIC-1.0 %ZnONPs-14.0 %TMP and RMGIC-2.0 %ZnONPs-14.0 %TMP groups showed the lowest cytotoxicity (p < 0.05) KW - Phosphate and zinc oxide nanoparticles KW - Glass ionomer PY - 2026 DO - https://doi.org/10.1016/j.jdent.2025.106307 SN - 0300-5712 VL - 165 SP - 1 EP - 10 PB - Elsevier Ltd. AN - OPUS4-65692 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ghadamyari, Marzieh A1 - Ebrahim Hosseini, Hossein A1 - Michálková, Monika A1 - de Camargo, Andréa Simone Stucchi A1 - Cao, Jiangkun A1 - Galusek, Dušan A1 - Chukova, Oksana A1 - Wondraczek, Lothar A1 - Jacobsohn, Luiz Gustavo A1 - Klement, Róbert T1 - Broadband visible emission in undoped K2ZnGeO4 by near UV and X-ray excitation N2 - Self-activated phosphors (SAP) have attracted significant attention for a wide range of applications, including lighting, displays, scintillators, lasers, luminescence-based sensors, bioimaging, drug delivery, and luminescent security inks. In this work, we report a new white emitting SAP, α-K2ZnGeO4, synthesized by high-temperature solid-state reaction. The phosphor crystallizes in a single-phase orthorhombic structure and consists of irregularly shaped particles. Under ultraviolet (UV) and X-ray excitation the sample exhibits broad yellowish-white emission spanning the 350–800 nm spectral range, with a long-wavelength tail extending into the near-infrared region, overlapping the biological window. Average lifetime values of 20.4 and 22.6 μs were determined from the fluorescence decay curves monitored at the centre of the band (550 nm), upon excitation at 272 and 377 nm, respectively. Additionally, the decay curve of a distinct spectral feature, peaked at 385 nm, was studied upon 272 nm excitation, yielding a lifetime of 2.3 μs. The role of structural defects (donors: VO and Zni; acceptors: VZn, VGe, and Oi) in the luminescence of α-K2ZnGeO4 was also investigated. Photoluminescence spectra recorded under 366 nm and 377 nm excitation yielded CIE 1931 chromaticity coordinates of (x, y) = (0.40213, 0.46943) and (0.39326, 0.47611), respectively. The values are almost identical and correspond to yellowish-white emission, highlighting the suitability of the material as a yellowish-white phosphor in white light-emitting diodes (wLEDs). KW - Broadband emitter KW - K2ZnGeO4 KW - X-ray excitation PY - 2026 DO - https://doi.org/10.1016/j.ceramint.2026.01.063 SN - 0272-8842 VL - 52 IS - 7 SP - 8658 EP - 8669 PB - Elsevier Ltd. AN - OPUS4-65691 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rex, Tobias A1 - Vilela, Raquel R. C. A1 - Bauer, Nadine A1 - Hepp, Alexander A1 - de Camargo, Andrea S. S. A1 - Kiefer, Friedemann A1 - Strassert, Cristian A. T1 - Host–Guest Nanoparticles Incorporating a Fluorophore-Conjugated Pt(II) Complex: A Ratiometric Dual Emitter Performing as a Self-Referenced Oxygen Reporter N2 - Ratiometric optical sensors, which provide real-time measurements by comparing the intensities of two spectrally separated emission bands, are highly effective for monitoring oxygen levels. By combining oxygen-independent and oxygensensitive emission characteristics, they offer accurate quantification, distinguishing them from other sensor types. In this work, we designed a ratiometric optical sensor concept based on a biscyclometalated platinum(II) complex coupled with an organic naphthalonitrile-based fluorophore and incorporated it into mesoporous silica nanoparticles. This encapsulation strategy significantly improved the stability and water-dispersibility of the otherwise hydrophobic coordination compound while preventing aggregation and enhancing its photophysical properties. Both the free molecule and its nanoparticle-encapsulated form were characterized, revealing high sensitivity to oxygen variations with the unique feature of self-referenced ratiometric readout. The sensor’s response was effectively measured at the single-particle level using photoluminescence microscopy, providing temporally and spatially resolved oxygen readouts. The versatility of the system was demonstrated across different experimental setups, including suspensions, solids, and agarose-embedded forms, highlighting is adaptability to a wide range of applications. This system holds significant promise for advanced oxygen monitoring, offering a reliable tool for high-resolution detection in complex environments with multiple orthogonal readouts. KW - Oxygen sensing KW - Ratiometric luminescence KW - Platinum (II) complex KW - Dual emitter probe KW - Mesoporous silica nanoprticles PY - 2026 DO - https://doi.org/10.1021/acsaom.5c00262 SN - 2771-9855 VL - 4 IS - 2 SP - 332 EP - 342 PB - American Chemical Society (ACS) AN - OPUS4-65689 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Saeed, A. M. A1 - Saied, M. A. A1 - Szymoniak, Paulina A1 - Altmann, Korinna A1 - Schönhals, Andreas A1 - Fahmy, Alaa T1 - High performance novel polyelectrolyte membrane consisting of polyvinyl alcohol-phenylsilanol-polypyrrole N2 - The synthesis of composite membranes based on PVA, PPy, and sulfonated–hydrolyzed TMPS was investigated for application in proton–exchange membrane fuel cells. FT–IR confirmed the hydrolysis of TMPS through the appearance of Si–OH vibrations, disappearance of Si–O–CH3 bands, reduced CH3 stretching intensity (2840 cm− 1), and successful sulfonation of the phenyl ring (1030 cm− 1). XPS verified the introduction of sulfonic acid groups by identifying S2p peaks between 166–170 eV. Scanning electron microscopy (SEM) showed an incorporation of PPy and that the membrane morphology altered by silanol leading to an increased surface roughness and inducing phase separation in comparison to pure PVA. The PVA–PPy–Si membrane which did not undergo phase separation demonstrated improved mechanical stability (maximum stress 5.91 MPa), reduced methanol uptake (22%, lower than Nafion’s 30%), and enhanced thermal resistance compared to PVA–PPy and PVA–Si. It also exhibited a high ion–exchange capacity (1.5mmol g− 1, exceeding Nafion® at 0.9mmol g− 1 ) and a proton conductivity of 0.036 S/cm, twice that of Nafion 117. These combined properties identify the PVA–PPy–Si composite as a promising high–performance polyelectrolyte membrane for fuel cell applications. KW - Polyelectrolyte membrane PY - 2026 DO - https://doi.org/10.1016/j.apsusc.2026.166495 SN - 1873-5584 VL - 731 SP - 1 EP - 11 PB - Elsevier B.V. AN - OPUS4-65627 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Suarez Ocano, Patricia T1 - Influence of heat-treatment-induced microstructural evolution on the Low Cycle Fatigue behavior of 316L stainless steel fabricated by Laser Powder Bed Fusion N2 - Additive manufacturing, particularly the laser powder bed fusion (PBF-LB/M) process, has gained significant attention in recent years due to its ability to produce complex geometries with enhanced mechanical properties. Among the various materials used, 316L stainless steel is highly favored for cyclically loaded components due to its exceptional mechanical strength, high-temperature performance, and corrosion resistance, making it widely applicable across various industries. 316L SS fabricated by PBF-LB/M (PBF-LB/M/316L) exhibits a unique hierarchical microstructure, with high density of low-angle grain boundaries (LAGBs), nano-dispersed silicates, chemical micro-segregations, and solidification-induced cellular structures. Particularly, the submicron-sized cellular features enriched with chromium (Cr) and molybdenum (Mo), along with high dislocation densities, contribute to a superior strength-ductility balance compared to conventionally manufactured 316L SS. The dispersed silicate particles act also as a strengthening phase, impeding dislocation movement and enhancing plastic deformation resistance. This study explores the effect of heat treatments on the low-cycle fatigue (LCF) behavior of PBF-LB/M/316L at room temperature (RT) and 600 °C. First, three heat treatment conditions were applied to the as-built material: 450 °C for 4 hours (HT450/4), 800 °C for 3 hours (HT800/3), and 900 °C for 1 hour (HT900/1) to investigate their influence on microstructural evolution. Microstructural analysis revealed that the HT450/4 condition preserved the cellular structure with high dislocation density, while the HT800/3 condition showed partial dissolution of cells together with reduction in segregated elements along the cell walls and a reduced dislocation density. The HT900/1 condition resulted in complete segregation and cellular structure dissolution with comparable dislocation density to HT800/3 while maintaining the crystallographic texture and grain morphology. Intermetallic χ phase was mostly observed at the grain boundaries in HT800/3, but not in HT900/1. Fully reversed LCF tests were conducted under strain-controlled conditions with a strain amplitude of 0.8 %. Tests were interrupted at specific intervals to analyze the interaction between hierarchical microstructural features and deformation mechanisms in the three heat-treated conditions. Due to the pronounced dislocation cell structures and elemental segregation, the microstructure of the HT450/4 condition significantly impact deformation and damage mechanisms during cyclic loading, which in turn, differ from the conventional produced counterparts. The results provide insights into the relationship between microstructural features and fatigue performance, highlighting key deformation and failure mechanisms under cyclic loading. T2 - FEMS 2025 EUROMAT 18th European Congress and Exhibition on Advanced Materials and Processes CY - Granada, Spain DA - 14.09.2025 KW - Additive manufacturing KW - 316L stainless steel KW - Heat treatments KW - Low Cycle Fatigue KW - Microstructure PY - 2025 AN - OPUS4-64238 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Agudo Jácome, Leonardo T1 - Low-Cycle Fatigue Behavior of Laser Powder Bed Fused Inconel 718 at Room and High Temperature N2 - The nickel-base superalloy Inconel 718 (IN718) is one of the most commonly used Ni-based superalloys for high temperature structural applications for its remarkable strength, as well as creep, fatigue, and corrosion resistance up to 650 °C. While IN718 has traditionally been employed as cast or wrought material, it is difficult to machine because of its high strength and toughness. The additive manufacturing of IN718 components made by metal AM has thus gained extensive attention to produce expensive near-net shaped components of high-temperature alloys such as IN718, for it saves material and costs in processing and machining steps. Among all metal additive manufacturing (AM) technologies, laser powder bed fusion (PBF-LB/M) is the most widespread, IN718 being one of the most common alloys produced with it. However, high cooling rates associated to the PBF-LB/M process, hinders the primary strengthening phases γ’’ and γ’ to form, as these cooling rates induce a dislocation cellular substructure, at which walls primary Laves phases bind segregating Nb, Ti and Mo. Many of the therefore needed heat-treatment strategies can then promote Laves-phase transformation into the stable δ phase along the cell and grain boundaries. Laves and δ phases, as well as grain-boundary primary carbides may have adverse effects on mechanical properties. The mostly needle-shaped δ phase was namely found to have a detrimental effect on creep rupture life while no direct effect on LCF fatigue life was evident. In this work room- and high-temperature (650 °C) low-cycle fatigue behavior of PBF-LB/M IN718 is investigated in the four-step heat-treated state and compared to wrought IN718. The microstructure of both materials is characterized across length scales via microscopy methods. The fatigue life at room temperature of the PBF-LB/M IN718 material is slightly lower than that for the wrought material, which is reversed at 650 °C. The cyclic stress response for both materials is marked by cyclic softening that is more pronounced at higher test temperatures. Multiple secondary cracks form at high strain amplitudes, at both room and high temperatures. High testing temperatures enhance specially crack formation at the transitions of regions between elongated grains and columns of stacked grains with ripple patterns in the PBF-LB/M material. Additional to this behavior, pronounced crack branching and deflection indicate that the cracks are controlled by sharp micromechanical gradients. T2 - EUROMAT 2025 CY - Granada, Spain DA - 14.09.2025 KW - Additive manufacturing KW - Low-cycle fatigue KW - Microstructural characterization KW - Ni-base superalloy PY - 2025 AN - OPUS4-64354 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Witte, Julien A1 - Treutler, Kai A1 - Schroepfer, Dirk A1 - Kannengiesser, Thomas A1 - Wesling, Volker T1 - Influence of microstructure on the machinability and surface integrity of additively manufactured iron aluminides N2 - The increasing global focus on energy and resource efficiency has stimulated a growing interest in additive manufacturing. AM offers economic advantages and enables an efficient use of materials. However, AM components often require subsequent mechanical post-processing, such as machining (e.g., milling), to achieve the final contours or surfaces. This is a particular challenge due to the heterogeneous and anisotropic nature of AM structures, which affect machining and the resulting component properties. High-performance materials such as iron aluminide represent a promising alternative to conventional high-temperature materials with a significant economic advantage. However, the strength and hardness properties, which are advantageous for applications in highly stressed lightweight components, pose a challenge for economical machining in addition to the AM microstructure properties. The difficult-to-cut material causes accelerated tool wear and insufficient surface quality. This study shows that crack-free additive manufacturing of the three-component system of iron-nickel-aluminum is possible, and advantages in terms of machinability compared to FeAl-AM components are achieved. The more homogeneous microstructure leads to a reduction in cutting forces, with positive effects on the machinability and optimized surface integrity. Ultrasonic assisted milling (USAM) offers great potential to address the major challenges posed by difficult-to-cut materials and additively manufactured weld structures. Therefore, this study focuses on assessing the transferability of previous positive results by USAM to the selected iron aluminide alloys. The machinability of the aluminides is analyzed by varying significant influencing variables in finish milling experiments and evaluated in terms of the loads on the tool and the resulting surface integrity. KW - Iron aluminide KW - Additive manufacturing KW - Machinability KW - Surface integrity KW - Ultrasonic-assisted milling process PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-656993 DO - https://doi.org/10.1007/s40194-026-02382-6 SN - 0043-2288 SP - 1 EP - 13 PB - Springer Science and Business Media LLC AN - OPUS4-65699 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wachsmuth, Janne A1 - Malikoutsakis, M. A1 - Savaidis, G. A1 - Savaidis, A. A1 - Bohse, Jürgen T1 - Corrosion and fatigue crack monitoring by means of acoustic emission for application in transportation means N2 - Corrosion damages and fatigue cracks are the main causes of structural failures in vessels and transport products. Acoustic emission is suggested as an alternative to the conventional inspection processes enabling continuous health monitoring of the structures. Comprehensive finite element analyses have been performed on the example of a 3-compartment road tanker taking the corresponding ADR design loads into account. The numerical results reveal various weld joints as the structure’s failure-critical hot spots. Welded plates made of fine grain steel were stressed by corrosion and fatigue. Damage development in the material was measured and analyzed by acoustic emission testing. It is shown that the different degradation mechanisms, corrosion and fatigue crack growth in welded areas, can be reliably detected by acoustic emission. In addition, principal differences of the acoustic emission signals depending on the degradation mechanism are also explored. KW - Acoustic emission KW - Health monitoring KW - Fatigue crack growth KW - Corrosion KW - Finite elements KW - Welds PY - 2012 SN - 1943-3514 VL - 5 IS - 1 SP - 9 EP - 17 PB - Global Scientech CY - Basking Ridge, NJ, USA AN - OPUS4-27610 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Fayis Kalady, Mohammed A1 - Schultz, Johannes A1 - Weinel, Kristina A1 - Wolf, Daniel A1 - Lubk, Axel T1 - Geometry-dependent localization of surface plasmons on random gold nanoparticle assemblies N2 - Assemblies of plasmonic nanoparticles (NPs) support hybridized modes of localized surface plasmons (LSPs), which delocalize in geometrically well-ordered arrangements. Here, the hybridization behavior of LSPs in geometrically completely disordered two-dimensional arrangements of Au NPs fabricated by an e-beam synthesis method is studied. Employing electron energy loss spectroscopy in a scanning transmission electron microscope and numerical simulations, the disorder-driven spatial and spectral localization of the coupled LSP modes that depends on the NP thickness is revealed. Below a NP thickness of 0.4 nm, localization increases toward higher hybridized LSP mode energies. In comparison, above 10 nm thickness, a decrease of localization toward higher mode energies is observed. In the intermediate thickness regime, a transition of the energy dependence of the localization between the two limiting cases, exhibiting a mode energy with minimal localization, is observed. It is shown that this behavior is mainly driven by the energy and thickness dependence of the polarizability of the individual NPs. KW - Gold Nanoparticles KW - Surface plasmons KW - Electron enerdy loss spectroscopy (EELS) KW - scanning transmission electron microscopy PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-647230 DO - https://doi.org/10.1103/44nk-6bp2 SN - 2643-1564 VL - 7 IS - 043053 EP - 4 PB - American Physical Society AN - OPUS4-64723 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hickel, Tilmann A1 - Waske, Anja A1 - Tehranchi, Ali A1 - Bhattacharya, Biswajit A1 - Stawski, Tomasz M. A1 - Fellinger, Tim-Patrick A1 - Mehmood, Asad A1 - Witt, Julia A1 - Ozcan, Ozlem A1 - Guilherme Buzanich, Ana A1 - Kumar, Sourabh A1 - Mishra, Rajesh Kumar A1 - Holzer, Marco A1 - Stucchi de Camargo, Andrea Simone A1 - Agudo Jácome, Leonardo A1 - Manzoni, Anna A1 - Fantin, Andrea A1 - John, Elisabeth A1 - Hodoroaba, Vasile-Dan A1 - Bührig, Sophia A1 - Murugan, Jegatheesan A1 - Marschall, Niklas A1 - George, Janine A1 - Darvishi Kamachali, Reza A1 - Maaß, Robert A1 - Emmerling, Franziska T1 - Chemically complex materials enable sustainable high-performance materials N2 - Chemically complex materials (CCMats) 􀀀 including high-entropy alloys, oxides, and related multi-principal element systems 􀀀 offer a paradigm shift in materials design by leveraging chemical diversity to simultaneously optimize functional, structural, and sustainability criteria. The vastness of the compositional and structural space in CCMats propels the field into an expanding exploratory state. To reconcile functional and structural performance across this immense parameter space remains an open challenge. This Perspective evaluates the opportunities and challenges associated with harnessing chemical complexity across a broad spectrum of applications, such as hydrogen storage, ionic conductors, catalysis, magnetics, dielectrics, semiconductors, optical materials, and multifunctional structural systems. It is delineated how three central design strategies: targeted substitution (SUB), defect engineering (DEF), and diversity management (DIV) enable the reconciliation of high functional performance with long-term structural stability and environmental responsibility. Advances in computational thermodynamics, microstructure simulations, machine learning, and multimodal characterization are accelerating the exploration and optimization of CCMats, while robust data infrastructures and automated synthesis workflows are emerging as essential tools for navigating their complex compositional space. By fostering cross-disciplinary knowledge transfer and embracing data-driven design, CCMats are poised to deliver next-generation materials solutions that address urgent technological, energy, and environmental demands. KW - Chemically complex materials KW - Structural stability KW - Functional performance KW - Design strategies KW - Sustainability PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-655598 UR - https://www.sciencedirect.com/science/article/pii/S1359028626000033?via%3Dihub DO - https://doi.org/10.1016/j.cossms.2026.101256 SN - 1359-0286 VL - 42 SP - 1 EP - 26 PB - Elsevier Ltd. CY - Amsterdam AN - OPUS4-65559 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Altmann, Korinna A1 - Abusafia, A A1 - Bannick, C-G A1 - Braun, U A1 - Crasselt, Claudia A1 - Dittmar, S A1 - Fuchs, M A1 - Gehde, M A1 - Hagendorf, C A1 - Heller, C A1 - Herper, D A1 - Heymann, S A1 - Kerndorff, A A1 - Knefel, M A1 - Jekel, M A1 - Lelonek, M A1 - Lunkenbein, T A1 - Obermaier, N A1 - Manhart, M A1 - Meurer, Maren A1 - Miclea, P-T A1 - Paul, A A1 - Richter, S A1 - Ricking, M A1 - Rohner, C A1 - Ruhl, A A1 - Sakai, Y A1 - Saravia Arzabe, C A1 - Scheid, C A1 - Schmitt, M A1 - Schnarr, M A1 - Schwertfirm, F A1 - Steinmetz, H A1 - Wander, Lukas A1 - Wiesner, Yosri A1 - Zechmeister, L T1 - RUSEKU - Repräsentative Untersuchungsstrategien für ein integratives Systemverständnis von spezifischen Einträgen von Kunststoffen in die Umwelt : Abschlussbericht N2 - Im Verbundprojekt RUSEKU wurde die Probenahme von Wasserproben entscheidend weiterentwickelt. Wichtig ist hierbei zu gewährleisten, dass genügend Merkmalsträger in jeder Probe untersucht werden. Es muss daher eine für den Probenahmeort repräsentative Beprobung hinsichtlich des Wasservolumens in Abhängigkeit der Partikelanzahl gewährleistet sein. Das Hauptaugenmerk lag im vorliegenden Projekt auf einer praxisnahen Beprobungsstrategie. Es wurden verschiedene Konzepte ausprobiert. • Grundsätzlich hat sich gezeigt, dass eine Stichprobe eine Momentaufnahme des MP-Massengehaltes zeigt. Es wird eine hohe Statistik, also eine Vielzahl an Messungen am gleichen Probenahmeort, benötigt, um eine valide Aussage über den MP-Gehalt zu machen. • Es zeigt sich, dass eine integrale Probenahme über mehrere Wochen mit dem SK routinemäßig möglich ist. Die erfassten MP-Massen sind reproduzierbar und robust. • Die DFZ ist für Stichproben geeignet. Partikel < 50 µm werden eventuell unterschätzt • Die fraktionierte Filtration kann für Stich- und Mischproben direkt im Feld genutzt werden. Fraktionen von 10 und 5 µm werden später im Labor Vakuum filtriert. Es erfolgt eine Fraktionierung der Probe mit Siebmaschenweiten von 1000, 500, 100, 50, 10 und 5 µm. • Die fraktionierte Filtration kann auch anschließend an die Beprobung mit dem SK zur Anwendung kommen. Wird die mit dem SK gewonnene Wasserprobe fraktioniert filtriert, kann neben einem MP-Gesamtgehalt auch eine Einschätzung über die Partikelgrößen gewonnen werden. • Für Wässer mit geringen Partikelzahlen wurde ein Messfiltertiegel entwickelt. Dieser hat eine Maschenweite von 6 µm. Seine Anwendung kann mögliche Verluste beim Transferieren vom Probenahmetool zum Messgefäß und mögliche Kontaminationen reduzieren. Die Optimierung der Probenahmestrategie wurde durch Modellversuche und Simulationen unterstützt. Modellversuche zum Sinkverhalten und Simulationen von MP in realen Gewässern verdeutlichten das komplexe Verhalten der Partikel. Es konnte gezeigt werden, dass Partikel ab einer bestimmten Größe (und kleiner) bei genügend starker Turbulenz sich in der Wassersäule unabhängig von ihrer Dichte verhalten und so auch MP mit kleiner Dichte (z.B. PE) in der gesamten Wassersäule zu finden sind. Es konnte mit dem TEM die Existenz von NP gezeigt werden. Ein wesentlicher Aspekt des RUSEKU Projektes war die Beprobung realer Kompartimente. Beprobt wurde neben Oberflächengewässern, das urbane Abwassersystem der Stadt Kaiserslautern, Waschmaschinenabwasser und Flaschenwasser. • In Oberflächengewässern wurde hauptsächlich PE gefunden. Je nach Probe und Gewässer konnten auch PP, PS, PET, PA, SBR und Acrylate nachgewiesen werden. • Im urbanen Abwassersystem der Stadt Kaiserslautern konnte an allen Probenahmestandorten MP nachgewiesen werden. Es wurde hauptsächlich PE, neben geringeren Mengen an PP, PS und SBR gefunden. Nach einem Regenereignis war der SBR Anteil deutlich erhöht. • Die Beprobung eines realen Wäschepostens, bestehend aus T-Shirts und Hemden mit PA/CO oder PES/CO Mischgewebe, zeigte einen PA- und PES-Austrag im Waschwasser. Der überwiegende Teil der detektierten Fasern ist aber auf Baumwolle zurückzuführen. Reine gravimetrische Messungen zur Detektion von MP führen zu einer starken Überschätzung. • In Flaschenwasser (PET-Flaschen) konnte MP detektiert werden. PET wurde nur im stillen Mineralwasser, nicht in Mineralwasser mit Kohlensäure gefunden werden. Teilweise wurde auch das MP-Material des Verschlusses im Wasser detektiert. • Für Luftproben konnte ein Aufbau zur größenselektiven Beprobung getestet werden. Neben der Probenahme hat das Projekt auch gezeigt, dass die TED-GC/MS geeignet für die MP-Detektion im Routinebetrieb ist. Die TED-GC/MS konnte weiter optimiert werden. Es wurden MP-Massen bestimmt. Im Projekt wurden erste realitätsnahe Referenzmaterialien für die MP Detektion hergestellt. Die Herstellung von realitätsnahen Polymeren in ausreichender Homogenität und Menge hat sich als große Herausforderung herausgestellt. KW - Mikroplastik KW - Probennahme KW - TED-GC/MS KW - Fraktionierte Filtration KW - Mikroplastikreferenzmaterial PY - 2022 SP - 1 EP - 201 AN - OPUS4-57800 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - In situ studies of mechanochemistry: a force of synthesis N2 - Recent results in the field of mechanisms and kinetics of mechanochemical reactions. T2 - Seminar GFZ Potsdam CY - Postdam, Germany DA - 28.03.2018 KW - In situ KW - XRD KW - Rietveld PY - 2018 AN - OPUS4-46992 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kabelitz, Anke T1 - In-situ characterisation of nucleation, growth, crystallisation and dissolution of nanoscaled iron oxides N2 - We present the synthesis of four mesoporous templated iron oxides: Ferrihydrite, Hematite, Maghemite, Magnetite/Maghemite and the influence of water on the crystallization mechanism and the kinetics. The absence of water stabilize the ferrihydrite structure. By monitoring the dissolution in situ by using a QCMB and ex situ microscopy we got details in the dissolution mechanism of ferrihydrite. T2 - Final Meeting of the CRC 1109 & Edith Flanigen Award Ceremony 2018 CY - Berlin, Germany DA - 10.10.2018 KW - Mesoporous KW - Iron oxide KW - Mechanism PY - 2018 AN - OPUS4-47010 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Yusenko, Kirill T1 - BAMline 2.0 – further technical developments for a broader multipurpose hard X-ray beamline at BESSY II N2 - We show further development of our beamline in the contexst of further itermational collaboration. T2 - PACC and AfSC CY - Accra, Ghana DA - 28.01.2019 KW - Synchrotron radiation PY - 2019 AN - OPUS4-47317 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - New insights in mechanochemical processes using real-time In situ investigations N2 - Mechanochemistry is a fast and efficient method applicable for the synthesis of new organic[1], metal-organic[2], and inorganic[3] compounds. The direct monitoring of milling reactions is still challenging. The underlying reaction mechanisms remain often unclear. In the last years, have established a tandem in situ approach for investigating mechanochemical reactions using time-resolved in situ XRD coupled with Raman spectroscopy.[4] Here, we present an in situ coupling of synchrotron XRD, Raman spectroscopy, and thermography allowing the observation of mechanochemical reactions in real time.[5] Information on the crystalline, molecular, and temperature state of the materials during grinding could be collected. The chemical composition of the reaction mixture was found to be directly correlated with changes in the temperature profile of the reaction. Furthermore, the presented setup allows the detection of crystalline, amorphous, eutectic as well as liquid intermediates. The resulting deeper kinetic and thermodynamic understanding of milling processes is the key for future optimization of mechanochemical syntheses. T2 - 5th International Conference "Fundamental Bases of Mechanochemical Technologies" CY - Novosibirsk, Russia DA - 25.06.2018 KW - Mechanochemistry KW - XRD KW - Kinetic KW - Coordination polymers PY - 2018 AN - OPUS4-46994 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Akhmetova, Irina T1 - Mechanochemical synthesis of metal phosphonates N2 - The exploration of metal phosphonates chemistry has gained great interest during the last decades, because of their structural diversity. Transition metal phosphonates are promising candidates for an application as electrocatalysts in oxygen evolution reactions (OER). Here, we present the in situ investigation of mechanochemical syntheses of different manganese phosphonates by synchrotron X-ray diffraction. Nitrilotri(methylenephosphonic acid) and N,N-Bis(phosphonomethyl)glycine were chosen as ligands. The liquid-assisted milling process can be divided into three steps, including an amorphous stage. One of the products has not been obtained by classical solution chemistry before. These metal phosphonates and/or their derivatives are considered to be active in electrochemical energy conversion. The verification of their applicability is one of the topics of our resent research. T2 - Fundamental Bases of Mechanochemical Technologies CY - Novosibirsk, Russia DA - 25.06.2018 KW - Metal phosphonates KW - Mechanochemistry KW - PXRD KW - Thermography PY - 2018 AN - OPUS4-46996 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Akhmetova, Irina T1 - In situ investigation of milling reactions and structure determination of the products using X-ray diffraction N2 - Mechanochemistry is a versatile approach for green and fast synthesis of pure substances. By milling the reactants, various organic, inorganic, and metal-organic compounds can be obtained in high yields. Although mechanochemistry is widely used, the underlying mechanisms are not fully understood making mechanochemical reactions difficult to predict. Metal phosphonates are metal-organic compounds accessible by grinding. Because of their structural diversity, the exploration of the chemistry of metal phosphonates has gained considerable interest during the last decades. Transition metal phosphonates are promising candidates for an application as electrocatalysts in oxygen evolution reaction (OER). Here, we present the in situ investigation of the mechanochemical synthesis of a manganese(II)-phosphonate by synchrotron X-ray diffraction and thermography. The product has not been obtained by classical solution chemistry before and its crystal structure was determined from PXRD data. The milling process can be divided into different steps, with the product crystallization corresponding with the highest temperature rise. The activity of this metal phosphonate towards OER was measured and is presented here. T2 - International School of Crystallography - 52nd Course: Quantum Crystallography CY - Erice, Italy DA - 1.06.2018 KW - Metal phosphonates KW - Mechanochemistry KW - PXRD KW - OER KW - Thermography PY - 2018 AN - OPUS4-46998 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kabelitz, Anke T1 - A02: In situ WAXS studies on the crystallization of Al 13 keggin clusters in water N2 - Polynuclear aluminium species (Al13 keggin cluster) find application in different areas like water purification [1], contaminant transport [2], and as pilling clays with high specific surface areas[3], due to their strong binding ability to aggregates and high positive charge. In the present contribution, we report on the in situ investigation of the Al13 sulfate synthesis by synchrotron wide-angle X-ray scattering (WAXS). Al13 cluster were crystallized by precipitating hydrolyzed aluminum solutions by the addition of sodium sulfate. The measurements were performed using a custom-made acoustic levitator as sample holder. The study provides information about the intermediates during the crystallization process. From the data, a mechanism was derived indicating the influence of the crystallization process. T2 - Final Meeting of the CRC 1109 & Edith Flanigen Award Ceremony 2018 CY - Berlin, Germany DA - 10.10.2018 KW - Crystallization KW - WAXS KW - Keggin Cluster PY - 2018 AN - OPUS4-47005 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauw, Brian Richard T1 - Laboratory x-ray scattering instruments as agile test-beds towards holistic experimentation N2 - Laboratory sources offer a unique advantage compared to synchrotron sources, largely in terms of freedom of operation. This freedom from user obligations, technology and software stacks and legacy decisions make the laboratory a very flexible place to develop and explore new ideas. The unparalleled availability furthermore allows for iterative improvement of instrumentation, sample environments and measurement methodologies to maximise the quality of the data obtained. This talk will highlight the use of the laboratory as an agile test-bed and development space, by giving examples of some complete and incomplete investigations undertaken in our laboratory over the last years. Furthermore, it will introduce the concept of holistic experimentation, where the laboratory provides broad-ranging support for materials science investigations. This means that we assist in the experimental preparation, perform the measurements, correction and analysis, and follow-up with assistance in interpretation of our analyses in light of the results from other techniques applied to the investigation. T2 - Invited talk at Diamond Light Source CY - Didcot, UK DA - 22.05.2024 KW - X-ray scattering KW - Methodology development KW - Laboratory management KW - Holistic experimentation KW - Laboratory automation KW - Nanostructural analysis PY - 2024 AN - OPUS4-60582 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauw, Brian Richard T1 - Glimpses of the Future : Oh my god it’s full of metadata! N2 - In this talk, the importance of metadata is underscored by real-world examples. Metadata is essential to alleviating the reproducibility crises in science. This imples that a wide range of metadata must be collected, with a heavy emphasis on the automated collection of such metadata. This must subsequently be organized in an intelligible, archival structure, when possible with units and uncertainties. Such metadata can aid in improving the usage efficiency of instrumentation, as is demonstrated on the MOUSE instrument. This metadata can now be used to connect the various aspects of the holistic experimental procedure to gain better insights on the materials structure. A second example shows the extraction and organization of such metadata from an automated materials development platform, collected during the synthesis of 1200 samples. These metadata from the synthesis can then be linked to the results from the analysis of these samples, to find direct correlations between the synthesis parameters and the final structure of the materials. T2 - Helmholtz Incubator Summer Academy - Next Level Data Science CY - Online meeting DA - 18.09.2023 KW - Metadata KW - Lab automation KW - Data provenance KW - High-throughput KW - Correlative analysis KW - MOUSE KW - X-ray scattering KW - Robotics PY - 2023 AN - OPUS4-58463 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Smales, Glen Jacob A1 - Pauw, Brian Richard T1 - DACHS/MOFs/AutoMOFs_4/Synthesis N2 - The DACHS (Database for Automation, Characterization and Holistic Synthesis) project aims to create completely traceable experimental data, covering syntheses, measurements, analyses, and interpretations. DACHS_MOFs focuses on the synthesis and characterisation of metal-organic frameworks, across multiple, automation-assisted experimental series (AutoMOFs), with the overall goal of producing reproducible MOF samples through tracking of the synthesis parameters. DACHS_MOFs is simultaneously used to test the DACHS principles. This upload contain synthesis data from AutoMOFs_4 in HDF5 format (.h5). Each .h5 file contains detailed information on the chemical, experimenal, and synthesis parameters used during the synthesis of a single AutoMOF sample. KW - Automation KW - Procedure KW - Synthesis KW - Traceability PY - 2024 DO - https://doi.org/10.5281/zenodo.11237899 PB - Zenodo CY - Geneva AN - OPUS4-61343 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Smales, Glen Jacob A1 - Pauw, Brian Richard T1 - DACHS/MOFs/AutoMOFs_1/Synthesis N2 - The DACHS (Database for Automation, Characterization and Holistic Synthesis) project aims to create completely traceable experimental data, covering syntheses, measurements, analyses, and interpretations. DACHS_MOFs focuses on the synthesis and characterisation of metal-organic frameworks, across multiple, automation-assisted experimental series (AutoMOFs), with the overall goal of producing reproducible MOF samples through tracking of the synthesis parameters. DACHS_MOFs is simultaneously used to test the DACHS principles. This upload contain synthesis data from AutoMOFs_1 in HDF5 format (.h5). Each .h5 file contains detailed information on the chemical, experimenal, and synthesis parameters used during the synthesis of a single AutoMOF sample. KW - Synthesis KW - Automation KW - Traceability KW - Procedure PY - 2024 DO - https://doi.org/10.5281/zenodo.11236031 PB - Zenodo CY - Geneva AN - OPUS4-60243 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Pauw, Brian Richard A1 - Smales, Glen Jacob A1 - Hörmann, Anja A1 - Moeez, Abdul A1 - Breßler, Ingo T1 - BAMresearch/HDF5Translator: A Framework for translating and transforming data between HDF5 files N2 - HDF5Translator is a Python framework for translating and transforming data between HDF5 files. It supports operations like unit conversion, dimensionality adjustments, and subtree copying, making it suitable for managing and manipulating a wide range of scientific datasets. KW - Measurement data conversion KW - Data conversion KW - HDF5 KW - NeXus KW - NXsas KW - Framework KW - Python KW - Methodology PY - 2024 DO - https://doi.org/10.5281/zenodo.10927639 PB - Zenodo CY - Geneva AN - OPUS4-59797 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Pauw, Brian Richard A1 - Laskina, Sofya A1 - Naik, Aakash A1 - Smales, Glen Jacob A1 - George, Janine A1 - Breßler, Ingo A1 - Benner, Philipp T1 - Jupyter notebook and VASP calculation details accompanying the manuscript: "Ultima Ratio: Simulating wide-range X-ray scattering and diffraction" N2 - Summary: This notebook and associated datasets (including VASP details) accompany a manuscript available on the ArXiv (https://doi.org/10.48550/arXiv.2303.13435) and hopefully soon in a journal as short communication as well. Most of the details needed to understand this notebook are explained in that paper with the same title as above. For convenience, the abstract is repeated here: Paper abstract: We demonstrate a strategy for simulating wide-range X-ray scattering patterns, which spans the small- and wide scattering angles as well as the scattering angles typically used for Pair Distribution Function (PDF) analysis. Such simulated patterns can be used to test holistic analysis models, and, since the diffraction intensity is presented coupled to the scattering intensity, may offer a novel pathway for determining the degree of crystallinity. The "Ultima Ratio" strategy is demonstrated on a 64-nm Metal Organic Framework (MOF) particle, calculated from $Q<0.01$\,$\mathrm{nm}^{-1}$ up to $Q\approx150$\,$\mathrm{nm}^{-1}$, with a resolution of 0.16\,\AA. The computations exploit a modified 3D Fast Fourier Transform (3D-FFT), whose modifications enable the transformations of matrices at least up to $8000^3$ voxels in size. Multiple of these modified 3D-FFTs are combined to improve the low-$Q$ behaviour. The resulting curve is compared to a wide-range scattering pattern measured on a polydisperse MOF powder. While computationally intensive, the approach is expected to be useful for simulating scattering from a wide range of realistic, complex structures, from (poly-)crystalline particles to hierarchical, multicomponent structures such as viruses and catalysts. KW - X-ray KW - Simulation KW - Scattering KW - MOUSE KW - Nanomaterials KW - XRD KW - SAXS KW - PDF KW - Total scattering KW - 3D Fourier transform KW - High resolution KW - FFT PY - 2023 DO - https://doi.org/10.5281/zenodo.7764044 PB - Zenodo CY - Geneva AN - OPUS4-57207 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mehri Sofiani, F. A1 - Chaudhuri, Somsubhro A1 - Elahi, S. A. A1 - Wallaert, E. A1 - Depover, T. A1 - De Waele, W. T1 - Accelerated laboratory simulation of corrosion pit evolution in low-carbon steel using phase-field guided overpotential application N2 - This study is performed to replicate field data of pit geometry evolution in the laboratory by accelerating pit evolution through the application of relatively high overpotential on low-carbon steel. A phase-field model is used to reduce the number of trials and errors in the laboratory. The effect of overpotential on pitting corrosion is studied in low-carbon steel in the electrolyte representative of the North Sea. Based on the results obtained through the numerical model, potentiostatic polarisation tests are performed, and a comparison is made between such accelerated tests and steel coupons collected from the field. The results of this comparison suggest that the pitting corrosion acceleration mechanism effectively produces surface conditions closely resembling those of naturally pitted steel. Additionally, it enables the investigation of the electrochemical characteristics of a stable pit over long-term exposure, where direct probing is challenging. This framework strives to mitigate the excessive costs of time-consuming coupon experiments by correlating accelerated pitting corrosion in short periods of time with actual pitting corrosion observed over the long term. KW - Pitting corrosion KW - Corrosion acceleration KW - Potentiodynamic tests KW - Phase-field KW - S355 PY - 2025 DO - https://doi.org/10.1016/j.engfailanal.2025.110352 SN - 1350-6307 VL - 184 SP - 1 EP - 20 PB - Elsevier CY - Oxford AN - OPUS4-64805 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Mohr, Gunther T1 - R&D insights into sustainable additive manufacturing for high-temperature applications (HTA) N2 - Im Rahmen des AM Forums Berlin 2026 wird durch diesen Vortrag ein Einblick in FuE-Aktivitäten der BAM auf dem Gebiet der additiven Fertigung für Hochtemperaturanwendungen gegeben. Es werden dabei insbesondere Aspekte der nachhaltigen Verwendung von Pulverausgangswerkstoff und der Einfluss von Sauerstoff im Pulverwerkstoff auf die Degradation resultierender mechanischer Eigenschaften von Probekörpern beleuchtet. Die präsentierten Arbeiten sind im Rahmen des Pro FIT Projektes HTA2.0 entstanden. T2 - 10. AM Forum 2026 CY - Berlin, Germany DA - 10.03.2026 KW - Additive Manufacturing KW - Sustainability KW - Powder recycling KW - Powder degradation PY - 2026 AN - OPUS4-65725 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hülagü, Deniz A1 - Hertwig, Andreas T1 - Correlative analysis of graphene: Advancing ellipsometry as a fast routine method N2 - Graphene (G) and graphene oxide (GO) are key materials for various applications, yet their structural and thickness inhomogeneities calls for rapid, reliable characterization. In this work, we performed a correlative analysis, combining spectroscopic (SE) and imaging ellipsometry (IE) with complementary microscopy techniques to investigate monolayer graphene and GO flakes on SiO₂/Si substrates. SEM, owing to its high resolution and excellent contrast, delivered a comprehensive overview of the monolayer graphene (Figure 1a) and enabled the clear identification of individual GO flakes (c). However, SEM does not provide layer-thickness information. In this case, SE served as a fast and non-destructive method capable of quantitative thickness determination through optical modeling, revealing a graphene layer thickness of 0.7 nm (b), corresponding to a monolayer. The GO flake identified by SEM was subsequently analyzed by AFM, a well-established technique providing nanoscale height profiles with high accuracy (d–f). AFM results further revealed flake thicknesses of a few monolayers. However, AFM is time-consuming, restricted to small scan areas, and does not offer a full overview of the sample. WLIM complemented these results by providing large-area imaging, enabling the visualization of multiple flakes simultaneously. Nevertheless, it is not able to quantify the exact thickness (e). In contrast, IE enabled non-destructive, substrate-independent thickness of GO flakes with single-atomic-layer precision and improved sensitivity, once the ellipsometer settings were optimized for material and thickness contrast and fixed during imaging, bridging the gap between overview imaging and quantitative nanoscale analysis (g–h). While SE provides non-destructive, quantitative thickness information for homogeneous monolayer graphene, GO flakes require imaging-based methods. Therefore, IE represents an attractive alternative, offering large-area maps of GO flakes together with local layer-thickness information. This correlative approach establishes a foundation for standardized, large-area quality assessment of such 2D materials. T2 - 13th Workshop on Spectroscopic Ellipsometry WSE 2026 CY - Genova, Italy DA - 09.02.2026 KW - Monolayer graphene KW - Graphene oxide KW - Correlative Analysis KW - SEM KW - Spectroscopic ellipsometry KW - Imaging ellipsometry KW - AFM PY - 2026 AN - OPUS4-65708 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Miliute, Aiste T1 - How experimental and computational methods allow us to design negative thermal expansion materials N2 - Combined experimental and computational methods allow a comprehensive understanding, design, and tailoring of material properties. We focus on a well-known negative thermal expansion (NTE) material, zirconium vanadate (ZrV2O7), and address its synthesis, characterisation, and computational validation of results. Experimental and computational X-ray diffraction and Raman spectroscopy data highlighted differences between phase-pure and multiphase ceramics. The total-scattering method enabled us to distinguish subtle differences in the material's structure. Based on ab initio simulated phonon data, we could interpret the Raman spectra, visualise Raman-active atomic vibrations, and gain deeper insight into the local structure. Computational models provided deeper insight and enabled further experimental improvements, while high-quality experimental data validated and improved the computational simulation strategy. T2 - CATS Special Guests III CY - Urcuqui, Ecuador DA - 06.03.2026 KW - NTE KW - Ab initio KW - PDF KW - Raman KW - XRD PY - 2026 AN - OPUS4-65714 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schaupp, Thomas A1 - Schröder, Nina A1 - Schröpfer, Dirk A1 - Kannengießer, Thomas T1 - Hydrogen-assisted cracking in GMA welding of high-strength structural steel - A new look into this issue at narrow groove N2 - Modern arc processes, such as the modified spray arc (Mod. SA), have been developed for gas metal arc welding of high-strength structural steels with which even narrow weld seams can be welded. High-strength joints are subjected to increasingly stringent requirements in terms of welding processing and the resulting component performance. In the present work, this challenge is to be met by clarifying the influences on hydrogen-assisted cracking (HAC) in a high-strength structural steel S960QL. Adapted samples analogous to the self-restraint TEKKEN test are used and analyzed with respect to crack formation, microstructure, diffusible hydrogen concentration and residual stresses. The variation of the seam opening angle of the test seams is between 30° and 60°. To prevent HAC, the effectiveness of a dehydrogenation heat treatment (DHT) from the welding heat is investigated. As a result, the weld metals produced at reduced weld opening angle show slightly higher hydrogen concentrations on average. In addition, increased micro- as well as macro-crack formation can be observed on these weld metal samples. On all samples without DHT, cracks in the root notch occur due to HAC, which can be prevented by DHT immediately after welding. KW - High-strength structural steel KW - Gas metal arc welding KW - Diffusible hydrogen KW - Hydrogen-assisted cracking KW - TEKKEN KW - Residual stresses KW - Weld metal cracking PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-527260 DO - https://doi.org/10.3390/met11060904 VL - 11 IS - 6 SP - 1 EP - 18 PB - MDPI CY - Basel AN - OPUS4-52726 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Engelking, Lorenz A1 - Madia, Mauro A1 - Schröpfer, Dirk A1 - Kruse, Julius A1 - Saliwan Neumann, Romeo A1 - Kannengießer, Thomas T1 - Influence of Ultrasonic-Assisted Milling on Surface Integrity and Fatigue Strength of a Low Alloy Steel N2 - The milling process significantly influences the surface integrity of metallic components through machining induced near surface residual stresses. Modern hybrid machining processes, such as ultrasonic-assisted milling (USAM), offer the potential to induce beneficial near-surface compressive residual stresses compared to the near-surface tensile residual stresses typically resulting from conventional milling (CM). This study investigates the effects of USAM compared to CM on the near-surface residual stress state and fatigue performance of a S355J2C low-alloy steel. Milling experiments and subsequent rotating bending tests revealed that USAM significantly reduces cutting force by approximately 45% and induces near-surface compressive re sidual stresses as low as −733MPa. This leads to a significant improvement in fatigue strength estimated in approximately 34% compared to polished specimens and 11% compared to the CM. These findings highlight the potential of USAM to enhance the fatigue performance of components made of steel. KW - Fatigue strength KW - Residual stress KW - Surface integrity KW - Surface roughness KW - Ultrasonic-assisted milling PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-657358 DO - https://doi.org/10.1111/ffe.70259 SP - 1 EP - 11 PB - Wiley AN - OPUS4-65735 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - George, Janine T1 - Robust Data Generation, Heuristics and Machine Learning for Materials Design N2 - Despite significant progress, computational materials design still faces major challenges—particularly when simulating advanced and chemically complex materials with the accuracy of density functional theory (DFT) or beyond.[1] To overcome these limitations, machine learning (ML) methods have gained considerable traction in recent years. We have developed robust data-generation strategies to support the creation and benchmarking of new ML models.[2] In this talk, I will highlight methods for large-scale quantum-chemical bonding analysis and workflows for ML interatomic potentials. Our work demonstrates that quantum-chemical bonding properties can be incorporated into ML models to predict phononic properties.[3] This approach enables large-scale validation of expected correlations—such as the link between bonding strength and force constants or thermal conductivities. Furthermore, we have built an automated training framework for machine-learned interatomic potentials (autoplex).[4] Initial workflows include random structure searches, suitable for general-purpose potentials, as well as specialized workflows targeting ML potentials with accurate phonon properties. While atomistic simulations are highly effective for certain material properties, others—such as magnetism or synthesizability—remain challenging. In these cases, promising strategies include benchmarking established ab initio methods against chemical heuristics or developing new ML models primarily based on experimental data.[5,6] T2 - MATSUS Spring 2026 CY - Barcelona, Spain DA - 24.03.2026 KW - Materials Design KW - High-througput KW - Bonding properties KW - Thermal conductivity KW - Amorphous materials KW - Crystallisation PY - 2026 AN - OPUS4-65734 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Suarez Ocano, Patricia T1 - Effect of the powder composition on the microstructure and mechanical properties of 316L stainless steel fabricated by laser powder bed fusion N2 - Additive manufacturing (AM) has seen rapid growth in recent decades, with Laser Powder Bed Fusion (PBF-LB/M) emerging as the leading technique for producing high-density, geometrically complex metal parts. Austenitic stainless steel 316L is one of the most studied alloys for PBF-LB/M due to its excellent strength, ductility, and corrosion resistance [1]. The microstructure formed during PBF-LB/M processing can improve certain mechanical properties compared to conventionally manufactured 316L [2]. However, the current 316L standards allow broad ranges for key alloying elements, particularly Cr and Ni. While such variations have little effect on conventionally produced alloys, emerging evidence shows that they can markedly alter the microstructure and mechanical properties in PBF-LB/316L—even within specification limits [3]. This study investigates through microstructural and thermodynamical assessment, how two powders of nominally standard 316L composition (Alloys A and B) respond to identical PBF-LB/M processing parameters. Despite identical printing conditions, Alloy A exhibited twice the grain size and five times higher low-angle grain boundary (LAGB) density compared to Alloy B . Conversely, Alloy B showed a significantly higher density of Σ3 twin boundaries, nearly absent in Alloy A. These microstructural differences are attributed primarily to variations in Cr and Ni content in the liquid, which may influence icosahedral short-range ordering (ISRO) mechanism [4]. ISRO potentially facilitates twin boundary formation, ultimately refining grain structure [5]. This work highlights the critical impact of compositional control on final part microstructures and consequent mechanical properties and emphasizes the need to reassess compositional tolerances for AM-specific applications. T2 - 5th Symposium on Materials and Additive Manufacturing (Additive 2026) CY - Kassel, Germany DA - 24.03.2026 KW - Additive manufacturing KW - 316L stainless steel KW - Chemical composition KW - Lcosahedral short-range ordering mechanism KW - Grain size PY - 2026 AN - OPUS4-65738 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, Hans A1 - Weidner, Steffen A1 - Scheliga, Felix T1 - Ring-Expansion Polymerization (REP) of L-lactide with cyclic Tin(II) Bisphenoxides N2 - Five new cyclic catalysts were prepared by a new synthetic method from tin(II)-2-ethyhexanoate and silylated catechols, silylated 2,2´dihydroxybiphenyl or silylated 1,1´-bisnaphthol. These catalysts were compared with regard to their usefulness as catalysts for the ring expansion polymerization (REP) of L-lactide in bulk at 160 °C, and with two different tin(IV) derivatives of 1,1´binaphthol. Best results were obtained using seven-membered cyclic tin(II)bisphenoxides, which yielded colorless cyclic poly(l-lactide)s free of racemization with weight average molecular weights (Mw) up to 305 000 g mol-1. Furthermore, these catalysts were active even at a lactide/catalyst ratio of 20 000/1. Our new results were superior to those obtained from all other previously published catalysts yielding cyclic poly(L-lactide). The seven-membered cycles also proved to be more active than tin(II) 2-ethylhexanoate with and without the addition of alcohol. KW - Lactide KW - Cyclization KW - Ring-expansion polymerization KW - Tin(II)octanoate KW - MALDI-TOF MS PY - 2019 DO - https://doi.org/10.1016/j.eurpolymj.2019.04.024 SN - 0014-3057 SN - 1873-1945 VL - 116 SP - 256 EP - 264 PB - Elsevier Ltd. AN - OPUS4-47794 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. R. A1 - Meyer, A. A1 - Weidner, Steffen T1 - High Tm Poly(l-lactide)s by Means of Bismuth Catalysts? N2 - One series of BiSub-catalyzed ring-opening polymerizations (ROPs) is per-formed at 160 °C for 3 days with addition of difunctional cocatalysts to find out, if poly(l-lactide) crystallizes directly from the reaction mixture. An analogous series is performed with monofunctional cocatalysts. High Tm crystal-lites (Tm > 190 °C) are obtained from all bifunctional cocatalysts, but not from all monofunctional ones. It is shown by means of SAXS measurements that the high Tm values are mainly a consequence of a transesterification–homogenization process across the lamellar surfaces resulting in thickness and smoothing of the surfaces. An unusual