Presence Of Micropollutants Research Articles

Relationship among micro-pollutants, economic growth, renewable energy, nanotechnology and ecological foot prints of China: evidence from panel data analysis.

An important concern is the availability of clean drinking water, which is an essential need for human survival. This issue arises due to the existence of hazardous micropollutants originating from various emission sources. Nanotechnology aids in the mitigation of micropollutants by assimilating and counteracting their effects, hence diminishing their influence on water and other ecosystems. The study investigates the relationship between nanotechnological progress, the adoption of renewable energy, environmental consequences, and economic growth in China, using the Environmental Kuznets Curve theory as a conceptual framework. The study employs panel cointegration tests to analyze structural breaks from 2000 to 2020. Nanotechnology is expected to reduce environmental degradation and the presence of micro-pollutants by increasing the use of renewable energy and promoting energy conservation. Nanotechnology is crucial for mitigating micro-pollutants and advancing sustainable development in this specific context. However, the literature also highlights the harmful consequences of nanoparticle emissions caused by nanotechnology on human and environmental health for a long duration, requiring more examination. This research is the first empirical inquiry into the relationship between improvements in nanotechnology, the use of renewable energy, economic growth, and ecological effect, all within the context of the Environmental Kuznets Curve theory. The results confirm the successful incorporation of all components with a focus on long-term outcomes. The findings suggest that the EKC hypothesis is relevant in China. In China, advancements in nanotechnology have a moderating effect on environmental degradation. The use of renewable energy sources in China enhances environmental circumstances. Given the offered empirical evidence, it is advisable for the government to have a leading role in the development of innovative nanotechnologies that have low emissions of nanoparticles. By using this approach, it will be possible to encourage the conservation of energy and the use of renewable sources in a more secure way, hence improving the effectiveness of sustainable development initiatives.

The influence of light intensities and micropollutants on the removal of total coliforms and E. coli from wastewater in a flat-panel photobioreactor

The presence of micropollutants and pathogens in sanitary wastewater and surface water is a growing concern that impacts public health, environmental balance and the maintenance of water supply services. To improve sanitary wastewater treatment, it is necessary to develop and improve sustainable technologies. Among the available options, microalgae-based systems stand out for their efficiency and generation of value-added byproducts. To study the impact of luminosity and the presence of micropollutants (13 selected) on the removal of E. coli and total coliforms from real anaerobically treated wastewater, a pilot flat-panel photobioreactor (50 L) was operated in batch mode in a tropical climate region. This is the first study to evaluate whether micropollutants interfere with coliform groups, considering a microalgae-based system and an experiment in a tropical climate region. E. coli had better removal (from 104 to 101 CFU 100 mL−1) than did total coliforms (from 104 to 103 CFU 100 mL−1). The removal of E. coli was more strongly linked to luminosity and temperature, while the removal of total coliforms was influenced by the presence of the selected micropollutants.

Adsorption Properties of Natural Zeolite Supported by Chitosan on Cd(II) in Micropolluted Irrigation Water.

This study utilized a 1% chitosan solution (dissolved in 2% acetic acid), with a chitosan-to-zeolite mass ratio of 0.005, to successfully prepare chitosan-loaded natural zeolite. The performance of chitosan-modified natural zeolite in the removal of low-concentration cadmium ions in the presence of micropollutants was investigated. The adsorbent was characterized using X-ray diffraction (XRD), Fourier transform infrared (FTIR), and scanning electron microscopy (SEM)/energy-dispersive spectroscopy (EDS) techniques. The impact of modified adsorbent dosage, pH value, contact time, temperature, and initial concentration on adsorption performance was discussed. Additionally, the adsorption kinetics, isotherms, and thermodynamics of cadmium on chitosan-modified zeolites were analyzed. The results indicated that the modified zeolite exhibited a dispersed and porous structure with increased surface area, average pore size, and total pore volume. Under the conditions of 25 °C, pH 6, a dosage of 8 g/L, and a 60 min adsorption reaction time, chitosan-loaded natural zeolite (CNZ) achieved a removal efficiency of over 94.51% for a 100 μg/L cadmium solution (in a 100 mL volume). The adsorption process followed the Langmuir model, suggesting monolayer adsorption. The adsorption kinetics followed a pseudo-second-order equation, indicating an exothermic process with an increase in entropy. Chitosan-loaded natural zeolite demonstrated improved adsorption capacity and effectively removed cadmium from water contaminated with micropollutants.

Assessing emerging and priority micropollutants in sewage sludge: environmental insights and analytical approaches

The application of sewage sludge (SS) in agriculture, as an alternative to manufactured fertilizers, is current practice worldwide. However, as wastewater is collected from households, industries, and hospitals, the resulting sludge could contaminate land with creeping levels of pharmaceuticals, pesticides, heavy metals, polycyclic aromatic hydrocarbons, and microplastics, among others. Thus, the sustainable management of SS requires the development of selective methods for the identification and quantification of pollutants, preventing ecological and/or health risks. This study presents a thorough evaluation of emerging and priority micropollutants in SS, through the lens of environmental insights, by developing and implementing an integrated analytical approach. A quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction method, coupled with gas chromatography and liquid chromatography, was optimized for the determination of 42 organic compounds. These include organophosphorus pesticides, organochlorine pesticides, pyrethroid pesticides, organophosphate ester flame retardants, polybrominated diphenyl ethers, polychlorinated biphenyls, and polycyclic aromatic hydrocarbons. The optimization of the dispersive-solid phase for clean-up, combined with the optimization of chromatographic parameters, ensured improved sensitivity. Method validation included assessments for recovery, reproducibility, limit of detection (LOD), and limit of quantification (LOQ). Recoveries ranged from 59.5 to 117%, while LODs ranged from 0.00700 to 0.271 µg g-1. Application of the method to seven SS samples from Portuguese wastewater treatment plants revealed the presence of sixteen compounds, including persistent organic pollutants. The quantification of α-endosulfan, an organochlorine pesticide, was consistently observed in all samples, with concentrations ranging from 0.110 to 0.571 µg g-1. Furthermore, the study encompasses the analysis of agronomic parameters, as well as the mineral and metal content in SS samples. The study demonstrates that the levels of heavy metals comply with legal limits. By conducting a comprehensive investigation into the presence of micropollutants in SS, this study contributes to a deeper understanding of the environmental and sustainable implications associated with SS management.Graphical

A technological approach using a metal-free immobilized photocatalyst for the removal of pharmaceutical substances from urban wastewaters

The presence of micropollutants (MPs) in aquatic compartments poses a great risk to the ecosystems and human health. Advanced oxidation processes (AOPs), such as light-induced systems employing a variety of powder optical semiconductors, have been widely investigated to remove MPs from water and wastewater. In this work, a metal-free photocatalyst (GCN-T) immobilized in the form of a film (GCN-T/PVDF) was activated by visible light (λexc = 417 nm) and successfully tested in both batch and continuous flow mode reactors for the degradation of two pharmaceutical model compounds (metoprolol and venlafaxine) spiked in ultrapure water (UP) and urban wastewater (WW) samples. A total removal of MPs was reached after 3 h reaction using GCN-T/PVDF film in a batch reactor. Under continuous mode operation, a steady state was attained after 2 h, with ca. 64 % removal for both MPs being obtained. The photocatalytic system was also examined using a non-spiked WW sample to study its performance to remove trace concentrations of these and other MPs in this type of complex matrix. MPs, such as bezafibrate, carbamazepine, diclofenac, isoproturon, and tramadol, were detected and efficiently degraded using the GCN-T/PVDF film. Finally, the ecotoxicity of the WW samples was also investigated using the aquatic invertebrate microcrustacean Daphnia magna. The results showed that the toxicity of WW samples decreases with the photocatalytic treatment.

Evaluation of hydrochar from peach stones for caffeine removal from aqueous medium and treatment of a synthetic mixture

ABSTRACT The presence of micropollutants, such as caffeine (CAF), has been detected throughout the world, since conventional treatment plants are not able to properly degrade them. CAF is a widely consumed stimulant, and has been demanding the development of efficient methodologies for its removal. Aiming at the agriculture waste valorization, a new hydrochar was developed based on chemical and thermal modification of peach stones (mod-PS) for CAF removal from water and from a synthetic mixture. The morphology, functional groups and surface electrical charge of the adsorbent were characterized by SEM, FTIR and zeta potential, respectively. Regarding CAF adsorption performance, the equilibrium time was reached at 480 min and the pseudo-second-order model presented the best fit for the experimental data. The maximum adsorption capacity was 68.39 mg g-1 (298 K) and the Langmuir model exhibited a better fit for the isothermal data. The thermodynamic properties confirmed that the process was exothermic, spontaneous and reversible. The main adsorption mechanisms were hydrogen bonds and π-interactions. The global removal efficiency was satisfactory in the synthetic mixture simulating real wastewater (67%). Therefore, the proposed new hydrochar has potential application as a low-cost adsorbent for CAF removal.

Micropollutants Removal from Water and Activated Carbon Regeneration by Combining Adsorption and Electro-Fenton

The presence of micropollutants in municipal wastewater effluents is a topic of major concern, as these pollutants end up in surface and ground waters. Currently, adsorption on activated carbon (AC) is used to remove these recalcitrant compounds. When saturated, the AC is generally either thermally regenerated or disposed of. Thermal regeneration is expensive and negatively affects the structure and adsorptive properties of the AC.Over the last decade, considerable attention has been directed towards the electrochemical advanced oxidation processes (eAOPs), due to their ability to remove a large range of organic pollutants from water even at very low concentrations [1]. eAOPs rely on the in-situ generation of powerful oxidants, such as HO• by electron transfer at the anode surface. However, these processes are limited by mass transfer and require high energy consumption.In this study, combined adsorption on granular activated carbon (GAC) and electro Fenton process (EF) is applied. The purpose of this coupled process is to overcome the mass transfer issue by pre-concentrating the compounds on AC and proposing a new AC regeneration method. During the EF the AC can directly be used as a cathode. Due to the electrostatic repulsions and oxidation process, the compounds are desorbed from the AC and oxidized by the HO• generated in the bulk. Material and Methods The adsorption cycles and EF experiments were performed in batch mode using deionized water (DW) and simulated wastewater (SWW) with caffeine as a model compound. Similar experimental steps and conditions as described in [2] are followed, using 1g of GAC, with pH=3, Fe2+= 0.15 mM, Na2SO4= 50mM, and a current intensity of 200 mA. To assess the degradation and mineralization of the caffeine, HPLC and TOC measurements were used, respectively. The regeneration efficiency was calculated by comparing the adsorption capacity of the AC after each regeneration cycle with its initial adsorption capacity. Results and Conclusions The efficiency of the process was discussed as regards (i) desorption of organic compounds and regeneration efficiency in DW and SWW, (ii) degradation and mineralization of organic compounds, and (iii) stability of GAC for several successive regeneration cycles. During the regeneration, over 80% of desorbed caffeine was degraded and 75% was mineralized due to the formed HO• by Fenton reaction and at the BDD anode surface (Fig.1). Furthermore, a recovery of the AC adsorption capacity by up to 50 % in PW and 37% in SWW was observed. These regeneration percentages decreased to 25% during the second cycle and then remained stable during the third and the fourth cycle. The incomplete regeneration is most likely due to remaining caffeine molecules at the AC [3], or a blockage of the carbon adsorption sites by formed degradation molecules. Hence, a longer treatment time might lead to higher efficiency. These hypotheses will be taken into consideration in future work to draw a clear conclusion on the regeneration phenomenon. The similar regeneration efficiencies and mineralization rates obtained during the 2nd,3rd, and 4th cycles indicate the stability of the GAC electrode.In conclusion, the results from this study illustrate that combined adsorption and EF is a suitable process for the removal of caffeine and regeneration of AC. The advantage of such a process is that part of the AC can be regenerated while over 75% of the desorbed compounds from the AC are mineralized, thus avoiding toxic effluents. This process is currently implemented as a continuous e-cell for sequential adsorption and EF regeneration.

Bioremoval of estrogens by laccase immobilized onto polyacrylonitrile/polyethersulfone material: Effect of inhibitors and mediators, process characterization and catalytic pathways determination

The presence of micropollutants in water, wastewater and soil are a global problem due to their persistent effect on ecosystems and human health. Although there are many methods of removal of environmental pollutants, they are often ineffective for degradation of pharmaceuticals, including estrogens. In presented work we proposed fabrication of electrospun material from polyacrylonitrile/polyethersulfone (PAN/PES) as a support for laccase immobilization by covalent binding. Oxidoreductase was attached to the electrospun fibers using polydopamine as a linker and produced system was used for degradation of two estrogens: 17β-estradiol (E2) and 17α-ethynylestradiol (EE2). It was shown that 92% of E2 and 100% of EE2 were degraded after 24 h of the process. Moreover, the effect of surfactants, metal ions and mediators on conversion efficiencies of estrogens was investigated and it was confirmed that immobilized enzyme possessed higher resistance to inhibitory agents as well as thermal and storage stability, compared to its native form. Finally, estrogenic activities of E2 and EE2 solutions decreased around 99% and 87%, respectively, after enzymatic conversion, that corresponds to significant reduction of the total organic carbon and formation of low-toxic final products of estrogens degradation.

Comparison of Acetaminophen Degradation by Laccases Immobilized by Two Different Methods via a Continuous Flow Microreactor Process Scheme.

The presence of micropollutants in wastewater is one of the most significant environmental challenges. Particularly, pollutants such as pharmaceutical residues present high stability and resistance to conventional physicochemical and biological degradation processes. Thus, we aimed at immobilizing a laccase enzyme by two different methods: the first one was based on producing alginate-laccase microcapsules through a droplet-based microfluidic system; the second one was based on covalent binding of the laccase molecules on aluminum oxide (Al2O3) pellets. Immobilization efficiencies approached 92.18% and 98.22%, respectively. Laccase immobilized by the two different methods were packed into continuous flow microreactors to evaluate the degradation efficiency of acetaminophen present in artificial wastewater. After cyclic operation, enzyme losses were found to be up to 75 µg/mL and 66 µg/mL per operation cycle, with a maximum acetaminophen removal of 72% and 15% and a retention time of 30 min, for the laccase-alginate microcapsules and laccase-Al2O3 pellets, respectively. The superior catalytic performance of laccase-alginate microcapsules was attributed to their higher porosity, which enhances retention and, consequently, increased the chances for more substrate–enzyme interactions. Finally, phytotoxicity of the treated water was lower than that of the untreated wastewater, especially when using laccase immobilized in alginate microcapsules. Future work will be dedicated to elucidating the routes for scaling-up and optimizing the process to assure profitability.

Synthesis of a biobased resin and its screening as an alternative adsorbent for organic and inorganic micropollutant removal.

The sol-gel route was used to synthesize a biophenolic resin from a blend of Kraft black liquor and condensed tannin. The biobased resin has an amorphous structure and diversified surface functional groups. The biomaterial thermal stability was improved by Kraft black liquor, which increased the fixed carbon yield by 19.78% in an oxidant medium and 9.07% in an inert medium. Moreover, the presence of fixed carbon and char is positively related to the material flame retardant property. Additionally, impedance measurements were used to understand the physical phenomena occurring at the polymeric matrix's interface and the material's final properties. The biobased resin characterization and the considerable increase in the presence of micropollutants in surface and water bodies suggest the new biomaterial application in the adsorption process. Thus, its adsorption capacity toward several organic and inorganic micropollutants and its effectiveness in complex water matrices were evaluated. Methylene blue was used as a model compound to assess the influence of the resin composition on the adsorption capacity, and the type H isotherm indicates the high affinity of the biobased resin toward the micropollutant. The adsorption occurs in multilayer by intermolecular interaction and electrostatic forces. The amount of Kraft black liquor favored the adsorption, and the adsorption capacity was greater than 1250mgg-1. When inorganic compounds were evaluated, the carboxyl and phenol groups favor the biomaterial affinity toward metal ions. Cu2+ and Ni2+ were completely removed from the contaminated water, and the adsorption capacity of the other inorganic compounds was: Pb2+ (36.97mgg-1), Al3+ (22.17mgg-1), Ba2+ (12.76mgg-1), Ag1+ (33.85mgg-1), and Fe2+ (19.44mgg-1). In contrast, the adsorption capacity of the organic micropollutants was: 2,4-D (3.09mgg-1), diuron (5.89mgg-1), atrazine (2.71mgg-1), diclofenac (2.04mgg-1), caffeine (5.79mgg-1), acetaminophen (4.80mgg-1), methylene Blue (106.66mgg-1), and methyl orange (30.48mgg-1). The results pointed that the adsorption efficiency of organic micropollutants increases with the distribution coefficient (logD), indicating the biobased resin affinity toward more lipophilic compounds and ionized species.

Biochar for the removal of detected micropollutants in South African domestic wastewater: a case study from a demonstration-scale decentralised wastewater treatment system in eThekwini

The presence of micropollutants, such as pharmaceuticals and personal care products, in surface and ground water has escalated globally, leading to adverse effects on aquatic organisms in receiving waters. Untreated or inadequately treated wastewater is the main source of micropollutants entering the environment. In South Africa, the consumption of antibiotics and antiretroviral drugs is relatively higher than other nations; however, little data exists on the identification and remediation of micropollutants in domestic wastewater. In this study, a novel method to detect and measure 71 micropollutants using online solid phase extraction liquid chromatography coupled to tandem mass spectrometry was developed. To test the method in the South African context, grab samples of the influent and anaerobically treated effluent (AF effluent) from a demonstration-scale decentralised wastewater treatment system in eThekwini (Durban) were taken over 3 consecutive days at 2 time points. The presence of 24 micropollutants was detected in the raw wastewater, with analgesics/anti-inflammatory drugs, antiretrovirals, and antibiotics showing the highest concentrations and with the majority of compounds still present in the AF effluent. One antibiotic, ciprofloxacin, exceeded its predicted no-effect concentration in all influent and AF effluent samples. This suggests that the anaerobic treatment of the raw wastewater was not effective in removing micropollutants. Preliminary data from lab-scale adsorption experiments using biochar produced from a set of 4 feedstocks – olive residues, tomato residues, rice husks, and the African palm tree Raphia farinifera – showed average removal rates for 4 compounds of up to 62%. The application of biochar is thus recommended as a secondary treatment step in decentralised wastewater treatment for the removal of micropollutants in South Africa.

Multi-site nanocomposite sorbent for simultaneous removal of diverse micropollutants from treated wastewater

Despite the advantages of maximizing treated wastewater (TWW) reuse, this practice brought upon the presence of micropollutants in edible plants, animals, and even humans, since many micropollutants are not completely removed by conventional treatment plants. Clay polymer nanocomposites (CPNs) have been proposed and widely studied in recent years as a promising sorbent for micropollutant removal. However, most of these studies report the development of a single CPN for the removal of specific micropollutants in batch experiments, usually from synthetic water, and do not compare to the removal by commercial sorbents. Here, we thoroughly investigated the adsorption mechanism of three chemically-diverse micropollutants; cationic, anionic, and non-ionic (metoprolol, diclofenac, and lamotrigine, respectively) from TWW by a CPN with a ‘loopy’ polymer configuration. The results suggest that both cation and anion exchange sites coexist on the CPN, and therefore anionic and cationic micropollutants adsorb simultaneously, and they do not compromise the adsorption of each other. The adsorption of the non-ionic micropollutant enhanced in the presence of the charged micropollutants due to a synergistic effect. These adsorption trends were also obtained for micropollutant filtration by CPN columns. Finally, we demonstrated the simultaneous filtration of effluent organic matter and an array of micropollutants from TWW by the CPN columns and compared it to the filtration by granular activated carbon (GAC). A cost-effective comparison indicates that the filtration by the CPN column is more efficient (ng pollutants/ sorbent cost) than by the GAC column.

Analysis of micropollutants in a marine outfall using network analysis and decision tree

The presence of micropollutants (MPs), including pharmaceutical, industrial, and pesticidal compounds, threatens both human health and the aquatic ecosystem. The development and extensive use of new chemicals have also inevitably led to the accumulation of MPs in aquatic environments. Recreational beaches are especially vulnerable to contamination, affecting humans and aquatic animals via the absorption of MPs in water during marine activities (e.g., swimming, sailing, and windsurfing). Additionally, marine outfalls in an urbanized coastal city can cause serious chemical and microbial pollution on recreational beaches, leading to an increase in adverse effects on public health and the ecological system. Therefore, the aim of this study was to, with the use of network and decision tree analyses, identify the features and factors that influence the change in MP concentrations in a marine outfall. These analyses were conducted to inspect the relationship between each MP and its hierarchical structure as well as hydrometeorological variables. Additionally, a risk analysis was conducted in this study in which the MPs were prioritized based on their optimized risk quotient values. During our monitoring of MP concentrations over time at the marine outfall, high concentrations of pharmaceutical and industrial compounds were detected when the tide level was low after rainfall. Furthermore, results of the risk analysis and the prioritization revealed that a total of 18 substances identified in our study posed a risk to the ecosystem; these include major ecotoxicologically hazardous substances such as telmisartan, mevinphos, and methiocarb. Results of the network analysis demonstrated distinct trends for pharmaceutical and industrial substances, whilst those for pesticide compounds were irregular. Additionally, the hierarchical structures for most MPs consisted of rainfall, tide level, and antecedent dry hours; this implies that these factors influence MP dynamics. These findings will be helpful for establishing chemical contamination management plans for recreational beaches in the future.

Micropollutant-loaded powdered activated carbon released from waste water treatment plants: a risk for sediment-dwelling organisms?

BackgroundIn order to protect aquatic environments and to reduce the presence of micropollutants in the global water cycle, wastewater treatment plants (WWTPs) often implement an additional treatment step. One of the most effective measures is the use of powdered activated carbon (PAC) as an adsorbent for micropollutants. This method provides sufficient elimination rates for several micropollutants and has been successfully employed in many WWTPs. Despite this success, there might be a drawback as the retention of the PAC in the WWTP can be challenging and losses of micropollutant-loaded PAC into the aquatic environment may occur. Upon emission, micropollutant-loaded PAC is expected to settle to the benthic zone of receiving waters, where sediment-dwelling organisms may ingest these particles. Therefore, the present study investigated possible adverse effects of micropollutant-loaded PAC from a WWTP as compared to unloaded (native) and diclofenac-loaded PAC on the sediment-dwelling annelid Lumbriculus variegatus.ResultsNative PAC induced the strongest effects on growth (measured as biomass) and reproduction of the annelids. The corresponding medium effective concentrations (EC50) were 1.7 g/kg and 1.8 g/kg, respectively. Diclofenac-loaded PAC showed lower effects with an EC50 of 2.5 g/kg for growth and EC50 of 3.0 g/kg for reproduction. Although tested at the same concentrations, the micropollutant-loaded PAC from the WWTP did not lead to obvious negative effects on the endpoints investigated for L.variegatus and only a slight trend of a reduced growth was detected.ConclusionWe did not detect harmful effects on L. variegatus caused by the presence of MP-loaded PAC from a WWTP which gives an auspicious perspective for PAC as an advanced treatment option.

Ozonation in view of micropollutant removal from biologically treated landfill leachate: Removal efficiency, [rad]OH exposure, and surrogate-based monitoring

The presence of micropollutants (MPs) in landfill leachate is attracting growing attention. Although ozonation is an effective oxidative treatment technique, knowledge of the removal efficiency and mechanisms of MPs from leachate by ozonation is scarce. In this work, biologically treated leachate spiked with carbamazepine, bisphenol A, atrazine, and alachlor was subjected to ozonation in a semi-continuous mode. No dissolved ozone was detected before 0.95 gO3/g DOC was dosed, indicating the specific initial ozone demand (IOD) of the leachate. This ozone dose was sufficient for a 99% removal of carbamazepine and bisphenol A, both characterized by a high ozone reactivity (kO3 > 104 M−1s−1). However, the more ozone-recalcitrant atrazine and alachlor were removed lower than 40%, indicating that commonly applied ozone doses (similar to IOD) are not sufficient for effective ozone-recalcitrant MPs removal. Given the importance of OH in removing such recalcitrant MPs, the OH formation was characterized by the ROH,O3 concept. The OH formation yield indicated by ROH,O3 value , increased with the applied ozone dose and varied between leachate samples due to the variation in organic composition, suggesting that it is impractical to predict MPs removal with OH formation yield information alone. As such, a surrogate-based model was proposed for the prediction of MPs abatement using spectroscopic measurements. The developed UVA254-based model exhibited a good predictive power for the abatement of ozone-recalcitrant MPs (R2 > 90%) in landfill leachates with different organic characteristics. This study provides valuable information for understanding occurring reactions and predicting MPs removal during landfill leachate ozonation.

A statistical assessment of micropollutants occurrence, time trend, fate and human health risk using left-censored water quality data

In recent years, the presence of micropollutants in drinking water has become an issue of growing global concern. Due to their low concentrations, monitoring databases are usually rich in censored data (e.g. samples with concentrations reported below the limit of quantification, LOQ) which are typically eliminated or replaced with a value arbitrarily chosen between 0 and LOQ. These conventional methods have some limitations and can lead to erroneous conclusions on: presence of micropollutants in the source water, treatment efficiencies, produced water quality and associated human health risk. In this work, an advanced approach, based on Maximum Likelihood Estimation method for left-censored data (MLELC), was applied on monitoring data of 19 contaminants (metals, volatile organic compounds, pesticides and perfluorinated compounds) in 5362 groundwater (GW) and 12,344 drinking water (DW) samples, collected from 2012 to 2017 in 28 drinking water treatment plants in an urbanized area. This study demonstrates the benefits of MLELC method, especially for high percentages of censored data. Data are used to build statistical distributions which can be effectively used for several applications, such as the time trend evaluation of GW micropollutant concentrations and the estimation of treatment removal efficiency, highlighting the adequacy or the need for an upgrade. Moreover, the MLELC method has been applied to assess the human health risk associated with micropollutants, indicating the high discrepancy in the estimations obtained with conventional methods, whose results do not follow precautionary or sustainability criteria.

Water Browning Controls Adaptation and Associated Trade-Offs in Phytoplankton Stressed by Chemical Pollution.

The acquisition of tolerance to an environmental stressor can result in organisms displaying slower growth after stress release. While well-grounded in the theory, empirical evidence of the trade-off between stress tolerance and organism fitness is scarce and blurred by the interaction with different environmental factors. Here, we report the effects of water browning on the responses, tolerance acquisition, and associated trade-offs in a population of microalgae exposed to sublethal concentrations of organic micropollutants over multiple generations. Our results show that dissolved organic matter (DOM) reduces toxic responses and modulates tolerance acquisition by the algae, possibly by complexing micropollutants. Microalgae that acquire tolerance allocate resources to fitness at the cost of reduced cell size. They yield higher productivity than nonadapted ones when grown in the presence of micropollutants but lower in their absence. The net trade-off was positive, indicating that adaptation can result in a higher productivity and fitness in tolerant species in recurrently stressed environments.

Biodegradation and adsorption of micropollutants by biological activated carbon from a drinking water production plant

The presence of micropollutants in surface water is a potential threat for the production of high quality and safe drinking water. Adsorption of micropollutants onto granular activated carbon (GAC) in fixed-bed filters is often applied as a polishing step in the production of drinking water. Activated carbon can act as a carrier material for biofilm, hence biodegradation can be an additional removal mechanism for micropollutants in GAC filters. To assess the potential of biofilm to biodegrade micropollutants, it is necessary to distinguish adsorption from biodegradation as a removal mechanism. We performed experiments at 5 °C and 20 °C with biologically active and autoclaved GAC to assess the biodegradation of micropollutants by the biofilm grown on the GAC surface. Ten micropollutants were selected as model compounds. Three of them, iopromide, iopamidol and metformin, were biodegraded by the GAC biofilm. Additionally, we observed that temperature can increase or decrease adsorption, depending on the micropollutant studied. Finally, we compared the adsorption capacity of GAC used for more than 100,000 bed volumes and fresh GAC. We demonstrated that used GAC shows a higher adsorption capacity for guanylurea, metformin and hexamethylenetetramine and only a limited reduction in adsorption capacity for diclofenac and benzotriazole compared to fresh GAC.

Screening of chemicals with binding activities of liver X receptors from reclaimed waters

Wastewater reclamation and reuse is considered an attractive and practical method for coping with water scarcity. However, the presence of micropollutants in reclaimed water, including endocrine disrupting chemicals (EDCs), is a major public health concern. This study attempted to identify unknown EDCs with liver X receptor (LXRα) agonist/antagonist activities in reclaimed wastewater, using nuclear receptors binding extraction coupled with high-resolution mass spectrometry (NRBE-HRMS). In total, 105 compounds in the reclaimed wastewater exhibited LXRα-binding activity. Among them, two previously unknown LXRα-antagonist compounds, catechol and 4-acetamidoantipyrine, were identified, based on authentic standards. The two LXRα-antagonist compounds exhibited weak LXRα-antagonist activities in a yeast two-hybrid assay. Catechol and 4-acetamidoantipyrine inhibited the β-galactosidase activity induced by 60 nM of TO901317 in an LXRα yeast assay, with IC20 values of 79,938.9 nM and 6286.4 nM, respectively. To the best of our knowledge, this is the first study to identify EDCs in reclaimed wastewater with LXRα-agonist/antagonist activity using the NRBE-HRMS method.

The potential of the organic micropollutants emission from swimming accessories into pool water

The potential leaching of organic micropollutants from swimming accessories was studied in the laboratory experiment. Seventeen different swimming accessories have been placed in various water matrices under different conditions in order to reproduce the actual environmental conditions of swimming pool water. The presence of micropollutants in water samples, after the exposure of swimming accessories, was assessed using indirect indicators (Total Organic Carbon and Phenol Index) and directly using a gas chromatograph coupled with a mass spectrometer with electron ionization. A wide range of organic compounds emitted from swimming accessories have been identified. The most common in tested samples was isophorone. The frequency of its occurrence in 50 swimming pools located in Poland was equal to 89% in concentrations ranged from 0.75 to 1.01 µg L−1 (below the concentration of 40 µg L−1, which is estimated to increase the cancer risk). Content of combined chlorine (1.52–3.16 mgCl2 L−1) in chlorinated matrices indicated a high potential for disinfection by products (DBPs) formation from organic matter emitted into pool water from swimming accessories. Ten of seventeen tested samples showed the toxic effect, measured as the bioluminescence inhibition of bacteria Aliivibrio fischeri.