26 research outputs found

    IMPACT OF LOW-RATE SUBSTRATE REMOVAL ON THE PERFORMANCE OF DENITRIFYING SYSTEMS

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    Strict effluent N criteria may also require the use of slowly biodegradable substrate as carbon source for denitrification. The paper draws attention to the fact that oxygen penetration through the surface of uncovered denitrification basins may significantly deteriorate the efficiency when substrate removal rate is low, whereas at high consumption rates this impact may prove to be negligible. Results of comparative lab-scale experiments carried out in both batch and continuous-flow operation revealed that the reason why denitrification rates are much more severely affected at low substrate consumption rates is the increased dissolved oxygen concentration that occurs due to the decreased ability of its removal. In the comparative batch experiments a zero-head-space reactor and a reactor with an open surface were applied using different samples of preclarified wastewater deriving from an existing treatment plant. In the continuous-flow experiment two differently arranged activated sludge systems were operated simultaneously, fed by a model wastewater containing peptone as carbon source. The total reactor volume serving predenitrification was identical in both arrangements; however, in one of the systems it was compartmentalized into three reactors. None of the reactors were covered in this experiment. The dissolved oxygen concentration raised significantly in both of the batch and continuous-flow experiments when the readily biodegradable substrate had been depleted. The results supported that in cases when readily denitrifiable carbon source is not in a pronounced excess, staging of anoxic reactors may significantly improve the efficiency of denitrification through maintaining relatively high substrate removal rate and thereby low oxygen concentration in the first basins

    The impact of temperature on the transformation of illicit drug biomarkers in wastewater

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    Temperature is one of the key factors, influencing the transformation kinetics of organic chemicals. In the context of wastewater-based epidemiology, however, temperature differences among sewer catchments and within the same catchment (due to, e.g., seasonal variations) have been neglected to date as a factor influencing the estimation of illicit drug consumption. In this study, we assessed the influence of temperature on the transformation of biomarkers in wastewater and its ensuing implications on the back-calculation of chemical consumption rate in urban catchments using the example of selected illicit drugs. Literature data, obtained in laboratory-scale experiments, on the stability of drug biomarkers in untreated wastewater at trace levels was systematically reviewed, and transformation rates obtained at different temperatures were collected. Arrhenius-based equations were fitted to empirical data and identified to describe the transformation of selected cocaine and morphine biomarkers at applicability temperature range (from 2–9 °C to 30–31 °C), with estimated exponential Arrhenius coefficients between 1.04 and 1.18. These empirically-derived relationships were used to assess the influence of temperature on the transformation of drug biomarkers during in-sewer transport and its effect on the back-calculation of drug consumption rate in hypothetical urban catchment scenario simulations. Up to 4-fold increase in removal efficiency was estimated when wastewater temperature increased from 15 °C to 25 °C. Findings from this study can help reducing the uncertainty intrinsic to wastewater-based epidemiology studies, and will be beneficial in comparing chemical consumption estimates from different catchments worldwide.</p

    Removal of pharmaceuticals in pre-denitrifying MBBR – Influence of organic substrate availability in single- and three-stage configurations

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    Due to the limited efficiency of conventional biological treatment, innovative solutions are being explored to improve the removal of trace organic chemicals in wastewater. Controlling biomass exposure to growth substrate represents an appealing option for process optimization, as substrate availability likely impacts microbial activity, hence organic trace chemical removal. This study investigated the elimination of pharmaceuticals in pre-denitrifying moving bed biofilm reactors (MBBRs), where biofilm exposure to different organic substrate loading and composition was controlled by reactor staging. A three-stage MBBR and a single-stage reference MBBR (with the same operating volume and filling ratio) were operated under continuous-flow conditions (18 months). Two sets of batch experiments (day 100 and 471) were performed to quantify and compare pharmaceutical removal and denitrification kinetics in the different MBBRs. Experimental results revealed the possible influence of retransformation (e.g., from conjugated metabolites) and enantioselectivity on the removal of selected pharmaceuticals. In the second set of experiments, specific trends in denitrification and biotransformation kinetics were observed, with highest and lowest rates/rate constants in the first (S1) and the last (S3) staged sub reactors, respectively. These observations were confirmed by removal efficiency data obtained during continuous-flow operation, with limited removal (<10%) of recalcitrant pharmaceuticals and highest removal in S1 within the three-stage MBBR. Notably, biotransformation rate constants obtained for non recalcitrant pharmaceuticals correlated with mean specific denitrification rates, maximum specific growth rates and observed growth yield values. Overall, these findings suggest that: (i) the long-term exposure to tiered substrate accessibility in the three-stage configuration shaped the denitrification and biotransformation capacity of biofilms, with significant reduction under substrate limitation; (ii) biotransformation of pharmaceuticals may have occurred as a result of cometabolism by heterotrophic denitrifying bacteria. (C) 2017 Elsevier Ltd. All rights reserved

    Reactor staging influences microbial community composition and diversity of denitrifying MBBRs- Implications on pharmaceutical removal

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    The subdivision of biofilm reactor in two or more stages (i.e., reactor staging) represents an option for process optimisation of biological treatment. In our previous work, we showed that the gradient of influent organic substrate availability (induced by the staging) can influence the microbial activity (i.e., denitrification and pharmaceutical biotransformation kinetics) of a denitrifying three-stage Moving Bed Biofilm Reactor (MBBR) system. However, it is unclear whether staging and thus the long-term exposure to varying organic carbon type and loading influences the microbial community structure and diversity. In this study, we investigated biofilm structure and diversity in the three-stage MBBR system (S) compared to a single-stage configuration (U) and their relationship with microbial functions. Results from 16S rRNA amplicon libraries revealed a significantly higher microbial richness in the staged MBBR (at 99% sequence similarity) compared to single-stage MBBR. A more even and diverse microbial community was selected in the last stage of S (S3), likely due to exposure to carbon limitation during continuous-flow operation. A core of OTUs was shared in both systems, consisting of Burkholderiales, Xanthomonadales, Flavobacteriales and Sphingobacteriales, while MBBR staging selected for specific taxa (i.e., Candidate division WS6 and Deinococcales). Results from quantitative PCR (qPCR) showed that S3 exhibited the lowest abundance of 16S rRNA but the highest abundance of atypical nosZ, suggesting a selection of microbes with more diverse N-metabolism (i.e., incomplete denitrifiers) in the stage exposed to the lowest carbon availability. A positive correlation (p &lt; 0.05) was observed between removal rate constants of several pharmaceuticals with abundance of relevant denitrifying genes, but not with biodiversity. Despite the previously suggested positive relationship between microbial diversity and functionality in macrobial and microbial ecosystems, this was not observed in the current study, indicating a need to further investigate structure-function relationships for denitrifying systems.</p

    Intermittent Aeration Suppresses Nitrite-Oxidizing Bacteria in Membrane-Aerated Biofilms:A Model-Based Explanation

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    Autotrophic ammonium oxidation in membrane-aerated biofilm reactors (MABRs) can make treatment of ammonium-rich wastewaters more energy-efficient, especially within the context of short-cut ammonium removal. The challenge is to exclusively enrich ammonium-oxidizing bacteria (AOB). To achieve nitritation, strategies to suppress nitrite-oxidizing bacteria (NOB) are needed, which are ideally grounded on an understanding of underlying mechanisms. In this study, a nitrifying MABR was operated under intermittent aeration. During eight months of operation, AOB dominated, while NOB were suppressed. On the basis of dissolved oxygen (DO), ammonium, nitrite, and nitrate profiles within the biofilm and in the bulk, a 1-dimensional nitrifying biofilm model was developed and calibrated. The model was utilized to explore the potential mechanisms of NOB suppression associated with intermittent aeration, considering DO limitation, direct pH effects on enzymatic activities, and indirect pH effects on activity via substrate speciation. The model predicted strong periodic shifts in the spatial gradients of DO, pH, free ammonia, and free nitrous acid, associated with aerated and nonaerated phases. NOB suppression during intermittent aeration was mostly explained by periodic inhibition caused by free ammonia due to periodic transient pH upshifts. Dissolved oxygen limitation did not govern NOB suppression. Different intermittent aeration strategies were then evaluated for nitritation success in intermittently aerated MABRs: both aeration intermittency and duration were effective control parameters

    Occurrence, characterisation and fate of (nano)particulate Ti and Ag in two Norwegian wastewater treatment plants

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    Due to their widespread application in consumer products, elemental titanium (e.g., titanium dioxide, TiO2) and silver (Ag), also in nanoparticulate form, are increasingly released from households and industrial facilities to urban wastewater treatment plants (WWTPs). A seven-day sampling campaign was conducted in two full-scale WWTPs in Trondheim (Norway) employing only primary treatment. We assessed the occurrence and elimination of Ti and Ag, and conducted size-based fractionation using sequential filtration of influent samples to separate particulate, colloidal and dissolved fractions. Eight-hour composite influent samples were collected to assess diurnal variations in total Ti and Ag influx. Measured influent Ti concentrations (up to 290 ÎŒg L−1) were significantly higher than Ag (0.7 ÎŒm). Removal efficiencies ≄70% were observed for both elements, requiring for one WWTP to account for the high Ti content (∌2 g L−1) in the flocculant. Nano- and micron-sized Ti particles were observed with scanning transmission electron microscopy (STEM) in influent, effluent and biosolids, while Ag nanoparticles were detected in biosolids only. Diurnal profiles of influent Ti were correlated to flow and pollutant concentration patterns (especially total suspended solids), with peaks during the morning and/or evening and minima at night, indicating household discharges as predominant source. Irregular profiles were exhibited by influent Ag, with periodic concentration spikes suggesting short-term discharges from one or few point sources (e.g., industry). Influent Ti and Ag dynamics were reproduced using a disturbance scenario generator model, and we estimated per capita loads of Ti (42–45 mg cap−1 d−1) and Ag (0.11 mg cap−1 d−1) from households as well as additional Ag load (14–22 g d−1) from point discharge. This is the first study to experimentally and mathematically describe short-term release dynamics and dry-weather sources of emissions of Ti and Ag in municipal WWTPs and receiving environments

    Bioaugmentation of activated sludge with <i>Achromobacter denitrificans</i> PR1 for enhancing the biotransformation of sulfamethoxazole and its human conjugates in real wastewater:Kinetic tests and modelling

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    Achromobacter denitrificans PR1 has previously shown potential to degrade the antibiotic sulfamethoxazole, whereby sulfamethoxazole biotransformation was stimulated in the presence of biogenic substrates. This study examined the biotransformation kinetics of sulfamethoxazole and its two main conjugates, N-4-acetyl-SMX and SMX-N-1-Glucuronide, by activated sludge and activated sludge bioaugmented with A. denitrificans PR1. SMX biotransformation under both anoxic and aerobic conditions was tested, with and without the addition of acetate as growth substrate, to understand the range of applicable conditions for bioaugmentation purposes. Biological process models, such as the pseudo-first order kinetic and cometabolic models, were also applied and, following the estimation of kinetic parameters, could well describe data measured in bioaugmented and non-bioaugmented AS batch experiments under various test conditions. Experimental and modelling results suggest that (i) retransformation of the two conjugates to SMX in AS occurred under both aerobic and anoxic conditions, and (ii) biotransformation kinetics of SMX can vary significantly depending on redox conditions, e.g., SMX was biotransformed by AS only under aerobic conditions. Notably, SMX biotransformation was significantly enhanced when PR1 was bioaugmented in AS. Addition of acetate as biogenic substrate is not necessary, as PR1 was capable of enhancing the SMX biotransformation by using the carbon sources present in wastewater. Overall, bioaugmentation by means of A. denitrificans PR1 could be a viable strategy for enhancing SMX removal in AS wastewater treatment plants (WWTPs)

    Wastewater-based epidemiology to assess pan-European pesticide exposure

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    Human biomonitoring, i.e. the determination of chemicals and/or their metabolites in human specimens, is the most common and potent tool for assessing human exposure to pesticides, but it suffers from limitations such as high costs and biases in sampling. Wastewater-based epidemiology (WBE) is an innovative approach based on the chemical analysis of specific human metabolic excretion products (biomarkers) in wastewater, and provides objective and real-time information on xenobiotics directly or indirectly ingested by a population. This study applied the WBE approach for the first time to evaluate human exposure to pesticides in eight cities across Europe. 24 h-composite wastewater samples were collected from the main wastewater treatment plants and analyzed for urinary metabolites of three classes of pesticides, namely triazines, organophosphates and pyrethroids, by liquid chromatography-tandem mass spectrometry. The mass loads (mg/day/1000 inhabitants) were highest for organophosphates and lowest for triazines. Different patterns were observed among the cities and for the various classes of pesticides. Population weighted loads of specific biomarkers indicated higher exposure in Castellon, Milan, Copenhagen and Bristol for pyrethroids, and in Castellon, Bristol and Zurich for organophosphates. The lowest mass loads (mg/day/1000 inhabitants) were found in Utrecht and Oslo. These results were in agreement with several national statistics related to pesticides exposure such as pesticides sales. The daily intake of pyrethroids was estimated in each city and it was found to exceed the acceptable daily intake (ADI) only in one city (Castellon, Spain). This was the first large-scale application of WBE to monitor population exposure to pesticides. The results indicated that WBE can give new information about the “average exposure” of the population to pesticides, and is a useful complementary biomonitoring tool to study population-wide exposure to pesticides
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