enthalpy-driven modification of the molecular weight distribution is found for samples that have crystallized during the polymerization. A third series of ROPs is performed at 170 °C for 2 h followed by annealing at 120 °C (2 h) to induce crystallization. Complete transformation of the resulting low Tm crystallites (Tm < 180 °C) into the high Tm crystallites by annealing at 170 °C for 1 d is not achieved, despite variation of the cocatalyst. KW - Polylactide KW - MALDI-TOF MS KW - Crystallization PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-522777 DO - https://doi.org/10.1002/macp.202100019 SN - 1022-1352 VL - 222 IS - 8 SP - 19 PB - Wiley AN - OPUS4-52277 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. R. A1 - Weidner, Steffen A1 - Meyer, A. T1 - About the Influence of (Non-)Solvents on the Ring Expansion Polymerization of l-Lactide and the Formation of Extended Ring Crystals N2 - Ring-expansion polymerizations (REPs) catalyzed by two cyclic tin catalysts(2-stanna-1.3-dioxa-4,5,6,7-dibenzazepine [SnBiph] and 2,2-dibutyl-2-stanna-1,3-dithiolane [DSTL) are performed at 140 °C in bulk. Small amounts (4 vol%) of chlorobenzene or other solvents are added to facilitate transesterification reactions (ring–ring equilibration) in the solid poly(l-lactide)s. In the mass range up to m/z 13 000 crystalline PLAs displaying a so-called saw-tooth pattern in the MALDI-TOF mass spectra are obtained indicating the formation of extended-ring crystals. The characteristics of extended-ring crystallites and folded-ring crystallites are discussed. Furthermore, extremely high melting temperatures (Tm’s up to 201.2 °C) and melting enthalpies (𝚫Hm’s up to 106 J g−1)) are found confirming that 𝚫Hmmax, the 𝚫Hm of a perfect crystal, is around or above 115 J g−1 in contrast to literature data. KW - Polylactide KW - MALDI-TOF MS KW - Ring-expansion polymerization KW - Crystals PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-565038 DO - https://doi.org/10.1002/macp.202200385 SN - 1022-1352 SP - 1 EP - 8 PB - Wiley VHC-Verlag AN - OPUS4-56503 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Weidner, Steffen A1 - Kricheldorf, H. R. T1 - SnOct2-catalyzed ROPs of L-lactide initiated by acidic OH- compounds: Switching from ROP to polycondensation and cyclization N2 - Ring-opening polymerizations (ROPs) of L-lactide are performed in bulk at 130°C with tin(II) 2-ethylhexanoate as catalyst and various phenols of differentacidity as initiators. Crystalline polylactides having phenyl ester end groups are isolated, which are almost free of cyclics. The dispersities and molecular weights are higher than those obtained from alcohol-initiated ROPs under identical conditions. Polymerizations at 160°C yield higher molecular weights than expected from the monomer/initiator ratio and a considerable fraction of cycles. The fraction of cycles increases with higher reactivity of the ester end group indicating that the cycles are formed by end-to-end cyclization. KW - Polylactide KW - MALDI-TOF MS KW - Polymerization PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-540250 DO - https://doi.org/10.1002/pol.20210823 SN - 2642-4150 VL - 60 IS - 5 SP - 785 EP - 793 PB - Wiley AN - OPUS4-54025 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Musl, O. A1 - Sulaeva, I. A1 - Sumerskii, I. A1 - Mahler, A.K. A1 - Rosenau, T. A1 - Falkenhagen, Jana A1 - Potthast, A. T1 - Mapping of the Hydrophobic Composition of Lignosulfonates N2 - Lignosulfonates are industrial biorefinery products that are characterized by significant variability and heterogeneity in their structural composition. Typically, they exhibit high dispersities in molar mass (molar mass distribution-MMD) and in functionalities (functionality-type distribution - FTD), which crucially affect their material usage. In terms of FTD, state-of-the-art Lignin analytics still rely mainly on the determination of functional group contents, which are statistical averages with limited explanatory power. In contrast, our online hydrophobic interaction chromatography−size-exclusion chromatography 2D-LC approach combines the determination of both MMD and FTD in a single measurement to provide a comprehensive picture of the characteristic composition of industrial lignosulfonates information hitherto inaccessible by state-of-the-art lignin analytics. In this way, the complex inter - relationships between these two important structural parameters can be studied in an unprecedented manner. In this study, we reveal the considerable differences in terms of hydrophobic composition and its dispersity present in a range of different industrial lignosulfonates - data desperately needed in tailoring and refining of lignosulfonate composition for material usage. KW - Lignosulfonates KW - Amphiphilicity KW - Hydrophobic interaction chromatography KW - Two-dimensional chromatography (2D-LC) KW - Charge-to-size-ratio PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-538612 DO - https://doi.org/10.1021/acssuschemeng.1c06469 VL - 9 IS - 49 SP - 16786 EP - 16795 PB - ASC Publications AN - OPUS4-53861 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. R. A1 - Weidner, Steffen A1 - Meyer, A. T1 - Poly(L-lactide): Optimization of Melting Temperature and Melting Enthalpy N2 - Twice recrystallized L-lactide was polymerized with a dozen of different tin or bismuth catalysts in bulk at 160°C for 24 h and was annealed at 150°C afterwards. In two cases Tm values above 197.0°C were obtained. The parameters causing a scattering of the DSC data were studied and discussed. The samples prepared with SnCl2, 2,2-dibutyl-2-stanna-1,3-ditholane (DSTL) or cyclic tin(II) bisphenyldioxide (SnBiph) were subject to annealing programs with variation of time and temperatures, revealing that the Tm´s did not increase. However, an increase of Hm was achieved with maximum values in the range of 93-96 J g-1 corresponding to crystallinities off around 90%. Further studies were performed with once recrystallized L-lactide. Again, those samples directly crystallized from the polymerization process showed the highest Tm values. These data were compared with the equilibrium Tm0 and Hm0 data calculated by several research groups for perfect crystallites. A Tm0 of 213+/-2°C and a Hm0 of 106 J g-1 show the best agreement with the experimental data. The consequences of annealing for the thickness growth of crystallites are discussed on the basis of SAXS measurements. Finally, a comparison of cyclic and linear poly L-lactide)s is discussed. KW - Polylactide KW - MALDI-TOF MS KW - Transesterification PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-538656 DO - https://doi.org/10.1039/D1MA00957E SP - 1 EP - 10 PB - Royal Society for Chemistry AN - OPUS4-53865 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Fink, Friedrich A1 - Emmerling, Franziska A1 - Falkenhagen, Jana T1 - Identification and Classification of Technical Lignins by means of Principle Component Analysis and k-Nearest Neighbor Algorithm N2 - The characterization of technical lignins is a key step for the efficient use and processing of this material into valuable chemicals and for quality control. In this study 31 lignin samples were prepared from different biomass sources (hardwood, softwood, straw, grass) and different pulping processes (sulfite, Kraft, organosolv). Each lignin was analysed by attenuated total reflectance Fourier transform infrared (ATR-FT-IR) spectroscopy. Statistical analysis of the ATR-FT-IR spectra by means of principal component analysis (PCA) showed significant differences between the lignins. Hence, the samples can be separated by PCA according to the original biomass. The differences observed in the ATR-FT-IR spectra result primarily from the relative ratios of the p-hydroxyphenyl, guaiacyl and syringyl units. Only limited influence of the pulping process is reflected by the spectral data. The spectra do not differ between samples processed by Kraft or organosolv processes. Lignosulfonates are clearly distinguishable by ATR-FT-IR from the other samples. For the classification a model was created using the k-nearest neighbor (k NN) algorithm. Different data pretreatment steps were compared for k=1…20. For validation purposes, a 5-fold cross-validation was chosen and the different quality criteria Accuracy (Acc), Error Rate (Err), Sensitivity (TPR) and specificity (TNR) were introduced. The optimized model for k=4 gives values for Acc = 98.9 %, Err = 1.1 %, TPR = 99.2 % and TNR = 99.6 %. KW - Classification KW - PCA KW - K-nearest neighbor KW - FT-IR KW - Technical lignin PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-533855 DO - https://doi.org/10.1002/cmtd.202100028 VL - 1 IS - 8 SP - 350 EP - 396 PB - Wiley-VCH GmbH AN - OPUS4-53385 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. R. A1 - Weidner, Steffen A1 - Meyer, A. T1 - High Tm linear poly(L-lactide)s prepared via alcohol-initiated ROPs of L-lactide N2 - Alcohol-initiated ROPs of L-lactide were performed in bulk at 160 °C for 72 h with variation of the catalyst or with variation of the initiator (aliphatic alcohols). Spontaneous crystallization was only observed when cyclic Sn(II) compounds were used as a catalyst. Regardless of initiator, high melting crystallites with melting temperatures (Tm) of 189–193 °C were obtained in almost all experiments with Sn(II) 2,2′-dioxybiphenyl (SnBiph) as catalyst, even when the time was shortened to 24 h. These HTm poly(lactide)s represent the thermodynamically most stable form of poly(L-lactide). Regardless of the reaction conditions, such