TY - JOUR A1 - Roesch, Philipp A1 - Vogel, Christian A1 - Kalbe, Ute A1 - Simon, Franz-Georg T1 - Entwicklung von PFAS-Summenparametern mittels Combustion Ion Chroma- tography (CIC) JF - Mitteilungen Umweltchemie Ökotox N2 - Wie können industriell synthetisierte Schadstoffe aus einer Stoffklasse quantifiziert werden, deren genauer Umfang unbekannt ist und auf mehrere tausend Verbindungen geschätzt wird? Im Falle der per- und polyfluorierten alkylierten Substanzen (PFAS) stellen sich Wissenschaftler*innen weltweit seit über zehn Jahren diese Frage. Neben der etablierten Methodik der Einzelstoffanalytik (engl. target analytic) existieren Summenparameteranalysen zur Quantifizierung organisch gebundener fluorierter Verbindungen in Umweltmedien und Konsumprodukten. An der Bundesanstalt für Materialforschung und -prüfung (BAM) beschäftigen wir uns mit der Weiterentwicklung von Summenparametermethoden am Beispiel von PFAS-belasteten Umweltkompartimenten wie Böden, Klärschlämmen und Gewässerproben sowie PFAS-haltigen Konsumgütern. In diesem Beitrag stellen wir zwei ausgewählte Fallbeispiele vor und diskutieren die Vor- und Nachteile der Methoden im Vergleich zur Einzelstoffanalytik. KW - PFAS KW - Combustion Ion Chromatography KW - LC-MS/MS KW - Water analysis KW - Environmental analysis KW - Sum parameter analysis PY - 2023 SN - 1618-3258 VL - 29 IS - 2 SP - 40 EP - 44 AN - OPUS4-57611 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Roesch, Philipp A1 - Witter, Philipp A1 - Vogel, Christian A1 - Kalbe, Ute A1 - Simon, Franz-Georg T1 - How to investigate potential emission sources of PFAS in consumer product materials? Comparative extraction approaches and sum parameter analysis by combustion ion chromatography (CIC) N2 - Besides classical per- and polyfluorinated alkylated substances (PFAS), side-chain fluorinated polymers (SFPs) are widely applied as efficient anti-wetting and anti-greasing coatings in various daily applicated consumer products such as outdoor apparel, carpetry or paper-based food contact materials. Although the fluorinated sidechains are chemically bound to a base polymer, their release can be triggered by environmental influences or wear-off, thus contribute as significant sources of PFAS in the environment. Since only little knowledge of PFAS and SFP composition in consumer products is available, a comprehensive analytical approach might be beneficial. T2 - SETAC Konferenz 2023 CY - Dublin, Ireland DA - 30.04.2023 KW - PFAS KW - Combustion Ion Chromatography KW - Comsumer good samples PY - 2023 AN - OPUS4-57422 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Roesch, Philipp A1 - Vogel, Christian T1 - micro-XRF und XANES-Analytik von PFAS N2 - Ergebnispräsentation über gesammelte Ergebnisse der Synchrotron F µ-XRF und -XANES Spektroskopischen Untersuchungen von PFAS und PFAS-haltigen Materialien T2 - Online-Seminar des Fortbildungsverbundes Boden und Altlasten Baden-Württemberg CY - Online meeting DA - 07.12.23 KW - PFAS KW - XANES KW - XRF KW - Röntgenspektroskopie KW - Synchrotron PY - 2023 AN - OPUS4-59077 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zweigle, J. A1 - Capitain, C. A1 - Simon, Fabian Michael A1 - Roesch, Philipp A1 - Bugsel, B. A1 - Zwiener, C. T1 - Non-extractable PFAS in functional textiles − Characterization by complementary methods: oxidation, hydrolysis, and fluorine sum parameters JF - Environmental Science: Processes & Impacts N2 - Per- and polyfluoroalkyl substances (PFAS) are widely used for durable water-repellent finishing of different fabrics and textiles like outdoor clothing, carpets, medical textiles and more. Existing PFAS extraction techniques followed by target analysis are often insufficient in detecting widely used side-chain fluorinated polymers (SFPs) that are barely or non-extractable. SFPs are typically copolymers consisting of a non-fluorinated backbone with perfluoroalkyl side-chains to obtain desired properties. We compared the accessible analytical information and performance of complementary techniques based on oxidation (dTOP assay, PhotoTOP), hydrolysis (THP assay), standard extraction, extractable organic fluorine (EOF), and total fluorine (TF) with five functional textiles and characterized 7 further textiles only by PhotoTOP oxidation. The results show that when applied directly to textile samples, oxidation by dTOP and PhotoTOP and also hydrolysis by the THP are able to capture large fractions of the TF in form of perfluoroalkyl side-chains present in the textiles while methods relying on extracts (EOF, target and non-target analysis) were much lower (e.g., factor ~25-50 lower). The conversion of large fractions of the measured TF into PFCAs or FTOHs from fluorinated side chains is in contrast to previous studies. Concentrations ranged from C8 (e.g. 580 µg/kg dw PFOS for Soil1), whereas the consumer product samples showed a more uniform distribution with regard to chain lengths from C4 to C8. Independent from quantified PFAS amounts via target analysis, µ-XRF mapping combined with µ-XANES spectroscopy was successfully applied to detect both point-specific concentration maxima and evenly distributed surface coatings of fluorinated organic contaminants in the corresponding samples. KW - PFAS KW - XRF KW - LC-MS/MS KW - XANES KW - Fluoride KW - Soil PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-576109 DO - https://doi.org/10.1039/D3EM00107E SN - 2050-7887 SP - 1 EP - 12 PB - Royal Society of Chemistry AN - OPUS4-57610 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -