1984
DOI: 10.1021/i300013a021
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Thermal behavior of some organic phosphates

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Cited by 35 publications
(23 citation statements)
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“…The basic idea is that the FRA could release free radicals (usually P or halogen containing) with flame-retardant effects on thermal decompose. The radicals can scavenge the active radicals (such as H• and OH•) to suppress the free radical chain reaction of combustion (Lhomme et al, 1984). Typical organophosphates, including trimethyl phosphate (TMP) (Lhomme et al, 1984), TEP (Lalia et al, 2010), diethyl ethylphosphonate (DEEP) (Feng et al, 2013), have been used as FRAs.…”
Section: Flame Retardant Additivementioning
confidence: 99%
“…The basic idea is that the FRA could release free radicals (usually P or halogen containing) with flame-retardant effects on thermal decompose. The radicals can scavenge the active radicals (such as H• and OH•) to suppress the free radical chain reaction of combustion (Lhomme et al, 1984). Typical organophosphates, including trimethyl phosphate (TMP) (Lhomme et al, 1984), TEP (Lalia et al, 2010), diethyl ethylphosphonate (DEEP) (Feng et al, 2013), have been used as FRAs.…”
Section: Flame Retardant Additivementioning
confidence: 99%
“…The results showed little degradation under these conditions (less than about 1% at 370°C for tricresyl phosphate [22]) but even at this temperature there were already traces of olefins, alkyl benzenes and condensed ring aromatic structures -all of which are soot precursors. In 1984 a paper was published [23] that not only identified the products of thermal/oxidative breakdown of phosphates but also attempted to postulate a pyrolysis mechanism (see Figure 6). For this study triphenyl phosphate, the most oxidatively stable aryl phosphate, was selected.…”
Section: Potential High-temperature Degradation Mechanismsmentioning
confidence: 99%
“…These are structures that are not produced under normal operating conditions but begin to form at specific elevated temperatures and whose presence in the degradation products could therefore indicate the approximate temperature to which small amounts of the fluid had been subjected. For example, fused ring structures, such as naphthalene, have been reported [23] as being formed from triphenyl phosphate at about 800°C. The fact that the pyrolysis takes place under non-oxidative conditions means that this may only be an approximate guide to the formation under operating conditions.…”
Section: Formation Of Other Volatile Materialsmentioning
confidence: 99%
“…At high temperature, OPCs will decompose into phosphoric or polyphosphoric acids and produce many radicals [15][16][17][18][19]. These species have good flame retardant performance to lignocellulosic materials and also can promote the carbonization of lignocellulosic materials.…”
Section: Introductionmentioning
confidence: 99%