TY - JOUR A1 - Schartel, Bernhard A1 - Perret, Birgit A1 - Dittrich, Bettina A1 - Ciesielski, M. A1 - Krämer, J. A1 - Müller, P. A1 - Altstädt, V. A1 - Zang, L. A1 - Döring, M. T1 - Flame retardancy of polymers: the role of specific reactions in the condensed phase N2 - Condensed-phase mechanisms play a major role in fire-retardant polymers. Generations of development have followed the concept of charring to improve fire properties. Whereas the principal reactions are believed to be known, the specific description for multicomponent systems is lacking, as is the picture across different systems. A two-step approach is proposed in general, and also presented in greater detail. The second step covers the specific reactions controlling charring, whereas the actual reactants are provided in the preceding step. This model consistently incorporates the variety of structure–property relationships reported. A comprehensive case study is presented on seven phosphorus flame retardants in two epoxy resins to breathe life into the two-step approach. KW - Charring KW - Epoxy KW - Flame retardancy KW - Pyrolysis KW - Thermogravimetric analysis (TGA) PY - 2016 DO - https://doi.org/10.1002/mame.201500250 SN - 1438-7492 SN - 1439-2054 VL - 301 IS - 1 SP - 9 EP - 35 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-35273 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Brehme, Sven A1 - Köppl, T. A1 - Schartel, Bernhard A1 - Altstädt, V. T1 - Competition in aluminium phosphinate-based halogen-free flame retardancy of poly(butylene terephthalate) and its glass-fibre composites N2 - Aluminium diethylphosphinate (AlPi-Et) and inorganic aluminium phosphinate with resorcinol-bis(di-2,6-xylyl phosphate) (AlPi-H+RXP) were compared with each other as commercially available halogen-free flame retardants in poly(butylene terephthalate) (PBT) as well as in glass-fibre-reinforced PBT (PBT/GF). Pyrolysis behaviour and flame retardancy performance are reported in detail. AlPi-H+RXP released phosphine at very low temperatures, which can become a problem during processing. AlPi-Et provided better limiting oxygen index (LOI) values and UL 94 ratings for bulk and PBT/GF than AlPi-H+RXP. Both flame retardants acted via three different flame-retardancy mechanisms in bulk as well as in PBT/GF, namely, flame inhibition, increased amount of char, and a protection effect of the char. AlPi-Et was more efficient in decreasing the total heat evolved of PBT in the cone calorimeter test. AlPi-H+RXP reduced the peak heat release rate of PBT more efficiently than AlPi-Et. An optimum loading of AlPi-Et in PBT/GF was found, which was below the supplier's recommendation. This loading provides a maximum increase in LOI and a maximum decrease in total heat evolved. KW - Aluminium phosphinate KW - Flame retardancy KW - Glass-fibre composite KW - Poly(butylene terephthalate) PY - 2014 DO - https://doi.org/10.1515/epoly-2014-0029 SN - 1618-7229 VL - 14 IS - 3 SP - 193 EP - 208 PB - De Gruyter CY - [S.l.] AN - OPUS4-30648 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pospiech, D. A1 - Fischer, O. A1 - Korwitz, A. A1 - Hoffmann, T. A1 - Köppl, T. A1 - Altstädt, V. A1 - Ciesielski, M. A1 - Döring, M. A1 - Brehme, Sven A1 - Schartel, Bernhard A1 - Vollmerhausen, D. T1 - Designed flame retardancy with phosphorus polymers N2 - Polymeric flame retardants offer the possibility to match effective flame retardancy with the requirements of new regulations. Synthesis, properties and efficiency in polymer matrices are discussed for two systems, epoxy resins as well as poly(butylene terephthalate). T2 - 25th Annual conference: Recent advances in flame retardancy of polymeric materials CY - Stamford, Connecticut, USA DA - 18.05.2014 KW - Flame retardancy KW - Phosphorus polymer KW - Poly(butylene terephthalate) KW - Epoxy resin PY - 2014 SP - 1 EP - 5 AN - OPUS4-30951 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yin, Huajie A1 - Dittrich, Bettina A1 - Farooq, Muhammad A1 - Kerling, S. A1 - Wartig, K.-A. A1 - Hofmann, D. A1 - Huth, Christian A1 - Okolieocha, C. A1 - Altstädt, V. A1 - Schönhals, Andreas A1 - Schartel, Bernhard T1 - Carbon-based nanofillers/poly(butylene terephthalate): thermal, dielectric, electrical and rheological properties N2 - The influence of distinct carbon based nanofillers: expanded graphite (EG), conducting carbon black (CB), thermally reduced graphene oxide (TRGO) and multi-walled carbon nanotubes (CNT) on the thermal, dielectric, electrical and rheological properties of polybutylene terephthalate (PBT) was examined. The glass transition temperature (Tg) of PBT nanocomposites is independent of the filler type and content. The carbon particles act as nucleation agents and significantly affect the melting temperature (Tm), the crystallization temperature (Tc) and the degree of crystallinity of PBT composites. PBT composites with EG show insulating behaviour over the tested concentration range of 0.5 to 2 wt.-% and hardly changed rheological behaviour. CB, CNT and TRGO induce electrical conductivity to their particular PBT composites by forming a conducting particle network within the polymer matrix. CNT reached the percolation threshold at the lowest concentration (<0.5 wt.-%), followed by TRGO (<1 wt.-%) and CB (<2 wt.-%). With the formation of a particle network, the flow behaviour of composites with CB, CNT and TRGO is affected, i.e., a flow limit occurs and the melt viscosity increases. The degree of influence of the carbon nanofillers on the rheological properties of PBT composites follows the same order as for electrical conductivity. Electrical and rheological results suggest an influence attributed to the particle dispersion, which is proposed to follow the order of EG<< CB