TY - CONF A1 - Strzelczyk, Rebecca T1 - Constant emitting reference material for emissions test procedures N2 - Since nowadays people spend most of their time indoors, a healthy environment is essential. Volatile organic compounds (VOCs) emitted from furniture and building materials are reported to cause health complaints. Therefore, the usage of low emitting materials will improve the indoor air quality. Quantitative VOC emission testing is usually conducted in emission test chambers under specified controlled conditions as described in DIN 16000-9 and DIN EN 16516. For reasons of quality control/quality assurance (QC/QA) and for a better comparability of test results from different laboratories, suitable emission reference materials (ERM) are needed. Here, it is important to have a homogenous material with known emission rates over a specific time. Different approaches can be found in literature, inter alia polymer films loaded with the target compound to be released again, or a lacquer material to which a VOC mixture is added. After curing of the lacquer, the material can be loaded into a test chamber. Drawback of those approaches are their relatively fast decreasing emission profiles. For QC/QA purposes according to the test standards, VOC sources with constant emission profiles are desirable. The EU-funded research project MetrIAQ “Metrology for the determination of emissions of dangerous substances from building materials into indoor air” is working on a multi-component ERM with an envisaged instability of ≤ 10 % in the emission rate over at least 14 days. Within a doctoral thesis porous materials are impregnated with VOCs. Supercritical CO2 is used as solvent. Thus, the impregnated material does not contain any solvent that may show a measurable amount of emission in the emission test chamber. Furthermore, CO2 has the benefits to have a good availability and low costs. For the selection of porous materials several properties like the pore size, the surface, and the interaction with the components in the atmosphere need to be considered. The impregnation method is optimised while the different porous materials are tested. For the selection of porous materials the pores need to be large enough for the VOC molecules, further influence of the pore size is tested. T2 - Healthy Buildings CY - Aachen, Germany DA - 11.06.2023 KW - VOC KW - Emission KW - Quality assurance KW - Reference material PY - 2023 AN - OPUS4-59842 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Taghavi Kalajahi, Sara T1 - Pilot Study of a Laboratory- Based Microbiologically Influenced Corrosion (MIC) Test Using Microbiological Consortia Sampled from the Field N2 - Experts widely agree that the verification of microbiologically influenced corrosion (MIC) require the use of multiple lines of evidence (MLOE), including metallurgical, microbiological, operational/historical and environmental/chemical aspects. Existing standards related to MIC, such as NACE TM0106, TMO212 and TM0194, primarily aim to offer guidance on gathering such evidence. Working Group 5 of Euro-MIC COST action 20130 (Achieving standardization) proposed a laboratory-based approach that directly confirms the capability of the sampled consortium of microorganisms, obtained from the specific field location under investigation, to increase and/or alter the corrosion processes. It is necessary to verify this laboratory approach by conducting it in different laboratories, performed by different scientist. In the current study, the experiments based on the laboratory protocol of WG5 were conducted at Endures’s laboratory using environmental samples (sediment and seawater) from the North Sea. Metal coupons (carbon steel C1010) were exposed to sediment and seawater samples with varying microbial inoculums and controls over 150 days. Microbial identification, corrosion product analysis, and surface morphology assessments were conducted using molecular and microscopy techniques. The results indicate distinct microbial influences, particularly in treatments containing yeast, which fostered heightened anaerobic activity, notably by sulfate-reducing bacteria (SRB). Weight loss measurements and surface analysis revealed elevated corrosion rates and susceptibility to pitting corrosion in microbial inoculum treatments, with yeast presence exacerbating corrosion processes. Elemental analysis confirmed the presence of iron sulfide in corrosion byproducts, affirming SRB activity. The findings emphasize the importance of employing a MLOE approach and investigating pitting corrosion to better understand the impact of microorganisms on metal corrosion in the marine environments. This study contributes to advancing knowledge in the field and developing standardization: the lab-to-field transition for MIC testing. T2 - MIC-STANDS CY - Lisbon, Portugal DA - 24.07.2024 KW - Microbiologically influenced corrosion (MIC), Multiple lines of evidence (MLOE) KW - Marine Corrosion KW - Achieving standardization PY - 2024 AN - OPUS4-61979 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Taghavi Kalajahi, Sara T1 - The effectiveness of cathodic protection (CP) on microbiologically influenced corrosion (MIC) control N2 - Cathodic protection (CP) is an electrochemical method, to manage corrosion in different industries, especially in buried and sub-merged environments. In those environments microorganisms are present and can affect the corrosion process and cause microbiologically influenced corrosion (MIC). Most of the industry standards recommend performing CP using -800 mV (Ag/AgCl), however, if microorganisms capable of initiating MIC are present, for instance sulfate reducing bacteria (SRB), it is recommended to use even more negative potentials. It is assumed that this will provide adequate protection of the metal. Currently there is no information or valid data in the context of CP, on the level of MIC threat and the extent to which more negative potentials can be used to provide adequate protection and not over-protection (due to hydrogen embrittlement threat). Conflicting statements can be found in the literature regarding the effectiveness of CP on MIC, from reducing biofilm attachment to increasing bacterial activity and biofilm attachment. Recently, the development and lower price of molecular microbiological methods (MMM) have opened the door for more effective studies of MIC mechanisms along with other electrochemical methods and surface analysis. In this work, the genetic functionality of biofilms formed in the laboratory under CP conditions is investigated using transcriptomics. Gene expression of SRB biofilms under different CP potentials (-800, -850 and -900 mV) will be studied; comparison with control will allow us to distinguish the specific genes that are differentially expressed, leading to a better understanding of the mechanism of CP to affect bacterial activity and diversity. Keywords - cathodic protection, microbiologically influenced corrosion, molecular microbial methods. T2 - IBBS CY - Berlin, Germany DA - 09.09.2024 KW - Microbiologically influenced corrosion PY - 2024 AN - OPUS4-61981 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Tang, Chi-Long T1 - Sub-4 nm particles from FFF-3D printing measured with the TSI 1 nm CPC and the Airmodus A11 nCNC N2 - Concerns have been raised as Fused Filament Fabrication (FFF) desktop 3D printer emits harmful ultrafine particles (dP < 100 nm) during operation in indoor spaces. However, the vast majority of previous emission studies have neglected the possible occurrence of sub-4 nm particles by using conventional condensation particle counter (CPC) for detection. Thus, the total particle emission could be systematically underestimated. This study has compared two diethylene glycol (DEG) based instruments to evaluate their suitability for measuring organic FFF particles in the sub-4 nm size range either as particle counter or as a particle size spectrometer. T2 - European Aerosol Conference 2024 CY - Tampere, Finland DA - 25.08.2024 KW - Air pollution KW - Emission testing KW - FFF-3D printing KW - Sub-4nm particles KW - Ultrafine particles PY - 2024 AN - OPUS4-60930 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ulbricht, Alexander T1 - Do Microbes like Additively Manufactured Aluminium? First Details of a Corrosion Test using Sulphate-Reducing Bacteria N2 - Additively manufactured metals become relevant for industrial application. Although many studies on wet corrosion of these metals have been conducted, to the authors knowledge no study seems to contain microbiological corrosion (MIC). In the presented study an experiment was conducted on PBF-LB/AlSi10Mg to test this material's susceptibility for MIC. The tested specimen were analysed using Computed Tomography before and after the MIC experiment to enable a detailed characterisation the damage on the specimens' global and local level. A global reduction of material was observed. In addition, localised damage along process inherent features of the materials microstructure was observed. T2 - Beiratssitzung TF Umwelt CY - Berlin, Germany DA - 17.03.2025 KW - Computed Tomography KW - Additive Manufacturing KW - Biocorrosion KW - Sulphate-reducing Bacteria KW - Microbially influenced corrosion PY - 2025 AN - OPUS4-62772 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ulbricht, Alexander T1 - Do Microbes like Additively Manufactured Aluminium? N2 - The use of laser-additively manufactured metallic components in the industrial sector is gaining traction, with the process now entering its application phase. Consequently, the materials are exposed to corrosive microbes, which this study examines in order to determine the implications of this exposure. Specifically, the study examines the exposure of laser powder bed fused AlSi10Mg (PBF-LB/AlSi10Mg) components to sulphate-reducing bacteria in an anaerobic environment. Is the specific PBF-LB microstructure a potential factor in determining or aiding biocorrosion? A prismatic specimen was exposed to sulphate-reducing bacteria (SRB) for two weeks. The sample was scanned by X-ray computed tomography (XCT) before and after SRB exposure. The two data sets were registered to each other (using the internal void distribution as markers, due to the corrosion of the specimen’s surface) to enable the evaluation of the corrosion damage. Virtual cuts of the 3D XCT reconstructions show a loss of volume and localised damage. The damage distribution aligns with the hatching pattern of laser exposure from laser powder bed fusion. T2 - Konferenz iCT 2026 CY - Linz, Austria DA - 10.02.2026 KW - Computed tomography KW - Biokorrosion KW - Additive manufacturing KW - PBF-LB KW - Laser powder bed fusion KW - Sulphate-reducing bacteria PY - 2026 AN - OPUS4-65570 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - Leaching behavior of Antimony in MSWI bottom ash N2 - Bottom ash (BA) from municipal solid waste incineration (MSWI) contains harmful substances such as heavy metals, chloride and sulfate which are mobilized in contact with water. Standardized leaching tests are used to measure the extent of mobilization. It is known that fresh bottom ash displays elevated concentrations of various heavy metals such as lead or zinc due to the formation of hydroxo complexes as a result of high pH values of 12 and above. Storage of BA is accompanied by ageing processes, mainly the reaction of CaO and Ca(OH)2 with CO2 leading to lower pH values in contact with water around 11. Usually heavy metals concentrations are minimum at these conditions. Knowledge of the long-term leaching behavior of potentially harmful substances is crucial for the assessment of the environmental compatibility of reusing municipal solid-waste incineration bottom ash (MSWI BA) in construction, i.e., as a road base layer. BA fractions obtained from wet-processing aiming at the improvement of environmental quality were used to investigate the mobility of relevant substances. Eluates from laboratory-scaled leaching procedures (column percolation and lysimeters) were analyzed to learn about the long-term release of substances. Unsaturated conditions and artificial rainwater were used in the lysimeter tests to simulate field conditions. In addition, batch test eluates were generated at usual liquid-to-solid ratios (L/S) for compliance testing purposes. A variety of cations and anions was measured in the eluates. The wet treatment reduces the leaching of chloride and particularly sulfate by more than 60%. The release of typical contaminants for the treated MSWI BA such as the heavy metals Cu and Cr was well below 1% in the conducted leaching tests. An increase in the Sb concentration was observed in the lysimeter experiments starting at L/S 0.75 L/kg and in the column experiment at L/S 4 L/kg is assumed to be related to decreasing concentrations of Ca and thus to the dissolution of sparingly soluble calcium antimonate. The same leaching mechanism applies with V, but the concentration levels observed are less critical regarding relevant limit values. However, on the long term the behavior of Sb could be problematic for the application of MSWI BA as secondary building material. T2 - MINEA Final Conference CY - Bologna, Italy DA - 20.02.2020 KW - Antimony KW - Bottom ash KW - Leaching KW - Solubility PY - 2020 AN - OPUS4-50450 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - Detection, quantification, and treatment of per- and polyfluoroalkyl substances (PFAS) in groundwater (DFEAT-PFAS) N2 - Over the past century, a range of synthetic compounds have been produced to improve humanity’s quality of life. These include pharmaceuticals, plastics, and other chemical compounds that possess properties making them potentially harmful when released to the environment (e.g., ecological and health impacts to humans and animals). Per- and polyfluoroalkyl substances (PFAS) are a large group of chemicals used in the formulations of thousands of consumer goods, including aqueous film-forming foams used to suppress aviation fires in training scenarios, non-stick cookware, fast-food wrappers, water-repellent fabrics, medical equipment, and plastic and leather products. Because of the recent regulations and restrictions on the use of long chain (≥C8) PFAS a significant shift in the industry towards short (C4-C7) and ultrashort (C1-C3) chain alternatives has been recognized the last years. Due to the high polarity and water solubility of ultrashort PFAS, the potential for bioaccumulation is low. However, the high persistence of ultrashort-chain PFAS will result in environmental accumulation, especially in aquatic environments, leading to potential risks for aquatic organisms and increased human external exposure through drinking water. Ultrashort PFAS like trifluoroacetic acid (TFA) are low to moderately toxic to a range of organisms. In addition, ultrashort PFAS can penetrate natural and anthropogenic barriers and eventually reach drinking water sources. Because common drinking water treatment techniques do not sufficiently remove them, they may reach human consumption. In the project we are focusing on detecting and removing PFAS, especially ultrashort-chain PFAS from contaminated groundwater. We are designing passive sampling devices, which can collect and monitor the temporal profile of PFAS species in groundwater. This will allow us to analyze PFAS contaminations in German and Israeli groundwater using state-of-the-art and novel analytical techniques and understand the extent of contamination. In addition to quantification, PFAS contaminated groundwater will be treated via a two-stage process to produce PFAS-free drinking water. As ultrashort-chain PFAS are difficult to analyze with the current target (LC-MS/MS) and sum parameter (AOF, EOF) analysis methods, we additionally using gas chromatography – mass spectrometry (GC-MS). Therefore, an analytical method based on GC-MS is in development to analyze the volatile ultrashort-chain PFAS (TFA, PFPrA, TFMS, PFEtS, PFPrS, trifluoroethanol, pentafluoropropanol and hexafluoro isopropanol) directly in contaminated groundwater samples with the headspace technique and in eluates of organic solvents from the developed passive sampler after direct injection. Moreover, a two-stages process is designed to increase the low concentrations found in groundwater using novel membranes processes such as closed-circuit reverse osmosis (CCRO) and mixed matrix composite nanofiltration membranes (MMCM). Next, the rejected streams containing higher concentrations of PFAS will be treated by coagulation, and the remaining PFAS adsorbed onto carbonaceous nanomaterials (CNMs). The DEFEAT-PFAS project will result in the development of novel tools to detect, quantify, and remove PFAS, especially ultrashort-chain PFAS from contaminated groundwater, and will acquire a new understanding of the extent of these contaminations. T2 - Dioxin Konferenz CY - Maastricht, Netherlands DA - 10.09.2023 KW - Ground water KW - Per- and Polyfluoroalkyl substances (PFAS) KW - Remediation PY - 2023 AN - OPUS4-58346 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - Combining DGT and 31P NMR spectroscopy to determine phosphorus species in soil N2 - The amount of plant-available phosphorus (P) in soil strongly influences the yield of plants in agriculture. Therefore, various simple chemical extraction methods have been developed to estimate the plant-available P pools in soil. More recently, several experiments with the DGT technique have shown that it has a much better correlation to plant-available P in soils than standard chemical extraction methods (e.g. calcium-acetate-lactate (CAL), Colwell, Olsen, water) when soils with different characteristics are considered. However, the DGT technique cannot give information on the plant-available P species in the soil. Therefore, we combined DGT with solution 31P nuclear magnetic resonance (NMR) spectroscopy. This was achieved by using a modified DGT device in which the diffusive layer had a larger pore size, the binding layer incorporated an adsorption material with a higher capacity, and the device had a larger exposure area. The spectroscopic investigation was undertaken after elution of the deployed DGT binding layer in a NaOH solution. Adsorption tests using solutions of known organic P compounds showed that a sufficient amount of these compounds could be adsorbed on the binding layer in order for them to be analyzed by solution 31P NMR spectroscopy. Furthermore, various intermediates of the hydrolysis of trimetaphosphate in soil could be also analyzed over time. T2 - DGT Konferenz CY - Paris, France DA - 11.10.2023 KW - Soil KW - Phosphorus KW - Plant-availability PY - 2023 AN - OPUS4-58574 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - Detection, quantification, and treatment of per- and polyfluoroalkyl substances (PFAS) in groundwater (DFEAT-PFAS) N2 - Per- and polyfluoroalkyl substances (PFAS) are a large group of chemicals used in the formulations of thousands of consumer goods. Because of the recent regulations and restrictions on the use of long chain (≥C8) PFAS a significant shift in the industry towards short (C4-C7) and ultrashort (C1-C3) chain alternatives has been recognized the last years. Due to the high polarity and water solubility of ultrashort PFAS, the potential for bioaccumulation is low. However, the high persistence of ultrashort-chain PFAS will result in environmental accumulation, especially in aquatic environments, leading to potential risks for aquatic organisms and increased human external exposure through drinking water. Ultrashort PFAS like trifluoroacetic acid (TFA) are low to moderately toxic to a range of organisms. In the project we are focusing on detecting and removing PFAS, especially ultrashort-chain PFAS from contaminated groundwater. Therefore, we suggest developing and optimizing short- and ultrashort-chain PFAS detection, quantification, and removal. We will design passive sampling devices, which can collect and monitor the temporal profile of PFAS species in groundwater. This will allow us to analyze PFAS contaminations in German and Israeli groundwater using state-of-the-art novel analytical techniques. In addition, contaminated groundwater will be treated via a two-stage process, designed to concentrate the relatively low PFAS concentrations by novel membrane processes including closed-circuit reverse osmosis (CCRO) and mixed matrix composite nanofiltration membranes (MMCM). Afterwards the rejected streams, containing higher concentrations of PFAS will be treated by coagulation and the remaining PFAS adsorbed onto carbonaceous nanomaterials (CNMs). T2 - SETAC Europe CY - Vienna, Austria DA - 11.05.2025 KW - Per- and polyfluoroalkyl substances (PFAS) KW - Groundwater KW - Remediation PY - 2025 AN - OPUS4-63095 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -