Cover image for Chemistry of ozone in water and wastewater treatment : from basic principles to applications
Title:
Chemistry of ozone in water and wastewater treatment : from basic principles to applications
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Publication Information:
London ; New York : IWA Pub., c2012
Physical Description:
ix, 302 p. : ill. ; 26 cm.
ISBN:
9781843393139

9781780400839
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30000010302780 TD461 S66 2012 Open Access Book Book
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30000010285344 TD461 S66 2012 Open Access Book Book
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Summary

Summary

Even though ozone has been applied for a long time for disinfection and oxidation in water treatment, there is lack of critical information related to transformation of organic compounds. This has become more important in recent years, because there is considerable concern about the formation of potentially harmful degradation products as well as oxidation products from the reaction with the matrix components. In recent years, a wealth of information on the products that are formed has accumulated, and substantial progress in understanding mechanistic details of ozone reactions in aqueous solution has been made. Based on the latter, this may allow us to predict the products of as yet not studied systems and assist in evaluating toxic potentials in case certain classes are known to show such effects.
Keeping this in mind, Chemistry of Ozone in Water and Wastewater Treatment: From Basic Principles to Applications discusses mechanistic details of ozone reactions as much as they are known to date and applies them to the large body of studies on micropollutant degradation (such as pharmaceuticals and endocrine disruptors) that is already available. Extensively quoting the literature and updating the available compilation of ozone rate constants gives the reader a text at hand on which his research can be based. Moreover, those that are responsible for planning or operation of ozonation steps in drinking water and wastewater treatment plants will find salient information in a compact form that otherwise is quite disperse. A critical compilation of rate constants for the various classes of compounds is given in each chapter, including all the recent publications.
This is a very useful source of information for researchers and practitioners who need kinetic information on emerging contaminants. Furthermore, each chapter contains a large selection of examples of reaction mechanisms for the transformation of micropollutants such as pharmaceuticals, pesticides, fuel additives, solvents, taste and odor compounds, cyanotoxins.
Authors: Prof. Dr. Clemens von Sonntag, Max-Planck-Institut für Bioanorganische Chemie, Mülheim an der Ruhr, and Instrumentelle Analytische Chemie, Universität Duisburg-Essen, Essen, Germany and Prof. Dr. Urs von Gunten, Eawag, Swiss Federal Institute of Aquatic Science and Technology, Dübendorf, and Ecole Polytechnique Federal de Lausanne, Lausanne, Switzerland.


Table of Contents

About the Authorsp. xi
Chapter 1 Historical background and scope of the bookp. 1
Chapter 2 Physical and chemical properties of ozonep. 7
2.1 Introductory Remarksp. 7
2.2 Generation of Ozonep. 8
2.3 Ozone Solubility in Waterp. 9
2.4 UV-VIS Spectrum of Ozonep. 10
2.5 Determination of the Ozone Concentrationp. 12
2.5.1 The N,N-diethyl-p-phenylenediamine (DPD) methodp. 12
2.5.2 The indigo methodp. 13
2.6 Methods for Measuring Ozone Kineticsp. 14
2.6.1 Ozone decay measurementsp. 15
2.6.2 Quenching of ozone with buten-3-olp. 16
2.6.3 Reactive absorptionp. 16
2.6.4 Competition kineticsp. 17
2.7 Reduction Potentials of Ozone and Other Oxygen Speciesp. 18
2.8 Stability of Ozone Solutionsp. 19
2.9 Reactivity of Ozonep. 19
2.9.1 pH dependence of ozone reactions and the "reactivity pK"p. 20
2.9.2 Multiple reaction sites within one moleculep. 21
Chapter 3 Ozone kinetics in drinking water and wastewaterp. 23
3.1 Stability of Ozone in Various Water Sourcesp. 23
3.2 Molecular Weight Distribution of Dissolved Organic Matterp. 31
3.3 Mineralisation and Chemical Oxygen Demandp. 33
3.4 Formation of Assimilable Organic Carbonp. 33
3.5 Formation and Mitigation of Disinfection By-productsp. 35
3.6 UV Absorbance of Dissolved Organic Matterp. 36
3.7 Relevance of Ozone Kinetics for the Elimination of Micropollutantsp. 37
3.8 Hydroxyl Radical Yield and OH-Scavenging Rate of Dissolved Organic Matterp. 39
3.9 Elimination of Ozone-Refractory Micropollutants by the *OH Routep. 40
3.10 Ozone-based Advanced Oxidation Processesp. 42
3.10.1 Peroxone processp. 42
3.10.2 UV photolysis of ozonep. 45
3.10.3 Reaction of ozone with activated carbonp. 46
Chapter 4 Inactivation of micro-organisms and toxicological assessment of ozone-induced products of micropollutantsp. 49
4.1 Disinfection Kineticsp. 49
4.2 Inactivation Mechanisms: Role of Membranes and DNAp. 52
4.3 Reactions with Nucleic Acid Componentsp. 53
4.4 Reaction with DNAp. 54
4.5 Application of Ozone for Disinfection in Drinking Water and Wastewaterp. 55
4.6 Toxicological Assessment of Ozone Induced Transformation Productsp. 55
4.7 Endocrine Disrupting Compoundsp. 56
4.7.1 Laboratory studiesp. 58
4.7.2 Full-scale studiesp. 59
4.8 Antimicrobial Compoundsp. 60
4.9 Toxicityp. 62
Chapter 5 Integration of ozonation in drinking water and wastewater process trainsp. 65
5.1 Historical Aspectsp. 65
5.1.1 Drinking waterp. 65
5.1.2 Municipal wastewaterp. 65
5.2 Drinking Water Treatment Schemes Including Ozonationp. 66
5.3 Micropollutants in Water Resources, Drinking Water and Wastewaterp. 70
5.4 Enhanced Wastewater Treatment with Ozonep. 72
5.5 Energy Requirements for Micropollutant Transformation in Drinking Water and Wastewaterp. 73
5.6 Source Controlp. 74
5.7 Reclamation of Wastewaterp. 75
5.8 Comparison of the Application of Ozone in the Urban Water Cyclep. 77
Chapter 6 Olefinsp. 81
6.1 Reactivity of Olefinsp. 81
6.2 The Criegee Mechanismp. 84
6.3 Partial Oxidationp. 87
6.4 Decay of the Ozonide via Free Radicalsp. 88
6.5 Detection of ¿-Hydroxyalkylhydroperoxidesp. 88
6.6 Ozone Reactions of Olefins-Products and Reactions of Reactive Intermediatesp. 89
6.6.1 Methyl- and halogen-substituted olefinsp. 89
6.6.2 Acrylonitrile, vinyl acetate, diethyl vinylphosphonate, vinyl phenyl sulfonate, vinylsulfonic acid and vinylene carbonatep. 91
6.6.3 Acrylic, methacrylic, fumaric, maleic and muconic acidsp. 92
6.6.4 Muconic acidsp. 96
6.6.5 Cinnamic acidsp. 98
6.6.6 Dichloromaleic acidp. 99
6.6.7 Pyrimidine nucleobasesp. 99
6.7 Micropollutants with Olefinic Functionsp. 102
Chapter 7 Aromatic compoundsp. 109
7.1 Reactivity of Aromatic Compoundsp. 109
7.2 Decay of Ozone Adductsp. 116
7.3 Ozone Reactions of Aromatic Compounds - Products and Reactions of Reactive Intermediatesp. 118
7.3.1 Methoxylated benzenesp. 118
7.3.2 Phenolsp. 121
7.4 Micropollutants with Aromatic Functionsp. 124
Chapter 8 Nitrogen-containing compoundsp. 131
8.1 Reactivity of Nitrogen-containing Compoundsp. 131
8.2 General Mechanistic Considerationsp. 138
8.2.1 Aliphatic aminesp. 138
8.2.2 Aromatic amines (anilines)p. 143
8.2.3 Nitrogen-containing heterocyclic compoundsp. 145
8.3 Micropollutants with Nitrogen-containing Functionsp. 146
8.3.1 The N-nitrosodimethylamine (NDMA) puzzlep. 156
Chapter 9 Reactions of sulfur-containing compoundsp. 161
9.1 Reactivity of Sulfur-containing Compoundsp. 161
9.2 Thiolsp. 162
9.3 Sulfides, Disulfides and Sulfinic Acidsp. 163
9.4 Sulfoxidesp. 165
9.5 Micropollutants Containing an Ozone-reactive Sulfurp. 166
Chapter 10 Compounds with C-H functions as Ozone-reactive sitesp. 169
10.1 Reactivity of Compounds with C-H Functions as Ozone-reactive Sitesp. 169
10.2 General Mechanistic Considerationsp. 171
10.3 Formate Ionp. 173
10.4 2-Methyl-2-Propanol (Tertiary Butanol)p. 175
10.5 2-Propanolp. 176
10.6 Carbohydratesp. 180
10.7 Dihydrogen Trioxide - Properties of a Short-lived Intermediatep. 182
10.8 Saturated Micropollutants Lacking Ozone-reactive Heteroatomsp. 184
Chapter 11 Inorganic anions and the peroxone processp. 185
11.1 Introductory Remarksp. 185
11.2 Hydroxide Ionp. 187
11.3 Hydroperoxide Ion - Peroxone Processp. 188
11.4 Fluoridep. 189
11.5 Chloridep. 190
11.6 Hypochloritep. 191
11.7 Chloritep. 192
11.8 Bromidep. 192
11.9 Hypobromitep. 193
11.10 Bromitep. 194
11.11 Iodidep. 194
11.12 Nitritep. 195
11.13 Azidep. 196
11.14 Hydrogen Sulfidep. 197
11.15 Hydrogen Sulfitep. 198
11.16 Bromate Formation and Mitigation in Water Treatmentp. 198
11.17 Bromide-catalysed Reactionsp. 201
11.18 Mitigation of Iodide-related Problemsp. 202
Chapter 12 Reactions with metal ionsp. 205
12.1 Reactivity of Metal Ionsp. 205
12.2 Arsenicp. 206
12.3 Cobaltp. 207
12.4 Copperp. 207
12.5 Ironp. 207
12.6 Leadp. 208
12.7 Manganesep. 208
12.8 Seleniump. 209
12.9 Silverp. 209
12.10 Tinp. 211
12.11 Metal Ions as Micropollutantsp. 211
Chapter 13 Reactions with free radicalsp. 213
13.1 Reactivity of Radicalsp. 213
13.2 Ozone Reactions with Reducing Radicalsp. 214
13.3 Ozone Reactions with Carbon-centered Radicalsp. 215
13.4 Ozone Reactions with Oxygen-centered Radicalsp. 217
13.5 Ozone Reactions with Nitrogen-and Sulfur-centred Radicalsp. 219
13.6 Ozone Reactions with Halogen-centred Radicalsp. 220
Chapter 14 Reactions of hydroxyl and peroxyl radicalsp. 225
14.1 Introductory Remarksp. 225
14.2 Hydroxyl Radical Reactionsp. 225
14.2.1 Addition reactionsp. 225
14.2.2 H-abstraction reactionsp. 227
14.2.3 Electron transfer reactionsp. 228
14.3 Determination of *OH Rate Constantsp. 229
14.4 Detection of *OH in Ozone Reactionsp. 230
14.5 Determination of *OH Yields in Ozone Reactionsp. 232
14.6 Formation of Peroxyl Radicalsp. 233
14.7 Redox Properties of Peroxyl Radicals and Reaction with Ozonep. 233
14.8 Unimolecular Decay of Peroxyl Radicalsp. 234
14.9 Bimolecular Decay of Peroxyl Radicalsp. 235
14.10 Reactions of Oxyl Radicalsp. 236
14.11 Involvement of *OH Radicals in Chlorate and Bromate Formationp. 237
14.11.1 Chlorate formationp. 237
14.11.2 Bromate formationp. 238
14.12 Degradation of Ozone-refractory Micropollutants by *OH/Peroxyl Radicalsp. 241
14.12.1 Saturated aliphatic compoundsp. 241
14.12.2 Aromatic compoundsp. 243
14.12.3 Chlorinated olefinsp. 245
14.12.4 Perfluorinated compoundsp. 248
Referencesp. 249
Indexp. 287