Kinetics on the decomposition of polychlorinated biphenyls with activated carbon-supported iron

被引:33
作者
Sun, Yifei [1 ]
Takaoka, Masaki [1 ]
Takeda, Nobuo [1 ]
Matsumoto, Tadao [1 ]
Oshita, Kazuyuki [1 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Urban & Environm Engn, Sakyo Ku, Kyoto 6068501, Japan
关键词
polychlorinated biphenyls; activated carbon; activated carbon-supported iron; decomposition; catalyst;
D O I
10.1016/j.chemosphere.2006.03.009
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The process of destroying polychlorinated biphenyls (PCBs) generates exhaust gases that contain low quantities of PCBs, which cannot be disposed of easily. Activated carbon (AC) can be used to adsorb residual PCBs after disposal of high-level PCBs. We examined the chemical reactivity of AC-supported iron as a catalyst to decompose PCB-153, and varied three decomposition parameters (temperature, time and iron concentration) under an atmosphere of either air or N-2. We measured the Brunauer Emmett Teller (BET) surface area and pore volume of AC to assess the adsorption capacity of AC before and after decomposition. At low temperatures the adsorption process was more important than the decomposition process. The decomposition process was completed within 30 and 60 min under air and N-2, respectively. The efficiency of PCB-153 decomposition at 350 degrees C for 120 min was similar to 100.0% and 97.1% under air and N-2, respectively. Analysis of inorganic chloride ions revealed that PCB-153 was effectively destroyed during decomposition. The differences between decomposition under air and N-2 reflected differences in BET surface and pore volume. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:183 / 189
页数:7
相关论文
共 20 条
[1]  
ACKERMAN DG, 1983, DESTRUCTION DISPOSAL
[2]   BOROHYDRIDE-ENHANCED DECHLORINATION OF CHLOROBENZENES AND TOLUENES [J].
EPLING, GA ;
FLORIO, EM .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1988, (03) :703-706
[3]   COPPER-CATALYZED DECHLORINATION HYDROGENATION OF POLYCHLORINATED DIBENZO-PARA-DIOXINS, POLYCHLORINATED DIBENZOFURANS, AND OTHER CHLORINATED AROMATIC-COMPOUNDS [J].
HAGENMAIER, H ;
BRUNNER, H ;
HAAG, R ;
KRAFT, M .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1987, 21 (11) :1085-1088
[4]  
Hosomi M., 2000, J JPN SOC WASTE MANA, V11, P197
[5]  
KAINUMA M, 2000, ENVIRON ENG RES, P477
[6]   Low-temperature conversion of NO to N2 by use of a novel Ni loaded porous carbon [J].
Miura, K ;
Nakagawa, H ;
Kitaura, R ;
Satoh, T .
CHEMICAL ENGINEERING SCIENCE, 2001, 56 (04) :1623-1629
[7]   Dechlorination of hexachlorobiphenyl by using potassium sodium alloy [J].
Miyoshi, K ;
Nishio, T ;
Yasuhara, A ;
Morita, M .
CHEMOSPHERE, 2000, 41 (06) :819-824
[8]   Control of micropore formation in the carbonized ion exchange resin by utilizing pillar effect [J].
Nakagawa, H ;
Watanabe, K ;
Harada, Y ;
Miura, K .
CARBON, 1999, 37 (09) :1455-1461
[9]  
Radovic L.R, 2001, Chemistry & Physics of Carbon
[10]  
RANDALL TL, 1980, J WATER POLLUT CON F, V52, P2117