TY - CONF A1 - Hübler, Daniela T1 - Tribological behavior and cutting performance of a NbC-Ni-WC-TiC cermet N2 - The addition of WC and TiC in a nickel bonded NbC cermet was investigated regarding the tribological behavior under dry oscillating sliding at different relative humidities φ and the cutting performance in dry cylindrical turning of C45E at different cutting speeds. NbC-12Ni-12WC-14TiC shows similar coefficient of friction f and wear rate compared to NbC-12Ni at φ = 2 %, but no pronounced decrease in f with increasing humidity. When turning C45E, NbC-12Ni-12WC-14TiC shows lower material removal VW compared to other NbC-based cermets, which can be attributed to inhomogeneities in the cutting material and a low hardness. T2 - 7th World Tribology Congress - WTC 2022 CY - Lyon, France DA - 11.07.2022 KW - Niobium carbide KW - NbC cermets KW - Tribology KW - Dry cylindrical turning PY - 2022 AN - OPUS4-56042 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Steinhäuser, Lorin A1 - Piechotta, Christian A1 - Westphalen, Tanja A1 - Kaminski, Katja T1 - Evaluation, comparison and combination of molecularly imprinted polymer solid phase extraction and classical solid phase extraction for the preconcentration of endocrine disrupting chemicals from representative whole water samples N2 - Estrogens are endocrine disrupting chemicals and of high concerns due to demonstrated harmful effects on the environment and low effect levels. For monitoring and risk assessment, several estrogens were included in the "watch list" of the EU Water Framework Directive which sets very low environmental quality standard (EQS) levels for Estrone (E1) and 17β-Estradiol (E2) of 0.4 ng L−1 and for 17α-Ethinylestradiol (EE2) of 0.035 ng L−1 requiring sensitive detection methods, as well as extensive sample preparation. A sensitive, derivatization-free, isotope dilution calibration HPLC-MS/MS method for a panel of 5 selected estrogens (including the 3 estrogens of the EU WFD watchlist), and a procedure for the reproducible preparation of a representative whole water matrix including mineral water, humic acids and solid particulate matter are presented. These are used in a diligent comparison of classical solid phase extraction (SPE) on hydrophilic-lipophilic balanced (HLB) phase to SPE on an estrogen-specific molecularly imprinted polymer phase (MISPE) for ultra-trace levels of the analytes (1–10 ng L−1). Additionally, a two-step procedure combining HLB SPE disks followed by MISPE is evaluated. The tow-step procedure provides superior enrichment, matrix removal and sample throughput while maintaining comparable recovery rates to simple cartridge SPE. Estimated method quantification limits (MQLs) range from 0.109–0.184 ng L−1 and thus meet EQS-levels for E1 and E2, but not EE2. The representative whole water matrix provides a reproducible comparison of sample preparation methods and lays the foundation for a certified reference material for estrogen analysis. The presented method will serve as the basis for an extended validation study to assess its use for estrogen monitoring in the environment. KW - Estrogens KW - Whole water samples KW - Molecular imprinted polymers KW - EU-WFD PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-563547 DO - https://doi.org/10.1016/j.talo.2022.100163 SN - 2666-8319 VL - 6 SP - 1 EP - 5 PB - Elsevier B.V. CY - Amsterdam, Niederlande AN - OPUS4-56354 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Stawski, Tomasz T1 - Particle-mediated origins of mesocrystalline disorder in calcium sulfate single crystals N2 - Calcium sulfate minerals are abundant in natural and engineered environments and they exist in the form of three hydrates: gypsum (CaSO4·2H2O), bassanite (CaSO4·0.5H2O), and anhydrite (CaSO4). Due to their relevance in natural and industrial processes, the formation pathways of these calcium sulfate phases from aqueous solution have been the subject of intensive research1. The state-of-the-art of the calcium sulfate formation mechanisms builds upon and goes beyond what we have come to appreciate in the astounding intricacy of other mineral formation processes from ions in aqueous solutions. The original, and rather naive, 'textbook' image of these phenomena, stemming from the adaptation of classical nucleation and growth theories, has increased in complexity due to the discovery of a variety of precursor and intermediate species2. These include solute clusters (e.g. prenucleation clusters, PNCs), liquid(-like) phases, as well as amorphous and nanocrystalline solids etc.. In this context, a number of studies have already revealed that nucleation in the CaSO4-H2O system is non-classical, where the formation of the different crystalline phases involves several steps including a common amorphous precursor1, 3, 4. In this contribution we show that the formation of the amorphous phase involves the aggregation of small primary particles into larger disordered aggregates exhibiting a "brick-in-the-wall" structure5, 6. The actual crystallization occurs by the restructuring and coalescence of the particles ("bricks") into a given calcium sulfate phase depending on the physicochemical conditions of the solution. Importantly, the rearrangement process does not continue until a (nearly-)perfect homogeneous single crystal is obtained. Instead it comes to a stop, or at least significantly slows down. Such a process thus yields a final imperfect mesocrystal, composed of smaller domains rather than a continuous crystal structure, within which the domains are separated by an amorphous (i.e. less ordered) calcium sulfate phase. Hence, the non-classical crystallization process of CaSO4 yields a final imperfect mesocrystal with an overall morphology resembling that of a single crystal, yet composed of smaller nano-domains. Importantly, these observations reveal that organic-free calcium sulfate mesocrystals grown by a particle mediated-pathway preserve in the final crystal structure a “memory” or “imprint” of their non-classical nucleation process, something that has been overlooked until now. Furthermore, the nano-scale misalignment of the structural sub-units within these crystals can propagate through the length-scales, and be expressed macroscopically as misaligned zones/domains in large single crystals. Indeed, by considering large anhydrite crystals from the famous Naica Mine (“Cueva de los cristales”) we observed a suite of correlated self-similar void defects spanning multiple length-scales7. These flaws, in the macroscopic crystal, stem from “seeds of imperfection” originating from a particle-mediated nucleation pathway. Hence, building a crystal could be viewed as Nature stacking blocks in a game of Tetris, whilst slowly forgetting the games core concept and failing to fill rows completely. T2 - ECCG: European Conference on Crystal Growth 7 CY - Paris, France DA - 25.07.2022 KW - Anhydrite KW - SAXS KW - Single crystal KW - Mesocrystal PY - 2022 AN - OPUS4-56276 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Frenzel, Olivia T1 - Identification of Metabolites and Transformation Products of Bisphenols N2 - Bisphenol A (BPA) is widely used in Polycarbonate (PC), Polyacrylic resins (PAR), Polysulfones (PSU), Epoxy resins (ER), and Polyetherimides (PEI). It is also used in recycled Polyvinyl chloride (PVC) [1–3]. These BPA-containing materials have a wide area of application, especially outside. All outdoor applications are exposed to a variety of environmental impacts, like temperature, solar radiation (physical influences), chemical influences (rain or ozone), biological influences (microorganisms), and mechanical influences (hail, sand). These impacts are damaging and aging the material which can be followed by leaching or migration of pollutants like Bisphenol A into the environment. Understanding the fate and behavior of the released pollutants is very important. Therefore, different transformation products of selected Bisphenols will be generated and analyzed. T2 - 33rd International Symposium on Chromatography – ISC 2022 CY - Budapest, Hungary DA - 18.09.2022 KW - Environment KW - Transformation products KW - Bisphenols KW - Metabolites KW - Wastewater PY - 2022 AN - OPUS4-56202 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Frenzel, Olivia T1 - Identification of transformation products and metabolites of selected Bisphenols N2 - Bisphenol A (BPA) is widely used in many Polymers. Many outdoor applications are made from BPA-based materials which are exposed to a variety of environmental impacts, like temperature, solar radiation, rain, and others. This could lead to damaging and aging of the material which might cause leaching or migration of pollutants into the environment. To understand the fate and behavior different transformation products of selected Bisphenols will be generated and analyzed. T2 - Umwelt2022 CY - Emden, Germany DA - 05.09.2022 KW - Environment KW - Bisphenols KW - Transformation products KW - Metabolites KW - Wastewater PY - 2022 AN - OPUS4-56203 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Neumann, Patrick P. T1 - Mobile Applications with Drones/Robots - Aerial- and Ground-based Gas Tomography N2 - Remote gas sensors mounted on mobile robots enable the mapping of gas distributions in large or poorly accessible areas. A challenging task however, is the generation of three-dimensional distribution maps from these spatially sparse gas measurements. To obtain high-quality reconstructions, the choice of optimal measuring poses is of great importance. Remote gas sensors, that are commonly used in Robot Assisted Gas Tomography (RAGT), require reflecting surfaces within the sensor’s range, limiting the possible sensing geometries, regardless of whether the robots are ground-based or airborne. By combining ground and aerial robots into a heterogeneous swarm whose agents are equipped with reflectors and remote gas sensors, remote inter-robot gas measurements become available, taking RAGT to the next dimension – releasing those constraints. In this paper, we demonstrate the feasibility of drone-to-drone measurements under realistic conditions and highlight the resulting opportunities. T2 - ISOCS Short Course Winter 2023 CY - Bormio, Italy DA - 16.01.2023 KW - Aerial robot KW - Ground robot KW - Gas tomography KW - Inter-robot measurements KW - Plume KW - TDLAS PY - 2023 AN - OPUS4-56872 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Vogel, Christian A1 - Simon, Franz-Georg A1 - Scholz, Philipp T1 - The chemical state of antimony and vanadium species in municipal solid waste incineration bottom ash N2 - Due to the large quantity as residual mineral waste, municipal solid waste incineration - bottom ash (MSWI-BA) is an interesting secondary raw material that can be utilized for road construction. However, leaching of chloride, sulfate and potentially hazardous heavy metals from MSWSI-BA into the environment may cause problems in utilization of it in civil engineering. In a previous study, we performed a long-term leaching test of MSWI-BA in a lysimeter for almost six years to investigate the efficiency of the treatment process on the release of hazardous substances. While concentrations of chloride, sulfate and the majority of the heavy metals started to decrease rapidly with progressive liquid-to-solid ratio (L/S), the ecotoxic hazardous elements antimony (Sb) and vanadium (V) behaved differently. To unravel these unusual release behaviors and the oxyanion-formation of Sb and V we will apply HERFD-XANES spectroscopy to analyze their chemical state. KW - Bottom ash KW - Antimony KW - Vanadium KW - XANES PY - 2023 DO - https://doi.org/10.15151/ESRF-ES-1020936484 PB - European synchroton Radiation Facility ESRF CY - Grenoble AN - OPUS4-56875 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Braymer, Joseph J. T1 - Cytosolic Fe/S Protein Biogenesis -a focus on [2Fe-2S] proteins- N2 - Iron-Sulfur (Fe/S) protein biogenesis in the cytosol is an essential process for the proper maturation of many proteins and enzymes required for cellular function. Between the two types of Fe/S cofactors, recent work has been uncovering the dependencies of [2Fe-2S] cluster on the known Fe/S protein biogenesis machineries and how they may be trafficked in the cytosol. New insights will here be discussed in addition to the discovery of a newly identified cytosolic [2Fe-2S] binding protein. T2 - DFG SPP1927 Final Meeting CY - Potsdam, Germany DA - 29.09.2024 KW - Metalloproteins KW - Iron-sulfur clusters KW - Spectroscopy KW - Yeast PY - 2024 AN - OPUS4-61516 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - INPR A1 - Langer, Carlotta A1 - Georgie, Yasmin Kim A1 - Porohovoj, Ilja A1 - Hafner, Verena Vanessa A1 - Ay, Nihat T1 - Analyzing Multimodal Integration in the Variational Autoencoder from an Information-Theoretic Perspective N2 - Human perception is inherently multimodal. We integrate, for instance, visual, proprioceptive and tactile information into one experience. Hence, multimodal learning is of importance for building robotic systems that aim at robustly interacting with the real world. One potential model that has been proposed for multimodal integration is the multimodal variational autoencoder. A variational autoencoder (VAE) consists of two networks, an encoder that maps the data to a stochastic latent space and a decoder that reconstruct this data from an element of this latent space. The multimodal VAE integrates inputs from different modalities at two points in time in the latent space and can thereby be used as a controller for a robotic agent. Here we use this architecture and introduce information-theoretic measures in order to analyze how important the integration of the different modalities are for the reconstruction of the input data. Therefore we calculate two different types of measures, the first type is called single modality error and assesses how important the information from a single modality is for the reconstruction of this modality or all modalities. Secondly, the measures named loss of precision calculate the impact that missing information from only one modality has on the reconstruction of this modality or the whole vector. The VAE is trained via the evidence lower bound, which can be written as a sum of two different terms, namely the reconstruction and the latent loss. The impact of the latent loss can be weighted via an additional variable, which has been introduced to combat posterior collapse. Here we train networks with four different weighting schedules and analyze them with respect to their capabilities for multimodal integration. KW - Multimodal Integration KW - Variational Autoencoder KW - Information Theory KW - Posterior Collapse PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-616420 DO - https://doi.org/10.48550/arXiv.2411.00522 SP - 1 EP - 17 PB - Cornell University CY - Ithaca, NY AN - OPUS4-61642 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hauschildt, Charlotte T1 - Development of methods to improve measurements of PFAS using GC-MS N2 - Per- and polyfluoroalkyl substances (PFAS) are a class of synthetically produced chemicals that includes an estimated 10.000 compounds. Known as “forever chemicals”, the characteristic feature is the complete or partial fluorination of the carbon chain. Due to the persistence, toxicity and ubiquitous occurrence, research has focused on the quali- and quantification of the most important compounds as well as on the investigation of toxicity and possible routes of entry over the last 10 years [1, 2]. Since 2022, four perfluorocarboxylic- and sulfonic acids have been regulated in food for the first time [3] . Liquid chromatography - mass spectrometry is the analytical standard used to test for PFAS, as the spectrum of detectable compounds is significantly more comprehensive than it is currently the case with gas chromatography - mass spectrometry (GC-MS). However, to be able to test for PFAS contamination in a more process-independent manner and to make the analysis more widely accessible, methods based on GC-MS are currently being developed. Since GC-MS methods only cover a fraction of the compounds belonging to the PFAS group so far, further development of the corresponding measurement methods is inevitable [2]. The here described project is part of the EU project 23IND13 ScreenFood [4]. The aim is to develop sensitive analytical GC-MS methods that contribute to an improved quali- and quantification of various PFAS (both currently regulated and emerging PFAS) in selected food and food packaging matrices. Of particular interest are native and recycled polymers such as PET. Besides, various techniques, including solvent-free variants such as TD-GC-MS, will be tested for a quick and easy analysis. This poster will present the overall project objectives and first results. The project (23IND13, ScreenFood) has received funding from the European Partnership on Metrology, co-financed from the European Union’s Horizon Europe Research and Innovation Programme and by the Participating States. T2 - 11th International Symposium on RECENT ADVANCES IN FOOD ANALYSIS (RAFA) CY - Prague, Czech Republic DA - 05.11.2024 KW - Per- and Polyfluoroalkyl Substances (PFAS) KW - Gas Chromatography - Mass Spectrometry (GC-MS) KW - EU Project KW - Food KW - Food Contact Material (FCM) PY - 2024 AN - OPUS4-61667 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hauschildt, Charlotte T1 - Method development for improved PFAS quantification using GC-MS N2 - Per- and polyfluoroalkyl substances (PFAS), commonly known as "forever chemicals”, are a class of man-made chemicals comprising an estimated 10.000 different compounds. The characteristic feature of PFAS is the complete or partial fluorination of the carbon chain. Due to the persistence, toxicity, and ubiquitous presence, research has focused on the identification and quantification of the most significant compounds, as well as exploring their toxicity and potential entry routes over the past decades [1,2]. Since 2022, four perfluorocarboxylic- and sulfonic acids have been regulated in food for the first time [3]. For the detection of PFAS liquid chromatography-mass spectrometry (LC-MS) is the standard analytical method, as it offers a much broader range of detectable compounds compared to gas chromatography-mass spectrometry (GC-MS). However, to enable more versatile testing and make PFAS analysis more widely accessible, new methods based on GC-MS are currently being developed. Since GC-MS methods only cover a fraction of the compounds belonging to the PFAS group so far, further development of the corresponding measurement methods is inevitable [2]. The work described here is part of the EU initiative 23IND13 ScreenFood [4]. Its goal is to develop sensitive GC-MS analytical methods to improve the identification and quantification of various PFAS - both those currently regulated and emerging - within selected food and food packaging matrices. Of particular interest are native and recycled polymers such as PET. Besides, various techniques, including solvent-free variants such as thermal desorption GC-MS, will be tested for a quick and easy analysis. This poster will present the project's main objectives and initial results. The project (23IND13, ScreenFood) has received funding from the European Partnership on Metrology, co-financed from the European Union’s Horizon Europe Research and Innovation Programme and by the Participating States. T2 - Adlershofer Forschungsforum (AFF) CY - Berlin, Germany DA - 11.11.2024 KW - Per- and Polyfluoroalkyl Substances (PFAS) KW - Gas Chromatography - Mass Spectrometry (GC-MS) KW - EU Project KW - Food KW - Food Contact Material (FCM) PY - 2024 AN - OPUS4-61668 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vo, P. H.N. A1 - Vogel, Christian A1 - Nguyen, H. T.M. A1 - Hamilton, B. R. A1 - Thai, P. K. A1 - Roesch, Philipp A1 - Simon, Franz-Georg A1 - Mueller, J. F. T1 - µ-X-ray fluorescence (XRF) and fluorine K-edge µ-X-ray absorption near-edge structure (XANES) spectroscopy for detection of PFAS distribution in the impacted concrete N2 - An improved understanding of the distribution of per- and polyfluoroalkyl substances (PFAS) in PFAS-impacted concrete is important for risk management and decontamination of PFAS. This study incorporates µ-X-ray fluorescence (µ-XRF) and fluorine K-edge µ-X-ray absorption near-edge structure (µ-XANES) spectroscopy to gain non-destructive insights into PFAS distribution in the impacted concrete. The μ-XRF and μ-XANES spectroscopy provided additional details on the detection of PFAS, which were not detected by the desorption electrospray ionization (DESI) imaging method conducted previously. The shorter chain PFAS were found on the top part of the concrete core (0.5 cm), and longer chain PFAS were mostly at the bottom part of the concrete core (5 cm). The inorganic fluorine fraction was also detected, and it likely hampered the detection of organic fluorine such as PFAS in the concrete. Thus, this non-destructive technique is an complementary approach to detect PFAS in contaminated concrete. KW - Beton KW - Per- and Polyfluoroalkyl substances (PFAS) KW - XANES spectroscopy PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-616711 DO - https://doi.org/10.1016/j.hazl.2024.100134 SN - 2666-9110 VL - 5 SP - 1 EP - 5 PB - Elsevier B.V. AN - OPUS4-61671 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Scharek, Vera T1 - Speciation Analysis of Organo-Tin in Environmental Samples via Electrothermal Vaporization/Inductively Coupled Plasma Mass Spectrometry N2 - Shipping plays a significant role in the global trade. However, it is negatively impacted by the unwanted accumulation of marine organisms on the ship hulls. To prevent