Published January 20, 2010 | Version v1
Journal article

Flame retardancy mechanisms of bisphenol A bis(diphenyl phosphate) in combination with zinc borate in bisphenol A polycarbonate/acrylonitrile-butadiene-styrene blends

  • 1. BAM Federal Institute for Material Research and Testing, Unter den Eichen 87, 12205 Berlin (Germany)
  • 2. BAM Federal Institute for Material Research and Testing, Richard-Willstaetter Str. 11, 12489 Berlin (Germany)

Description

Bisphenol A polycarbonate/acrylonitrile-butadiene-styrene (PC/ABS) with and without bisphenol A bis(diphenyl phosphate) (BDP) and 5 wt.% zinc borate (Znb) were investigated. The pyrolysis was studied by thermogravimetry (TG), TG-FTIR and NMR, the fire behaviour with a cone calorimeter applying different heat fluxes, LOI and UL 94. Fire residues were examined with NMR. BDP affects the decomposition of PC/ABS and acts as a flame retardant in the gas and condensed phases. The addition of Znb results in an additional hydrolysis of PC. The fire behaviour is similar to PC/ABS, aside from a slightly increased LOI and a reduced peak heat release rate, both caused by borates improving the barrier properties of the char. In PC/ABS + BDP + Znb, the addition of Znb yields a borate network and amorphous phosphates. Znb also reacts with BDP to form alpha-zinc phosphate and borophosphates that suppress the original flame retardancy mechanisms of BDP. The inorganic-organic residue formed provides more effective flame retardancy, in particular at low irradiation in the cone calorimeter, and a clear synergy in LOI, whereas for more developed fires BDP + Znb become less effective than BDP in PC/ABS with respect to the total heat evolved.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.tca.2009.10.007

Additional details

Identifiers

DOI
10.1016/j.tca.2009.10.007;
PII
S0040-6031(09)00364-5;

Publishing Information

Journal Title
Thermochimica Acta
Journal Volume
498
Journal Issue
1-2
Journal Page Range
p. 92-99
ISSN
0040-6031
CODEN
THACAS

Optional Information

Copyright
Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.