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Potassium ion signaling mediates microbial communication in electroactive biofilms within microbial fuel cells (MFCs), but its role in nitrogen removal remains unclear. This study investigated the impact of inhibiting potassium signaling on nitrogen removal in MFCs using tetraethylammonium chloride (TEA) as an inhibitor. Results demonstrated that 5 mM and 10 mM TEA reduced the maximum power generation of MFCs from 77.95 mW/cm 2 to 57.18 mW/cm 2 and 48.23 mW/cm 2 , respectively. Correspondingly, total nitrogen (TN) removal efficiency was decreased from 46.57 ± 1.01% to 35.93 ± 0.63% and 38.97 ± 0.74%, respectively. This decline was attributed to inhibited potassium ion signaling, which compromised the electrochemical performance of the MFC and hindered the nitrogen removal process. The relative abundance of exoelectrogen Geobactor decreased from 15.37% to 5.17% and 8.05%, while the relative abundance of cathodic nitrifying bacteria Nitrosomonas decreased from 17.87% to 4.92% and 3.63% under 5 mM and 10 mM TEA. These findings underscore the crucial role of potassium ion signaling in enhancing the bioelectrochemical nitrogen removal process in MFCs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Inc.)

Deep dewatering of Waste Activated Sludge (WAS) through mechanical processes remains inefficient, primarily due to the formation of a stable hydrogen bonding network between the biopolymers and water, which consequently leads to significant water trapped by Extracellular Polymeric Substances (EPS). In this study, a novel and recyclable treatment for WAS based on Ionic Liquids (ILs) was established, named IL-biphasic aqueous system (IL-ABS) treatment. Specifically, the IL-ABS formed in WAS facilitated rapid and efficient in-situ deep dewatering while concurrently recovering hydroxyapatite. The water content decreased from an initial 98.27 % to 65.35 % with IL-ABS, formed by 1-Butyl-3-methylimidazolium bromide (BmimBr) and K 3 PO 4 synthesized from waste H 3 PO 4 . Moreover, the recycled BmimBr maintaining the water content of the dewatered sludge consistently between 65.61 % and 67.25 % across five cycles, exhibited remarkable reproducibility. Through three-dimensional excitation-emission matrix, lactate dehydrogenase analyses and confocal laser scanning microscopy, the high concentration of BmimBr in the upper phase effectively disrupted the cells and EPS, which exposed protein and polysaccharide on the EPS surface. Subsequently, the K 3 PO 4 in the lower phase led to an enhanced salting-out effect in WAS. Furthermore, FT-IR analysis revealed that K 3 PO 4 disrupted the original hydrogen bonds between EPS and water. Then, BmimBr formed numerous hydrogen bonds with the sludge flocs, leading to deep dewatering and agglomeration of the sludge flocs during the unique phase separation process of IL-ABS. Notably, sludge-derived hydroxyapatite product exhibited remarkable adsorption capacity for prevalent heavy metal contaminants such as Pb 2+ , Cd 2+ and Cu 2+ , with efficiencies comparable to those of commercial hydroxyapatite, thereby achieving the resource utilization of waste H 3 PO 4 . Moreover, economic calculations demonstrated the suitability of this novel treatment. This innovative treatment exhibits potential for practical applications in the non-mechanical deep dewatering of WAS., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Field-scale trials were conducted to remove cadmium (Cd) from paddy soil by using recycled hydroxyapatite modified biochar (HBC) plus low-level CaCl 2 washing. Synergistic reduction efficiencies of total and available Cd in soil (45.6 % and 36.8 %) were achieved by the combined amendments compared with only HBC or CaCl 2 . The release of Cd from soil particulates was facilitated by CaCl 2 washing and the increased soluble Cd in soil water (hardly removed by drainage) could be removed efficiently by recycled HBC adsorption. Significantly decreases in Cd translocation and accumulation in rice plants benefited from the decrease of Cd level and availability in soil and the increase of available silicon (Si). As a result, Cd contents in early/late rice grains decreased by ~85 % and met the Chinese national food standard. SOM, CEC, and soil nutrients after remediation were increased due to 10 %-15 % of HBC residual. Grain yields of the early and late rice increased by 34.1 % and 9.91 %, respectively. The collected HBC (>85 % of the total used HBC) was in-situ regenerated and could be used in the next field trials. The generated wastewater together with drainage from field treatment could be reused as irrigation water after the treatment with a small-scale reclamation ecosystem. The work provides a novelty remediation strategy for Cd-contaminated paddy soil. The noticeable remediation efficiency for Cd reduction in soil and grains, and improved productivity-relevant soil properties have important implications for paddy soil with poor fertility, severe desilicification, and Cd contamination in South China whereas the application of biochar or chemical washing alone did not., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Hemin has attracted considerable interest as an efficient catalyst recently, however, its direct application is inefficient due to severe molecular aggregation. Immobilizing hemin on various supports is a feasible approach to address this issue. In this work, a CNTs-hemin catalyst was prepared by loading hemin onto multiwalled carbon nanotubes (CNTs) through ball milling. Compared with hemin, CNTs-hemin demonstrates remarkably enhanced performance in the peroxymonosulfate system, with a 650-fold improvement of apparent rate constant, reaching 97.8% degradation of sulfathiazole