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Efficiency of wollastonite and ammonium polyphosphate combinations on flame retardancy of polystyrene
Author(s) -
Quach YenThiHai,
Ferry Laurent,
Sonnier Rodolphe,
Lopez Cuesta JoséMarie
Publication year - 2013
Publication title -
polymers for advanced technologies
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.61
H-Index - 90
eISSN - 1099-1581
pISSN - 1042-7147
DOI - 10.1002/pat.3057
Subject(s) - ammonium polyphosphate , materials science , thermogravimetric analysis , cone calorimeter , char , chemical engineering , polystyrene , combustion , polyphosphate , ammonium dihydrogen phosphate , thermal stability , calorimetry , pyrolysis , fire retardant , analytical chemistry (journal) , phosphate , composite material , organic chemistry , chemistry , polymer , fertilizer , physics , engineering , thermodynamics
The thermal and fire properties of polystyrene (PS) flame retarded by a system composed of ammonium polyphosphate (APP) and wollastonite (W) were investigated by thermogravimetric analysis, pyrolysis‐combustion flow calorimeter, pyrolysis gas chromatography mass spectrometry, cone calorimetry and epiradiator. The combustion residues were observed by scanning electron microscopy/energy dispersive X‐ray spectroscopy and analyzed by X‐ray diffraction. The combination of both additives enables increasing the thermal stability of PS while increasing simultaneously the high temperature residue. The peak of HRR was also significantly reduced while time to ignition varied depending on the composition. It was shown that the degradation pathway of PS was affected by the presence of the additives implying a reduction of the effective heat of combustion. In the condensed phase, APP decomposition promotes char formation and favors the reactivity between phosphorus and silicate. A layer composed of char, W and a mixture of calcium and silicon phosphate is formed at the sample surface during combustion. This layer is cohesive enough to limit the release of combustible gases to the gas phase. Moreover, the thermally stable protective layer reaches high temperature enabling the re‐irradiation of a part of the incident heat flux. The flame retardancy of PS is thus enhanced. Copyright © 2012 John Wiley & Sons, Ltd.