the so-called bio-fouling, antifoulant paints containing the organometallic compound tributyltin (TBT) have been used on ship hulls since the 1960s. Compared to the generally considered non-toxic inorganic tin, the endocrine disruptor TBT leads to the endangerment of non-target organisms. The most prominent effects are imposex in snails and shell deformation in oysters. This resulted in a global ban by the International Maritime Organization in 2008. Nevertheless, recent studies have found alarmingly high concentrations in sediment. Organotin compounds (OTCs) are known to persist and accumulate in marine sediments, posing a long-term threat to the environment. Once released from the ship hull, TBT gets effectively absorbed into the sediment. Under anaerobic conditions and the absence of light, the half-life is extended up to several decades. The resuspension and transport of sediment remobilizes butyltin compounds, making them bioavailable even in distant regions. The monitoring of OTCs in sediment is inevitable to conduct a comprehensive risk assessment and a thorough monitoring of pollution. Conventionally, species-specific analysis of OTCs involves (gas-)chromatographic separation after extraction and pre-concentration of the analytes. However, the sample preparation is time-consuming, chemical-intensive, and prone to species-transformation, respectively incomplete extraction. In this context, electrothermal vaporization coupled with inductively coupled plasma-mass spectrometry (ETV/ICP-MS) shows high potential as a rapid and chemical-saving screening tool for OTCs in environmental samples. The main challenge for obtaining correct, quantitative data with direct solid sampling techniques like ETV/ICP-MS is the application of a suitable calibration strategy. In this context, a new quantification method based on on-line isotope dilution analysis has been developed and validated by a reference material with certified OTC content. Our approach overcomes matrix effects while being compatible with commercially available ETV systems. Using an optimized multi-step ETV temperature program, the full separation of OTCs, inorganic tin, and major matrix components could be achieved. Since its use as a screening tool, analyzing OTCs as a sum parameter is beneficial and can complement chromatographic approaches. T2 - European Symposium on Analytical Spectrometry (ESAS) CY - Warsaw, Poland DA - 24.06.2024 KW - Organotin compounds KW - Sediment KW - Electrothermal Vaporization KW - Inductively coupled plasma-mass spectrometry PY - 2024 AN - OPUS4-61621 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Scharek, Vera T1 - Screening for tin-based environmental Pollutants in Sediment via ETV/ICP-MS N2 - Shipping plays a significant role in the global trade. However, it is negatively impacted by the unwanted accumulation of marine organisms on the ship hulls. Antifoulant paints containing the organometallic compound tributyltin (TBT) have been used to prevent the so-called fouling on ship hulls since the 1960s. Compared to the generally considered non-toxic inorganic tin, the endocrine disruptor TBT affects the biological fitness of non-target organisms. The most prominent effects are imposex in snails and shell deformation in oysters. This resulted in a global ban by the International Maritime Organization in 2008, but recent studies have found alarmingly high concentrations in sediment. Once TBT is released from the ship hull, it gets effectively absorbed into the sediment. Under anaerobic conditions and the absence of light, the half-life is extended up to several decades. The resuspension and transport of sediment remobilizes tin organic compounds (OTCs), making them bioavailable even in distant regions. To conduct a comprehensive risk assessment, it is necessary to monitor OTCs in sediment. Conventionally, species-specific analysis of OTCs involves (gas-)chromatographic separation after extraction and pre-concentration of the analytes. However, the sample preparation is time-consuming, chemical-intensive, and prone to species-transformation, respectively incomplete extraction. In this context, electrothermal vaporization coupled with inductively coupled plasma-mass spectrometry (ETV/ICP-MS) shows potential as a fast and automatable screening tool for OTCs in environmental samples. In this study, an ETV/ICP-MS method for the speciation analysis of OTC in environmental samples has been developed. The method was validated by spiking experiments using an OTC-containing, respectively OTC-free certified reference material. With a single ETV temperature program, the full separation of OTCs, inorganic tin, and potentially interfering major matrix components were achieved in three different sediment matrices. Co-vaporization of the individual OTC species could be observed. However, when used as a screening tool for environmental monitoring sum parameter analysis of OTC is beneficial. In conclusion, ETV/ICP-MS, is a fast and convenient tool for monitoring metal-based pollutants at ppb level in the environment. T2 - Analytica conference 2024 CY - Munich, Germany DA - 09.04.2024 KW - Organotin compounds KW - Sediment KW - Electrothermal Vaporization KW - Inductively coupled plasma-mass spectrometry PY - 2024 AN - OPUS4-61622 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Zuliani, T. T1 - Advancing Stable and Long-lived Radiogenic Isotope Ratio Measurements of Environmental Pollutants N2 - The isotopic compositions of elements vary in the environment due to processes such as radioactive decay, cosmic ray spallation, mass-dependent and mass-independent fractionation, and different anthropogenic sources such as industrial activities, nuclear weapon testing, nuclear accidents, as well as natural phenomena long-range atmospheric and water transport, climate change, etc. Isotope ratio data obtained by mass spectrometry now plays an important role as tracers of a multitude of processes in Earth and environmental sciences. Inductively coupled plasma mass spectrometry (ICP-MS) is a widely used technique for detecting variations in isotopic abundances in e.g., environmental samples. Recent advancements in mass spectrometric instrumentation have significantly enhanced sensitivity and precision, enabling the reliable detection of even minute variations in the isotopic composition of most elements with more than one natural isotope. However, to fully realize these new capabilities, a significant analytical challenge remains due to a vast number of analyte/matrix combinations, concomitant matrix effects, spectral interferences, and instrumental isotopic fractionation that must be characterized before and during the measurements. Success in developing new and improved methods for stable and long-lived radiogenic isotope ratio measurements by mass spectrometric methods depends on improvements in the reduction and quantification of uncertainties associated with sample preparation, instrumentation, and external calibration. The goal of this presentation is to show the key findings of the European Partnership on Metrology project “Metrology for the harmonisation of measurements of environmental pollutants in Europe” - MetroPOEM (https://www.npl.co.uk/euramet/metropoem), with a focus on the ICP-MS techniques used for isotope ratio measurements. Several elements were used as model systems for the development and optimisation of sample preparation and measurement procedures, including Li, B, Cr, Cd, Ni, Sb, Pb, and U. Isotope ratios of these elements determined by multi-collector ICP-MS, sector field ICPMS, quadrupole ICP-MS, and ICP-MS/MS will be assessed and compared. Data on their performance will be presented and assessed in terms of accuracy and precision. Comprehensive uncertainty budgets for the determination of the isotope ratios of the selected elements by different calibration approaches will be presented. The presented results will highlight the potential of recent advances in ICP-MS technology. T2 - 11th Nordic Conference on Plasma Spectrochemistry CY - Loen, Norway DA - 09.06.2024 KW - Isotope analysis KW - ICP-MS KW - Measurement uncertainty PY - 2024 AN - OPUS4-61599 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schlegel, Moritz-C. T1 - Considerations for an overall Material Efficiency Index N2 - The material efficiency of products is increasingly addressed in the consumer communication of manufacturers (associations) and as well by policy makers. For instance, EU policies, such as the European Green Deal or the Circular Economy Action Plan, include and indicate sustainability measures related to material efficiency. The strategies and measures address product efficiency far beyond energy efficiency, which has been prioritized and effectively improved due to past policy measures. Now the material efficiency of products is to be increased by considering aspects such as durability, reparability and recyclability. The European Commission has already started to address these material efficiency topics in regulations within the Ecodesign regulatory framework. There is also discussion where and how sustainable product characteristics can be labelled for the information of consumers. A regulation has been passed that requires an energy label including a repairability index for smartphones starting in 2025. Further product groups and product properties such as recyclability and use of post-consumer recycled material might follow. So, the question arises: Should information be combined to reduce the complexity for consumers? Is there potential to develop a consumer labelling including additional sustainability aspects of products such as reuse, refurbishing, remanufacturability? This study analyses opportunities to better flag recyclability, recycled content, durability and reparability. Since the indices are intended to direct consumption toward the most material- and resource-efficient products, the study also presents an approach how these indices could be merged into an overall material efficiency index - possibly a starting point for minimum material efficiency requirements or a labelling opportunity under upcoming Ecodesign-related regulations. T2 - EEDAL'24 - 12th International Conference on Energy Efficiency in Domestic Appliances and Lighting CY - Kitakyushu, Japan DA - 07.10.2024 KW - Material efficiency KW - Recyclability KW - Durability KW - Reparability KW - Ecodesign KW - ESPR PY - 2024 AN - OPUS4-61653 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Melzer, Michael T1 - Good practice definitions for DCCs on temperature- and humidity quantities N2 - Automation in metrological traceability of measurements bears high potential for a more effective quality management with less human interaction and reduced risks from manual data processing. However, this can only be achieved, if the metrological data from the calibration service is provided in a machine-readable and machine-interpretable format. With the provision of an XML-schema for digital calibration certificates (DCCs), PTB has defined a comprehensive frame for machine-readable reports that is applicable to calibrations of arbitrary quantities and methods. In order to increase the interoperability of DCCs, further harmonization needs to be established, especially within the communities of specific measurement quantities. This allows for a straight-forward automation in the processing of DCCs independent from the issuing laboratory. Recently, the German Calibration Service (DKD) has started to compile quantity-specific as well as overarching good practice definitions for DCCs in its various technical committees. The committee for temperature and humidity quantities set the focus on good practice for calibrations according to its guidelines DKD-R 5-1 for resistance thermometers (e.g. Pt100) and DKD-R 5-8 for hygrometers for the direct measurement of relative humidity, first. Here, for several specific expressions, e.g. the used temperature scales (e.g. ITS-90 vs. thermodynamic temperature), the impact of hysteresis and self-heating or the calibration medium used, related XML code implementations are defined and tested. Another important aspect to achieve machine-interpretability of information in a DCC are refType definitions. RefTypes are key semantic providing attributes that are used in the XML code if no unique structure is available in the DCC scheme for a particular information that should still be associated with a specific meaning. Hence, they represent “bookmarks” for the algorithms interpreting good practice DCCs and therefore it is vital that they have a fixed wording. For the case of temperature and humidity calibrations, several refType denotations together with their meanings and allowed locations in the DCC-schema were defined, respectively. These refType definitions will be available in an online refType repository that is hosted by the DKD and can be incorporated into good practice DCCs for validation. The good practice definitions for temperature and humidity DCCs introduced in this contribution will be thoroughly described and published in an open access DKD expert report that is also equipped with validated DCC templates for most common calibration items and procedures. Since most of the added values of an automated metrological traceability are provided on the receiving side of DCCs, specific use cases are currently acquired for temperature and humidity calibrations, respectively. These pilot applications are especially intended to demonstrate the potential of DCC utilization for the industrial metrology and quality management. T2 - IMEKO 2024 XXIV World Congress CY - Hamburg, Germany DA - 26.08.2024 KW - Digital Calibration Certificate KW - QI-digital KW - Digital Metrology KW - Calibration KW - Temperature quantities PY - 2024 UR - https://www.imeko2024.org/home AN - OPUS4-61870 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kilic, Özge T1 - Tracking collective behavioural responses of termites with machine learning pose estimation software N2 - Termites, as eusocial insects, exhibit complex social behaviors critical to their ecological roles. This study employs cutting-edge machine learning techniques, specifically SLEAP pose estimation software, to investigate the interactions of *Reticulitermes flavipes* within controlled environments. By leveraging advanced tracking methods, this research addresses challenges such as track breaks in movement data and uses custom coding solutions to ensure accurate reconnections, preserving the continuity and reliability of individual and group behavior analyses. Custom-designed 3D-printed habitats facilitate controlled observations, while machine learning enables the annotation and tracking of key body segments (mandible, thorax, and abdomen). This approach provides granular insights into colony dynamics, highlighting task differentiation and social clustering. Future applications include the development of automated, continuous recording setups and expanded experiments to examine the impact of varying environmental conditions. This interdisciplinary work, combining biology and data science, advances our understanding of termite social systems and paves the way for predictive simulations of their activity. Such insights contribute to ecological management strategies and deepen our knowledge of collective animal behaviors. T2 - ASAB 2024 CY - Exeter, United Kingdom DA - 21.04.2024 KW - Machine learning KW - Artifical Intelligent KW - Social behaviour KW - 3D Printing KW - Pose estimation KW - Tracking PY - 2024 AN - OPUS4-61830 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Oberbeckmann, Sonja T1 - The Microplastic Microbiome N2 - Microplastics represent man-made and newly emerging surfaces in our ecosystems, where they interact with microorganisms. The ecosystem in focus of this presentation will be the aquatic environment. It will be portrayed, which microorganisms use microplastics as a habitat, how environmental factors shape this colonization, and why the biodegradation of plastics in the ocean is an overall unlikely process. We will also discuss whether potentially pathogenic microorganisms use microplastics as a raft. Finally, possible adaptation mechanisms of plastic-colonizing microorganisms will be presented, such as the production of photoreactive molecules. The microplastic microbiome has a large potential to harbor so far unknown species with curious traits, representing an exciting research topic for the future. T2 - Geomicrobiological and Geochemical Colloquium, GFZ CY - Potsdam, Germany DA - 20.02.2024 KW - Microplastics KW - Microbiome KW - Biofilm PY - 2024 AN - OPUS4-60203 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ladu, Luana T1 - Making the transition to a sustainable and circular bioeconomy N2 - This presentation provides an introduction and intermediate results of the Horizon-Europe STAR4BBS project.It focuses on how to maximize the potential of Sustainability Certification Schemes (SCS) and labels to support a successful transition to a sustainable bio-based economy by assessing their effectiveness, robustness, and credibility. T2 - Sustainability Transition Assessment Rules for Bio-Based Systems (STAR4BBS) CY - Rome, Italy DA - 17.05.2024 KW - Sustainability Certificaiton Schemes KW - Quality Infrastructure KW - Governance indicators KW - Robust certification schemes PY - 2024 AN - OPUS4-60211 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dudziak, Mateusz A1 - Bhatia, Riya A1 - Dey, Rohit A1 - Ullrich, Matthias S. A1 - Schartel, Bernhard T1 - Phosphor-enriched wastewater products as sustainable flame retardant in PLA N2 - Revolutionizing our polymer industry for adaption to a sustainable carbon circular economy has become one of today’s most demanding challenges. Exploiting renewable resources to replace fossil-fuel—based plastics with biopolymers such as poly(lactic acid) (PLA) is inevitable while using waste streams as a raw material resource at least is promising. When it comes to using PLA as technical polymer, its high flammability must be addressed by flame retardants compatible with the thermoplastic processing of PLA and its compostability. This study proposes microalgae enriched with phosphorus from wastewater (P-Algae) as an elegant way towards a kind of sustainable organophosphorus flame retardant. The concept is demonstrated by investigating the processing, pyrolysis, flammability, and fire behavior of PLA/P-Algae, while varying the P-Algae content and comparing P-Algae with four alternative bio-fillers (phosphorylated lignin, biochar, thermally treated sewage sludge, and metal phytate) with different P-contents as meaningful benchmarks. T2 - EcoFRam2024 CY - Valencia, Spain DA - 22.05.2024 KW - PLA KW - Flame retardancy KW - Phosphorylated algae KW - Wastewater flame retardants KW - Zink phytate KW - Phosphorylated lignin KW - Thermally treated sludge PY - 2024 AN - OPUS4-60142 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR ED - Imbert, E. ED - Ladu, Luana T1 - Special issue "Metrics for sustainable chemistry" N2 - This special issue addresses the current need to enhance the conceptual and empirical implementation of sustainability assessment methodologies and related metrics within the GSC (Green and Sustainable Chemistry), collecting 7 papers. KW - Green and sustainable chemistry (GSC) KW - Special issue KW - Sustainability assessment methodologies PY - 2022 UR - https://www.sciencedirect.com/journal/current-opinion-in-green-and-sustainable-chemistry/special-issue/103FS5FCQ68 SN - 2452-2236 SP - 100160 EP - 100844 PB - Elsevier CY - Amsterdam AN - OPUS4-60022 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Leube, Peter T1 - Quantification of ultrashort per- and polyfluoroalkyl substances (PFAS) in water samples via headspace gas chromatography-mass spectrometry (GC-MS) - a method development N2 - Per- and polyfluoroalkyl substances (PFAS) were classified as a group of highly concerning chemicals over the last decades. Because of the high persistence of PFAS, their previous use led to contamination of the environment and human population. Due to ongoing use and incomplete remediation or destruction methods, the PFAS background in the environment is growing continuously. The presence of ultrashort PFAS (with ≤3 carbon atoms) in the environment is often overlooked despite their contributions to PFAS levels. These compounds may directly contaminate the environment and arise from degradation of polyfluorinated compounds as well as incomplete PFAS destruction in certain industrial processes. Nonetheless, few approaches for targeted analysis of ultrashort PFASs have been developed, except for trifluoroacetic acid (TFA). Beside liquid (LC-MS/MS), supercritical fluid (SFC-MS/MS), and ion chromatography (IC-MS)-based systems, gas chromatography coupled with mass spectrometry (GC-MS) is a promising method for detection and quantification of ultrashort PFAS. The goal of this study was to develop a simple headspace GC-MS method for the quantification of ultrashort perfluorocarboxylic acids (PFCAs) and polyfluorinated alcohols (PFOHs) in water samples. In contrast to PFOHs, functionalization of PFCAs was required for quantification. This was done by esterification with methanol at 80 °C, which can be carried out directly in the headspace GC-MS system. Moreover, several parameters were optimized to achieve a low limit of quantification (LOQ) for the analytes used: i) The ratio of the aqueous solution, methanol, and available gas phase within the analysis vessel, ii) the concentration of additional acid in esterification mixtures of PFCAs, iii) shaking frequency and iv) shaking time before analysis. After optimizing the procedure, we were able to quantify ultrashort PFCAs and PFOHs. Thus, our developed headspace GC-MS method has the potential to be used as an alternative target analysis for ultrashort-chain PFCAs and PFOHs in various water samples (groundwater, wastewater). T2 - SETAC Europe 34th Annual Meeting CY - Seville, Spain DA - 05.05.2024 KW - Ultrashort PFAS KW - Headspace GC-MS KW - Perfluorocarboxylic acid (PFCA) KW - Polyfluorinated alcohol (PFOH) PY - 2024 AN - OPUS4-60042 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ronen, A. A1 - Panglisch, S. T1 - Detection, Quantification and Treatment of Per and Polyfluoroalkyl substances (PFAS) in Groundwater N2 - The research project focuses on tackling the detection, measurement, and elimination of per- and polyfluoroalkyl substances (PFAS) from polluted groundwater, with a particular emphasis on addressing short (C4-C7) and ultrashort (C1-C3) chain PFAS. Given the widespread use of PFAS in various products, they are commonly found in groundwater near industrial and military sites in Germany and Israel. Moreover, recent regulations limiting the use of long chain PFAS have led industries to shift towards shorter chain alternatives. Hence, our efforts are geared towards refining detection, quantification, and removal methods for short and ultrashort chain PFAS. In terms of detection, ww are developing passive sampling devices capable of collecting and tracking the temporal distribution of PFAS species in groundwater. This will enable us to analyze contaminations in German and Israeli groundwater using cutting-edge analytical techniques. Additionally, contaminated groundwater will undergo a two-stage treatment process aimed at concentrating the relatively low PFAS concentrations using innovative membrane technologies such as closed-circuit reverse osmosis and mixed matrix composite nanofiltration membrane adsorbers. Subsequently, the streams containing higher PFAS concentrations will be treated through coagulation, with the remaining PFAS being adsorbed onto carbonaceous nanomaterials. The outcome of this research will include the creation of advanced tools for detecting, measuring, and eliminating PFAS from polluted groundwater, while also enhancing our understanding of the scope of these contaminations. T2 - German Israeli Water Technology Status Seminar CY - Koblenz, Germany DA - 18.06.2024 KW - Ground water KW - Per- and Polyfluoroalkyl substances (PFAS) KW - Remediation PY - 2024 AN - OPUS4-60328 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ben Efraim, R. T1 - Comparison of PFAS Adsorption and Electro-Sorption Using Pristine and Functionalized MWCNTs N2 - Per- and polyfluoroalkyl substances (PFAS) have been extensively utilized in various industrial processes, resulting in elevated concentrations in landfills and drinking water reservoirs. Despite recognizing that shortchained PFAS are harmful, they are often overlooked. Short-chain PFAS are more challenging to remove via adsorption and membrane separation processes, and their detection is complex, thus creating a critical gap in understanding their environmental impact. To improve their environmental monitoring, we aim to improve short-chain PFAS adsorption and electro-sorption on novel carbon-based adsorbers such as pristine and functionalized multi-walled carbon nanotubes (MWCNTs) and assess their adsorption mechanisms. Based on the obtained result, we aim to develop a PFAS passive sampling device. T2 - German Israeli Water Technology Status Seminar CY - Koblenz, Germany DA - 18.06.2024 KW - Ground water KW - Per- and Polyfluoroalkyl substances (PFAS) KW - Sorption PY - 2024 AN - OPUS4-60329 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Leube, Peter T1 - Quantification of ultrashort per- and polyfluoroalkyl substances (PFAS) in water samples via headspace gas chromatographymass spectrometry (GC-MS) - a method development N2 - Ultrashort PFAS (≤ 3 carbon atoms) were overlooked for a long time in analytical monitoring. Beside through the use of these substances, they contribute to the PFAS background in the environment through (environmental/ bio-) degradation and incomplete destruction3 of PFAS with longer carbon chains or other fluorinated compounds. As part of the German-Israeli Cooperation in Water Technology Research project „Detection, quantification, and treatment of per- and polyfluoroalkyl substances in groundwater“ (DEFEAT-PFAS), we are developing an as simple as possible direct headspace (HS-)GC-MS method to detect trifluoroacetic acid (TFA) and perfluoropropanioc acid (PFPrA), as well as trifluoroethanol (TFEtOH), pentafluoropropanol(PFPrOH) and hexafluoroiospropanol (HFIP) in water samples. Here we present the results of the PFAS mentioned in spiked ultrapure water solutions. T2 - German Israeli Water Technology Status Seminar CY - Koblenz, Germany DA - 18.06.2024 KW - Ground water KW - Per- and Polyfluoroalkyl substances (PFAS) KW - Gas chromatography - mass spectrometry (GC-MS) PY - 2024 AN - OPUS4-60330 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ronen, A. A1 - Vogel, Christian A1 - Leube, Peter A1 - Ben Efraim, R. A1 - Nir, O. A1 - Chaudhary, M. A1 - Futterlieb, M. A1 - Panglisch, S. T1 - DEFEAT-PFAS: Detection, Quantification, and Treatment of Per- and Polyfluoroalkyl Substances (PFAS) in Groundwater N2 - The research project focuses on tackling the detection, measurement, and elimination of per- and polyfluoroalkyl substances (PFAS) from polluted groundwater, with a particular emphasis on addressing short (C4-C7) and ultrashort (C1-C3) chain PFAS. Given the widespread use of PFAS in various products, they are commonly found in groundwater near industrial and military sites in Germany and Israel. Moreover, recent regulations limiting the use of long chain PFAS have led industries to shift towards shorter chain alternatives. Hence, our efforts are geared towards refining detection, quantification, and removal methods for short and ultrashort chain PFAS. In terms of detection, ww are developing passive sampling devices capable of collecting and tracking the temporal distribution of PFAS species in groundwater. This will enable us to analyze contaminations in German and Israeli groundwater using cutting-edge analytical techniques. Additionally, contaminated groundwater will undergo a two-stage treatment process aimed at concentrating the relatively low PFAS concentrations using innovative membrane technologies such as closed-circuit reverse osmosis and mixed matrix composite nanofiltration membrane adsorbers. Subsequently, the streams containing higher PFAS concentrations will be treated through coagulation, with the remaining PFAS being adsorbed onto carbonaceous nanomaterials. The outcome of this research will include the creation of advanced tools for detecting, measuring, and eliminating PFAS from polluted groundwater, while also enhancing our understanding of the scope of these contaminations. T2 - German Israeli Water Technology Status Seminar CY - Koblenz, Germany DA - 18.06.2024 KW - Ground water KW - Per- and Polyfluoroalkyl substances (PFAS) KW - Remediation PY - 2024 UR - https://indico.scc.kit.edu/event/4029/attachments/7552/12045/Proceedings_Ger-Isr-Coop_Status-Seminar-2024.pdf SP - 33 EP - 36 AN - OPUS4-60331 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dudziak, Mateusz A1 - Schartel, Bernhard T1 - Phosphor-enriched wastewater products as sustainable flame retardant in PLA N2 - Revolutionizing our polymer industry for adaption to a sustainable carbon circular economy has become one of today’s most demanding challenges. Exploiting renewable resources to replace fossil-fuel—based plastics with biopolymers such as poly(lactic acid) (PLA) is inevitable while using waste streams as a raw material resource at least is promising. When it comes to using PLA as technical polymer, its high flammability must be addressed by flame retardants compatible with the thermoplastic processing of PLA and its compostability. This study proposes microalgae enriched with phosphorus from wastewater (P-Algae) as an elegant way towards a kind of sustainable organophosphorus flame retardant. The concept is demonstrated by investigating the processing, pyrolysis, flammability, and fire behavior of PLA/P-Algae, while varying the P-Algae content and comparing P-Algae with four alternative bio-fillers (phosphorylated lignin, biochar, thermally treated sewage sludge, and metal phytate) with different P-contents as meaningful benchmarks. T2 - Polymers for Sustainable Future CY - Prague, Czech Republic DA - 24.06.2024 KW - PLA KW - Flame Retardancy KW - Thermally Treated Sludge KW - Phosphorylated Algae KW - Zink Phytate KW - Wastewater Flame Retardants KW - Phosphorylated Lignin PY - 2024 AN - OPUS4-60619 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - PFAS analysis by fluorine K-edge XANES spectroscopy and thermal and mechanochemical treatment N2 - Per- and polyfluoroalkyl substances (PFAS) are a large group of more than 12,000 organofluorine surfactants. As a result of continuous and prolific use, mainly in aviation firefighting foams, thousands of industrial and military installations have been found to contain contaminated soil, groundwater and surface water. . Current decontamination strategies of PFAS-burdened soils mainly consist of adsorption methods using adsorbents for fixation of PFAS in the ground. A second option is the utilization of a “pump and treat” process, cycling polluted soils through a washing plant leading to the concentration of the pollutants in the fine fraction. Both approaches are cost-intensive and not intended for the direct decomposition of all PFAS contaminants. Furthermore, the contaminated adsorbants have to be safely thermal treated for recovery. Hence, there is a great demand for innovative developments, dealing with new strategies of tackling the PFAS problem. Previously, mechanochemical treatment of polychlorinated organic compounds in soils showed an efficient dechlorination. Thus, we investigated mechanochemical treatment of PFAS contaminated soils with various additives in a ball mill. T2 - SEMICON CY - Tokyo, Japan DA - 12.12.2024 KW - Mechanochemical treatment KW - Per- and Polyfluoroalkyl substances (PFAS) KW - XANES spectroscopy KW - Thermal treatment PY - 2024 AN - OPUS4-62183 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Fuentes, Elsa A1 - Prieto, Beatriz T1 - Effect of climate change on phototrophic biofilms colonizing granitic rocks and their biodeteriogenic activity. N2 - Material cultural heritage from NW of the Iberian Peninsula is linked to the use or presence of granite, whether in historical buildings, sculptures, archaeological sites or any other artistic manifestation. This resistant material has the ideal physical characteristics that favor its longevity, but, like any material exposed to the environment, it is susceptible to deterioration. To this respect, environmental changes due to climate change and global change may modify biological colonization-substrate interactions. The main objective of the present research was to analyse the effects of Climate Change, more specifically changes in water availability, increased temperature, increased CO2 concentrations and changes in UV-B radiation patterns, on the survival and biodeteriogenic activity of phototrophic biofilms on granite heritage and the consequences for the built heritage. Both field and laboratory work were carried out. Field studies were conducted on three rural churches to characterise the current biological colonization. A higher proportion of algae than cyanobacteria was identified, with the genera Trentepohlia and Desmococcus standing out among the former. The most common current fungi are lichenised fungi, but black fungal genera such as Catenulostroma, Rhinocladiella and Knufia were also identified. Bacterial genera related to the production of sphinganes, EPS, carotenoids and some causing the so-called pink discolouration are also present. The effect of climate change on the growth and physiological state of the organisms was analysed in the laboratory. For this purpose, mixed biofilms were developed in the laboratory and exposed to changing conditions of temperature, water availability, CO2 and UV-B. A reduction in growth was observed with increasing water restriction, although in the initial colonization process, rock bioreceptivity was shown to be a more important aspect in favoring anchorage and retention of organisms. Temperature was shown to have a growth-enhancing effect when water availability was low, whereas an increase in CO2 only resulted in increased growth under conditions of high-water availability. Increased UV-B produced a reduction in growth, especially at the highest dose (equivalent to the current dose of a west-facing wall in southern Portugal, which is considered as high), while little difference in the physiological state of the organisms was observed at the current doses in Galicia (considered as medium) and southern Ireland (considered as low). Clear changes in microbial composition were observed, with a trend towards increased or greater resistance of cyanobacteria to higher temperature, lower water availability and higher UV-B doses. In addition, all these changes in development, physiological and microbial composition had an effect on the predominant pigments, tending towards more yellowish-brownish colourations, and on the ability of the organisms to generate biodeterioration by affecting ion concentrations on water solutions by enhancing their consumption or adhesion which lead to granite deterioration. Future work should take into account the combination of a greater number of climatic parameters simultaneously and also the possible resistances associated with the nature of the SAB community studied. T2 - 19th International Biodeterioration and Biodegradation Symposium CY - Berlin, Germany DA - 09.09.2024 KW - Biofilm KW - Granite KW - Climate change KW - Biodeterioration KW - Cultural heritage PY - 2024 AN - OPUS4-62271 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meermann, Björn T1 - Analytical Approaches for PFAS Sum-parameter Analysis – From Materials to Environment N2 - PFAS sind emerging pollutants und sind omnipräsent – sowohl in vielen Produkten als auch in der Umwelt. Aufgrund der Vielzahl an verschiedenen Verbindungen werden dringend neue Analytische Methoden zum Nachweis der PFAS benötigt. Im Rahmen meines eingeladenen Vortrags werden neue elementanalytische Summenparameterverfahren, die in meinem Fachbereich entwickelt wurden, vorgestellt. T2 - Analytisches Seminar Uni Duisburg Essen CY - Duisburg, Germany DA - 26.02.2024 KW - PFAS KW - HR-CS-GFMAS KW - Sum parameter PY - 2024 AN - OPUS4-62240 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meermann, Björn T1 - Analytical Approaches for PFAS Sum-parameter Analysis – From Materials to Environment N2 - PFAS sind emerging pollutants und sind omnipräsent – sowohl in vielen Produkten als auch in der Umwelt. Aufgrund der Vielzahl an verschiedenen Verbindungen werden dringend neue Analytische Methoden zum Nachweis der PFAS benötigt. Im Rahmen meines eingeladenen Vortrags werden neue elementanalytische Summenparameterverfahren, die in meinem Fachbereich entwickelt wurden, vorgestellt. T2 - GDCh Kolloquium CY - Freiberg, Germany DA - 29.05.2024 KW - PFAS KW - HER-CS-GFMAS KW - Evolution of pollution PY - 2024 AN - OPUS4-62241 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meermann, Björn T1 - Element Analytical Methods for a Sustainable Transformation of our Society N2 - Ressourcenknappheit benötigt alternative Strategien, um auch nachfolgenden Generationen eine lebenswerte Welt zu erhalten und einen guten Lebensstandard zu gewährleisten. Ein wesentlicher Beitrag hierzu wird die Transformation unserer Gesellschaft hin zu einer Kreislaufwirtschaft (CEco) sein. Bisher ist unsere Wirtschaft nicht dahingehend ausgelegt – ein wesentlicher Beitrag muss seitens der Analytischen Chemie kommen – nur hierüber können Qualitätsstandards und –kontrolle gewährleistet werden Im Rahmen meines eigeladenen Vortrags werden elementanalytisch Methoden, die in meinem Fachbereich entwickelt/angewendet werden, für eine CEco vorgestellt. T2 - Analytica Conference CY - Munich, Germany DA - 11.04.2024 KW - PFAS KW - HR-CS-GFMAS KW - Sum parameter PY - 2024 AN - OPUS4-62242 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meermann, Björn T1 - Discrete element and isotope analytical methods for a sustainable transformation of our society N2 - Ressourcenknappheit benötigt alternative Strategien, um auch nachfolgenden Generationen eine lebenswerte Welt zu erhalten und einen guten Lebensstandard zu gewährleisten. Ein wesentlicher Beitrag hierzu wird die Transformation unserer Gesellschaft hin zu einer Kreislaufwirtschaft (CEco) sein. Bisher ist unsere Wirtschaft nicht dahingehend ausgelegt – ein wesentlicher Beitrag muss seitens der Analytischen Chemie kommen – nur hierüber können Qualitätsstandards und –kontrolle gewährleistet werden. Im Rahmen meines eigeladenen Vortrags werden elementanalytisch Methoden, die in meinem Fachbereich entwickelt/angewendet werden, für eine CEco vorgestellt. T2 - Summer school CY - Poland DA - 31.07.2024 KW - Elemental analysis KW - Division 1.1 KW - Environment - material PY - 2024 AN - OPUS4-62245 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Heide, K. A1 - Nolze, Gert A1 - Völksch, G. A1 - Heide, G. T1 - Boracite Mg3[B7O13Cl] from the Zechstein salt deposits N2 - Among the borates in the Middle European Zechstein Salt Succession boracite Mg3[B7O13Cl] is the most common mineral in quantity and local distribution. An exceptional enrichment is observed in Stassfurt Serie Z2) in the Stassfurth seam K2H. Boracite is to be found in two varieties: individual crystals in cubic, tetrahedral or dodecahedral habit on the one hand and fibrous crystals so-called “stassfurtite” on the other hand. The formation conditions such widely spread borates in the salt succession are ambiguous in two respects. First of all the synthetic formation of boracites is to be made by hydrothermal or melt conditions. Both processes can be suspended for the salt succession. Furthermore the cubic modification is stable above 265°C for the Mg-boracite. The cubic, tetrahedral or dodecahedral habit could be used as a geothermometer, but such conditions can be exclude by the paragenetic minerals, esp. carnallite (MgKCl3 x 6H2O). The chemical composition of orthorhombic, pseudo-cubic boracite depends on the location. Pure Mg-boracite in hexahedral habit and in fibrous habit, so-called “stassfurtite”, occurs in the North Harz region, whereas the Fe-, Mn-, Mg-boracite appears in the South Harz region. Until now the source of boron, the time of formation of crystals, but also the reasons for the differences in habit of the single hexahedral crystals are still unclear. The formation during a diagenetic/metamorphic process is evident. However, the preferred formation in Stassfurt seam could be an indication for the boron enrichment in an early diagenetic process. Furthermore permit the determination of the thermal stability and the volatile content of crystals conclusions to the chemical composition of the fluid. The observed variation suggests that the condition of crystal growth as well as the chemical composition of fluid repeatedly changed over the time. Randomly occuring xenomorpheous anhydrite and magnesite inclusions within single boracite crystals have been interpreted as an indication to factors of chemical milieu during the formation of crystals. The reversible phase transition temperature of the boracite is a linearly function of the iron and manganese content and varies from 265°C for Mg-boracite to 330°C for Fe(Mn)-boracite. The thermal decomposition of boracite is determined by two processes. The decomposition started with a boron-chlorine release (BOCl?), having a maximum rate at 1050°C. Additionally to this release one observes a simultaneous emission of H2O, HCl, HF, CO2 , N2 , SO2 , H2 , and hydro carbons. The results give evidence for the aged approach of a secondary formation of boracite within the complete Stassfurt seam, possibly in connection with the formation of salt diapirs in the Jura and Cretaceous period. The wider environmental distribution of borates is an indication of chemical transport processes within the salt succession. This should be a more important issue in the discussion about the utilisation of salt diapirs for the storage of nuclear waste. KW - Borate KW - Boracite KW - Thermal behaviour KW - Electron backscatter diffraction KW - Energy-dispersive x-ray spectroscopy PY - 2013 DO - https://doi.org/10.1524/zkri.2013.1633 VL - 228 SP - 467 EP - 475 PB - Oldenbourg Wissenschaftsverlag, München AN - OPUS4-37982 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Reith, F. A1 - Fairbrother, L. A1 - Nolze, Gert A1 - Wilhelmi, O. A1 - Clode, P. L. A1 - Gregg, A. O. A1 - Parsons, J. E. A1 - Wakelin, S. A. A1 - Pring, A. A1 - Hough, R. A1 - Southam, G. A1 - Brugger, J. T1 - Nanoparticle factories: Biofilms hold the key to gold dispersion and nugget formation N2 - Biofilms living on gold (Au) grains play a key role in the biogeochemical cycle of Au by promoting the dispersion of Au via the formation of Au nanoparticles as well as the formation of secondary biomorphic Au. Gold grains from Queensland, Australia, are covered by a polymorphic, organic-inorganic layer that is up to 40 μm thick. It consists of a bacterial biofilm containing Au nanoparticles associated with extracellular polymeric substances as well as bacterioform Au. Focused ion beam (FIB) sectioning through the biofilm revealed that aggregates of nanoparticulate Au line open spaces beneath the active biofilm layer. These aggregates (bacterioform Au type 1) resulted from