TY - JOUR A1 - Seefeldt, Henrik A1 - Dümichen, Erik A1 - Braun, Ulrike T1 - Flame retardancy of glass fiber reinforced high temperature polyamide by use of aluminum diethylphosphinate: thermal and thermo-oxidative effects N2 - Glass fiber reinforced polyamide (PA) 6T/DT flame retarded with aluminum diethylphosphinate (AlPi) was tested to assess its flame retardant properties. Models for the decomposition of PA 6T/DT with and without AlPi are presented. Thermal decomposition was measured by performing TGA with Fourier transform infrared (FTIR) spectroscopy and FTIR spectroscopy in the condensed phase. Fire behavior was studied using a cone calorimeter and flammability was tested with UL 94 and the limiting oxygen index. AlPi works as an effective flame retardant for glass fiber reinforced PA 6T/DT materials, acting in the gas phase. Also observed was condensed-phase action, which occurs especially under oxidative conditions before the samples ignite. KW - Flame retardancy KW - High tmeperature polyamide 6T/DT KW - Aluminum phosphinate KW - Degradation PY - 2013 U6 - https://doi.org/10.1002/pi.4497 SN - 0959-8103 SN - 1097-0126 SN - 0007-1641 VL - 62 IS - 11 SP - 1608 EP - 1616 PB - Wiley InterScience CY - Chichester, West Sussex AN - OPUS4-29386 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Braun, Ulrike A1 - Deglemann, P. A1 - Krämer, R. A1 - Sturm, Heinz A1 - Senz, R. A1 - Rybak, Thomas A1 - Schneider, Michael A1 - Kukofka, Tobias T1 - Investigation of the Degradation Mechanism of Transition Metal Doped Polyamides and Polyesters T2 - PDDG CY - Paris, France DA - 2013-09-01 PY - 2013 AN - OPUS4-29078 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Elert, Anna Maria A1 - Braun, Ulrike A1 - Bannick, Claus Gerhard A1 - Eisentraut, Paul T1 - Identification of microplastics in the environment N2 - The worldwide produced plastic amount was about 314 m tones in 2013. A content of about 5-12 m tones of plastic products is estimated to attain to the environment. There, they are exposed to environmental aging conditions like UV light, abrasion, water, oxidation etc. and degrade to small particles. If the particles reach a dimension < 5 mm they are called microplastic. Today microplastic is almost ubiquitary and was found in the aquatic as well as in the terrestrial environment. The main representatives are polyethylene (PE), polypropylene (PP), polystyrene (PS) and polyethylene terephthalat (PET). Analyzing microplastics in environmental samples turned out to be very challenging, due to the fact that there are only a few synthetic particles beside a huge number of natural. Furthermore, the different polymers particles vary in their shape, their density and their chemical characteristics. Until now, there is no standard procedure for sampling, concentration and analyzing. We developed a thermal decomposition method for analyzing micro plastics in environmental samples. The method is a combination of a thermal extraction on solid-phase adsorption agents with a subsequent analysis of the decomposition products by thermal desorption gas chromatography mass spectrometry. In contrast to more established methods, such as IR or Ramen spectroscopy, our method enables measurements within few hours and gives an integration result of polymer specific decomposition products. Therefore, it is possible to identify and to quantify polymers in environmental matrices. The use of the method is demonstrated for various polymers (PE, PP, PS, PET) in spiked and first time also in real environmental samples. T2 - MoDeSt 2016 CY - Krakau, Poland DA - 04.09.2016 KW - Microplastic PY - 2016 AN - OPUS4-37314 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Braun, Ulrike A1 - Dümichen, Erik A1 - Barthel, Anne-Kathrin A1 - Bannick, Claus Gerhard T1 - Charakterisierung von Mikroplastik Partikeln aus Umweltproben N2 - Durch den stetig steigenden Einsatz von Plastikprodukten sind unerwünschte Kunststofffunde in verschiedenen Umweltmatrices mittlerweile allgegenwärtig. Besonderes Interesse erfahren die Kunststoffpartikel von einer Größe kleiner 5 mm, sogenannte Mikroplastik (MP) Partikel. Es werden aktuell Risiken für Mensch und Umwelt diskutiert, die von diesen Partikeln ausgehen. T2 - Wasser 2016 - Jahrestagung der Wasserchemischen Gesellschaft CY - Bamberg, Deutschland DA - 02.05.2016 KW - Mikroplastik KW - Polymere KW - Polyethylen (PE) KW - Polystyrol (PS) KW - Poly(ethylenterephthalat) (PET) PY - 2016 SN - 978-3-936028-94-2 SP - 74 EP - 76 PB - Wasserchemische Gesellschaft CY - Mülheim an der Ruhr, Germany AN - OPUS4-36782 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Braun, Ulrike A1 - Deglemann, P. A1 - Krämer, R. T1 - The impact of metal oxide particles on the thermal and thermo-oxidative degradation of polyamide 66 T2 - MoDeSt 2014 CY - Portorož, Slovenia DA - 2014-08-31 PY - 2014 AN - OPUS4-31501 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Braun, Ulrike T1 - Decomposition gas analysis of polymers by thermogravimetry solid-phase extraction thermal desorption gas chromatography mass spectrometry (TGA-SPE/TDS-GC-MS) T2 - GEFTA 2014 (Gesellschaft für Thermische Analyse e. V.) CY - Berlin, Germany DA - 2014-09-16 PY - 2014 AN - OPUS4-31502 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dümichen, Erik A1 - Braun, Ulrike A1 - Senz, R. A1 - Fabian, G. A1 - Sturm, Heinz T1 - Assessment of a new method for the analysis of decomposition gases of polymers by a combining thermogravimetric solid-phase extraction and thermal desorption gas chromatography mass spectrometry N2 - For analysis of the gaseous thermal decomposition products of polymers, the common techniques are thermogravimetry, combined with Fourier transformed infrared spectroscopy (TGA–FTIR) and mass spectrometry (TGA–MS). These methods offer a simple approach to