Belastung des Neusiedler Sees mit anthropogenen Spurenstoffen: Überlegungen zu Herkunft und Verhalten

In this paper, we first present the contamination of Lake Neusiedl with anthropogenic trace substances regulated at national or EU level. Second, we identify main emission pathways for selected substances into the River Wulka and Lake Neusiedl and identify the potential environmental behaviour of trace substances in the aquatic system. Even if a comprehensive monitoring of all regulated substances in the lake is at present still missing, we can assume the compliance with environmental quality standards for most of them based on measurements carried out in the River Wulka and from biota-monitoring in the lake. For some substances quality criteria are not or probably not met, for others a final diagnosis is currently not possible due to analytical constraints. Depending on the examined substance, effluents from waste water treatment plants, agricultural erosion or atmospheric deposition on the lake surface may be the dominant pathway of contamination into the River Wulka and Lake Neusiedl. Besides specific considerations for individual substances, taking into account the enormous number of anthropogenic trace substances that are released into the environment, Lake Neusiedl must be regarded as especially vulnerable to this kind of contamination. The high vulnerability mainly derives from the lake acting as a substance-sink. Persistent chemicals which enter the lake may concentrate in the water of the lake or may be stored in the sediments of the reed belt, from where they might be mobilized later on. Even if many of the highly persistent chemicals are removed from the lake water through degradation or conversion to metabolites, little is known about the end products of this conversion and they cannot be monitored completely because of their high number. As a basis for the development of strategies for a long-term and efficient management of the lake, a regular monitoring of trace substances in lake and reed belt should be reinforced considerably to detect any undesirable developments as early as possible.EU-Projekt ATHU53 REBEN5225361

Occurrence and levels of micropollutants across environmental and engineered compartments in Austria

Occurrence and concentration of a broad spectrum of micropollutants are investigated in Austrian river catchments, namely polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs), organotin compounds, perfluoroalkyl acids (PFAAs) and metals. The parallel analysis across multiple environmental and engineered compartments sheds light on the ratio of dissolved and particulate transport and on differences in concentration levels between point and diffuse emission pathways. It is found that some PAHs and organotins are present in rivers, groundwater and bulk deposition at higher concentrations than in municipal wastewater effluents. Among PFAAs and metals, highest concentrations were recorded either in atmospheric deposition or in discharges from wastewater treatment plants. The relevance of the analysis across compartments is best shown by the case of perfluorooctanesulfonic acid (PFOS). Despite municipal wastewater effluents being the emission pathway with highest concentrations, this study reveals that not only rivers, but also atmospheric deposition and groundwater sometimes exceed the environmental quality standard for surface waters. Moreover, this work reveals partially counterintuitive patterns. In rivers with treated wastewater discharges, increasing levels of dissolved compounds were measured at rising flow conditions, whereas the opposite would be expected owing to the dilution effect. This might derive from the mobilisation from soil or suspended particulate matter or rather find its explanation in high concentrations in atmospheric deposition. These hypotheses require however being tested through targeted studies. Additional future research includes the analysis of how regional or catchment specific characteristics might alter the relative importance of different emission pathways, and the modelling of emission and river loads to assess their relative contribution to river pollution.Federal Ministry of Sustainability and Tourism (BMNT)6366531

Effect of ozonation on the biodegradability of urban wastewater treatment plant effluent

The present work aimed to study the effect of ozonation on the organic sum parameters linked to enhanced biodegradability. Laboratory experiments were conducted with the effluent of four Austrian urban wastewater treatment plants with low food to microorganism ratios and different matrix characteristics. Biochemical oxygen demand over 5 days (BOD5) was measured before ozonation and after application of different specific ozone doses (Dspec) (0.4, 0.6 and 0.8 g O3/g DOC). Other investigated organic parameters comprised chemical oxygen demand (COD), dissolved organic carbon (DOC), UV absorption at 254 nm (UV254), which are parameters that are applied in routine wastewater analysis. Carbamazepine and benzotriazole were measured as reference micropollutants. The results showed a dose-dependent increase in biological activity after ozonation; this increase was linked to the enhanced biodegradability of substances that are recalcitrant to biodegradation in conventional activated sludge treatment. The highest relative change was determined for BOD5, which already occurred between 0 and 0.4 g O3/g DOC for all samples. Increasing the Dspec to 0.6 and 0.8 g O3/g DOC resulted in a less pronounced increase. DOC was not substantially decreased after ozonation, which was consistent with a low reported degree of mineralization, while partial oxidation led to a quantifiable decrease in COD (7 to 17%). Delta UV254 and the decline in specific UV absorption after ozonation clearly correlated with Dspec. In contrast, for COD and biodegradable DOC (BDOC), a clear dose-response pattern was identified only after exposure to BOD5 measurement. Indications for improved biodegradability were further supported by the rise in the BOD5/COD ratio. The results indicated that subsequent biological processes have a higher degradation potential after ozonation. The further reduction in biodegradable organic carbon emission by the combination of ozonation and biological post treatment represents another step towards sustainable water resource management in addition to micropollutant abatement.19

Optimization of Ozonation and Peroxone Process for Simultaneous Control of Micropollutants and Bromate in Wastewater

The final publication is available via https://doi.org/10.2166/wst.2018.170.The study aims to simultaneously control micropollutants and bromate formations by using ozonation and peroxone process. The batch experiments were run with variations in specific ozone dose (SOD) and hydrogen peroxide-to-ozone (H2O2/O3) ratio. Based on the removal by ozonation and peroxone, micropollutants were categorized into three groups: non-reactive compounds (i.e. amidotrizoate), moderately reactive compounds (i.e. metoprolol, acesulfame potassium, bezafibrate, and benzotriazole), and highly reactive compounds (i.e. carbamazepine and diclofenac). For ozonation and peroxone process, the removals for highly reactive compounds and moderately reactive compounds were 82–99% and 29–99%, respectively. The removal of amidotrizoate was not observed in this study. The effect of ozonation on micropollutant removals was similar to the peroxone process. However, differences in bromate formation were observed. Bromate formation depended on the SOD, while addition of hydrogen peroxide suppressed the bromate formation. The peroxone process at the H2O2/O3 ratio of 0.3 was recommended to bromide-containing water below 100 µg·L−1 for simultaneous control of micropollutants and bromate. Enhancement in micropollutant removals, except for the non-reactive groups, was achieved with either higher SOD or the addition of hydrogen peroxide to ozonation. The micropollutant removal predicted from the second-order kinetic reaction with ozone and •OH exposures was higher than the observed data

Capillary electrophoresis for continuous nitrogen quantification in wastewater treatment processes

The final publication is available via https://doi.org/10.1016/j.talanta.2018.11.056.A water quality analyzer based on the working principle of capillary electrophoresis (CE) was developed to determine ionic inorganic nitrogen compounds contained in wastewater samples. The instrument provides simultaneous quantification of anions and cations by superimposing hydrodynamic pumping with electrokinetic motion. It features a single separation capillary with contactless conductivity detection and a sequential injection manifold for fluid handling. Dynamic adaption of the system calibration was enabled by the use of a high precision pressure regulator to cover a wide measurement range showing low relative standard deviations (< 2 %) and high measurement accuracy comparable to conventional wastewater analyzers. The prototype is transportable, integrated in a 19 in. rack and connected to a membrane filter system developed for direct sample aspiration in the wastewater process. For operation on site, only a power supply and a network connection for remote control is necessary. Continuous operation was demonstrated over 24 h at the aeration tank of a pilot scale wastewater treatment plant at TU Wien and a good correlation with laboratory results was achieved. At this time, there is no device available, on the market, to analyze all nitrogen species in one assembly with limited hardware complexity and chemical demand. This entails a significant step forward towards automated water quality monitoring with respect to the implementation of new advanced wastewater treatment technologies.366371

Valorisation of cheese whey as substrate and inducer for recombinant protein production in E. coli HMS174(DE3)

Every year worldwide around 190 million tons of cheese whey are generated resulting in a huge environmental burden. We recently published a study where we showed that E. coli strain HMS174(DE3) can be cultivated using only lactose as C-source and inducer. Motivated by the results we investigated using a concentrated whey feed instead of the lactose feed. Spray drying whey and dissolving the powder allowed preparation of a 40-fold concentrated whey containing 91% lactose and 81% protein of the original whey. Cultivations using the concentrated whey feed instead of a defined lactose feed revealed 39% higher growth rates, 24% higher biomass yields and even higher specific product titers for the model enzymes, flavanone 3-hydroxylase and chalcone 3- hydroxylase. Our strategy simultaneously provides a cheap substrate for large-scale production of technical enzymes and an excellent opportunity for cheese whey valorization, reducing the biological burden resulting from whey wastewaters.Fonds zur Förderung der Wissenschaftlichen Forschung

Ozone as oxidizing agent for the total oxidizable precursor (TOP) assay and as a preceding step for activated carbon treatments concerning per- and polyfluoroalkyl substance removal

Several thousands of highly persistent per- and polyfluoroalkyl substances (PFAS) exist and it is therefore challenging to analytically determine a larger spectrum of these compounds simultaneously in one sample. It is even more difficult to efficiently remove mobile PFAS in wastewater treatment plants (WWTPs) to protect the receiving waters. The total oxidizable precursor (TOP) assay is an approach that enables the detection of the total PFAS content in a sample via oxidation of precursors, followed by subsequent analysis of the perfluoroalkyl acid (PFAA) concentration before and after oxidative processes. Activated carbon combined with a preceding ozonation step is considered a promising tool for the removal of micropollutants but considering PFAS removal efficiencies in effluents for this process combination more information is required. The focus of the study was to implement and assess the TOP assay with ozone as oxidizing agent to estimate the total PFAS content in a WWTP effluent. Additionally, granular activated carbon (GAC) and powdered activated carbon (PAC) with a preceding ozonation step was tested for the removal efficiencies for 22 PFAS. For the TOP assay the obtained accordance in molarity using spiked tap water as quality control was 95.2% (15 mg O3/L) and 99.1% (6 mg O3/L). Applying the TOP assay, an estimated total PFAS content of 840 ng/L was determined in the respective effluent, which was 91.1% higher than obtained by target PFAS analysis, implying the presence of unknown precursors not included in common monitoring. While all treatment techniques that included ozone or a preceding ozonation step solely transformed precursors and long-chain perfluoroalkyl acids (PFAA, i.e., >C9) to shorter congeners, PAC was the only tested water treatment application that was able to remove 19.3% of the total PFAS molarity.1343

To analyze or to throw away? On the stability of excitation-emission matrices for different water systems

Fluorescence spectroscopy has numerous applications to characterize natural and human-influenced water bodies regarding dissolved organic matter (DOM) and contamination. Analyzing samples in a timely manner is crucial to gaining valid and reproducible excitation-emission matrices (EEM) but often difficult, specifically in transnational projects with long transport distances. In this study, eight samples of different water sources (tap water, differently polluted rivers, and wastewater treatment plant (WWTP) effluents) were stored under standardized conditions for 59 days and analyzed regularly. With this data set, the sample and fluorescence spectra stability was evaluated. Established analysis methods such as peak picking and fluorescence metrics were compared over time and benchmarked against dissolved organic carbon (DOC) and a maximal change of 10% in terms of their variability. Additional high-performance liquid chromatography (HPLC) data to identify single organic compounds provides insights into these DOM alterations and allows for conclusions about the underlying biological processes. Our results corroborate in a systematic way that the higher the organic or microbial load, the faster the sample must be processed. For all water sources, considerable changes were found between days zero and one, indicating a potential systematic bias between in-situ and laboratory measurements. The absolute signals of individual peaks vary substantially after only a few days. In contrast, relative metrics are robust for a much longer time. For specific metrics, when filtered and stored under cool and dark conditions, tap water may be stored for up to 59 days, non-polluted river water for up to 31–59 days, and WWTP effluents for up to 14–59 days. The storability thus depends both on the specific water source and the analytical plan. By systematizing our understanding of how the specific water source and DOM concentration determine the stability of samples during storage, these conclusions facilitate efforts to establish a standardized protocol

Desorption of Organic Micropollutants from Loaded Granular Activated Carbon

©2020 by the authors.The loading of granular activated carbon (GAC) is influenced by the amount of water treated and the concentrations of adsorbates present in the water matrix. Through extraction experiments, we aimed to investigate the total adsorbed mass of eight organic micropollutants by using ethanol as solvent and the maximum possible concentrations, due to the desorption of organic micropollutants, in water. Three different drying methods and the impact of the contact time, GAC particle size, and GAC/solvent ratio were investigated. Although no significant differences between the drying methods could be observed, the chosen contact time and particle size had a significant impact on the amount of organic micropollutants extracted. Lower GAC/solvent ratios positively affected the extraction yield. The masses extracted in ethanol were compared with the cumulated masses calculated from 72 feed and effluent samples, collected during filter operation, resulting in extraction yields between 0.5% and 30%. The composition of extracted micropollutants in ethanol reflected the concentrations in feed water of the pilot-scale filter. Desorption in water was mostly influenced by the solubility of the investigated micropollutants. The same substances found in the supernatants inf the experiments could also be identified in the backwash water of the filter.1202