in 5 min. High-valent iron-oxo porphyrin cation ((Porp) +• Fe IV =O) radicals are proposed as the dominant reactive species in the CNTs-hemin/peroxymonosulfate system instead of sulfate radicals (SO 4 •- ), hydroxyl radicals (•OH), superoxide radicals (O 2 •- ) and singlet oxygen ( 1 O 2 ). More in-depth mechanisms reveal that the strong electron transfer between CNTs and hemin promotes the generation of (Porp) +• Fe IV =O radicals through a heterolysis pathway. This research enriches the understanding of the catalytic mechanism of supported biomimetic catalysts for PMS activation and provides a perspective on the role of support materials for catalytic activity., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Here the role of microplastic size on dissolved organic matter, leaching compounds and microbial community during anaerobic sludge digestion was evaluated. Compared to that without the addition of polyvinyl chloride (PVC), during the 30 days' incubation, the anaerobic sludge digestion by adding PVC at the size of 75 μm and the concentration of 2.4 g/g volatile solids (VS) showed a 8.5% lower cumulative methane production, while a 17.9% higher cumulative methane production was noted by adding PVC at the size of 3000 μm and the concentration of 2.4 g/g VS. A long-term fed-batch laboratory-scale fermenter test for 147 days further testified, that higher removal efficiencies of total solids, volatile solids, and total chemical oxygen demand, and higher methane production were noted by adding PVC (2.4 g/g VS, 3000 μm) into the fermenter. More interestingly, higher concentrations of proteins, polysaccharides, volatile fatty acids, and soluble microbial by-products component were noted in the liquid phase of sludge drawn from the fermenter added with PVC since the biomass therein showed higher efficiencies of solubilization, hydrolysis, acidification, and methanogenesis. Moreover, as identified from the fermenter added with PVC, dibutyl phthalate (DBP) was the most predominant leaching phthalates compound, although the biomass therein showed a 93.4% anaerobic biodegradability of DBP. The leaching of DBP drove the predominance of microbial community towards Synergistota and Methanosaeta. More irregular elliptical shallow dimples were noted on the PVC surface after 147 days' incubation, accompanied with abundances of Proteobacteria, Actinobacteriota, Chloroflexi, Methanosaeta and Methanobacterium. The results from this study showed that the size of microplastic was a crucial factor in evaluating its impact on anaerobic sludge digestion., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Low concentrations of antibiotics can regulate the formation of electroactive biofilms, however, the underlying mechanisms, especially the composition and spatial distribution of extracellular polymeric substances (EPS) and their effects on extracellular electron transfer (EET) process, have not been fully deciphered. Here, the response of EPS of Geobacter sulfurreducens biofilm to low concentrations of tetracycline (μg L -1 to mg L -1 ) was explored, and the impact of such EPS variations on EET efficiency was further elucidated by transcriptomic analysis. Results showed that 0.05 mg L -1 of tetracycline achieved both beneficial quantitative and spatial regulation of redox-active proteins and non-conducting exopolysaccharides in EPS, while higher concentrations induced negative effects. Moreover, 1 mg L -1 of tetracycline upregulated multiple exopolysaccharide biosynthesis-related genes, indicating a stress response for cell-protection, while 0.05 mg L -1 of tetracycline upregulated most direct EET-related gene expressions, resulting in the promoted EET efficiency. Furthermore, 0.05 mg L -1 of tetracycline selectively enriched Geobacter (45.55% vs 19.55% in control, respectively) from mixed inoculum. This research provides a new insight of how antibiotics at low concentrations regulated EET process through modulation of EPS., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

This study systematically evaluated phosphorus (P) solubilization from pyrochar and hydrochar derived from both raw sludge and iron-rich sludge. The data indicated, that an increase in thermal treatment temperature and the presence of iron promoted the accumulation of P in both pyrochar (derived at 300, 500, and 800 °C) and hydrochar (derived at 100, 200, and 280 °C). After incubating pyrochar and hydrochar with a phosphate solubilizing microorganism (PSM) (Pseudomonas aeruginosa) for 30 days, PSM significantly promoted the solubilization of P in pyrochar and hydrochar synthesized at low temperatures rather than those at high temperatures, with a 59 % increase for the pyrolysis of raw sludge at 300 °C than that pyrolyzed at 800 °C and a 62 % increase for the hydrothermal treatment of raw sludge at 100 °C than that treated at 280 °C. And the phenomena were more obvious on the char samples derived from iron-rich sludge. The mass balance of different P species in the solid and liquid phases indicated that after incubating with PSM for 30 days, NaOH-P was the main P solubilized from the solid phase of pyrochar and HCl-P was the main P solubilized from the solid phase of hydrochar. Considering P availability to plants, the preliminary economic analysis indicated that the hydrothermal treatment of iron-rich sludge at 100 °C showed the highest economic benefits for P recovery, with the net cost of 28.79 USD/ton wet sludge. This study was useful in giving novel insights into the reuse of char samples as P fertilizer, and also suggested the importance of Pseudomonas aeruginosa and other bacteria in sludge application, particularly in terms of P solubilization., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

This study investigated a novel sodium iron chlorophyllin-H 2 O 2 (SIC-H 2 O 2 ) sludge pretreatment strategy before anaerobic digestion to enhance methane production. The efficiencies and mechanism of the proposed strategy to enhance sludge biodegradability were explored. The SIC-H 2 O 2 pretreatment could enhance the oxidation performance for sludge floc disintegration to dissociate TB-EPS into S-EPS increased SCOD to 521.38 mg/L. The increase of solubilization and release of EPS with the pretreatment facilitate the biogas production at 702 L kg -1 VS, which was 3-folds of the control and significantly higher than other pretreatments. The result of excitation-emission matrix and parallel factor (EEM-PARAFAC) analysis showed that the SIC-H 2 O 2 pretreatment enhanced the dissociation of TB-EPS fractions, especially the protein-like and soluble microbial by-product-like substances. Electron paramagnetic resonance (EPR) results provided evidence for homolytic catalysis H 2 O 2 for the generation OH and the production of high-valent (Por)Fe IV (O) intermediates. Synergistic effects of reactive oxygen species (OH, H 2 O 2 and /HO 2 ) and (Por)Fe IV (O) enhanced the EPS disintegration during SIC-H 2 O 2 pretreatment. The mixed-acid type fermentation provided continuous VFAs supply under the enrichment of Chloroflexi and Actinobacteria and multiplication Methanosaeta also promoted methane production. This research provides a feasible pretreatment strategy increase sludge biodegradability and enhance biogas production in the anaerobic digestion process., (Copyright © 2021. Published by Elsevier Inc.)

The utilization of recycled biochar combined with chemical leaching is an appropriate method to remove cadmium (Cd) from paddy soil. Some Cd-rich soil clay particulates (particulate Cd) are reported to be removed via biochar adsorption and the potential impact of biochar on soil properties need further study. The removal efficiencies and mechanisms of Cd from soil by using floatable hydroxyapatite modified biochar (HBC) combined with CaCl 2 were studied. Synergetic removal efficiencies of total Cd (46.5%) and bioavailable Cd (37.9%) from the paddy soil were achieved with 2% HBC and 1 mM CaCl 2 . The increased soluble Cd in soil pore water by CaCl 2 leaching could be efficiently adsorbed on HBC, and removed by HBC collection, reducing the risk of the residual soluble Cd in soil pore water to rice plants caused by the inefficient drainage in the field. The suspendability of clay particulates in overlying water was little affected by the low-level CaCl 2 based on Derjaguin-Landau-Verwey-Overbeek (DLVO) calculation. Moreover, low-level CaCl 2 facilitated the accumulation of particulate Cd on the floating HBC via decreasing the interaction energy (by 25%) between clay particulates and HBC. HBC-mediated Cd migration contributed ~70% of total Cd removal, while soluble and particulate Cd removed through the drainage accounted for ~30%. Soil clay proportion maintained at 25.3% due to the replenishment of HBC residues. In addition, soil nutrient and physicochemical conditions were improved with HBC residues. This work provides a novel soil remediation method by using floatable biochar combined with low-level CaCl 2 for Cd-contaminated paddy soil remediation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Biological wastewater treatment generates a large quantity of sewage sludge that requires proper treatments. In this study, the biochar pyrolyzed by sludge conditioned with Fenton's reagent and lime (referred to as Fenton-lime system) was first used as an efficient silicon fertilizer for rice cultivation. When the pyrolysis temperature was 750 °C, the dissolved silicon and available silicon contents in biochar derived from sludge conditioned with Fenton-lime system were much higher than those in raw sludge derived biochar without conditioning (3.49 vs. 0.72, 77.25 vs. 2.33 mg/g dry solid, respectively). The enhanced available silicon content was attributed to the newly formed calcium aluminosilicate from the reactions between the added lime and silicon-rich phases in sludge. The rice cultivated with biochar derived from Fenton-lime conditioned sludge showed improved biomass of stem and root by 76.85% and 36.11%, respectively, compared to blank group without the addition of Si source. Heavy metals and the reactive oxygen species (ROS) accumulation in rice were not observed after a culture period of 30 days in the application of sludge-derived biochar as silicon fertilizer. This study provides a promising approach for sewage sludge recycling as an efficient silicon fertilizer in silicon-deficiency land., Competing Interests: Declaration of competing interest We wish to confirm that there are no known conflicts of interest associated with this publication and there has been no significant financial support for this work that could have influenced its outcome. We confirm that we have given due consideration to the protection of intellectual property associated with this work and that there are no impediments to publication, including the timing of publication, with respect to intellectual property. In so doing we confirm that we have followed the regulations of our institutions concerning intellectual property., (Copyright © 2021. Published by Elsevier B.V.)

Microplastic accumulation in agricultural soils can stress plants and affects quality of the products. Current research on the effects of microplastics on plants is not consistent and the underlying mechanisms are yet unknown. Here, the molecular mechanisms of the stress response were investigated via metabolomic and transcriptomic analyses of rice Oryza sativa L. II Y900 and XS123 under the exposure of polystyrene microplastics (PS-MPs) in a field study. Distinct responses were obtained in these two rice subspecies, showing decreased head rice yield by 10.62% in Y900 and increase by 6.35% in XS123. The metabolomics results showed that PS-MPs exposure inhibited 29.63% of the substance accumulation-related metabolic pathways and 43.25% of the energy expenditure-related metabolic pathways in the Y900 grains; however, these related pathways were promoted in the XS123 grains. The transcriptomics results indicated that the expression of genes encoding proteins involved in the tricarboxylic acid cycle in the Y900 grains was inhibited, but it was enhanced in the XS123 grains. The XS123 subspecies could response against microplastic exposure stress through the metabolite accumulation and energy expenditure pathways, while the Y900 could not. The results provide insight into the perturbation of rice grains in farmlands with microplastics contamination., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Deep dewatering of sewage sludge pretreated with advanced oxidation processes (AOPs) is a strategy for efficient sludge reduction and subsequent disposal. The pretreatment and dewatering performance of sludge conditioned with three types of AOPs (Fe 2+ /H 2 O 2 , Fe 2+ /Ca(ClO) 2 , and Fe 2+ /Na 2 S 2 O 8 ), compared with sludge conditioned with traditional conditioner (Fe 3+ /CaO), were investigated in both bench and pilot-scale tests. All of those conditioner systems could reduce the water content of dewatered sludge cake to below 60 wt% in bench-scale (about 16 kg raw sludge per round) and pilot-scale (approximate 800 kg raw sludge per round) diaphragm filter press dewatering. Compared with raw sludge, the deep-dewatering filtrate after different conditioning and dewatering processes had higher ammonia nitrogen (NH 4 + -N) and chemical oxygen demand (COD) contents due to the degradation of organic matter, and much lower total phosphorus (TP) content due to the formation of iron phosphate precipitate. A better biodegradability (i.e. higher BOD 5 /COD ratio) was found in the deep-dewatering filtrate of sludge conditioned with Fe 2+ /H 2 O 2 (25.2 %) and Fe 2+ /Ca(ClO) 2 (17.4 %). Most of the heavy metals (Cr, Cu, Ni, and Pb) (>79 wt%) have remained in the dewatered sludge cake, and most of the Cl element (>90 wt%) in the sludge pretreated by Fe 2+ /Ca(ClO) 2 and Fe 3+ /CaO was kept in the filtrate, rather than the dewatered sludge cake. Based on the pilot-scale experimental results, if all the filtrate in the deep-dewatering process returned to the influent of WWTP, the loading ratios of TP, NH 4 + -N, COD in the four conditioner systems were less than 3 wt%. The above results proved that the AOPs conditioned sludge could achieve deep-dewatering in pilot-scale and the direct recirculation of deep-dewatering filtrate to the influent of wastewater treatment plant was feasible., (Copyright © 2021 Elsevier Inc. All rights reserved.)

The electrogeneration of H 2 O 2 and electro-regeneration of ferrous are conflicting matters in electro-Fenton system. In this research, the degradation of Rhodamine B, methyl orange (MO) and 4-chlorophenol (4-CP) was investigated using a novel dual-cathode microbial fuel cell (MFC) electro-Fenton (EF) hybrid system. An air-cathode of an EF system was used for H 2 O 2 electrogeneration and a carbon felt cathode of a MFC was used to accelerate Fe 2+ regeneration. Synergistic improvement of MFC power generation and the degradation of the above refractory organics through EF reaction was achieved. The EF air-cathode was fabricated by adopting activated carbon/graphite powder mixture and PVDF binder, which showed higher H 2 O 2 generation but slower Fe 3+ reduction rate than MFC carbon felt cathode. The Rhodamine B removal rate constant and mineralization current efficiency of the MFC coupled EF were 64% and 42% higher than that of uncoupled EF, respectively. The MFC-EF coupled system also exhibited significantly higher removal efficiency for MO and 4-CP than that of un-coupled EF system. Moreover, the power density of MFC was greatly enhanced by coupling EF due to higher Fe 3+ /Fe 2+ redox potential than oxygen reduction., (Copyright © 2021 Elsevier B.V. All rights reserved.)

