Elimination of organic micropollutants in a municipal wastewater treatment plant upgraded with a full-scale post-ozonation followed by sand filtration.

The removal efficiency for 220 micropollutants was studied at the scale of a municipal wastewater treatment plant (WWTP) upgraded with post-ozonation followed by sand filtration. During post-ozonation, compounds with activated aromatic moieties, amine functions, or double bonds such as sulfamethoxazole, diclofenac, or carbamazepine with second-order rate constants for the reaction with ozone >10(4) M(-1) s(-1) at pH 7 (fast-reacting) were eliminated to concentrations below the detection limit for an ozone dose of 0.47 g O3 g(-1) dissolved organic carbon (DOC). Compounds more resistant to oxidation by ozone such as atenolol and benzotriazole were increasingly eliminated with increasing ozone doses, resulting in >85% removal for a medium ozone dose (approximately 0.6 g O3 g(-1) DOC). Only a few micropollutants such as some X-ray contrast media and triazine herbicides with second-order rate constants <10(2) M(-1) s(-1) (slowly reacting) persisted to a large extent. With a medium ozone dose, only 11 micropollutants of 55 detected in the secondary effluent were found at >100 ng L(-1). The combination of reaction kinetics and reactor hydraulics, based on laboratory-and full-scale data, enabled a quantification of the results by model calculations. This conceptual approach allows a direct upscaling from laboratory- to full-scale systems and can be applied to other similar systems. The carcinogenic by-products N-nitrosodimethylamine (NDMA) (< or =14 ng L(-1)) and bromate (<10 microg L(-1)) were produced during ozonation, however their concentrations were below or in the range of the drinking water standards. Furthermore, it could be demonstrated that biological sand filtration is an efficient additional barrier for the elimination of biodegradable compounds formed during ozonation such as NDMA. The energy requirement for the additional post-ozonation step is about 0.035 kWh m(-3), which corresponds to 12% of a typical medium-sized nutrient removal plant (5 g DOC m(-3)).

[1]  Jeyong Yoon,et al.  Oxidative degradation of N-nitrosodimethylamine by conventional ozonation and the advanced oxidation process ozone/hydrogen peroxide. , 2007, Water research.

[2]  Adriano Joss,et al.  Scrutinizing pharmaceuticals and personal care products in wastewater treatment. , 2004, Environmental science & technology.

[3]  Christoph Ort,et al.  Model-based evaluation of reduction strategies for micropollutants from wastewater treatment plants in complex river networks. , 2009, Environmental science & technology.

[4]  B. Kasprzyk-Hordern,et al.  N-nitrosodimethylamine (NDMA) formation during ozonation of dimethylamine-containing waters. , 2008, Water research.

[5]  Francisco Omil,et al.  Kinetics of triclosan oxidation by aqueous ozone and consequent loss of antibacterial activity: relevance to municipal wastewater ozonation. , 2007, Water research.

[6]  Christoph Ort,et al.  JEM spotlight: Monitoring the treatment efficiency of a full scale ozonation on a sewage treatment plant with a mode-of-action based test battery. , 2009, Journal of environmental monitoring : JEM.

[7]  A Joss,et al.  Are we about to upgrade wastewater treatment for removing organic micropollutants? , 2008, Water science and technology : a journal of the International Association on Water Pollution Research.

[8]  Gun-Young Park,et al.  Oxidation of pharmaceuticals during ozonation and advanced oxidation processes. , 2003, Environmental science & technology.

[9]  Shane A Snyder,et al.  Effect of ozone exposure on the oxidation of trace organic contaminants in wastewater. , 2009, Water research.

[10]  S. Kunikane,et al.  Formation of N-nitrosodimethylamine (NDMA) by ozonation of dyes and related compounds. , 2008, Chemosphere.

[11]  Carsten K Schmidt,et al.  N,N-dimethylsulfamide as precursor for N-nitrosodimethylamine (NDMA) formation upon ozonation and its fate during drinking water treatment. , 2008, Environmental science & technology.

[12]  Oliver A.H. Jones,et al.  Questioning the excessive use of advanced treatment to remove organic micropollutants from wastewater. , 2007, Environmental science & technology.

[13]  U. Gunten Ozonation of drinking water: part II. Disinfection and by-product formation in presence of bromide, iodide or chlorine. , 2003 .

[14]  U. Gunten Ozonation of drinking water: part I. Oxidation kinetics and product formation. , 2003 .

[15]  T. Ternes,et al.  Ozonation of carbamazepine in drinking water: identification and kinetic study of major oxidation products. , 2005, Environmental science & technology.

[16]  Adriano Joss,et al.  Oxidation of pharmaceuticals during ozonation of municipal wastewater effluents: a pilot study. , 2005, Environmental science & technology.

[17]  J. Hoigne,et al.  Characterization Of Water Quality Criteria for Ozonation Processes. Part II: Lifetime of Added Ozone , 1994 .

[18]  T. Ternes,et al.  Removal of estrogenic activity and formation of oxidation products during ozonation of 17alpha-ethinylestradiol. , 2004, Environmental science & technology.

[19]  M. Jekel,et al.  Ozonation and Advanced Oxidation of Wastewater: Effect of O3 Dose, pH, DOM and HO•-Scavengers on Ozone Decomposition and HO• Generation , 2006 .

[20]  Hideshige Takada,et al.  Removal of selected pharmaceuticals and personal care products (PPCPs) and endocrine-disrupting chemicals (EDCs) during sand filtration and ozonation at a municipal sewage treatment plant. , 2007, Water research.

[21]  Martin Krauss,et al.  Kinetic assessment and modeling of an ozonation step for full-scale municipal wastewater treatment: micropollutant oxidation, by-product formation and disinfection. , 2011, Water research.

[22]  O. Köster,et al.  Mechanistic and kinetic evaluation of organic disinfection by-product and assimilable organic carbon (AOC) formation during the ozonation of drinking water. , 2006, Water research.

[23]  Norman Nowotny,et al.  Quantification and modeling of the elimination behavior of ecologically problematic wastewater micropollutants by adsorption on powdered and granulated activated carbon. , 2007, Environmental science & technology.

[24]  Adriano Joss,et al.  Removal of pharmaceuticals and fragrances in biological wastewater treatment. , 2005, Water research.

[25]  Martin Krauss,et al.  Occurrence and removal of N-nitrosamines in wastewater treatment plants. , 2009, Water research.

[26]  T. Hutchinson,et al.  A review of the effects of bromate on aquatic organisms and toxicity of bromate to oyster (Crassostrea gigas) embryos. , 1997, Ecotoxicology and environmental safety.

[27]  Michael C. Dodd,et al.  Oxidation of antibacterial compounds by ozone and hydroxyl radical: elimination of biological activity during aqueous ozonation processes. , 2009, Environmental science & technology.

[28]  Martin Kampmann,et al.  Ozonation: a tool for removal of pharmaceuticals, contrast media and musk fragrances from wastewater? , 2003, Water research.

[29]  J. Dewulf,et al.  Ozonation of ciprofloxacin in water: HRMS identification of reaction products and pathways. , 2008, Environmental science & technology.

[30]  W. Giger,et al.  Environmental exposure assessment of fluoroquinolone antibacterial agents from sewage to soil. , 2003, Environmental science & technology.

[31]  Shane A. Snyder,et al.  Role of membranes and activated carbon in the removal of endocrine disruptors and pharmaceuticals , 2007 .

[32]  Robert C Andrews,et al.  Formation of N-nitrosamines from eleven disinfection treatments of seven different surface waters. , 2008, Environmental science & technology.

[33]  Urs von Gunten,et al.  Degradation Kinetics of Atrazine and Its Degradation Products with Ozone and OH Radicals: A Predictive Tool for Drinking Water Treatment , 2000 .