TY - CONF A1 - Schröder, Hartmut A1 - Munz, Martin A1 - Böhning, Martin A1 - Lorenz, Edelgard A1 - Kneip, Gisela T1 - New method for testing the resistance to oxidation - Application and Evaluation: Polyolefinic Products T2 - EUROCORR 2006 CY - Maastricht, The Netherlands DA - 2006-09-25 PY - 2006 N1 - Serientitel: EFC-Event – Series title: EFC-Event IS - 280 SP - 1 EP - 8 PB - European Federation of Corrosion CY - Maastricht AN - OPUS4-13706 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Schröder, Hartmut A1 - Munz, Martin A1 - Böhning, Martin T1 - A new method for testing and evaluating the long-tIme resistance to oxidation of polyolefinic products T2 - 13th International Plastics Additives and Compounding Conference "Addcon World 2007" CY - Frankfurt/M. DA - 2007-09-05 PY - 2007 SN - 978-1-84735-018-3 IS - Paper 7 SP - 1 EP - 10 CY - Shawbury AN - OPUS4-15762 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schröder, Hartmut A1 - Munz, Martin A1 - Böhning, Martin T1 - A new method for testing and evaluating the long-time resistance to oxidation of polyolefinic products N2 - A report is presented on the development of a test for determining the long-term oxidation resistance of polyolefin materials, which is accelerated not only by elevated temperatures but also by increased oxygen pressure and a stirred aqueous medium. The method permits durability tests to be carried out at markedly lower temperatures with reasonable testing durations and significantly reduced diffusion limited oxidation effects and allows for physical and chemical impacts of aqueous media. Oxidative durability can be assessed by autoclave immersion exposures at three different temperatures (60, 70 and 80 degrees C) and 50 bar oxygen pressure and at 80 degrees C and two different oxygen pressures (usually 10 and 20 bar). Accelerated test data are evaluated by modified Arrhenius equations with the application of a three-dimensional regression analysis. The application of the test method to various materials, including PP non-woven materials and geosynthetics is demonstrated. 10 refs. KW - Polyolefin KW - Testing KW - Oxidation KW - Durability KW - Geosynthetics PY - 2008 SN - 0967-3911 SN - 1478-2391 VL - 16 IS - 1 SP - 71 EP - 79 PB - RAPRA Technology Ltd. CY - Shrewsbury AN - OPUS4-17187 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Böhning, Martin A1 - Niebergall, Ute A1 - Adam, Adeline A1 - Stark, Wolfgang T1 - Impact of biodiesel sorption on mechanical properties of polyethylene N2 - The time-dependent sorption of biodiesel in a typical polyethylene for container applications is investigated in comparison to conventional diesel fuel at three different temperatures. In this context, the desorption behavior is also addressed. Subsequently, the effects of both penetrants on mechanical properties are characterized in terms of impact strength and dynamic-mechanical analysis. The discussion of property changes is firstly based on the sorption kinetics of biodiesel and diesel, which is determined by immersion experiments allowing for the calculation of respective diffusion coefficients. Changes in impact strength as determined by the Charpy method are further characterised in more detail by analyzing the fracture surfaces, and correlated with results of dynamic-mechanical analysis. KW - Biodiesel KW - Fuel sorption KW - Desorption KW - Impact strength KW - Dynamic-mechanical analysis KW - PE-HD PY - 2014 DO - https://doi.org/10.1016/j.polymertesting.2013.12.003 SN - 0142-9418 VL - 34 SP - 17 EP - 24 PB - Elsevier Science CY - Amsterdam [u.a.] AN - OPUS4-30096 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Frasca, Daniele A1 - Schulze, Dietmar A1 - Böhning, Martin A1 - Krafft, Bernd A1 - Schartel, Bernhard T1 - Multilayer graphene chlorine isobutyl isoprene rubber nanocomposites: influence of the multilayer graphene concentration on physical and flame-retardant properties N2 - In recent years, different nanoparticles have been proposed and successfully introduced as nanofillers in rubber nanocomposites. In this study, multilayer graphene (MLG) is proposed as a nanoparticle that functions efficiently at low concentrations. MLG consists of just 10 or so graphene sheets. Chlorine isobutyl isoprene rubber (CIIR)/MLG nanocomposites with different MLG loadings were prepared using an ultrasonically assisted solution mixing procedure followed by two-roll milling. The incorporation of MLG provides a clear improvement in the rheological, mechanical, curing, and gas barrier properties of the nanocomposites. Adding only 3 phr ofMLGto CIIR increased the Young’s modulus by more than two times and reduced the permeability ofO2 andCO2 by 30%. Higher nanofiller concentrations yielded further improvement in the properties of the nanocomposites. Moreover, CIIR/MLG nanocomposites showed reduced flammability. KW - Graphene KW - Rubber KW - Nanocomposites KW - Flammability KW - Reinforcement PY - 2016 DO - https://doi.org/10.5254/rct.15.84838 SN - 0035-9475 VL - 89 IS - 2 SP - 316 EP - 334 AN - OPUS4-37595 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yin, Huajie A1 - Chapala, P. A1 - Bermeshev, M. A1 - Schönhals, Andreas A1 - Böhning, Martin T1 - Molecular Mobility and Physical Aging of a Highly Permeable Glassy Polynorbornene as Revealed by Dielectric Spectroscopy N2 - Polymeric membranes represent a cost- and energy efficient solution for gas separation. Recently superglassy polymers with high free volume outperform many conventional dense polymers in terms of gas permeability and selectivity. However, such polymers are prone to pronounced physical aging, resulting in a dramatic reduction in the gas permeability. Molecular mobility of polymer segments plays an important role in the physical aging and the gas transport performance of polymeric membranes. Molecular mobility and physical aging of a representative superglassy polynorbornene with very high gas permeability, PTCNSi2g, was monitored by using dielectric spectroscopy with state-of-the-art high-resolution analyzers. This work helps to shed some light on the structure−property relationship of superglassy polymers on a molecular level and to provide practical “design rules” for the development of high performance polymers for gas separation. KW - Molecular mobility KW - Gas separation membrane KW - Broadband dielectric spectroscopy KW - Polymer KW - Physical ageing PY - 2017 DO - https://doi.org/10.1021/acsmacrolett.7b00456 SN - 2161-1653 VL - 6 IS - 8 SP - 813 EP - 818 PB - ACS CY - Washington DC, USA AN - OPUS4-41354 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Characterization of gas sorption in glassy polymers combining experimental and molecular modeling techniques T2 - American Chemical Society (ACS) Spring Meeting CY - New Orleans, LA, USA DA - 2008-04-06 PY - 2008 AN - OPUS4-17402 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hao, Ning A1 - Böhning, Martin A1 - Wohlrab, Sebastian A1 - Schönhals, Andreas T1 - Polymer Based Nanocomposites with PhenethylPOSS as Nanofilter Investigated by Dielectric Spectroscopy and Gas Transport Measurements N2 - Polyhedral oligomeric silsesquioxane with phenethyl substituents (PhenethylPOSS) as nanofiller was incorporated within Poly(bisphenol A carbonate) (PBAC) as matrix. Dielectric spectroscopy proved an almost complete miscibility of PhenethylPOSS up to 7 wt. %. At higher concentrations phase separation yields composites with a PBAC-rich matrix and POSS-rich domains which posses well shaped interfaces. The nanocomposites were also investigated with respect to their gas transport behaviour. An increase of the gas permeability was found at higher PhenethylPOSS concentrations, which is due to the phase separated structure. KW - Dielectric measurements KW - Nanocomposites KW - Permeation KW - Polycarbonates KW - Polyhedral oligomeric silsesquioxanes PY - 2008 DO - https://doi.org/10.1002/masy.200850712 SN - 1022-1360 SN - 0258-0322 SN - 1521-3900 VL - 267 IS - 1 SP - 69 EP - 73 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-17751 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Atomistic simulation of gas sorption isotherms in a polymer of intrinsic microporosity (PIM-1) T2 - EUROMEMBRANE 2009 Conference CY - Montpellier, France DA - 2009-09-06 PY - 2009 AN - OPUS4-20103 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Retzlaff, J. A1 - Bronstein, Z. A1 - Müller-Rochholz, J. A1 - Böhning, Martin A1 - Robertson, Daniela A1 - Schröder, Hartmut T1 - Oxidative resistance of geosynthetics: practical aspects and developments of testing at elevated temperature and oxygen pressure N2 - Service life of geosynthetics made of polyolefin materials is mainly limited by oxidative degradation. Durability of polyolefin products depend on formulation, morphology resulting from manufacturing, design and particularly on the antioxidants used. Although the fundamental oxidative reactions are known, the complex effect of geosynthetic characteristics and external influences mean that durability assessments require practical tests. The assessment of oxidative durability involves exposure to accelerating conditions as well as the material characterisation with respect to the state of stabilisation and/or degradation (e.g. by tensile testing and/or oxidation induction time). The autoclave test developed by BAM for durability assessments of polyolefin geosynthetics is based on the simultaneous application of moderately elevated temperatures (up to 80 degrees Celsius) and elevated oxygen pressures (up to 5.0 MPa) in combination with a surrounding aqueous medium. Thus this test method provides several advantages in comparison to conventional oven testing, especially with respect to test duration, impact of surrounding environment and the potential to differentiate and rank oxidative resistance between products of very different dimensions (surface/volume) and stabilisation. In view of the increasing demand for durability assessments of geosynthetic products with lifetimes significantly exceeding 25 years, the contribution is focused on practical aspects concerning implementation and optimisation of test procedures, conditions and evaluation of results. Furthermore, advanced approaches based on multiple exposure conditions will also be included and corresponding calculations of expected service life in typical applications will be evaluated with respect to significance and repeatability. Thereby involved standards and recommendations - such as EN ISO 13438, Part C or EAG-EDT - are considered. T2 - EuroGeo4, 4th European Geosynthetics Conference CY - Edinburgh, UK DA - 2008-09-07 KW - Ageing KW - Degradation KW - HDPE KW - Laboratory test KW - Oxidation KW - Polypropylene PY - 2008 IS - Paper 178 SP - 1 EP - 4 AN - OPUS4-18423 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Retzlaff, J. A1 - Müller-Rochholz, J. A1 - Klapperich, H. A1 - Böhning, Martin T1 - The behaviour of geosynthetics under cyclic load N2 - Whenever geosynthetics are used to reinforce or stabilise infrastructural elements such as road- and railways, bridge abutments, run- and taxiways on airports or to protect coastlines of canals and other steep slopes they may be exposed to cyclic loads. Therefore, a reduction factor for dynamic effects on the geosynthetic tensile strength has been included into the calculation of the Long Term Design Strength (LTDS). An approach to assess the behaviour of geosynthetics is to adopt Woehler- or Smith graphs and Haigh-diagrams for polymers. This is because an endurance limit for polymers, which defines an infinite life under a defined cyclic load, has not been seen so far. A huge amount of mechanical testing is needed to predict the behaviour of geosynthetics against this particular background. To reduce these efforts while getting an indication of the cyclic effect on geosynthetics, a combined method of mechanical and chemical analysis has been developed. The pure tensile strength tests to determine the residual strength after cyclic stress has been amended by IR-spectroscopy and Differential Scanning Calorimetry (DSC). In this context the chain change model of PET has been proven as valid for cyclic loads as well, which helps to define the endurance limit of materials made out of PET. For polyolefins such as PP and PE, a limit for the maximum alternating load has been identified at the point of the stress strain graph where the actual and the numerical stress of a material diverge from each other. Cyclic tensile strength tests have been carried out in a hydraulic test frame. The test parameters have been set to simulate the service life of a railway bed trafficked by high speed trains (ICE). T2 - EuroGeo4, 4th European Geosynthetics Conference CY - Edinburgh, UK DA - 2008-09-07 KW - Cyclic load KW - Dynamic loads KW - Laboratory test KW - Reduction factor KW - Reinforcement KW - Stiffness PY - 2008 IS - Paper 179 SP - 1 EP - 7 AN - OPUS4-18425 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böhning, Martin T1 - Charakterization of gas sorption in glassy polymers using experimental and molecular modeling techniques T2 - 14th International Conference "Polymeric Materials" CY - Halle (Saale), Germany DA - 2010-09-15 PY - 2010 AN - OPUS4-22104 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hölck, Ole A1 - Böhning, Martin A1 - Heuchel, M. A1 - Siegert, M.R. T1 - Gas-induced structural changes in polymeric membrane materials combining experiment, phenomenological models and simulation KW - Polymer KW - Gas transport KW - Dilation KW - Plasticization KW - Free volume molecular modelling PY - 2006 DO - https://doi.org/10.1016/j.desal.2006.03.283 SN - 0011-9164 VL - 200 IS - 1-3 SP - 166 EP - 168 PB - Elsevier CY - Amsterdam AN - OPUS4-13730 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hölck, Ole A1 - Siegert, M.R. A1 - Heuchel, M. A1 - Böhning, Martin T1 - CO2 Sorption Induced Dilation in Polysulfone: Comparative Analysis of Experimental and Molecular Modeling Results N2 - Experimental sorption and dilation data of the polysulfone/CO2 system at 308 K and pressures up to 50 bar were measured utilizing a gravimetric sorption balance and a dilatometer based on a capacitive distance sensor. The data of this glassy polymer/gas system were subjected to a thorough kinetic analysis on the basis of a viscoelastic model, which allows the separation of the diffusive/elastic fraction of the sorption/dilation process from the slower relaxational part. The results were interpreted in terms of the common dual mode sorption model and the site distribution model of Kirchheim. Detailed atomistic packing models of the same polymer/gas system were created for two reference states with regard to concentration and swelling. The CO2 sorption isotherms of the packing models corresponding to these two swelling states, calculated using GCMC simulations, could be combined in order to interpolate the gas uptake over the intermediate pressure range with good agreement to the experimental data. The elastic part of the gas induced dilation is successfully described by MD simulations and derived partial molar volumes are in satisfying agreement with experimental findings. Finally, the free volume of the packing models is probed and the obtained size distribution of the free volume elements is compared to the results of the analysis of experimental data according to the site distribution model. KW - Sorption KW - Dilation KW - Dual mode sorption model KW - Site distribution model KW - Molecular modelling KW - Polysulfone PY - 2006 SN - 0024-9297 SN - 1520-5835 VL - 39 IS - 26 SP - 9590 EP - 9604 PB - American Chemical Society CY - Washington, DC AN - OPUS4-14405 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hao, Ning A1 - Böhning, Martin A1 - Goering, Harald A1 - Schönhals, Andreas T1 - Nanocomposites of Polyhedral Oligomeric Phenethylsilsesquioxanes and Poly(bisphenol A carbonate) as Investigated by Dielectric Spectroscopy N2 - Nanocomposites were prepared by solution blending of polyhedral oligomeric silsesquioxane with phenethyl substituents (PhenethylPOSS) into poly(bisphenol A carbonate) (PBAC). The nanocomposites were investigated by dielectric spectroscopy, differential scanning calorimetry (DSC) and density measurements. PhenethylPOSS shows one relaxation process, the α-relaxation, confirmed by DSC investigations. PBAC shows a β-relaxation at lower and an α-relaxation at higher temperatures. With increasing PhenethylPOSS content the α-relaxation of the composites shifts to lower temperatures. Thus, incorporation of PhenethylPOSS leads to a plasticization of PBAC due to a decrease of the packing density which is rationalized by density measurements. For higher concentrations of PhenethylPOSS (>10 wt %) the α-relaxation of the polycarbonate matrix splits into two peaks. Moreover, close to the α-relaxation of PhenethylPOSS a third process is observed. These results indicate a phase separation into a PBAC matrix with a few percents of molecularly solved POSS and POSS-rich domains. These POSS-rich domains are surrounded by an interfacial layer of PBAC having a higher concentration of POSS than the matrix. A phase diagram is deduced providing a miscibility criterion. For the phase separated nanocomposites an interfacial polarization phenomena is observed. Using a simplified model the time constant of this process is correlated with the size of the PhenethylPOSS-rich domains and theire increasing size with the increase of the concentration of POSS. KW - Polyhedral oligomeric silsesquioxane (POSS) KW - Polymer-based nanocomposites KW - Broadband dielectric spectroscopy KW - Interfacial polarisation PY - 2007 SN - 0024-9297 SN - 1520-5835 VL - 40 IS - 8 SP - 2955 EP - 2964 PB - American Chemical Society CY - Washington, DC AN - OPUS4-14768 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -