TY - JOUR A1 - Malefioudaki, Mariella A1 - Misra, Archismita A1 - Sbeity, Nadja A1 - Zueco-Vincelle, Juan A1 - Laguna-Bercero, Miguel A. A1 - Koerdt, Andrea A1 - Martín-Rapún, Rafael A1 - Mitchell, Scott G. T1 - Multifunctional polyoxomolybdate ionic liquid coatings for mitigating microbiologically influenced corrosion N2 - Corrosion of metals and other materials in marine environments poses significant economic, operational, safety, and environmental challenges across the oil and gas industry, the renewable energy sector, and maritime infrastructure. Microbiologically influenced corrosion (MIC) accounts for a substantial portion of this corrosion, with sulfate-reducing bacteria (SRB) and methanogenic archaea (MA) being key contributors. Conventional methods such as cathodic polarization have proven insufficient in mitigating the colonization of corrosive microbial communities in real marine environments, requiring the development of alternative, broad-spectrum antimicrobial strategies to prevent such biofilm formation. Recently, molybdate has emerged as a potential alternative to traditional biocides and nitrate. Our hypothesis is polyoxometalate-ionic liquids (POM-ILs), which exhibit antimicrobial and anticorrosion properties, could have a broader spectrum of antimicrobial activity than demonstrated until now and could be capable of shielding and protecting sensitive metal surfaces from the extreme acidic environments produced by MIC microorganisms. Here we show how two prototype polyoxomolybdate-based POM-ILs, [(CH3(CH2)6)4N]2[Mo6O19] and [(CH3(CH2)6)4N]4[Mo8O26], demonstrated antimicrobial activity at microgram per millilitre concentrations, prevented biofilm formation on metal surfaces, and provided resistance to corrosive acidic environments. Furthermore, impedance measurements were commensurate with electron microscopy studies showing that POM-IL-coated brass coupons withstood extremely corrosive environments. These proof-of-concept results demonstrate how multi-functional POM-IL coatings represent promising MIC mitigation solutions by providing a hydrophobic acid-resistant and biocidal protective layer that prevents biocolonisation and acidic corrosion by MIC microorganisms. KW - Polyoxometalates KW - Ionic liquid KW - Microbiologically influenced corrosion KW - Corrosion KW - Heritage preservation PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-631951 DO - https://doi.org/10.1039/d5mh00373c SN - 2051-6347 VL - 12 IS - 13 SP - 4648 EP - 4661 PB - Royal Society of Chemistry (RSC) CY - Cambridge AN - OPUS4-63195 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dimitrijević, Stevan P. A1 - Dimitrijević, Silvana B. A1 - Koerdt, Andrea A1 - Ivanović, Aleksandra A1 - Stefanović, Jelena A1 - Stanković, Tanja A1 - Gerengi, Husnu T1 - Comparison of Corrosion Resistance of Cu and Cu72Zn28 Metals in Apricot Fermentation Liquid N2 - The production of fruit brandies is based on distilling fermented fruit juices. Distillation equipment is usually made of copper. In traditional manufacturing, it consists of a boiler (batch) distiller, a boiler (pot), a steam pipe, and a condenser, all of which are made of pure copper. This study determined the corrosion parameters for copper (Cu) and Cu72Zn28 (in wt%) alloy in fermented apricot juice at room temperature. The fermentation process examined in this research utilized natural strains of yeast and bacteria, supplemented by active dry yeast Saccharomyces cerevisiae strains. This research used the following methods: open circuit potential (OCP), linear polarization resistance (LPR), and Tafel extrapolation to identify corrosion parameters. Cu had a 3.8-times-lower value of corrosion current density than brass, and both were within the range of 1–10 μA·cm−2, with an excellent agreement between LRP and Tafel. This study proved that Cu is an adequate material for the distillation of fruit brandies from a corrosion perspective. Despite this, there are occasional reports of corrosion damage from the field. Significant corrosion impacts can arise, as evidenced by laboratory tests discussed in this paper. In the absence of a highly corrosive environment, this study indicates that, to some extent, microbiologically influenced corrosion (MIC) can influence the degradation of the equipment material. KW - MIC KW - Metall KW - Envitonment PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-628911 DO - https://doi.org/10.3390/ma18061253 SN - 1996-1944 VL - 18 IS - 6 SP - 1 EP - 17 PB - MDPI AG AN - OPUS4-62891 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mallikarjun, Jhenkhar A1 - Gorbushina, Anna A1 - Kuzyakov, Yakov A1 - Koester, Moritz A1 - Castro, Rodrigo A1 - Yudina, Anna A1 - Abdallah, Khaled A1 - Matus, Francisco J. A1 - Dippold, Michaela A. T1 - Post-fire recovery of temperate and mediterranean ecosystems: An interplay between fire severity, soil nutrients, and vegetation from early-stage to decadal-scale dynamics N2 - Wildfires strongly alter soil properties, which in turn affect ecosystem recovery over extended periods, though long-term impacts are less certain. This study investigated a 14-year post-fire chronosequence in Chile’s mediterranean and temperate humid forests, revealing ecosystem-specific soil properties and nutrient recovery mechanisms. By analysing sites at successional stages, the chronosequence approach assessed temporal changes and ecosystem recovery, revealing long-term wildfire effects on soil dynamics and nutrients recovery. Wildfires raised soil bulk density to 0.9 g cm−3 in humid temperate and 1.2 g cm−3 in mediterranean ecosystems. Mediterranean soils experienced greater compaction from organic matter loss, soil aggregate destruction, ash-clogged pores, and topsoil erosion. Soil texture shifts were ecosystem-dependent: mediterranean soils increased 10–12 % in clay and silt through ash redistribution and aggregation, while temperate soils saw sand content rise by 0.74 % and 0.32 % yearly at 0–5 and 5–10 cm depths from thermal disaggregation and erosion. Ground vegetation recovers quickly, but physical soil properties like bulk density require over 14 years to return to pre-fire conditions. In humid temperate forests, ash input initially increased soil pH (4.8 to 5.8), reducing acidity, mitigating aluminium toxicity, while increasing nutrient availability. Base cation stocks increased in mediterranean woodlands (e.g., Ca: up to 0.41 Mg ha−1 y−1) due to ash retention, lower leaching, and ash infiltration into subsoil. Nutrient stocks in humid forests recovered slowly (Ca: 0.087–0.13 Mg ha−1 y−1) due to rainfall-driven leaching and low subsoil reserves. Carbon and N losses were restricted to the litter horizon in temperate forests, recovering via fire-resistant tree inputs, whereas mediterranean soils suffered severe C and N depletion from vegetation loss, erosion, and low N fixation. Fire effects and recovery are ecosystem-specific, shaped by landscape, geology, hydrology, and vegetation resilience. Understanding how fire regimes affect soil and nutrient recovery is vital for improving projections in fire-prone regions. KW - Historical fire & Wildfire KW - Nutrients Ecosystem recovery & Vegetation succession KW - Chronosequence approach KW - Losses of nutrients & Nutrients stocks KW - Wildfire PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-642918 DO - https://doi.org/10.1016/j.catena.2025.109431 SN - 0341-8162 VL - 260 SP - 1 EP - 13 PB - Elsevier B.V. AN - OPUS4-64291 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kleinbub, Sherin A1 - Braymer, Joseph J A1 - Pfeiffer, Friedhelm A1 - Dyall-Smith, Mike A1 - Spirgath, Kristin A1 - Alfaro-Espinoza, Gabriela A1 - Koerdt, Andrea T1 - From Genes to Black Rust: Genomic insights into corrosive methanogens N2 - Within the past ten years, genetic evidence has been increasing for the direct role that microbes play in microbiologically influenced corrosion (MIC), also known as biocorrosion or biodeterioration. One prominent example is the correlation between the corrosion of metal and the presence of genes encoding an extracellular [NiFe]-hydrogenase (MIC hydrogenase) in the methanogenic archaeon, Methanococcus maripaludis. In this study, DNA sequencing and bioinformatic analysis were used to classify the MIC hydrogenase as belonging to a core set of genes, the MIC core, found so far in Methanococci and Methanobacteria classes of methanogens. Genetic evidence is provided for the mobilization of the MIC core via multiple mechanisms, including a horizontal gene transfer event from Methanobacteria to Methanococci and a newly described MIC-transposon. A detailed comparison of M. maripaludis genomes further pointed to the relevance that cell wall modifications involving N-glycosylation of S-layer proteins and the MIC hydrogenase likely play in methanogen-induced MIC (Mi-MIC). Microscopic analysis of corrosive methanogens encoding the MIC core indicated that Methanobacterium-affiliated strain IM1 can form extensive biofilms on the surface of corrosion products whereas individual cells of M. maripaludis Mic1c10 were only found localized to crevices in the corrosion layer. An updated model of Mi-MIC involving two modes of action is presented, which predicts that the propensity of cells to adhere to iron surfaces directly influences the rate of corrosion due to the localization of the MIC hydrogenase at the metal-microbe interface. KW - Biocorrosion KW - Hydrogenases KW - Metalloprotein KW - Microbes PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-649425 DO - https://doi.org/10.1093/femsmc/xtaf018 SN - 2633-6685 VL - 6 SP - 1 EP - 19 PB - Oxford University Press (OUP) AN - OPUS4-64942 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Duarte-Ruiz, D. A1 - Saßnick, H.-D. A1 - Ferreira De Araujo, F. A1 - Gentzmann, Marie A1 - Huthwelker, T. A1 - Cocchi, C T1 - X-ray absorption spectroscopy of scandium oxide polymorphs N2 - Scandium oxide (Sc2O3) is a rare-earth oxide with significant potential in key technological areas, but due to its limited supply a deep understanding of its characteristics in different crystalline phases is still missing. Here, we present a combined experimental and ab initio X-ray absorption spectroscopy investigation of Sc2O3 focusing on excitations from the O K-edge and the Sc L2,3-edge. While measurements are performed on a cubic sample, the most stable phase under ambient conditions, six different polymorphs are computed, including two high-pressure phases with a trigonal and monoclinic lattice in addition to the cubic phase, as well as three computationally predicted structures. Our analysis of the structural and electronic properties reveals significant similarities between the cubic polymorph and the high-pressure trigonal phase, while the monoclinic crystal exhibits distinct features. The spectra simulated for these similar phases from the solution of the Bethe–Salpeter equation show very good agreement with measurements. Additional comparison with results computed in the independent-particle approximation highlights the dominant role of electron–hole correlations in shaping the absorption features, particularly at the O K-edge, where a common pattern with the features of other sesquioxides is identified. Our findings offer new insight into the spectral fingerprints of Sc2O3 polymorphs, aiding in situ characterization and informing sustainable materials management. KW - Scandium PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-650806 DO - https://doi.org/10.1039/d5ra06446e VL - 15 IS - 56 SP - 47814 EP - 47825 AN - OPUS4-65080 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Poliakova, A. A1 - Ciotti, G. A1 - Helman-Wazny, Agnieszka A1 - Fromm, J. T1 - Phytolith assemblages from palm leaves and palm-leaf manuscripts: what is the difference and what it could mean? N2 - We studied freshly collected, dried and herbarized leaf fragments of two palms, namely Borassus flabellifer L. and Corypha umbraculifera L., most commonly used for palm-leaf manuscript (PLM) production in South (S) and Southeast Asia (SE) in order to reveal differences in their phytolith assemblages. For each of the two palms, 25 leaf samples were taken from the two Indian states of Kerala and Tamil Nadu. Dried leaf material was obtained from the fresh one by drying the leaves in air. Herbarium samples were obtained from two independent herbaria, specimen origin comprises S and SE Asia with the main focus on South India and Sri Lanka. Additionally, 25 manuscripts made of Borassus flabellifer leaves and 25 manuscripts made of Corypha umbraculifera leaves were investigated for phytoliths. All manuscripts are preliminary dated back to between the 16th and the beginning of the 20th century CE; most of them assumedly were produced in S India (Tamil Nadu and Kerala), Sri Lanka, Burma or Indonesia. Phytolith assemblages significantly differed between fresh, dry and herbarized palm leaves in comparison to PLM material, both qualitatively and quantitatively (mean r2 = - 0.61 ± 9.3 for Borassus samples and r2 = - 0.75 ± 5.3 for Corypha samples, at p < 0.001). Fifty-three phytolith types described for PLM material were not observed in any of the fresh, dry or herbarized palm-leaf samples. Geographical analysis of PLM-specific phytoliths suggests that the combination of those phytoliths could be region-related. In this paper, we prove that the methods of palaeoecological reconstructions based on detailed microscopy of the PLMs surface and phytolith analysis applied in combination with methods of mathematical and computer data analysis can contribute to answer the questions posed by material codicology by revealing lost manuscript production recipes and by studying manuscript provenance in terms of the geographical origin of the artefacts. Our approach can potentially open a new perspective for palaeoecological studies expanding their traditional scope and making them applicable to a new research field. KW - Palm-leaf manuscripts KW - Material codicology KW - Palaeoecology PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-652517 DO - https://doi.org/10.3389/fpls.2024.1482790 SN - 1664-462X VL - 15 SP - 1 EP - 29 PB - Frontiers Media SA AN - OPUS4-65251 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stohl, Leonie A1 - Tonon, Chiara A1 - Cook, Jake A1 - Gorbushina, Anna A1 - Dehn, Frank A1 - von Werder, Julia T1 - Understanding bioreceptivity of concrete: realistic and accelerated weathering experiments with model subaerial biofilms N2 - Vertical greening systems are a promising solution to the increasing demand for urban green spaces, improving environmental quality and addressing biodiversity loss. This study facilitates the development microbially greened algal biofilm facades, which offer a low maintenance vertical green space. The study focuses on concrete as a widely used building material and explores how physical surface characteristics impact its bioreceptive properties. Concrete samples, produced from the same mix but differing in surface structure, were subjected to a laboratory weathering experiment to assess their bioreceptivity. A novel inoculation method was employed, involving a single initial inoculation with either alga ( Jaagichlorella sp.) alone, or a model biofilm consisting of a combination of the alga ( Jaagichlorella sp.) with a fungus ( Knufia petricola). The samples underwent four months of weathering in a dynamic laboratory setup irrigated with deionized water to observe subaerial biofilm attachment and growth. The formation of subaerial biofilms was monitored with high resolution surface imaging, colorimetric measurements and Imaging Pulse Amplitude Modulated Fluorometry (Imaging PAM-F), with Imaging PAM-F proving the most effective. Statistical analysis revealed that by impacting surface pH value and water retention capability, surface structures significantly influence microbial growth and that the concrete’s bioreceptivity can be influenced through thoughtful design of the materials surface. The inoculation of algae combined with a fungus facilitated the formation of a stable subaerial biofilm, enabling algae to colonize a surface structure that it could not colonize alone. This finding highlights the importance of modelling synergistic interactions present in natural biofilms. KW - Bioreceptivity KW - Concrete KW - Biofilm PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-653105 DO - https://doi.org/10.1617/s11527-025-02864-x SN - 1359-5997 VL - 59 IS - 2 SP - 1 EP - 18 PB - Springer Science and Business Media LLC AN - OPUS4-65310 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Walsh, Michael A1 - Schenk, Gerhard A1 - Robinson, Nicole A1 - John, Samuel A1 - Dayananda, Buddhi A1 - Krishnan, Vithya A1 - Adam, Christian A1 - Hermann, Ludwig A1 - Schmidt, Susanne T1 - The Circular Phosphorus Economy: Agronomic Performance of Recycled Fertilizers and Target Crops N2 - ABSTRACTBackgroundThe circular phosphorus (P) economy addresses economic and environmental penalties inherent to the current linear P economy. Phosphorus sources recovered from waste steams (recyclates) offer an alternative to conventional fertilizers.AimThis research aimed to assess the agronomic performance of P recyclates derived from wastewater (hazenite, struvite), treated sewage sludge ash (SSA) and compost (FOGO food organics/garden organics) with crops previously characterized for P use efficiency (PUE).MethodsPhosphorus was supplied as granules and benchmarked against conventional fertilizers or mineral solution. Grown in controlled conditions, crops received recyclates individually or as amalgamates, with or without additional water‐soluble P. We quantified P uptake, yield and phytate content, and calculated agronomic performance indicators.ResultsResults revealed that (1) crop genotypes with purportedly lower or higher PUE showed similar performance when grown with limiting P supply and/or less soluble P recyclates, (2) crop performance improved when less soluble P recyclates were combined with water‐soluble P, (3) crops produced similar yield and biomass when supplied with an organo‐mineral formulation, hazenite, or conventional fertilizer, (4) grain accumulated higher levels of the antinutrient phytate with excess soluble P.ConclusionWe conclude that suitably formulated P recyclates can supplement or replace conventional fertilizers, and that fertilizer design should consider the solubility of recyclates and a crop's ability to access less soluble P. This adds to the growing body of evidence that well‐formulated next‐generation fertilizers can efficiently nourish crops. Integrating insights from controlled experiments and field trials is a cost‐effective strategy to actualize the circular P economy. KW - Recycling fertilizer KW - Phosphate recovery KW - Sewage sludge ash KW - Struvite KW - Hazenite PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-627116 DO - https://doi.org/10.1002/jpln.202400299 SP - 1 EP - 14 PB - Wiley AN - OPUS4-62711 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Leers, K. A1 - Arnold, U. A1 - Herzel, Hannes A1 - Adam, Christian A1 - Burkhardt, J. T1 - Thermochemically Treated Sewage Sludge Ash From Pilot-Scale Production as P-Fertilizer for Spring Wheat and Maize in Different Soil Conditions N2 - Background P-fertilizers made from sewage sludge ash (SSA) may be suitable substitutes for rock phosphate (RP)-based fertilizers and contribute to sustainable use of waste. In this context, the thermochemical AshDec treatment of SSA (TC-SSA) has been continuously improved and has emerged as a possible method to produce plant-available and low-pollutant P-fertilizers. Aim Evaluation of the P-fertilizer efficacy of TC-SSA produced in pilot trials in vegetation experiments with different plants, soils, and fertilizer doses. Methods TC-SSA was tested in pot experiments for spring wheat and maize on different soils and at two doses (0.2 and 0.4 g fertilizer P pot−1) and is compared to untreated SSA (USSA), RP, Struvite, triple superphosphate (TSP), and a control without P-fertilization (Zero P). Pot experiments are complemented by an analysis of fertilizer P-solubility. Results P-solubility of SSA with different extraction methods increased due to the thermochemical treatment, whereas the water-insoluble property remained. In contrast to RP or USSA, TC-SSA enriched calcium–acetate–lactate extractable soil P to the same extent as TSP. Plant biomass and P-uptake increased with TC-SSA compared to Zero P, RP, and USSA and were in most cases equal to TSP fertilization under different soil conditions. In contrast, the effects of RP and USSA varied among soils but, mostly, did not exceed plant biomass and P-uptake of the unfertilized control. Conclusion TC-SSA has an increased fertilizer efficacy compared to USSA and is an effective P-fertilizer for spring wheat and maize in different soil conditions. KW - Phosphorus KW - Fertilizer KW - Thermochemical KW - Maize PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-648251 DO - https://doi.org/10.1002/jpln.70035 SN - 1522-2624 VL - 189 IS - 1 SP - 81 EP - 93 PB - Wiley-VCH AN - OPUS4-64825 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meiers, Emelie A1 - Scholl, Juliane A1 - Droas, Morten A1 - Vogel, Christian A1 - Leube, Peter A1 - Sommerfeld, Thomas A1 - Bagheri, A. A1 - Adam, Christian A1 - Seubert, A. A1 - Koch, Matthias T1 - Development and evaluation of analytical strategies for the monitoring of per- and polyfluoroalkyl substances from lithium-ion battery recycling materials N2 - Per- and polyfluoroalkyl substances (PFAS) are well-known as “forever chemicals” and persistent pollutants released by different anthropogenic sources. The potential release of PFAS from accumulating electronic waste and lithium-ion battery (LIB) recycling activities has gained increasing attention in the past years. This creates a need for analytical methods tailored for the determination of PFAS out of environmental matrices related to the named activities or directly out of the concerned materials. In this work, analytical strategies for the monitoring of PFAS in LIB recycling materials were explored for a group of legacy perfluoro sulfonic- and carbonic acids (PFSA and PFCA) and of fluorinated sulfonylimides suspected to be LIB electrolyte ingredients. These analytical strategies comprehend PFAS target approaches with a herein optimized liquid chromatography tandem mass spectrometry (LC–MS/MS) method equipped with a HILIC (hydrophilic interaction liquid chromatography) column in combination with the TOP (total oxidizable precursor) assay and an adapted sample preparation method for high-matrix LIB recycling materials. The validated target method was applied to a set of LIB recycling materials: end-of-life batteries, black masses from hydrometallurgical recycling, and gas absorption solutions from thermal treatment of black masses as part of the recycling procedure. Investigation results show that the LIB industry can be connected to the release of both “LIB”-PFAS, such as the target sulfonylimides, and “already-legacy” PFAS, like the PFSA and PFCA. Especially, the presence of trifluoroacetic acid (TFA) as an emerging pollutant in every investigated LIB material type underlines the threat of PFAS emissions from LIB waste and recycling activities. KW - Per- and polyfluoroalkyl substances (PFAS) KW - Battery PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-647015 DO - https://doi.org/10.1007/s00216-025-06165-8 SN - 1618-2642 VL - 417 SP - 6567 EP - 6583 PB - Springer Science and Business Media LLC AN - OPUS4-64701 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -