Hydroxyl radical production via the photo-Fenton reaction in the presence of fulvic acid

被引:161
作者
Southworth, BA [1 ]
Voelker, BM [1 ]
机构
[1] MIT, Dept Civil & Environm Engn, Cambridge, MA 02139 USA
关键词
D O I
10.1021/es020757l
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The photo-Fenton reaction, the reaction of photoproduced Fell) with H2O2 to form the highly reactive hydroxyl radical (OH.), could be an important source of OH. in sunlit natural waters. To determine if the photo-Fenton reaction is significant in mildly acidic surface waters, we conducted experiments simulating conditions representative of natural freshwaters using solutions of standard fulvic acid and amorphous iron oxide at pH 6.0. A probe method measuring (CO2)-C-14 produced by the reaction of C-14-labeled formate with OH. was used to detect small OH. production rates without otherwise influencing the chemical reactions occurring in the experiments. Net H2O2 accumulation was simultaneously measured using an acridinium ester chemiluminescence method. Measured losses of H2O2 by reaction with Fe(II) in dark experiments produced approximately the expected quantities of OH.. The difference between H2O2 accumulation in the presence and absence of Fe(III) in fulvic acid solutions exposed to light was interpreted as the loss of H2O2 by reaction with photoproduced Fe(II), consistent with measured OH. production rates. The Fe ligand desferrioxamine mesylate eliminated both OH. production and H2O2 photoloss induced by Fe. Our results imply that when Fe is a major sink of H2O2, the photo-Fenton reaction is likely to be the most important source of OH., leading to a significant sink of organic compounds in a wide variety of sunlit freshwaters.
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页码:1130 / 1136
页数:7
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[1]   Photochemical oxygen consumption in marine waters: A major sink for colored dissolved organic matter? [J].
Andrews, SS ;
Caron, S ;
Zafiriou, OC .
LIMNOLOGY AND OCEANOGRAPHY, 2000, 45 (02) :267-277
[2]  
[Anonymous], ENV CHEM LAKES RESER
[3]   PHOTOMETRIC-METHOD FOR THE DETERMINATION OF LOW CONCENTRATIONS OF HYDROGEN-PEROXIDE BY THE PEROXIDASE CATALYZED OXIDATION OF N,N-DIETHYL-P-PHENYLENEDIAMINE (DPD) [J].
BADER, H ;
STURZENEGGER, V ;
HOIGNE, J .
WATER RESEARCH, 1988, 22 (09) :1109-1115
[4]   Atrazine degradation in irradiated iron oxalate systems: Effects of pH and oxalate [J].
Balmer, ME ;
Sulzberger, B .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1999, 33 (14) :2418-2424
[5]  
Balzani V., 1970, PHOTOCHEMISTRY COORD
[6]   Nitrate-induced photolysis in natural waters: Controls on concentrations of hydroxyl radical photo-intermediates by natural scavenging agents [J].
Brezonik, PL ;
Fulkerson-Brekken, J .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (19) :3004-3010
[7]   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
[8]   PHOTO-REDUCTION OF IRON IN THE EPILIMNION OF ACIDIC LAKES [J].
COLLIENNE, RH .
LIMNOLOGY AND OCEANOGRAPHY, 1983, 28 (01) :83-100
[9]   PHOTOCHEMICAL FORMATION OF H2O2 IN NATURAL-WATERS EXPOSED TO SUNLIGHT [J].
COOPER, WJ ;
ZIKA, RG ;
PETASNE, RG ;
PLANE, JMC .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1988, 22 (10) :1156-1160
[10]   PHOTOCHEMICAL FORMATION OF HYDROGEN-PEROXIDE IN SURFACE AND GROUND WATERS EXPOSED TO SUNLIGHT [J].
COOPER, WJ ;
ZIKA, RG .
SCIENCE, 1983, 220 (4598) :711-712