TY - JOUR A1 - Böhning, Martin A1 - Tidjani, Adams A1 - Wald, Oliver A1 - Brzezinka, Klaus-Werner A1 - Turky, Gamal A1 - Goering, Harald A1 - Schartel, Bernhard A1 - Schönhals, Andreas T1 - Dielectric and gas transport properties of polypropylene-clay nanocomposites T2 - Frühjahrstagung des Arbeitskreises Festkörperphysik bei der DPG CY - Regensburg, Germany DA - 2002-03-11 PY - 2002 SN - 0420-0195 SN - 0372-5448 SN - 0343-9216 IS - CPP 5.4 SP - 425 CY - Bad Honnef AN - OPUS4-2036 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Gas transport and molecular mobility in polymer/POSS nanocomposites T2 - Euromembrane 2006 CY - Taormina, Italy DA - 2006-09-24 PY - 2006 AN - OPUS4-11214 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Investigation of swollen polymer/gas-systems: atomistic packing models based on experimental properties T2 - Frühjahrstagung der Deutschen Physikalischen Ges. / AKF Condensed Matter CY - Dresden, Germany DA - 2006-03-26 PY - 2006 AN - OPUS4-11316 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Gas Transport and Molecular Mobility in Polymer Based Nanocomposite Systems T2 - 1st International Conference on Advanced Materials and their application, National Research Centre, Physics Division CY - Cairo, Egypt DA - 2005-12-12 PY - 2005 AN - OPUS4-10976 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Small Molecules in Polymers and Polymer based Nanocomposites - Molecular Probes for Material Characterization and Design T2 - Polydays 2004 (Berliner Polymerentage); Universität Potsdam, Campus "Am Neuen Palais" CY - Potsdam, Germany DA - 2004-10-04 PY - 2004 AN - OPUS4-7297 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin A1 - Goering, Harald T1 - Preparation and Characterisation of Nanoscaled Nanostructured Materials T2 - Nanofair 2004 CY - Karlsruhe, Germany DA - 2004-11-22 PY - 2004 AN - OPUS4-7296 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin A1 - Robertson, Daniela A1 - Schröder, Hartmut T1 - Autoclave testing: a new approach for the evaluation of oxidative long-term resistance of geosynthetics N2 - Oxidative long time resistance is essential for many polyolefin based products, especially if repair or exchange is not possible as encountered in many building and geotechnical applications. Current regulations and recommendations for geosynthetics cover mainly the needs of a maximum lifetime of 25 years, though many applications require longer lifetimes up to 100 years and more. Reliable testing of the long time oxidation resistance is complicated by the complex interplay of physicochemical processes and reactions in combination with the need of relatively short testing durations, usually not exceeding 12 months. Thus for conventional atmospheric oven testing, the use of temperatures higher than 100 °C is inevitable, making conclusive Arrhenius extrapolations often questionable. Practical assessments of oxidative durability consist of exposures under accelerated ageing conditions with subsequent characterization of exposed material samples with respect to their residual stabilization and/or their mechanical properties. The autoclave test combines exposures at elevated temperatures with higher oxygen pressures and is performed with material samples immersed in a well defined aqueous medium representing critical environments in geosynthetic applications and including extraction of additives. Under these conditions meaningful results can be obtained within reasonable testing durations at only moderately elevated temperatures up to 80 °C. Application of different physicochemical methods, such as tensile testing, OIT /HP-OIT and analysis of residual antioxidant content (ICOT), in order to determine the time dependent degradation behaviour, reveal valuable information about mechanisms and effectiveness of the used antioxidants. Corresponding results for exposures at different temperatures and oxygen pressures are the basis for a 3D-extrapolation in order to estimate the expected service life. Different empirical models are presented and discussed with respect to their practical impact. T2 - EuroGeo4, 4th European Geosynthetics Conference CY - Edinburgh, UK DA - 2008-09-07 KW - Ageing KW - Degradation KW - Geotextiles KW - Polyolefin KW - Polypropylene KW - Oxidative resistance KW - Lifetime prediction PY - 2008 IS - Paper 143 SP - 1 EP - 8 AN - OPUS4-18424 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Heuchel, M. A1 - Hölck, Ole A1 - Böhning, Martin A1 - Siegert, R. A1 - Hofmann, D. ED - Qi, Y. ED - H.E. Fang, ED - N. Reynolds, ED - Liu, Z.-K. T1 - Knowledge-based approach to gas sorption in glassy polymers by combining experimental and molecular simulation techniques N2 - We present a method which allows to calculate gas sorption in complex polymers where, as slow processes, gas induced plasticization and volume dilation are important factors. Since the relaxational swelling of the polymer matrix that is observed at elevated gas concentrations takes hours or days, the swelling process is orders of magnitudes too slow to simulate the respective molecular dynamics in reasonable time and effort. To address this apparent incompatibility of experiment and simulation, we use single representative reference states from experiment and construct atomistic packing models according to these specifications. Gas sorption of CO2 and CH4 was successfully calculated on polysulfone, a 6FDA-polyimide, and a polymer of intrinsic microporosity, PIM-1, at 308 K and pressures up to 50 bar. T2 - MRS Fall Meeting 2008 - Symposium W - Computational Materials Design via Multiscale Modeling CY - Boston, MA, USA DA - 2008-12-01 KW - Gas sorption KW - Molecular modelling KW - Simulation KW - Glassy polymers PY - 2009 DO - https://doi.org/10.1557/PROC-1130-W06-10 VL - 1130 SP - W06 EP - W10 AN - OPUS4-19106 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Gas sorption in glassy polymers - Comparative characterization using experimental and molecular modeling techniques T2 - EUROMEMBRANE 2009 Conference CY - Montpellier, France DA - 2009-09-06 PY - 2009 AN - OPUS4-20018 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Böhning, Martin A1 - Hölck, Ole A1 - Heuchel, M. A1 - Hofmann, D. T1 - Characterization of gas sorption in glassy polymers combining experimental and molecular modeling techniques KW - Glassy Polymers KW - Gas Sorption KW - Molecular Modelling KW - Diffusion PY - 2008 SN - 0743-0515 VL - 98 SP - 875 EP - 876 PB - Division of Polymeric Materials Science and Engineering, American Chemical Society CY - Washington, DC AN - OPUS4-17485 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Autoclave testing - a new approach for the evaluation of oxidative long-term resistance of geosynthetics T2 - 4th European Geosynthetics Conference CY - Edinburgh, Scotland DA - 2008-09-07 PY - 2008 AN - OPUS4-18295 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Gas transport in glassy polymers and PNCs - experiment, analysis, modeling of diffusion, sorption and dilation T2 - Workshop: Polymers, University of Zagreb, Faculty of Mechanical Engineering and Naval Architecture, Laboratory for Non-Metals CY - Zagreb, Croatia DA - 2012-05-23 PY - 2012 AN - OPUS4-25969 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Gas transport in glassy polymers and PNCs - experiment, analysis, modeling of diffusion, sorption and dilation T2 - Workshop: Nanostructured and Nanocomposite Membranes for Gas und Vapour Separation CY - Cetraro, Italy DA - 2012-05-15 PY - 2012 AN - OPUS4-26631 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Correlation of gas diffusivity and local chain mobility in polycarbonate/POSS nanocomposites as determined by broadband dielectric relaxation spectroscopy T2 - Euromembrane 2012 CY - London, England DA - 2012-09-23 PY - 2012 AN - OPUS4-26629 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Kinetic analysis of gas sorption and gas induced dilation and relaxation behaviour of PIM-1 compared to other glassy polymers T2 - Euromembrane 2012 CY - London, England DA - 2012-09-23 PY - 2012 AN - OPUS4-26630 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Frasca, Daniele A1 - Schulze, Dietmar A1 - Wachtendorf, Volker A1 - Krafft, Bernd A1 - Morys, Michael A1 - Böhning, Martin A1 - Rybak, Thomas T1 - Multilayer graphene rubber nanocomposites N2 - Multilayer Graphene (MLG), a nanoparticle with a specific surface of BET = 250 m²/g and thus made of only approximately 10 graphene sheets, is proposed as a nanofiller for rubbers. When homogenously dispersed, it works at low loadings enabling the replacement of carbon black (CB), increase in efficiency, or reduction in filler concentration. Actually the appropriate preparation yielded nanocomposites in which just 3 phr are sufficient to significantly improve the rheological, curing and mechanical properties of different rubbers, as shown for Chlorine-Isobutylene-Isoprene Rubber (CIIR), Nitrile-Butadiene Rubber (NBR), Natural Rubber (NR), and Styrene-Butadiene Rubber (SBR). A mere 3 phr of MLG tripled the Young’s modulus of CIIR, an effect equivalent to 20 phr of carbon black. Similar equivalents are observed for MLG/CB mixtures. MLG reduces gas permeability, increases thermal and electrical conductivities, and retards fire behavior. The later shown by the reduction in heat release rate in the cone calorimeter. The higher the nanofiller concentration is (3 phr, 5 phr, and 10 phr was investigated), the greater the improvement in the properties of the nanocomposites. Moreover, the MLG nanocomposites improve stability of mechanical properties against weathering. An increase in UV-absorption as well as a pronounced radical scavenging are proposed and were proved experimentally. To sum up, MLG is interesting as a multifunctional nanofiller and seems to be quite ready for rubber development. T2 - TOP 2016, VIII International Conference on “Times of Polymers and Composites” CY - Naples, Italy DA - 19.06.2016 KW - Graphene KW - Nanocomposite KW - Rubber PY - 2016 SN - 978-0-7354-1390-0 DO - https://doi.org/10.1063/1.4949621 SN - 0094-243X SN - 1551-7616 VL - 1736 SP - 020046, 1 EP - 4 PB - AIP AN - OPUS4-36864 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Konnertz, Nora A1 - Ding, Yi A1 - Harrison, W.J. A1 - Budd, P.M. A1 - Schönhals, Andreas A1 - Böhning, Martin T1 - Molecular mobility of the high performance membrane polymer PIM-1 as investigated by dielectric spectroscopy N2 - The increasing demand for energy efficient separation processes fosters the development of new high performance polymers as selective separation layers for membranes. PIM-1 is the archetypal representative of the class of polymers of intrinsic microporosity (PIM) which are considered most promising in this sector, especially for gas separations. Since their introduction, PIMs stimulated a vast amount of research in this field and meanwhile evolved to the state of the art in membrane technology for gas separation. The major obstacle for extending the practical membrane application is their strong tendency to physical aging. For the first time, investigations by broadband dielectric spectroscopy (BDS) addressing molecular dynamics and conductivity in PIM 1 are presented. As chain packing during film formation from the casting solution and physical aging are key factors determining the separation performance of PIMs as membrane materials, characterization of the molecular mobility in such materials as revealed by BDS will provide valuable information for further development and optimization. KW - PIM-1 KW - BDS broadband dielectric spectroscopy KW - Relaxation KW - Membrane PY - 2016 DO - https://doi.org/10.1021/acsmacrolett.6b00209 SN - 2161-1653 VL - 5 IS - 4 SP - 528 EP - 532 PB - ACS American Chemical Society CY - Washington, DC, USA AN - OPUS4-35798 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Konnertz, Nora A1 - Böhning, Martin A1 - Schönhals, Andreas A1 - Ding, Yi T1 - Molecular mobility and gas transport properties of PIM-1 and nano composites based on PIM-1 and phenethylPOSS N2 - Polymers with intrinsic microporosity are of highly interest in the field of gas separation membranes. Especially the first synthesized PIM-1 shows extraordinary permeabilities and selectivities. Unfortunately, PIM-1 tends to physical aging and loses its good properties. Physical aging is related to the molecular mobility of PIM-1 which was here investigated by broadband dielectric spectroscopy (BDS). Besides the studies on pure PIM-1 a polyhedral oligomeric silsesquioxane with phenethyl substituents (PhenethylPOSS) was used as nanofiller (0 - 40 wt-%) in the PIM-1 matrix to improve the gas transport properties and prevent physical aging. The molecular mobility of the solution casted nano composite films was analyzed by BDS as well. Furthermore, gas transport properties were determined with the time lag method (0 - 20 bar) in a temperature range of 35°C to 65°C with N2, O2, CH4 and CO2. T2 - 80. Jahrestagung der DPG und DPG-Frühjahrstagung CY - Regensburg, Germany DA - 06.03.2016 KW - PIM-1 PY - 2016 AN - OPUS4-35541 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Niebergall, Ute A1 - Zanotto, M. A1 - Wachtendorf, Volker A1 - Böhning, Martin T1 - Impact of biodiesel sorption on tensile properties of PE-HD for container applications N2 - In previous papers, we investigated the influence of biodiesel or diesel on mechanical properties of a high-density polyethylene (PE-HD) for tank applications using Charpy impact tests and dynamicmechanical analysis (DMA). In this work, covering two more PE-HD materials, we extend our study to addressing the tensile properties, especially changes of Young's modulus, after immersion in biodiesel or diesel at 60 °C. As we cover sorption and desorption behavior, during desorption, i.e. storage at 60 °C in a circulating air oven, ageing or degradation phenomena were also observed and characterized in some detail using spectral reflectance measurements and FT-IR spectroscopy. The results obtained here support the concept of co-oxidation, i.e. the faster oxidation of the PE-HD matrix if the samples were previously saturated with biodiesel, itself easily oxidizable. KW - polyethylene KW - biodiesel KW - biofuels KW - sorption KW - plasticization KW - degradation PY - 2016 DO - https://doi.org/10.1016/j.polymertesting.2016.01.025 SN - 0142-9418 VL - 50 SP - 315 EP - 324 PB - Elsevier AN - OPUS4-35369 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Agroui, K. A1 - Collins, G. A1 - Oreski, G. A1 - Böhning, Martin A1 - Hadj Arab, A. A1 - Ouadjaout, D. T1 - Effect of crosslinking on EVA-based encapsulant properties during photovoltaic module fabrication process N2 - The key objective of this work is to create a comprehensive comparison between experimental analysis methods for detecting crosslinking reaction in EVA encapsulant material during PV module fabrication process. Several analytical methods, spanning from classical gel content extraction measurements over different thermo-analytic and mechanical approaches to spectroscopic analysis as Thermally Stimulated Current (TSC), have been investigated as to their ability to reveal the crosslinking state of ethylene vinyl acetate (EVA). The basic results show that TSC complements perfectly other thermal analysis methods like as Differential Scanning Calorimetry (DSC), Dynamic Mechanical Thermal Analysis (DMTA) to determine fundamental properties of EVA such as molecular mobility characteristics and also to monitor the crosslinking reaction. Exothermic peak as revealed by DSC analysis can be used to estimate the crosslinking rate of EVA during PV module encapsulation process as fast quality control test. ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ L'objectif principal de ce travail est de permettre une meilleure compréhension entre les différentes techniques analyses expérimentales pour détecter la réaction de réticulation au niveau de l’encapsulant Ethylène-Vinyle Acétate (EVA), durant le process de fabrication d'un module PV. Plusieurs méthodes d'analyse, allant du test classique d'extraction du taux de gel aux différentes techniques d'analyses thermomécaniques ainsi que les techniques d'analyse de spectroscopie comme le courant stimulé thermiquement (TSC), ont été étudiés pour permettre de révéler le phénomène de la réaction de réticulation de l'encapsulant l'EVA. Les résultats de base montrent que la TSC complète parfaitement d'autres méthodes d'analyses thermiques comme la calorimétrie différentielle à balayage (DSC), l'analyse mécanique dynamique (DMTA) pour déterminer les propriétés fondamentales de l'EVA. Ces techniques permettent de déterminer les caractéristiques relatives à la mobilité moléculaire et aussi pour mieux mettre en évidence la réaction de réticulation. Le pic exothermique comme révélé par l'analyse par DSC, peut être utilisé pour estimer le taux de réticulation de l'EVA au cours du process d'encapsulation du module PV comme un test rapide de contrôle de qualité. KW - EVA KW - Photovoltaic module KW - Crosslinking process KW - Thermal properties KW - Mechanical properties PY - 2015 SN - 1112-2242 VL - 18 IS - 2 SP - 303 EP - 314 AN - OPUS4-34994 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zorn, R. A1 - Yin, Huajie A1 - Lohstroh, W. A1 - Harrison, W. A1 - Budd, P.M. A1 - Pauw, Brian Richard A1 - Böhning, Martin A1 - Schönhals, Andreas T1 - Anomalies in the low frequency vibrational density of states for a polymer with intrinsic microporosity - the Boson peak of PIM-1 N2 - Polymers with intrinsic microporosity are promising candidates for the active separation layer in gas separation membranes. Here, the vibrational density of states (VDOS) for PIM-1, the prototypical polymer with intrinsic microporosity, is investigated by means of inelastic neutron scattering. The results are compared to data measured for a more conventional high-performance polyimide used in gas separation membranes (Matrimid). The measured data show the characteristic low frequency excess contribution to VDOS above the Debye sound wave level, generally known as the Boson peak in glass-forming materials. In comparison to the Boson peak of Matrimid, that of PIM-1 is shifted to lower frequencies. This shift is discussed considering the microporous, sponge-like structure of PIM-1 as providing a higher compressibility at the molecular scale than for conventional polymers. For an annealed PIM-1 sample, the Boson peak shifts to higher frequencies in comparison to the un-annealed sample. These changes in the VDOS of the annealed PIM-1 sample are related to changes in the microporous structure as confirmed by X-ray scattering. KW - Polymers KW - Boson peak KW - Neutron scattering KW - Physical aging KW - Polymer of intrinsic microporosity PY - 2018 DO - https://doi.org/10.1039/C7CP07141H SN - 1463-9076 SN - 1463-9084 VL - 20 IS - 3 SP - 1355 EP - 1363 PB - The Royal Society of Chemistry AN - OPUS4-43808 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yin, Huajie A1 - Chua, Y. Z. A1 - Yang, B. A1 - Schick, C. A1 - Harrison, W. A1 - Budd, P. A1 - Böhning, Martin A1 - Schönhals, Andreas T1 - First clear cut experimental evidence for a glass transition in a polymer with intrinsic microporosity: PIM-1 N2 - Polymers with intrinsic microporosity (PIMs) represent a novel, innovative class of materials with great potential in various applications from high-performance gas separation membranes to electronic devices. Here for the first time, for PIM-1, as the archetypal PIM, fast scanning calorimetry provides definitive evidence for a glass transition (Tg=715 K, heating rate 3·10^4 K/s) by decoupling the time-scales responsible for glass transition and decomposition. As the rigid molecular structure of PIM-1 prevents any conformational changes, small-scale bend and flex fluctuations must be considered the origin of its glass transition. This result has strong implications for the fundamental understanding of the glass transition and for the physical aging of PIMs and other complex polymers, both topical problems of materials science. KW - Polymers with intrinsic microporosity KW - Fast Scanning Calorimetry PY - 2018 DO - https://doi.org/10.1021/acs.jpclett.8b00422 SN - 1948-7185 VL - 9 IS - 8 SP - 2003 EP - 2008 PB - ACS AN - OPUS4-44683 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Thuy, Maximilian A1 - Niebergall, Ute A1 - Oehler, H. A1 - Alig, I. A1 - Böhning, Martin T1 - Evaluation of the damaging effect of crop protection formulations on high density polyethylene using the Full Notch Creep Test N2 - Four typical high-density polyethylene container materials were used to investigate damage or stress cracking behavior in contact with model liquids for crop protection products. These model liquids are established in German regulations for the approval of dangerous goods containers and consist of typical admixtures used for crop protection products but without biological active ingredients. This study is performed with the standardized method of Full Notch Creep Test, adapting the media temperature to 40 °C according to the usual conditions where these test liquids are applied. The two model liquids differ into a water-based solution and a composition based on different organic solvents which are absorbed by the material up to significant levels. Therefore, extensive sorption measurements are performed. The fracture surfaces obtained are analyzed in detail not only by light microscopy, but also by laser scanning microscopy as well as scanning electron microscopy. Influence of pre-saturation and applied stress are addressed by respective systematic series of experiments. KW - Polyethylene KW - Full Notch Creep Test KW - Environmental Stress Cracking KW - Fracture PY - 2021 DO - https://doi.org/10.1016/j.polymer.2021.123853 SN - 0032-3861 VL - 228 SP - 123853 PB - Elsevier Ltd. AN - OPUS4-52686 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Environmental Stress Cracking in PE-HD – Assessment of Crack Propagation and Mechanisms by Optical Methods N2 - Slow crack growth (SCG) under the influence of external fluid media, usually termed environmental stress cracking (ESC), is still one of the most frequent origins of severe damage and failure of polymeric materials. For polyethylene (PE) this is relevant for mass products, like bottles for consumer products, but also for high-performance materials for pipes or industrial packaging, including containers for chemicals and other dangerous goods. Especially for high-density polyethylene (PE-HD) the susceptibility to SGC and ESC is depending on the complex interplay between molecular weight and architecture and the resulting semicrystalline morphology, especially the formation of tie-molecules. A reliable assessment of the resistance against this damage phenomenon is essential for demanding as well as safety-critical applications and has to take into account suitable testing methodologies and conditions in combination with environmental media reflecting the properties representative for typical fillings and relevant components causing ESC. In this context a better understanding of different influencing factors, such as sorption, swelling or surface activity is necessary together with a detailed characterization of different stages of crack propagation and underlying mechanisms. Therefor well-established testing methods, such as the Full Notch Creep Test (FNCT), were complemented by detailed fracture surface analysis using e.g. LSM and SEM in combination with a time-dependent optical monitoring of the progressing crack growth. For the crack growth also the ratio of fibrillated craze zone to crack opening is important for the deeper understanding of crack propagation and related material parameters which can be additionally addressed by X-ray computed tomography. T2 - 34th Polymer Degradation Disscussion Group (PDDG) Conference CY - Dubrovnik, Croatia DA - 12.06.2023 KW - Polyethylen KW - Full Notch Creep Test KW - Environmental Stress Cracking KW - Fracture Surface Analysis PY - 2023 AN - OPUS4-57711 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Strommer, Bettina A1 - Battig, Alexander A1 - Schulze, Dietmar A1 - Agudo Jácome, Leonardo A1 - Schartel, Bernhard A1 - Böhning, Martin T1 - Shape, orientation, interaction, or dispersion: valorization of the influence factors in natural rubber nanocomposites N2 - The addition of nanoparticles as reinforcing fillers in elastomers yields nanocomposites with unique property profiles, which opens the door for various new application fields. Major factors influencing the performance of nanocomposites are studied by varying the type and shape of nanoparticles and their dispersion in the natural rubber matrix. The industrial applicability of these nanocomposites is put into focus using two types of graphene and a nanoscale carbon black, all commercially available, and scalable processing techniques in the form of a highly filled masterbatch production via latex premixing by simple stirring or ultrasonically assisted dispersing with surfactant followed by conventional two-roll milling and hot pressing. Different processing and measurement methods reveal the potential for possible improvements: rheology, curing behavior, static and dynamic mechanical properties, swelling, and fire behavior. The aspect ratio of the nanoparticles and their interaction with the surrounding matrix prove to be crucial for the development of superior nanocomposites. An enhanced dispersing method enables the utilization of the improvement potential at low filler loadings (3 parts per hundred of rubber [phr]) and yields multifunctional rubber nanocomposites: two-dimensional layered particles (graphene) result in anisotropic material behavior with strong reinforcement in the in-plane direction (157% increase in the Young's modulus). The peak heat release rate in the cone calorimeter is reduced by 55% by incorporating 3 phr of few-layer graphene via an optimized dispersing process. KW - Graphene KW - Natural rubber KW - Nanocomposites KW - Anisotropy KW - Fire behavior PY - 2023 DO - https://doi.org/10.5254/rct.23.77961 SN - 0035-9475 SN - 1943-4804 VL - 96 IS - 1 SP - 40 EP - 58 PB - Allen Press CY - Lawrence (KA), USA AN - OPUS4-57568 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Erdmann, Maren A1 - Kleinbub, Sherin A1 - Wachtendorf, Volker A1 - Schütter, Jan David A1 - Niebergall, Ute A1 - Böhning, Martin A1 - Koerdt, Andrea T1 - Photo-oxidation of PE-HD affecting polymer/fuel interaction and bacterial attachment N2 - In the present study, a simple approach was used to investigate the effect of UV-exposure on two high density Polyethylene materials (PE-HD), commonly used for storage tanks, on fuel sorption behavior and colonization by microorganisms. The aim was to investigate whether the sorption behavior of the fuels (diesel/biodiesel) and the colonization by microorganisms, frequently occurring in the fuel, is affected and may lead to undesirable or safety-relevant material changes. We showed that the UV-irradiation leads to significant changes of the sorption behavior due to chemi-crystallization and crosslinking. The fuel Sorption is affected by the UV-induced formation of polar carbonyl and hydroxyl groups predominantly occurring at the surface. With respect to microbial colonization behavior for Bacillus subtilis and Pseudomonas aeruginosa, isolated from a contaminated diesel sample, differences of the initial adhesion could be shown depending on the initial type of polyethylene as well as on the degree of UV-induced degradation. KW - High density polyethylene KW - Bacterial attachment KW - UV-irradiation KW - Fuel sorption PY - 2020 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-510001 DO - https://doi.org/10.1038/s41529-020-0122-1 VL - 4 IS - 1 SP - Article number: 18 PB - Nature Partner Journals AN - OPUS4-51000 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Curing behavior of EVA-based encapsulants for photovoltaic applications T2 - 11. Schwarzheider Kunststoffkolloquium CY - Schwarzheide, Germany DA - 2011-09-21 PY - 2011 AN - OPUS4-24936 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Robertson, Daniela A1 - Schröder, Hartmut A1 - Böhning, Martin A1 - Brummermann, K. A1 - Kaundinya, I. A1 - Saathoff, F. T1 - Test method for the assessment of the service life of polymeric geosynthetic barriers (GBR-P) for road tunnels N2 - This paper is dealing with a systematic investigation to evaluate the testing method “autoclave test” for the assessment of the oxidative durability of polyolefin-based GBR-P products applied in road tunnel construction. The aim was to derive suitable exposure conditions and criteria for a practical testing procedure with regard to service lifetimes up to 100 years. The screening test (index test) according to DIN EN ISO 13438 developed in the BAM was applied in extended form and amended by a basic characterization, as well as complementary analyses, following autoclave exposure. The time dependency of some of the products and the so called lifetime parameter of one product were investigated and compared with the results of conventional oven tests. Based on the results of the research program some conclusions and practical outlooks were concluded. T2 - Euro GEO 5 - 5th European geosynthetics congress CY - Valencia, Spain DA - 16.09.2012 KW - Durability KW - Oxidation KW - Acceleration ageing KW - GBR-P PY - 2012 SN - 978-0415-64340-5 VL - 1 IS - Topic: Transport SP - 150 EP - 154 AN - OPUS4-27312 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Maximilian, Thuy A1 - Spyrantis, Alexander A1 - Böhning, Martin A1 - Niebergall, Ute A1 - Maaß, Robert T1 - Spatially resolved roughness exponent in polymer fracture N2 - The fracture surface of slow and continuous crack propagation during environmental stress cracking of a semicrystalline polyethylene exhibits isotropic roughness exponents at the local scale but resolved across the macroscopic fracture surface a clear position dependence is found. The spatially resolved roughness exponent admits values in the range between 0.1 and 0.4, demonstrating nontrivial exponents in the small length-scale regime. Instead, they vary across the fracture surface according to the stress-state distribution, which suggests that the exponents are intimately linked to the locally dominating dissipation processes during craze cracking. KW - Plasticity KW - Fracture KW - Material failure KW - Mechanical deformation PY - 2022 DO - https://doi.org/10.1103/PhysRevMaterials.6.L090601 VL - 6 IS - 9 SP - 1 EP - 7 PB - American Physical Society CY - USA, Maryland AN - OPUS4-55797 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Erdmann, Maren A1 - Böhning, Martin A1 - Niebergall, Ute T1 - Physical and chemical effects of biodiesel storage on high-density polyethylene: Evidence of co-oxidation N2 - The physical and chemical effects of diesel and biodiesel fuels on two high-density polyethylene (PE-HD) types were investigated. Both semi-crystalline PE-HD are common thermoplastic materials for container and storage tank applications. Biodiesel, a composition of unsaturated fatty acid esters from renewable resources, was chosen as it is regarded a possible green alternative to fossil fuels. The study aims at identifying significant differences between biodiesel and conventional diesel fuels based on the differences in the chemical nature of the two. The physical effects of the fuels on the polymer at first comprises the sorption behavior, i.e. kinetics and final equilibrium concentration. Not only are both fuels absorbed by the amorphous phase of the semi-crystalline PE-HD, they also induce a plasticization effect that modifies the molecular mobility and therefore also the characteristic yielding properties, manifest in the obtained stress-strain curves. The chemical effects related to degradation phenomena is investigated by a long-term storage scenario using partially immersed tensile test specimens in diesel and biodiesel. We were able to confirm the proposed co-oxidation mechanism by Richaud et al. for polyethylene-unsaturated penetrant systems on a larger scale based on practical tensile tests. One of the investigated polyethylene grades subjected to tensile drawing showed a significant loss of plastic deformation and the onset of premature failure after 150 days of storage in biodiesel. Further biodiesel storage showed a systematically reduced elongation at break before necking. None of these effects were observed in diesel. Oxidation of fuels and polymer after progressing storage times were analyzed by the evolution of carbonyl species in FT-IR/ATR spectroscopy. KW - Biodiesel KW - Degradation KW - Long-term storage KW - Sorption KW - Diesel PY - 2019 DO - https://doi.org/10.1016/j.polymdegradstab.2019.01.018 SN - 0141-3910 VL - 161 IS - 1 SP - 139 EP - 149 PB - Elsevier CY - Amsterdam AN - OPUS4-47268 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yin, Huajie A1 - Chapala, P. A1 - Bermeshev, M. A1 - Pauw, Brian Richard A1 - Schönhals, Andreas A1 - Böhning, Martin T1 - Influence of Trimethylsilyl Side Groups on the Molecular Mobility and Charge Transport in Highly Permeable Glassy Polynorbornenes N2 - Superglassy polymers with a large fractional free volume have emerged as novel materials with a broad range of applications, especially in the field of membrane separations. Highly permeable addition-type substituted polynorbornenes with high thermal resistance and chemical stability are among the most promising materials. The major obstacle for extending the practical membrane application is their strong tendency to physical aging, leading to a partial decline in their superior transport performance over time. In the present study, broadband dielectric spectroscopy with complementary X-ray scattering techniques were employed to reveal changes in microporous structure, molecular mobility, and conductivity by systematic comparison of two polynorbornenes with different numbers of trimethylsilyl side groups. Their response upon heating (aging) was compared in terms of structure, dynamics, and charge transport behavior. Furthermore, a detailed analysis of the observed Maxwell−Wagner−Sillars polarization at internal interfaces provides unique information about the microporous structure in the solid films. The knowledge obtained from the experiments will guide and unlock potential in synthesizing addition-type polynorbornenes with versatile properties. KW - Dielectric spectroscopy KW - Molecular mobility KW - Electrical conductivity KW - Gas separation membranes PY - 2019 DO - https://doi.org/10.1021/acsapm.9b00092 SN - 2637-6105 VL - 1 IS - 4 SP - 844 EP - 855 PB - ACS CY - Washington DC AN - OPUS4-47838 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yin, Huajie A1 - B, Yang A1 - Chua, Y. Z. A1 - Szymoniak, Paulina A1 - Carta, M A1 - Malpass-Evans, R A1 - McKeown, N A1 - Harrison, W A1 - Budd, P A1 - Schick, C A1 - Böhning, Martin A1 - Schönhals, Andreas T1 - Effect of backbone rigidity on the glass transition of polymers of in-trinsic microporosity probed by fast scanning calorimetry N2 - Polymers of Intrinsic Microporosity (PIMs) of high performance have developed as materials with a wide application range in gas separation and other energy-related fields. Further optimization and long-term behavior of devices with PIMs require an understanding of the structure-property relationships including physical aging. In this context the glass transi-tion plays a central role, but with conventional thermal analysis a glass transition is usually not detectable for PIMs be-fore their thermal decomposition. Fast scanning calorimetry provides evidence of the glass transition for a series of PIMs, as the time scales responsible for thermal degradation and for the glass transition are decoupled by employing ultrafast heating rates of tens of thousands K s-1. The investigated PIMs were chosen considering the chain rigidity. The estimated glass transition temperatures follow the order of the rigidity of the backbone of the PIMs. KW - Polymers of intrinsic microporosity KW - Fast scanning calormetry PY - 2019 DO - https://doi.org/10.1021/acsmacrolett.9b00482 SN - 2161-1653 VL - 8 IS - 8 SP - 1022 EP - 1028 PB - ACS Publications AN - OPUS4-48617 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Böhning, Martin A1 - Frasca, Daniele A1 - Schulze, Dietmar A1 - Schartel, Bernhard ED - Yaragalla, S. ED - Kumar Mishra, R. ED - Thomas, S. ED - Kalarikkal, N. ED - Maria, H. J. T1 - Multilayer Graphene/Elastomer Nanocomposites N2 - Elastomers are usually reinforced by large amount of fillers like carbon black (CB) or silica in order to improve various mechanical properties, such as Young’s modulus, hardness, tear resistance, abrasion resistance, and gas barrier properties. In recent years, such improvements were also obtained by using nanoparticles at significantly lower filler loadings. Graphene is a twodimensional (2D) sheet of a thickness in the atomic scale, composed of a honeycomb structure of sp2 carbon atoms. Besides significant mechanical reinforcement, graphene harbors the potential to be used as a multifunctional filler, as it can also increase the conductivity and weathering stability of elastomer matrices. Ultraviolet (UV) irradiation and oxidative agents can lead to the degradation of elastomers due to a multistep photooxidative process, including the formation of radicals. Carbon-based fillers have an influence on these reactions, as they can absorb UV radiation and act as radical scavengers. This chapter summarizes the results of our larger project on multilayer graphene (MLG)/elastomer nanocomposites, previously published, which present a comprehensive case study of MLG as a multifunctional nanofiller in elastomer/graphene nanocomposites. Different elastomeric matrices are compared in order to demonstrate the outstanding impact of MLG as a general benefit. The dependency of this effect on concentration is discussed in detail. Taking into account the key role of dispersion, different mixing procedures are compared, evaluating a facile implementation of graphene nanocomposites into conventional rubber processing. Finally, the most probable commercial uses of MLG nanofillers in combination with conventional CB are studied. The nanocomposites were prepared in the kg scale in order to obtain enough specimens to investigate various properties of the uncured and vulcanized rubbers at the highest quality level, including rheology, curing, morphology, several mechanical properties, abrasion, conductivity, gas permeation, burning behavior, and weathering stability. The structure property relationships are asserted and questioned, for example, by investigating the radical scavenging ability or aspect ratio of the MLG. This chapter illustrates the state of the art of graphene/rubber nanocomposites targeted for commercial mass applications. KW - Nanocomposite KW - Graphene KW - Rubber KW - Reinforcement KW - Durability KW - Masterbatch KW - Gas Barrier Properties KW - Conductivity PY - 2019 SN - 978-0-12-817342-8 SP - 139 EP - 200 PB - Elsevier AN - OPUS4-47408 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Characterization of high-performance membrane polymers for gas separation using broadband dielectric spectroscopy N2 - In recent years superglassy polymers exhibiting intrinsic microporosity established a new perspective for a number of applications, especially for gas separation membranes as These polymers Combine extremely high permeabilities with attractive selectivities. The essential factor governing the structure Formation in the solid film or layer is either a contorted rigid Backbone (polymers of intrinsic microporosity - PIMs) or extremely bulky side groups (polynorbornenes and polytricyclonenenes). For a deeper understanding of both types of such high-Performance polymers for gas separation membranes and their further development broadband dielectric spectroscopy (BDS) can provide a substantial contribution. BDS addresses molecular relaxations characterizing the dynamics of the solid polymer as a major factor determining the gas transport properties but also the physical aging behavior which is an essential issue for such polymers. BDS is applied on PIMs where fluctuations of molecular dipoles connected to the backbone can be directly monitored. Furthermore, also polynorbornenes were investigated which carry no dipole moment in their repeat unit - the high resolution of modern equipment allows for the detailed analysis also for very small dielectric losses originating from partially oxidized moieties or marginal catalyst residues. Additionally, from interfacial polarization phenomena, such as Maxwell-Wagner-Sillars (MWS) polarization due to blocking of charge carriers at internal interfacial boundaries on a mesoscopic length scale, valuable information on the intrinsic microporosity and its changes induced by physical aging can be obtained. Finally, also conductivity can be characterized in detail in such polymeric systems revealing contributions of interactions of aromatic moieties (π-π-stacking) or the drift motion of charge carriers. These features also determine the structure formation in the solid state. T2 - 257th ACS National Meeting - Symposium "Transport in Polymer Membranes" CY - Orlando, FL, USA DA - 31.03.2019 KW - polymers KW - gas separation membranes KW - polynorbornenes KW - polymers of intrinsic microporosity KW - dielectric spectroscopy KW - molecular mobility PY - 2019 AN - OPUS4-48142 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jaunich, Matthias A1 - Böhning, Martin A1 - Braun, Ulrike A1 - Teteris, G. A1 - Stark, W. T1 - Investigation of the curing state of ethylene/vinyl acetate copolymer (EVA) for photovoltaic applications by gel content determination, rheology, DSC and FTIR N2 - The cure behaviour of a specific ethylene vinyl acetate material as used for encapsulation of photovoltaic modules was analysed by rheometer, differential scanning calorimetry and Fourier transform infrared spectroscopy to test for a suitable replacement for the laborious determination of gel content. The results show that all applied methods are capable of describing the effects of the cross-linking process. Some provide results very similar to those yielded by analysis of the insoluble content, but the question remains as to whether indirect methods should be preferred over the direct measurement of physical properties, e.g. as performed by the curemeter. A material stored for one year was also tested to demonstrate the effect of extended storage on cure behaviour and how this is detected by different methods. This complements the other methods, which were clearly able to detect the different cure behaviour of the aged EVA, whereas determination of the gel content could not. KW - Photovoltaic cell encapsulation KW - EVA KW - Incoming goods control KW - Insoluble content KW - Rheometer PY - 2016 DO - https://doi.org/10.1016/j.polymertesting.2016.03.013 SN - 0142-9418 VL - 52 IS - 1 SP - 133 EP - 140 PB - Elsevier Ltd. CY - Oxford, UK AN - OPUS4-35918 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - von der Ehe, Kerstin A1 - Jaunich, Matthias A1 - Wolff, Dietmar A1 - Böhning, Martin A1 - Goering, Harald T1 - Radiation induced structural changes of (U)HMW polyethylene with regard to its application for radiation shielding N2 - The special properties of high molecular weight polyethylene (HMW-PE) and ultra high molecular weight polyethylene (UHMW-PE) result basically from their extreme chain lengths and their high degree of crystallinity. As high-performance polymers, they are used for a variety of applications. UHMW-PE in particular is often utilized for endoprothesis (due to its excellent slip and wear properties) and due to its high hydrogen content as a neutron moderator in casks for storage and transport of radioactive materials. To prepare the material for instance for its use as a total joint replacement, it is exposed to radiation for several reasons, such as sterilization and crosslinking, leading to partial improvement of the mechanical properties (e.g. fracture toughness, crack propagation resistance, wear resistance) and better chemical stability. To be applicable for long term radiation shielding purposes for instance over a period of 40 years, PE has to withstand any type of degradation affecting safety relevant aspects. The scope of our investigation comprises an estimation of the radiation impact on the molecular and supra molecular structure of two types of PE and to what extent these changes are detectable by thermo-analytical (TA) methods, such as Differential Scanning Calorimetry (DSC), Thermo Mechanical Analysis (TMA), Dynamic Mechanical Analysis (DMA) and Thermo Gravimetric Analysis (TGA). Additionally FT-IR spectroscopy as well as density and gas sorption measurements were carried out. Due to the poor solubility of HMW-PE and UHMW-PE, some classical analytical techniques are not applicable. But TA-methods represent a feasible approach to detect structural and morphological features of these materials as well as changes caused by external influences, such as thermal treatment and/or irradiation. With the combination of the applied TA-techniques it is possible to distinguish between crosslinking and degradation. T2 - PATRAM 2010 - 16th International symposium on the packaging and transport of radioactive materials CY - London, UK DA - 2010-10-03 PY - 2010 SP - 1 EP - 8 (T25/Paper 173) AN - OPUS4-24621 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wolff, Dietmar A1 - von der Ehe, Kerstin A1 - Jaunich, Matthias A1 - Böhning, Martin T1 - Performance of neutron radiation shielding material (U)HMW-PE influenced by gamma radiation N2 - Due to their extreme high hydrogen contents high molecular weight (HMW-) and ultra-high molecular weight (UHMW-) polyethylene (PE) are a comprehensible choice as neutron radiation shielding material in thick walled metallic casks for storage and transport of radioactive materials. For this application it has to be taken into consideration that gamma radiation – that is a direct consequence of inserting radioactive material in such casks – has a high influence on the molecular structure of polyethylene. In order to be applicable for long-term neutron radiation shielding purposes during the whole storage period (in Germany for instance up to 40 years) PE has to withstand any type of degradation affecting safety relevant aspects. The scope of our work comprises an estimation of the influence of gamma radiation and temperature on the molecular and supra molecular structure of (U)HMW-PE used as cask components for neutron radiation shielding. Therefore it was investigated to what extent these changes are detectable by a combination of conventional polymer characterization techniques such as Differential Scanning Calorimetry (DSC), Thermo Mechanical Analysis (TMA), Dynamic Mechanical Analysis (DMA), and Thermo Gravimetric Analysis (TGA). Additionally optical (FTIR) and weighing methods were applied. For UHMWPE the results are compared with those published for similar UHMW-PE material that is used in medical technology. For this application, gamma irradiation is applied deliberately for purposes such as sterilization and crosslinking, the latter leading to partial improvement of mechanical properties and better chemical stability. As a result the so far observed structural changes of the irradiated material are not safety relevant for the application of polyethylene as neutron shielding material; moreover, some properties actually improve via irradiation. T2 - PSAM 11 ESREL 2012 - 11th International probabilistic safety assessment and management conference & The annual european safety and reliability conference CY - Helsinki, Finland DA - 25.06.2012 KW - (U)HMW-PE KW - Gamma irradiation KW - Shielding material KW - Cask for storage and transport of radioactive materials PY - 2012 SP - 1 EP - 8 AN - OPUS4-26176 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - von der Ehe, Kerstin A1 - Jaunich, Matthias A1 - Böhning, Martin A1 - Goering, Harald A1 - Wolff, Dietmar T1 - Detection of structural changes of (U)HMW-PE induced by gamma irradiation T2 - 14th International conference "Polymeric materials" CY - Halle (Saale), Germany DA - 2010-09-15 PY - 2010 SN - 978-3-86829-282-4 SP - 1 EP - 6 PB - Druck-Zuck GmbH CY - Halle / Saale AN - OPUS4-21997 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Jaunich, Matthias A1 - Kömmling, Anja A1 - Böhning, Martin A1 - Silbernagl, Dorothee T1 - Comparison of ageing behavior of O-ring seals under hydrogen and air N2 - Elastomeric seals are essential components in the infrastructure which prevent leakage of gas and ensure proper function of technical devices and are therefore highly safety relevant. For proper function a remaining resilience and tolerance to pressure changes is required. The ageing of elastomers is an undesirable but inevitable process leading to a limited lifetime of rubber products such as seals. Independent of the application, as e.g. automotive, piping or container applications, a long lifetime or at least a timely exchange of a seal before occurrence of critical failure is desired. Hydrogen is a key element for the energy turnaround and therefore the compatibility of seals with hydrogen is essential. In addition to the effect of hydrogen uptake and release, which might also cause destructive effects such as rapid gas decompression, ageing at high temperature under hydrogen atmosphere is of interest too. Most of the existing work is addressing the performance of new materials and comprises only very limited investigations concerning long-term use and the behaviour of aged materials in contact with hydrogen. As ageing can lead to substantial changes of material properties, it must be evaluated whether these changes are beneficial or deteriorating for the component function. In this work we present and compare results of the characterization of three sealing materials (EPDM, HNBR, FKM) after ageing at high temperature under hydrogen and air. Despite the common assumption that ageing under hydrogen atmosphere should be less severe for the material in comparison to air ageing, this is not the case for every material. T2 - ASME PVP2025, Pressure Vessels & Piping Conference CY - Montreal, Quebec, Canada DA - 20.07.2025 KW - Aging KW - Seal KW - Compression set KW - Atomic force microscopy PY - 2025 SP - 1 EP - 7 AN - OPUS4-63889 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zaghdoudi, M. A1 - Kömmling, Anja A1 - Böhning, Martin A1 - Jaunich, Matthias T1 - Ageing of elastomers in air and in hydrogen environment - A comparative study N2 - EPDM, HNBR and FKM materials were exposed at 150 ◦C to air under atmospheric pressure and to hydrogen at 50 bar for different ageing times. All measurements after hydrogen exposure were conducted on samples in degassed condition to assess irreversible effects resulting from that exposure and to compare them to those after ageing in air. Density, hardness, tensile properties, compression set, and hydrogen permeability of all samples were analysed. In both ageing environments, HNBR exhibited the most significant changes of material properties. However, for both EPDM and HNBR, considerably less severe ageing effects were observed under hydrogen in comparison to ageing in air. On the other hand, FKM showed about the same low level of deterioration in both ageing environments but exhibited poor resistance against damage due to rapid gas decompression in hydrogen environment that can lead to seal failure. The obtained results may serve as a guidance toward a better understanding for design and utilisation of elastomeric materials in future hydrogen infrastructure components. KW - Rapid gas decompression KW - Condensed matter physics KW - Hydrogen KW - Sustainability and the environment KW - Rubber sealing KW - Renewable energy PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-597417 DO - https://doi.org/10.1016/j.ijhydene.2024.03.053 SN - 0360-3199 SN - 1879-3487 VL - 63 SP - 207 EP - 216 PB - Elsevier CY - Oxford AN - OPUS4-59741 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Wolff, Dietmar A1 - von der Ehe, Kerstin A1 - Jaunich, Matthias A1 - Böhning, Martin A1 - Goering, Harald ED - Yamamoto, T. T1 - (U)HMWPE as neutron radiation shielding materials: impact of gamma radiation on structure and properties N2 - Due to their extreme high hydrogen contents, high molecular weight (HMW-) and ultra-high molecular weight (UHMW-) polyethylene (PE) are a comprehensible choice as neutron radiation shielding material in casks for storage and transport of radioactive materials. But as a direct consequence of inserting radioactive material in such casks, gamma radiation occurs. Hence, the impact of gamma radiation on the molecular structure of polyethylene has to be taken into consideration. Consequently, PE has to withstand any type of gamma radiation induced degradation affecting safety relevant aspects in order to be applicable for long term neutron radiation shielding purposes during the whole storage period (in Germany, for instance, up to 40 years). The scope of our investigation comprises an estimation of the impact of gamma radiation and temperature on the molecular and supra molecular structure of the two types of PE used as neutron radiation shielding cask components. A further point which is worth exploring is to what extent these changes are detectable by conventional analysis methods. Therefore, thermoanalytical measurements were performed such as differential scanning calorimetry (DSC), thermo mechanical analysis (TMA), dynamic mechanical analysis (DMA), and thermo gravimetric analysis (TGA). Additionally optical and weighing methods were applied. With those methods it is possible to detect structural changes in polyethylene induced by exposure to gamma radiation. The observed amounts of changes of the irradiated material are not safety relevant for the application of polyethylene as neutron radiation shielding material; moreover, some properties actually improve via irradiation. KW - HMW-PE KW - UHMW-PE KW - Gamma irradiation KW - Neutron radiation shielding material PY - 2013 SN - 978-0-8031-7533-4 DO - https://doi.org/10.1520/STP103980 N1 - Serientitel: STP – Series title: STP VL - 25 IS - STP 1547 SP - 211 EP - 227 AN - OPUS4-27931 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - The glass transition temperature of Polymers of Intrinsic Microporosity (PIMs) as determined by fast scanning calorimetry N2 - Polymers of intrinsic microporosity (PIMs) have recently emerged as novel materials for a broad range of high-performance applications from gas separation to electronic devices. The very rigid, contorted polymer chains show only limited molecular mobility and therefore pack inefficiently giving rise to intrinsic microporosity with pore sizes generally smaller than 1 nm resulting in BET surface areas larger than 700 m2/g. Using conventional thermal analysis techniques, no glass transition temperature (Tg) of PIMs could be unambiguously detected up to now. Employing fast scanning calorimetry (FSC) based on a one chip sensor, decoupling the time scales responsible for the glass transition and the thermal decomposition is a reliable strategy to overcome this limitation. The FSC device is capable to heat and cool a small sample (ng-range) with ultrafast rates of several ten thousand K/s. Evidence of a glass transition is obtained for a series of PIMs with different chain rigidities. Local small-scale fluctuations are held responsible for the glass transition of highly rigid PIMs rather than segmental motions as in conventional polymers. T2 - International Polymer Processing Society (PPS) - Europe-Africa 2019 Regional Conference (PPS2019) CY - Pretoria, South Africa DA - 18.11.2019 KW - Polymers KW - Polymers of intrinsic microporosity KW - Glass transition KW - Fast scanning calorimetry PY - 2019 AN - OPUS4-49957 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Musil, B. A1 - Böhning, Martin A1 - Johlitz, M. A1 - Lion, A. T1 - On the inhomogenous chemo-mechanical ageing behaviour of nitrile rubber: experimental investigations, modelling and parameter identification N2 - Elastomers are used in almost all areas of industrial applications, such as tires, engine mounts, bridge bearings, seals or coatings. During their use in operation, they are exposed to different environmental influences. These include, in particular, climatic factors such as air oxygen, high temperatures, light (UV radiation) and the influence of media (e.g. oils, fuels). A very important result of these factors is the chemical ageing of elastomers. In this case, the elastomer degenerates and changes its chemical structure in the aged regions, which leads to an irreversible change in the material properties in connection with the reduction in its usability. In this paper, chemical ageing of nitrile butadiene rubber (NBR) is investigated. Especially in case of thermo-oxidative ageing at elevated operating temperatures, the ageing processes run inhomogeneously. These effects are known as diffusion-limited oxidation (DLO) and are associated with the diffusion–reaction behaviour of atmospheric oxygen with the elastomer network. For these reasons, NBR samples are artificially aged in air and subjected to different experimental methods, which are presented and discussed. Additional results from inhomogeneous mechanical tests and permeation tests indicate the causes of the DLO-effect, show the influence of chemical ageing and are subsequently used for parameter identification in relation to the diffusion–reaction equation. A continuum-mechanical modelling approach is also presented here, which describes the finite hyperelasticity, diffusion–reaction processes as well as chemical degradation and reformation of the elastomer network. This multifield problem leads to a system of partial and ordinary differential equations and constitutive equations and is solved within the finite element method. KW - Rubber KW - Ageing KW - Gas permeability KW - DLO KW - NBR PY - 2019 DO - https://doi.org/10.1007/s00161-019-00791-1 SN - 0935-1175 SN - 1432-0959 VL - 32 IS - 1 SP - 127 EP - 146 PB - Springer CY - Heidelberg AN - OPUS4-48560 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Erdmann, Maren A1 - Kupsch, Andreas A1 - Müller, Bernd R. A1 - Hentschel, Manfred P. A1 - Niebergall, Ute A1 - Böhning, Martin A1 - Bruno, Giovanni ED - Erdmann, Maren T1 - Diesel-induced transparency of plastically deformed high-density polyethylene N2 - High-density polyethylene becomes optically transparent during tensile drawing when previously saturated with diesel fuel. This unusual phenomenon is investigated as it might allow conclusions with respect to the material behavior. Microscopy, differential scanning calorimetry, density measurements are applied together with two scanning X-ray scattering techniques: wide angle X-ray scattering (WAXS) and X-ray refraction, able to extract the spatially resolved crystal orientation and internal surface, respectively. The sorbed diesel softens the material and significantly alters the yielding characteristics. Although the crystallinity among stretched regions is similar, a virgin reference sample exhibits strain whitening during stretching, while the diesel-saturated sample becomes transparent. The WAXS results reveal a pronounced fiber texture in the tensile direction in the stretched region and an isotropic orientation in the unstretched region. This texture implies the formation of fibrils in the stretched region, while spherulites remain intact in the unstretched parts of the specimens. X-ray refraction reveals a preferred orientation of internal surfaces along the tensile direction in the stretched region of virgin samples, while the sample stretched in the diesel-saturated state shows no internal surfaces at all. Besides from stretching saturated samples, optical transparency is also obtained from sorbing samples in diesel after stretching. KW - PE-HD Sorption KW - Cavitation KW - Diesel Fuel KW - X-ray refraction KW - WAXS KW - Internal Surfaces KW - Crystal Texture PY - 2019 DO - https://doi.org/10.1007/s10853-019-03700-8 SN - 1573-4803 SN - 0022-2461 VL - 54 IS - 17 SP - 11739 EP - 11755 PB - Springer US CY - US AN - OPUS4-48226 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schilling, Markus A1 - Marschall, Niklas A1 - Niebergall, Ute A1 - Wachtendorf, Volker A1 - Böhning, Martin T1 - Unveiling Effects of Biodiesel and Diesel on Environmental Stress Cracking of PE-HD N2 - The behavior of high‐density polyethylene with respect to resistance against environmental stress cracking (ESC) is usually regarded as an inherent material property being specific for respective types of PE‐HD and tested using standardized methods, conditions, and also standard testing liquids (usually aqueous surfactant solutions). On the other hand, for practical applications the ESC behavior of those polymeric materials, commonly used for pipes or containers, in contact with other liquids (e.g., fuels) is often of relevant interest, but for a reasonable assessment, where consistent benchmark data for a direct comparison are often missing, it is essential to determine the actually prevailing failure mode and classify it related to crack propagation or other mechanisms. Using the well‐established Full Notch Creep Test, which favorably allows for a detailed microscopic fracture surface analysis after failure, the behavior of two typical PE‐HD types for container applications is investigated in biodiesel and diesel and compared to a standard surfactant solution. This enables a clear identification of characteristic features of the interaction of biodiesel and diesel as sorptive fuels in contact with the polymer, revealing the complex interplay of sorption and plasticization as well as ESC inducing effects on PE‐HD, which could be clearly shown for both fuels. KW - Biodiesel KW - Confocal laser scanning microscopy (LSM) KW - Diesel KW - Full notch creep test (FNCT) KW - Plasticization PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-650525 DO - https://doi.org/10.1002/pen.70239 SN - 0032-3888 SP - 1 EP - 16 PB - Wiley CY - Hoboken (NJ) AN - OPUS4-65052 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Schartel, Bernhard A1 - Richter, K. H. A1 - Böhning, Martin ED - Morgan, A. B. ED - Wilkie, C. A. ED - Nelson, G. L. T1 - Synergistic use of talc in halogen-free flame retarded polycarbonate/Acrylonitrile-butadiene-styrene blends N2 - Pyrolysis, flammability, fire behavior, melt viscosity, and gas diffusion of bisphenol A polycarbonate/acrylonitrile-butadiene-styrene (PC/ABS) were investigated, with bisphenol A bis(diphenyl phosphate) (BDP), with 10 wt.% talc and with BDP in combination with 5, 10 and 20 wt.% talc, respectively. Compared to PC/ABS, PC/ABS + BDP results in an increased decomposition temperature of PC, a higher char yield, a significantly increased LOI, a V-0 classification in UL 94, a reduced peak heat release rate (pHRR), and a reduced total heat release (THR) in the cone calorimeter. This efficient flame retardancy is due to mechanisms in both the gas and condensed phases. PC/ABS + 10 wt.% talc shows a decrease in the PC decomposition temperature. The fire behavior is improved in part compared to PC/ABS, with an increased LOI and reduced pHRR. PC/ABS + BDP + 10 wt.% talc shows a strong synergism in LOI, a V-0 classification, and a decrease in pHRR, whereas THR is slightly increased compared to PC/ABS + BDP. Talc decreases the gas diffusion and enhances the flow limit for low shear rates, both of which influence the pyrolysis and flammability results. Further, talc improves the protection properties of the fire residues. Nevertheless it also partly suppresses flame inhibition and the charring effect of BDP. The synergism between BDP and talc in LOI is obtained even for low talc loadings in PC/ABS + BDP + talc, whereas for higher loadings saturation is observed. KW - Flame retardancy KW - PC/ABS KW - Aryl phosphate KW - Talc PY - 2012 SN - 978-0-8412-2780-4 DO - https://doi.org/10.1021/bk-2012-1118.ch002 N1 - Serientitel: ACS Symposium Series – Series title: ACS Symposium Series VL - 1118 IS - Chapter 2 SP - 15 EP - 36 PB - Oxford University Press AN - OPUS4-27563 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -