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Thermal Degradation of Organophosphorus Flame Retardants

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Publisher MDPI
Date 2022 Nov 26
PMID 36433056
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Abstract

The development of new organophosphorus flame retardants for polymeric materials is spurred by relatively low toxicity, effectiveness, and demand for replacement of more traditional materials. To function, these compounds must decompose in a degrading polymer matrix to form species which promote modification of the solid phase or generate active radical moieties that escape to the gas phase and interrupt combustion propagating reactions. An understanding of the decomposition process for these compounds may provide insight into the nature of flame retardant action which they may offer and suggest parameters for the synthesis of effective new organophosphorus flame retardants. The thermal degradation of a series of organophosphorus esters varying in the level of oxygenation at phosphorus-alkyl phosphate, aryl phosphate, phosphonate, phosphinate-has been examined. Initial degradation in all cases corresponds to elimination of a phosphorus acid. However, the facility with which this occurs is strongly dependent on the level of oxygenation at phosphorus. For alkyl phosphates elimination occurs rapidly at relatively low temperature. The same process occurs at somewhat higher temperature for aryl phosphates. Elimination of a phosphorus acid from phosphonate or phosphinate occurs more slowly and at much higher temperature. Further, the acids formed from elimination rapidly degrade further to evolve volatile species.

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References
1.
Darnerud P . Brominated flame retardants as possible endocrine disrupters. Int J Androl. 2008; 31(2):152-60. DOI: 10.1111/j.1365-2605.2008.00869.x. View

2.
Liang S, Hemberger P, Neisius N, Bodi A, Grutzmacher H, Levalois-Grutzmacher J . Elucidating the thermal decomposition of dimethyl methylphosphonate by vacuum ultraviolet (VUV) photoionization: pathways to the PO radical, a key species in flame-retardant mechanisms. Chemistry. 2014; 21(3):1073-80. DOI: 10.1002/chem.201404271. View

3.
Behnisch P, Hosoe K, Sakai S . Brominated dioxin-like compounds: in vitro assessment in comparison to classical dioxin-like compounds and other polyaromatic compounds. Environ Int. 2003; 29(6):861-77. DOI: 10.1016/s0160-4120(03)00105-3. View

4.
Hamers T, Kamstra J, Sonneveld E, Murk A, Kester M, Andersson P . In vitro profiling of the endocrine-disrupting potency of brominated flame retardants. Toxicol Sci. 2006; 92(1):157-73. DOI: 10.1093/toxsci/kfj187. View

5.
Howell B, Daniel Y . Incorporation of Comonomer -5-(Diphenylphosphato)Isosorbide-2--Acrylate to Generate Flame Retardant Poly(Styrene). Polymers (Basel). 2019; 11(12). PMC: 6960599. DOI: 10.3390/polym11122038. View