Occurrence and migration of microplastics and plasticizers in different wastewater and sludge treatment units in municipal wastewater treatment plant

● Reduce the quantifying MPs time by using Nile red staining. ● The removal rate of MPs and PAEs in wastewater and sludge were investigated. ● MPs and PAEs were firstly analyzed during thermal hydrolysis treatment. ● The removal of PAEs from wastewater and sludge was mainly biodegradation. Microplastics (MPs) and plasticizers, such as phthalate esters (PAEs), were frequently detected in municipal wastewater treatment plants (MWTP). Previous research mainly studied the removal of MPs and PAEs in wastewater. However, the occurrence of MPs and PAEs in the sludge was generally ignored. To comprehensively investigate the occurrence and the migration behaviors of MPs and PAEs in MWTP, a series of representative parameters including the number, size, color, shape of MPs, and the concentrations of PAEs in wastewater and sludge were systematically investigated. In this study, the concentrations of MPs in the influent and effluent were 15.46±0.37 and 0.30±0.14 particles/L. The MP removal efficiency of 98.1% was achieved and about 73.8% of MPs were accumulated in the sludge in the MWTP. The numbers of MPs in the sludge before and after digestion were 4.40±0.14 and 0.31±0.01 particles/g (dry sludge), respectively. Fourier Transform Infrared Spectroscopy (ATR FT-IR) analysis showed that the main types of MPs were polyethylene terephthalate (PET), polypropylene (PP), polyethylene (PE), and polystyrene (PS). Six PAEs, including phthalate (DMP), diethyl phthalate (DEP), diisobutyl phthalate (DIBP), ortho dibutyl phthalate (DBP), butyl benzyl phthalate (BBP), and bis(2-ethyl) hexyl phthalate (DEHP), were detected in the MWTP. The concentrations of total PAEs (ΣPAEs) in the influent and effluent were 76.66 and 6.28 µg/L, respectively. The concentrations of ΣPAEs in the sludge before and after digestion were 152.64 and 31.70 µg/g, respectively. In the process of thermal hydrolysis, the number and size of MPs decreased accompanied by the increase of the plasticizer concentration.     

Microbial biodegradation of plastics: Challenges,opportunities, and a critical perspective

● Health hazards of plastic waste on environment are discussed. ● Microbial species involved in biodegradation of plastics are being reviewed. ● Enzymatic biodegradation mechanism of plastics is outlined. ● Analytical techniques to evaluate the plastic biodegradation are presented. The abundance of synthetic polymers has increased due to their uncontrolled utilization and disposal in the environment. The recalcitrant nature of plastics leads to accumulation and saturation in the environment, which is a matter of great concern. An exponential rise has been reported in plastic pollution during the corona pandemic because of PPE kits, gloves, and face masks made up of single-use plastics. The physicochemical methods have been employed to degrade synthetic polymers, but these methods have limited efficiency and cause the release of hazardous metabolites or by-products in the environment. Microbial species, isolated from landfills and dumpsites, have utilized plastics as the sole source of carbon, energy, and biomass production. The involvement of microbial strains in plastic degradation is evident as a substantial amount of mineralization has been observed. However, the complete removal of plastic could not be achieved, but it is still effective compared to the pre-existing traditional methods. Therefore, microbial species and the enzymes involved in plastic waste degradation could be utilized as eco-friendly alternatives. Thus, microbial biodegradation approaches have a profound scope to cope with the plastic waste problem in a cost-effective and environmental-friendly manner. Further, microbial degradation can be optimized and combined with physicochemical methods to achieve substantial results. This review summarizes the different microbial species, their genes, biochemical pathways, and enzymes involved in plastic biodegradation.     

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.     

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.     

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.     

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.     

Co-pyrolysis of oil sludge with hydrogen-rich plastics in a vertical stirring reactor: Kinetic analysis,emissions, and products

● Collaborative treatment of plastics and OS was established to improve oil quality. ● PE addition successfully improved OS pyrolysis process by deploying H/C_eff ratio. ● Higher H/C_eff ratio promoted cracking to obtain more gas and light oil fractions. ● The degradation of PE and OS was promoted each other under their temperature range. Pyrolysis is an effective method to treat oily sludge (OS) due to its balance between oil recovery and nonhazardous disposal. However, tank bottom OS contains a high content of heavy fractions, which creates obstacles for pyrolysis due to the high activation energy. The incomplete cracking of macromolecules and secondary polymerization decreases the oil quality and causes coking during the operation process. This study introduced polyethylene (PE) into OS to deploy the H/C_eff ratio of feedstocks for pyrolysis. A strong interaction between OS and PE during copyrolysis could be observed from the TG/DTG curves. PE tightly participated in OS degradation, while OS also promoted PE degradation at high temperature. Apparent pits were generated in solid residues from copyrolysis, which was attributed to the uniform and violent gas release. In addition to HCN, other nitrogenous and sulphurous pollutants were inhibited. Accordingly, more gas products were attained after PE addition with more value-added compositions of alkanes and alkenes. Although the oil yield decreased after PE addition, the oil products from copyrolysis possessed higher heating values and higher contents of light fractions with short chains as well as paraffins. Consequently, copyrolysis of OS and PE significantly improved the pyrolysis process and resulted in high oil quality.     

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.     

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.     

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 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.     

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.     

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.     

Characterization and variation of dissolved organic matter in composting: a critical review

● Effect of composting approaches on dissolved organic matter (DOM). ● Effect of composting conditions on the properties of DOM. ● Character indexes of DOM varied in composting. ● The size, hydrophobicity, humification, and electron transfer capacity increased. ● The hydrophilicity, protein-like materials, and aliphatic components reduced. As the most motive organic fraction in composting, dissolved organic matter (DOM) can contribute to the transfer and dispersal of pollutants and facilitate the global carbon cycle in aquatic ecosystems. However, it is still unclear how composting approaches and conditions influence the properties of compost-derived DOM. Further details on the shift of DOM character indexes are required. In this study, the change in properties of compost-derived DOM at different composting approaches and the effect of composting conditions on the DOM characteristics are summarized. Thereafter, the change in DOM character indexes’ in composting was comprehensively reviewed. Along with composting, the elements and spectral properties (chromophoric DOM (CDOM) and fluorescent DOM (FDOM)) were altered, size and hydrophobicity increased, and aromatic-C and electron transfer capacity were promoted. Finally, some prospects to improve this study were put forward. This paper should facilitate the people who have an interest in tracing the fate of DOM in composting.     

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.     

Current scenario and challenges of plastic pollution in Bangladesh: a focus on farmlands and terrestrial ecosystems

● A global snapshot of plastic waste generation and disposal is analysed. ● Effect of plastic pollution on environment and terrestrial ecosystem is reviewed. ● Ecotoxicity and food security from plastic pollution is discussed. Plastic is considered one of the most indispensable commodities in our daily life. At the end of life, the huge ever-growing pile of plastic waste (PW) causes serious concerns for our environment, including agricultural farmlands, groundwater quality, marine and land ecosystems, food toxicity and human health hazards. Lack of proper infrastructure, financial backup, and technological advancement turn this hazardous waste plastic management into a serious threat to developing countries, especially for Bangladesh. A comprehensive review of PW generation and its consequences on environment in both global and Bangladesh contexts is presented. The dispersion routes of PW from different sources in different forms (microplastic, macroplastic, nanoplastic) and its adverse effect on agriculture, marine life and terrestrial ecosystems are illustrated in this work. The key challenges to mitigate PW pollution and tackle down the climate change issue is discussed in this work. Moreover, way forward toward the design and implementation of proper PW management strategies are highlighted in this study.     

Screening of indicator pharmaceuticals and personal care products in landfill leachates: a case study in Shanghai,China

● A systematic framework was developed to identify i-PPCPs for landfill leachate. ● The wide-scope target analysis offered a basis for comprehensive i-PPCP screening. ● Source-specificity and representativeness analysis helped to refine i-PPCPs. ● Erythromycin, gemfibrozil and albendazole were identified as i-PPCPs for leachate. Identifying potential sources of pharmaceuticals and personal care products (PPCPs) in the environment is critical for the effective control of PPCP contamination. Landfill leachate is an important source of PPCPs in water; however, it has barely been involved in source apportionment due to the lack of indicator-PPCPs (i-PPCPs) in landfill leachates. This study provides the first systematic framework for identifying i-PPCPs for landfill leachates based on the wide-scope target monitoring of PPCPs. The number of target PPCPs increased from < 20 in previous studies to 68 in the present study. Fifty-nine PPCPs were detected, with median concentrations in leachate samples ranging from below the method quantification limit (MQL) to 41 μg/L, and 19 of them were rarely reported previously. A total of 29 target compounds were determined to be PPCPs of high concern by principal component analysis according to multiple criteria, including occurrence, exposure potential, and ecological effect. Coupled with source-specificity and representativeness analysis, erythromycin, gemfibrozil, and albendazole showed a significant difference in their occurrence in leachate compared to other potential sources (untreated and treated municipal wastewater and livestock wastewater) and correlated with total PPCP concentrations; these were recommended as i-PPCPs for leachates. Indicator screening procedure can be used to develop a sophisticated source apportionment method to identify sources of PPCPs from adjacent landfills.     

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.     

Low-temperature caproate production,microbial diversity,and metabolic pathway in xylose anaerobic fermentation

● Converting xylose to caproate under a low temperature of 20 °C by MCF was verified. ● Final concentration of caproate from xylose in a batch reactor reached 1.6 g/L. ● Changing the substrate to ethanol did not notably increase the caproate production. ● Four genera, including Bifidobacterium , were revealed as caproate producers. ● The FAB pathway and incomplete RBO pathway were revealed via metagenomic analysis. Mixed culture fermentation (MCF) is challenged by the unqualified activity of enriched bacteria and unwanted methane dissolution under low temperatures. In this work, caproate production from xylose was investigated by MCF at a low temperature (20 °C). The results showed that a 9 d long hydraulic retention time (HRT) in a continuously stirred tank reactor was necessary for caproate production (~0.3 g/L, equal to 0.6 g COD/L) from xylose (10 g/L). The caproate concentration in the batch mode was further increased to 1.6 g/L. However, changing the substrate to ethanol did not promote caproate production, resulting in ~1.0 g/L after 45 d of operation. Four genera, Bifidobacterium, Caproiciproducens, Actinomyces, and Clostridium_sensu_stricto_12, were identified as the enriched caproate-producing bacteria. The enzymes in the fatty acid biosynthesis (FAB) pathway for caproate production were identified via metagenomic analysis. The enzymes for the conversion of (C_n+2)-2,3-Dehydroxyacyl-CoA to (C_n+2)-Acyl-CoA (i.e., EC 1.3.1.8 and EC 1.3.1.38) in the reverse β-oxidation (RBO) pathway were not identified. These results could extend the understanding of low-temperature caproate production.     

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.