TY - GEN A1 - Schartel, Bernhard A1 - Bartholmai, Matthias A1 - Braun, Ulrike ED - Le Bras, M. T1 - Barrier effects for the fire retardancy of polymers T2 - 9th European Meeting on Fire Retardancy and Protection of Materials CY - Lille, France DA - 2003-09-15 KW - Fire retardancy KW - Nanocomposites KW - Red Phosphorus KW - Mg(OH)2 KW - Cone Calorimeter KW - LOI PY - 2005 SN - 0-85404-582-1 VL - 9 SP - 264 EP - 275 PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-7377 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Kunze, Ralf A1 - Bartholmai, Matthias A1 - Neubert, Dietmar A1 - Schriever, Robert T1 - TG-MS and TG-FTIR applied for an unambiguous thermal analysis of intumescent coatings N2 - Thermogravimetry (TG), thermogravimetry coupled with mass spectroscopy (TG-MS) and thermogravimetry coupled with Fourier transform infrared spectroscopy (TG-FTIR) were used to characterise the thermo-oxidative behaviour of two intumescent coating materials. The temperature dependence, the corresponding volatile products and the amount of residue of the different processes were determined. Using both TG-MS and TG-FTIR results in an unambiguous interpretation of the volatile products. Characteristics such as the influence of endothermic reactions, the release of non-flammable gases, the dehydrogenation enhancing the char formation and the stability of the cellular char were discussed in detail. It was demonstrated, that TG, TG-MS and TG-FTIR are powerful methods to investigate mechanisms in intumescent coatings and that they are suitable methods in respect to quality assurance and unambiguous identification of such materials. KW - Intumescent coating materials KW - TG KW - TG-FTIR KW - TG-MS PY - 2002 DO - https://doi.org/10.1023/A:1022272707412 SN - 1388-6150 SN - 1418-2874 SN - 0368-4466 SN - 1572-8943 VL - 70 IS - 3 SP - 897 EP - 909 PB - Kluwer Academic Publ. CY - Dordrecht AN - OPUS4-2133 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Braun, Ulrike A1 - Schwarz, U. A1 - Reinemann, S. T1 - Fire Retardancy of Polypropylene/Flax Blends N2 - A comprehensive characterization of the thermal and the fire behaviour is presented for polypropylene (PP) flax compounds containing ammonium polyphosphate (APP) and expandable graphite as fire retardants. Thermogravimetry coupled with an evolved gas analysis (TG-FTIR) was performed to ensure a significant thermal analysis. The fire response under forced flaming conditions was studied using a cone calorimeter. The external heat flux was varied between 30 and 70 kW m-2 so that the results could be evaluated for different fire scenarios and tests. Different flammability tests (UL 94, limiting oxygen index, glow wire test, GMI 60261) were performed and the results compared with the cone calorimeter data. The different char forming mechanisms are described and the resulting fire retardancy is classified. The successful and ecological friendly fire retardancy is a technological breakthrough for PP/flax biocomposites. KW - Biosomposites KW - Flame retardancy KW - Flax PY - 2003 DO - https://doi.org/10.1016/S0032-3861(03)00692-X SN - 0032-3861 SN - 1873-2291 VL - 44 IS - 20 SP - 6241 EP - 6250 PB - Springer CY - Berlin AN - OPUS4-2640 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bartholmai, Matthias A1 - Schriever, Robert A1 - Schartel, Bernhard T1 - Influence of external heat flux and coating thickness on the thermal insulation properties of two different intumescent coatings using cone calorimeter and numerical analysis N2 - Polymeric intumescent coatings are fire protective materials that increase their thermal resistance when exposed to high temperatures to prevent building structures from damage. The idea of the investigation was to develop a simple test method to determine the time dependent thermal conductivity of intumescent coatings. Therefore steel plates were coated with two different intumescent systems. During cone calorimeter tests the temperature at the back side of the coated plates was measured. These results were used to calculate the time dependent thermal resistance of the protective layer with the simulation program IOPT2D for different external heat fluxes and different layer thickness. KW - Intumescent coatings KW - Thermal resistance KW - Cone calorimetry KW - Numerical analysis PY - 2003 DO - https://doi.org/10.1002/fam.823 SN - 0308-0501 SN - 1099-1018 VL - 27 IS - 4 SP - 151 EP - 162 PB - Heyden CY - London AN - OPUS4-2633 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bartholmai, Matthias A1 - Schartel, Bernhard T1 - Layered silicate polymer nanocomposites: new approach or illusion for fire retardancy? Investigations of the potentials and the tasks using a model system N2 - Polymeric nanocomposites are discussed as one of the most promising advanced materials whose nanoscale effects can be exploited for industry. Layered silicate polypropylene-graft-maleic anhydride nanocomposites are investigated as a model to clarify the potential of such materials in terms of fire retardancy. The nanostructure is characterized using transmission electron microscopy (TEM) and shear viscosity. The fire behavior is characterized using different external heat fluxes in cone calorimeter, limiting oxygen index and UL 94 classification. A comprehensive fire behavior characterization is presented which enables an assessment of the materials’ potential with respect to different fire scenarios and fire tests. The influence of morphology and the active mechanisms are discussed, such as barrier formation and changed melt viscosity. To our knowledge, it is the first attempt to illuminate the concept’s strengths, such as the reduction of flame spread, and weaknesses, such as the lack of influence on ignitability, in a clear, comprehensive and detailed manner. KW - Fire retardancy KW - Nanocomposites KW - Cone Calorimeter KW - LOI KW - UL94 KW - Flame retardance KW - poly(propylene) (PP) KW - Organoclay PY - 2004 UR - http://www3.interscience.wiley.com/cgi-bin/jissue/109085890 SN - 1042-7147 SN - 1099-1581 VL - 15 IS - 7 SP - 355 EP - 364 PB - John Wiley & Sons, Ltd. CY - Chichester AN - OPUS4-3706 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard A1 - Wachtendorf, Volker A1 - Krüger, Simone A1 - Hennecke, Manfred T1 - Chemiluminescence - An advanced method for small extent, early stages and accelerated testing of the thermooxidative degradation in polymers T2 - Makromolekulares Kolloquium Freiburg CY - Freiburg im Breisgau, Germany DA - 2000-02-24 PY - 2000 SP - 45 CY - Freiburg im Breisgau AN - OPUS4-2435 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard A1 - Wachtendorf, Volker A1 - Damerau, T. A1 - Hennecke, Manfred ED - Spadaro, G. T1 - Photooxidative and thermooxidative degradation of conjugated polymers T2 - 1st International Conference on Polymer Modification, Degradation and Stabilisation (MoDeSt 2000) CY - Palermo, Italy DA - 2000-09-03 PY - 2000 SN - 0969-806X VL - 63 IS - 1 PB - Pergamon CY - Oxford AN - OPUS4-2436 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard A1 - Kunze, Ralf A1 - Neubert, Dietmar T1 - ZnS as Fire Retardant in PVC-P T2 - 2nd International Conference on Polymer Modification, Degradation and Stabilisation (MoDeSt) CY - Budapest, Hungary DA - 2002-06-30 PY - 2002 VL - 82 IS - 2 PB - Elsevier CY - Orlando, Fla. AN - OPUS4-2437 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Grell, M. A1 - Long, X. A1 - Bradley, D. A1 - Bernius, M. A1 - Chamberlin, T. A1 - Inbasekaran, M. A1 - Woo, E. P. A1 - Hennecke, Manfred A1 - Schartel, Bernhard A1 - Wachtendorf, Volker T1 - A liquid crystalline mainchain conjugated polymer for polarized electroluminescence applications T2 - 4th European Conference on Molecular Electronics (ECME 97) CY - Cambridge, England, UK DA - 1997-09-07 PY - 1997 CY - Stuttgart AN - OPUS4-2432 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Schartel, Bernhard A1 - Krüger, Simone A1 - Wachtendorf, Volker A1 - Hennecke, Manfred T1 - Chemiluminescence - A promising new testing method for plastic optical fibres? T2 - 7th International Plastic Optical Fibres Conference (POF-7) CY - Berlin, Germany DA - 1998-10-05 PY - 1998 SN - 3-905084-55-4 VL - 7 SP - 248 EP - 249 PB - AKM AG CY - Basel AN - OPUS4-2433 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard A1 - Wachtendorf, Volker A1 - Grell, M. A1 - Bradley, D. A1 - Hennecke, Manfred ED - Gerhard-Multhaupt, R. T1 - Polarized fluorescence and orientational order parameters of a liquid crystalline conjugated polymer T2 - European Conference on Macromolecular Physics: Molecular Orientation in Polymers, Generation, Characterisation, Application CY - Potsdam, Germany DA - 1999-09-30 PY - 1999 N1 - Serientitel: Europhysics conference abstracts – Series title: Europhysics conference abstracts IS - 23H SP - 46 CY - Potsdam AN - OPUS4-2434 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hartwig, A. A1 - Pütz, D. A1 - Schartel, Bernhard A1 - Bartholmai, Matthias A1 - Wendschuh-Josties, M. T1 - Combustion behaviour of epoxide based nanocomposites with ammonium and phosponium bentonites N2 - The influence of different organobentonites on the decomposition and the combustion behaviour of an epoxy resin were examined. The epoxy resin is a cationically polymerised cycloaliphatic epoxy resin flexibilised with poly(tetrahydrofuran) (PTHF), with hydroxyl endgroups. The bentonite was modified with either an ammonium or a phosphonium salt. The thermal decomposition of the PTHF induced by the initiator, used for the cationic polymerisation, did neither take place for the nanocomposite based on the ammonium bentonite nor for that based on the phosphonium bentonite. This improved decomposition characteristic lead to a larger time to ignition for both kinds of nanocomposites compared to the not modified polymer, which is not the case for other polymer/clay nanocomposites described in the literature. The fire behaviour was investigated using limiting oxygen index (LOI), a horizontal burner test and a cone calorimeter. The forced flaming conditions in the cone calorimeter were varied using different external heat fluxes between 30 and 70 kW · m-2. The fire behaviour of the nanocomposites was improved in comparison to the polymer, and phosphonium bentonite was superior to ammonium bentonite. The main mechanism is a barrier formation resulting in a reduction of the fire growth rate, which was more pronounced in the case of high external heat fluxes. KW - Cationic polymerisation KW - Clay KW - Combustion KW - Degradation KW - Epoxide KW - Nanocomposite PY - 2003 DO - https://doi.org/10.1002/macp.200300047 SN - 1022-1352 SN - 1521-3935 VL - 204 IS - 18 SP - 2247 EP - 2257 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-2801 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Tidjani, Adams A1 - Wald, Oliver A1 - Pohl, M.-M. A1 - Hentschel, Manfred P. A1 - Schartel, Bernhard T1 - Polypropylene-graft-maleic anhydride-nanocomposites: I-Characterization and thermal stability of nanocomposites produced under nitrogen and in air N2 - The morphology and thermal behaviour of polypropylene–graft–maleic anhydride (PP–g–MA) layered silicate (montmorillonite) nanocomposites were investigated using X-ray diffraction, transmission electron microscopy, differential scanning calorimetry and thermogravimetry. The study focuses on the influence of the presence of oxygen during the preparation of PP–g–MA–nanocomposite using two different modified clays. The nanocomposites show tactoid, intercalated and exfoliated structures side by side with different dominant states depending on the clay used and on the processing conditions. The systems are described as multi-component blends rather than binary blends since the organic ions do not only change the mixing behaviour, but also influence material properties. Beside the physical barrier property of the clay layers also chemical processes were found to play an important role. KW - Polypropylene-graft-maleic anhydride KW - Montmorillonites KW - Nanocomposites KW - X-ray KW - Thermal stability PY - 2003 DO - https://doi.org/10.1016/S0141-3910(03)00174-5 SN - 0141-3910 SN - 1873-2321 VL - 82 IS - 1 SP - 133 EP - 140 PB - Applied Science Publ. CY - London AN - OPUS4-2773 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Schartel, Bernhard A1 - Braun, Ulrike A1 - Schwarz, U. A1 - Reinemann, S. ED - Lewin, M. T1 - Fire Retarded Polypropylene/Flax Biocomposites T2 - 14th Conference on Recent Advances in Flame Retardancy of Polymeric Materials ; 14th Annual BCC Conference on Flame Retardancy CY - Stamford, CT, USA DA - 2003-06-02 KW - Fire retardancy KW - PP/Flax Biocomposite KW - Expandable Graphite KW - Ammonium Polyphosphate KW - TG-FTIR KW - Cone Calorimeter PY - 2003 SN - 1-569-65930-3 VL - 14 SP - 219 EP - 228 PB - BCC CY - Norwalk, Conn. AN - OPUS4-2815 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Braun, Ulrike A1 - Schartel, Bernhard T1 - Fire Retardancy Mechanisms of Red Phosphorus in Thermoplastics N2 - The thermal decomposition and the fire behavior of glass fiber reinforced polyamide 66 (PA-66) and high impact polystyrene (HIPS) containing red phosphorus (P4) were investigated. For glass fiber reinforced PA-66, P4 promotes char formation in the condensed phase. Barrier effects and the reduction of combustible volatiles were identified as fire retardancy mechanisms. For HIPS, P4 acts in the gas phase, mainly trapping radicals. The heat release per mass loss polymer is reduced due to an incomplete combustion. T2 - 12th International Conference Additives 2003 CY - San Francisco, CA, USA DA - 2003-04-06 PY - 2003 UR - http://www.executive-conference.com/conferences/archives/abstracts2003/add03_abs5b.html SP - 1(?) EP - 10(?) PB - ECM CY - Plymouth, Mich. AN - OPUS4-2502 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Braun, Ulrike T1 - Fire Retardancy Mechanisms of Phosphorus in Thermoplastics KW - Fire retardancy KW - Red Phosphorus KW - Cone Calorimeter KW - TG-FTIR KW - TG-MS KW - HIPS KW - PBT KW - PA 66 PY - 2004 SN - 0743-0515 VL - 91 SP - 152 EP - 153 PB - Division of Polymeric Materials Science and Engineering, American Chemical Society CY - Washington, DC AN - OPUS4-3971 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard A1 - Bartholmai, Matthias A1 - Braun, Ulrike T1 - Residue, Charring and Intumescence N2 - The exploration of condensed phase mechanisms such as charring and intumescence has been pushed forward in the last decades, since it is believed that focusing on these concepts will bring materials closer to an efficient and ecologically friendly fire retardancy. They promise to concentrate efficient fire retardancy at the key position between pyrolysis zone and gas phase. Examples of residue/char forming and intumescent materials are used to illustrate the influence of mass and heat barrier effects on the fire behavior of materials and general results are presented. A comprehensive understanding of the mechanisms and structure-property relationships in fire retardancy is presented. KW - Fire retardancy KW - Nanocomposites KW - Red Phosphorus KW - Intumescence KW - Cone Calorimeter PY - 2006 SN - 1-59623-221-8 VL - XV SP - 15 EP - 21 PB - BCC Research CY - Norwalk, Conn. AN - OPUS4-4068 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Red Phosphorus, Nanocomposites and Intumescence Catings - Three Examples of Advanced Fire Retardancy T2 - SFB Kolloquium am Institut für Makromolekulare Chemie, Albert-Ludwigs Universität Freiburg CY - Freiburg, Germany DA - 2003-10-29 PY - 2003 AN - OPUS4-4056 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Fire Retardancy of Polymers: Science between Macromolecular Chemistry and Fire Engineering T2 - Hochpolymer- und Kunststoffkolloquium, Technische Universität Darmstadt CY - Darmstadt, Germany DA - 2003-10-30 PY - 2003 AN - OPUS4-4057 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Fire Retardancy of Polymers T2 - Bayer AG CY - Dormagen, Germany DA - 2003-11-04 PY - 2003 AN - OPUS4-4058 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Fire Behavior Assessment of Nanocomposites T2 - Nanocomposites 2003 CY - San Francisco, CA, USA DA - 2003-11-10 PY - 2003 AN - OPUS4-4059 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Fire retardancy of Polymers Using Barrier Effects T2 - 8. Rudolstädter Kunststofftag CY - Rudolstadt, Germany DA - 2003-05-21 PY - 2003 AN - OPUS4-4045 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Fire retardancy of Polypropylene/Flax Blends T2 - 14th Annual BCC Conference on Flame Retardancy; Recent Advances in Flame Retardancy of Polymeric Materials CY - Stamford, CT, USA DA - 2003-06-02 PY - 2003 AN - OPUS4-4046 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Flammschutz von Polymeren durch Oberflächenmodifizierung T2 - Habilitänden-Workshop 2003, GDCH Fachgruppe Makromolekulare Chemie CY - Düsseldorf, Germany DA - 2003-07-14 PY - 2003 AN - OPUS4-4047 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Fire Retardancy of Polymers T2 - BASF AG CY - Ludwigshafen am Rhein, Germany DA - 2003-09-11 PY - 2003 AN - OPUS4-4048 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Barier Effects for the Fire Retardancy of Polymers T2 - 9th European Meeting on Fire Retardancy and Protection of Materials, FRPM '03 CY - Lille, France DA - 2003-09-17 PY - 2003 AN - OPUS4-4049 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - red phosphorus, nanocomposites and Intumescence Coatings - Three Examples of Advanced Fire Retardancy T2 - SFB Kolloquium am Institut für Makromolekulare Chemie, Albert-Ludwigs Universität Freiburg CY - Freiburg, Germany DA - 2003-10-29 PY - 2003 AN - OPUS4-4050 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Combustion Behaviour and Fire Retardancy of Polymers T2 - Clariant GmbH CY - Hürth, Germany DA - 2003-02-04 PY - 2003 AN - OPUS4-4044 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Brandverhalten und Flammschutz von Polymeren T2 - ITC-CPV Institutskolloquium des Forschungszentrums Karlsruhe CY - Karlsruhe, Germany DA - 2004-07-27 PY - 2004 AN - OPUS4-4176 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Fire Retardancy Mechanisms of Phosphorus in Thermoplastics T2 - 228th ACS National Meeting, Fall 2004 CY - Philadelphia, PA, USA DA - 2004-08-22 PY - 2004 AN - OPUS4-4177 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Flammschutz von Polymeren T2 - Institutskolloquium des Instituts für Polymerforschung IPF CY - Dresden, Germany DA - 2004-04-30 PY - 2004 AN - OPUS4-4170 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Residue, Charring and Intumescence T2 - 15th Annual BCC Conference on Flame Retardancy; Recent Advances in Flame Retardancy of Polymeric Materials CY - Stamford, CT, USA DA - 2004-06-06 PY - 2004 AN - OPUS4-4171 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard ED - Troitzsch, J. T1 - Untersuchungen von Wirkmechanismen - ein Beitrag zur gezielten Optimierung von Polymer-Flammschutzmittel-Systemen T2 - 7. Fachtagung Kunststoffe, Brandschutz und Flammschutzmittel, Neue Entwicklungen und Anwendungen CY - Würzburg, Deutschland DA - 2004-12-01 KW - Fire retardancy KW - Nanocomposites KW - Cone Calorimeter KW - Red Phosphorus KW - Intumescence PY - 2004 SP - D1 EP - D11 PB - SKZ CY - Würzburg AN - OPUS4-5286 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Braun, Ulrike A1 - Schartel, Bernhard T1 - Effect of Red Phosphorus and Melamine Polyphosphate on the Fire Behavior of HIPS N2 - Pyrolysis and fire behavior of high impact polystyrene (HIPS) containing red phosphorus and melamine polyphosphate were investigated. The thermal and thermo-oxidative decomposition were characterized using thermogravimetry coupled with FTIR and MS, respectively. The fire behavior was monitored with a cone calorimeter using different external heat fluxes and determining the LOI. Red phosphorus reduced the heat release in HIPS due to radical trapping in the gas phase. The reduction in effective heat of combustion was accompanied by an increase of incomplete combustion products such as smoke and carbon monoxide. Melamine polyphosphate in HIPS acted in the condensed phase with barrier formation. The heat release rate was reduced, whereas the total heat evolved, smoke and carbon monoxide formation were not influenced significantly. Using both fire retardants, the resulting fire retardancy was characterized mainly by superposition. KW - HIPS KW - Red Phosphorus KW - TG-FTIR KW - TG-MS KW - Cone Calorimeter KW - LOI KW - Fire retardancy KW - Melamine Polyphosphate PY - 2005 DO - https://doi.org/10.1177/0734904105043451 SN - 0734-9041 SN - 1530-8049 VL - 23 IS - 1 SP - 5 EP - 30 PB - Sage CY - London AN - OPUS4-5287 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Untersuchungen von Wirkmechanismen - ein Beitrag zur gezielten Optimierung von Polmer-Flammschutzmittel-Systemen T2 - 7. Fachtagung des SKZ "Brandschutz und Flammschutzmittel" CY - Würzburg, Germany DA - 2004-12-01 PY - 2004 AN - OPUS4-5283 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Some comments on the use of cone calorimeter data T2 - Developments in Calorimetry Workshop CY - London, England DA - 2006-02-16 PY - 2006 AN - OPUS4-12109 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Mechanisms of phosphorus flame retardants T2 - Fire Retardants 2006 CY - London, England DA - 2006-02-14 PY - 2006 AN - OPUS4-12110 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Schartel, Bernhard A1 - Braun, Ulrike T1 - Mechanisms of Phosphorous Flame Retardants T2 - 12th International Flame Retardants 2006 Conference CY - London, England, UK DA - 2006-02-14 PY - 2006 SN - 0-9541216-7-8 SP - 153 EP - 154 PB - Interscience Communications CY - London AN - OPUS4-12078 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Knoll, Uta A1 - Hartwig, A. A1 - Pütz, D. T1 - Phosphonium-modified layered silicate epoxy resins nanocomposites and their combinations with ATH and organo-phosphorus fire retardants N2 - Phosphonium-modified layered silicate epoxy resin nanocomposites were evaluated by testing the thermal/thermo-mechanical properties [differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), torsional pendulum, Sharpy toughness], flammability (limiting oxygen index LOI) and fire behavior (cone calorimeter with different irradiations). The morphology of the composites was determined using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The drying conditions of phosphonium-modified layered silicate were varied in order to improve the nanocomposite formation and properties. The results were compared with using a commercial ammonium-modified montmorillonite. Enhanced nanocomposite formation was found for the commercial systems due to the amount of excess surfactant, but this effect was overcompensated through the advanced morphology of the phosphonium-modified systems. Several fire retardancy mechanisms and their specific influence on the different fire properties, such as ignitability, flammability, flame spread, total heat release (fire load), and the production of CO and smoke were discussed comprehensively. The main mechanism of layered silicate is a barrier formation influencing the flame spread in developing fires. Several minor mechanisms are significant, but important fire properties such as flammability or fire load are hardly influenced. Hence combinations with aluminum hydroxide and organo-phosphorus flame retardants were evaluated. The combination with aluminum hydroxide was a promising approach since it shows superposition in properties such as the fire load and only in some properties very little antagonism. The combination with an organo-phosphorus flame retardant disillusions, since it was characterized mainly by antagonism. KW - Flame retardance KW - Nanocomposites KW - Organoclay KW - Epoxy resin KW - Cone calorimeter PY - 2006 DO - https://doi.org/10.1002/pat.686 SN - 1042-7147 SN - 1099-1581 VL - 17 IS - 4 SP - 281 EP - 293 PB - John Wiley & Sons, Ltd. CY - Chichester AN - OPUS4-12519 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Wirkmechanismen von phosphorhaltigen Flammschutzmitteln T2 - SKZ-Fachtagung Kunststoffe, Brandschutz und Flammschutzmittel, Neue Entwicklungen und Anwendungen CY - Würzburg, Germany DA - 2006-06-21 PY - 2006 AN - OPUS4-12502 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Cone calorimeter: A tool for the research and development of polymeric materials T2 - Kolloquium des Department "Materialien und Systeme zum Schutz und Wohlbefinden des menschlichen Körpers" der Eidgenössischen Materialprüfungs- und Forschungs-Anstalt (EMPA) CY - St. Gallen, Switzerland DA - 2006-06-01 PY - 2006 AN - OPUS4-12503 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Wirkmechanismen von phosphorhaltigen Flammschutzmitteln T2 - 8. SKZ-Fachtagung "Kunststoffe, Brandschutz und Flammschutzmittel" CY - Würzburg, Deutschland DA - 2006-06-21 PY - 2006 SP - D1-D6, 1-16 PB - SKZ CY - Würzburg AN - OPUS4-12537 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Perez, R.M. A1 - Sandler, J.K.W. A1 - Altstädt, V. A1 - Hoffmann, T. A1 - Pospiech, D. A1 - Ciesielski, M. A1 - Döring, M. A1 - Braun, Ulrike A1 - Knoll, Uta A1 - Schartel, Bernhard T1 - Effective halogen-free flame retardants for carbon fibre-reinforced epoxy composites N2 - DOPO-based flame retardants with tailored chemical structures are proposed for carbon fibre reinforced epoxy composites. Critical properties related to the fracture toughness are maintained, effectively allowing the use of such compounds in composites for demanding applications. KW - Fire retardancy KW - DOPO KW - Epoxy resin KW - LOI KW - UL94 PY - 2006 DO - https://doi.org/10.1007/s10853-006-0134-4 SN - 0022-2461 SN - 1573-4803 VL - 41 IS - 15 SP - 4981 EP - 4984 PB - Springer Science + Business Media B.V. CY - New York, USA AN - OPUS4-12641 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Braun, Ulrike A1 - Knoll, Uta A1 - Schartel, Bernhard A1 - Hoffmann, T. A1 - Pospiech, D. A1 - Artner, J. A1 - Ciesielski, M. A1 - Döring, M. A1 - Perez-Graterol, R. A1 - Sandler, J.K.W. A1 - Altstädt, V. T1 - Novel Phosphorus-Containing Poly(ether sulfone)s and Their Blends with an Epoxy Resin: Thermal Decomposition and Fire Retardancy N2 - Summary: The decomposition of novel phosphorus-containing poly(oxyphenylene-sulfonyl-phenylene-oxy-diphenyl phenylene phosphine oxide) (PSU_I), 2,5-dihydroxy-1-biphenylene-phosphine oxide based polysulfone (PSU_II), poly(sulfonyl-diphenylphenylene phosphonate) (PSU_P) and bisphenol A-based polysulfone (PSU) is studied. The influence of the chemical structure, charring and phosphorus release is discussed based on the mass loss, kinetics and products. The pyrolysis and fire behaviour of blends with epoxy resin (EP) are studied. For EP-PSU_II, phosphorus initiates water elimination and changes the decomposition pathway of EP. The fire behaviour of EP-PSU shows some improvements, whereas the heat release rate is crucially reduced for EP-PSU_II due to simultaneous char formation and flame inhibition. KW - Epoxy KW - Flame retardance KW - High performance polymers KW - Polysulfones KW - Thermogravimetric analysis (TGA) PY - 2006 DO - https://doi.org/10.1002/macp.200600182 SN - 1022-1352 SN - 1521-3935 VL - 207 IS - 16 SP - 1501 EP - 1514 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-12650 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Fire Retardancy of Textiles: Fundamentals, Mechanisms, Requirements T2 - Internationale Chemiefasertagung CY - Dornbirn, Austria DA - 2005-09-21 PY - 2005 AN - OPUS4-10974 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Some Comments on Fire Retardancy Mechanisms in Polymer Nanocomposites T2 - 8th International Symposium on Polymers for Advanced Technologies CY - Budapest, Hungary DA - 2005-09-12 PY - 2005 AN - OPUS4-10977 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Some Comments on Fire Retardancy Mechanisms in Polymer Nanocomposites T2 - 10th European Meeting on Fire Retardancy and Protection of Materials (10th European Conference on Fire Retardant Polymers), FRPM '05, BAM, Berlin CY - Berlin, Germany DA - 2005-09-07 PY - 2005 AN - OPUS4-10978 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Assessing the performance of intumescent coatings using bench-scaled cone calorimeter T2 - European Coatings Conference - Fire Retardant Coatings CY - Berlin, Germany DA - 2006-09-14 PY - 2006 AN - OPUS4-13780 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pawlowski, Kristin A1 - Schartel, Bernhard T1 - Mechanisms of Aryl Phosphates as Flame Retardants in PC/ABS N2 - The pyrolysis and the fire behaviour of PC/ABS containing various aryl phosphates and their combinations with aluminium hydroxide oxide, talc and zinc borate were investigated. Main interest was focused on the flame retardant effect and mechanism of aryl phosphates (e.g. BDP) in PC/ABS, especially in combination with the other additives. Therefore the thermal and thermo oxidative decomposition was characterised by the means of thermogravimetry analysis and thermogravimetry coupled with infrared Fourier transform spectroscopy (TG-FTIR). The results were verified with further methods, e.g. pyrolysis-gaschromatography/mass spectroscopy (Py-GC/MS). Kinetic analysis and evolved gas analysis were used to study the pyrolysis mechanisms and to expose existent synergisms in the combined systems. The fire behaviour was investigated by cone calorimeter. The flammability was determined by LOI and UL 94. The chemical compositions of the residues were also examined. T2 - 17th Annual BCC Conference on Flame Retardancy CY - Stamford, CT, USA DA - 2006-05-22 KW - Aryl Phosphate KW - TG-FTIR KW - PC/ABS KW - Cone Calorimeter KW - Fire retardancy PY - 2006 SN - 1-59623-221-8 VL - 17 SP - 132 EP - 142 PB - BCC Research CY - Norwalk, Conn. AN - OPUS4-13982 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Bartholmai, Matthias A1 - Knoll, Uta T1 - Some comments on the main fire retardancy mechanisms in polymer nanocomposites N2 - Barrier formation and increasing the melt viscosity are addressed as the two main general fire retardancy mechanisms of polymer nanocomposites. They result in specific impacts on fire properties that consequentially cause varying flame retardancy efficiency in different fire tests. The barrier formation retards mainly flame spread (peak of heat release rate) in developing fires, but does not reduce fire load (total heat evolved), ignitability or flammability (limiting oxygen index, UL 94). Furthermore, this flame retardancy effect increases with increasing irradiation and vanishes with decreasing irradiation. The increased melt viscosity prevents dripping, which is beneficial or disadvantageous depending on the fire test used. In some test, it become the dominant influence, transforming self-extinguishing samples into flammable materials or causing wicking. Advantages and the limits are sketched comprehensively for exploiting the main general fire retardancy mechanisms of polymer nanocomposites. It is concluded that barrier formation and changing the melt viscosity in nanocomposites are not sufficient for most applications, but must be accompanied by additional mechanisms in special systems or in combination with other flame retardants. KW - Flame retardance KW - Nanocomposites KW - Organoclay KW - Cone calorimeter KW - Flammability PY - 2006 DO - https://doi.org/10.1002/pat.792 SN - 1042-7147 SN - 1099-1581 VL - 17 IS - 9-10 SP - 772 EP - 777 PB - John Wiley & Sons, Ltd. CY - Chichester AN - OPUS4-13868 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Braun, Ulrike A1 - Balabanovich, Aliaksandr A1 - Schartel, Bernhard A1 - Knoll, Uta A1 - Artner, J. A1 - Ciesielski, M. A1 - Döring, M. A1 - Perez, R. A1 - Sandler, J.K.W. A1 - Altstädt, V. A1 - Hoffmann, T. A1 - Pospiech, D. T1 - Influence of the oxidation state of phosphorus on the decomposition and fire behaviour of flame-retarded epoxy resin composites N2 - A systematic and comparative evaluation of the pyrolysis of halogen-free flame-retarded epoxy resins containing phosphine oxide, phosphinate, phosphonate, and phosphate (phosphorus contents around 2.6 wt.%) and the fire behaviour of their carbon fibre composites is presented. Decomposition pathways are proposed based on the thermal analysis (TG), TG coupled with evolved gas analysis (TG-FTIR), kinetics and analysis of the residue with FTIR and XPS. All organophosphorus-modified hardeners containing phenoxy groups lead to a reduced decomposition temperature and mass loss step for the main decomposition of the cured epoxy resin. With increasing oxidation state of the phosphorus the thermally stable residue increases, whereas the release of phosphorus-containing volatiles decreases. The flammability of the composites was investigated with LOI and UL 94 and the fire behaviour for forced-flaming conditions with cone calorimeter tests performed using different irradiations. The flame retardancy mechanisms are discussed. With increasing oxidation state of the phosphorus additional charring is observed, whereas the flame inhibition, which plays the more important role for the performance of the composites, decreases. The processing and the mechanical performance (delamination resistance, flexural properties and interlaminar bonding strength) of the fibre-reinforced composites containing phosphorus were maintained at a high level and, in some cases, even improved. The potential for optimising flame retardancy while maintaining mechanical properties is highlighted in this study. KW - Fire retardant KW - Composites KW - Organophosphorus-containing epoxy resin PY - 2006 DO - https://doi.org/10.1016/j.polymer.2006.10.022 SN - 0032-3861 SN - 1873-2291 VL - 47 IS - 26 SP - 8495 EP - 8508 PB - Springer CY - Berlin AN - OPUS4-14054 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Perez, R.M. A1 - Sandler, J.K.W. A1 - Altstädt, V. A1 - Hoffmann, T. A1 - Pospiech, D. A1 - Artner, J. A1 - Ciesielski, M. A1 - Döring, M. A1 - Balabanovich, Aliaksandr A1 - Schartel, Bernhard T1 - Effective halogen-free flame retardancy for a monocomponent polyfunctional epoxy using an oligomeric organophosphorus compound N2 - Oligomeric organo-phosphorus flame retardants are proposed for a monocomponent polyfunctional epoxy resin system (RTM6) without significantly deteriorating the overall performance of the resulting material. KW - DOPO KW - Epoxy resin KW - Fire retardancy KW - LOI PY - 2006 DO - https://doi.org/10.1007/s10853-006-1079-3 SN - 0022-2461 SN - 1573-4803 VL - 41 IS - 24 SP - 8347 EP - 8351 PB - Springer Science + Business Media B.V. CY - New York, USA AN - OPUS4-14112 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Perez, R.M. A1 - Sandler, J.K.W. A1 - Altstädt, V. A1 - Hoffmann, T. A1 - Pospiech, D. A1 - Ciesielski, M. A1 - Döring, M. A1 - Braun, Ulrike A1 - Balabanovich, Aliaksandr A1 - Schartel, Bernhard T1 - Novel phosphorus-modified polysulfone as a combined flame retardant and toughness modifier for epoxy resins N2 - A novel phosphorus-modified polysulfone (P-PSu) was employed as a combined toughness modifier and a source of flame retardancy for a DGEBA/DDS thermosetting system. In comparison to the results of a commercially available polysulfone (PSu), commonly used as a toughness modifier, the chemorheological changes during curing measured by means of temperature-modulated DSC revealed an earlier occurrence of mobility restrictions in the P-PSu-modified epoxy. A higher viscosity and secondary epoxy-modifier reactions induced a sooner vitrification of the reacting mixture; effects that effectively prevented any phase separation and morphology development in the resulting material during cure. Thus, only about a 20% increase in fracture toughness was observed in the epoxy modified with 20 wt.% of P-PSu, cured under standard conditions at 180 °C for 2 h. Blends of the phosphorus-modified and the standard polysulfone (PSu) were also prepared in various mixing ratios and were used to modify the same thermosetting system. Again, no evidence for phase separation of the P-PSu was found in the epoxy modified with the P-PSu/PSu blends cured under the selected experimental conditions. The particular microstructures formed upon curing these novel materials are attributed to a separation of PSu from a miscible P-PSu–epoxy mixture. Nevertheless, the blends of P-PSu/PSu were found to be effective toughness/flame retardancy enhancers owing to the simultaneous microstructure development and polymer interpenetration. KW - Flame retardants KW - Phosphorus-modified polysulfone KW - Fracture toughness PY - 2007 SN - 0032-3861 SN - 1873-2291 VL - 48 IS - 3 SP - 778 EP - 790 PB - Springer CY - Berlin AN - OPUS4-14515 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bartholmai, Matthias A1 - Schartel, Bernhard T1 - Assessing the performance of intumescent coatings using bench-scaled cone calorimeter and finite difference simulations N2 - A method was developed to assess the heat insulation performance of intumescent coatings. The method consists of temperature measurements using the bench-scaled experimental set-up of a cone calorimeter and finite difference simulation to calculate the effective thermal conductivity dependent on time/temperature. This simulation procedure was also adapted to the small scale test furnace, in which the standard time-temperature curve is applied to a larger sample and thus which provides results relevant for approval. Investigations on temperature and calculated effective thermal conduction were performed on intumescent coatings in both experimental set-ups using various coating thicknesses. The results correspond to each other as well as showing the limits of transferability between both fire tests. It is shown that bench-scaled cone calorimeter tests are a valuable tool for assessing and predicting the performance of intumescent coatings in larger tests relevant for approval. The correlation fails for processes at surface temperatures above 750°C, which are not reached in the cone calorimeter, but are attained in the small scale furnace set-up. KW - Intumescent coatings KW - Cone calorimetry KW - Numerical analysis KW - Small scale test furnace PY - 2007 SN - 0308-0501 SN - 1099-1018 VL - 31 IS - 3 SP - 187 EP - 205 PB - Heyden CY - London AN - OPUS4-14645 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Balabanovich, Aliaksandr A1 - Braun, Ulrike A1 - Knoll, Uta A1 - Artner, J. A1 - Ciesielski, M. A1 - Döring, M. A1 - Perez, R. A1 - Sandler, J.K.W. A1 - Altstädt, V. A1 - Hoffmann, T. A1 - Pospiech, D. T1 - Pyrolysis of Epoxy Resins and Fire Behavior of Epoxy Resin Composites Flame-Retarded with 9,10-Dihydro-9-oxa-10-phosphaphenanthrene-10-oxide Additives N2 - The pyrolysis of an epoxy resin and the fire behavior of corresponding carbon fiber-reinforced composites, both flame-retarded with either 10-ethyl-9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide or 1,3,5-tris[2-(9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide-10-)ethyl]1, 3,5-triazine-2,4,6(1H,3H,5H)-trione, are investigated. The different fire retardancy mechanisms are discussed, and their influence on the fire properties assessed, in particular for flammability (limiting oxygen index, UL 94) and developing fires (cone calorimeter with different external heat fluxes of 35, 50, and 70 kW m-2). Adding the flame retardants containing 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide affects the fire behavior by both condensed phase and gas phase mechanisms. Interactions between the additives and the epoxy resin result in a change in the decomposition pathways and an increased char formation. The release of phosphorous products results in significant flame inhibition. The fire properties achieved are thus interesting with respect to industrial exploration. KW - Flame retardance KW - Thermosets KW - Composites KW - Thermogravimetric analysis (TGA) KW - Pyrolysis KW - High performance polymers KW - Epoxy resin PY - 2007 SN - 0021-8995 SN - 1097-4628 VL - 104 IS - 4 SP - 2260 EP - 2269 PB - Wiley InterScience CY - Hoboken, NJ AN - OPUS4-14573 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Development of fire retarded materials - The use of the Cone Calorimeter and the Pyrolysis Combustion Flow Calorimeter T2 - 17. Ulm-Freiberger Kalorimetrietage CY - Freiberg, Germany DA - 2007-03-28 PY - 2007 AN - OPUS4-14688 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Schartel, Bernhard ED - Morgan, A. ED - Wilkie, C. T1 - Considerations regarding specific impacts of the principal fire retardancy mechanisms in nanocomposites KW - Nanocomposites KW - Fire retardancy KW - Layered silicate KW - Cone calorimeter KW - Multiwall carbon nanotubes KW - LOI KW - UL 94 PY - 2007 SN - 978-0-471-73426-0 IS - Kap. 5 SP - 107 EP - 129 PB - John Wiley & Sons, Ltd. CY - New York AN - OPUS4-14844 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pawlowski, Kristin A1 - Schartel, Bernhard T1 - Flame retardancy mechanisms of bisphenol A bis(diphenyl phosphate) in polycarbonate/acrylonitrile-butadiene-styrene blends T2 - FRPM07 - 11th European Meeting on Fire Retardant Polymers CY - Bolton, England DA - 2007-07-04 PY - 2007 AN - OPUS4-15000 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Hull, T.R. T1 - Development of fire-retarded materials-Interpretation of cone calorimeter data N2 - There is little consensus within the fire science community on interpretation of cone calorimeter data, but there is a significant need to screen new flammability modified materials using the cone calorimeter. This article is the result of several discussions aiming to provide guidance in the use and interpretation of cone calorimetry for those directly involved with such measurements. This guidance is essentially empirical, and is not intended to replace the comprehensive scientific studies that already exist. The guidance discusses the fire scenario with respect to applied heat flux, length scale, temperature, ventilation, anaerobic pyrolysis and set-up represented by the cone calorimeter. The fire properties measured in the cone calorimeter are discussed, including heat release rate and its peak, the mass loss and char yield, effective heat of combustion and combustion efficiency, time to ignition and CO and smoke production together with deduced quantities such as FIGRA and MARHE. Special comments are made on the use of the cone calorimeter relating to sample thickness, textiles, foams and intumescent materials, and the distance of the cone heater from the sample surface. Finally, the relationship between cone calorimetry data and other tests is discussed. KW - Cone calorimetry KW - Heat release KW - Fire retardant PY - 2007 SN - 0308-0501 SN - 1099-1018 VL - 31 IS - 5 SP - 327 EP - 354 PB - Heyden CY - London AN - OPUS4-15069 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Perez, R.M. A1 - Sandler, J.K.W. A1 - Altstädt, V. A1 - Hoffmann, T. A1 - Pospiech, D. A1 - Artner, J. A1 - Ciesielski, M. A1 - Döring, M. A1 - Balabanovich, Aliaksandr A1 - Knoll, Uta A1 - Braun, Ulrike A1 - Schartel, Bernhard T1 - Novel Phosphorus-containing Hardeners with Tailored Chemical Structures for Epoxy Resins: Synthesis and Cured Resin Properties N2 - A comparative evaluation of systematically tailored chemical structures of various phosphorus-containing aminic hardeners for epoxy resins was carried out. In particular, the effect of the oxidation state of the phosphorus in the hardener molecule on the curing behavior, the mechanical, thermomechanical, and hot-wet properties of a cured bifunctional bisphenol-A based thermoset is discussed. Particular attention is paid to the comparative pyrolysis of neat cured epoxy resins containing phosphine oxide, phosphinate, phosphonate, and phosphate (with a phosphorus content of about 2.6 wt %) and of the fire behavior of their corresponding carbon fiber-reinforced composites. Comparatively faster curing thermosetting system with an enhanced flame retardancy and adequate processing behavior can be formulated by taking advantage of the higher reactivity of the phosphorus-modified hardeners. For example, a combination of the high reactivity and of induced secondary crosslinking reactions leads to a comparatively high Tg when curing the epoxy using a substoichiometric amount of the phosphinate-based hardener. The overall mechanical performance of the materials cured with the phosphorus-containing hardeners is comparable to that of a 4,4-DDS-cured reference system. While the various phosphorus-containing hardeners in general provide the epoxy-based matrix with enhanced flame retardancy properties, it is the flame inhibition in the gas phase especially that determines the improvement in fire retardancy of carbon fiber-reinforced composites. In summary, the present study provides an important contribution towards developing a better understanding of the potential use of such phosphorus-containing compounds to provide the composite matrix with sufficient flame retardancy while simultaneously maintaining its overall mechanical performance on a suitable level. KW - Flame retardance KW - Organo-phosphorus compounds KW - Fracture toughness PY - 2007 SN - 0021-8995 SN - 1097-4628 VL - 105 IS - 5 SP - 2744 EP - 2759 PB - Wiley InterScience CY - Hoboken, NJ AN - OPUS4-15071 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Accurate use of cone calorimeter data: Some food for thought T2 - FRPM07 - 11th European Meeting on Fire Retardant Polymers CY - Bolton, England DA - 2007-07-04 PY - 2007 AN - OPUS4-15060 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Braun, Ulrike T1 - Comprehensive fire behaviour assessment of polymeric materials based on cone calorimeter investigations N2 - Bench scale performance based cone calorimeter investigations were conducted on glass fibre reinforced polyamide 66 (PA-66) and high impact polystyrene (HIPS) materials. Red phosphorus and magnesium hydroxide were used as fire retardants. Dilution, heat sink, barrier and charring mechanisms are considered to be active in the condensed phase. Dilution, cooling and flame poisoning mechanisms are discussed for the gas phase. Cone calorimeter data are used to give a comprehensive fire behaviour assessment in terms of the propensity to cause a quick growing fire and of the propensity to cause a fire of long duration. The external heat flux is varied between 30 and 75 kW/m2 so that the results for combustion behaviour and flame retardancy, respectively, are valid for different fire scenarios and fire tests. Results on the intrinsic contribution of the steady heat release rate per unit area reveal information about the flammability behaviour. UL 94 results are predicted in close correspondence to UL 94 experiments. PY - 2003 DO - https://doi.org/10.1515/epoly.2003.3.1.177 SN - 1618-7229 IS - 013 SP - 1 EP - 14 PB - De Gruyter CY - [S.l.] AN - OPUS4-15852 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Pawlowski, Kristin A1 - Schartel, Bernhard T1 - Flame retardancy mechanisms of triphenyl phosphate, resorcinol bis(diphenyl phosphate) and bisphenol A bis(diphenyl phosphate) in polycarbonate/acrylonitrile-butadiene-styrene blends N2 - The flame retardancy mechanisms of three aryl phosphates, triphenyl phosphate (TPP), resorcinol bis(diphenyl phosphate) (RDP) and bisphenol A bis(diphenyl phosphate) (BDP), in a polycarbonate/acrylonitrile-butadiene-styrene (PC/ABS) blend are investigated and compared. Further, the influence of polytetrafluorethylene (PTFE) on viscosity and thermal decomposition is discussed in the systems PC/ABS and PC/ABS + BDP. Mechanisms are proposed based on the results of various methods. Thermogravimetric analysis, Fourier transform infrared spectroscopy and kinetics are used to study the pyrolysis. The fire behaviour is studied by means of cone calorimeter measurements at different heat fluxes and the flammability is specified by limiting oxygen index (LOI) and UL 94. Rheology measurements are used to illuminate the changed dripping behaviour due to PTFE. TPP shows only a gas phase action. RDP shows mainly a gas phase action and some condensed phase action. BDP shows a crucial condensed phase action in addition to a gas phase action. TPP and RDP are somewhat superior in terms of flammability (LOI), whereas BDP shows superior performance in forced flaming combustion (cone calorimeter). Synergistic effects between PTFE and BDP are found. KW - Aryl phosphates KW - PC/ABS KW - Flame retardant KW - Pyrolysis KW - Flammability KW - TG-FTIR PY - 2007 DO - https://doi.org/10.1002/pi.2290 SN - 0959-8103 SN - 1097-0126 SN - 0007-1641 VL - 56 IS - 11 SP - 1404 EP - 1414 PB - Wiley InterScience CY - Chichester, West Sussex AN - OPUS4-15857 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Phosphorus-containing polymeric materials: The impact of pyrolysis on flame retardancy T2 - interflam2007 - 11th International Conference on Fire Science and Engineering CY - London, England DA - 2007-09-03 PY - 2007 AN - OPUS4-15829 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Artner, J. A1 - Ciesielski, M. A1 - Ahlmann, M. A1 - Walter, O. A1 - Döring, M. A1 - Perez, R.M. A1 - Altstädt, V. A1 - Sandler, J.K.W. A1 - Schartel, Bernhard T1 - A novel and effective synthetic approach to 9,10-Dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) Derivatives N2 - Starting from trivalent 10-alkoxy-10H-9-oxa-10-phosphaphenanthrenes, a broad range of DOPO derivatives was synthesized via transesterification with aliphatic alcohols and subsequent Michaelis-Arbuzov rearrangement using catalytic amounts of p-toluenesulfonic acid methylester. Due to the considerable differences in the nature of the alcohols employed, several procedures for processing them are presented. KW - DOPO KW - Flame retardant KW - Michaelis-Arbuzov rearrangement KW - Transesterification PY - 2007 DO - https://doi.org/10.1080/10426500701407417 SN - 1042-6507 SN - 0308-664X VL - 182 IS - 9 SP - 2131 EP - 2148 PB - Taylor & Francis CY - Philadelphia, USA AN - OPUS4-15705 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Braun, Ulrike A1 - Schartel, Bernhard A1 - Fichera, Mario Augusto A1 - Jäger, Christian T1 - Flame retardancy mechanisms of aluminium phosphinate in combination with melamine polyphosphate and zinc borate in glass-fibre reinforced polyamide 6,6 N2 - The fire retardancy mechanisms of aluminium diethylphosphinate in combination with melamine polyphosphate and zinc borate was analysed in glass-fibre reinforced polyamide 6,6. The influence of phosphorus compounds on the polyamide decomposition pathways was characterized using thermal analysis (TG), evolved gas analysis (TG–FTIR), and FTIR–ATR analysis of the residue. The Lewis acid–base interactions between the flame retardants, the amide unit, and the metal ions control the decomposition. The flammability (LOI, UL 94) and performance under forced-flaming conditions (cone calorimeter using different irradiations) were investigated. Fire residues were analysed with FTIR–ATR, SEM–EDX, and NMR. Aluminium phosphinate in polyamide 6,6 acts mainly by flame inhibition. Melamine polyphosphate shows some fuel dilution and a significant barrier effect. Using a combination of aluminium phosphinate and melamine polyphosphate results in some charring and a dominant barrier effect. These effects are improved in the presence of zinc borate due to the formation of boron–aluminium phosphates instead of aluminium phosphates. KW - Flame retardancy KW - Polyamide 6,6 KW - Metal phosphinate KW - Melamine polyphosphate KW - Zinc borate PY - 2007 SN - 0141-3910 SN - 1873-2321 VL - 92 IS - 8 SP - 1528 EP - 1545 PB - Applied Science Publ. CY - London AN - OPUS4-15707 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Pawlowski, Kristin A1 - Lyon, R.E. T1 - Pyrolysis combustion flow calorimeter: A tool to assess flame retarded PC/ABS materials? N2 - The pyrolysis combustion flow calorimeter (PCFC) as a tool for assessing the flammability of a polycarbonate (bisphenol A)/acrylonitrile–butadiene–styrene (PC/ABS) blend containing different flame retardants and additives was investigated. Strategies are proposed for analysing multi-step decomposition. The heat release capacity (HRC) and total heat release (HR), obtained by PCFC, are related to the char yield and the heat of complete combustion of the volatiles. Physical affects such as dripping, wicking, and sample thickness are not described, nor are chemical effects such as flame inhibition because pyrolysis and combustion are forced to completion on a small (milligram) sample. Varying the combustion temperature or oxygen concentration results in incomplete combustion as occuring in real fires. The correlations with flammability (UL 94, LOI) and forced flaming combustion in a cone calorimeter are discussed. The best correlation is found between HR and LOI. Reasonable correlation exists between HRC and char residue with the LOI and for HRC and HR with peak heat release rate (pHRR) in the cone calorimeter. Combining results from PCFC with those from oxygen bomb or cone calorimeter tests yields an additional understanding of fire behaviour. KW - Pyrolysis combustion flow calorimeter KW - Flammability KW - Combustion KW - Flame retardancy KW - PC/ABS PY - 2007 DO - https://doi.org/10.1016/j.tca.2007.05.021 SN - 0040-6031 SN - 1872-762X VL - 462 IS - 1-2 SP - 1 EP - 14 PB - Elsevier CY - Amsterdam AN - OPUS4-15734 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard A1 - Braun, Ulrike A1 - Pawlowski, Kristin T1 - Phosphorus-Containing Polymeric Materials: The Impact of Pyrolysis on Flame Retardancy T2 - 11th International Conference "INTERFLAM 2007" CY - London, UK DA - 2007-09-03 KW - Flame Retardancy KW - Fire Retardancy KW - Flame Retardants KW - Decompositiion pathways KW - Pyrolysis KW - Phosphorus PY - 2007 SN - 978-0-9541216-8-6 SN - 978-0-9541216-9-3 SP - 71 EP - 78 PB - Interscience Communications Limited CY - London, UK AN - OPUS4-15761 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Braun, Ulrike A1 - Knoll, Uta A1 - Bartholmai, Matthias A1 - Goering, Harald A1 - Neubert, Dietmar A1 - Pötschke, P. T1 - Mechanical, Thermal, and Fire Behavior of Bisphenol A Polycarbonate/Multiwall Carbon Nanotube Nanocomposites N2 - Nanocomposites of bisphenol A polycarbonate with 2, 4, 6, and 15 wt% multiwall carbon nanotubes (MWNT) and their use in fire retardancy are investigated. Their thermal behavior and pyrolysis are characterized using thermogravimetry, differential scanning calorimeter, oscillatory shear rheology, and dynamic mechanical analysis. The flammability is addressed using LOI and UL 94; the fire behavior, with a cone calorimeter using different irradiation. With increasing MWNT content the storage modulus is increased (10-20%) and melt viscosity increases by several orders of magnitude, particularly for low shear rates. The melt flow, dripping, and deformation during fire are hindered, which influences UL 94 and cone calorimeter results. The peak heat release rate is reduced up to 40-50% due to an improved barrier for small amounts (2 wt%) of MWNT and for low irradiation, whereas the effect is reduced for increasing irradiation and nearly vanishes for increasing filling. Adjuvant but also deleterious mechanisms result in the complex dependency on the MWNT content. Significant flame retardancy effects are specific and limited to only some fire properties. This study allows the materials' potential for implementation in different fire scenarios and tests to be assessed and provides insight into active mechanisms. KW - Flame retardancy KW - Nanocomposite KW - Carbon multiwall nanotube (MWNT) KW - Cone Caorimeter KW - Flammability PY - 2008 DO - https://doi.org/10.1002/pen.20932 SN - 0032-3888 SN - 1548-2634 VL - 48 IS - 1 SP - 149 EP - 158 PB - Wiley CY - Hoboken, NY AN - OPUS4-16365 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard ED - Troitzsch, J. T1 - Entwicklung von flammgeschützten Polymerwerkstoffen - Interpretation von Cone Calorimeter Daten T2 - 9. SKZ-Fachtagung "Kunststoffe, Brandschutz und Flammschutzmittel" CY - Würzburg, Deutschland DA - 2007-12-05 KW - Flammschutz von Polymeren KW - Fire Retardancy KW - Cone Calorimeter PY - 2007 N1 - Sprachen: Deutsch/Englisch - Languages: German/English SP - 1 EP - 25 PB - SKZ CY - Würzburg AN - OPUS4-16487 LA - mul AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Entwicklung von flammgeschützten Polymerwerkstoffen - Interpretation von Cone Calorimeter Daten T2 - 9. SKZ-Fachtagung Kunststoffe, Brandschutz und Flammschutzmittel. Neue Entwicklungen und Anwendungen CY - Würzburg, Germany DA - 2007-12-05 PY - 2007 AN - OPUS4-16476 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Phosphorus-containing flame retarded polymeric materials T2 - Makromolekulares Kolloquium Freiburg CY - Freiburg, Germany DA - 2008-02-28 PY - 2008 AN - OPUS4-16702 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Braun, Ulrike A1 - Balabanovich, Aliaksandr A1 - Artner, J. A1 - Ciesielski, M. A1 - Döring, M. A1 - Perez, R.M. A1 - Sandler, J.K.W. A1 - Altstädt, V. T1 - Pyrolysis and fire behaviour of epoxy systems containing a novel 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide-(DOPO)-based diamino hardener N2 - Highly soluble 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide-(DOPO)-based diamino hardener (2), bearing its amino groups directly on the DOPO framework, is investigated with respect to its use as a reactive flame retardant in thermosets. A mechanism for decomposition of the corresponding phosphorus-modified epoxy resin system based on a diglycidylether of bisphenol A DGEBA and 2 (DGEBA/2) is proposed and compared to the systems using DGEBA and 4,4'-diaminodiphenylsulfon (DGEBA/DDS) and to a similar system based on the structurally comparable non-reactive DOPO-based compound (DGEBA/DDS/1). Additive 1 changed the decomposition characteristics of the epoxy resin only slightly and phosphorus was released. Incorporating 2 induces two-step decomposition and most of the phosphorus remains in the residue. Furthermore, the fire behaviour of neat epoxy resin systems and a representative carbon fibre-reinforced composite based on DGEBA, DDS and 2 (DGEBA/DDS/2) were examined and compared to that of the analogous composite systems based on DGEBA/DDS and DGEBA/DDS/1. Based on different flame retardancy mechanisms both the reactive compound 2 and the additive compound 1 improve flammability (increase in LOI >13% and achieving V-1 behaviour) of the epoxy resin and composites. Under forced flaming only the flame inhibition of the additive compound 1 acts sufficiently. Lastly, the superior key mechanical properties of the epoxy resin and composite based on 2 are sketched. KW - Decomposition KW - DOPO KW - Flame retardancy KW - Composites KW - Thermosets PY - 2008 DO - https://doi.org/10.1016/j.eurpolymj.2008.01.017 SN - 0014-3057 SN - 1873-1945 VL - 44 IS - 3 SP - 704 EP - 715 PB - Elsevier CY - Oxford AN - OPUS4-16708 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gallo, Emanuela A1 - Fan, Z. A1 - Schartel, Bernhard A1 - Greiner, A. T1 - Electrospun nanofiber mats coating - new route to flame retardancy N2 - A novel route toward halogen-free fire retardancy of polymers through innovative surface coating is described. Nanofiber mats based on polyimide are deposited on PA66 through electrospinning. Scanning electron microscopy is used to characterize the nanofibers. Cone calorimeter tests were performed to evaluate the fire performance. Because of their low thermal conductivity, electrospun nanofiber mats act not only as sacrificial layers but also as a protective surface that delays ignition. The effect is influenced by the fiber diameters and the imidization. KW - Electrospinning KW - Polyimide KW - Nanofibers KW - Fire retardancy PY - 2011 DO - https://doi.org/10.1002/pat.1994 SN - 1042-7147 SN - 1099-1581 VL - 22 IS - 7 SP - 1205 EP - 1210 PB - John Wiley & Sons, Ltd. CY - Chichester AN - OPUS4-24093 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Composites and Fire: A Journey from 1 nm to 50 cm T2 - 13th European Meeting on Fire retardant Polymers, FRPM CY - Alessandria, Italy DA - 2011-06-26 PY - 2011 AN - OPUS4-24069 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Development of Fire-Retarded Materials - Interpretation of Cone Calorimeter Data T2 - Sixth International Conference on Composites In Fire CY - Newcastle upon Tyne, England DA - 2011-06-09 PY - 2011 AN - OPUS4-23898 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Perret, Birgit A1 - Schartel, Bernhard T1 - TGA-FTIR: Von der Untersuchung der Pyrolyse zur Aufklärung von Flammschutzmechanismen KW - TGA-FTIR KW - Flammschutz KW - Pyrolyse PY - 2010 VL - 32 SP - 16 EP - 19 AN - OPUS4-23904 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Perret, Birgit A1 - Schartel, Bernhard T1 - TGA-FTIR: From the investigation of pyrolysis to the elucidation of fire retardancy mechanisms KW - TGA-FTIR KW - Flammschutz KW - Pyrolyse PY - 2010 VL - 32 SP - 16 EP - 19 AN - OPUS4-23905 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Perret, Birgit A1 - Schartel, Bernhard T1 - TGA-FTIR: Détermination des mécanismes ignifuges par l´étude de la pyrolyse KW - TGA-FTIR KW - Flammschutz KW - Pyrolyse PY - 2010 VL - 32 SP - 16 EP - 19 AN - OPUS4-23906 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yu, D. A1 - Kleemeier, M. A1 - Wu, Guang Mei A1 - Schartel, Bernhard A1 - Liu, W.Q. A1 - Hartwig, A. T1 - The absence of size- dependency in flame retarded composites containing low-melting organic-inorganic glass and clay: Comparison between micro- and nanocomposites N2 - Due to optimised processing of epoxy based composite materials containing a low-melting organic–inorganic glass together with an organo clay, the size of the glass particles could be successfully reduced. Thus truly nano-dispersed composites were obtained, with glass particles in the range of 10 nm to 200 nm. The small particle size allowed efficient interaction of glass particles and organo clay layers. The flame retardancy as well as the thermo-mechanical properties were tested, and the results showed that the low-melting glass led to a remarkable reduction of peak heat release rate by forming an enhanced barrier layer. Nevertheless no further improvement could be achieved by lowering the particle size to the nanometre region. For good flame retardancy a microdispersion of the low-melting glass was already sufficient. KW - Epoxy resin KW - Nanocomposites KW - Low-melting glass KW - Clay KW - Flame retardancy PY - 2011 DO - https://doi.org/10.1016/j.polymdegradstab.2011.06.003 SN - 0141-3910 SN - 1873-2321 VL - 96 IS - 9 SP - 1616 EP - 1624 PB - Elsevier Ltd. CY - London AN - OPUS4-24211 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yu, D. A1 - Kleemeier, M. A1 - Wu, Guang Mei A1 - Schartel, Bernhard A1 - Liu, W.Q. A1 - Hartwig, A. T1 - Phosphorus and silicon containing low-melting organic-inorganic glasses improve flame retardancy of epoxy/clay composites N2 - New low-melting organic–inorganic glassy polymers containing phosphorus and silicon are synthesized by the reaction between phenylphosphonic acid and methyltrichlorosilane or methyltriethoxysilane. They possess both low-softening points and high onset decomposition temperatures, which are favorable for preparing flame retardant composites. Although the glass by itself is sensitive to water, the composites are not significantly affected in that way. For glass/clay/epoxy composites glass transition temperature (Tg) as well as storage modulus increase with the glass amount. The glasses improve flame retardancy significantly due to flame inhibition and the formation of fire residue working as protection layer during burning. The total heat evolved is reduced by 23–28% for using 5–15 wt.% glass and the maximum HRR even by 58–48%. The latter effect decreases with increasing glass amount due to an adulterate residue deformation. The combination of glass and clay is proposed as a possible route to enhance flame retardancy. KW - Clay KW - Epoxy resin KW - Flame retardancy KW - Organic-inorganic polymer KW - Low-melting glass PY - 2011 DO - https://doi.org/10.1002/mame.201100014 SN - 1438-7492 SN - 1439-2054 VL - 296 IS - 10 SP - 952 EP - 964 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-24516 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Brehme, Sven A1 - Schartel, Bernhard A1 - Bykov, Y. A1 - Ciesielski, M. A1 - Döring, M. A1 - Fischer, O. A1 - Pospiech, D. A1 - Köppl, T. A1 - Altstädt, V. T1 - Flame retardancy mechanisms and performance of a halogen-free phosphorus polyester in PBT N2 - PET-P-DOPO is a phosphorus-containing polyester prepared from the glycol ether of the hydroquinone derivative of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) and dimethyl terephthalate. PET-P-DOPO and a blend of PBT with PET-PDOPO were investigated with respect to pyrolysis and fire behavior. PET-P-DOPO achieves a V-0 rating in the UL 94 test and exhibits a high LOI of 39.3%. The outstanding flame-retardant properties of PET-P-DOPO are the result of three different mechanisms (flame inhibition, charring and a protection effect of the intumescent char) that are active in PET-P-DOPO. The fire load and the peak of heat release rate (pHRR) are reduced to 34% and 17%, respectively. The char exhibits an intumescent multicellular structure enabling it to act as an efficient protection layer. As PET-P-DOPO is immiscible with PBT, the blend shows a lower breaking elongation than pure PBT. Compared to pure PET-P-DOPO, the flame retardancy of the blend is decreased according to the fraction of PET-P-DOPO used. Nevertheless, the flame-retardancy of PET-P-DOPO in the blend was good enough to compete with PBT flame-retarded by AlPi-Et (aluminum diethylphosphinate) that was used as a Benchmark. KW - PBT KW - DOPO KW - Flame retardancy PY - 2011 SN - 1-59623-795-3 SP - 1 EP - 15 CY - Wellesley, USA AN - OPUS4-24617 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Gezielte Entwicklung flammgeschützter Polymerwerkstoffe T2 - 11. Schwarzheider Kunststoffkolloquium CY - Schwarzheide, Germany DA - 2011-09-21 PY - 2011 AN - OPUS4-24651 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gallo, Emanuela A1 - Schartel, Bernhard A1 - Acierno, Domenico A1 - Russo, P. T1 - Flame retardant biocomposites: Synergism between phosphinate and nanometric metal oxides N2 - The known flame-retardant synergism between phosphorus-based additives and metal oxides, already used for petroleum-based plastics, has been extended to bio-based materials. The pyrolysis and the flame-retardancy properties of aluminium phosphinate (AlPi) in combination with nanometric iron oxide and antimony oxide on a poly(3-hydroxy-butyrate-co-3-hydroxyvalerate)/poly(butylene adipate-co-terephthalate) (PHBV/PBAT) blend were investigated. Better fire retardancy, ascribed to increases in intermediate char, favoured improvements in the UL 94 classification. Both the phosphorus and the nanofiller components participate simultaneously in the flame-retardancy mechanism: the first acting as flame inhibition in the gas phase, and the second promoting cross-linking in the solid phase. Redox reactions between iron oxide and the phosphinate additive were confirmed by XRD analysis and provided further evidence of the activity of metal compounds. KW - Aliphatic biopolyesters KW - Metal oxide KW - Flame retardancy KW - Aluminium phosphinate PY - 2011 DO - https://doi.org/10.1016/j.eurpolymj.2011.04.001 SN - 0014-3057 SN - 1873-1945 VL - 47 IS - 7 SP - 1390 EP - 1401 PB - Elsevier CY - Oxford AN - OPUS4-23889 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard ED - Gibson, A.G. T1 - Fire retardancy in composites: a journey from nano to intermediate scale N2 - The fire behaviour of composites clearly differs in comparison to polymers. Even though fibres and inorganic particles may be inert with respect to pyrolysis, they are clearly not with respect to fire behaviour. They change heat absorption and transfer within the Condensed phase, the melt flow/dripping behaviour of pyrolysing melts, the amount and properties of the fire residue and so on. Flame retardancy concepts tailored to composites are needed. Furthermore tasks that are specific for composites such as the structural integrity in fire get into the focus. Thus understanding of fire behaviour and flame retardancy mechanisms in composites is a key for target-oriented future development. The field is illuminated by Spotlights on different length scales. The examples are taken from different projects carried out in the group of the authors in the recent years. Flame retardancy mechanisms in nanocomposites are discussed, advanced halogen-free flame retardants for carbon and glass fibre composites presented as well as an approach to mechanical intermediate scale testing of carbon fibre composites under fire. T2 - Composites in fire 6 - 6th International conference on composites in fire CY - Newcastle, UK DA - 09.06.2011 KW - Flame retardancy KW - Composite KW - Composite and fire KW - Flame retardants PY - 2011 SN - 978-0-9540459-9-9 SP - 55 EP - 62 PB - CompositeLink (Consultants) Limited AN - OPUS4-23857 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yu, D. A1 - Kleemeier, M. A1 - Wu, Guang Mei A1 - Schartel, Bernhard A1 - Liu, W.Q. A1 - Hartwig, A. T1 - A low melting organic-inorganic glass and its effect on flame retardancy of clay/epoxy composites N2 - A low-melting organic-inorganic glass with a high molecular weight soluble in solvents was synthesized by hydrolytic polycondensation of phenyltriethoxysilane followed by a subsequent heat treatment. Softening point and thermostability were strongly increased after heat treatment. The composites of glass/epoxy and glass/clay/epoxy were studied with respect to their thermal properties, fire behavior and mechanical properties. Heat release rate as measured by cone calorimetry was remarkably reduced in the presence of glass, relative to neat epoxy resin and polymer/clay composites. The combination of glass and clay is a promising approach. It showed mainly superposition and even synergistic effects in some fire properties for higher filler concentrations due to the formation of an enhanced barrier. The structure of residue was investigated by transmission electron microscopy (TEM). KW - Low-melting glass KW - Clay KW - Epoxy resin PY - 2011 DO - https://doi.org/10.1016/j.polymer.2011.03.033 SN - 0032-3861 SN - 1873-2291 VL - 52 IS - 10 SP - 2120 EP - 2131 PB - Elsevier Ltd. AN - OPUS4-23858 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gallo, Emanuela A1 - Schartel, Bernhard A1 - Braun, Ulrike A1 - Russo, P. A1 - Acierno, Domenico T1 - Fire retardant synergisms between nanometric Fe2O3 and aluminium phosphinate in poly(butylene terephthalate) N2 - The pyrolysis and the flame retardancy of poly(butylene terephthalate) (PBT) containing aluminum diethylphosphinate (AlPi) and nanometric Fe2O3 were investigated using thermal analysis, evolved gas analysis (Thermogravimetry-FTIR), flammability tests (LOI, UL 94), cone calorimeter measurements and chemical analysis of residue (FTIR). AlPi mainly acts as a flame inhibitor in the gas phase, through the release of diethylphosphinic acid. A small amount of Fe2O3 in PBT promotes the formation of a carbonaceous char in the condensed phase. The combination of 5 and 8 wt% AlPi, respectively, with 2 wt% metal oxides achieves V-0 classification in the UL 94 test thanks to complementary action mechanisms. Using PBT/metal oxide nanocomposites shows a significant increase in the flame retardancy efficiency of AlPi in PBT and thus opens the route to surprisingly sufficient additive contents as low as 7 wt%. KW - Poly(butylene terephthalate) (PBT) KW - Flammability KW - Metal oxide KW - Nanocomposite KW - Aluminum diethylphosphinate PY - 2011 DO - https://doi.org/10.1002/pat.1774 SN - 1042-7147 SN - 1099-1581 VL - 22 IS - 12 SP - 2382 EP - 2391 PB - John Wiley & Sons, Ltd. CY - Chichester AN - OPUS4-24915 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Towards Evidence-based Development of Flame Retarded Polymers T2 - Polymer- und Kunststoff Kolloquium CY - Darmstadt, Germany DA - 2011-11-24 PY - 2011 AN - OPUS4-24933 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Köppl, T. A1 - Brehme, Sven A1 - Wolff-Fabris, F. A1 - Altstädt, V. A1 - Schartel, Bernhard A1 - Döring, M. T1 - Structure-property relationships of halogen-free flame-retarded poly(butylene terephthalate) and glass fiber reinforced PBT N2 - Flame retardancy for thermoplastics is a challenging task where chemists and engineers work together to find solutions to improve the burning behavior without strongly influencing other key properties of the material. In this work, the halogen-free additives aluminum diethylphosphinate (AlPi-Et) and a mixture of aluminum phosphinate (AlPi) and resorcinol-bis(di-2,6-xylyl phosphate) (AlPi-H + RXP) are employed in neat and reinforced poly(butylene terephthalate) (PBT), and the morphology, mechanical performance, rheological behavior, and flammability of these materials are compared. Both additives show submicron dimensions but differ in terms of particle and agglomerate sizes und shapes. The overall mechanical performance of the PBT flame-retarded with AlPi-Et is lower than that with AlPi-H-RXP, due to the presence of larger agglomerates. Moreover, the flow behavior of the AlPi-Et/PBT materials is dramatically changed as the larger rod-like primary particles build a percolation threshold. In terms of flammability, both additives perform similar in the UL 94 test and under forced-flaming combustion. Nevertheless, AlPi-Et performs better than AlPi-H + RXP in the LOI test. The concentration required to achieve acceptable flame retardancy ranges above 15 wt %. KW - Polyesters KW - Fibers KW - Morphology KW - Structure–property relations KW - Flame retardance PY - 2012 DO - https://doi.org/10.1002/app.34910 SN - 0021-8995 SN - 1097-4628 VL - 124 IS - 1 SP - 9 EP - 18 PB - Wiley InterScience CY - Hoboken, NJ AN - OPUS4-25253 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Thin fire protection coatings: Is there any alternative to intumescence? T2 - European coatings conference: Fire redardant coatings V CY - Berlin, Germany DA - 2012-03-13 PY - 2012 AN - OPUS4-25612 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - FUNgraphen - Vorstellung der Forschungsziele T2 - 4. Jahrestagung inno.CNT CY - Bayreuth, Germany DA - 2012-01-30 PY - 2012 AN - OPUS4-25613 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Towards Evidence-based Development of Flame Retarded Polymers T2 - 243th ACS National Meeting Spring 2012 CY - San Diego, CA, USA DA - 2012-03-25 PY - 2012 AN - OPUS4-25716 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bier, A.K. A1 - Bognitzki, M. A1 - Schmidt, A. A1 - Greiner, A. A1 - Gallo, Emanuela A1 - Klack, Patrick A1 - Schartel, Bernhard T1 - Synthesis, properties, and processing of new siloxane-substituted poly(p-xylylene) via CVD N2 - The synthesis of a disiloxane-functionalized [2.2]paracyclophane and its polymerization to the corresponding siloxane-substituted poly(p-xylylene) via chemical vapor deposition (CVD) has been described. Because of the enhanced solubility of the siloxane substituted poly(p-xylylene) analysis of the molecular structure by NMR, molecular weight, and polydispersity by gel permeation chromatography (GPC), and processing by film casting as well as nanofiber formation by electrospinning was possible. Structural isomers were found by NMR which was expected due to the isomeric mixture of the precursor. High molecular weights at moderate polydispersities were found by GPC which was unexpected for a vapor phase deposition polymerization. The amorphous morphology in combination with a low glass transition temperature led to high elongation at break for the siloxane substituted poly(p-xylylene). Significant difference for the wetting versus water was found for as-deposited films, solution cast films, and nanofibers obtained by electrospinning with contact angles up to 135° close to superhydrophobic behavior. KW - Poly(p-xylylene) KW - Siloxane functionalized PPX KW - Chemical vapor deposition KW - Difunctionalized [2.2]paracyclophanes KW - Gorham process PY - 2012 DO - https://doi.org/10.1021/ma2021369 SN - 0024-9297 SN - 1520-5835 VL - 45 IS - 2 SP - 633 EP - 639 PB - American Chemical Society CY - Washington, DC AN - OPUS4-25466 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hörold, Andreas A1 - Schartel, Bernhard A1 - Trappe, Volker A1 - Korzen, Manfred A1 - Naumann, Maurice T1 - Structural integrity in fire: an intermediate-scale approach T2 - ECCM15 - 15th European conference on composite materials CY - Venice, Italy DA - 2012-06-24 KW - Intermediate-scale test method KW - Structural integrity investigation KW - Fully developed fire KW - Carbon fibre reinforced plastics CFRP PY - 2012 SN - 978-88-88785-33-2 SP - 1 EP - 8(?) AN - OPUS4-26380 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lorenzetti, A. A1 - Modesti, M. A1 - Gallo, Emanuela A1 - Schartel, Bernhard A1 - Besco, S. A1 - Roso, M. T1 - Synthesis of phosphinated polyurethane foams with improved fire behaviour N2 - Both alkylphosphinates and inorganic phosphinates (based on sodium, calcium, magnesium or zinc) have been recently proposed as flame retardants for polyesters, polyamides and polyurethane foams as well. The main aim of this work was to compare the flame retardant effectiveness of inorganic (already proofed in PU foams) and organic phosphinates in PU foams which have never been used in polyurethane (PU) foams. The thermal stability in nitrogen and air as well as limiting oxygen index and cone calorimeter behaviour have been studied to assess the effectiveness of such flame retardants in PU foams. The results obtained showed that both inorganic and organic phosphinates are effective in enhancing fire behaviour of PU foams since they improve thermal stability, LOI and fire performance. Cone calorimetry highlighted the flame inhibition action in the gas phase due to the release of phosphorus-containing molecules. The better results obtained for inorganic phosphinate are probably related to the better quality of the char layer developed during burning, but may also be related to the higher phosphorus content of such flame retardant with respect the other ones. It was also verified that both inorganic and organic phosphinate containing N-synergic compound showed a fuel dilution effect, deriving from water and/or ammonia release in the gas phase. KW - Phosphinate KW - Polyurethane foam KW - Flame retardancy KW - Fire behaviour PY - 2012 DO - https://doi.org/10.1016/j.polymdegradstab.2012.07.026 SN - 0141-3910 SN - 1873-2321 VL - 97 IS - 11 SP - 2364 EP - 2369 PB - Applied Science Publ. CY - London AN - OPUS4-26735 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Brehme, Sven A1 - Köppl, T. A1 - Schartel, Bernhard A1 - Fischer, O. A1 - Altstädt, V. A1 - Pospiech, D. A1 - Döring, M. T1 - Phosphorus polyester - an alternative to low-molecular-weight flame retardants in poly(butylene terephthalate)? N2 - Pyrolysis, fire behaviour and mechanical properties of a blend of poly(butylene terephthalate) (PBT) with a phosphorus polyester (PET-P-DOPO) are investigated and compared with PBT/aluminium diethylphosphinate (AlPi-Et) composites. The PBT/PET-P-DOPO is immiscible and exhibits gas-phase and condensed-phase activity, whereas AlPi-Et in PBT results mainly in flame inhibition. Only higher loadings of AlPi-Et yield significant condensed-phase activity. Using the same phosphorus content, PBT/PET-P-DOPO and PBT/AlPi-Et exhibit similar reductions in fire load (22%) and flame spread (17% assessed by fire growth rate, FIGRA), compared with PBT. In contrast to AlPi-Et, the addition of PET-P-DOPO does not decrease the tensile strength of PBT. Thus, PET-P-DOPO is an interesting alternative to low-molecular-weight flame retardants. KW - Aluminium phosphinate KW - Blends KW - 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide KW - Flame retardance KW - Polyesters PY - 2012 DO - https://doi.org/10.1002/macp.201200072 SN - 1022-1352 SN - 1521-3935 VL - 213 IS - 22 SP - 2386 EP - 2397 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-26982 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Despinasse, Marie-Claire A1 - Schartel, Bernhard T1 - Influence of the structure of aryl phosphates on the flame retardancy of polycarbonate/acrylonitrile-butadiene-styrene N2 - The impact of the chemical structure of four different aryl bisphosphates on the flame retardancy of bisphenol A polycarbonate/acrylonitrile–butadiene–styrene blends (PC/ABS) was investigated. The impact of the bridging unit was studied, by comparing bisphenol A bis(diphenyl phosphate) BDP with biphenyl bis(diphenyl phosphate) BBDP and hydroquinone bis(diphenyl phosphate) HDP; as well as the influence of an aromatic substitution by comparing BBDP with biphenyl bis (di-2,6-xylyl phosphate) BBXP. The blends were investigated in terms of pyrolysis (thermogravimetry TG, TG coupled with Fourier transformed infrared spectroscopy (FTIR) and mass spectrometry (MS)) and fire performance (cone calorimeter, LOI, UL 94). The decomposition temperature of the flame retardant is a main parameter enabling a condensed phase interaction with PC decomposition products. The phosphate esters reacting with phenolic groups during pyrolysis were shown to increase cross-linking and reduce the hydrolysis/alcoholysis of the carbonate group. Variation of the aromatic substitution with the use of biphenyl bis (di-2,6-xylyl phosphate) led to reduced performance, highlighting the importance of the reactivity of the flame retardant with the decomposing PC. KW - Bisphenol A polycarbonate/acrylonitrile–butadiene–styrene (PC/ABS) KW - Flame retardancy KW - Flammability KW - Phosphate esters KW - Pyrolysis PY - 2012 DO - https://doi.org/10.1016/j.polymdegradstab.2012.07.005 SN - 0141-3910 SN - 1873-2321 VL - 97 IS - 12 SP - 2571 EP - 2580 PB - Applied Science Publ. CY - London AN - OPUS4-26969 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Fire Retardant Composites: A Journey from Nano to Intermediate Scale T2 - Trends im Brandschutz und innovative Flammschutzmittel bei Kunststoffen CY - Würzburg, Germany DA - 2012-05-23 PY - 2012 AN - OPUS4-26489 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gallo, Emanuela A1 - Schartel, Bernhard A1 - Acierno, Domenico A1 - Cimino, F. A1 - Russo, P. T1 - Tailoring the flame retardant and mechanical performances of natural fiber-reinforced biopolymer by multi-component laminate N2 - The potential of a multi-component laminate composite material in terms of improved flame retardancy and adequate mechanical performance is discussed. A double-layer system based on a biodegradable polyhydroxyalkanoates blend was obtained by compression molding. A thin halogen-free flame-retarded layer was located at the top of a kenaf-fiber-reinforced core. Kenaf fibers acted as a carbonization compound promoting charring and building up a superficial insulating layer that protected the material throughout combustion. The impact of different skin/core thickness on the thermal and fire properties was investigated. Synergistic flame retardancy occurs in the cone calorimeter. Chemical and fire investigations confirmed a changed pyrolysis behavior in multicomponent materials. Promising results are obtained in terms of mechanical performance: higher flexural and impact properties were observed in the single fiber-reinforced layer. KW - A. Fibres KW - A. Layered structures KW - D. Thermal analysis KW - D. Mechanical testing PY - 2013 DO - https://doi.org/10.1016/j.compositesb.2012.07.005 SN - 1359-8368 VL - 44 IS - 1 SP - 112 EP - 119 PB - Elsevier CY - Oxford [u.a.] AN - OPUS4-26741 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard T1 - Composites in Fire: Fire Behaviour Tailored for Differnt Applications T2 - Interflam 2013, 13 th International Conference and Exhibition on Fire Science and Engineering CY - London, England DA - 2013-06-24 PY - 2013 AN - OPUS4-28766 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -