Investigation of the Iron-Peroxo Complex in the Fenton Reaction: Kinetic Indication, Decay Kinetics, and Hydroxyl Radical Yields

被引:61
作者
Wiegand, Hanna Laura [1 ]
Orths, Christian Timon [1 ]
Kerpen, Klaus [1 ]
Lutze, Holger Volker [1 ,2 ,3 ]
Schmidt, Torsten Claus [1 ,2 ,3 ]
机构
[1] Univ Duisburg Essen, Instrumental Analyt Chem, Univ Str 5, D-45141 Essen, Germany
[2] Univ Duisburg Essen, Ctr Water & Environm Res ZWU, Univ Str 2, D-45141 Essen, Germany
[3] IWW Water Ctr, Moritzstr 26, D-45476 Mulheim, Germany
关键词
ADVANCED OXIDATION PROCESSES; WASTE-WATER TREATMENT; HYDROGEN-PEROXIDE; PHOTO-FENTON; FERRIC IONS; AQUEOUS-SOLUTION; FERROUS-IONS; PH; REAGENT; ACID;
D O I
10.1021/acs.est.7b03706
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The Fenton reaction describes the reaction of Fe(II) with hydrogen peroxide. Several researchers proposed the formation of an intermediate iron-peroxo complex but experimental evidence for its existence is still missing. The present study investigates formation and lifetime of this intermediate at various conditions such as different Fe(II)-concentrations, absence vs presence of a hydroxyl radical scavenger (dimethyl sulfoxide, DMSO), and different pH values. Obtained results indicate that the iron-peroxo complex is formed under all experimental conditions. Based on these data, stability of the iron-peroxo complex could be examined. At pH 3 regardless of [Fe(II)](0) decay rates, for the iron-peroxo complex of about SO s(-1) were determined in absence and presence of DMSO. Without DMSO and [Fe(II)](0) = 300 mu M variation of pH yielded decay rates of about 70 s(-1) for pH 1 and 2 and of about 50 s(-1) at pH 3 and 4. Hence, the iron-peroxo complex becomes more stable with increasing pH. Furthermore, pH-dependent hydroxyl radical yields were determined to investigate whether the increasing stability of the intermediate complex may indicate a different reaction of the iron-peroxo complex which might yield Fe(IV) instead of hydroxyl radical formation as suggested in literature. However, it was found that hydroxyl radicals were produced proportionally to the Fe (II)-concentration.
引用
收藏
页码:14321 / 14329
页数:9
相关论文
共 67 条
[21]   Effect of pH on the oxidation rate of organic compounds by FeII/H2O2.: Mechanisms and simulation [J].
Gallard, H ;
de Laat, J ;
Legube, B .
NEW JOURNAL OF CHEMISTRY, 1998, 22 (03) :263-268
[22]   Spectrophotometric study of the formation of iron(III)-hydroperoxy complexes in homogeneous aqueous solutions [J].
Gallard, H ;
De Laat, J ;
Legube, B .
WATER RESEARCH, 1999, 33 (13) :2929-2936
[23]  
GLAZE WH, 1987, OZONE-SCI ENG, V9, P335
[24]   THE FENTON REAGENTS [J].
GOLDSTEIN, S ;
MEYERSTEIN, D ;
CZAPSKI, G .
FREE RADICAL BIOLOGY AND MEDICINE, 1993, 15 (04) :435-445
[25]   Oxidation of iron(II) nanomolar with H2O2 in seawater [J].
González-Davila, M ;
Santana-Casiano, JM ;
Millero, FJ .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2005, 69 (01) :83-93
[26]   On the catalysis of hydroperoxide. [J].
Haber, F ;
Weiss, J .
NATURWISSENSCHAFTEN, 1932, 20 :948-950
[27]  
Haber F., 1935, P ROYAL SOC LONDON, VA147, P332
[28]   THE RATE CONSTANT OF THE REACTION BETWEEN FERROUS IONS AND HYDROGEN PEROXIDE IN ACID SOLUTION [J].
HARDWICK, TJ .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1957, 35 (05) :428-436
[29]   Iron-catalyzed oxidation of arsenic(III) by oxygen and by hydrogen peroxide: pH-dependent formation of oxidants in the Fenton reaction [J].
Hug, SJ ;
Leupin, O .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (12) :2734-2742
[30]   pH dependence of Fenton reagent generation and As(III) oxidation and removal by corrosion of zero valent iron in aerated water [J].
Katsoyiannis, Ioannis A. ;
Ruettimann, Thomas ;
Hug, Stephan J. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (19) :7424-7430