Plastic materials and water sources actively select and shape wastewater plastispheres over time

● Wastewater MPs exhibited resistomes and therefore health threats. ● High density of alkB gene indicates both HDPE and PET can be utilized by microbes. ● Plastics and waters actively selected and shaped the plastispheres over time. ● A broader phylogenetic spectrum of MHET-degrading microorganisms was annotated. The daily use of plastics presents a serious pollution issue due to their extremely slow degradation. Microplastics and the biofilm that grows on plastics (i.e., the plastisphere) are important subsets of plastic wastes. Many studies have been conducted to reveal the structures of the plastispheres, the driving factors for the formation of the plastisphere, and the ability of the plastispheres to degrade plastics in a variety of water bodies. However, the plastispheres related to wastewater are understudied. In this study, we used a microcosmic strategy to study the evolution of the plastispheres associated with microplastics (MPs) over time in wastewater. We found that plastic materials and water sources did not actively select and shape the plastispheres at an early stage, but the active selection for a unique niche of the plastisphere occurred after 14 d of growth. In addition, we confirmed that the alkB gene was densely present, and metagenomics showed some additional chemical reactions, which suggests that MPs are consumed by the microbes in the plastispheres. Additionally, metagenomics identified some metagenome-assembled genomes (MAGs) associated with high-density polyethylene (HDPE) and polyethylene terephthalate (PET). The identification of HDPE-associated MAGs and PET-associated MAGs further supports the notion that the selection for a unique niche of the plastisphere is driven by plastic materials and water sources (in this study, after 14 d of growth). Our discoveries bring new views on the behavior of the wastewater-associated plastisphere, especially how long it takes a wastewater plastisphere to form.     

Salinity exchange between seawater/brackish water and domestic wastewater through electrodialysis for potable water

● Present a general concept called “salinity exchange”. ● Salts transferred from seawater to treated wastewater until completely switch. ● Process demonstrated using a laboratory-scale electrodialysis system. ● High-quality desalinated water obtained at ~1 mL/min consuming < 1 kWh/m ³ energy. Two-thirds of the world’s population has limited access to potable water. As we continue to use up our freshwater resources, new and improved techniques for potable water production are warranted. Here, we present a general concept called “salinity exchange” that transfers salts from seawater or brackish water to treated wastewater until their salinity values approximately switch, thus producing wastewater with an increased salinity for discharge and desalinated seawater as the potable water source. We have demonstrated this process using electrodialysis. Salinity exchange has been successfully achieved between influents of different salinities under various operating conditions. Laboratory-scale salinity exchange electrodialysis (SEE) systems can produce high-quality desalinated water at ~1 mL/min with an energy consumption less than 1 kWh/m³. SEE has also been operated using real water, and the challenges of its implementation at a larger scale are evaluated.     

Evaluating the impact of sulfamethoxazole on hydrogen production during dark anaerobic sludge fermentation

● SMX promotes hydrogen production from dark anaerobic sludge fermentation. ● SMX significantly enhances the hydrolysis and acidification processes. ● SMX suppresses the methanogenesis process in order to reduce hydrogen consumption. ● SMX enhances the relative abundance of hydrogen-VFAs producers. ● SMX brings possible environmental risks due to the enrichment of ARGs. The impact of antibiotics on the environmental protection and sludge treatment fields has been widely studied. The recovery of hydrogen from waste activated sludge (WAS) has become an issue of great interest. Nevertheless, few studies have focused on the impact of antibiotics present in WAS on hydrogen production during dark anaerobic fermentation. To explore the mechanisms, sulfamethoxazole (SMX) was chosen as a representative antibiotic to evaluate how SMX influenced hydrogen production during dark anaerobic fermentation of WAS. The results demonstrated SMX promoted hydrogen production. With increasing additions of SMX from 0 to 500 mg/kg TSS, the cumulative hydrogen production elevated from 8.07 ± 0.37 to 11.89 ± 0.19 mL/g VSS. A modified Gompertz model further verified that both the maximum potential of hydrogen production (P_m) and the maximum rate of hydrogen production (R_m) were promoted. SMX did not affected sludge solubilization, but promoted hydrolysis and acidification processes to produce more hydrogen. Moreover, the methanogenesis process was inhibited so that hydrogen consumption was reduced. Microbial community analysis further demonstrated that the introduction of SMX improved the abundance of hydrolysis bacteria and hydrogen-volatile fatty acids (VFAs) producers. SMX synergistically influenced hydrolysis, acidification and acetogenesis to facilitate the hydrogen production.     

