Removal Of Micropollutants Research Articles

Enhanced removal of pesticide micropollutant and bacteria using solar light-assisted Ag-doped TiO2: prospects for environmental and health impacts.

Pesticide micropollutants like 4-chlorophenol (4CP) and E. coli bacteria represent a substantial hazard, impacting both the environment and human health. This study delves into the effectiveness of Ag-doped TiO2 (Ag@TiO2) in removing both 4CP and E. coli. Ag@TiO2 has demonstrated remarkable effectiveness in removing 4CP under both solar and visible light conditions, earning degradation efficiencies of 91.3% and 72.8%, respectively. Additionally, it demonstrates outstanding photodegradation efficiency for 4CP (98.8%) at an initial concentration of 1mgL-1. Moreover, Ag@TiO2 exhibited substantially higher removal performance for 4CP (81.6%) compared to TiO2 (27.6%) in wastewater. Analysis of the radicals present during the photodegradation process revealed that ·O2- primarily drives the decomposition of 4CP, with h+ and ·OH also playing significant roles in the oxidation reactions of the pollutant. Interestingly, even under dark conditions, Ag@TiO2 exhibited the capability to eliminate approximately 20% of E. coli, a percentage that increased to over 96% under solar light. In addition, the prospects for environmental and health impacts of utilizing Ag@TiO2 for pesticide micropollutant removal and bacteria were discussed.

Unraveling the role of Mn(V)/Mn(III) in the enhanced permanganate oxidation under Vis-LED radiation

A novel approach of visible light-emitting diode (Vis-LED) radiation was employed to activate permanganate (Mn(VII)) for efficient organic micropollutant (OMP) removal. The degradation rates of OMPs by Vis-LED/Mn(VII) were 2–5.29 times higher than those by Mn(VII) except for benzoic acid and atrazine. Increasing wavelengths (445–525 nm) suppressed the degradation of diclofenac (DCF) and 4-chlorophenol (4-CP) owing to the decreased quantum yields of Mn(VII). Comparatively, light intensity and Mn(VII) dosage had a positive effect on the degradation of DCF and 4-CP. Experimental data revealed that Mn(V) dominated the DCF degradation whereas Mn(III) was the active oxidant in the 4-CP degradation. Mn(V) and Mn(III) formed from the photo-decomposition of Mn(VII), meanwhile, Mn(III) also formed from the Mn(V) photo-decomposition. The increase in solution pH inhibited DCF degradation but had a positive impact on 4-CP degradation, mainly due to the changing speciation of DCF and 4-CP. Inorganic anions (Cl− and HCO3−) had little impact on DCF and 4-CP degradation, while humic acid (HA) showed a positive impact because of the π-π interaction between HA and DCF/4-CP. The transformation products of DCF and 4-CP were identified and transformation pathways were proposed. Finally, the Vis-LED/Mn(VII) exhibited great degradation performance in various authentic waters. Overall, this study boosts the development of Mn(VII)-based oxidation processes.

Heterostructure g-C3N4/Bi2MoO6 PVDF nanofiber composite membrane for the photodegradation of steroid hormone micropollutants

Photocatalytic membrane reactors (PMRs) are a promising technology for micropollutant removal. Sunlight utilization and catalyst surface sites limit photodegradation. A poly(vinylidene fluoride) (PVDF) nanofiber composite membrane (NCM) with immobilized visible-light-responsive g-C3N4/Bi2MoO6 (BMCN) were developed. Photodegradation of steroid hormones with the PVDF-BMCN NCM was investigated with varying catalyst properties, operating conditions, and relevant solution chemistry under solar irradiation. Increasing CN ratio (0–65 %) enhanced estradiol (E2) degradation from 20 ± 10 to 75 ± 7 % due to improved sunlight utilization and photon lifetime. PVDF nanofibers reduced self-aggregation of catalysts. Hydraulic residence time and light intensity enhanced the photodegradation. With the increasing pH value, the E2 removal decreased from 84 ± 4 to 67 ± 7 % owing to electrical repulsion and thus reduced adsorption between catalysts and E2. A removal of 96 % can be attained at environmentally relevant feed concentration (100 ng.L–1) with a flux of 60 L.m−2.h−1, irradiance of 100 mW.cm−2, and 1 mg.cm−2 BMCN65 loading. This confirmed that heterojunction photocatalysts can enhance micropollutants degradation in PMRs.

Membrane hybrid system assembled with MXene@h-BN for efficient typical pharmaceuticals removal and self-cleaning: Synergetic effect on adsorption-photocatalytic process

Membrane filtration is regarded as one of the promising technologies for water treatment. However, insufficient micropollutants removal and membrane fouling still limited the further application. Herein, this study engineered a novel membrane hybrid system integrating typical pharmaceuticals removal and membrane self-cleaning by assembled layered MXene and hexagonal boron nitride (h-BN). By doping a small amount of MXene into h-BN (mass ratio of 1 to 10), the synergetic process of adsorption and photocatalytic degradation were achieved. Based on experimental and density functional theory (DFT) calculation results, the chemisorption-photodegradation performance of the membrane hybrid system assembled with 1/10 MXene@h-BN was significantly enhanced due to the termination group and conductive property of MXene. In addition, trimethoprim (TMP) degradation by the above membrane followed the Langmuir–Hinshelwood model, indicating pollutants removal initiated not only on the membrane surface but also in the bulk solution under simulated solar irradiation. This phenomenon was attributed to the generation of •OH and 1O2 by forming Ohmic contact with altered internal band structure. The durability and practical experiments with secondary effluent from local wastewater treatment were also tested. The exceptional self-cleaning performance of the membrane hybrid system assembled with 1/10 MXene@h-BN was demonstrated by lower membrane fouling and maintaining durability even after five cycles. Furthermore, the performance (both pollutants removal and flux) of the modified membrane for secondary effluent treatment was also considerable, validating its potential for practical application. Owing to the excellent features, the membrane assembled with MXene@h-BN is anticipated to be an ideal candidate for advanced wastewater treatment.

Impact of long-term temperature shifts on activated sludge microbiome dynamics and micropollutant removal

Micropollutants removal efficiency strongly vary across different aerobic wastewater treatment plants, resulting in their frequent detection in surface and ground waters. Seasonal temperature variation is a major factor influencing plant performance, but it is still unclear how prolonged periods of temperature change impact microbiome and micropollutant biotransformation. This work investigates the effect of long-term temperature variation on the microbial dynamics in an activated sludge system, and the impact on micropollutant biotransformation. Sequencing batch reactors were used as model system and 4–40 °C temperature range was studied. 16S rRNA amplicon sequencing showed that temperature drives microbial structure (gDNA) and activity (RNA), rather than time, and this was stronger below 15 °C and above 25 °C. The microbial community was richest and more diverse at 20 °C, while rarer and more specific taxa became predominant over time, at more extreme temperatures. This suggested that less abundant taxa might be responsible for maintaining the biotransformation capability in the activated sludge at extreme temperatures. Micropollutant biotransformation rates mostly deviated from the classic Arrhenius model below 15 °C and above 25 °C, indicating that prolonged exposure to temperature changes leads to temperature-induced taxonomic shifts, resulting in the emerging of different sets of biotransformation pathways over different temperature ranges.

Conjugated Microporous Polymers-Based Catalytic Membranes with Hierarchical Channels for High-Throughput Removal of Micropollutants.

Engineering a catalytic membrane capable of efficiently removing emerging organic microcontaminants under ultrahigh flux conditions is of significance for water purification. Herein, drawing inspiration from the functional attributes of lymphatic vessels involved in immunosurveillance and fluid transport with minimal energy consumption, a novel hierarchical porous catalytic membrane is engineered. This membrane, based on an innovative nitrogen-rich conjugated microporous polymer (polytripheneamine, PTPA), is synthesized using an electrospinning coupled in situ polymerization approach. The resulting bioinspired membrane with hierarchical channels comprises a thin layer (≈1.7µm) of crosslinked PTPA nanoparticles covering the interconnected electrospun nanofibers. This unique design creates an intrinsic microporous angstrom-confined system capable of activating peroxymonosulfate (PMS) to generate 98.7% singlet oxygen (1O2), enabling durable and highly efficient degradation of microcontaminants. Additionally, the presence of a thin layer of mesoporous structure between PTPA nanoparticles and macroporous channels within the interwoven nanofibers enhances mass transfer efficiency and facilitates high flux rates. Notably, the prepared hierarchical porous organic catalytic membrane demonstrates enduring high-efficiency degradation performance with a superior permeance (>95% and >2500 L m-2 h-1 bar-1) sustained over 100 h. This work introduces an innovative pathway for the design of high-performance catalytic membranes for the removal of emerging organic microcontaminants.

Estrogenic compounds in drinking water: A systematic review and risk analysis

Estrogenic compounds are the endocrine disruptors that receive major attention because of their ability to imitate the natural female hormone, 17β-estradiol and cause adverse effects on the reproductive system of animals. The presence of estrogenic compounds in drinking water is a warning to assess the risks to which human beings are exposed. The present work has the objectives of carrying out a systematic review of studies that investigated estrogenic compounds in drinking water around the world and estimate the human health and estrogenic activity risks, based on the concentrations of each compound reported. The systematic review returned 505 scientific papers from the Web of Science®, SCOPUS® and PubMED® databases and after careful analysis, 45 papers were accepted. Sixteen estrogenic compounds were identified in drinking water, from the classes of hormones, pharmaceutical drugs and personal care products, plasticizers, corrosion inhibitors, pesticides and surfactants. Di-(2-ethylhexyl) phthalate (DEHP) was the compound found at the highest concentration, reaching a value of 1.43 mg/L. Non-carcinogenic human health risk was classified as high for 17α-ethynilestradiol and DEHP, medium for dibutyl phthalate, and low for bisphenol A. The estrogenic activity risks were negligible for all the compounds, except DEHP, with a low risk. None of the estrogenic compounds presented an unacceptable carcinogenic risk, due to estrogenic activity. However, the risk assessment did not evaluate the interactions between compounds, that occurs in drinking water and can increase the risks and adverse effects to human health. Nonetheless, this study demonstrates the need for improvement of drinking water treatment plants, with more efficient technologies for micropollutant removal.

Pilot scale removal of organic micropollutants by combining ozonation with powdered activated carbon

ABSTRACT Pilot experiments were conducted to assess the removal of organic micropollutants from biologically treated wastewater at a municipal wastewater treatment plant in Sweden. Powdered activated carbon (PAC) was combined with a low dose of ozone added directly before the PAC contact tank, enabling ozone to react simultaneously with the PAC and the wastewater contaminants. This combination of ozone and PAC was compared to PAC or ozone alone. The process, which included coagulation/flocculation and ballasted high-rate lamella sedimentation, proved to be both robust and efficient for the removal of micropollutants. The addition of 1.3 mg PAC/mg DOC resulted in a 73% average reduction of micropollutants. With the addition of 0.13 mg O3/mg DOC, the reduction increased to 83%, which was similar to the outcome with the addition of 26 mg PAC/mg DOC without ozone. The process configuration and operating conditions did not lead to any detectable bromate formation despite relatively high influent bromide levels. The estimated operating costs for combining PAC with a low dose of ozone were significantly lower than for applying a higher PAC dose. Thus, this way of combining PAC with ozone seems to have several advantages with respect to treatment efficiency and operation.

Manipulating singlet oxygen generation on Co nanoclusters-confined g-C3N4 macroscopic beads for boosted water decontamination

Reducing the migration distance of reactive oxygen species (ROS) and enhancing interfacial electron transfer represent effective approaches for enhancing the reactivity of heterogeneous catalysts, albeit still posing significant challenges. Herein, we successfully synthesized ultrasmall cobalt nanoclusters-confined g-C3N4 macroscopic beads with N-doped carbon dots (Co/NC@CN beads). Compared to unconfined Co/C and Co/C@CN beads, Co/NC@CN beads demonstrated remarkable utilization efficiency of PMS (84.3%), achieving complete degradation of TC within 20 min at a rate of 162.1 min-1·M-1, surpassing most reported catalysts. Besides, Co/NC@CN beads predominantly generated singlet oxygen (1O2), ensuring efficient removal of micropollutants with resistance to pH and complex water bodies. Experiments have proven that the strong interaction between Co clusters and g-C3N4 beads containing NC dots facilitated the generation of interfacial electron transfer by optimizing the electronic structure of Co nanoclusters, thereby Co/NC@CN beads could capture electrons from tetracycline (TC) and PMS molecules towards dissolved oxygen (DO) to form O2·-, which subsequently converted into 1O2. More importantly, the efficiency of the flow-through unit in the continuous degradation of TC with zero discharge was substantiated by long-term experiments, and its performance could be restored through a straightforward low-temperature carbonization process. This study offers a universal design framework for the creation of various confined macroscopic beads, enabling the achievement of highly effective wastewater treatment.

Modelling competitive adsorption of organic micropollutants onto powdered activated carbon in continuous stirred tank reactors for advanced wastewater treatment

This work investigates the validation and application of a competitive model approach for full-scale wastewater treatment plants (WWTP) with external recirculation of partially loaded powdered activated carbon (PAC) for removal of organic micropollutants (OMP). It is based on the ideal adsorbed solution theory (IAST) for multisolute mixtures combined with calibration of fictive organic components and correction of single-solute model parameters for OMP by use of the tracer model (TRM). Adsorption kinetics are represented by a pseudo first order reaction (PFO) and compared to mass transfer calculated with the homogenous surface diffusion model (HSDM). Model validation with operational data from two different WWTPs showed a strong dependency of model results on the batch sample quality used for model calibration. In contrast, the kinetic approach is of less importance for predicting full-scale OMP removal with long PAC sludge retention times. Further model application demonstrated that external PAC recirculation significantly improves the OMP removal with regard to both adsorption capacity and compensation of competitive effects of Dissolved Organic Carbon (DOC).

Modulating the channel structure of iron-based catalysts with β-cyclodextrin for enhanced degradation of 2,4,6-trichlorophenol via peroxymonosulfate activation: Performance, mechanism and transformation pathways

Rationally regulating the structure of catalysts in Fenton-like reactions provides abundant opportunities for the efficient remediation of organic micropollutants from the aqueous environment, yet it is challenging to achieve superior reactivity and the catalytic mechanisms have rarely been systematically elucidated. Herein, we present a simple strategy to synthesize confined catalysts with different pore-size distributions by modulating the proportion of β-cyclodextrin (β-CD) with a cavity. The degradation performance of the confined catalyst MCF with the smallest pore size (5.9 nm) was remarkably enhanced compared to the unconfined catalyst NCF, mainly by 1O2 and electron transfer. As the cavity content increases, the reactivity displayed an unexpected volcanic peak tendency. The pseudo-first-order reaction constant of MCF was 2.6 times higher than that of HCF (8.2 nm) in Fenton-like oxidation with peroxymonosulfate (PMS). Comparative control experiments demonstrated that the appropriate structure can significantly facilitate the diffusion and degradation process of pollutants that are adsorbed in the confined channels. The MCF/PMS system exhibited strong adaptability to coexisting ions and pH in the water matrix, and the intermediate products were harmless to the environment. This unusual catalytic mechanism and the structural regulation strategy will establish new insights into boosting the catalytic performance for the efficient removal of organic micropollutants.

