4.7 Article

Theoretical study on pyrolysis mechanism of decabromodiphenyl ether (BDE-209) using DFT method

Journal

CHEMOSPHERE
Volume 310, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2022.136904

Keywords

BDE-209; Pyrolysis mechanism; DFT method; PBDD; Fs; Debromination reaction; Cyclization reaction

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This study investigated the thermal degradation mechanism of BDE-209 using density functional theory method and found that the primary degradation reactions involved cleaving the ether bond and the C-Br bond. The formation of hexabromobenzene and low-brominated diphenyl ethers were observed as major products. The results obtained in this study provide valuable information for the treatment and reuse of waste plastics containing BDE-209.
Decabromodiphenyl ether (BDE-209), as a brominated flame retardant (BFR), is widely applied to various consumer products due to its superior performance and affordable pricing to improve the flame resistance of materials. To better comprehend the pyrolysis behavior of BDE-209 and the evolution process of main pyrolysis products, the thermal degradation mechanism of BDE-209 was studied using density functional theory (DFT) method at the theoretical level of M06/cc-pVDZ, and thermodynamic parameters were calculated in this paper. Unimolecular degradation was dominated by cleavage of the ether linkage, which results in a high yield of hexabromobenzene, and fission of the ortho-position C-Br bond is the main competitive reaction channel. In the system of BDE-209 + H, the pyrolysis reaction is majorly characterized by debromination, leading to the for-mation of considerable HBr and low-brominated diphenyl ethers. Additionally, the hydrogen-derived splitting of the ether bond acts as a mainly competitive channel, which is the source of polybromophenols and poly-bromobenzenes. The formation of polybrominated dibenzofuran (PBDF) derives from the cyclization reaction of ortho-phenyl-type radicals, which are readily generated through the ortho-position Br atom abstraction by H radical. The formation of polybrominated dibenzo-p-dioxin (PBDD) involves the ortho-C-O coupling reaction of polybromophenoxy radicals, debromination reaction, and cyclization reaction. And the total yield of PBDD/Fs was significantly increased when H was involved. Results presented in this work will provide the helpful in-formation for the treatment and reuse of BDE-209-containing waste plastics through using pyrolysis technology.

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