Hyperbranched Polyphosphoesters, -di/amidates and –amides as Novel Flame Retardants for Epoxy Resins: Understanding the Role of Chemical Composition

  • The use of phosphorus-containing flame retardants as a viable alternative to their widely used halogen-containing counterparts has been the source of much recent research. As the search for an effective flame retardant for specific polymeric systems continues, a new class of flame retardants have shown promising results, namely hyperbranched polyphosphoesters and their derivatives. These macromolecules promise to combine the effects of complex, hyperbranched structures with the flame retarding effects of phosphorus, enabling a high miscibility and processability, as well as a lower impact on glass transition temperature and decreased diffusion from the polymer matrix. These and other functions enable them to act as multifunctional additives. In recent times, phosphorus-based hyperbranched materials and their efficacy as flame retardants have been described in literature. Often, the inclusion of nitrogen atoms into the chemical surrounding of phosphorus has lead to reports ofThe use of phosphorus-containing flame retardants as a viable alternative to their widely used halogen-containing counterparts has been the source of much recent research. As the search for an effective flame retardant for specific polymeric systems continues, a new class of flame retardants have shown promising results, namely hyperbranched polyphosphoesters and their derivatives. These macromolecules promise to combine the effects of complex, hyperbranched structures with the flame retarding effects of phosphorus, enabling a high miscibility and processability, as well as a lower impact on glass transition temperature and decreased diffusion from the polymer matrix. These and other functions enable them to act as multifunctional additives. In recent times, phosphorus-based hyperbranched materials and their efficacy as flame retardants have been described in literature. Often, the inclusion of nitrogen atoms into the chemical surrounding of phosphorus has lead to reports of increased flame retarding performance through synergistic effects. However, a comprehensive study of the relationship between nitrogen and phosphorus in hyperbranched polymers is lacking. The aim of this work is to determine the efficacy of novel, phosphorus-based hyperbranched polymers compared to other, commercially available, previously studied flame retardants and to investigate the molecular flame retarding mechanism of these complex structured macromolecules. Among one of the key aspects here is the modification of the O:N ratio of the phosphorus-containing repeating units of these hyperbranched polymers. The newly described synthesis route yields trifunctional monomers of the desired composition, which undergo an A2+B3-type polymerization via radical thiol-ene reactions, producing polyphosphoesters, -amidates, -diamidates, or -amides, respectively. By precisely tailoring the nitrogen and oxygen ratio in the chemical surrounding of phosphorus, a more comprehensive picture of the structure-property relationship of these materials may be gained. Furthermore, by adjusting the aromaticity of the hydrocarbon moieties in these trifunctional monomers, an optimization of flame retarding properties, such as increased charring, is aimed to be achieved. Additionally, the trifunctional monomers themselves act as low molecular weight fire retardants; therefore, by comparing the performance of these monomers to their high molecular weight, hyperbranched, polymeric counterparts, an understanding of the role of molecular architecture in designing a more effective flame retardant can be gained. Finally, several epoxy resin matrices, common in high-tech industrial applications, are investigated in the interest of comprehending the interaction between these novel hyperbranched flame retardant additives and their surrounding polymeric matrix. In order to determine the flame retardancy mechanism of these materials, a multi-methodological approach is selected, thus offering a high volume of correlating data. Using Fourier-transform infrared spectroscopy (FTIR) coupled with thermogravimetric analysis (TGA), as well as pyrolysis combustion flow calorimetry (PCFC), provides evidence of mass loss processes, their respective decomposition products, and the heat released by volatiles in the gas phase during pyrolysis, while hot-stage FTIR offers information of the decomposition products occurring in the condensed phase. Limiting oxygen index (LOI) and UL-94 help to quantify and categorize the materials’ flammability, while the use of a cone calorimeter offers valuable insight into the fire behavior in forced flaming conditions, providing heat release rates, smoke and CO/CO2 production, amount of residue, and other important indices. Finally, the use of differential scanning calorimetry (DSC) provides information of material properties such as glass transition temperatures, and the implementation of blooming tests serves to examine the reduction of molecular mobility in the matrix. By varying the architecture of the flame retardants – in the O:N ratio of the chemical surrounding of phosphorus and in the aromatic composition of the monomers’ hydrocarbon moieties – and by comparing low versus high molecular weight species in varied epoxy resin matrices, as well as through the use of a multi-methodological approach, new insight into the use and the mode of action of these components as flame retardants for modern materials can be won.zeige mehrzeige weniger

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Metadaten
Autor*innen:Alexander Battig
Koautor*innen:J. Markwart, M. M. Velencoso, F. R. Wurm, Bernhard Schartel
Dokumenttyp:Posterpräsentation
Veröffentlichungsform:Präsentation
Sprache:Englisch
Jahr der Erstveröffentlichung:2017
DDC-Klassifikation:Technik, Medizin, angewandte Wissenschaften / Ingenieurwissenschaften / Ingenieurbau
Freie Schlagwörter:Epoxy resin; Flame retardant; Hyperbranched polymer; Phosphoester; Phosphor(di)amidate; Phosphoramide
Veranstaltung:FRPM 2017, 16th European Meeting on Fire Retardant Polymeric Materials
Veranstaltungsort:Manchester, UK
Beginndatum der Veranstaltung:03.07.2017
Enddatum der Veranstaltung:06.07.2017
Verfügbarkeit des Dokuments:Datei im Netzwerk der BAM verfügbar ("Closed Access")
Datum der Freischaltung:11.07.2017
Referierte Publikation:Nein
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