The impact of different voltage application modes on biodegradation of chloramphenicol and shift of microbial community structure

● Presented coupled system enhanced biodegradation of antibiotic chloramphenicol. ● HRT and electrical stimulation modes were key influencing factors. ● Electrical stimulation had little effect on the chloramphenicol metabolic pathway. ● Microbial community structure varied with the voltage application mode. Exoelectrogenic biofilms have received considerable attention for their ability to enhance electron transfer between contaminants and electrodes in bioelectrochemical systems. In this study, we constructed anaerobic-aerobic-coupled upflow bioelectrochemical reactors (AO-UBERs) with different voltage application modes, voltages and hydraulic retention times (HRTs). In addition, we evaluated their capacity to remove chloramphenicol (CAP). AO-UBER can effectively mineralize CAP and its metabolites through electrical stimulation when an appropriate voltage is applied. The CAP removal efficiencies were ~81.1%±6.1% (intermittent voltage application mode) and 75.2%±4.6% (continuous voltage application mode) under 0.5 V supply voltage, which were ~21.5% and 15.6% greater than those in the control system without voltage applied, respectively. The removal efficiency is mainly attributed to the anaerobic chamber. High-throughput sequencing combined with catabolic pathway analysis indicated that electrical stimulation selectively enriched Megasphaera, Janthinobacterium, Pseudomonas, Emticicia, Zoogloea, Cloacibacterium and Cetobacterium, which are capable of denitrification, dechlorination and benzene ring cleavage, respectively. This study shows that under the intermittent voltage application mode, AO-UBERs are highly promising for treating antibiotic-contaminated wastewater.     

Genome-resolved metagenomic analysis reveals different functional potentials of multiple Candidatus Brocadia species in a full-scale swine wastewater treatment system

● Four Ca. Brocadia species were observed during the spontaneously enrichment. ● Novel anammox species SW510 and SW773 dominated the full-scale ecosystem. ● Urease and cyanase genes were detected in the new anammox genomes. ● Functional differentiation potentially facilitated co-occurrence of anammox species. The increasing application of anammox processes suggests their enormous potential for nitrogen removal in wastewater treatment facilities. However, the functional potentials and ecological differentiation of cooccurring anammox species in complex ecosystems have not been well elucidated. Herein, by utilizing functional reconstruction and comparative genome analysis, we deciphered the cooccurring mechanisms of four Candidatus Brocadia species that were spontaneously enriched in a full-scale swine wastewater treatment system. Phylogenetic analysis indicated that species SW172 and SW745 were closely related to Ca. Brocadia caroliniensis and Ca. Brocadia sapporoensis, respectively, whereas the dominant species SW510 and SW773, with a total average abundance of 34.1%, were classified as novel species of the genus Ca. Brocadia. Functional reconstruction revealed that the novel species SW510 can encode both cytochrome cd₁-type nitrite reductase and hydroxylamine oxidase for nitrite reduction. In contrast, the detected respiratory pentaheme cytochrome c nitrite reductase and acetate kinase genes suggested that SW773 likely reduced nitrite to ammonium with acetate as a carbon source. Intriguingly, the presence of genes encoding urease and cyanase indicated that both novel species can use diverse organic nitrogen compounds in addition to ammonia and nitrite as substrates. Taken together, the recovery and comparative analysis of these anammox genomes expand our understanding of the functional differentiation and cooccurrence of the genus Ca. Brocadia in wastewater treatment systems.     

Differences in distributions,assembly mechanisms,and putative interactions of AOB and NOB at a large spatial scale

● Nitrifiers in WWTP were investigated at large spatial scale. ● AOB populations varied greatly but NOB populations were similar among cities. ● Drift dominated both AOB and NOB assembling processes. ● DO did not show a significant effect on NOB. ● NOB tended to cooperate with AOB and non-nitrifying microorganisms. Ammonia-oxidizing bacteria (AOB) and nitrite-oxidizing bacteria (NOB) play crucial roles in removing nitrogen from sewage in wastewater treatment plants (WWTPs) to protect water resources. However, the differences in ecological properties and putative interactions of AOB and NOB in WWTPs at a large spatial scale remain unclear. Hence, 132 activated sludge (AS) samples collected from 11 cities across China were studied by utilizing 16S rRNA gene sequencing technology. Results indicated that Nitrosomonas and Nitrosospira accounted for similar ratios of the AOB community and might play nearly equal roles in ammonia oxidation in AS. However, Nitrospira greatly outnumbered other NOB genera, with proportions varying from 94.7% to 99.9% of the NOB community in all WWTPs. Similar compositions and, hence, a low distance–decay turnover rate of NOB (0.035) across China were observed. This scenario might have partly resulted from the high proportions of homogenizing dispersal (~13%). Additionally, drift presented dominant roles in AOB and NOB assembling mechanisms (85.2% and 81.6% for AOB and NOB, respectively). The partial Mantel test illustrated that sludge retention time and temperature were the primary environmental factors affecting AOB and NOB communities. Network results showed that NOB played a leading role in maintaining module structures and node connections in AS. Moreover, most links between NOB and other microorganisms were positive, indicating that NOB were involved in complex symbioses with bacteria in AS.     

Adsorption behavior of imidacloprid pesticide on polar microplastics under environmental conditions: critical role of photo-aging

● Small molecular chains formed on photo-aged polylactic acid microplastics (MPs). ● Oxygen-containing functional groups generated on photo-aged polyamide MPs. ● Photo-aging has the opposite influence on the imidacloprid adsorption on two MPs. ● Electrostatic interactions and hydrogen bonds were the main mechanisms. ● High pH value and low ionic strength increase the adsorption capacity. The photo-aging behavior of microplastics (MPs) in natural environment has become a global concern. The ultraviolet radiation has enough energy to change the polymer structure and physical-chemical properties of MPs. Less attention has focused on the interactions of the photo-aged polar and biodegradable MPs with organic pollutants. This work investigated the structural properties of aged polar polyamide (PA) MPs and biodegradable polylactic acid (PLA) MPs exposed to ultraviolet irradiation and their adsorption behavior and mechanism for neonicotinoid insecticide imidacloprid (IMI). The results showed that the MPs had extensive changes in surface morphology and chemical properties after photo-aging. The C–N bond of PA MPs was disrupted to form more carbonyl groups. The oxygen-containing functional groups on the surface of aged PLA MPs were broken and generated relatively smaller molecules. The adsorption capacity of IMI on PA MPs decreased by 19.2 %, while the adsorption capacity of IMI on PLA MPs increased by 41.2 % after photo-aging. This depended on the natural structure of the MPs and their ability to absorb ultraviolet light. The electrostatic interactions, hydrogen bonds, van der Waals interactions, and polar-polar interactions were the main adsorption mechanisms of IMI on MPs. High initial solution pH and low ionic strength favored the adsorption of IMI by altering charge distribution on the MPs surface. The formation of the humic acid-IMI complexes decreased the concentration of IMI in the water phase and further decreased the adsorption on MPs. These results are enlightening for a scientific comprehension of the environmental behavior of the polar MPs.     

Highly efficient and selective removal of phosphate from wastewater of sea cucumber aquaculture for microalgae culture using a new adsorption-membrane separation-coordinated strategy

● A new adsorption-membrane separation strategy is used for phosphate removal. ● PVC/Zr-BT shows a selective adsorption ability to low-concentration phosphate. ● Low concentration of P below 0.05 mg/L was achieved in actual wastewater treatment. ● Algal biomass production served as a demonstration of phosphorus recycling. Enhanced phosphorus treatment and recovery has been continuously pursued due to the stringent wastewater discharge regulations and a phosphate supply shortage. Here, a new adsorption-membrane separation strategy was developed for rational reutilization of phosphate from sea cucumber aquaculture wastewater using a Zr-modified-bentonite filled polyvinyl chloride membrane. The as-obtained polyvinyl chloride/Zr-modified-bentonite membrane was highly permeability (940 L/(m²·h)), 1–2 times higher than those reported in other studies, and its adsorption capacity was high (20.6 mg/g) when the phosphate concentration in water was low (5 mg/L). It remained stable under various conditions, such as different pH, initial phosphate concentrations, and the presence of different ions after 24 h of adsorption in a cross-flow filtration system. The total phosphorus and phosphate removal rate reached 91.5% and 95.9%, respectively, after the membrane was used to treat sea cucumber aquaculture wastewater for 24 h and no other water quality parameters had been changed. After the purification process, the utilization of the membrane as a new source of phosphorus in the phosphorus-free f/2 medium experiments indicated the high cultivability of economic microalgae Phaeodactylum tricornutum FACHB-863 and 1.2 times more chlorophyll a was present than in f/2 medium. The biomass and lipid content of the microalgae in the two different media were similar. The innovative polyvinyl chloride/Zr-modified-bentonite membrane used for phosphorus removal and recovery is an important instrument to establish the groundwork for both the treatment of low concentration phosphate from wastewater as well as the reuse of enriched phosphorus in required fields.     

Ozonation of aromatic monomer compounds in water: factors determining reaction outcomes

● p- CNB and IBP were selected, to explore factors determining ozonation outcomes. ● •OH contributed only 50 % to IBP removal, compared to the 90 % for p -CNB removal. ● IBP achieved fewer TOC removal and more by-product types and quantities. ● A longer ring-opening distance existed during the degradation of IBP. ● Multiple positions on both branches of IBP were attacked, consuming more oxidants. For aromatic monomer compounds (AMCs), ozonation outcomes were usually predicted by the substituents of the benzene ring based on the electron inductive effect. However, the predicted results were occasionally unreliable for complex substituents, and other factors caused concern. In this study, p-chloronitrobenzene (p-CNB) and ibuprofen (IBP) were selected for ozonation. According to the electron inductive theory, p-CNB should be less oxidizable, but the opposite was true. The higher rates of p-CNB were due to various sources of assistance. First, the hydroxyl radical (•OH) contributed 90 % to p-CNB removal at pH 7.0, while its contribution to IBP removal was 50 %. Other contributions came from molecular O₃ oxidation. Second, p-CNB achieved 40 % of the total organic carbon (TOC) removal and fewer by-product types and quantities, when compared to the results for IBP. Third, the oxidation of p-CNB started with hydroxyl substitution reactions on the benzene ring; then, the ring opened. However, IBP was initially oxidized mainly on the butane branched chain, with a chain-shortening process occurring before the ring opened. Finally, the degradation pathway of p-CNB was single and consumed fewer oxidants. However, both branches of IBP were attacked simultaneously, and three degradation pathways that relied on more oxidants were proposed. All of these factors were determinants of the rapid removal of p-CNB.     

Electrocatalytic biofilm reactor for effective and energy-efficient azo dye degradation: the synergistic effect of MnOx/Ti flow-through anode and biofilm on the cathode

● MnO _x /Ti flow-through anode was coupled with the biofilm-attached cathode in ECBR. ● ECBR was able to enhance the azo dye removal and reduce the energy consumption. ● Mn^IV=O generated on the electrified MnO _x /Ti anode catalyzed the azo dye oxidation. ● Aerobic heterotrophic bacteria on the cathode degraded azo dye intermediate products. ● Biodegradation of intermediate products was stimulated under the electric field. Dyeing wastewater treatment remains a challenge. Although effective, the in-series process using electrochemical oxidation as the pre- or post-treatment of biodegradation is long. This study proposes a compact dual-chamber electrocatalytic biofilm reactor (ECBR) to complete azo dye decolorization and mineralization in a single unit via anodic oxidation on a MnO_x/Ti flow-through anode followed by cathodic biodegradation on carbon felts. Compared with the electrocatalytic reactor with a stainless-steel cathode (ECR-SS) and the biofilm reactor (BR), the ECBR increased the chemical oxygen demand (COD) removal efficiency by 24 % and 31 % (600 mg/L Acid Orange 7 as the feed, current of 6 mA), respectively. The COD removal efficiency of the ECBR was even higher than the sum of those of ECR-SS and BR. The ECBR also reduced the energy consumption (3.07 kWh/kg COD) by approximately half compared with ECR-SS. The advantages of the ECBR in azo dye removal were attributed to the synergistic effect of the MnO_x/Ti flow-through anode and cathodic biofilms. Catalyzed by Mn^IV=O generated on the MnO_x/Ti anode under a low applied current, azo dyes were oxidized and decolored. The intermediate products with improved biodegradability were further mineralized by the cathodic aerobic heterotrophic bacteria (non-electrochemically active) under the stimulation of the applied current. Taking advantage of the mutual interactions among the electricity, anode, and bacteria, this study provides a novel and compact process for the effective and energy-efficient treatment of azo dye wastewater.     

Electro-conductive crosslinked polyaniline/carbon nanotube nanofiltration membrane for electro-enhanced removal of bisphenol A

● A crosslinked polyaniline/carbon nanotube NF membrane was fabricated. ● Electro-assistance enhanced the removal rate of the NF membrane for bisphenol A. ● Intermittent voltage-assistance can achieve nearly 100% removal of bisphenol A. ● Membrane adsorption–electro-oxidation process is feasible for micropollutant removal. Nanofiltration (NF) has attracted increasing attention for wastewater treatment and potable water purification. However, the high-efficiency removal of micropollutants by NF membranes is a critical challenge. Owing to the adsorption and subsequent diffusion, some weakly charged or uncharged micropollutants, such as bisphenol A (BPA), can pass through NF membranes, resulting in low removal rates. Herein, an effective strategy is proposed to enhance the BPA removal efficiency of a crosslinked polyaniline/carbon nanotube NF membrane by coupling the membrane with electro-assistance. The membrane exhibited a 31.9% removal rate for 5 mg/L BPA with a permeance of 6.8 L/(m²·h·bar), while the removal rate was significantly improved to 98.1% after applying a voltage of 2.0 V to the membrane. Furthermore, when BPA coexisted with humic acid, the membrane maintained 94% removal of total organic carbon and nearly 100% removal of BPA at 2.0 V over the entire filtration period. Compared to continuous voltage applied to the membrane, an intermittent voltage (2.0 V for 0.5 h with an interval of 3.5 h) could achieve comparable BPA removal efficiency, because of the combined effect of membrane adsorption and subsequent electrochemical oxidation. Density functional theory calculations and BPA oxidation process analyses suggested that BPA was adsorbed by two main interactions: π–π and hydrogen-bond interactions. The adsorbed BPA was further electro-degraded into small organic acids or mineralized to CO₂ and H₂O. This work demonstrates that NF membranes coupled with electro-assistance are feasible for improving the removal of weakly charged or uncharged micropollutants.     

Property-performance relationship of core-shell structured black TiO2 photocatalyst for environmental remediation

● Properties and performance relationship of CSBT photocatalyst were investigated. ● Properties of CSBT were controlled by simply manipulating glycerol content. ● Performance was linked to semiconducting and physicochemical properties. ● CSBT (W:G ratio 9:1) had better performance with lower energy consumption. ● Phenols were reduced by 48.30% at a cost of $2.4127 per unit volume of effluent. Understanding the relationship between the properties and performance of black titanium dioxide with core-shell structure (CSBT) for environmental remediation is crucial for improving its prospects in practical applications. In this study, CSBT was synthesized using a glycerol-assisted sol-gel approach. The effect of different water-to-glycerol ratios (W:G = 1:0, 9:1, 2:1, and 1:1) on the semiconducting and physicochemical properties of CSBT was investigated. The effectiveness of CSBT in removing phenolic compounds (PHCs) from real agro-industrial wastewater was studied. The CSBT synthesized with a W:G ratio of 9:1 has optimized properties for enhanced removal of PHCs. It has a distinct core-shell structure and an appropriate amount of Ti³⁺ cations (11.18%), which play a crucial role in enhancing the performance of CSBT. When exposed to visible light, the CSBT performed better: 48.30% of PHCs were removed after 180 min, compared to only 21.95% for TiO₂ without core-shell structure. The CSBT consumed only 45.5235 kWh/m³ of electrical energy per order of magnitude and cost $2.4127 per unit volume of treated agro-industrial wastewater. Under the conditions tested, the CSBT demonstrated exceptional stability and reusability. The CSBT showed promising results in the treatment of phenols-containing agro-industrial wastewater.     

Factors affecting the distribution of microplastics in soils of China

● Microplastic (MP) abundance in soil of China was highly heterogeneous. ● MP abundance was higher near large rivers and central land affected by monsoons. ● MP abundance was correlated with longitude, mulching film, and average temperature. ● Factors suitable for predicting MP pollution using models were discussed. Microplastics (MPs) are found worldwide in high abundance, posing a potential threat to ecosystems. Despite the ubiquity of MPs in the environment, very little is known about the regional distribution of MPs and underlying factors affecting this distribution in the field, which likely include human activity, but also features of the environment itself. Here, out of a total of 1157 datapoints investigated in 53 Chinese studies, 9.68% datapoints were removed as outliers in the heterogeneity analysis. This review revealed that the abundance of MPs was highly heterogeneous. In addition, microplastic (MP) distribution maps based on China demonstrated that the highest abundance of MPs tended to occur near large rivers and central land affected by the intersection of two monsoons. The model-fitting and previous studies showed that MP abundance in China was correlated with longitude, agricultural mulching film usage per capita, temperature, and precipitation. However, due to the heterogeneity of MPs and the low matching degree between the current environmental data and the sampling points, this pattern was not as evident as reported in any single study. Factors affecting the distribution of MPs can not be captured by linear relationships alone, and systematic selection of suitable environmental factors and further model optimization are needed to explore the cause of MP pollution in soil. Overall, this review revealed an uneven distribution of MPs and serves as a reference for model prediction to assess and control plastic pollution in natural soil environments.     

Removal of ammonium and nitrate through Anammox and FeS-driven autotrophic denitrification

● Simultaneous NH₄⁺/NO₃^– removal was achieved in the FeS denitrification system ● Anammox coupled FeS denitrification was responsible for NH₄⁺/NO₃^– removal ● Sulfammox, Feammox and Anammox occurred for NH₄⁺ removal ● Thiobacillus, Nitrospira , and Ca. Kuenenia were key functional microorganisms An autotrophic denitrifying bioreactor with iron sulfide (FeS) as the electron donor was operated to remove ammonium (NH₄⁺) and nitrate (NO₃⁻) synergistically from wastewater for more than 298 d. The concentration of FeS greatly affected the removal of NH₄⁺/NO₃⁻. Additionally, a low hydraulic retention time worsened the removal efficiency of NH₄⁺/NO₃⁻. When the hydraulic retention time was 12 h, the optimal removal was achieved with NH₄⁺ and NO₃⁻ removal percentages both above 88%, and the corresponding nitrogen removal loading rates of NH₄⁺ and NO₃⁻ were 49.1 and 44.0 mg/(L·d), respectively. The removal of NH₄⁺ mainly occurred in the bottom section of the bioreactor through sulfate/ferric reducing anaerobic ammonium oxidation (Sulfammox/Feammox), nitrification, and anaerobic ammonium oxidation (Anammox) by functional microbes such as Nitrospira, Nitrosomonas, and Candidatus Kuenenia. Meanwhile, NO₃⁻ was mainly removed in the middle and upper sections of the bioreactor through autotrophic denitrification by Ferritrophicum, Thiobacillus, Rhodanobacter, and Pseudomonas, which possessed complete denitrification-related genes with high relative abundances.     

A critical review on thermodynamic mechanisms of membrane fouling in membrane-based water treatment process

● Fundamentals of membrane fouling are comprehensively reviewed. ● Contribution of thermodynamics on revealing membrane fouling mechanism is summarized. ● Quantitative approaches toward thermodynamic fouling mechanisms are deeply analyzed. ● Inspirations of thermodynamics for membrane fouling mitigation are briefly discussed. ● Research prospects on thermodynamics and membrane fouling are forecasted. Membrane technology is widely regarded as one of the most promising technologies for wastewater treatment and reclamation in the 21st century. However, membrane fouling significantly limits its applicability and productivity. In recent decades, research on the membrane fouling has been one of the hottest spots in the field of membrane technology. In particular, recent advances in thermodynamics have substantially widened people’s perspectives on the intrinsic mechanisms of membrane fouling. Formulation of fouling mitigation strategies and fabrication of anti-fouling membranes have both benefited substantially from those studies. In the present review, a summary of the recent results on the thermodynamic mechanisms associated with the critical adhesion and filtration processes during membrane fouling is provided. Firstly, the importance of thermodynamics in membrane fouling is comprehensively assessed. Secondly, the quantitative methods and general factors involved in thermodynamic fouling mechanisms are critically reviewed. Based on the aforementioned information, a brief discussion is presented on the potential applications of thermodynamic fouling mechanisms for membrane fouling control. Finally, prospects for further research on thermodynamic mechanisms underlying membrane fouling are presented. Overall, the present review offers comprehensive and in-depth information on the thermodynamic mechanisms associated with complex fouling behaviors, which will further facilitate research and development in membrane technology.     

A hybrid fuel cell for water purification and simultaneously electricity generation

● A novel hybrid fuel cell (F-HFC) was fabricated. ● Pollutant degradation and synchronous electricity generation occurred in F-HFC. ● BiOCl-NH₄PTA photocatalyst greatly improved electron transfer and charge separation. ● Pollutant could act as substrate directly in ambient conditions without pretreatment. ● The mechanism of the F-HFC was proposed and elucidated. The development of highly efficient energy conversion technologies to extract energy from wastewater is urgently needed, especially in facing of increasing energy and environment burdens. Here, we successfully fabricated a novel hybrid fuel cell with BiOCl-NH₄PTA as photocatalyst. The polyoxometalate (NH₄PTA) act as the acceptor of photoelectrons and could retard the recombination of photogenerated electrons and holes, which lead to superior photocatalytic degradation. By utilizing BiOCl-NH₄PTA as photocatalysts and Pt/C air-cathode, we successfully constructed an electron and mass transfer enhanced photocatalytic hybrid fuel cell with flow-through field (F-HFC). In this novel fuel cell, dyes and biomass could be directly degraded and stable power output could be obtained. About 87 % of dyes could be degraded in 30 min irradiation and nearly 100 % removed within 90 min. The current density could reach up to ~267.1 μA/cm²; with maximum power density (P_max) of ~16.2 μW/cm² with Rhodamine B as organic pollutant in F-HFC. The power densities were 9.0 μW/cm², 12.2 μW/cm², and 13.9 μW/cm² when using methyl orange (MO), glucose and starch as substrates, respectively. This hybrid fuel cell with BiOCl-NH₄PTA composite fulfills the purpose of decontamination of aqueous organic pollutants and synchronous electricity generation. Moreover, the novel design cell with separated photodegradation unit and the electricity generation unit could bring potential practical application in water purification and energy recovery from wastewater.     

Technologies for pollutant removal and resource recovery from blackwater: a review

● Blackwater is the main source of organics and nutrients in domestic wastewater. ● Various treatment methods can be applied for resource recovery from blackwater. ● Blackwater treatment systems of high integration and efficiency are the future trend. ● More research is needed for the practical use of blackwater treatment systems. Blackwater (BW), consisting of feces, urine, flushing water and toilet paper, makes up an important portion of domestic wastewater. The improper disposal of BW may lead to environmental pollution and disease transmission, threatening the sustainable development of the world. Rich in nutrients and organic matter, BW could be treated for resource recovery and reuse through various approaches. Aimed at providing guidance for the future development of BW treatment and resource recovery, this paper presented a literature review of BWs produced in different countries and types of toilets, including their physiochemical characteristics, and current treatment and resource recovery strategies. The degradation and utilization of carbon (C), nitrogen (N) and phosphorus (P) within BW are underlined. The performance of different systems was classified and summarized. Among all the treating systems, biological and ecological systems have been long and widely applied for BW treatment, showing their universality and operability in nutrients and energy recovery, but they are either slow or ineffective in removal of some refractory pollutants. Novel processes, especially advanced oxidation processes (AOPs), are becoming increasingly extensively studied in BW treatment because of their high efficiency, especially for the removal of micropollutants and pathogens. This review could serve as an instructive guidance for the design and optimization of BW treatment technologies, aiming to help in the fulfilment of sustainable human excreta management.     

A pyrazine based metal-organic framework for selective removal of copper from strongly acidic solutions

● pz-UiO-66 was synthesized facilely by a solvothermal method. ● Efficient capture of copper from highly acidic solution was achieved by pz-UiO-66. ● pz-UiO-66 exhibited excellent selectivity and capacity for copper capture. ● Pyrazine-N in pz-UiO-66 was shown to be the dominant adsorption site. The selective capture of copper from strongly acidic solutions is of vital importance from the perspective of sustainable development and environmental protection. Metal organic frameworks (MOFs) have attracted the interest of many scholars for adsorption due to their fascinating physicochemical characteristics, including adjustable structure, strong stability and porosity. Herein, pz-UiO-66 containing a pyrazine structure is successfully synthesized for the efficient separation of copper from strongly acidic conditions. Selective copper removal at low pH values is accomplished by using this material that is not available in previously reported metal–organic frameworks. Furthermore, the material exhibits excellent adsorption capacity, with a theoretical maximum copper uptake of 247 mg/g. As proven by XPS and FT-IR analysis, the coordination of pyrazine nitrogen atoms with copper ions is the dominant adsorption mechanism of copper by pz-UiO-66. This work provides an opportunity for efficient and selective copper removal under strongly acidic conditions, and promises extensive application prospects for the removal of copper in the treatment for acid metallurgical wastewater.     

Responses of microbial interactions to elevated salinity in activated sludge microbial community

● Salinity led to the elevation of NAR over 99.72%. ● Elevated salinity resulted in a small, complex, and more competitive network. ● Various AOB or denitrifiers responded differently to elevated salinity. ● Putative keystone taxa were dynamic and less abundant among various networks. Biological treatment processes are critical for sewage purification, wherein microbial interactions are tightly associated with treatment performance. Previous studies have focused on assessing how environmental factors (such as salinity) affect the diversity and composition of the microbial community but ignore the connections among microorganisms. Here, we described the microbial interactions in response to elevated salinity in an activated sludge system by performing an association network analysis. It was found that higher salinity resulted in low microbial diversity, and small, complex, more competitive overall networks, leading to poor performance of the treatment process. Subnetworks of major phyla (Proteobacteria, Bacteroidetes, and Chloroflexi) and functional bacteria (such as AOB, NOB and denitrifiers) differed substantially under elevated salinity process. Compared with subnetworks of Nitrosomonadaceae, Nitrosomonas (AOB) made a greater contribution to nitrification under higher salinity (especially 3%) in the activated sludge system. Denitrifiers established more proportion of cooperative relationships with other bacteria to resist 3% salinity stress. Furthermore, identified keystone species playing crucial roles in maintaining process stability were dynamics and less abundant under salinity disturbance. Knowledge gleaned from this study deepened our understanding of microbial interaction in response to elevated salinity in activated sludge systems.     

Simple fabrication of carboxymethyl cellulose and κ-carrageenan composite aerogel with efficient performance in removal of fluoroquinolone antibiotics from water

● A composite aerogel was simply obtained to remove various fluoroquinolones (FQs). ● The structural and textural properties of this composite aerogel are improved. ● Its adsorption capacity was improved at a low content of coexisting Cu²⁺ or Fe³⁺ ion. ● Two substructural analogs of FQs are compared to explore the adsorption mechanisms. ● This aerogel after saturated adsorption can be reused directly for Cu²⁺ adsorption. 3D composite aerogels (CMC-CG) composed of carboxymethyl cellulose and κ-carrageenan were designed and fabricated using the one-pot synthesis technique. The optimized CMC-CG showed a good mechanical property and a high swelling ratio due to its superior textural properties with a proper chemically cross-linked interpenetrating network structure. CMC-CG was utilized for the removal of various fluoroquinolones (FQs) from water and exhibited high adsorption performance because of effective electrostatic attraction and hydrogen bonding interactions. Ciprofloxacin (CIP), a popular FQ, was used as the representative. The optimized CMC-CG had a theoretically maximal CIP uptake of approximately 1.271 mmol/g at the pH of 5.0. The adsorption capacity of CMC-CG was improved in the presence of some cations, Cu²⁺ and Fe³⁺ ions, at a low concentration through the bridging effect but was reduced at a high concentration. The investigation of adsorption mechanisms, based on the adsorption kinetics, isotherms and thermodynamic study, Fourier transform infrared spectrometry and X-ray photoelectron spectroscopy analyses before and after adsorption, and changes in the adsorption performance of CMC-CG toward two molecular probes, further indicated that electrostatic attraction was the dominant interaction rather than hydrogen bonding in this adsorption. CMC-CG after saturated adsorption of CIP could be easily regenerated using a dilute NaCl aqueous solution and reused efficiently. Moreover, the disused aerogel could still be reused as a new adsorbent for effective adsorption of Cu²⁺ ion. Overall, this study suggested the promising applications of this composite aerogel as an eco-friendly, cost-effective, and recyclable adsorbent for the efficient removal of FQs from water.