Heating of BDE-209 and BDE-47 in plant oil in presence of o,p'-DDT or iron(III) chloride can produce monochloro-polybromo diphenyl ethers.
Heating of BDE-209 and BDE-47 in plant oil in presence of o,p'-DDT or iron(III) chloride can produce monochloro-polybromo diphenyl ethers.
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DOI:
10.1016/j.fct.2012.02.040
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发表时间:
2012-05
期刊:
影响因子:
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通讯作者:
Paul Bendig;M. Blumenstein;W. Vetter
中科院分区:
文献类型:
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作者:
Paul Bendig;M. Blumenstein;W. Vetter
Heating processes of food can alter the concentrations and composition of organohalogen compounds. In this study the fate of two polybrominated diphenyl ether (PBDE) congeners, decabromodiphenyl ether (BDE-209) and 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) was analyzed when heated in plant oil with and without additional compounds. When the PBDEs were heated in pure plant oil, no transformation was observed. Heating of decabromodiphenyl ether (BDE-209) together with ortho,para′-dichlorodiphenyltrichloroethane (o,p′-DDT) or iron(III) chloride in plant oil resulted in the formation of monochloro–nonabromodiphenyl ethers (Br9Cl-DEs). Almost 10% of the initial amount of BDE-209 was transferred into Br9Cl-DEs. Heating BDE-47 in the presence of iron(III) chloride produced two monochlorinated transformation products which were tentatively identified as 2,2′,4-tribromo-4′-chlorodiphenyl ether (4′-Cl-BDE-17) and 2,4,4′-tribromo-2′-chlorodiphenyl ether (2′-Cl-BDE-28). However, the reactivity was smaller and no Br→Cl exchange was observed with o,p′-DDT. The conditions used in our experiments (200°C; heating 30min–3h) indicate that such reactivity may also occur during cooking of fish, meat and other food samples.