Yang Long , Liming Tai , Shi Yan , Yan Zhu , Jinbao Huang , Li Jin , Yaqing Cai , Hong Wang , Xinsheng Li , Hao Cheng
{"title":"十溴联苯醚的降解机理:与活性自由基的反应及多溴二苯并对二恶英和二苯并呋喃的形成化学","authors":"Yang Long , Liming Tai , Shi Yan , Yan Zhu , Jinbao Huang , Li Jin , Yaqing Cai , Hong Wang , Xinsheng Li , Hao Cheng","doi":"10.1016/j.jaap.2025.107139","DOIUrl":null,"url":null,"abstract":"<div><div>Although decabromodiphenyl ether (BDE-209) has been banned from production and use as a brominated flame retardant, its threat to human and ecological environment cannot still be ignored. Nevertheless, the mechanism of BDE-209 initiated by reactive radicals in the thermochemical decomposition process remains unknown. The density functional theory method is used to study the thermochemical decomposition behavior of BDE-209, with reactive radical reactions, and the formation mechanism of polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs). The results show that BDE-209 is not prone to self-decomposition due to its high bond dissociation energy (249.6 ∼ 281.4 kJ/mol) and HOMO-LUMO energy gap (7.10 eV). The reaction of BDE-209 with three active free radicals, including •H, Br•, and •OH, usually results in a variety of hypobromated products or important intermediates at low reaction energy barriers (52.9, 54.3, 50.4 kJ/mol). At 600 K, the branching ratio of H-abstraction reaction in the reaction system of •H and BDE-209 is 67.5 %. At 300 K, the reaction rate constant of BDE-209 with Br• to form P2 and IM2 is 4.14 × 10<sup>−17</sup> cm<sup>3</sup> molecule<sup>−1</sup> s<sup>−1</sup>. The branching ratio of BDE-209 + •OH → P9 + Br• is 40.3 % at 400 K. The OH-addition and OH-abstraction reactions of BDE-209 form octabromodibenzo-p-dioxin, which is further debrominated to form PBDDs. <em>Ortho</em>-phenyl-type radical generated by eliminating <em>ortho</em>-Br is a crucial precursor radical for the formation of PBDD/Fs. The most favorable reaction pathway for the subsequent degradation of <em>ortho</em>-phenyl-type radical is IM10 → <strong>TS38</strong> → IM13. The participation of polymer materials increases the production of toxic PBDD/Fs. This is because the free radicals formed by the chain scission of the polymer can easily extract the <em>ortho</em>-Br atom of BDE-209, thereby promoting the formation of the precursor (<em>ortho</em>-phenyl radical) of PBDD/Fs. Furthermore, the degradation mechanism of BDE-209 induced by active free radicals is explored to help control the formation of toxic substances during thermal treatment.</div></div>","PeriodicalId":345,"journal":{"name":"Journal of Analytical and Applied Pyrolysis","volume":"190 ","pages":"Article 107139"},"PeriodicalIF":5.8000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Degradation mechanism of decabromodiphenyl ether: Reaction with reactive radicals and formation chemistry of polybrominated dibenzo-p-dioxins and dibenzofurans\",\"authors\":\"Yang Long , Liming Tai , Shi Yan , Yan Zhu , Jinbao Huang , Li Jin , Yaqing Cai , Hong Wang , Xinsheng Li , Hao Cheng\",\"doi\":\"10.1016/j.jaap.2025.107139\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Although decabromodiphenyl ether (BDE-209) has been banned from production and use as a brominated flame retardant, its threat to human and ecological environment cannot still be ignored. Nevertheless, the mechanism of BDE-209 initiated by reactive radicals in the thermochemical decomposition process remains unknown. The density functional theory method is used to study the thermochemical decomposition behavior of BDE-209, with reactive radical reactions, and the formation mechanism of polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs). The results show that BDE-209 is not prone to self-decomposition due to its high bond dissociation energy (249.6 ∼ 281.4 kJ/mol) and HOMO-LUMO energy gap (7.10 eV). The reaction of BDE-209 with three active free radicals, including •H, Br•, and •OH, usually results in a variety of hypobromated products or important intermediates at low reaction energy barriers (52.9, 54.3, 50.4 kJ/mol). At 600 K, the branching ratio of H-abstraction reaction in the reaction system of •H and BDE-209 is 67.5 %. At 300 K, the reaction rate constant of BDE-209 with Br• to form P2 and IM2 is 4.14 × 10<sup>−17</sup> cm<sup>3</sup> molecule<sup>−1</sup> s<sup>−1</sup>. The branching ratio of BDE-209 + •OH → P9 + Br• is 40.3 % at 400 K. The OH-addition and OH-abstraction reactions of BDE-209 form octabromodibenzo-p-dioxin, which is further debrominated to form PBDDs. <em>Ortho</em>-phenyl-type radical generated by eliminating <em>ortho</em>-Br is a crucial precursor radical for the formation of PBDD/Fs. The most favorable reaction pathway for the subsequent degradation of <em>ortho</em>-phenyl-type radical is IM10 → <strong>TS38</strong> → IM13. The participation of polymer materials increases the production of toxic PBDD/Fs. This is because the free radicals formed by the chain scission of the polymer can easily extract the <em>ortho</em>-Br atom of BDE-209, thereby promoting the formation of the precursor (<em>ortho</em>-phenyl radical) of PBDD/Fs. Furthermore, the degradation mechanism of BDE-209 induced by active free radicals is explored to help control the formation of toxic substances during thermal treatment.</div></div>\",\"PeriodicalId\":345,\"journal\":{\"name\":\"Journal of Analytical and Applied Pyrolysis\",\"volume\":\"190 \",\"pages\":\"Article 107139\"},\"PeriodicalIF\":5.8000,\"publicationDate\":\"2025-04-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Analytical and Applied Pyrolysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0165237025001925\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Analytical and Applied Pyrolysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0165237025001925","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Degradation mechanism of decabromodiphenyl ether: Reaction with reactive radicals and formation chemistry of polybrominated dibenzo-p-dioxins and dibenzofurans
Although decabromodiphenyl ether (BDE-209) has been banned from production and use as a brominated flame retardant, its threat to human and ecological environment cannot still be ignored. Nevertheless, the mechanism of BDE-209 initiated by reactive radicals in the thermochemical decomposition process remains unknown. The density functional theory method is used to study the thermochemical decomposition behavior of BDE-209, with reactive radical reactions, and the formation mechanism of polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs). The results show that BDE-209 is not prone to self-decomposition due to its high bond dissociation energy (249.6 ∼ 281.4 kJ/mol) and HOMO-LUMO energy gap (7.10 eV). The reaction of BDE-209 with three active free radicals, including •H, Br•, and •OH, usually results in a variety of hypobromated products or important intermediates at low reaction energy barriers (52.9, 54.3, 50.4 kJ/mol). At 600 K, the branching ratio of H-abstraction reaction in the reaction system of •H and BDE-209 is 67.5 %. At 300 K, the reaction rate constant of BDE-209 with Br• to form P2 and IM2 is 4.14 × 10−17 cm3 molecule−1 s−1. The branching ratio of BDE-209 + •OH → P9 + Br• is 40.3 % at 400 K. The OH-addition and OH-abstraction reactions of BDE-209 form octabromodibenzo-p-dioxin, which is further debrominated to form PBDDs. Ortho-phenyl-type radical generated by eliminating ortho-Br is a crucial precursor radical for the formation of PBDD/Fs. The most favorable reaction pathway for the subsequent degradation of ortho-phenyl-type radical is IM10 → TS38 → IM13. The participation of polymer materials increases the production of toxic PBDD/Fs. This is because the free radicals formed by the chain scission of the polymer can easily extract the ortho-Br atom of BDE-209, thereby promoting the formation of the precursor (ortho-phenyl radical) of PBDD/Fs. Furthermore, the degradation mechanism of BDE-209 induced by active free radicals is explored to help control the formation of toxic substances during thermal treatment.
期刊介绍:
The Journal of Analytical and Applied Pyrolysis (JAAP) is devoted to the publication of papers dealing with innovative applications of pyrolysis processes, the characterization of products related to pyrolysis reactions, and investigations of reaction mechanism. To be considered by JAAP, a manuscript should present significant progress in these topics. The novelty must be satisfactorily argued in the cover letter. A manuscript with a cover letter to the editor not addressing the novelty is likely to be rejected without review.