Role of cupric ions in the H2O2/UV oxidation of humic acids

被引:42
作者
Liao, CH [1 ]
Lu, MC [1 ]
Su, SH [1 ]
机构
[1] Chia Nan Univ Pharm & Sci, Dept Environm Engn & Hlth, Tainan, Taiwan
关键词
cupric ions; humic acids; hydrogen peroxide; ultraviolet light; metal complexation;
D O I
10.1016/S0045-6535(00)00580-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The purpose of this study is to reveal the role of cupric ions as a natural water contaminant in the H2O2/UV oxidation of humic acids. Humic acids are naturally occurring organic matter and exhibit a strong tendency of complexation with some transition metal ions. Chlorination of humic acids causes potential health hazards due to formation of trihalomethane (THM). The removal of THM precursors has become an issue of public concern. The H2O2/UV process is capable of mineralizing humic acids due to formation of a strong oxidant, hydroxyl radicals, in reaction solution. Experiments were conducted in a re-circulated photoreactor. Different cupric concentrations (0-3.8 mg/l) and different pH values (4-9) were controlled to determine their effects on the degradation of humic acids, I-TV light absorbance at 254 nm, and H2O2. The presence of cupric ions inhibits humic mineralization and decreases the rate of destruction of humic acids which absorb UV light at 254 mn. On the other hand, the higher the cupric concentration, the lower the H2O2 decomposition rate. In the studied pH range, the minimum of total organic carbon (TOC) removal occurs at pH = 6 in the presence of 2.6 mg/l of cupric ions; both acidification (pH = 4) and alkaline condition (pH = 9) lead to a better removal of TOC. It is inferred from this study that the cupric-complexed form of humic acids is more refractory than the non-complexed one. (C) 2001 Elsevier Science Ltd. Ail rights reserved.
引用
收藏
页码:913 / 919
页数:7
相关论文
共 26 条
[1]  
Aiken G., 1985, Humic Substance in Soil, Sediment, and Water
[2]  
[Anonymous], AQUATIC CHEM KINETIC
[3]   THE PHOTOLYSIS OF HYDROGEN PEROXIDE AT HIGH LIGHT INTENSITIES [J].
BAXENDALE, JH ;
WILSON, JA .
TRANSACTIONS OF THE FARADAY SOCIETY, 1957, 53 (03) :344-356
[4]  
BETTS K, 1998, ENV SCI TECHNOL NEWS, P546
[5]   THE PHOTOOXIDATION OF PROPIONIC-ACID BY OXYGEN IN THE PRESENCE OF TIO2 AND DISSOLVED COPPER IONS [J].
BIDEAU, M ;
CLAUDEL, B ;
FAURE, L ;
KAZOUAN, H .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1992, 67 (03) :337-348
[6]   THE INFLUENCE OF DISSOLVED METAL-IONS ON THE PHOTOCATALYTIC DEGRADATION OF PHENOL IN AQUEOUS TIO2 SUSPENSIONS [J].
BREZOVA, V ;
BLAZKOVA, A ;
BOROSOVA, E ;
CEPPAN, M ;
FIALA, R .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 1995, 98 (02) :109-116
[7]   PHOTOCATALYTIC OXIDATION IN AQUEOUS TITANIUM-DIOXIDE SUSPENSIONS - THE INFLUENCE OF DISSOLVED TRANSITION-METALS [J].
BUTLER, EC ;
DAVIS, AP .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1993, 70 (03) :273-283
[8]   CRITICAL-REVIEW OF RATE CONSTANTS FOR REACTIONS OF HYDRATED ELECTRONS, HYDROGEN-ATOMS AND HYDROXYL RADICALS (.OH/.O-) IN AQUEOUS-SOLUTION [J].
BUXTON, GV ;
GREENSTOCK, CL ;
HELMAN, WP ;
ROSS, AB .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1988, 17 (02) :513-886
[9]  
CHANG CJ, 1993, J CHEM TECHNOL BIOT, V57, P355
[10]  
CROZES G, 1995, JAWWA, V87, P79