high melting crystallites were never obtained when Sn(II) 2-ethylhexanoate (SnOct2) was used as catalyst. SAXS measurements evidenced that formation of HTm poly(L-lactide) involves growth of the crystallite thickness, but chemical modification of the crystallite surface (smoothing) seems to be of greater importance. A hypothesis, why the “surface smoothing” is more effective for crystallites of linear chains than for crystallites composed of cycles is discussed. KW - Polylactide KW - MALDI-TOF MS KW - Ring-opening polymerization PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-524330 DO - https://doi.org/10.1039/d1ra01990b VL - 11 IS - 23 SP - 14093 EP - 14102 PB - Royal Society of Chemistry AN - OPUS4-52433 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. R. A1 - Weidner, Steffen T1 - ROP of L-lactide and ε-caprolactone catalyzed by tin(ii) andtin(iv) acetates–switching from COOH terminated linear chains to cycles N2 - The catalytic potential of tin(II)acetate, tin(IV)acetate, dibutyltin-bis-acetate and dioctyl tin-bis-acetate was compared based on polymerizations of L-lactide conducted in bulk at 160 or 130°C. With SnAc2 low-Lac/Cat ratios (15/1–50/1) were studied and linear chains having one acetate and one carboxyl end group almost free of cyclics were obtained. Higher monomer/catalyst ratios and lower temperatures favored formation of cycles that reached weight average molecular weights (Mw's) between 100,000 and 2,500,000. SnAc4 yielded mixtures of cycles and linear species under all reaction conditions. Dibutyltin- and dioctyl tin bis-acetate yielded cyclic polylactides under most reaction conditions with Mw's in the range of 20,000–80,000. Ring-opening polymerizations performed with ε-caprolactone showed similar trends, but the formation of COOH-terminated linear chains was significantly more favored compared to analogous experiments with lactide. The reactivity of the acetate catalysts decreased in the following order: SnAc2> SnAc4>Bu2SnAc2~Oct2SnAc2 KW - Polylactide KW - MALDI-TOF MS KW - Catalyst KW - Ring-opening polymerization KW - Tin acetates PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-521923 DO - https://doi.org/10.1002/pol.20200866 VL - 59 IS - 5 SP - 439 EP - 450 PB - Wiley Online Library AN - OPUS4-52192 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. R. A1 - Scheliga, F. A1 - Weidner, Steffen T1 - What does conversion mean in polymer science? N2 - The definition of the term “conversion” is discussed for a variety of polymer syntheses. It is demonstrated that in contrast to organic and inorganic chemistry several different definitions are needed in polymer science. The influence of increasing conversion on structure and topology of homo- and Copolymers is illustrated. Chain-growth polymerizations, such as radical polymerization or living anionic polymerizations of vinyl monomers, condensative chain polymerization, two and three-dimensional step-growth polymerizations, ring–ring or chain–chain equilibration and chemical modification of polymers are considered. KW - Polymers KW - Polymerization KW - Conversion KW - Polycondensation PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-523597 DO - https://doi.org/10.1002/macp.202100010 VL - 222 IS - 8 SP - 10 PB - Wiley VCH AN - OPUS4-52359 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. R. A1 - Weidner, Steffen A1 - Falkenhagen, Jana T1 - The role of transesterifications in reversible polycondensations and a reinvestigation of the Jacobson-Beckmann-Stockmayer experiments N2 - The polycondensations of adipic acid and 1,10-decanediol catalyzed by toluene sulfonic acid (TSA) were reinvestigated using MALDI TOF mass spectrometry and NMR spectroscopy. Unexpected reactions of TSA were detected along with incomplete conversion of the monomers. Furthermore, transesterification reactions of end-capped poly(1,10-decanediol adipate) and end-capped poly(ε-caprolactone) catalyzed by TSA were studied. Despite the quite different (ionic) reaction mechanisms, it was found that for polycondensations performed in bulk intermolecular transesterification is more efficient than the intramolecular “back-biting”; this scenario was not considered in the Jacobson–Stockmayer theory of reversible polycondensations. These results also confirm that the Jacobson–Stockmayer explanation of reversible polycondensations solely on the basis of ring chain equilibration is not only devoid of any experimental evidence, but also in contradiction to the results elaborated in this work. KW - Polylactide KW - MALDI-TOF MS KW - Polycondensation PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-543402 DO - https://doi.org/10.1039/d1py01679b SN - 1759-9962 SP - 1 EP - 9 PB - RSC Publ. CY - Cambridge AN - OPUS4-54340 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. R. A1 - Weidner, Steffen A1 - Scheliga, F. T1 - Ring-Expansion Polymerization of 𝝐-Caprolactone, Glycolide, and l-lactide with a Spirocyclic Tin(IV) Catalyst Derived from or 2,2′-Dihydroxy-1,1′-Binaphthyl – New Results and a Revision N2 - In contrast to other cyclic tin bisphenoxides, polymerizations of glycolide and l-lactide with the spirocyclic tin(IV) bis-1,1′-bisnapthoxide yield linear chains having a 1,1′-bisnapthol end group and no cycles. In the case of l-lactide, LA/Cat ratio and temperature are varied and at 160 °C or below, all polylactides mainly consist of even-numbered chains. A total predominance of even-numbered chains is also found for homopolymerization of glycolide, or the copolymerization of glycolide and l-lactide, when conducted <120 °C. Linear chains having a bisnaphthol end group are again the main reaction products of ring-expansion polymerizations (REP) of 𝝐-caprolactone, but above 150 °C cycles are also formed. KW - Polylactide KW - MALDI-TOF MS KW - Polymerization PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-541931 DO - https://doi.org/10.1002/macp.202100308 VL - 222 IS - 24 SP - 1 EP - 10 PB - Wiley VCH GmbH AN - OPUS4-54193 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Chandna, Sanjam A1 - Povolotsky, Tatyana L. A1 - Nie, Chuanxiong A1 - Schwartz, Sophia A1 - Wedepohl, Stefanie A1 - Quaas, Elisa A1 - Ludwig, Kai A1 - Boyakova, Yulia A1 - Bhatia, Sumati A1 - Meyer, Klas A1 - Falkenhagen, Jana A1 - Haag, Rainer A1 - Block, Stephan T1 - Lignin-Based Mucus-Mimicking Antiviral Hydrogels with Enzyme Stability and Tunable Porosity N2 - Mucus is a complex hydrogel that acts as a defensive and protective barrier in various parts of the human body. Therise in the level of viral infections has underscored the importance of advancing research into mucus-mimicking hydrogels for theefficient design of antiviral agents. Herein, we demonstrate the gram-scale synthesis of biocompatible, lignin-based virus-bindinginhibitors that reduce waste and ensure long-term availability. The lignin-based inhibitors are equipped with sulfate moieties, whichare known binding partners for many viruses, including SARS-CoV-2 and herpes viruses. In addition, cross-linking the synthesizedinhibitors yielded hydrogels that mimicked native mucus concerning surface functionality and rheology. The degree of sulfationexhibits a very strong impact on the mesh size distribution of the hydrogels, which provides a new means to fine-tune the steric andelectrostatic contributions of the virus−hydrogel interaction. This feature strongly impacts the sequestration capability of the lignin-based hydrogels, which is demonstrated by infection inhibition assays involving human herpes simplex virus 1, influenza A viruses,and the bacterium Escherichia coli (E. coli). These measurements showed a reduction in plaque-forming units (HSV-1) and colony-forming units (E. coli) by more than 4 orders of magnitude, indicating the potent inhibition by the lignin-based hydrogels KW - Lignin functionalization KW - Mucus-mimicking hydrogels PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-625301 DO - https://doi.org/10.1021/acsami.4c18519 SP - 1 EP - 14 PB - American Chemical Society (ACS) CY - USA AN - OPUS4-62530 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Falkenhagen, Jana A1 - Dalgic, Mete-Sungur A1 - Weidner, Steffen T1 - Quantitative MALDI-TOF Mass Spectrometry of Star-Shaped Polylactides Based on Chromatographic Hyphenation N2 - The end groups of three- and four-arm star-shaped polylactides (PLA) with trimethylolpropane and pentaerythritol core structures were functionalized with acetic acid. Reaction products with different degrees of functionalization were analyzed by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. Additional gradient elution liquid adsorption chromatography (GELAC) measurements were performed to determine the degree of functionalization. This technique enabled clear separation and sufficient quantification of the formed species. These chromatographic data could be used inversely to quantify mass spectrometric results, which are usually biased by the unknown ionization probabilities of different polymer end group structures. Our results showed that, in this particular case, the peak intensity in the MALDITOF mass spectra can be used to semiquantitatively determine the degree of functionalization in incompletely functionalized multiarm PLA. KW - Polylactides KW - MALDI-TOF-MS KW - Gradient elution liquid adsorption chromatography PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-625292 DO - https://doi.org/10.1021/jasms.4c00491 SN - 1879-1123 SP - 1 EP - 9 PB - American Chemical Society (ACS) AN - OPUS4-62529 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -