TY - CONF A1 - Martins, Marta S. S. T1 - Ceramic tapes as fire protective coatings for CFRP composites N2 - Ceramic tapes with different chemical compositions were produced by tape casting technology. Unlike the traditional solvent-based slurries, we have used eco-friendly water based formulations. These thin coatings were afterwards used as top layer on 6-layered carbon fibre epoxy composites as intended fire protective coatings. Tape C, containing cellulose fibres, has demonstrated to be the most effective coating regarding the fire reaction behaviour. These coatings are attractive in the sense that: Their composition can be more or less tailored, there are easily impregnated with epoxy resin, and they are extremely flexible, and can therefore be used in a wide range of applications. T2 - COST MP1105 Final Conference Innovations in Flame Retardancy of Textiles and Related Materials CY - Poznan, Poland DA - 27.04.2016 KW - Composites KW - Fire retardancy KW - Laminates KW - Carbon fibres PY - 2016 AN - OPUS4-36871 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Scarfato, Paola A1 - Incarnato, L. A1 - Di Maio, L. A1 - Dittrich, Bettina A1 - Schartel, Bernhard T1 - Influence of a novel organo-silylated clay on the morphology, thermal and burning behavior of low density polyethylene composites N2 - The functionalization of a natural sodium montmorillonite (MMT) with (3-glycidyloxypropyl)trimethoxysilane by a silylation procedure is presented, and its use as nanofiller in the melt compounding of low density polyethylene (LDPE) nanocomposites. In particular, the effects on the thermal stability and flame retardant properties of melt compounded LDPE nanocomposites are analyzed, with and without magnesium hydroxide (MH) as an additional conventional flame retardant. The purpose was to investigate possible synergistic effects between the two inorganic fillers on fire behavior. The obtained organosilylated clay showed higher interlayer spacing than the original MMT and good thermal stability, higher than that of many commercial organoclays modified with alkylammonium salts. Its addition to LDPE allowed the production of hybrids with nanoscale dispersion of the filler, as demonstrated by X-ray diffraction. The simultaneous presence of MH, which strongly interacts with the nanoclay, hindered intercalation of the polymer chains between the clay galleries and clay layer exfoliation within the LDPE resin. The investigation of the thermal and burning behavior of the LDPE nanocomposites indicated that the organosilylated clay alone shows only a limited residual protection layer effect. In combination with MH the nanocomposites have a small adverse effect on the reaction to small flame as measured by the Oxygen index and UL 94 testing, and, surprisingly, no effect on the peak heat release rate in the cone calorimeter. The quality of the fire residue was lacking on the microscopic scale. The ternary LDPE/MH/ organoclay systems investigated did not open the door to reducing MH content in halogen-free flame retardant LDPE yet, but demand further research. KW - Nano structures KW - Polymer-matrix composites KW - High-temperature properties KW - Thermoplastic resin KW - Burning behavior KW - Fire retardancy PY - 2016 DO - https://doi.org/10.1016/j.compositesb.2016.05.053 SN - 1359-8368 VL - 98 SP - 444 EP - 452 PB - Elsevier AN - OPUS4-36865 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - THES A1 - Shabir Mahr, Muhammad T1 - Wood modification with titania and silica based precursors - a novel approach to prepare multifunctional sol-gel derived TiO2 / SiO2 wood-inorganic composites N2 - This dissertation is devoted to explicitly investigate the suitability of titania and silica based precursors for wood modification. Novel TiO2 / SiO2 wood inorganic composites were prepared by two-step process. In first step, freshly prepared precursor solutions of silicon and titanium alkoxides were vacuum impregnated (one or more cycles) to oven dried pine sapwood (Pinius sylvestris L.). Precursor solutions with nano-scaled species and particulates (TiO2 and SiO2) were soaked by the entire wood matrix during this step. In (second) subsequent curing step, these penetrating liquids transformed into respective gel layers and depositions therein by sol-gel processing (in-situ hydrolysis-condensation). Sol-gel based depositions were evenly covered on the cell walls in the form of thin layers. These gel films were not crack-free however; very few cracks were visible in the gel coatings present within the wood matrix of composites prepared with precursors of low alkoxide content. In addition, the gels were randomly distributed, found to be mainly deposited in the wood cell lumen and also localized in the cell walls as ESEM-EDX mapping revealed. The impregnated samples show an increase in mass and volume expressed as weight percent gain (WPG) and bulking (B). Both of the parameters are decisive for tailoring a number of physical properties of the resultant composites. In general, moisture and water sorption capacities were decreased by 43 to 50 % while anti-swelling efficiency (ASE) and bending strength (MOE) of the precursor-modified wood (composite) were increased up to 34 % and 41 % respectively, when compared to unmodified wood. These improvements are attributed mainly to gel depositions in the wood structure that physically interact with the wood matrix consequently narrowing the main flow passages there and reinforcing strengths of the fiber. These materials show superior resistance against fire of different scenarios. In small scale fire, their flame was retarded markedly (up to 78 % in optimum case) in comparison to wood controls as studied by oxygen index test (LOI). Cone calorimetric investigations revealed their better fire retardancy in terms of time resolved heat release rates (HRR) in the developing fire scenario. A remarkable reduction of 40 % in the second peak of HRR was achieved through sol-gel treatment. Furthermore, fire hazards such as CO and total smoke production were considerably lowered for these materials. Beside these improvements, reductions in first peak HRR and in fire load (total heat evolved) were not worth considering in compliance to fire retardancy principles. In relation to the mechanism of protection, it can be concluded that stable gel layer (independence of material loading) inside the wood retards markedly the proceeding combustion processes (oxidation) after first pyrolysis by improving the overall protection properties of the fire residue. These materials show excellent resistance against bio-deterioration. Almost full decay protection was achieved against wood destroying brown rot fungi (Coniophora puteana and Poria placenta) in 10 weeks laboratory trials only with 1 mass% loadings (WPG). Mass loss in prolonged test (16 weeks) was similar to 10 week lasted test indicating that protection is permanent. In addition, composites imparted moderate resistances against soft rot fungi and very minor one against surface blue stain. The lowering in moisture content that discourages fungal colonization, gel layer that provides better shielding against fungal exposure and un-hydrolyzed alkoxides (organics) that probably induce biocidal effects are the main reasons for protection against biological attack in these materials. Composites are utmost leach resistant because of the insolubility of gel depositions in water as well as due to their fixture into the wood matrix. In addition to this intrinsic property, gel precipitates can also reduce substantially (70 to 80 %) the release of hazardous active agents (e.g. CuCl2) of wood preservatives into the environment. This anti-leaching effect is supposed to be due to the reduced ion mobility of active agents inside the wood by their encapsulations into the gel matrix, lowering of water penetration into the wood depths as well as due to the internal covering action of the gel layer. In short, it can be assessed that TiO2 / SiO2 based sol-gel precursor treatment of wood has a possibility to be commercialize in near future due to easy handling and non-toxic nature of the precursor used. Resultant end products (composites) are also novel and promising multifunctional materials that can be used for multi-purposes in relation to use class 3 (outdoor but without ground contact according to EN 335 2006) environments. KW - Precursor solutions KW - Sol-gel process KW - Gel depositions KW - Wood modification KW - Composite materials KW - Fire retardancy KW - Cone calorimeter KW - Flammability KW - Anti-fungal efficacy KW - Brown rot fungi KW - Soft rot fungi KW - Leach resistance PY - 2013 SN - 978-3-95404-570-9 SP - 1 EP - 110 PB - Cuvillier CY - Göttingen AN - OPUS4-29988 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Sturm, Heinz A1 - Schartel, Bernhard A1 - Weiß, André A1 - Braun, Ulrike T1 - SEM/EDX: Advanced investigation of structured fire residues and residue formation N2 - Heterogeneous, gradual or structured morphology of fire residues plays an important role in fire retardancy of polymers. A scanning electron microscope with an attached energy dispersive X-ray spectrometer (SEM/EDX) is highlighted as a powerful tool for the advanced characterization of such complex fire residues, since it offers high resolution in combination with both good depth of field and analysis of chemical composition. Two examples are presented: First, comprehensive SEM/EDX investigation on a complex structured fire residue of glass fibre reinforced polyamide 6,6 (PA 66-GF) flame retarded by diethylaluminium phosphinate, melamine polyphosphate and some zinc borate. A multilayered surface crust (thickness ~ 24 µm) covers a rather hollow area stabilized by GF glued together. The resulting efficient thermal insulation results in self-extinguishing before pyrolysis is completed, even under forced-flaming combustion. Second, sophisticated, quasi online SEM/EDX imaging of the formation of residual protection layer in layered silicate epoxy resin nanocomposites (LSEC). Burning specimens were quenched in liquid nitrogen for subsequent analyses. Different zones were distinguished in the condensed phase characterized by distinct processes such as melting and ablation of organic material, as well as agglomeration, depletion, exfoliation and reorientation of the LS. KW - Fire residue KW - SEM/EDX KW - Fire retardancy KW - PA 66 KW - Layered silicate KW - Diethylaluminium phosphinate PY - 2012 DO - https://doi.org/10.1016/j.polymertesting.2012.03.005 SN - 0142-9418 VL - 31 IS - 5 SP - 606 EP - 619 PB - Elsevier CY - Amsterdam AN - OPUS4-25802 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Weiß, André A1 - Sturm, Heinz A1 - Kleemeier, M. A1 - Hartwig, A. A1 - Vogt, C. A1 - Fischer, R.X. T1 - Layered silicate epoxy nanocomposites: formation of the inorganic-carbonaceous fire protection layer N2 - The layered silicate (LS) modification and processing parameters applied control the morphology of the LS/polymer composites. Here, increasing the surface area of the LS particles by using alternative drying processes increases dispersion towards a more typical nanocomposite morphology, which is a basic requirement for promising flame retardancy. Nevertheless, the morphology at room temperature does not act itself with respect to flame retardancy, but serves as a prerequisite for the formation of an efficient surface protection layer during pyrolysis. The formation of this residue layer was addressed experimentally for the actual pyrolysis region of a burning nanocomposite and thus our results are valid without any assumptions or compromises on the time period, dimension, surrounding atmosphere or temperature. The formation of the inorganic-carbonaceous residue is influenced by bubbling, migration, reorientation, agglomeration, ablation, and perhaps also delamination induced thermally and by decomposition, whereas true sintering of the inorganic particles was ruled out as an important mechanism. Multiple, quite different mechanisms are relevant during the formation of the residue, and the importance of each mechanism probably differs from one nanocomposite system to another. The main fire protection effect of the surface layer in polymer nanocomposites based on non-charring or nearly non-charring polymers is the increase in surface temperature, resulting in a substantial increase in reradiated heat flux (heat shielding). KW - Nanocomposite KW - Fire retardancy KW - Epoxy resin KW - Fire behavior KW - Flammability PY - 2011 DO - https://doi.org/10.1002/pat.1644 SN - 1042-7147 SN - 1099-1581 VL - 22 IS - 12 SP - 1581 EP - 1592 PB - John Wiley & Sons, Ltd. CY - Chichester AN - OPUS4-24916 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 - JOUR A1 - Brehme, Sven A1 - Schartel, Bernhard A1 - Goebbels, Jürgen A1 - Fischer, O. A1 - Pospiech, D. A1 - Bykov, Y. A1 - Döring, M. T1 - Phosphorus polyester versus aluminium phosphinate in poly(butylene terephthalate) (PBT): Flame retardancy performance and mechanisms N2 - Pyrolysis and fire behaviour of a phosphorus polyester (PET-P-DOPO) have been investigated. The glycol ether of the hydroquinone derivative of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide was used as a reactive halogen-free flame retardant in PET-P-DOPO. PET-P-DOPO is proposed as an alternative to poly(butylene terephthalate) (PBT) with established halogen-free additives. It exhibits a high LOI (39.3%) and achieves V-0 classification in the UL 94 test. Three different mechanisms (flame inhibition, charring and a protection effect by the intumescent char) contribute to the flame retardancy in PET-P-DOPO and were quantified with respect to different fire risks. The fire load was reduced by 66% of the PBT characteristic. The reduction is the superposition of the relative reduction due to flame inhibition (factor 0.625) and charring (factor 0.545). The peak of heat release rate (pHRR) was reduced by 83% due to flame inhibition, charring and the protection properties of the char (factor 0.486). The strength of all three mechanisms is in the same order of magnitude. The intumescent multicellular structure enables the char to act as an efficient protection layer. PBT flame-retarded with aluminium diethylphosphinate was used as a benchmark to assess the performance of PET-P-DOPO absolutely, as well as versus the phosphorus content. PET-P-DOPO exhibits superior fire retardancy, in particular due to the additional prolongation of the time to ignition and increase in char yield. PET-P-DOPO is a promising alternative material for creating halogen-free flame-retarded polyesters. KW - Poly(butylene terephthalate) (PBT) KW - Fire retardancy KW - Aluminium phosphinate KW - 9,10-Dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) PY - 2011 DO - https://doi.org/10.1016/j.polymdegradstab.2011.01.035 SN - 0141-3910 SN - 1873-2321 VL - 96 IS - 5 SP - 875 EP - 884 PB - Applied Science Publ. CY - London AN - OPUS4-23469 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Braun, Ulrike A1 - Wachtendorf, Volker A1 - Geburtig, Anja A1 - Bahr, Horst A1 - Schartel, Bernhard T1 - Weathering resistance of halogen-free flame retardance in thermoplastics N2 - The influence of weathering on the fire retardancy of polymers is investigated by means of a cone calorimeter test, before and after artificial weathering. The surface degradation was monitored using different techniques (ATR–FTIR, microscopy, colour measurement). Different kinds of polymeric materials were chosen, all as they are used in practice: polycarbonate (PC) blends, polyamide (PA) and polypropylene (PP) flame-retarded with arylphosphate, melamine cyanurate (MC) and intumescent formulation based on ammonium polyphosphate (APP), respectively. All samples show material degradation at the surface due to weathering. No significant weathering influence occurs on the flame retardancy when it is a bulk property, as was observed for aryl phosphates in PC blends and MC in PA. When the fire retardancy is dominated by a surface mechanism, dependence on the duration of weathering is detected: for intumescent formulations based on ammonium APP in PP, a worsening in the formation of the intumescent network was observed. KW - Fire retardancy KW - Weathering resistance KW - Degradation KW - Intumescence KW - Cone calorimeter PY - 2010 DO - https://doi.org/10.1016/j.polymdegradstab.2010.08.020 SN - 0141-3910 SN - 1873-2321 VL - 95 IS - 12 SP - 2421 EP - 2429 PB - Applied Science Publ. CY - London AN - OPUS4-22612 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Perret, Birgit A1 - Schartel, Bernhard A1 - Stöß, K. A1 - Diederichs, J. A1 - Ciesielski, M. A1 - Döring, M. A1 - Krämer, J. A1 - Altstädt, V. ED - Lewin, M. T1 - Novel phosphorus-based flame retardants for epoxy resins and carbon fiber composites: Decomposition mechanisms and fire behavior T2 - 21st Annual conference on recent advances on flame retardancy of polymeric materials CY - Stamford, USA DA - 2010-05-24 KW - DOPO KW - Fire retardancy KW - Flammability KW - Pyrolysis KW - Epoxy resin KW - Composites PY - 2010 SN - 1-59623-619-1 VL - 21 SP - 134 EP - 145 PB - BCC Research AN - OPUS4-22162 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard T1 - Phosphorus-based flame retardancy mechanisms - Old hat or a starting point for future development? N2 - Different kinds of additive and reactive flame retardants containing phosphorus are increasingly successful as halogen-free alternatives for various polymeric materials and applications. Phosphorus can act in the condensed phase by enhancing charring, yielding intumescence, or through inorganic glass formation; and in the gas phase through flame inhibition. Occurrence and efficiency depend, not only on the flame retardant itself, but also on its interaction with pyrolysing polymeric material and additives. Flame retardancy is sensitive to modification of the flame retardant, the use of synergists/adjuvants, and changes to the polymeric material. A detailed understanding facilitates the launch of tailored and targeted development. KW - Fire retardancy KW - Red phosphorus KW - Phosphate KW - Phosphonate KW - Phosphinate KW - Phosphine oxide KW - Flame inhibition KW - Charring KW - Intumescence PY - 2010 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-220368 DO - https://doi.org/10.3390/ma3104710 SN - 1996-1944 VL - 3 IS - 10 SP - 4710 EP - 4745 PB - MDPI CY - Basel AN - OPUS4-22036 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Kempel, Florian A1 - Schartel, Bernhard A1 - Hofmann-Böllinghaus, Anja A1 - Butler, K.M. A1 - Onate, E. A1 - Idelsohn, S.R. A1 - Rossi, R. A1 - Marti, J.M. T1 - Numerical simulation of polymeric materials in UL 94 test: Competition between gasification and melt flow/dripping T2 - Interflam 2010 - 12th International conference CY - Nottingham, UK DA - 2010-07-05 KW - Particle finite element method (PFEM) KW - UL 94 KW - Fire retardancy KW - PC/ABS KW - Melt flow KW - Dripping PY - 2010 SN - 978-0-9541216-5-5 N1 - Geburtsname von Hofmann-Böllinghaus, Anja: Hofmann, A. - Birth name of Hofmann-Böllinghaus, Anja: Hofmann, A. VL - 1 SP - 721 EP - 730 PB - Interscience Communications CY - London, UK AN - OPUS4-21670 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schartel, Bernhard A1 - Braun, Ulrike T1 - Understanding Fire Retardancy Mechanisms in Composites: A Key for Future Development T2 - 5th International Conference on Composites In Fire (CIF5) CY - Newcastle upon Tyne, United Kingdom DA - 2008-07-10 KW - Fire retardancy KW - Composites KW - Flame Retardants KW - Phosphinate PY - 2008 SP - 01-1 - 01-10 CY - Newcastle upon Tyne, UK AN - OPUS4-17716 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Braun, Ulrike A1 - Knoll, Uta A1 - Neubert, Dietmar A1 - Schartel, Bernhard ED - Schartel, Bernhard T1 - Fire Retarding Mechanisms of Red Phosphorus in Polybutylenterephthalate (PBT) in Combination with Melamine Cyanurate or Zinc Oxide KW - Fire retardancy KW - Polyester KW - Red phosphorus KW - Thermal analysis KW - Cone calorimeter PY - 2007 SN - 978-3-8334-8873-3 SP - 35 EP - 49 PB - Books on Demand GmbH CY - Norderstedt AN - OPUS4-17662 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN 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 - Braun, Ulrike A1 - Schartel, Bernhard ED - Schartel, Bernhard T1 - Flame retardant epoxy resin system for liquid composite moulding applications KW - Epoxy resin KW - Fire retardancy PY - 2007 SN - 978-3-8334-8873-3 SP - 69 EP - 84 PB - Books on Demand GmbH CY - Norderstedt AN - OPUS4-17627 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 - 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 - 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 - 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 - 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 - Bartholmai, Matthias A1 - Knoll, Uta T1 - Some comments on the use of cone calorimeter data N2 - The cone calorimeter has become one of the most important and widely used instruments for the research and development of fire retarded polymeric materials. The paper addresses three important ways in which the principal setup influences the results — factors which sometimes do not receive due consideration when drawing conclusions. The paper discusses in detail the impact on cone calorimeter results of the choice of external heat flux, the influence on the peak of heat release rate of sample thickness and thermal feedback from the back of the sample, and the influence on irradiance of the horizontal and vertical distances from the cone heater. KW - Cone Calorimeter KW - Fire retardancy KW - Fire testing KW - Nanocomposites KW - Intumescence PY - 2005 DO - https://doi.org/10.1016/j.polymdegradstab.2004.12.016 SN - 0141-3910 SN - 1873-2321 VL - 88 IS - 3 SP - 540 EP - 547 PB - Applied Science Publ. CY - London AN - OPUS4-7211 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Pötschke, P. A1 - Knoll, Uta A1 - Abdel-Goad, M. T1 - Fire behaviour of polyamide 6/multiwall carbon nanotube naocomposites N2 - Nanocomposites of polyamide 6 with 5 wt.% multiwall carbon nanotubes are investigated to clarify their potential as regards the fire retardancy of polymers. The nanocomposites are investigated using SEM, electrical resistivity, and oscillatory shear rheology. The pyrolysis is characterized using thermal analysis. The fire behaviour is investigated with a cone calorimeter using different external heat fluxes, by means of the limiting oxygen index and the UL 94 classification. The fire residue is characterized using SEM. The comprehensive fire behaviour characterization not only allows the materials’ potential for implementation in different fire scenarios and fire tests to be assessed, but also provides detailed insight into the active mechanisms. The increased melt viscosity of the nanocomposites and the fibre-network character of the nanofiller are the dominant mechanisms influencing fire performance. The changes are found to be adjuvant with respect to forced flaming conditions in the cone calorimeter, but also deleterious in terms of flammability. KW - Carbon Nanotubes KW - Nanocomposites KW - Flame retardancy KW - Rheology KW - Thermal Analysis KW - Fire retardancy KW - Cone Calorimeter PY - 2005 DO - https://doi.org/10.1016/j.eurpolymj.2004.11.023 SN - 0014-3057 SN - 1873-1945 VL - 41 IS - 5 SP - 1061 EP - 1070 PB - Elsevier CY - Oxford AN - OPUS4-7142 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Schartel, Bernhard ED - Okamoto, M. T1 - Fire retardancy based on polymer layered silicate nanocomposites KW - Fire retardancy KW - Nanocomposites KW - Cone Calorimeter KW - LOI KW - UL94 KW - Rheology PY - 2004 SN - 4-88231-479-7 SP - 242 EP - 257 PB - CMC Publ. AN - OPUS4-5497 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 - JOUR A1 - Braun, Ulrike A1 - Schartel, Bernhard T1 - Flame Retardant Mechanisms of Red Phosphorus and Magnesium Hydroxide in High Impact Polystyrene N2 - The flame retardant mechanisms of red phosphorus, magnesium hydroxide and red phosphorus combined with magnesium hydroxide were studied in high impact polystyrene by means of comprehensive decomposition studies and combustion tests. The study is intended to illuminate prerequisites and the potential of red phosphorus as a fire retardant for hydrocarbon polymers in the condensed phase and in the gas phase. Thermal and thermo-oxidative decomposition, decomposition kinetics and the product gases evolved were characterized using thermogravimetry coupled with Fourier transform infrared spectroscopy and mass spectroscopy, respectively. Fire behaviour was investigated with a cone calorimeter using different external heat fluxes, whereas the flammability was determined by limited oxygen indices. The combustion residues were analysed using XPS. Red phosphorus reduced the heat release in HIPS due to radical trapping in the gas phase. Magnesium hydroxide influenced fire behaviour by heat sink mechanisms, release of water and the formation of a magnesia layer acting as a barrier. The combination of both flame retardants in HIPS nearly resulted in a superposition. A slight synergy in barrier characteristics was due to the formation of magnesium phosphate, whereas a slight anti-synergism occurred in flammability and in the gas phase action. The latter effect is controlled by a decreased fuel rate due to the barrier layer rather than by an initiation of red phosphorus oxidation in the condensed phase. KW - Fire retardancy KW - Polystyrene KW - Pyrolysis KW - TG-FTIR KW - Red Phosphorus KW - Mg(OH)2 KW - Cone Calorimeter KW - Additives KW - Thermogravimetric analysis PY - 2004 DO - https://doi.org/10.1002/macp.200400255 SN - 1022-1352 SN - 1521-3935 VL - 205 IS - 16 SP - 2185 EP - 2196 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-4488 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 - 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 - 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 - 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 - JOUR A1 - Schartel, Bernhard A1 - Kunze, Ralf A1 - Neubert, Dietmar A1 - Tidjani, Adams T1 - ZnS as fire retardant in plasticised PVC N2 - The flame retardant effect of zinc sulphide (ZnS) in plasticised poly(vinyl chloride) (PVC-P) materials was investigated. PVC-P containing different combinations of additives such as 5% ZnS, 5% of antimony oxide (Sb2O3) and 5% of mixtures based on Sb2O3 and ZnS were compared. The thermal degradation and the combustion behaviour were studied using thermogravimetry (TG), coupled with FTIR (TG-FTIR) or with mass spectroscopy (TG-MS), and a cone calorimeter, respectively. A detailed and unambiguous understanding of the decomposition and release of the pyrolysis products was obtained using both TG-MS and TG-FTIR. The influence of ZnS, Sb2O3 and the corresponding mixtures on the thermal decomposition of PVC-P was demonstrated. Synergism was observed for the combination of the two additives. The combustion behaviour (time to ignition, heat release, smoke production, mass loss, CO production) was monitored versus external heat fluxes between 30 and 75 kW m-2 with the cone calorimeter. Adding 5% of ZnS has no significant influence on the fire behaviour of PVC-P materials beyond a dilution effect, whereas Sb2O3 works as an effective fire retardant. Synergism of ZnS and Sb2O3 allows the possibility of replacing half of Sb2O3 by ZnS to reach equivalent fire retardancy. KW - PVC KW - ZnS KW - Fire retardancy KW - TG-FTIR KW - Cone calorimeter PY - 2002 DO - https://doi.org/10.1002/pi.845 SN - 0959-8103 SN - 1097-0126 SN - 0007-1641 VL - 51 IS - 3 SP - 213 EP - 222 PB - Wiley InterScience CY - Chichester, West Sussex AN - OPUS4-1291 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Kunze, Ralf A1 - Neubert, Dietmar T1 - Red Phosphorus-Controlled Decomposition for Fire Retardant PA 66 N2 - The thermal degradation and the combustion behavior of glass fiber-reinforced PA 66 materials containing red phosphorus were investigated. Thermogravimetry (TG), TG coupled with FTIR, and TG coupled with mass spectroscopy were used to investigate the thermal decomposition. The flame retardant red phosphorus was investigated with respect to the decomposition kinetics and the release of volatile products. The combustion behavior was characterized using a cone calorimeter. Fire risks and fire hazards were monitored versus external heat fluxes between 30 and 75 kW/m2. Red phosphorus acts in the solid phase and its efficiency depends on the external heat flux. The use of red phosphorus results in an increased amount of residue and in a corresponding decrease in total heat release. The decrease of the mass loss rate peak results in a corresponding decrease of the peak heat release. With increasing external heat flux applied the first effect on the total heat release decreases linearly, whereas the second effect on the peak heat release expands linearly. The investigation provides insight into the mechanisms of how the fire retardant PA 66 is achieved by red phosphorus controlling the degradation kinetics. Taking into account that a decrease of the volatile products also leads to a decrease of heat production in the flame zone and that the char acts as heat transfer barrier, a reduced pyrolysis temperature is suggested as a further feedback effect. T2 - 8th European Conference on fire retardant polymers CY - Alessandria, Italy DA - 2001-06-24 KW - PA 66 KW - Red phosphorus KW - Fire retardancy KW - TG-FTIR KW - Cone calorimeter PY - 2002 DO - https://doi.org/10.1002/app.10144 SN - 0021-8995 SN - 1097-4628 VL - 83 IS - 10 SP - 2060 EP - 2071 PB - Wiley InterScience CY - Hoboken, NJ AN - OPUS4-1234 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -