The dynamic thermo-oxidative degradation of expandable graphite (EG)-based
intumescent halogen-free flame retardant (HFFR) LLDPE blends in the condens
ed phase at 300 or 400 degreesC has been studied in situ by real time Fouri
er transform infrared spectroscopy. The kinetic characteristics and dynamic
changes of various kinds of pyrolysis products during the thermo-oxidative
degradation were examined extensively for several LLDPE/EG blends with dif
ferent HFFR additives, such as the phosphorus-nitrogen compound NP28, ammon
ium polyphosphate (APP), red phosphorus (RP), and zinc berate (ZB). It has
been found (i) that the dynamic monitoring of the LLDPE/EG/HFFR blends duri
ng the pyrolysis shows that the breakdown of LLDPE main chains and formatio
n of various kinds of carbonyl products increase with increasing thermo-oxi
dation time and temperature; the latter have been identified as carboxylic
acids, ketone, lactone and cyclic anhydrides; (ii) that the fast formation
rate and high initial concentrations of P-O-P and P-O-C products in the pho
sphorus-containing HFFR systems have a crucial importance for decreasing th
e thermo-oxidative degradation rate of LLDPE efficiently (the NP28 system i
s the most efficient in the present study); and (iii) that the pyrolysis te
mperature has a significant effect on the efficiency of flame retardants, w
hich requires the LLDPE/EG/HFFR formulation should be optimized at certain
temperature range in order to form compact intumescent charred layers immed
iately at the beginning of the thermo-oxidative degradation of the LLDPE bl
ends. (C) 2001 Elsevier Science Ltd. All rights reserved.