PCDD/DF formations by the heterogeneous thermal reactions of phenols and their TiO2 photocatalytic degradation by batch-recycle system

被引:14
作者
Muto, H
Saitoh, K
Funayama, H
机构
[1] Akita Univ, Environm Res Ctr, Akita 0108543, Japan
[2] Tohkem Prod Co, Akita 0100065, Japan
[3] Akita Natl Coll Technol, Akita 0118511, Japan
关键词
PCDD/DFs; thermal formation; photodecomposition; phenol; 2,4,5-TCP; sol-gel method; batch-recycle reactor; TiO2 thin film;
D O I
10.1016/S0045-6535(00)00552-X
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/DFs) formation by the thermal reactions of phenols with CuCl2 under oxygen flux were carried out in relation to their formation mechanisms. To evaluate the effect of photocatalytic degradation of titanium dioxide (TiO2) thin film prepared by the sol-gel method. the photocatalysis of PCDD/DFs in acetonitrile/water solution by batch-recycle system was conducted. For the thermal reaction system of powder mixtures of 2,4,5-trichlorophenol (2,4,5-TCP) and CuCl2,the formation rates were 8.1 mug/g-2,4,5-TCP/min for total PCDD/DFs and 6.9 mug/g-2,4,5-TCP/min for PCDDs, and total PCDD/DF rate was higher by approximately 40 fold compared to phenol vapor/oxygen/CuCl2 powder system. For the system of 2,4,5-TCP, PCDDs were mainly formed via ortho-phenoxyphenols (POP) intermediate by the condensation of 2,4,5-trichlorophenate. For PCDD/DF photocatalytic degradations, most PCDD congeners photodecomposed rapidly and the rates presented more than 70% (as dechlorination rates of 76% for PCDDs) at 24 h after irradiation, using PCDD/DFs formed with 2,4,5-TCP. The rate constants were in the order of 4.8-6.1 x 10(-3) min(-1), assuming the pseudo-first-order reactions for their low levels. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:129 / 136
页数:8
相关论文
共 21 条
[1]   BIOAVAILABILITY AND TRANSFORMATION OF HIGHLY CHLORINATED DIBENZO-P-DIOXINS AND DIBENZOFURANS IN ANAEROBIC SOILS AND SEDIMENTS [J].
ADRIAENS, P ;
FU, QZ ;
GRBICGALIC, D .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (09) :2252-2260
[2]   DETERMINATION OF CHLORODIBENZODIOXINS AND CHLORODIBENZOFURANS DISCHARGED FROM SEVERAL MUNICIPAL INCINERATORS IN JAPAN [J].
ASADA, S ;
MATSUSHITA, H ;
MORITA, M ;
HAMADA, Y .
CHEMOSPHERE, 1987, 16 (8-9) :1907-1910
[3]   ATMOSPHERIC LIFETIMES OF DIBENZO-PARA-DIOXINS AND DIBENZOFURANS [J].
ATKINSON, R .
SCIENCE OF THE TOTAL ENVIRONMENT, 1991, 104 (1-2) :17-33
[4]   PREPARATION OF QUALITATIVE STANDARD MIXTURES OF POLYCHLORINATED DIBENZO-P-DIOXINS AND DIBENZOFURANS BY ULTRAVIOLET AND GAMMA-IRRADIATION OF OCTACHLORO COMPOUNDS [J].
BUSER, HR .
JOURNAL OF CHROMATOGRAPHY, 1976, 129 (DEC22) :303-307
[6]   ENVIRONMENTAL PHOTOCHEMISTRY OF POLYCHLORINATED DIBENZOFURANS (PCDFS) AND DIBENZO-PARA-DIOXINS (PCDDS) - A REVIEW [J].
CHOUDHRY, GG ;
WEBSTER, GRB .
TOXICOLOGICAL AND ENVIRONMENTAL CHEMISTRY, 1987, 14 (1-2) :43-61
[7]  
DULLIN D, 1986, ENVIRON SCI TECHNOL, V20, P72
[8]  
FORSTER CJB, 1992, ENVIRON SCI TECHNOL, V26, P502
[9]   CHEMICAL AND TOXICOLOGICAL EVALUATIONS OF ISOLATED AND SYNTHETIC CHLORO DERIVATIVES OF DIBENZO-RHO-DIOXIN [J].
HIGGINBOTHAM, GR ;
HUANG, A ;
FIRESTONE, D ;
VERRETT, J ;
RESS, J ;
CAMPBELL, AD .
NATURE, 1968, 220 (5168) :702-+
[10]  
HIRAOKA M, 1994, ORGANOHALOGEN COMPOU, V19, P275