Efficient peracetic acid activation by high-index facets of Cu2O under simulated solar light: The crucial role of uncoordinated Cu atoms

Tuning the facets of transition-metal catalysts to achieve effective micropollutant removal via peracetic acid (PAA) activation is a promising approach. However, within this process, the correlation between PAA activation and the atomic arrangement of the exposed facets is ambiguous. Herein, we present a comprehensive study wherein a series of Cu2O materials, with typical high-index facets ({211}, {311}, and {332}) and low-index facets ({100}, {110}, and {111}), were synthesized. These materials were used to investigate facet-dependent PAA activation for tetracycline (TC) degradation under simulated solar light irradiation. The results demonstrate that Cu2O with high-index {332} facets exhibit the optimal TC degradation (96.65 % within 20 min), and its kobs values are 1.52 and 2.01 times those of Cu2O with {311} and {211} facets, respectively. Detailed identification of the active species proved that •OH, 1O2, and the electron transfer process induced by the reactive Cu (I)–PAA* complexes were involved in TC degradation. In contrast to the {211} and {311} facets, PAA demonstrated a heightened tendency for adsorption and activation into active species on the {332} facets because of the denser uncoordinated Cu atoms. In addition, the facet heterojunction composed of {332} and {100} facets was conducive to the separation of photogenerated electron-hole pairs and charge migration, thus promoting the Cu(II)/Cu(I) cycle. In the practical applicability evaluation, Cu2O with {332} facets effectively removed multiple pollutants as well as actual pharmaceutical wastewater. This study provides a novel strategy for PAA activation by regulating the exposed facets of the catalyst.

Navigating the balance between nanofiltration and oxidation to remove organic micropollutants from wastewater treatment plant effluent

The removal of organic micropollutants (OMPs) from wastewater treatment plant effluent is becoming more important due to the adverse effects of these compounds on the environment. To overcome the limitations of currently available technologies, this study proposes a combination of hollow fiber membrane filtration with advanced oxidation to remove OMPs. The possible synergy between these processes was investigated. The nanofiltration membrane ensures the removal of organic matter and thus an improvement of transmittance, after which oxidation with UV/H2O2 of the permeate can remove OMPs more effectively and at a significantly lower energy consumption than without a membrane. Six membranes were evaluated with a pure water permeability between 6.7 and 106 Lm−2 h−1 bar−1 and a MgSO4 retention ranging from 0.93 to 0. The molecular weight cut-off (MWCO) varied from 250 Da to more than 10 kDa. The measured MWCO can depend strongly on the applied flux. The UV-transmittance of NF permeate of treated wastewater was investigated experimentally to be between 97% and 50%. These values were used for an estimation of the specific energy consumption (SEC) for the membrane and the oxidation step, resulting in a combined SEC of 0.17–0.18 kWhm−3 for 70 or 80% removal of OMPs, respectively. Remarkably, this lowest SEC was not found for the combination with the most dense membrane, but for a slightly more open membrane. The reported SEC is comparable to the total energy consumption required for ozonation and adsorption, while producing clean water with a double barrier, high transmittance and 70–80% removal of OMPs.

Recent Advancement in Emerging MXene-Based Photocatalytic Membrane for Revolutionizing Wastewater Treatment.

MXene-based photocatalytic membranes provide significant benefits for wastewater treatment by effectively combining membrane separation and photocatalytic degradation processes. MXene represents a pioneering 2D photocatalyst with a variable elemental composition, substantial surface area, abundant surface terminations, and exceptional photoelectric performance, offering significant advantages in producing high-performance photocatalytic membranes. In this review, an in-depth overview of the latest scientific progress in MXene-based photocatalytic membranes is provided. Initially, a brief introduction to the structure and photocatalytic capabilities of MXene is provided, highlighting their pivotal role in promoting the photocatalytic process. Subsequently, in pursuit of the optimal MXene-based photocatalytic membrane, critical factors such as the morphology, hydrophilicity, and stability of MXenes are meticulously taken into account. Various preparation strategies for MXene-based photocatalytic membranes, including blending, vacuum filtration, and dip coating, are also discussed. Furthermore, the application and mechanism of MXene-based photocatalytic membranes in micropollutant removal, oil-water separation, and antibacterial are examined. Lastly, the challenges in the development and practical application of MXene-based photocatalytic membranes, as well as their future research direction are delineated.

Reactive layered hydroxide membrane for advanced water treatment: Micropollutant degradation and antifouling potential

The effective removal of micropollutants by water treatment technologies remains a significant challenge. Herein, we develop a CoFe layered double hydroxide (CoFeLDH) catalytic membrane for peroxymonosulfate (PMS) activation to achieve efficient micropollutant removal with improved mass transfer rate and reaction kinetics. This study found that the CoFeLDH membrane/PMS system achieved an impressive above 98% degradation of the probe chemical ranitidine at 0.1 mM of PMS including five more micropollutants (Sulfamethoxazole, Ciprofloxacin, Carbamazepine, Acetaminophen and Bisphenol A) at satisfactory level (above 80%). Moreover, significant improvements in water flux and antifouling properties were observed, marking the membrane as a specific advancement in the removal of membrane fouling in water purification technology. The membrane demonstrated consistent degradation efficiency for several micropollutants and across a range of pH (4–9) as well as different anionic environments, thereby showing it suitability for scale-up application. The key role of reactive species such as SO4•–, and O2• − radicals in the degradation process was elucidated. This is followed by the confirmation of the occurrence of redox cycling between Co and Fe, and the presence of CoOH+ that promotes PMS activation. Over the ten cycles, the membrane could be operated with a flux recovery of up to 99.8% and maintained efficient performance over 24 h continuous operation. Finally, the efficiency in degrading micropollutants, coupled with reduced metal leaching, makes the CoFeLDH membrane as a promising technology for application in water treatment.

Deciphering the role of extracellular polymeric substances in the adsorption and biotransformation of organic micropollutants during anaerobic wastewater treatment

Extracellular polymeric substances (EPS) participate in the removal of organic micropollutants (OMPs), but the primary pathways of removal and detailed mechanisms remain elusive. We evaluated the effect of EPS on removal for 16 distinct chemical classes of OMPs during anaerobic digestion (AD). The results showed that hydrophobic OMPs (HBOMPs) could not be removed by EPS, while hydrophilic OMPs (HLOMPs) were amenable to removal via adsorption and biotransformation of EPS. The adsorption and biotransformation of HLOMPs by EPS accounted up to 19.4 ± 0.9 % and 6.0 ± 0.8 % of total removal, respectively. Further investigations into the adsorption and biotransformation mechanisms of HLOMPs by EPS were conducted utilizing spectral, molecular dynamics simulation, and electrochemical analysis. The results suggested that EPS provided abundant binding sites for the adsorption of HLOMPs. The binding of HLOMPs to tryptophan-like proteins in EPS formed nonfluorescent complexes. Hydrogen bonds, hydrophobic interactions and water bridges were key to the binding processes and helped stabilize the complexes. The biotransformation of HLOMPs by EPS may be attributed to the presence of extracellular redox active components (c-type cytochromes (c-Cyts), c-Cyts-bound flavins). This study enhanced the comprehension for the role of EPS on the OMPs removal in anaerobic wastewater treatment.

Selected Micropollutant Removal from Municipal Wastewater

Micropollutants belong to various groups of chemicals. One of the most diverse and large group of them are pharmaceuticals. The presence of pharmaceutical residues in wastewater poses a significant challenge to water quality and environmental health. This paper provides an overview of recent advancements in the removal of pharmaceuticals from water, focusing on various treatment processes and their effectiveness in eliminating micropollutants. Through a review of the literature, including studies on ozonation, UV irradiation, sulfate radical-based technologies, and photocatalytic processes, insights into degradation mechanisms and optimal conditions for their removal are synthesized. Additionally, with new legislation mandating the monitoring of selected micropollutants and the implementation of quaternary treatment in wastewater treatment plants, the paper discusses prospects for future research and recommendations for effective pharmaceutical removal. Key actions include conducting comprehensive laboratory and pilot trials, implementing quaternary treatment of wastewater, continuously monitoring water quality, investing in research and development, and promoting collaboration and knowledge sharing among stakeholders. By embracing these strategies, we can work towards safeguarding water resources and protecting public health from the adverse effects of pharmaceutical contamination.

Ozone Strong Water Dosing as Optimized Ozonation Process for Micropollutants Reduction in Wastewater Treatment Plants

ABSTRACT Growing concern over potential ecotoxicological problems caused by micropollutants (MPs) in water has led to the application of adsorptive and oxidative advanced treatment technologies at European wastewater treatment plants (WWTPs). Direct dosage of gaseous ozone via diffusers or pump-injection systems is the most common large-scale process applied in water and wastewater treatment. Studies point out that MP removal may take place via the direct, very selective reaction with the ozone molecule as well as the indirect reaction with the very reactive but nonselective hydroxyl radicals. Several process parameters and set-ups may affect the MPs elimination and inhibit or even cause the formation of transformation products (TPs) such as bromate. This work compares an alternative ozone application procedure (the so-called ‘ozone strong water’ dosing – OSW) with standard systems regarding MP elimination, ozone consumption, reaction time, and required plant space. A full-scale OSW system was installed and operated at the WWTP Duisburg-Vierlinden. A significant reduction in the time required to achieve the maximum possible elimination was observed for all six MPs investigated, with a hydraulic reaction time of 8 min. According to a theoretical calculation, the reactor volume could be reduced by two-thirds of the installed volume.

Biological degradation of organic micropollutants in GAC filters–temporal development and spatial variations

The capacity for organic micropollutant removal in granular activated carbon (GAC) filters for wastewater treatment changes over time. These changes are in general attributed to changes in adsorption, but may in some cases also be affected by biological degradation. Knowledge on the degradation of organic micropollutants, however, is scarce. In this work, the degradation of micropollutants in several full-scale GAC and sand filters was investigated through incubation experiments over a period of three years, using 14C-labeled organic micropollutants with different susceptibilities to biological degradation (ibuprofen, diclofenac, and carbamazepine), with parallel 16S rRNA gene sequencing. The results showed that the degradation of diclofenac and ibuprofen in GAC filters increased with increasing numbers of bed volumes when free oxygen was available in the filter, while variations over filter depth were limited. Despite relatively large differences in bacterial composition between filters, a degradation of diclofenac was consistently observed for the GAC filters that had been operated with high influent oxygen concentration (DO >8 mg/L). The results of this comprehensive experimental work provide an increased understanding of the interactions between microbial composition, filter material, and oxygen availability in the biological degradation of organic micropollutants in GAC filters.

Occurrence of micropollutants in rural domestic wastewater in Zhejiang Province, China and corresponding wastewater-based epidemiology analysis

By 2021, rural regions in China were occupied by over 500 million residents, generating an annual volume of 19.5 billion m3 of rural domestic wastewater (RDW). This study aimed to investigate the occurrence and removal of micropollutants (MPs) in RDW treatment facilities and to perform a corresponding wastewater-based epidemiology analysis (WBE). Our findings indicated the significantly high levels of influent MPs, particularly pharmaceuticals, such as ofloxacin and diclofenac being most prevalent (ranging from several to tens of μg/L) across different facilities. After various treatments, regular water indexes in the effluent, like NH3 -N and COD, have basically satisfied the local discharge standard. However, the concentration of certain dominant MPs in effluent remained notably high, ranging from hundreds of ng/L to several μg/L. The risk quotients of MPs like diclofenac, ciprofloxacin, ofloxacin, sulfamethoxazole, diuron, and isoproturon were all above 1 in the effluent, signifying significant hazards to aquatic organisms. The quantitative meta-analysis revealed higher average standardized removal efficiency for membrane bioreactor (MBR) treatment (-11 %) compared to anaerobic/anoxic/aerobic (A2O) treatment (11 %), indicating the higher efficiency of MBR treatment in outperforming the A2O as a secondary treatment. Additionally, employing biofilter as a tertiary treatment proved to be more effective as compared to flocculation-air flotation and artificial wetlands. Moreover, the results of WBE analysis showed that diclofenac and ofloxacin emerged as the most commonly used pharmaceuticals (of seven), with consumption levels recorded at 1222 and 517 mg/(d·103 capita), with daily defined doses per day per 103 capita of 12.2/1000 and 1.29/1000, respectively. This study addresses the existing knowledge gaps regarding the occurrence and removal of MPs in RDW and offers valuable insights into pharmaceutical consumption patterns in rural regions, thereby improving our understanding of public health.