Organic Micropollutants Research Articles

Interfacial engineering of BiVO4/PANI p-n heterojunction for enhanced photocatalytic degradation of p-nitrophenol: Pathway, toxicity evaluation and mechanistic insights

The presence of organic micro-pollutants (OMPs) in the water sources is a major threat to the aquatic and human health and also affects the wastewater treatment process. p-Nitrophenol (p-NP), has been extensively used as raw materials in various chemical industries. The present study focused on the development of BiVO4/PANI nanocomposites (NCs) for enhanced photocatalytic degradation of p-NP under visible light irradiation. The morphology, chemical composition and crystallinity of the prepared NCs was characterized by XRD, XPS, FE-SEM, RAMAN, EIS and TEM, and the optical properties of the NCs were determined by UV–vis DRS, and PL analysis. Compared to the bare BiVO4 and PANI, the NCs showed a better performance against p-NP (98.25 %) and had good cycle stability (91.91 % after six cycles). The enhance photocatalytic performance of the NCs is ascribed to the synergistic effect and the p-n heterojunction formed between BiVO4 and PANI. Furthermore, several tests were done to determine the effect of pH, NCs and p-NP concentrations and influence of various ions were also studied. Scavenger experiments revealed that •OH, and h+ contributed significantly in the degradation process of p-NP. The intermediate metabolites were identified, and toxicity of the by-products was elucidated by using GC–MS and ECOSAR program respectively. The reusability of the material was assessed by repeating the degradation experiment for 6 consecutive cycles. This work underlines the promising potential of BiVO4/PANI NCs for efficient treatment of toxic pollutants bearing wastewater.

From shower to table: fate of organic micropollutants in hydroponic systems for greywater treatment and lettuce cultivation

ABSTRACT This study evaluated the dual functionality of hydroponic systems to grow edible crops while treating greywater (GW) containing 20 organic micropollutants (OMPs). Various conditions with differing nutrient contents were tested: raw GW, GW with struvite, and GW with commercial nutrient solution. System performance was assessed with plant growth and standard parameters and OMP removal. After 4-week exposure, all conditions produced healthy-looking plants, proving GW as a viable hydroponic growth medium. However, only the condition with commercial solution yielded plants comparable to the biotic control, indicating the necessity of nutrient supplementation. Effluent from conditions with well-developed plants met the requirements of the European water reuse legislation (EU 2020/741) for scenarios B–D (food crops not in direct contact with the reclaimed water and industrial crops), and had the highest OMP removal, showcasing the effectiveness of the system for OMP treatment. Estimated calculations of OMP detected in leaves (10/20 OMP detected, predominantly positive and small) resulted in calculated potential human health risks through lettuce intake for two compounds: atenolol and epoxycarbamazepine. These findings support a continued evaluation of the behavior of other OMPs and their transformation products in water–plant systems, and their consideration in legislation on water reuse and food safety.

Ultrasound-assisted extractive-catalytic removal of micro-organic pollutants in liquid hydrocarbon fuels using highly active ZnO nanoparticles supported zinc-substituted phosphotungstate

To produce ultra-low sulfur diesel (ULSD), it is necessary to remove compounds such as 2-methylthiophene and 3-methylthiophene that cannot be isolated by conventional industrial methods. This paper presents, a phosphotungstate catalyst improved with zinc atoms placed on the surface of super active zinc oxide nanoparticles and is able to switch between two phases using a hydrophobic ionic liquid (transfer agent). Here, is a description of the synthesis of the α-keggin type hybrid nanocatalyst and its application for the removal of 2- methylthiophene and 3-methylthiophene. The nanocatalyst was subjected to various characterization techniques, including Fourier Transform Infrared Spectrometer (FTIR), X-ray diffraction (XRD), Scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) Surface Area Analysis, Barrett-Joyner-Halenda (BJH) pore size and volume analysis and Energy-dispersive X-ray analysis(EDAX). The optimized conditions for the ultrasound-assisted extractive-catalytic oxidative desulfurization (UA-ECODS) process were determined using a statistical design, specifically the Box-Behnken design (BBD), which was proposed as a plan for designing experiments and studying the behavior of the parameters. The optimal conditions, which encompass four parameters, namely ultrasonic time, reactor temperature, amount of nanocatalyst, and oxidant concentration, are archived as 14.43 min, 40.52 °C, 86.27 mg catalyst, and 24 % H2O2 Respectively. The results indicated that the removal efficiency was higher for 2- methylthiophene than 3-methylthiophene. The paper concludes that the UA-ECODS method utilizing the synthesized nanocatalyst is a promising and effective approach for desulfurizing of liquid hydrocarbon fuels.

Rational design of a hydrophilic nanoarray-structured electro-Fenton membrane for antibiotics removal and fouling mitigation: An intensified catalysis process in an oxygen vacancy‐mediated cathodic microreactor

Electro-Fenton membranes (EFMs) can synchronously realize organic micropollutants destruction and fouling mitigation in a single filtration process with the assistance of hydroxyl radicals (•OH). Herein, a nanoarray-structured EFM (NS-EFM) was designed by assembling Fenton reactive CoFe-LDH nanowires using a low-temperature hydrothermal method. Combined with a defect-engineering strategy, the oxygen vacancies (OVac) in the CoFe-LDH nanoarrays were tailored by manipulating the stoichiometry of cations to optimize the Fenton reactivity of NS-EFMs. The optimized NS-EFM demonstrated exceptional sulfamethoxazole (SMX) removal (99.4%) and fast degradation kinetics (0.0846 min−1), but lower energy consumption (0.22 kWh m−3 per log removal of SMX). In-depth mechanism analysis revealed that the intrinsic electronic properties of OVac endowed NS-EFM with enhanced reactivity and charge transferability at metallic active sites of CoFe-LDH, thereby intensifying •OH generation. Besides, the nanoarray-structured NS-EFM built a confined microreactor space, leading to expedited •OH microflow to SMX. Meanwhile, the hydrophilic nature of CoFe-LDH nanoarrays synergistically contributed to the high flux recovery (95.0%) and minimal irreversible membrane fouling (5.0%), effectively alleviating membrane fouling within pores and on surfaces. This study offers insights into the potential of defect engineering as a foundational strategy in the design of EFMs, significantly advancing the treatment of organic pollutants and control of membrane fouling.

Investigation of organic micropollutant pollution in İzmit Bay: a comparative study of passive sampling and instantaneous sampling techniques.

In this study, we used a comprehensive array of sampling techniques to examine the pollution caused by organic micropollutants in İzmit Bay for the first time. Our methodology contains spot seawater sampling, semi-permeable membrane devices (SPMDs) passive samplers for time-weighted average (TWA), and sediment sampling for long-term pollution detection in İzmit Bay, together. Additionally, the analysis results obtained with these three sampling methods were compared in this study. Over the course of two seasons in 2020 and 2021, we deployed SPMDs for 21days in the first season and for 30days in the second season. This innovative approach allowed us to gather sea water samples and analyze them for the presence of polycyclic aromatic hydrocarbons (Σ15 PAHs), polychlorinated biphenyls (Σ7 PCBs), and organochlorine pesticides (Σ11 OCPs). Using SPMD-based passive sampling, we measured micropollutant concentrations: PAHs ranged from 1963 to 10342pg/L in 2020 and 1338 to 6373pg/L in 2021; PCBs from 17.46 to 61.90pg/L in 2020 and 8.37 to 78.10pg/L in 2021; and OCPs from 269.2 to 8868pg/L in 2020 and 141.7 to 1662pg/L in 2021. Our findings revealed parallels between the concentrations of PAHs, PCBs, and OCPs in both SPMDs and sediment samples, providing insights into the distribution patterns of these pollutants in the marine ecosystem. However, it is worth noting that due to limited data acquisition, the suitability of spot sampling in comparison to instantaneous sampling remains inconclusive, highlighting the need for further investigation and data collection.

Identifying organic micropollutants' transformation products from the soil dissipation experiment by non-targeted high-resolution mass spectrometry approach: Can we gain more than transformation product identity?

Risk assessment of environmental hazards originating from xenobiotics extensively used worldwide (e.g., pharmaceuticals, bisphenols, or preservatives) requires a combined study of their effects, mobility, dissipation mechanisms, and subsequent transformation product identification and evaluation. We have developed an efficient accelerated solvent extraction method for a broad range of micropollutants of variable physical-chemical properties in soils to enable more accurate hazard characterisation. Micropollutant recoveries from freeze-dried soils were 60–120%, with the exception of atorvastatin, fexofenadine, and telmisartan, which had reduced recoveries (40–66%). The observed matrix effect ranged from −26% to 17% and was corrected by the matrix matching standard for quantitative analysis. The method allows sensitive and reliable determination of a wide range of analytes in soil samples and, consequently, qualitative analysis of transformation products (TP) with variable physicochemical properties. We identified TPs of five compounds (venlafaxine, telmisartan, valsartan, atorvastatin, and sertraline) by applying suspect and non-targeted data analyses. To our knowledge, the transformation product of atorvastatin was reported for the first time. All others were found in soil or other matrices. Valsartan (formed valsartan acid) and atorvastatin (transformed probably by oxidative decarboxylation of beta, delta dihydroxy heptanoic acid chain to propionic acid) were modified to a relatively large extent. All other compounds identified were only hydroxylated (sertraline and telmisartan) or demethylated (venlafaxine). We estimated the stability and presence of the identified TPs based on the constructed time trends and the ratio between TP formation and degradation rates. We demonstrated how valuable a non-targeted approach can be for complex evaluation of the fate and effect of soil pollutants.

Fast sintering of titania monoliths for photocatalytic degradation of organic micropollutants

Scalable solutions to efficiently remove organic micropollutants from water are urgently needed to address the significant adverse health effects their accumulation causes on the environment and in humans. Solutions based on slurries of titania (TiO2) nanoparticles, while effective in the lab, cannot be scaled up due to cost and environmental concerns. Conversely, titania monolithic structures are not photoactive as high sintering temperatures result in the predominance of the non-photoactive rutile phase. In this work the combination of 3D printing and fast sintering allowed, for the first time, to obtain titania monoliths which are mechanically stable and retain their photoactivity. The latter arises from the anatase-rich composition of the monoliths, a result not possible using convectional sintering methods. To demonstrate their photoactivity, the porous monoliths were used in a recirculating flow reactor to degrade primidone, a widely used drug and ubiquitous micropollutant. Results for the best performing monolith showed a quantum yield value of 1.1 × 10−5and an electrical energy per order value of 13 kWh m−3, both significantly outperforming literature data. These results show a clear route to scaling-up the fabrication of photocatalytically active titania monoliths capable of effectively degrading organic micropollutants in water, whose presence is a major health and environmental hazard.

Reusable and inductively regenerable magnetic activated carbon for removal of organic micropollutants from secondary wastewater effluents

This work introduces a new sustainable alternative of powdered activated carbon (PAC) - magnetically harvestable and reusable after regeneration via inductive heating - for the adsorptive removal of organic micropollutants (OMP) from secondary wastewater effluents. For this purpose, two commercial PACs - lignite “L” (1187 m2/g) and coconut “C”-based (1524 m2/g) - were modified with magnetic iron oxide following two different synthesis approaches: infiltration (“infiltr”) and surface deposition (“depos”) route. The resulting magnetic powdered activated carbons (mPAC) and their precursor PACs were fully characterized before application. The iron oxide content of the modified “L” and “C” samples was ∼30 % and ∼20 %, respectively. Iron oxide gives the PAC beneficial magnetic properties for easy magnetic separation and simultaneously acts as an inductively heatable agent for the carbon regeneration. The infiltrated samples displayed better inductive heating performance and regeneration than their deposited counterparts. Tests with real wastewater showed fast adsorption kinetics of the organic load following the pseudo-second-order kinetic model. Adsorption isotherms were compliant with the Freundlich isotherm model. Sample “L-infiltr” had the best overall adsorption performance throughout 5 reuse cycles when intermediately inductively regenerated (<3 % drop in organics removal per cycle with intermediate regeneration vs. ∼10 % drop per cycle without regeneration). The treated supernatant was additionally tested for 31 representative organic micropollutants and their transformation products (pharmaceuticals, personal care products, industrial chemicals, etc.), where 26 OMPs had consistently high removal (>85 %) throughout 5 cycles with intermediate regeneration and for 28 OMPs the total adsorption efficiency dropped by <5 % after 5 cycles.

N-doped carbon polyhedron-modified Co@N-doped carbon nanotube with enhanced [formula omitted] production for selective removal of organic pollutants

Persulfate-based advanced oxidation process dominated by singlet oxygen (1O2) shows potential for targeted degradation of organic pollutants but the regulation of 1O2 generation is still challenging. In this study, N-doped carbon polyhedron-modified Co@N-doped carbon nanotube (NCP/Co@NCNT) were successfully fabricated. The as-obtained NCP/Co@NCNT demonstrated a much enhanced 1O2 production in activating peroxymonosulfate (PMS) because of the nanoconfinement effect of metallic Co nanoparticles encapsulated in NCNT, which was further confirmed by density functional theory calculations. The NCP/Co@NCNT/PMS system has excellent catalytic performance and is capable of removing 97 % of carbamazepine (CBZ) in 55 min (Catalyst: 0.1 g/L, CBZ: 20 mg/L, PMS: 0.5 g/L). Quantitative structure–activity relationship (QSAR) analysis uncovered a positive correlation between the oxidation kinetics of organic pollutants and their EHOMO. Specifically, pollutants with higher EHOMO are more easily oxidized in the 1O2-dominated NCP/Co@NCNT/PMS system. Furthermore, the generated intermediates exhibited low toxicity in the system with 1O2 as the primary active species. This study offers an effective approach to prepare catalysts for the selective elimination of organic micropollutants in complex water environments.

Insights into the enhanced oxidation of organic micropollutants by single-atom Cu catalyst activated peroxydisulfate: Valence-dominated nonradical pathway

Herein, we anchored Cu atoms with four N atoms into waste adsorbent-based biochar (SACu30@NC) containing both Cu(I) and Cu(II) to explore the role of different Cu valences for PDS activation mechanism. The atomic Cu was identified as the active site, and Cu(III) and electron shuttle process dominated organics degradation in SACu30@NC/PDS system. Therein, Cu(I) preferred to activate the adsorbed PDS to produce Cu(III) (Cu(I)N4-PDS→Cu(II)N4-SO4•-→Cu(III)N4-SO42-), whereas PDS adsorbed on Cu(II) surface was more likely to extract electrons from organic pollutants directly. Benefiting from non-radical process, SACu30@NC exhibited selective and anti-interference performance for organic pollutants in complex matrixes. The promising catalytic activity of SACu30@NC (BPA=50 mg/L, 100% within 180 min) with low Cu leaching (<0.1 mg/L) in continuous-flow experiments further revealed the potential of SACu30@NC for practical applications. This work provides new insights into the PDS activation mechanism by single-atom Cu catalysts and develops an efficient approach for practical wastewater purification.

Mechanically treated Mn2O3 triggers peracetic acid activation for superior non-radical oxidation of micropollutants: Identification of reactive complexes

This study used a simple mechanical ball milling strategy to significantly improve the ability of Mn2O3 to activate peracetic acid (PAA) for sustainable and efficient degradation of organic micropollutant (like bisphenol A, BPA). BPA was successfully removed and detoxified via PAA activation by the bm-Mn2O3 within 30 min under neutral environment, with the BPA degradation kinetic rate improved by 3.4 times. Satisfactory BPA removal efficiency can still be achieved over a wide pH range, in actual water and after reuse of bm-Mn2O3 for four cycles. The change in hydrophilicity of Mn2O3 after ball milling evidently elevated the affinity of Mn2O3 for binding to PAA, while the reduction in particle size exposed more active sites contributing partially to catalytic oxidation. Further analysis revealed that BPA oxidation in the ball mill-treated Mn2O3 (bm-Mn2O3)/PAA process mainly depends on the bm-Mn2O3-PAA complex (i.e., Mn(III)−OO(O)CCH3) mediated non-radical pathway rather than R-O• and Mn(IV). Especially, the existence of the Mn(III)-PAA complex was definitely verified by in situ Raman spectroscopy and in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). Simultaneously, density functional theory calculations determined that PAA adsorbs readily on manganese sites thereby favoring the formation of Mn(III)−OO(O)CCH3 complexes. This study advances an in-depth understanding of the underlying mechanisms involved in the manganese oxide-catalyzed activation of PAA for superior non-radical oxidation of micropollutants.

Peracetic acid activated by nickel cobaltite as effective oxidizing agent for BPA and its analogues degradation

The presented research concerns the use of nickel cobaltite nanoparticles (NiCo2O4 NPs) for the heterogeneous activation of peracetic acid and application of NiCo2O4-PAA system for degradation 10 organic micropollutants from the group of bisphenols. The bisphenols removal (initial concentration 1 μM) process was optimized by selecting the appropriate process conditions. The optimal amount of catalyst (115 mg/L), peracetic acid (PAA) concentration (7 mM) and pH (7) were determined using response surface analysis in the Design of Experiment. Then, NiCo2O4 NPs were used to check the possibility of reuse in subsequent oxidation cycles. The work also attempts to explain the mechanism of oxidation of the studied micropollutants. The participation of the sorption process on the catalyst was excluded and based on the experiments with radical scavengers it can be concluded that the oxidation proceeds in a radical pathway, mainly with participation of O2•- radicals. Experiments conducted in real water matrices exhibit low impact on degradation efficiency. Toxicity tests with green alga Acutodesmus obliquus and aquatic plant Lemna minor showed that post-reaction mixture influenced growth and the content of photosynthetic pigments in concentration dependent manner.

Organic Micropollutants in the Agricultural Chain of Production of Strawberries by Irrigation with Treated Wastewater and Assessment of Human Health Implications

Treated water reuse is vital for sustainable water management and reducing the strain on freshwater resources, particularly in agriculture, which has a great impact on freshwater withdrawal. Despite the benefits, the reuse of treated wastewater carries risks due to residual chemical and microbiological contaminants, such as the organic micropollutants polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs), which are not fully removed by current treatment processes and can affect plant growth and human health when used for irrigation. This study focuses on monitoring the PAHs and PCBs in wastewater used for irrigating strawberries, assessing their transfer to crops and potential health risks. The effluents of four wastewater treatment plants were monitored for two years (2017 and 2018) and used to irrigate strawberries grown in plot installations. Effective and robust analytical methodologies (60–99% recoveries, optimal reproducibility) were developed for wastewater and strawberry analysis. The analysis of the treated wastewaters showed the presence of residual PAH and PCB concentrations at hundreds of ng/L. The strawberry crops were further analyzed to measure the PAHs and PCBs. Since two PAHs were present in strawberries, a risk assessment was performed (EPA methodology), finding that the residual contamination of treated waters does not pose a significant health risk, for both adults and children, through the consumption of fruits.

Quenching residual H2O2 from UV/H2O2 with granular activated carbon: A significant impact of bicarbonate

UV/H2O2 has been used as an advanced oxidation process to remove organic micropollutants from drinking water. It is essential to quench residual H2O2 to prevent increased chlorine demand during chlorination/chloramination and within distribution systems. Granular activated carbon (GAC) filter can quench the residual oxidant and eliminate some of the dissolved organic matter. However, knowledge on the kinetics and governing factors of GAC quenching of residual H2O2 from UV/H2O2 and the mechanism underlying the enhancement of the process by HCO3− is limited. Therefore, this study aimed to analyse the kinetics and influential factors, particularly the significant impact of bicarbonate (HCO3−). H2O2 decomposition by GAC followed first-order kinetics, and the rate constants normalised by the GAC dosage (kn) were steady (1.6 × 10−3 L g−1 min−1) with variations in the GAC dosage and initial H2O2 concentration. Alkaline conditions favour H2O2 quenching. The content of basic groups exhibited a stronger correlation with the efficiency of GAC in quenching H₂O₂ than did the acidic groups， with their specific kn values being 8.9 and 2.4 min−1 M−1, respectively. The presence of chloride, sulfate, nitrate, and dissolved organic matter inhibited H2O2 quenching, while HCO3− promoted it. The interfacial hydroxyl radical (HO•) zones were visualised on the GAC surface, and HCO3− addition increased the HO• concentration. HCO3− increased the concentration of persistent free radicals (PFRs) on the GAC surface, which mainly contributed to HO• generation. A significant enhancement of HCO3− on H2O2 quenching by GAC was also verified in real water. This study revealed the synergistic mechanism of HCO3− and GAC on H2O2 quenching and presents the potential applications of residual H2O2 in the H2O2-based oxidation processes.

Magnetic nanoparticle loading and application of weak magnetic field to reconstruct the cake layer of coagulation-ultrafiltration process to achieve efficient antifouling: Performance and mechanism analysis

Abandoning the costly development of new membrane materials and instead directly remodeling the naturally occurring cake layer constitutes a dynamic, low-cost, long-lasting, and proactive strategy to "fight fouling with fouling". Several optimization strategies, including coagulation/modified magnetic seed loading and applying a weak magnetic force (0.01T) at the ultrafiltration end, improved the anti-fouling, retention, and sieving performances of conventional ultrafiltration process during the treatment of source water having complex natural organic matter (NOMs) and small molecule micropollutants. Two modified magnetic seeds we prepared were composite nano-seed particles (Fe3O4@SiO2-NH2 (FS) and Fe3O4@SiO2@PAMAM-NH2 (FSP)). Aim of the study was to regulate the formation of cake layer via comprehensive testing of the antifouling properties of optimized processes and related mechanistic studies. It was found to be essential to enhance the interception of xanthate and tryptophan proteins in the cake layer for improving the anti-fouling performance based on the correlation and redundancy analyses, while the use of modified magnetic seeds and magnetic field showed a significant positive impact on water production. Blockage modeling demonstrated the ability to form a mature cake layer during the initial filtration stage swiftly. This mitigated the risk of irreversible fouling caused by pore blockage during the early stage of coagulation-ultrafiltration. Morphologically, the reconstructed cake layer exhibited elevated surface porosity, an internal cavity channel structure, and enhanced roughness that can promote increased water flux and retention of water impurities. These optimized the maturity of the cake layer in both time and space. Density Functional Theory (DFT), Extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory, and Modified Extended Derjaguin-Landau-Verwey-Overbeek (MDLVO) calculations indicated aggregation behavior of matter on the cake layer to be enhanced effectively due to magnetic seed loading. This is mainly due to the strengthening of polar interactions, including hydrogen bonding, π-π* conjugation, etc., which can happen between the cake layer loaded with FSP and the organic matter. Under the influence of a magnetic field, magnetic force energy (VMF) significantly impacts the system by eliminating energy barriers. This research will provide innovative strategies for effectively purifying intricate source water through ultrafiltration while controlling membrane fouling.

Expression of Concern: Study on the removal of organic micropollutants from aqueous and ethanol solutions by HAP membranes with tunable hydrophilicity and hydrophobicity (Chemosphere, Vol. 174, May 2017, Pages 380–389)

Expression of Concern: Study on the removal of organic micropollutants from aqueous and ethanol solutions by HAP membranes with tunable hydrophilicity and hydrophobicity (Chemosphere, Vol. 174, May 2017, Pages 380–389)

High resolution mass spectrometry-based screening for the comprehensive investigation of organic micropollutants in surface water and wastewater from Pasto city, Colombian Andean highlands

The complexity of the aquatic environment scenario, including the impact of urban wastewater, together with the huge number of potential hazardous compounds that may be present in waters, makes the comprehensive characterization of the samples an analytical challenge, particularly in relation to the presence of organic micropollutants (OMPs). Nowadays, the potential of high-resolution mass spectrometry (HRMS) for wide-scope screening in environmental samples is out of question. Considering the physicochemical characteristics of OMPs, the coupling of liquid (LC) and gas chromatography (GC) to HRMS is mandatory. In this work, we have explored the combined use of LC and GC coupled to Quadrupole-Time-of-Flight Mass Spectrometry (QTOF MS) for screening of surface water and wastewater samples from Pasto (Nariño), a town of the Colombian Andean highlands (average altitude 2527 m), located in an important agricultural area. The upper basin of the Pasto River is impacted by phytosanitary products used in different crops, whereas the domestic wastewater is directly discharged into the river without any treatment, enhancing the anthropogenic impact on the water quality. The OMP searching was made by target (standards available) and suspect (without standards) approaches, using home-made databases containing >2000 compounds. Up to 15 pesticides (7 insecticides, 6 fungicides and 2 herbicides) were identified in the sampling point of the Pasto River up to the town, while no pharmaceuticals were found at this site, illustrating the impact of agriculture practices. On the contrary, 14 pharmaceuticals (7 antibiotics and 3 analgesics, among others) were found in river samples collected in the middle and down to the town sites, revealing the impact of the urban population. Interestingly, some transformation products, including metabolites, such as carbofuran-3-hydroxy and 4-acetylamino antipyrine were identified in the screening. Based on these data, future monitoring will apply target quantitative LC-MS/MS methods for the most relevant compounds identified.

Efficient removal of 2,4,6-trinitrotoluene (TNT) from industrial/military wastewater using anodic oxidation on boron-doped diamond electrodes

With growing public concern about water quality particular focus should be placed on organic micropollutants, which are harmful to the environment and people. Hence, the objective of this research is to enhance the security and resilience of water resources by developing an efficient system for reclaiming industrial/military wastewater and protecting recipients from the toxic and cancerogenic explosive compound—2,4,6-trinitrotoluene (TNT), which has been widely distributed in the environment. This research used an anodic oxidation (AO) process on a boron-doped diamond (BDD) electrode for the TNT removal from artificial and real-life matrices: marine water and treated wastewater. During experiments, TNT concentrations were significantly decreased, reaching the anodic degradation efficiency of above 92% within two hours and > 99.9% after six hours of environmental sample treatment. The presented results show the great potential of AO performed on BDD anodes for full-scale application in the industry and military sectors for TNT removal.

Effects of running time on biological activated carbon filters: water purification performance and microbial community evolution.

Ozone-biologically activated carbon (BAC) filtration is an advanced treatment process that can be applied to remove recalcitrant organic micro-pollutants in drinking water treatment plants (DWTPs). In this study, we continuously monitored a new and an old BAC filter in a DWTP for 1year to compare their water purification performance and microbial community evolution. The results revealed that, compared with the new filter, the use of the old BAC filter facilitated a slightly lower rate of dissolved organic carbon (DOC) removal. In the case of the new BAC filter, we recorded general increases in the biomass and microbial diversity of the biofilm with a prolongation of operating time, with the biomass stabilizing after 7months. For both new and old BAC filters, Proteobacteria and Acidobacteria were the dominant bacterial phyla. At the genus level, the microbial community gradually shifted over the course of operation from a predominance of Herminiimonas and Hydrogenophaga to one predominated by Bradyrhizbium, Bryobacter, Hyphomicrobium, and Pedomicrobium, with Bradyrhizobium being established as the most abundant genus in the old BAC filter. Regarding spatial distribution, we detected reductions in the biomass and number of operational taxonomic units with increasing biofilm depth, whereas there was a corresponding increase in microbial diversity. However, compared with the effects of time, the influence of depth on the composition of the biofilm microbial community was considerably smaller. Furthermore, co-occurrence network analysis revealed that the microbial community network of the new filter after 11months of operation was the most tightly connected, although its modular coefficient was the lowest of those assessed. We speculate that the positive and negative interactions within the network may be attributable to symbiotic or competitive relationships among species. Moreover, there may have been a significant negative interaction between SWB02 and Acidovorax, plausibly associated with a competition for substrates.

A Sustainable Banana Peel Activated Carbon for Removing Pharmaceutical Pollutants from Different Waters: Production, Characterization, and Application.

Due to the growing concerns about pharmaceutical contamination and its devastating impact on the economy and the health of humans and the environment, developing efficient approaches for removing such contaminants has become essential. Adsorption is a cost-effective technique for removing pollutants. Thus, in this work, banana peels as agro-industrial waste were utilized for synthesizing activated carbon for removing pharmaceuticals, namely amoxicillin and carbamazepine from different water matrices. The chemically activated carbon by phosphoric acid (H3PO4) was carbonized at temperatures 350 °C, 450 °C and 550 °C. The material was characterized by several techniques such as scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS), Fourier transform infrared spectroscopy (FTIR), Boehm titration, point of zero charge (pHPZC), BET surface area (SBET), the proximate and ultimate analyses, X-ray powder diffraction (XRD), and thermos-gravimetric analysis (TGA). The SEM of banana peel activated carbon (BPAC) depicted a semi-regular and heterogeneous morphology, characterized by an abundance of pores with diverse forms and sizes. Boehm titration revealed an increase in the amounts of acidic groups by 0.711 mmol/g due to activation by H3PO4. FTIR recorded different peaks suggesting significant modifications in the spectroscopic characteristics of the BPAC surface due to the successful activation and adsorption of the pollutant molecules. The pHpzc of BPAC was calculated to be 5.005. The SBET surface area dramatically increased to 911.59 m2/g after the activation. The optimum conditions were 25 °C, a materials dosage of 1.2 g/L, a saturation time of 120 min, a pollutants mixture of 25 mg/L, and a pH of 5. Langmuir exhibits a slightly better fit than Freundlich with a low value of the residual sum of squares (SSE) and the data were better fitted to the pseudo-second-order kinetic. Furthermore, the efficacy of BPAC in eliminating pharmaceuticals from Milli Q water, lake water, and wastewater was successfully investigated over the seven cycles. The results of the present work highlighted a potential usage of agro-industrial waste in eliminating organic micropollutants while exhibiting sustainable management of this waste.