the decomposition mechanism, especially for small decomposition molecules. Complex spectra of gaseous mixtures are very often hard to identify because of overlapping signals. In this paper a new method is described to adsorb the decomposition products during controlled conditions in TGA on solid-phase extraction (SPE) material: twisters. Subsequently the twisters were analysed with thermal desorption gas chromatography mass spectrometry (TDS–GC–MS), which allows the decomposition products to be separated and identified using an MS library. The thermoplastics polyamide 66 (PA 66) and polybutylene terephthalate (PBT) were used as example polymers. The influence of the sample mass and of the purge gas flow during the decomposition process was investigated in TGA. The advantages and limitations of the method were presented in comparison to the common analysis techniques, TGA–FTIR and TGA–MS. KW - TDS-GC-MS KW - TGA-FTIR KW - TGA-MS KW - Degradation KW - Polymer KW - Solid-phase extraction PY - 2014 U6 - https://doi.org/10.1016/j.chroma.2014.05.057 SN - 0021-9673 VL - 1354 SP - 117 EP - 128 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-31046 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Braun, Ulrike A1 - Senz, R. T1 - Investigation of a flame retardant high-temperature polyamide T2 - Tag der Chemie CY - Berlin, Germany DA - 2010-06-16 PY - 2010 AN - OPUS4-21522 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Braun, Ulrike T1 - Analyzing the thermal- and thermo-oxidative degradation of polymers by a combination of thermal solid-phase extraction and thermal desorptiion (TED-GC-MS) T2 - Interantional Summit on Current Trends in Mass Spectrometry CY - New Orleans, USA DA - 2015-07-13 PY - 2015 AN - OPUS4-33758 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Wendt-Potthoff, Katrin A1 - Schulze, Michaela A1 - Kuhlicke, Ute A1 - Neu, Thomas T1 - Mikrobielle Besiedlung von Mikroplastik aus kommerziellen Produkten T2 - Fluss. Stadt. Land. Gewässer im Wandel - Jahrestagung der Deutschen Gesellschaft für Limnologie und der deutschsprachigen Sektionen der SIL CY - Essen, Deutschland DA - 2015-09-21 PY - 2015 AN - OPUS4-34288 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Erdmann, Maren A1 - Braun, Ulrike A1 - Trappe, Volker A1 - Sturm, Heinz T1 - Non Isothermal Cure Kinetics of an Epoxy/Amine Resin by In Situ Near Infrared Spectroscopy T2 - PDDG 2015 CY - Stockholm, Sweden DA - 2015-08-30 PY - 2015 AN - OPUS4-34505 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bannick, Claus Gerhard A1 - Bierl, R. A1 - Braun, Ulrike A1 - Brand, K. A1 - Dümichen, Erik A1 - Jekel, M. A1 - Klein, S. A1 - Knepper, T.P. A1 - König, F. A1 - Miklos, D. A1 - Rechenberg, B. A1 - Steffens, I. T1 - Mikroplastik in der aquatischen Umwelt - Ein Beitrag zur aktuellen Diskussion in Deutschland N2 - Plastics are important materials in households and industry and therefore a crucial part of our everyday life. Since the beginning of the 1970s the occurrence of plastic particles in coastal waters has been explicitly described. Meanwhile, besides the marine environment, microplastics were also detected in other environmental media, biota and water management facilities. This work gives an overview of the occurrence and first known effects of microplastics in the environment. Furthermore, current scientific proceedings are considered and pending issues are discussed. In this regard it is of central importance to develop an environmentally comprehensive, harmonized scientific proceeding for miroplastics, which enables an evaluation of relevant material flows in adaption to necessary assessment concepts. N2 - Kunststoffe sind wichtige Werkstoffe und heutzutage aus Haushalt und Wirtschaft nicht mehr wegzudenken. Seit Anfang der 1970er-Jahre wird das Vorkommen von Kunststoffpartikeln in Küstengewässern beschrieben. Inzwischen ist Mikroplastik nicht nur im marinen Bereich, sondern auch in weiteren Umweltkompartimenten, Biota und technischen Einrichtungen der Wasserwirtschaft nachgewiesen worden, in dieser Arbeit wird ein Überblick über das Vorkommen von Mikroplastik in der aquatischen Umwelt und ersten bekannten Auswirkungen gegeben. Darüber hinaus werden die aktuellen Untersuchungsverfahren von Probenahme, Probenaufbereitung und Analytik betrachtet und offene fragen diskutiert. Zentral erscheint in diesem Zusammenhang die Entwicklung einer harmonisierten medienübergreifenden Untersuchungsmethodik, die eine Auswertung relevanter Stoffströme ermöglicht und auf notwendige Bewertungskonzepte abgestimmt ist. KW - Water management KW - Plastics KW - Microplastics KW - Environment KW - Analysis KW - Mikroplastik KW - Kunststoff KW - Wasserwirtschaft KW - Analytik KW - Umwelt PY - 2015 SN - 0083-6915 VL - 113 IS - 1 SP - 7 EP - 14 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-33105 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Braun, Ulrike T1 - Prüfung der Beständigkeit von Kunststoffen im täglichen Gebrauch - thermische Analyseverfahren und Anwendungen an der Bundesanstalt für Materialforschung und -prüfung T2 - Campus Bizz, Hochschule Hamm-Lippstadt CY - Hamm-Lippstadt, Deutschland DA - 2014-12-16 PY - 2014 AN - OPUS4-32334 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dümichen, Erik A1 - Barthel, Anne-Kathrin A1 - Braun, Ulrike A1 - Bannick, Claus Gerhard A1 - Brand, K. A1 - Jekel, M. A1 - Senz, R. T1 - Analysis of polyethylene microplastics in environmental samples, using a thermal decomposition method N2 - Small polymer particles with a diameter of less than 5 mm called microplastics find their way into the environment from polymer debris and industrial production. Therefore a method is needed to identify and quantify microplastics in various environmental samples to generate reliable concentration values. Such concentration values, i.e. quantitative results, are necessary for an assessment of microplastic in environmental media. This was achieved by thermal extraction in thermogravimetric analysis (TGA), connected to a solid-phase adsorber. These adsorbers were subsequently analysed by thermal desorption gas chromatography mass spectrometry (TDS-GC-MS). In comparison to other chromatographic methods, like pyrolyse gas chromatography mass spectrometry (Py-GC-MS), the relatively high sample masses in TGA (about 200 times higher than used in Py-GC-MS) analysed here enable the measurement of complex matrices that are not homogenous on a small scale. Through the characteristic decomposition products known for every kind of polymer it is possible to identify and even to quantify polymer particles in various matrices. Polyethylene (PE), one of the most important representatives for microplastics, was chosen as an example for identification and quantification. KW - Microplastic KW - Identification and quantification of polymers KW - Thermogravimetric analysis KW - Evolved gas analysis KW - Gas chromatography mass spectroscopy PY - 2015 U6 - https://doi.org/10.1016/j.watres.2015.09.002 SN - 0043-1354 VL - 85 SP - 451 EP - 457 PB - Elsevier Ltd. CY - Amsterdam AN - OPUS4-34337 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dümichen, Erik A1 - Braun, Ulrike A1 - Kraemer, R. A1 - Deglmann, P. A1 - Senz, R. T1 - Thermal extraction combined with thermal desorption: A powerful tool to investigate the thermo-oxidative degradation of polyamide 66 materials N2 - Using thermogravimetric analysis (TGA) with a solid-phase adsorber for thermal extraction, followed by subsequently analysing the adsorber with thermo-desorption gas chromatography mass spectrometry (TDS-GC–MS) enables measurement of polymer degradation under oxidizing atmosphere, and the identification of certain complex hydrocarbon degradation products by chromatographic separation and defined mass patterns. This technique, thermal-extraction desorption gas chromatography mass spectrometry (TED-GC–MS) was used to investigate the thermo-oxidative degradation of PA 66 and PA 66 doped with 2 wt% of metal oxide particles. In TGA pure PA 66 formed more residue under an oxidizing atmosphere than an inert one. In contrast to the measurements under inert atmosphere, several condensed aromatic species containing nitrogen could be identified in thermo-oxidative measurements. These degradation products were formed through condensation reactions of primary amides originating from imide hydrolysis. The formation of such highly condensed species also causes higher char formation. Four metal oxides have shown an impact on the thermo-oxidative degradation of PA 66: Fe2O3 on η-Al2O3 < pure Fe2O3 = Fe2O3 on γ-Al2O3 < pure ZnO. For ZnO even a char-stabilizing effect could be observed. A catalytic effect of these metal oxides causes more condensed cyclopentanone and pyridine derivates. Thus, more water is formed and released, resulting in increased hydrolysis of the imides and degradation at lower temperatures. KW - PA 66 KW - Metal oxide particles KW - Thermo-oxidation KW - Thermogravimetry KW - Solid-phase extraction PY - 2015 U6 - https://doi.org/10.1016/j.jaap.2015.08.006 SN - 0165-2370 SN - 1873-250X VL - 115 SP - 288 EP - 298 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-34338 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Braun, Ulrike A1 - Barthel, Anne-Kathrin A1 - Bannick, Claus Gerhard T1 - Methoden zur Identifizierung und Quantifizierung von Mikroplastik in der Umwelt T2 - Fluss. Stadt. Land - Gewässer im Wandel - Jahrestagung der Deutschan Gesellschaft für Limnologie und der deutschsprachigen Sektion der SIL CY - Essen, Deutschland DA - 2015-09-21 PY - 2015 AN - OPUS4-34310 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dümichen, Erik A1 - Javdanitehran, M. A1 - Erdmann, Maren A1 - Trappe, Volker A1 - Sturm, Heinz A1 - Braun, Ulrike A1 - Ziegmann, G. T1 - Analyzing the network formation and curing kinetics of epoxy resins by in situ near-infrared measurements with variable heating rates N2 - Near-infrared spectroscopy (NIR) turned out to be well suited for analyzing the degree of cure for epoxy systems. In contrast to dynamic scanning calorimetry (DSC), where the released heat of reaction determines the degree of epoxy conversion indirectly, NIR spectroscopy is able to determine the conversion directly by analyzing structural changes. Therefore, a new heatable NIR cell was equipped with an integrated thermocouple, which enables the real sample temperature to be controlled and monitored in situ during epoxy curing. Dynamic scans at different heating rates were used for kinetic modelling, to define kinetic parameters and to predict real curing processes. The kinetic models and their parameters were validated with an isothermal and a more complex multi-step curing scenario. Two available commercial epoxy systems based on DGEBA were used with an anhydride and with an amine hardener. NIR results were compared with DSC data. The simulated conversion predicted with a model fitted on the basis of NIR and DSC dynamic scans showed good agreement with the conversion measured in the isothermal curing validation test. Due to the proven reliability of NIR in measuring the reaction progress of curing, it can be considered a versatile measurement system for in situ monitoring of component production in the automotive, aerospace and wind energy sectors. KW - Epoxy resins KW - Curing kinetics KW - Near-infrared spectroscopy KW - DSC PY - 2015 U6 - https://doi.org/10.1016/j.tca.2015.08.008 SN - 0040-6031 SN - 1872-762X VL - 616 SP - 49 EP - 60 PB - Elsevier CY - Amsterdam AN - OPUS4-34187 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dümichen, Erik A1 - Braun, Ulrike A1 - Sturm, Heinz A1 - Kraemer, R. A1 - Deglmann, P. A1 - Gaan, S. A1 - Senz, R. T1 - A new molecular understanding of the thermal degradation of PA 66 doped with metal oxides: Experiment and computation N2 - The thermal molecular degradation of polyamide 66 (PA 66) doped with (partially supported) metal oxide particles (Fe2O3, ZnO, Al2O3) was investigated qualitatively and quantitatively using common analysis techniques like thermogravimetry coupled with IR-spectroscopic evolved gas analysis (TGA-FTIR). Using pyrolysis coupled with gas chromatography mass spectrometry (Py-GC-MS), qualitative conclusions were drawn about the complex hydrocarbon products. However, the combination of TGA with solid-phase extraction, followed by thermal desorption gas chromatography mass spectrometry (TED-GC-MS), allows qualitative and even semi-quantitative conclusions about the decomposition pathway of PA 66 in the presence of various metal oxide particles. The investigations under inert conditions showed that the presence of metal particles increases the rate of decarboxylation and deamination reactions, as well as the formation rate of cyclopentanone and pyridine derivatives. These species are a consequence of various condensation reactions. The condensation reactions release a large amount of water, thus triggering the hydrolysis of PA 66. Molecular thermal degradation mechanisms were developed for the main decomposition as well as for the condensation reactions and supported by quantum chemical calculations. The catalytic effect of the metal oxides in PA 66 increases in the following order: PA 66 = PA 66 – Al2O3 < PA 66 – Fe2O3 < PA 66 – ZnO. KW - PA 66 KW - Metal oxide particles KW - Thermal degradation KW - Solid-phase extraction KW - Molecular modeling PY - 2015 U6 - https://doi.org/10.1016/j.polymdegradstab.2015.07.011 SN - 0141-3910 SN - 1873-2321 VL - 120 SP - 340 EP - 356 PB - Elsevier Ltd. CY - London AN - OPUS4-33806 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Erdmann, Maren A1 - Trappe, Volker A1 - Sturm, Heinz A1 - Braun, Ulrike A1 - Dümichen, Erik T1 - Cure conversion of structural epoxies by cure state analysis and in situ cure kinetics using nondestructive NIR spectroscopy N2 - Non-isothermal heating rate kinetics was applied to two epoxy resin systems. In situ near-infrared (NIR) measurements were taken with a heatable NIR cell which allowed the cure to be monitored by characteristic absorption bands. An autocatalyzed reaction of the nth order was shown to describe the epoxy conversion curves. Differential Scanning Calorimetry (DSC) was used as a complementary method. The kinetic models developed by both NIR and DSC are in good accordance with experimental epoxy conversion in the in situ NIR setup for single and multiple cure temperature ramps. A linear calibration curve of the characteristic absorption bands of epoxy normalized to aromatic vibrations was introduced. The curing degree of structural epoxies that were cured according to an industrial temperature cure profile was determined by NIR using the calibration curve. The epoxy conversions of the structural components showed good agreement with the experimental in situ NIR. Several degrees of cure for structural specimens were evaluated by NIR and residual reaction enthalpy by DSC. We present the non-destructive NIR spectroscopy as an alternative to determine fast and non-destructive epoxy conversion, particularly suitable for high degrees of cure on structural components. KW - Epoxy resin KW - Curing kinetics KW - In situ near-infrared (NIR) spectroscopy KW - Differential scanning calorimetry (DSC) PY - 2017 UR - http://www.sciencedirect.com/science/article/pii/S0040603117300205 U6 - https://doi.org/10.1016/j.tca.2017.01.010 SN - 0040-6031 SN - 1872-762X VL - 650 SP - 8 EP - 17 PB - Elsevier B.V. AN - OPUS4-39123 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Eisentraut, Paul A1 - Braun, Ulrike T1 - Fast identification of microplastics using thermal extractions methods N2 - A new and full automated system for the analysis of microplastics in environmental samples is presented. T2 - BAM-BfR Seminar 2018 CY - Berlin, Germany DA - 15.02.2018 KW - Mikroplastik KW - TED KW - Thermal degradation PY - 2018 AN - OPUS4-44179 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dümichen, Erik A1 - Eisentraut, Paul A1 - Celina, M. A1 - Braun, Ulrike T1 - Automated thermal extraction-desorption gas chromatography mass spectrometry: A multifunctional tool for comprehensive characterization of polymers and their degradation products N2 - The TED-GC-MS analysis is a two-step method. A sample is first decomposed in a thermogravimetric analyzer (TGA) and the gaseous decomposition products are then trapped on a solid-phase adsorber. Subsequently, the solid-phase adsorber is analyzed with thermal desorption gas chromatography mass spectrometry (TDU-GC-MS). This method is ideally suited for the analysis of polymers and their degradation processes. Here, a new entirely automated System is introduced which enables high sample throughput and reproducible automated fractioned collection of decomposition products. Strengths and limitations of the system configuration are elaborated via three examples focused on practical challenges in materials analysis and identification: i) separate analysis of the components of a wood-plastic-composite material, ii) quantitative determination of weight concentration of the constituents of a polymer blend and iii) quantitative analysis of model samples of microplastics in suspended particulate matter. KW - Thermal extraction-desorption gas chromatography mass spectrometry KW - Analysis KW - Polymers KW - Microplastics KW - Automation PY - 2019 U6 - https://doi.org/10.1016/j.chroma.2019.01.033 VL - 1592 SP - 133 EP - 142 PB - Elsevier CY - Amsterdam AN - OPUS4-48287 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Javdanitehran, M. A1 - Berg, D. Ch. A1 - Dümichen, Erik A1 - Ziegmann, G. ED - Javdanitehran, M. T1 - An iterative approach for isothermal curing kinetics modelling of an epoxy resin system N2 - In this work a novel iterative method for isothermal cure kinetic modelling of an epoxy resin system using differential scanning calorimetry (DSC) technique is presented. To reach the isothermal cure temperature, the sample has to be heated up from ambient temperature. This is commonly done with very high heat-up rates to minimise the time the sample reacts at temperatures other than the desired one. However, during heat up with high heating the amount of released energy rates cannot be measured directly because the shape of baseline is unknown. This means that the cure state at the beginning of the isothermal stage is unknown. For fast curing systems this unknown cure state causes significant inaccuracies in cure kinetics modelling. The presented iterative approach attempts to estimate the released enthalpy during heat-up of an isothermal run through an iterative numerical modelling of the heat-up phase. In each iteration the algorithm starts by estimating the enthalpy released during heat-up based on the recorded temperature profile and the calibrated model of the previous iteration. At the same time, it estimates the degree of cure at the end of the heat-up phase. Once the initial cure state is known the total heat of enthalpy can be recalculated for the current iteration. Subsequently the degree of cure and curing rate are re-evaluated with the newly estimated total enthalpy and used for determining the kinetics parameters. This is done by simultaneous fitting of the selected model to all experimental heat flow curves using a non-linear nonrestricted multivariable fitting method. The model with these new parameters is used again to estimate the released enthalpy and cure degree during the heat-up phase. The described loop is repeated until a predefined convergence criterion is satisfied. For modelling the reaction kinetics, the Kamal–Sourour equation accompanied with Rabinowitch approach to consider the diffusion effects is used. The diffusion reaction rate is modelled by the free volume model proposed by Huguenin and Klein. DiBenedetto model is applied to predict the Evolution of glass transition temperature against the degree of cure. In order to compensate the effect of the Initial values in the model’s calibration, the algorithm is implemented in a routine, which assesses the quality of the fitting and consequently selects the cure kinetics parameter. The described algorithm and the Routine are implemented in MATLAB. This paper demonstrates the application of this approach for using cure kinetics modelling to predict the degree of cure and the glass transition temperature. It supports the obtained results with validation tests using isothermal, dynamic and combined temperature profiles. KW - Epoxy resins KW - Curing kinetics KW - DSC KW - Isothermal PY - 2016 U6 - https://doi.org/10.1016/j.tca.2015.11.014 VL - 2016 IS - 623 SP - 72 EP - 79 PB - Elsevier B.V. AN - OPUS4-35719 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Campbell, C. G. A1 - Jordon Astorga, D. A1 - Dümichen, Erik A1 - Celina, M. T1 - Thermoset materials characterization by thermal desorption or pyrolysis based gas chromatography-mass spectrometry methods N2 - Thermoset materials characterization is often limited to solid state analytical techniques such as IR, NMR, DSC, TGA and mechanical testing. Alternatively, their off-gassing behavior can also be evaluated using GC based techniques such as TD-GC-MS, allowing this method to be applied to thermoset materials analyses such as identification, aging characterization, and formulation optimization. As an overview, common thermoset materials were evaluated by analyzing their gaseous degradation products via TGA-based pyrolysis and subsequent TD-GC-MS for the identification of representative volatile signatures. It is thereby possible to distinguish different classes of phenolic materials or cured epoxy resins, as well as their amine or anhydride curatives. Additionally, this method enabled quantification of a volatile fragment (bisphenol A, BPA) which is associated with oxidation of epoxy/amine thermoset materials. The amount of evolved BPA increased linearly with aging time and this trend exhibits linear Arrhenius behavior over the temperature range (80–125 °C) studied, in agreement with oxidation sensitivies based on oxygen consumption data. Further, TD-GC-MS was used to explore how off-gassing of residual anhydride curative from an epoxy/anhydride material depends on formulation stoichiometry. Even in formulations that theoretically contained enough epoxy to consume all anhydride (1:1 stoichiometry), an imperfect final cure state resulted in residual anhydride which could evolve from the material. For such materials, a slightly epoxy-rich formulation is required to ensure that the material contains no residual unreacted anhydride. Analysis of volatiles generated by thermal exposure is an attractive characterization approach enabling compositional analysis as well as complementary diagnostics for materials degradation. KW - Polymer analysis/characterization KW - Thermal desorption mass spectrometry KW - Thermoset composition KW - Volatiles from thermosets KW - Degradation signatures PY - 2020 U6 - https://doi.org/10.1016/j.polymdegradstab.2019.109032 VL - 174 SP - 109032 PB - Elsevier Ltd. AN - OPUS4-50435 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dümichen, Erik A1 - Eisentraut, Paul A1 - Bannick, Claus Gerhard A1 - Barthel, Anne-Kathrin A1 - Senz, R. A1 - Braun, Ulrike T1 - Fast identification of microplastics in complex environmental samples by a thermal degradation method N2 - In order to determine the relevance of microplastic particles in various environmental media, comprehensive investigations are needed. However, no analytical method exists for fast identification and quantification. At present, optical spectroscopy methods like IR and RAMAN imaging are used. Due to their time consuming procedures and uncertain extrapolation, reliable monitoring is difficult. For analyzing polymers Py-GC-MS is a standard method. However, due to a limited sample amount of about 0.5 mg it is not suited for analysis of complex sample mixtures like environmental samples. Therefore, we developed a new thermoanalytical method as a first step for identifying microplastics in environmental samples. A sample amount of about 20 mg, which assures the homogeneity of the sample, is subjected to complete thermal decomposition. The specific degradation products of the respective polymer are adsorbed on a solid-Phase adsorber and subsequently analyzed by thermal Desorption gas chromatography mass spectrometry. For certain identification, the specific degradation products for the respective polymer were selected first. Afterwards real environmental samples from the aquatic (three different rivers) and the terrestrial (bio gas plant) systems were screened for microplastics. Mainly polypropylene (PP), polyethylene (PE) and polystyrene (PS) were identified for the samples from the bio gas plant and PE and PS from the rivers. However, this was only the first step and quantification measurements will follow. KW - Microplastics KW - Thermal desorption KW - Gas chromatography PY - 2017 U6 - https://doi.org/10.1016/j.chemosphere.2017.02.010 SN - 0045-6535 SN - 1879-1298 IS - 174 SP - 572 EP - 584 PB - Elsevier AN - OPUS4-40235 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Eisentraut, Paul A1 - Dümichen, Erik A1 - Ruhl, A. A1 - Jekel, M. A1 - Albrecht, M. A1 - Gehde, M. A1 - Braun, Ulrike T1 - Two Birds with One Stone-Fast and Simultaneous Analysis of Microplastics: Microparticles Derived from Thermoplastics and Tire Wear N2 - Analysis of microplastic particles (MP) in environmental samples needs sophisticated techniques and is time intensive due to sample preparation and detection. An alternative to the most common (micro ) spectroscopic techniques, FTIR or Raman spectroscopy, are the thermoanalytical methods, where specific decomposition products can be analyzed as marker compounds for different kind of plastics types and mass contents. Thermal extraction desorption gas chromatography mass spectrometry (TED-GC-MS) allows the fast identification and quantification of MP in environmental samples without sample preparation. Whereas up to now only the analysis of thermoplastic polymers was realized, this is the first time that even the analysis of tire wear (TW) content in environmental samples is possible. Various marker compounds for TW were identified. They include characteristic decomposition products of elastomers, antioxidants and vulcanization agents. Advantages and drawbacks of these marker substances were evaluated. Environmental samples from street run off were exemplarily investigated and presented. KW - TED-GC-MS KW - Microplastic KW - Tire wear PY - 2018 U6 - https://doi.org/10.1021/acs.estlett.8b00446 VL - 5 IS - 10 SP - 608 EP - 613 PB - American Chemical Society AN - OPUS4-46460 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Braun, Ulrike A1 - Eisentraut, Paul T1 - Thermal extraction/desorption-gas chromatography-mass spectroscopy: A powerful tool for analyzing the degradation and decomposition of polymers N2 - Due to the high molecular weights the analysis of polymers is difficult to carry out. Their dissolution is usually limited and the vapor pressure is very low. However, the degradation of a polymer leads usually to smaller compounds which then enable volatile analysis to aid in the characterization of the degradation or decomposition mechanism. The type and the amount of these smaller degradation products is characteristic for the momentary stage of the degradation process. With thermal desorption coupled to gas chromatography with mass spectrometry (TDS-GC-MS) the polymers can be heated from ambient temperatures to approximately 300 °C. During the heating process small volatile products with a molecular mass up to 350 - 400 m/z were first cryogenic trapping, reheated under controlled conditions and finally separated through a chromatographic column and identified with mass spectrometry. For instance clear differences in the released volatile species of Polypropylene (PP) can be observed depending on the progress of accelerated aging. In combination with a Thermogravimetric analyzer (TGA) the samples can be heated up to 1000 °C under inert as well oxidative atmosphere. This leads to a complete thermal-pyrolytic or thermo-oxidative degradation of the whole material and a release of degradation fragments over a range of Mw. These fragments enable conclusions for the underlying degradation or decomposition pathways. For coupling to GC-MS a solid-phase adsorption agent can be coupled to the exhaust of the TGA. This adsorption agent is usually a PDMS species that is capable to adsorb compounds with a wide range of polarities. After the thermal extraction the solid-phase adsorption agent will be analyzed by TDS-GC-MS. Therefore, it is possible to determine the species and amounts of the released complex thermal or thermo-oxidative degradation products in detail. This approach offers overall advantageous over existing volatile analytical methods. Thus, it was possible to determine new thermal and thermo-oxidative degradation mechanism pathways of a well-known material like Polyamide 66 (PA 66). Further example is the unique analysis of small polymer particles, which can be identified and quantified in complex environmental samples. This is our current focus of R&D activities within the framework of the analysis of microplastics in the environment. In the present work we will present a new, automatized set up of this method. T2 - PDDG CY - Taormina, Sicily, Italy DA - 04.09.2017 KW - Thermal desorption KW - Thermal extraction PY - 2017 AN - OPUS4-41910 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dümichen, Erik A1 - Eisentraut, Paul A1 - Bannick, Claus Gerhard A1 - Barthel, Anne-Kathrin A1 - Braun, Ulrike A1 - Senz, R. T1 - Fast identification of microplastics in complex environmental samples by a thermal degradation method N2 - n order to determine the relevance of microplastic particles in various environmental media, comprehensive investigations are needed. However, no analytical method exists for fast identification and quantification. At present, optical spectroscopy methods like IR and RAMAN imaging are used. Due to their time consuming procedures and uncertain extrapolation, reliable monitoring is difficult. For analyzing polymers Py-GC-MS is a standard method. However, due to a limited sample amount of about 0.5 mg it is not suited for analysis of complex sample mixtures like environmental samples. Therefore, we developed a new thermoanalytical method as a first step for identifying microplastics in environmental samples. A sample amount of about 20 mg, which assures the homogeneity of the sample, is subjected to complete thermal decomposition. The specific degradation products of the respective polymer are adsorbed on a solid-phase adsorber and subsequently analyzed by thermal desorption gas chromatography mass spectrometry. For certain identification, the specific degradation products for the respective polymer were selected first. Afterwards real environmental samples from the aquatic (three different rivers) and the terrestrial (bio gas plant) systems were screened for microplastics. Mainly polypropylene (PP), polyethylene (PE) and polystyrene (PS) were identified for the samples from the bio gas plant and PE and PS from the rivers. However, this was only the first step and quantification measurements will follow. KW - Thermal Degradation KW - Microplastic PY - 2017 U6 - https://doi.org/10.1016/j.chemosphere.2017.02.010 VL - 174 SP - 572 EP - 584 PB - Elsevier Ltd. AN - OPUS4-42143 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Deußing, G. A1 - Dümichen, Erik A1 - Braun, Ulrike T1 - Polymeranalytik Intelligent kombiniert N2 - Durch die intelligente Anbindung an die Stir Bar Sorptive Extraction (SBSE) lassen sich Zersetzungsprodukte der thermogravimetrischen Analyse (TGA) von Polymeren auf effiziente Weise anreichern, auftrennen und mittels GC/MS identifizieren. KW - Thermische Degradation KW - Mikroplastik PY - 2016 UR - http://www.gerstel.cn/de/GA51_Polymeranalytik.htm IS - 51 SP - 9 EP - 11 PB - Gerstel AN - OPUS4-42146 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Deußing, G. A1 - Dümichen, Erik A1 - Braun, Ulrike T1 - Der Fänger im Spülgas N2 - Durch die intelligente Anbindung an eine in der GC/MS gängige Extraktionstechnik (SBSE) lassen sich Zersetzungsprodukte der thermogravimetrischen Analyse (TGA) von Polymeren auf effiziente Weise anreichern, anschließend trennen und sicher identifizieren. KW - Polymeranalytik KW - Thermische Extraktion PY - 2015 UR - http://www.laborpraxis.vogel.de/so-erweitern-sie-die-moeglichkeiten-der-tga-a-490995/index2.html UR - https://files.vogel.de/vogelonline/vogelonline/issues/6773.pdf SN - 0344-1733 VL - 39 IS - 6 SP - 24 EP - 27 PB - Vogel Business Media AN - OPUS4-42149 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dümichen, Erik A1 - Eisentraut, Paul A1 - Braun, Ulrike T1 - Polymere und Mikroplastik in der Umwelt N2 - Es wird ein neues und voll automatisiertes Verfahren vorgestellt für die Analyse von Mikroplastik in der Umwelt. KW - Mikroplastik KW - TED PY - 2017 SN - 0016-3538 VL - 61 IS - 9 SP - 24 EP - 27 PB - Wiley AN - OPUS4-42170 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - THES A1 - Dümichen, Erik T1 - Einsatz neuer thermoanalytischer Verfahren zur Untersuchung thermischer und thermo-oxidativer Degradationsmechanismen sowie dem Netzwerkaufbau von Polymeren N2 - Die Anwendung thermoanalytischer Methoden für die Polymercharakterisierung hat aufgrund der makromolekularen Struktur von Polymere Vorteile. Es wurden zwei neue thermoanalyti-sche Verfahren entwickelt und deren Einsatz anhand von Anendungsbeispielen demons-triert, sowie mit etablierten, thermoanalytischen Methoden verglichen. Für die thermische- und thermo-oxidative Zersetzungsgasanalytik wurde die Thermogravi-metrie (TGA) gekoppelt mit der Thermodesoptions-Gaschromatographie-Massenspektrometrie (TDS-GC-MS). Die Zersetzungsgase der TGA wurden dafür über ei-nen Festphasenadsorber geleitet, auf dem eine repräsentative Auswahl von polymerspezifi-schen Analyten adsorbiert wurde. Die thermische Extraktion der Analyten erfolgte in der TDS-GC-MS. Dies ermöglichte die Trennung der Analyten sowie die eindeutige Identifizie-rung mittels charakteristischer Massenfragmentmuster. Sie wurde als TED-GC-MS bezeichnet. Es stellte sich heraus, dass sie sich besonders für die Analyse von komplexen Kohlen-wasserstoffgemischen mit Molmassen von mehr als 100 g/mol eignet. In Kombination mit anderen Kopplungstechniken wie beispielsweise die TGA-FTIR/MS, die speziell für die Ana-lyse von kleineren Molekülen verwendet wurde, konnten neue grundlegende Zersetzungs-mechanismen entwickelt werden. Es wurde beispielsweise sichtbar, dass sowohl bei der thermischen als auch bei der thermo-oxidativen Degradation von Polyamid 66 (PA 66) Kon-densationsreaktionen eine wichtige Rolle spielen. Die Methode erwies sich darüber hinaus als besonders geeignet für die Identifizierung und Quantifizierung von Polymeren in Umweltproben. Es entstand dazu eine erste grundlegende Arbeit für die quantitative Bestimmung von Polyethylen (PE) Mikroplastik in Umweltproben. Im zweiten Teil der Arbeit wurde eine steuerbare beheizbare Zelle eingeführt. Mit ihr war es möglich, mit Hilfe der Nahinfrarotspektroskopie (NIR), sich verändernde Netzwerkstrukturen während der Härtung sichtbar zu machen. Vergleichend dazu wurden etablierte, kalorische Messungen durchgeführt. Somit konnten für verschiedene Epoxidsysteme die Aushärtegrade während der Härtung mit variablen Heizraten bestimmt werden. Dadurch konnten Aushär-tungskinetiken erstellt werden, die durch isotherme und komplexe Aushärtungsszenarien validiert wurden. KW - Thermische Methoden KW - Polymer KW - Analytik PY - 2016 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:188-fudissthesis000000100982-9 UR - http://www.diss.fu-berlin.de/diss/receive/FUDISS_thesis_000000100982 SP - 1 EP - 65 PB - FU Berlin CY - Berlin AN - OPUS4-42171 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik A1 - Braun, Ulrike T1 - Neue Verfahren zur Untersuchung der Polymerdegradation und Aushärtung N2 - Es werden neue analytische Verfahren für die thermische und thermo-oxidative Degradation von Polymeren dargestellt sowie für die Analyse des Netzwerkaufbaus von Epoxidharzen. CY - Hochschule Hamm-Lippstadt DA - 16.12.2014 KW - Polymeranayltik PY - 2014 AN - OPUS4-42154 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Elert, Anna Maria A1 - Becker, Roland A1 - Dümichen, Erik A1 - Eisentraut, Paul A1 - Falkenhagen, Jana A1 - Sturm, Heinz A1 - Braun, Ulrike T1 - Comparison of different methods for MP detection: What can we learn from them, and why asking the right question before measurments matters? N2 - In recent years, an increasing trend towards investigating and monitoring the contamination of the environment by microplastics (MP) (plastic pieces < 5 mm) has been observed worldwide. Nonetheless, a reliable methodology that would facilitate and automate the monitoring of MP is still lacking. With the goal of selecting practical and standardized methods, and considering the challenges in microplastics detection, we present here a critical evaluation of two vibrational spectroscopies, Raman and Fourier transform infrared (FTIR) spectroscopy, and two extraction methods: thermal extraction desorption gas chromatography mass spectrometry (TED-GC-MS) and liquid extraction with subsequent size exclusion chromatography (SEC) using a soil with known contents of PE, PP, PS and PET as reference material. The obtained results were compared in terms of measurement time, technique handling, detection limits and requirements for sample preparation. The results showed that in designing and selecting the right methodology, the scientific question that determines what needs to be understood is significant, and should be considered carefully prior to analysis. Depending on whether the object of interest is quantification of the MP particles in the sample, or merely a quick estimate of sample contamination with plastics, the appropriate method must be selected. To obtain overall information about MP in environmental samples, the combination of several parallel approaches should be considered. KW - Microplastics KW - FTIR imaging KW - Raman imaging KW - TED-GC-MS KW - SEC KW - Analysis and identification PY - 2017 U6 - https://doi.org/10.1016/j.envpol.2017.08.074 SN - 0269-7491 SN - 1873-6424 VL - 231 IS - 2 SP - 1256 EP - 1264 PB - Elsevier AN - OPUS4-42157 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dümichen, Erik T1 - Neue Verfahren zur Untersuchung der Polymerdegradation und Aushärtung N2 - Es werden neue analytische Verfahren für die thermische und thermo-oxidative Degradation von Polymeren dargestellt sowie für die Analyse des Netzwerkaufbaus von Epoxidharzen. T2 - Sonderkolloquium des Adolf-Martens-Fonds e. V. CY - Berlin, Germany DA - 30.05.2017 KW - Poymeranalytik KW - Thermische Degradation PY - 2017 AN - OPUS4-42159 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Braun, Ulrike A1 - Eisentraut, Paul A1 - Altmann, Korinna A1 - Kittner, Maria A1 - Dümichen, Erik A1 - Thaxton, K. A1 - Kleine-Benne, E. A1 - Anumol, T. T1 - Accelerated Determination of Microplastics in Environmental Samples Using Thermal Extraction Desorption-Gas Chromatography/Mass Spectrometry (TED-GC/MS) N2 - There is growing interest in quantifying microplastics in environmental samples. This application note presents a thermal extraction desorption-gas chromatography/mass spectrometry (TED-GC/MS) method that is well suited to automation and increased sample throughput. The method is also able to detect all particle sizes in the sample as long as the limit of detection (LOD) is reached and allows analysis of larger samples of 15 to 25 mg or more. Samples were decomposed by thermogravimetric analysis (TGA), and the gaseous decomposition products were trapped on a solid-phase sorbent, followed by thermal desorption‑gas chromatography/mass spectrometry (TD-GC/MS) using an Agilent 5977B GC/MSD coupled to an Agilent 7890B GC. Target microplastic particle (MP) polymers were identified in environmental samples including surface water, finished compost, house dust, and drinking water. Quantification of MP polymers in environmental samples provided LODs of 0.06 to 2.2 μg, allowing the detection of MPs in trace amounts with sample weights of up to 1 g. Method repeatability was adequate for reliable quantification with RSDs of approximately 6 to 12%. KW - Environment KW - Microplastic particles KW - TED-GC/MS KW - Mass content KW - Thermoanalytical PY - 2020 VL - 2020 SP - 1 EP - 8 PB - Agilent Technologies Inc. CY - USA AN - OPUS4-51672 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -