Dechlorination of polychlorinated dibenzo- p-dioxins catalyzed by noble metal catalysts under mild conditions

Dechlorination of polychlorinated dibenzo- p-dioxins such as 2,7-dichlorodibenzo- p-dioxin (2,7-DCDD) and 1,2,6,7-tetrachlorodibenzo- p-dioxin (1,2,6,7-TCDD) was carried out in a solution of NaOH in 2-propanol in the presence of carbon-supported noble metal catalyst (Pd/C or Rh–Pt/C) at temperatures...

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Published inChemosphere (Oxford) Vol. 46; no. 4; pp. 507 - 510
Main Authors Ukisu, Yuji, Miyadera, Tatsuo
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 2002
Elsevier
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Summary:Dechlorination of polychlorinated dibenzo- p-dioxins such as 2,7-dichlorodibenzo- p-dioxin (2,7-DCDD) and 1,2,6,7-tetrachlorodibenzo- p-dioxin (1,2,6,7-TCDD) was carried out in a solution of NaOH in 2-propanol in the presence of carbon-supported noble metal catalyst (Pd/C or Rh–Pt/C) at temperatures between 23 and 35 °C. At initial concentrations of 140–240 μg/ ml , 2,7-DCDD and 1,2,6,7-TCDD were efficiently converted to a chlorine-free product, dibenzo- p-dioxin (DD), in high yield (60–80%). The conversion of 2,7-DCDD and 1,2,6,7-TCDD and the yield of DD were hardly affected by the atmosphere (N 2 or air). We postulate that the displacement of aromatic chlorines by hydrogen selectively occurs on the catalyst, involving hydrogen-transfer from 2-propanol to the substrates.
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ISSN:0045-6535
1879-1298
DOI:10.1016/S0045-6535(01)00170-9