How to efficiently improve waste activated sludge (WAS) dewaterability is a common challenge in WAS treatment and management throughout world. The interaction energy of sludge flocs is of great importance for sludge dewaterability. In this study, the relationship among the repulsive force of sludge flocs, hydrophilic/hydrophobic characteristics of sludge flocs, and sludge dewaterability have been quantitatively and qualitatively investigated based on extended Derjaguin-Landau-Verwey-Overbeek theory for the first time. The energy barrier of sludge flocs has good correlations with sludge dewaterability (p < 0.05). Trivalent cations (Al 3+ and Fe 3+ ) and Fenton's reagent reduced the interfacial free energy (ΔG) from 9.4 mJ/m 2 of raw sludge to -34.2 (Al 3+ ), -60.5 (Fe 3+ ), and -63.2 (Fenton) mJ/m 2 , respectively, indicating that the hydrophilic surfaces of the sludge flocs converted to hydrophobic (△G < 0), and decreasing Lewis acid-base interaction energy (W AB ) of sludge flocs. In addition, most of the trivalent cations (Al 3+ and Fe 3+ ) were attached to sludge flocs, leading to neutralize negative charges and mitigate electrostatic interaction energy (W R ) of sludge flocs. The reduction of W AB and W R eliminated energy barrier of sludge flocs and repulsive force between sludge flocs. In comparison, monovalent (Na + and K + ) and bivalent (Ca 2+ and Mn 2+ ) cations cannot completely change the hydrophilic surface characteristic and negative charge of sludge flocs. The existed energy barrier prevented sludge flocs to agglomerate with each other, thus resulting in a worse dewaterability. This study illustrated that reducing interaction energy of sludge flocs played a critical role to improve sludge dewaterability., (Copyright © 2020 Elsevier Inc. All rights reserved.)

A hybrid sludge conditioning strategy with electrooxidation and Fe(II) addition was used for heavy metal removal from sewage sludge and industrial sludge, with simultaneous sludge dewatering and stabilization. With the addition of 82 mg/g DS Fe(II) and treatment time of 4.5 h, heavy metal removals of 72.95% and 78.49% for Cu, 66.29% and 84.26% for Zn, and 36.52% and 36.99% for Pb were achieved from sewage sludge and industrial sludge samples respectively. The system pH decreased to 2.33 and 2.98 and the oxidation-reduction potential (ORP) values increased to 435.90 mV and 480.60 mV in sewage sludge and industrial sludge samples, respectively, which was conducive to the desorption and dissolution of heavy metals from sludge structures and the degradation of the organic compounds that complexed with heavy metals. In addition, the hybrid conditioning process demonstrated excellent dewatering performance due to the efficient electrochemical disintegration of sludge flocs together with the coagulation of sludge particles by Fe(III) generated via electrooxidation. The strong acidic and oxidative environment produced by the enhanced electrooxidation process was also responsible for pathogen inactivation., (Copyright © 2020 Elsevier B.V. All rights reserved.)

A hybrid electrochemical process with Ca(ClO) 2 addition for simultaneous sludge dewaterability, stabilization and phosphorus fixation was proposed. Under optimal conditions (150 mg/g VS Ca(ClO) 2 , 15 V), the capillary suction time (CST) and specific resistance to filtration (SRF) were decreased by 88% and 92%, respectively. Efficient sludge stabilization with E. coli colonies of less than 1000 MPN/g TS was achieved. Phosphorus of 99% was removed from the filtrate and successfully fixed in the sludge cake and on the electrode surface. The integration of electrochemical and hypochlorite oxidation could effectively degrade the tightly bound extracellular polymeric substances (TB-EPS) structure with a total organic carbon (TOC) reduction of 52%. Besides, the disintegration of microbial cell envelopes was also achieved, with a reduction of living cell fraction of 98%. Furthermore, system pH could be maintained at near neutral (7.45) and the conversion of Fe(II) to Fe(III) was also facilitated with the addition of Ca(ClO) 2 , resulting in improved electrocoagulation process for enhanced sludge dewatering and phosphorus fixation. The multifunctional effects were achieved with the cooperated extracellular electrooxidation for EPS destruction and the active chlorine for intracellular microbial cell disintegration. This research provides a promising strategy for integrated sludge treatment and recycling for possible land utilization., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Although polyhalogenated carbazoles (PHCZs) can be generated and detected in drinking water, their occurrence and potential health risks to humans via drinking water ingestion are not well known. In this study, 11 PHCZs were screened in drinking water samples from Wuhan, the most populous city in central China. The total concentration of PHCZs could be up to 53.48 ng/L with a median level of 8.19 ng/L, which was comparable to polychlorinated biphenyls and poly- and perfluoroalkyl substances reported in the literatures for drinking water. Composition profiles revealed that 3,6-dichlorocarbazole, 3-chlorocarbazole, 3-bromocarbazole and 3,6-dibromocarbazole were the predominant PHCZ congeners in the tested samples. Regional differences in the levels and patterns of PHCZs suggested that anthropogenic releases should be the dominant source compared to natural generation. Boiling of the water samples caused no significant change in PHCZs concentrations after correcting the volume change due to evaporation. Potential health risks associated to the levels of PHCZs in drinking water were assessed using the toxic equivalent (TEQs) method. The estimated daily intake of PHCZs via drinking water ingestion is up to 0.38 pg-TEQ/kg body weight/day for infants, nearly 4.5 times higher than that for adults, and appears to reach the maximum permissible concentration set by certain authority agencies. Overall, drinking water ingestion represents an important exposure pathway for PHCZs. This is the first comprehensive study on the abundance and health risks of PHCZs in drinking water., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

A novel method to enhance sludge dewaterability with ammonium sulfate ((NH 4 ) 2 SO 4 ) was proposed, and the potential reuse of dewatered sludge cake and filtrate as nitrogen fertilizers was evaluated. Compared with raw sludge, 87.91% reduction of capillary suction time (CST) and 88.02% reduction of specific resistance to filtration (SRF) after adding 80% (m/m) (NH 4 ) 2 SO 4 were achieved, with 38.49% of protein precipitated simultaneously. The (NH 4 ) 2 SO 4 dose destroyed cell membrane, resulting in the release of intracellular water by converting bound water into free water, thus enhancing sludge dewaterability. In the solid phase, the content of protein-N increased, and larger protein aggregates were formed. The (NH 4 ) 2 SO 4 dose destroyed the hydration shell, making proteins to exhibit hydrophobic interactions, and to be aggregated, and precipitated from the liquid phase. When incubated Pennisetum alopecuroides L. with the dewatered sludge cake and filtrate after dewatering and conditioning with (NH 4 ) 2 SO 4 , the germination rate of grass seed and shoot lengths both increased while compared with those incubated with dewatered sludge cake and filtrate of the raw sludge. This study might provide insights into sustainable sludge treatment by integrating sludge dewatering and the potential reuse of dewatered sludge cake and filtrate as nitrogen fertilizer via treatment with (NH 4 ) 2 SO 4 ., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Fe-rich biochar with multivalent iron compounds (Fe 0 , Fe 0.95 C 0.05 , Fe 3 O 4 , and FeAl 2 O 4 ) pyrolyzed from sludge cake conditioned with Fenton's reagent and red mud was utilized as an efficient Fenton catalyst for the degradation of 4-chlorophenol (4-CP). Effects of pyrolysis temperature and sludge conditioner composition on the transformation of iron compounds were studied. Both homogeneous Fenton reaction initiated by Fe 2+ leached from both low-valent Fe 0 and Fe 0.95 C 0.05 , and heterogeneous Fenton reaction initiated by solid iron phases of Fe 3 O 4 and FeAl 2 O 4 were revealed to contribute to the degradation of 4-CP. The removal efficiency of 4-CP remained 100% after five successive degradation rounds. The homogeneous Fenton reaction mainly works in the first degradation round, and the heterogeneous Fenton reaction dominates in subsequent degradation rounds. The findings of this study suggest that sewage sludge derived Fe-rich biochar could be utilized as an efficient Fenton catalyst for recalcitrant organics degradation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

The novel catalyst LaCu 0.5 Fe 0.5 O 3-δ with oxygen vacancies (OVs) was prepared and demonstrated excellent stability and activity for the degradation of bisphenol A. The removal rate of 92.1 % and H 2 O 2 utilization efficiency of 70.4 % were obtained due to the efficient hydroxyl radical generation mediated by OVs. The density functional theory calculation showed that the substitution of Cu and formation of OVs significantly increases the charge density near the active sites. Bader charge analysis revealed that the charge offset accelerated the reduction of Fe. The elevation of electron transfer efficiency also promotes the valence transition of copper and iron atoms. The reversible electronic transition between Fe 2+ ⇆ Fe 3+ , Cu + ⇆ Cu 2+ and Cu 2+ ⇆ Fe 2+ involved in this reaction were considered to be enhanced and the homolytic bond clearage of H 2 O 2 was simultaneously promoted, facilitated by the electron-rich region combined with OVs on the surface of LaCu 0.5 Fe 0.5 O 3-δ ., Competing Interests: Declaration of Competing Interest The authors declare no competing financial interest., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Biogas and phosphorus recovery from waste activated sludge (WAS) with sequential homogeneous protocatechuic acid (PCA) enhanced Fenton pretreatment, anaerobic digestion (AD) and microbial electrolysis cell (MEC) were investigated. The cumulation of biogas production of WAS-Fenton-AD was 330.4 mL/g VS, which was 2.05-fold of the control without pretreatment (WAS-AD) during anaerobic digestion. Biogas production of 178 mL/L/d from WAS-Fenton-AD-MEC was achieved, which was 5.23-fold of the WAS-MEC, 2.28-fold of WAS-Fenton-MEC and 1.46-fold of WAS-AD-MEC, respectively. Enhanced phosphorus recovery in form of struvite reached 1.72 g/g TS (18.03% of total P) with a purity of 74.4%. Microbial community richness and diversity analysis revealed that the pretreatment process under circumneutral condition improved the diversity of microbial community, which was consisted of Bacteroidetes (33.90%), Proteobacteria (33.14%), and Chloroflexi (10.14%), compared to a majority of Firmicutes (70.81%) in WAS-AD. This study provides a feasible strategy for the recovery of biogas combined with phosphorus from WAS., (Copyright © 2019 Elsevier B.V. All rights reserved.)

MFC toxicity sensor has major hindrances that limit its practical application, such as the poor concentration-response relationship and inferior recovery capability after high toxicity shock. Till now, the direct influence of intrinsic properties on the performance of MFC toxicity sensor has not been well understood. Quorum sensing (QS) is a cell-to-cell communication strategy that indirectly affects the intrinsic properties of electroactive biofilms. In this work, commercially available QS autoinducers (AHLs) were applied to MFC toxicity sensor to manipulate anode biofilm for better sensing performance. The results showed that the addition of AHLs (C6-HSL, 3-OXO-C12-HSL) led to higher sensing linearity to a wider range of Pb 2+ . The voltage of MFC sensors with AHLs addition fully recovered even after 10 mg/L Cu 2+ shock, indicating an enhanced recovery capability of MFC toxicity sensor. It was found that higher live/dead cells ratio and increased exoelectrogen Geobacter abundance were responsible for the superior sensing linearity and recovery capability of MFC toxicity sensor. Our work presented a novel and effective way to advance the process of MFC toxicity sensor application from the perspective of EABs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. I would like to declare on behalf of my co-authors that the work described was original research that has not been published previously, and not under consideration for publication elsewhere., (Copyright © 2019 Elsevier Inc. All rights reserved.)

A facile one-pot solvothermal method was applied to synthesize a magnetic biochar composite (MB) using phoenix tree leaves-derived biochar as the carbon matrix. The structure of MB was optimized by varying the load ratio and particle size of Fe 3 O 4 nanoparticles on biochar. Time-dependent structure and composition evolution of solid and liquid phases during heterogeneous solvothermal process were investigated to understand the formation mechanism of MB. Firstly, Fe 2+ /Fe 3+ ions were coordinated by oxygen-containing groups on biochar and part of them were hydrolyzed to form iron hydroxides. Then, those iron-containing precursors were thermally decomposed and reduced to iron oxides; and finally Fe 3 O 4 nanoparticles were generated. The MB had an adsorption capacity for Cr(VI) of 55.0 mg/g in an aqueous solution, which exceeds those of biochar (39.8 mg/g) and Fe 3 O 4 nanoparticles (26.5 mg/g). The adsorption mechanism study reveals that biochar as a carbon skeleton mainly provided binding sites for Cr(VI) and electron-donor groups for reduction of Cr(VI), while Fe 3 O 4 nanoparticles mainly involved in the immobilization of newly formed Cr(III) through formation of Fe(III)-Cr(III) hydroxide. MB exhibited a stable structure with a lower Fe leakage at pH 2.0 than that of a comparable magnetic biochar sample prepared by conventional co-precipitation method. Recycling experiments suggested that MB could keep 84% of its initial removal capability for Cr(VI) even after seven cycles. The results indicate that solvothermal method is a promising alternative to prepare magnetic biochar for adsorption of heavy metal-containing wastewater., (Copyright © 2019 Elsevier B.V. All rights reserved.)

In this study, a method to reduce the emission of NO x precursors (e.g., hydrogen cyanide (HCN) and ammonia (NH 3 )) while simultaneously reclaim more plant-available P was proposed through pyrolyzing ferric sludge (sludge conditioned by Fenton's reagents) rather than raw sludge. The nitrogen and phosphorus transformation at different pyrolysis temperatures was investigated. The results indicated that in comparison with the pyrolysis of raw sludge, the remaining iron compounds in ferric sludge can fix char-N in more stable forms (e.g., appearance of pyrrole-N at 900 °C). The secondary cracking of amine-N compounds in tar-N (e.g., 81.67% increase of amine-N at 900 °C) can be inhibited. Hence, more amine-N was remained and less heterocyclic-N and nitrile-N compounds were generated in tarN. Less generation of NH 3 -N and HCN-N was also observed in NO x precursors (e.g., 5.46% decrease of NH 3 -N and 6.91% decrease of HCN-N at 900 °C). Moreover, the results of X-ray diffractometry, liquid 31 P nuclear magnetic resonance spectroscopic, X-ray photoelectron spectroscopic, and chemical analyses collectively indicated that iron present in ferric sludge also favored reclamation of more plant-available P. In comparison with the pyrolysis of raw sludge, an increase in the total phosphorus pool was noted (18.06-36.26 versus 15.54-30.59 mg g -1 dry solids). A decrease in mobility with the predominant P as sodium hydroxide (NaOH)-P, and an increase in plant-available P can be also obtained. This study indicated that pyrolysis of ferric sludge was a feasible way to simultaneously reduce emission of NO x precursors, reclaim plant-available P, and reuse ferric sludge., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Massive realgar tailings abandoned in mining areas in China have caused serious arsenic (As) pollution seeking for urgent disposal. Stabilization treatment is a feasible strategy, however, stabilization technologies for realgar tailings, that are Fe-deficient, Ca-rich and S-rich, have not been well developed to date. In this study, we conducted a pilot-scale stabilization treatment of realgar tailings via ferrous sulfate addition to evaluate the transformation of As during stabilization. We found that Si, As, Ca, and S were the predominant elements in the raw realgar tailings with a low content of Fe, and realgar (As II 4 S 4 ) and pharmacolite (CaHAs V O 4 ·2H 2 O) were the main As-bearing minerals. After the ferrous sulfate treatment, the As leaching concentration of realgar tailings was successfully reduced from 135 mg/L to a level below the Chinese regulatory limit (2.5 mg/L). Based on the results of leaching tests, sequential extraction analysis, XRD, SEM-EDS, XPS, and thermodynamic modeling, we concluded that ferrous sulfate addition enhanced the transformation of Ca-As and S-As species to more stable Fe-As species, e.g., crystalline symplesite and amorphous Fe-As complex. Dissolution of pharmacolite was facilitated by H + and SO 4 2- derived from the hydrolysis and oxidation of ferrous sulfate, and oxidation of realgar could be promoted by reactive oxygen species (ROSs) from Fe(II) oxygenation. This study improved our understanding of As transformation pathways in realgar tailings during ferrous sulfate treatment, which could serve as an alternative scheme for realgar tailings stabilization., (Copyright © 2019 Elsevier B.V. All rights reserved.)

In this study, the long-term stability of Cr(VI) in the FeSO 4 and H 2 SO 4 (FeSO 4 -H 2 SO 4 ) treated chromite ore processing residue (COPR) after 400 curing days and the stabilization mechanisms were investigated. FeSO 4 -H 2 SO 4 treatment significantly reduced toxicity characteristic leaching procedure (TCLP) and synthetic precipitation leaching procedure (SPLP) Cr(VI) concentrations to lower than the regulatory limit of 1.5mgL -1 (HJ/T 301-2007, China EPA) even for the samples curing 400days, achieving an outstanding long-term stability. Our independent leaching tests revealed that H + and SO 4 2- have synergistic effect on promoting the release of Cr(VI), which would make Cr(VI) easier accessed by Fe(II) during stabilization. The contributions of H + and SO 4 2- to Cr(VI) release ratio were 25%-44% and 19%-38%, respectively, as 5mol H 2 SO 4 per kg COPR was used. X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and alkaline digestion analyses were also employed to interpret the possible stabilization mechanism. Cr(VI) released from COPR solid was reduced to Cr(III) by Fe(II), and then formed stable Fe x Cr (1-x) (OH) 3 precipitate. This study provides a facile and reliable scheme for COPR stabilization, and verifies the excellent long-term stability of the FeSO 4 -H 2 SO 4 treated COPR., (Copyright © 2016 Elsevier B.V. All rights reserved.)

A conjugated oligoelectrolyte (COE), which spontaneously aligns within cell membranes, was shown to completely inhibit H2 uptake by Geobacter sulfurreducens in microbial electrolysis cells. Coulombic efficiencies that were 490±95%, due to H2 recycling between the cathode and microorganisms on the anode, were reduced to 86±2% with COE addition. The use of the COE resulted in a 67-fold increase in H2 gas recovery, and a 4.4-fold increase in acetate removal. Current generation, H2 recovery and COD removals by Geobacter metallireducens, which cannot use H2, were unaffected by COE addition. These results show that this COE is an effective H2 uptake inhibitor, and that it can enable improved and sustained H2 gas recovery in this bioelectrochemical system., (Copyright © 2015 Elsevier B.V. All rights reserved.)