Degradation of BTEX and PAHs by Co(II) and Cu(II)-based radical-generating systems

被引:26
作者
Gabriel, J
Baldrian, P
Verma, P
Cajthaml, T
Merhautová, V
Eichlerová, I
Stoytchev, I
Trnka, T
Stopka, P
Nerud, F
机构
[1] Inst Microbiol ASCR, Lab Biochem Wood Rotting Fungi, Prague 14220 4, Czech Republic
[2] Charles Univ Prague, Fac Sci, Dept Organ Chem, Prague 12000, Czech Republic
[3] Inst Inorgan Chem ASCR, Rez 25068, Czech Republic
关键词
cobalt; copper; BTEX; PAH; EPR; ROS; free radicals; hydrogen peroxide; degradation;
D O I
10.1016/j.apcatb.2004.02.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Copper(II) or cobalt(II)/ligand/hydrogen peroxide systems were used for degradation of benzene, toluene, ethylbenzene, xylenes (BTEX), and polycylic aromatic hydrocarbons. The most efficient systems were Cu/glucaric acid/H2O2 and CU/D-arabinono-1,4-lactone/H2O2 for the degradation of BTEX. All compounds were completely degraded within 1 h. Co/ascorbic acid/H2O2 system was the most effective for polycyclic aromatic hydrocarbons (PAHs) degradation. More than 95% of anthracene, pyrene, benzo[k]fluoranthene, benzo[a]pyrene and dibenzo[a,h]anthracene were degraded during a 1 h incubation at 22 degreesC. Oxidation of anthracene led to the formation of 9, 10-anthracenedione, 1,4-anthracenedione, and phthalic acid. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:159 / 164
页数:6
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