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The research was done with partial filling micellar electrokinetic chromatography, microemulsion electrokinetic chromatography, and ultra-high performance liquid chromatography. The study focuses on determination of male and female steroids from cold and hot tap water of households in Helsinki City. The district ' s raw water is made run from Paijanne Lake through a water tunnel to the purification plants in Helsinki area. The effluents delivered from the plants to households as tap water were sampled and used for the study. They were concentrated with solid phase extraction to exceed the detection limits of the three methods. With partial filling method the limits were 0.50, 0.48, 0.33, and 0.50 mg/L for androsterone, testosterone, progesterone, and testosterone-glucuronide, respectively. In microemulsion method the limit values were 1.33, 1.11, and 0.40 mg/L for androsterone, testosterone, and progesterone, respectively, and 0.83, 0.45, and 0.50 mg/L for hydrocortisone, 17-alpha-hydroxyprogesterone, and 17-alpha-methyltestosterone, respectively. In the tap water samples, progesterone concentrations represented the highest values being 0.22 and 1.18 ng/L in cold and hot water, respectively. They also contained testosterone (in all samples), its glucuronide metabolite (in 25% of the samples), and androstenedione (in 75% of the samples). The ultra-high liquid chromatographic method with mass spectrometric detection was used for identification of the steroids at mu g/L level. (c) 2021 Elsevier B.V. All rights reserved.

Acetaminophen (paracetamol) (PAR) is one of the most popular non-steroidal anti-inflammatory drugs (NSAIDs) with analgesic and antipyretic properties consumed worldwide and often detected in the aquatic environment. Due to the fact that PAR induces oxidative stress in mammals, the aim of this study was to evaluate if similar effects were observed in oysters Crassostrea gigas, given their economic and ecological importance and world-wide distribution. Oysters were exposed for 1, 4 and 7 days to two different sublethal PAR concentrations (0, 1 and 100 mu g L-1). Cell viability, DNA damage in hemocytes and enzymatic activities of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidases (GPx), glutathione reductase (GR), glucose 6-phosphate dehydrogenase (G6PDH) and glutathione S-transferases (GST) were evaluated in oyster gills. In addition, changes at transcriptional level of Cu/Zn superoxide distnutase (SOD), catalase-like (CAT-like), cytochrome P450 genes (CYP30C1, CYP2AU2, CYP3071A1, CYP356A1), glutathione S-transferase isoforms (GST-omega and GST-pi-like), cyclooxygenase (COX), fatty acid binding proteins-like (FABP-like), and caspase genes were evaluated in oyster gills and digestive gland. No changes in cell viability and DNA damage were observed in oysters exposed to both PAR concentrations. Similarly, no significant changes were detected in the major antioxidant enzymes (except for auxiliary enzyme GR) in oyster gills, suggesting that changes in GR activity are enough to counteract a potential oxidative stress in C. gigas gills under these experimental conditions. Furthermore, changes at transcriptional level are concentration and tissue dependent. PAR elicited an inhibition of CYP30C1, CYP3071A1 and FABP-like transcripts highlighting their role in drug metabolism, transport and detoxification of PAR in the gills. GST transcript levels were type, tissue and concentration-dependent. GST-pi-like was down-regulated in oyster gills exposed to the lowest PAR concentration and up-regulated in the digestive gland of oysters exposed to the highest PAR concentration. However, GST-omega transcript levels were lower only in oysters digestive gland exposed to the lowest PAR concentration. Therefore, changes at transcriptional level were more sensitive to assess the exposure to PAR at environmental relevant concentrations. project UNIVERSAL - MCTI/CNPq [14/2012 (483028/21012-6)] MSC grant PEC-PG/CNPq CNPq [307467/2013-9] PVE-CNPq [406104/2013-1]

WOS: 000405643200003, In this Article, a new electrochemical sensor based on molecular imprinting polymer (MIP) and platinum nanoparticles (Pt NPs)/carbon nitride nanotubes (C3N4 NTs) nanocomposite was developed for atrazine (ATR) analysis. First, the structures of prepared nanocomposites and surfaces were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and energy dispersive X-ray analysis (EDX). After the characterization studies, ATR-imprinted glassy carbon electrode (GCE) based on Pt NPs/C3N4 NTs nanocomposite was developed by 100 mM phenol containing 25 nM ATR: The linearity range and the detection limit of the molecular imprinted sensor were calculated as 1.0 X 10(-12)-1.0 X 10(-10) and 1.5 X 10(-13) M, respectively. In addition, the voltammetric sensor was applied to wastewater samples with high recovery.

Current research is the first part of the BIOMETAL DEMO project, funded by the European Union, focusing on the development of complementary and modular biotreatment processes for the removal of metal ions from industrial effluents (issued from mining industry, surface treatment and ceramics). Metal bio-precipitation (in form of metal sulfides and metal phosphates) using sulfate-reducing bacteria (SRB), phytase and phosphatase enzymes, biosorption using sugar-beet pulp, algal biomass and alginate- or chitosan-based composites (immobilizing polyethyleneimine derivatives by encapsulation) have been extensively studied using synthetic and industrial effluents. These preliminary results allow designing a treatment flow-sheet including pre-treatment of the effluent using biologically-assisted precipitation followed by biosorption (for mining effluents that contain sulfate anions). For surface treatment and ceramics effluents, bio-precipitation combined with biosorption processes and physicochemical pretreatment followed by biosorption process represent, respectively, a promising solution. The carbon-source for the SRB process, the optimization of process parameters and the biosorbents have been selected taking into account both the technical performance and the economic viability. (C) 2016 Elsevier B.V. All rights reserved. European Union's Seventh Framework Programme (FP7) [619101] info:eu-repo/semantics/publishedVersion

A joint action of ssDNA aptamers and electrochemistry is a key element in developing successful biosensing platforms, since aptamers are capable of binding various targets with high specificity, and electrochemistry is one of the most sensitive techniques for on-site detections. A continuous search for improved immobilization and sensing strategies of aptamers on transducer surfaces resulted in the strategy presented in this article. The strategy is based on the covalent attachment of gold nanoparticles on the surface of glassy carbon electrodes through sulfhydryl-terminated monolayer, acting as a glue to connect AuNPs on the electrode. The covalently attached gold nanoparticles modified glassy carbon electrodes have been applied for the efficient immobilization of thiolated ssDNA probes, with a surface coverage of about 8.54 × 10 13 molecules cm −2 which was 7-fold higher than that on the electrochemically deposited gold nanoparticles. Consequently, improved sensitivity, good reproducibility and stability are achieved for electrochemical aptasensor. Combined with the high affinity and specificity of an aptamer, a simple, novel, rapid, sensitive and label-free electrochemical aptasensor was successfully fabricated for ofloxacin (OFL) detection. The linear dynamic range of the sensor varies between 5 × 10 −8 to 2 × 10 −5 M OFL with a detection limit of 1 × 10 −9 M OFL. A potential application in environmental monitoring was demonstrated by using this sensing strategy for the determination of OFL in (experimentally spiked) real samples such as tap water and effluent of sewage treatment plant. The proposed nanoaptasensor combines the advantages of the covalent attachment of neatly arranged AuNPs (enlarged active surface area and strengthened electrochemical signal) and the elimination of labels for the amplified detection of OFL, with the covalent attachment of highly specific aptamers to the surface of the modified electrode.

Nanoparticles, namely titanium dioxide (TiO2), are emerging contaminants widely used to commercial and industrial applications, are a potential hazard and can cause damage to environment and human health due to their toxicity. Therefore, their removal from the water is urgent to minimize or eliminate the adverse environmental and human effects. This work, investigates the efficiency of conventional coagulation/flocculation/sedimentation (C/F/S) from drinking water treatment to remove TiO2 nano particles (NPs) from surface waters, and pretends to understand if the removal of TiO2 NPs affects the ability of C/F/S to remove natural organic matter (NOM) and turbidity, and consequently affects the quality of the treated water. Results show that TiO2 NPs removal is high (>90%) for all the waters studied (hydrophobic and hydrophilic waters) and the treated water quality is not compromised (turbidity, Ti and Al concentrations, pH and conductivity are below the national and international guidelines). In addition, TiO2 initial concentrations, ranging between 0.2 and 10 mg/L, have not a significant impact on NPs removal by C/F/S. Therefore, the widely used polyaluminium based coagulants are effective in the removal of TiO2 NPs by conventional C/F/S treatment, but removal is strongly influenced by the water characteristics. Hydrophobic waters need a higher coagulant dose than hydrophilic waters to achieve the same TiO2 NPs removals, as well as water with higher UV254nm values. The principal mechanism involved in TiO2 NPs removal is charge neutralisation. (C) 2016 Elsevier Ltd. All rights reserved. Portuguese Foundation of Science and Technology [SFRH/BD/100402/2014]

Palm oil mill effluent (POME) is well known as agricultural wastewater that has a high potential as a medium for microalgal growth due to its high macro- and micronutrient content. The cyanobacterium Arthrospira platensis is considered as a species with a high C-phycocyanin (C-PC) content which is important for fine chemical and pharmaceutical applications. However, cultivation of A. platensis on POME to produce economically feasible amounts of C-PC has not been well explored. For this, environmental, nutritional, and cultivation modes (batch, semi-continuous) were varied to optimize C-PC productivity when cultivated at various POME concentrations. Arthrospira platensis was found to grow well on POME. Highest biomass and C-PC concentrations were found on 30–100% POME. Central composite rotatable design (CCRD) response surface methodology demonstrated that C-PC productivity was influenced by urea addition at the optimum salinity. The highest C-PC productivity was found on 100% POME during semi-continuous cultivation, while the addition of phosphorus and urea did not significantly improve C-PC productivity. By applying semi-continuous cultivation with 50% POME at the first stage and 100% POME at the second stage, a similarly high C-PC productivity (4.08 ± 1.3 mg L−1 day−1) was achieved as compared with (artificial) Zarrouk medium during batch cultivation. We conclude that, when using a two-stage semi-continuous cultivation process, A. platensis can produce economically feasible amounts of C-PC when cultivated on 100% POME.

The biodegradation of the nylon-6 precursor caprolactam by a strain of Pseudomonas jessenii proceeds via ATP-dependent hydrolytic ring-opening to 6-aminohexanoate. This non-natural ω-amino acid is converted to 6-oxohexanoic acid by an aminotransferase (PjAT) belonging to the fold type I PLP enzymes. To understand the structural basis of 6-aminohexanoatate conversion, we solved different crystal structures and determined the substrate scope with a range of aliphatic and aromatic amines. Comparison with the homologous aminotransferases from Chromobacterium violaceum (CvAT) and Vibrio fluvialis (VfAT) showed that the PjAT enzyme has the lowest KM values (highest affinity) and highest specificity constant (kcat /KM ) with the caprolactam degradation intermediates 6-aminohexanoate and 6-oxohexanoic acid, in accordance with its proposed in vivo function. Five distinct three-dimensional structures of PjAT were solved by protein crystallography. The structure of the aldimine intermediate formed from 6-aminohexanoate and the PLP cofactor revealed the presence of a narrow hydrophobic substrate-binding tunnel leading to the cofactor and covered by a flexible arginine, which explains the high activity and selectivity of the PjAT with 6-aminohexanoate. The results suggest that the degradation pathway for caprolactam has recruited an aminotransferase that is well adapted to 6-aminohexanoate degradation. This article is protected by copyright. All rights reserved.

Agriculture has been implicated as a potential driver of human infectious diseases. However, the generality of disease-agriculture relationships has not been systematically assessed, hindering efforts to incorporate human health considerations into land-use and development policies. Here we perform a meta-analysis with 34 eligible studies and show that people who live or work in agricultural land in Southeast Asia are on average 1.74 (CI 1.47–2.07) times as likely to be infected with a pathogen than those unexposed. Effect sizes are greatest for exposure to oil palm, rubber, and non-poultry based livestock farming and for hookworm (OR 2.42, CI 1.56–3.75), malaria (OR 2.00, CI 1.46–2.73), scrub typhus (OR 2.37, CI 1.41–3.96) and spotted fever group diseases (OR 3.91, CI 2.61–5.85). In contrast, no change in infection risk is detected for faecal-oral route diseases. Although responses vary by land-use and disease types, results suggest that agricultural land-uses exacerbate many infectious diseases in Southeast Asia., Here, Shah et al. perform a meta-analysis and show that people who live or work in agricultural land in Southeast Asia are on average 1.7 times more likely to be infected with a pathogen than controls, suggesting that agricultural land-use increases infectious disease risk.

Since the advent of soap, personal hygiene practices have revolved around removal, sterilization, and disinfection—both of visible soil and microscopic organisms—for a myriad of cultural, aesthetic, or health-related reasons. Cleaning methods and products vary widely in their recommended use, effectiveness, risk to users or building occupants, environmental sustainability, and ecological impact. Advancements in science and technology have facilitated in-depth analyses of the indoor microbiome, and studies in this field suggest that the traditional “scorched-earth cleaning” mentality—that surfaces must be completely sterilized and prevent microbial establishment—may contribute to long-term human health consequences. Moreover, the materials, products, activities, and microbial communities indoors all contribute to, or remove, chemical species to the indoor environment. This review examines the effects of cleaning with respect to the interaction of chemistry, indoor microbiology, and human health. Published version

The use of organic amendments in agriculture is a common practice due to their potential to increase crop productivity and enhance soil health. Indeed, organic amendments of different origin and composition (e.g., animal slurry, manure, compost, sewage sludge, etc.) can supply valuable nutrients to the soil, as well as increase its organic matter content, with concomitant benefits for soil health. However, the application of organic amendments to agricultural soil entails a variety of risks for environmental and human health. Organic amendments often contain a range of pollutants, including heavy metals, persistent organic pollutants, potential human pathogens, and emerging pollutants. Regarding emerging pollutants, the presence of antibiotic residues, antibiotic-resistant bacteria, and antibiotic-resistance genes in agricultural amendments is currently a matter of much concern, due to the concomitant risks for human health. Similarly, currently, the introduction of microplastics to agricultural soil, via the application of organic amendments (mainly, sewage sludge), is a topic of much relevance, owing to its magnitude and potential adverse effects for environmental health. There is, currently, much interest in the development of efficient strategies to mitigate the risks associated to the application of organic amendments to agricultural soil, while benefiting from their numerous advantages. J.U. was the recipient of a predoctoral fellowship from the Department for Economic Development and Infrastructures of the Basque Government

Using periodic density functional theory calculations combined with four dispersion-correction schemes, we have investigated the adsorption of phenol, toluene and water for various cation-exchanged faujasite zeolites. In the context of purifying the biofuels derived from the catalytic cracking of lignocellulosic bio-oils in a fluid catalytic cracking (FCC) unit, our aim was to find a suitable material with a higher affinity for phenol versus toluene and water, which are also present in the biofuel charge. In order to identify the most promising adsorbent materials, we have undertaken a full screening of monovalent cations which can be incorporated into the faujasite-type zeolite (FAU). We have evidenced that phenol can be adsorbed in two modes: O-interaction (where phenol is adsorbed via its oxygen) and π-interaction (where phenol is adsorbed via its aromatic ring). The screening of the interaction energies of the different exchanged zeolites showed that over HFAU the phenol is selectively adsorbed via O-interaction, contrary to what is observed over alkali and transition metal exchanged zeolites where the π-interaction dominates for the adsorption of phenol, leading to weaker interaction with the zeolite compared to toluene. On the Lewis modeled acid sites, namely the defect Lewis acid site (D-LAS) and the extraframework Lewis acid site (EX-LAS), the two interaction modes of phenol show almost equivalent interaction energies. In terms of selectivity, HFAU is the most selective to phenol adsorption towards O-interaction even in the presence of toluene and H2O molecules. Both adsorption modes of phenol present a higher interaction energy than those of toluene and H2O once adsorbed over an EX-LAS. The alkali and metallic cations have a high affinity for toluene molecules, which prohibit their use for the biofuel purification process.

Chitin is an abundant polysaccharide primarily produced as an industrial waste stream during the processing of crustaceans. Despite the limited applications of chitin, there is interest from the medical, agrochemical, food and cosmetic industries because it can be converted into chitosan and partially acetylated chitosan oligomers (COS). These molecules have various useful properties, including antimicrobial and anti-inflammatory activities. The chemical production of COS is environmentally hazardous and it is difficult to control the degree of polymerization and acetylation. These issues can be addressed by using specific enzymes, particularly chitinases, chitosanases and chitin deacetylases, which yield better-defined chitosan and COS mixtures. In this review, we summarize recent chemical and enzymatic approaches for the production of chitosan and COS. We also discuss a design-of-experiments approach for process optimization that could help to enhance enzymatic processes in terms of product yield and product characteristics. This may allow the production of novel COS structures with unique functional properties to further expand the applications of these diverse bioactive molecules.

Mesoporous silica-coated solid phase microextraction (SPME) Arrow systems were developed for capturing of low-molecular-weight aliphatic amines (LMWAAs) from complicated sample matrices. Specifically, silicas of type MCM-41, SBA-15 and KIT-6 were chosen as substrates to afford size-exclusion selectivity. They possess ordered multidimensional pore-channel structures and mesopore sizes between 3.8 and 8.2 nm. Their surface acidity was enhanced by grafting them with a layer of titanium hydrogenphosphate (-TP). This enhanced the chemical selectivity for basic LMWAAs. The siliceous coatings increased the extraction of ethylamine, diethylamine (DEA) and triethylamine (TEA) by factors of 18.6–102.5, 4.8–10.8 and 2.6–4.0, respectively, when compared to the commercial SPME Arrow with polydimethylsiloxane/divinylbenzene coating. Among them, the MCM-41 and MCM-41-TP coated SPME Arrows demonstrated exceptional selectivity towards LMWAAs that were quantified by gas chromatography-mass spectrometry (GC-MS). The total peak area ratios of LMWAAs/ten competing compounds were 25.4 and 36.3, respectively. The extraction equilibrium was reached within 20–30 min. The MCM-41 and MCM-41-TP derived SPME Arrows gave very similar results (18.4 ± 2.1–376 ± 12 ng g−1 to DEA and TEA) when applied to urban mushroom samples. SPME Arrow with MCM-41 coatings followed by GC-MS was applied also to the analysis of atmospheric air and urine samples resulting in high selectivity due to the size and mesoporous structure of the functionalized silica, and its chemical interactions with the LMWAAs. Graphical abstractScheme of synthesis of the MCM-41 silicas, and the preparation of solid phase microextraction Arrow coatings. They were employed for selective capturing of aliphatic amines from complex sample matrices, followed by gas chromatography-mass spectrometry. Electronic supplementary material The online version of this article (10.1007/s00604-019-3523-5) contains supplementary material, which is available to authorized users.

Antibiotic resistance and its environmental component are gaining more attention as part of combating the growing healthcare crisis. The One Health framework, promulgated by many global health agencies, recognizes that antimicrobial resistance is a truly inter-domain problem in which human health, animal agriculture, and the environment are the core and interrelated components. This prospectus presents the status and issues relevant to the environmental component of antibiotic resistance, namely, the needs for advancing surveillance methodology: the environmental reservoirs and sources of resistance, namely, urban wastewater treatment plants, aquaculture production systems, soil receiving manure and biosolid, and the atmosphere which includes longer range dispersal. Recently, much work has been done describing antibiotic resistance genes in various environments; now quantitative, mechanistic, and hypothesis-driven studies are needed to identify practices that reduce real risks and maintain the effectiveness of our current antibiotics as long as possible. Advanced deployable detection methods for antibiotic resistance in diverse environmental samples are needed in order to provide the surveillance information to identify risks and define barriers that can reduce risks. Also needed are practices that reduce antibiotic use and thereby reduce selection for resistance, as well as practices that limit the dispersal of or destroy antibiotic-resistant bacteria or their resistance genes that are feasible for these varied environmental domains.

Most of the nutrients in municipal wastewater originate from urine. Nevertheless, chemical fertilizers are commonly used in the agriculture instead of urine. There are some problems related to the direct utilization of urine, such as micropollutants present in urine, odour and storage of large volume of urine. In wastewater, phosphorus may contribute significantly to the pollution of the aquatic systems. Therefore, wastewater treatment techniques are mainly focusing on removing phosphorus. Phosphorus is collected in the sludge either by a chemical or by a biological process. With the growing concern of micropollutants present, which are in the sludge, the use of sludge in agriculture has been gradually decreasing. It means that the phosphorus content in sludge is not recycled efficiently whereas the use of limited mineral phosphorus resources is growing. To overcome these issues, urine could be collected separately and struvite could be produced. This may recover about 90 % of phosphate in urine. In this paper, the use of human urine and struvite as a fertilizer in the agriculture and the production of struvite is discussed. Results showed that the struvite could be an effective natural fertilizer.

© 2019 Tech Science Press. This paper evaluates the adsorption capacity of chemically sugarcane bagasses with sodium hydroxide (SHS), citric acid (CAS), tartaric acid (TAS) and unmodified sugarcane bagasse (SB) for cadmium adsorption in water environment. The results prove adsorption capacity for Cd (II) increases after chemical modification and the adsorption fits perfectly with the Langmuir isotherm. CAS had the highest maximum adsorption capacity of 45.45 mg/g followed by TAS with 38.46 mg/g and SHS with 29.41 at optimum pH 5.0 and 120 minutes equilibrium time while 1 g SB removed 18.8 mg Cd (II) in the same conditions. The kinetics study of the process followed a pseudo-second-order rate expression, that indicated a strong interaction between the biosorbents and adsorbate. The sugarcane bagasse and modified sugarcane bagasse were characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) analysis. The chemical modification was confirmed by the presence of carboxyl and esters groups created at 1,738 cm-1. The estimation of acid groups in modified materials shows the enhancement of this group after modification. On the other hand, desorption studies showed the high leaching of cadmium ion from the biosorbent leading to the efficient re-utilization of materials. ispartof: JOURNAL OF RENEWABLE MATERIALS vol:7 issue:5 pages:415-428 status: published

The nanoporous oxide 12CaO ⋅ 7Al2O3 (C12A7) offers the possibility of capturing large concentrations of environmentally damaging extra-framework species in its nanopores. Using density functional theory with a dispersion correction, we predict the structures and energetics of some heavy metals (Cr, Ni, Cu, Zn, Cd, Hg, and Pb) trapped by the stoichiometric and electride form of C12A7. In the stoichiometric form, while Zn, Cd, Hg, and Pb are encapsulated weakly, Cr, Ni, and Cu exhibit strong encapsulation energies. The electride form of C12A7 shows a significant enhancement in the encapsulation of Cr, Ni, Cu, and Pb. Successive encapsulation of multiple Cr, Ni, Cu, and Pb as single species in adjacent cages of C12A7 is also energetically favorable.

The present study investigates the photocatalytic degradation of three quinolone antibiotics (i.e., Flumequine (FLU), Oxolinic Acid (OA) and Nalidixic Acid (NA)) in mono-, binary and ternary compound systems. The closed-loop step photo-reactor and TiO2 impregnated on cellulosic paper as supported photo-catalyst in presence of UV light irradiation were used. The degradation of FLU occurred within 4 h. A 65.4% mineralization of OA was observed in a mono-compound system, due to the fast conversion of these main by-products formed. Besides, the investigation of the contribution of free radicals revealed the involvement of hole (h(+)), O-2(center dot-), but mainly "OH on the degradation of OA. The second-order kinetic rate constants calculated relative to the contribution of (OH)-O-center dot radicals on the degradation of OA was 4.03 x 10(9) M(-1)s(-1), whereas for that of NA was 4.42 x 10(9) M(-1)s(-1), thus underscoring that (OH)-O-center dot coproduct is the primary reactive species implicated in the photocatalytic degradation of these compounds on TiO2/cellulosic paper catalysts. The mono-compound system shows a higher degradation rate compared to multi-compound system (binary and ternary) which explained by the competitive adsorption of antibiotics on the available active sites of photocatalyst surface. Overall, the constant photocatalytic rates are higher following this order: mono compound system > ternary mixture >binary mixture. The catalyst was characterized by mean of FTIR, HR-TEM and XRD. The SiO2-binder role was discussed in details based on the atomic distribution of elements on the cellulose fibers as shown by the EDS atomic mapping. (C) 2019 Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.

Urine contains sufficient phosphorus (P) to consider P recycling form urine as an interesting strategy. In this study, the potential of MgAl or ZnAl layered double hydroxides (LDHs) to be used in such recovery was assessed. LDHs are anion exchangers with a high P selectivity, and P-loaded LDHs have demonstrated fertiliser potential. A critical factor for efficient P recycling with LDH is the stability of these materials, which can be compromised by urinary citrate, complexing aluminium (Al3+) and by the low pH of fresh urine dissolving the alkaline LDHs. Different phase pure ZnAl and MgAl LDHs were synthesised by coprecipitation in scenarios of varying synthesis pH and Mg/Al or Zn/Al ratios. The obtained materials were incubated in P solutions at different pH, with or without citrate in full factorial combinations, and in fresh and stored human urine. The P sorption capacities increased for LDHs synthesised at lower pH, at increasing Al content and for sorption solutions with lower pH. These trends are explained by an increased anion exchange capacity (AEC) and by P speciation (charge) in the LDHs, an interpretation supported by XRD measurements. The P capacity reached 61mg P/g LDH, which equals 85% of the theoretical LDH exchange capacity. Only 1g LDH is required to remove 90% of P from 1L urine and evidence is found that sorption, not struvite precipitation, is the P removal mechanism involved. The ZnAl LDHs were equally effective in P uptake compared to the MgAl LDHs, but the ZnAl materials showed more irreversible P sorption in contrast with the high desorption yields (53mg P/g) of the MgAl LDHs. Therefore, the large potential of MgAl LDHs for P recovery from urine is supported by this study. ispartof: SCIENCE OF THE TOTAL ENVIRONMENT vol:682 pages:437-446 ispartof: location:Netherlands status: published

Assessing global water quality issues requires a multi-pollutant modelling approach. We discuss scientific challenges and future directions for such modeling. Multi-pollutant river models need to integrate information on sources of pollutants such as plastic debris, nutrients, chemicals, pathogens, their effects and possible solutions. In this paper, we first explain what we consider multi-pollutant modelling. Second, we discuss scientific challenges in multi-pollutant modelling relating to consistent model inputs, modelling approaches and model evaluation. Next, we illustrate the potential of global multi-pollutant modelling for hotspot analyses. We show hotspots of river pollution with microplastics, nutrients, triclosan and Cryptosporidium in many sub-basins of Europe, North America and South Asia. Finally, we reflect on future directions for multi-pollutant modelling, and for linking model results to policy-making.

Over the past decade, the health care sector has become increasingly aware of the impact of pharmaceutical emissions to the environment. Yet, it remains unclear which compounds are the most relevant to address and at what point emission control is most effective. This study presents a modelling framework to prioritize pharmaceuticals based on their relative risks for aquatic organisms, using purchase and prescription data from hospitals. The framework consists of an emission prediction module and a risk prioritization module. The emission prediction module accounts for three different routes of intake (oral, intravenous, rectal), for non-patient consumption, and for delayed athome excretion due to relatively long half-lives or prescription durations of selected pharmaceuticals. We showcase the modelling framework with 16 pharmaceuticals administered at two Dutch academic hospitals. Predictions were validated with experimental data from passive sampling in the sewer system. With the exception of metformin, all predictions were within a factor of 10 from measurements. The risk prioritization module ranks each pharmaceutical based on its predicted relative risk for aquatic organisms. The resulting prioritization suggests that emission mitigation strategies should mainly focus on antibiotics and non-steroidal anti-inflammatory drugs (NSAIDs).

The treatment of nitrogen-deficient agriculture wastewater, arising from the vegetable and fruit processing, is a significant problem that limits the efficiency of its biological treatment. This study evaluates the effectiveness of the symbiotic co-culture of Azospirillum brasilense and Scenedesmus sp., under two nitrogen levels (8.23 mg L&minus, 1 and 41.17 mg L&minus, 1) and mixing systems (aeration and magnetic stirring), aiming to simultaneously use the N-deficient media for their growth while producing biomass for biofuels. Microalgae growth and biomass composition, in terms of protein, carbohydrate and fatty acid contents, were evaluated at the end of the exponential growth phase (15 days after inoculation). Results show that the symbiotic co-culture of microalgae-bacteria can be effectively performed on nitrogen-deficient media and has the potential to enhance microalgae colony size and the fatty acid content of biomass for biofuels. The highest biomass concentration (103 &plusmn, 2 mg&middot, L&minus, 1) was obtained under aeration, with low nitrogen concentration, in the presence of A. brasilense. In particular, aeration contributed to, on average, a higher fatty acid content (48 &plusmn, 7% dry weight (DW)) and higher colony size (164 &plusmn, 21 &micro, m2) than mechanical stirring (with 39 &plusmn, 2% DW and 134 &plusmn, m2, respectively) because aeration contribute to better mass transfer of gases in the culture. Also, co-culturing contributed in average, to higher colony size (155 &plusmn, m2) than without A. brasilense (143 &plusmn, m2). Moreover, using nitrogen deficient wastewater as the culture media can contribute to decrease nitrogen and energy inputs. Additionally, A. brasilense is approved and already extensively used in agriculture and wastewater treatment, without known environmental or health issues, simplifying the biomass processing for the desired application.

With the growth in production and use of chemicals and the fact that many end up in the aquatic environment, there is an increasing need for advanced water treatment technologies that can remove chemicals of emerging concern (CECs) from water. The current lack of a homogenous approach for testing advanced water treatment technologies hampers the interpretation and evaluation of CEC removal efficiency data, and hinders informed decision making by stakeholders with regard to which treatment technology could satisfy their specific needs. Here a data evaluation framework is proposed to improve the use of current knowledge in the field of advanced water treatment technologies for drinking water and wastewater, consisting of a set of 9 relevance criteria and 51 reliability criteria. The two criteria sets underpin a thorough, unbiased and standardised method to select studies to evaluate and compare CEC removal efficiency of advanced water treatment technologies in a scientifically sound way. The relevance criteria set was applied to 244 papers on removal efficiency, of which only 20% fulfilled the criteria. The reliability criteria were applied to the remaining papers. In general these criteria were fulfilled with regards to information on the target compound, the water matrix and the treatment process conditions. However, there was a lack of information on data interpretation and statistics. In conclusion, a minority of the evaluated papers are suited for comparison across techniques, compounds and water matrixes. There is a clear need for more uniform reporting of water treatment studies for CEC removal. In the future this will benefit the selection of appropriate technologies., Water Research, 161, ISSN:0043-1354, ISSN:1879-2448