the reprecipitation of dissolved Au, and their internal growth structures provide direct evidence for coarsening of the Au grains. At the contact between the polymorphic layer and the primary Au, bacterioform Au type 2 is present. It consists of solid rounded forms into which crystal boundaries of underlying primary Au extend, and is the result of dealloying and Ag dissolution from the primary Au. This study demonstrates that (1) microbially driven dissolution, precipitation, and aggregation lead to the formation of bacterioform Au and contribute to the growth of Au grains under supergene conditions, and (2) the microbially driven mobilization of coarse Au into nanoparticles plays a key role in mediating the mobility of Au in surface environments, because the release of nanoparticulate Au upon biofilm disintegration greatly enhances environmental mobility compared to Au complexes only. KW - Nanomaterial KW - Gold KW - Electron backscatter diffraction PY - 2010 DO - https://doi.org/10.1130/G31052.1 VL - 38 IS - 9 SP - 843 EP - 846 PB - Geological Society of America AN - OPUS4-37995 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schoknecht, Ute T1 - Leaching of biocides from organic coatings N2 - Biocide leaching was investigated for acrylate and polymer based coatings containing biocides either as liquid formulations or microcapsules. Laboratory and field tests indicate similar relations of results on carbendazim, diuron, terbutryn and OIT from different coatings in laboratory and field experiments. Emissions were higher in EN 16105 laboratory tests than from vertically installed test specimens exposed to weathering, and slower for microencapsulated biocides. Competing processes that cause losses of active substances can occur in both tests, but to a higher degree in field experiments. Emission curves related to runoff water were similar in repeated field experiments. Relative humidity, temperature and global radiation were identified as meteorological factors that affect leaching by complex interaction besides the amount of driving rain. T2 - Advances in Coatings Technology CY - Sosnowiec, Poland DA - 08.11.2016 KW - Biocide KW - Coating KW - Leaching PY - 2016 AN - OPUS4-38234 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schoknecht, Ute A1 - Mathies, Helena A1 - Wegner, R. A1 - Uhlig, S. A1 - Baldauf, H. A1 - Colson, B. T1 - Leaching of biocides from organic coatings N2 - Biocide leaching was investigated for acrylate and vinyl acetate based coatings containing biocides either as liquid formulations or microcapsules. Laboratory and field tests indicate similar relations of results on carbendazim, diuron, terbutryn and OIT from different coatings in laboratory and field experiments. Emissions were higher in EN 16105 laboratory tests than from vertically installed test specimens exposed to weathering, and slower for microencapsulated biocides. Competing processes that cause losses of active substances can occur in both tests, but to a higher degree in field experiments. Emission curves related to runoff water were similar in repeated field experiments. Relative humidity, temperature and global radiation were identified as meteorological factors that affect leaching by complex interaction besides the amount of driving rain. T2 - 12th International Conference 'Advances in Coatings Technology ACT´16' CY - Sosnowiec, Poland DA - 08.11.2016 KW - Biocide KW - Leaching KW - Coating PY - 2016 SN - 978‒83‒63555‒50‒4 SP - Paper 51, 1 EP - 10 AN - OPUS4-38236 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bartholmai, Matthias A1 - Neumann, Patrick P. T1 - Leak detection with linear soil gas sensors under field conditions - First experiences running a new measurement technique N2 - A 400 m² soil test field with gas injection system was built up, which enables an experimental validation of linear gas sensors for specific applications and gases in an application-relevant scale. Several injection and soil watering experiments with carbon dioxide (CO2) at different days with varying boundary conditions were performed indicating the potential of the method for, e.g., rapid leakage detection with respect to Carbon Capture and Storage (CCS) issues. T2 - IEEE Sensors 2016 CY - Orlando, FL, USA DA - 30.10.2016 KW - Soil test field KW - Membrane-based linear gas sensor KW - Leak detection KW - Field conditions PY - 2016 AN - OPUS4-38247 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Lehnik-Habrink, Petra T1 - Human influences on forest soil - pollution with PAH, PCB and OCP in Germany N2 - While organic pollutants have been extensively studied in urban and agricultural areas, data from forested regions are relatively rare. Within the framework of a forest soil inventory in Germany polycyclic aromatic hydrocarbons (PAH), polychlorinated biphenyls (PCB) and organochlorine pesticides (OCP) were analyzed in 1500 soil samples taken from 3 soil horizons at 447 sites. An analytical protocol was developed and validated for the simultaneous extraction and measurement of all analytes in humic rich soil at trace level range. It included pressurized liquid extraction (PLE) and a two step cleanup procedure consisting of gel permeation chromatography (GPC) followed by solid phase extraction (SPE). Quantification was carried out using gas chromatography combined with mass spectrometry (GC-MS). In line with the monitoring campaign a comprehensive quality assurance concept was implemented to guarantee constant analytical measurement conditions for two years. The protocol is applicable for field laboratories with a high level of automation and for analyzing high sample amounts. At most sampling sites pollutant concentrations gradually decrease with depth. Only few spots showed highest concentrations in the upper mineral soil. In the O-horizon the sum concentrations of 16 PAHs range from 104 to 14.000 µg/kg, of 6 PCBs from <1 to 106 µg/kg and the sum of DDT and metabolites range from <1 to ca. 4.000 µg/kg. The observed concentration of PAH, PCB and OCP reflect an ubiquitous background contamination at most sites. Relatively high concentrations of PAH and PCB are related to industrial areas and peak concentrations only of PAH are associated with open cast mining of brown coal areas. The spatial distribution of the contents of DDT and metabolites in German forest soils can clearly be attributed to historic application. A contribution of ubiquitous background pollution derived from long-range atmospheric transport is likely for some compounds in the studied area, e.g., DDT in the western part of Germany. The results generally reflect the distribution of POPs in densely populated and industrialized countries located in temperate regions]. T2 - International network of environmental forensics CY - Oerebro, Sweden DA - 27.06.2016 KW - Forest soil KW - Organic pollution KW - Spatial distribution PY - 2016 AN - OPUS4-38598 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Lehnik-Habrink, Petra T1 - Evaluation of suitability of PLE, soxhlet, and shaking for extraction of POPs from soil N2 - The occurrence of persistent organic pollutants like polychlorinated biphenyls (PCB) and organochlorine pesticides (OCP) in the environment is still a matter of concern, even years after their use was abolished. Hence, threshold values are regulated by law which reference a number of national and international standards for determination of said contaminants. In this context, soil is an especially difficult matrix, because several defining parameters can vary in a wide range. Organic matter content in particular has a crucial influence on extractability of contaminants because it largely governs formation of non-extractable or bound residues. For this study, four soils of different total organic carbon (TOC) content were generated from uncontaminated reference soil (RefeSol 01-A) and compost which were spiked to contaminant levels representative of the Bundes-Bodenschutz-Verordnung (BBodSchV). These test materials were extracted using accelerated solvent extraction (ASE), Soxhlet extraction, and liquid-liquid extraction. For the latter method, samples were initially extracted for 15 minutes employing acetone. The follow-up extraction step was carried out using cyclohexane and the extraction time varied between 15 minutes and 16 hours. After clean-up, extracts were analysed via gas chromatography-mass spectrometry (GC MS) and with a gas chromatograph equipped with an electron capture detector (GC ECD). Statistical analysis of the experimental values showed that recovery was not dependent on matrix TOC content. Also, no clear preference for a single method could be detected. Concerning liquid-liquid-extraction, it is merely observed that prolonged extraction time results in slightly higher recoveries, while moderate extraction times appear to yield the most robust results. Although Soxhlet and ASE show high recoveries, they also lead to larger standard deviations and are not suitable for determination of thermolabile pesticides. In addition to recovery by different extraction methods, the agreement of values obtained by ECD and MS was evaluated. For ECD, standard deviations are generally higher but overall the values obtained by MS and ECD are comparable. T2 - International network of environmental forensics CY - Oerebro, Sweden DA - 27.06.2016 KW - Pesticides KW - PCB KW - Organic matter KW - Comparison extraction methods PY - 2016 AN - OPUS4-38605 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Lehnik-Habrink, Petra T1 - Comparison of extraction methods for analysis of OCP and PCB in soils N2 - The determination of organochlorine pesticides (OCP) and polychlorinated biphenyls is challenging because they are strongly physical and chemical bound to soil organic matter. There are various valid standards for the determination of these analytes in soil that differ especially in the extraction method and extraction time. In order to make profound assessments concerning the extraction efficiency seven extraction procedures namely pressurized liquid extraction (PLE), soxhlet and shaking with different extraction times 0.5 h, 1 h, 3 h, 6 h and 16 h were compared. For the study four soils of different total organic carbon (TOC) content were generated from uncontaminated reference soil and compost which were spiked to contaminant levels representative of the Bundes-Bodenschutz-Verordnung. Clean-up and measurement conditions using gas chromatography with mass spectrometry (GC-MS) were kept constant. Statistically analysis of the experimental values showed that recovery rates were not dependent on matrix TOC content. In consideration of measurement uncertainties of 10% - 20% for the determination of OCP and PCB in soil no differences in the efficiency between the tested extraction procedures could be observed. T2 - ISO Meeting CY - Paris, France DA - 24.10.2016 KW - Standardization KW - PCB KW - OCP KW - Extraction methods PY - 2016 AN - OPUS4-38611 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Philipp, Rosemarie T1 - Traceable measurements for monitoring critical pollutants under the European Water Framework Directive (WFD) 2000/60/EC N2 - The European Water Framework Directive (WFD) 2000/60/EC specifies a list of 33 priority water pollutants. For these substances, Environmental Quality Standards (EQS), equivalent to the maximum allowable concentrations, had been defined at very low levels. EQS values refer to the whole water body, i.e. include contaminants which are associated to suspended solids or colloids present in the natural water. For several priority pollutants primary analytical methods capable of measuring the target analytes at EQS level in natural water are still missing. The project has developed and validated such methods for three selected compounds, namely Tributyltin (TBT), Polybrominated Diphenylether (PBDE) and Polycyclic Aromatic Hydrocarbons (PAH). KW - Water polluntants KW - Monitoring KW - Water analysis KW - Tributyltin KW - Polybrominated diphenylether KW - Polycyclic aromatic hydrocarbons PY - 2016 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-386230 SP - 1 EP - 3 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-38623 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kreutzbruck, Marc T1 - Prospects of the metal magnetic memory technique N2 - Prospects and Restrictions of the Metal Magnetic Memory Technique T2 - 69th-IIW-Meeting CY - Melbourne, Australia DA - 12.07.2016 KW - Metal magnetic memory KW - Magnetic field KW - GMR sensor KW - Microstructure PY - 2016 AN - OPUS4-38133 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Piechotta, Christian T1 - Characterization of new disinfection by-products of polycyclic musks (AHTN and HHCB) and their metabolites N2 - The polycyclic musks 6-Acetyl-1,1,2,4,4,7-hexamethyltetraline (AHTN) and 1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-ɣ-2-benzopyran (HHCB) are widely used fragrances in cosmetics, products of daily care and cleaning products for households and industry. They are in the focus of interest due to their estrogenic potential. Both compounds can be found at low μg/L concentrations in surface water where they are introduced mainly by sewage treatment plants supplied by municipal wastewater. In order to disinfect wastewater in sewage treatment plants or water in swimming pools, chlorine can be added to water as gas or hypochlorite solution. This disinfectant has a high oxidation potential resulting in the formation of disinfection by-products, the estrogenicity and toxicity of which might differ from their precursor. In this work the behaviour of AHTN and HHCB upon treatment with sodium hypochlorite solution was investigated and chlorinated possible disinfection by-products could be identified as well as a carboxylic acids and lactones derived from AHTN and HHCB. The identified species were characterized by GC-MS, LC-MSn and 1H-NMR. The elucidated structures of potential disinfection by-products are verified by X-ray crystallography. Finally the estrogenicity between the parent analytes and generated transformation products were compared. For that task, MCF-7 assay has been chosen for being most relevant to humans. Moreover metabolism studies were carried out using AHTN, HHCB and their disinfection by-products. T2 - ISEB 2016 CY - Barcelona, Spain DA - 30.05.2016 KW - AHTN PY - 2016 AN - OPUS4-38523 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Piechotta, Christian T1 - Traceability for mercury measurements - MeTra N2 - The aim of this work is to develop measurement procedures to provide full traceability and robust uncertainty statements for dissolved elemental mercury (Hg(0)), inorganic mercury (Hg(II)) and methyl-mercury (MeHg) in freshwater and sea water, and inorganic mercury (Hg(II)) and methyl-mercury (MeHg) in biota. Accurate measurements with low uncertainties e.g. <50 % at the EQS level are required to assess concentration levels and trends in these important environmental reservoirs for mercury. In particular this work aims to: Develop and validate primary measurement procedures for Hg speciation (Hg(II), MeHg and Hg(0)) in fresh and sea waters at sub-ng levels in the presence of suspended particular matter and/or colloidal fractions, Apply the developed IDMS procedures in water in order to evaluate possible artefacts associated with sample collection and preparation, preserving speciation and/or correcting for possible post-sampling interconversions, Develop and validate primary measurement procedures for the accurate quantification of Hg(II) and MeHg in biota, using samples from the Federal Environmental Specimen Bank, Apply the developed IDMS procedures in biota in order to evaluate the effect of different treatments for fish sample preparation. T2 - EMRP MeTra Meeting CY - Geel, Belgium DA - 01.02.2016 KW - Methyl mercury PY - 2016 AN - OPUS4-38519 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Maierhofer, Christiane A1 - Kind, Thomas A1 - Köpp, Christian A1 - Helmerich, Rosemarie T1 - CHEF - Cultural heritage protection against flooding N2 - CHEF provides knowledge about flood protection of cultural heritage objects and directly supports the European Floods Directive by giving recommendations on how to assess the vulnerability of monuments. A comprehensive analysis of protective measures BEFORE, DURING and AFTER a flood has been carried out within the project, including technical and administrational measures. An overview of these measures is given, followed by recommendations on how to establish the most effective protective strategies. KW - Cultural heritage KW - Flood protection KW - Flood risks PY - 2011 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-385463 SP - 1 EP - 3 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-38546 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Simon, Franz-Georg A1 - Bandow, Nicole T1 - Significance of cadmium from artists‘ paints to agricultural soil and the food chain N2 - An Annex XV restriction dossier for cadmium in artists’ paints was submitted by an EU member state to the European Chemicals Agency ECHA. By cleaning used brushes under the tap cadmium can enter the food chain via waste water treatment and subsequent agricultural application of the sewage sludge. It was estimated that 110 kg Cd per year is spread on agricultural land via this exposure route. Other sources of Cd amount to almost 120 tons per year. The mobility of Cd from pigments was studied in a field-like scenario by leaching experiments using soil samples amended with sewage sludge and spiked with Cd pigments in percolation columns. The redox conditions were confirmed to be the decisive factor for the release of Cd. The release of Cd from artists’ paints was in most cases 1% or lower in the experiments performed. Cd from artists’ paints in sewage sludge applied in agriculture will be mobilized for intake by crops or to leaching either by oxidation of sulfide to sulfate or by dissolution at lower pH values. The quantity of Cd from artists’ paints calculated in the restriction dossier is however negligible compared to other sources of Cd to agricultural soil. Therefore ECHA did not consider the proposed restriction to be the most appropriate EU wide measure to address the negligible level of risk. In the presentation sources of Cd on agricultural land will be discussed together with possible policy instruments to mitigate such emissions. T2 - 9th International Cadmium Conference CY - Lisbon, Portugal DA - 26.10.2016 KW - Cadmium KW - REACH KW - leaching PY - 2016 UR - http://www.conference.cadmium.org/ SP - 9 EP - 10 AN - OPUS4-38473 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Carl, Peter T1 - A bead suspension array for measuring emerging pollutants and anthropogenic markers in wastewater. N2 - The assessment of water quality demands for high-throughput and multi-target compatible analytical methods. On the one hand, the influence of sewage on natural surface waters must be routinely monitored - according to the European Water Framework Directive. On the other hand, estimation of removal efficiencies of pollutants, such as drug residues, is in the focus of industrial and public wastewater treatment. Immunoassays, such as ELISA, are often applied in this area owing to their cost-efficiency and high-throughput capability. However, it is only possible to measure a single analyte in one measurement. In contrast, array technology is capable for measuring multiple substances in parallel. Here we present a four-plex bead-based flow cytometric assay for measuring three drugs (carbamazepine, an anti-epileptic drug, diclofenac, an antiphlogistic and caffeine, a psychoactive substance) and the bile acid isolithocholic acid, which is proposed to be used as a fecal marker. In this suspension array core-shell particles, consisting of a polystyrene core and a silica shell are used. They can be easily encoded with a fluorophore which is introduced to the core and functionalized with amino groups on the surface for creating binding sites for antibodies: Therefore, the marker substances are bound to the amino groups via NHS chemistry. For the determination of the pollutants, the beads are incubated with a mixture of the analyte-specific antibodies. The antibodies undergo a competitive reaction to bind the immobilised molecules on the surface of the beads or the free analyte in the solution, respectively. Bound antibodies can then be visualized via fluorophore-labelled secondary antibodies. For read-out a flow cytometer is used to virtually separate the different encoded beads and to measure the resulting signal intensity of the immunoassay. In order to obtain highly selective binding of the antibodies, we investigated different types of surface modifications to overcome unspecific binding, finding that a PEG-based surface is suitable to support our immunoassay format. The resulting multiplexing assay is appropriate to detect the marker substances in the low µg/L range. T2 - The Singlet Oxygen Strategy: From Singlet Oxygen to Sustainable Oxidation CY - Gent, Belgium DA - 15.06.2016 KW - Bead-based assay KW - Small-molecule sensors KW - Immunoassay KW - Anthropogenic markers KW - Wastewater PY - 2016 AN - OPUS4-36753 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Braun, Ulrike T1 - General aspects of polymers and and polymers in environment N2 - The presentation addresses first general aspects of polymers and polymers in environment (definitions, types, phases, morphology, density) and than summarise the possibilities of analysis. T2 - 1. meeting of ISO/TC 61/SC 5/AHG "microplastics" CY - Berlin, Germany DA - 12.04.2016 KW - Microplastics KW - Polymers PY - 2016 AN - OPUS4-36758 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -