Formation rates of polychlorinated dibenzofurans and dibenzo-p-dioxins from polycyclic aromatic hydrocarbons, activated carbon and phenol

被引:39
作者
Iino, F
Imagawa, T
Takeuchi, M
Sadakata, M
Weber, R
机构
[1] Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Natl Inst Resources & Environm, Tsukuba, Ibaraki 3058569, Japan
[3] Ishikawajima Harima Heavy Ind Co Ltd, Yokohama, Kanagawa 2358501, Japan
关键词
polychlorinated dibenzo-p-dioxins; polychlorinated dibenzofurans; polycyclic aromatic hydrocarbons; de novo synthesis; formation rate;
D O I
10.1016/S0045-6535(99)00209-X
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The formation rates of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) from polycyclic aromatic hydrocarbons (PAHs), activated carbon, and phenol were compared. The heat treatment at 300 degrees C of all tested PAH on silica in the presence of CuCl2 preferred PCDFs over PCDDs. Perylene reproducibly gave a higher yield of PCDFs than activated carbon gave under the same conditions. The formation rate of PCDFs from perylene could be higher than the values in this study because the residence time of perylene in the reactor is shorter than that of activated carbon. PCDDs were mainly formed from phenol. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2749 / 2756
页数:8
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