Magnetic MoS2/Fe3O4 composite as an effective activator of persulfate for the degradation of tetracycline: performance, activation mechanisms and degradation pathways.

The activated persulfate (PS) process could produce sulfate radical (SO4·-) and rapidly degrade organic pollutants. The application of Fe3O4 as a promising PS activator was limited due to the rapid conversion of Fe2+ to Fe3+ on its surface. Mo4+ on MoS2 surface could be used as a reducing site to convert Fe3+ to Fe2+, but the separation and recovery of MoS2 was complex. In this study, MoS2/Fe3O4 was prepared to accelerate the Fe3+/Fe2+ cycle on Fe3O4 surface and achieved efficient separation of MoS2. The results showed that MoS2/Fe3O4 was more effective for PS activation compared to Fe3O4 or MoS2, with a removal efficiency of 91.8% for 20 mg·L-1 tetracycline (TC) solution under the optimal conditions. Fe2+ and Mo4+ on MoS2/Fe3O4 surface acted as active sites for PS activation with the generation of SO4•-, •OH, •O2-, and 1O2. Mo4+ acted as an electron donor to promote the Fe3+/Fe2+ cycling and thus improved the PS activation capability of MoS2/Fe3O4. The degradation pathways of TC were inferred as hydroxylation, ketylation of dimethylamino group and C-N bond breaking. This study provided a promising activated persulfate-based advanced oxidation process for the efficient degradation of TC by employing MoS2/Fe3O4 as an effective activator.

Z-scheme heterojunction composed of Fe-doped g-C3N4 and Bi2MoO6 for photo-fenton degradation of antibiotics over a wide pH range: Activity and toxicity assessment.

In photo-Fenton technology, the narrower pH range limits its practical application for antibiotic wastewater remediation. Therefore, in this study, a Z-scheme heterojunction photo-Fenton catalyst was constructed by Fe-doped graphite-phase carbon nitride in combination with bismuth molybdate for the degradation of typical antibiotics. Fe doping can shorten the band gap and increase visible-light absorption. Simultaneously, the constructed Z-scheme heterojunction provides a better charge transfer pathway for the photo-Fenton reaction. Within 30 min, Fe3CN/BMO-3 removed 95.54% of tetracycline hydrochloride (TC), and its remarkable performance was the higher Fe3+/Fe2+ conversion efficiency through the decomposition of H2O2. The Fe3CN/BMO-3 catalyst showed remarkable photo-Fenton degradation performance in a wide pH range (3.0-11.0), and it also had good stability in the treatment of TC wastewater. Furthermore, the order of action of the active species was h+ > ·O2- > 1O2 > ·OH, and the toxicity assessment suggested that Fe3CN/BMO-3 was effective in reducing the biotoxicity of TC. The catalyst proved to be an economically feasible and applicable material for antibiotic photo-Fenton degradation, and this study provides another perspective on the application of elemental doping and constructed heterojunction photo-Fenton technology for antibiotic water environmental remediation.

Facile fabrication of nanocellulose-supported membrane composited with modified carbon nitride and HKUST-1 for efficient photocatalytic degradation of formaldehyde.

As a cellulose-derived material, nanocellulose possesses unique properties that make it an ideal substrate for various functional composite materials. In this study, we developed a novel composite membrane material capable of adsorbing and photo-catalyzing formaldehyde by immobilizing HKUST-1 (copper open framework composed of 1,3,5-benzenetricarboxylic acid) onto NFC (Nano-fibrillated cellulose) membranes and subsequently loading modified carbon nitride. The synthesized CNx@HN composite membrane (consisting of NFC membrane with anchored HKUST-1 and modified g-C3Nx nanosheets) was thoroughly characterized, and its photocatalytic degradation performance towards low concentrations of formaldehyde (3.0 mg/m3) was investigated. The results demonstrated that HKUST-1's porous nature exhibited a concentrated adsorption capacity for formaldehyde, while the modified CNx (Modified g-C3Nx nanosheets) displayed robust photocatalytic degradation of formaldehyde. The synergistic effect of HKUST-1 and modified CNx on the NFC membrane significantly enhanced the efficiency of formaldehyde degradation. Under xenon lamp irradiation, CNx@HN-5 achieved a total removal efficiency of 86.9 % for formaldehyde, with a photocatalytic degradation efficiency of 48.45 %, showcasing its exceptional ability in both adsorption and photocatalytic degradation of formaldehyde. Furthermore, after 10 cycles of recycling, the composite membrane exhibited excellent stability for the photocatalytic degradation process. Therefore, this study presents a green and facile strategy to fabricate nanocellulose-supported composite membranes with great potential for practical applications in formaldehyde degradation.

Bi(â ¢) and Ce(â £) functionalized carbon nitride photocatalyst for antibiotic degradation: Synthesis, toxicity, and mechanism investigations.

Graphite-phase carbon nitride (g-C3N4) has shown great potential for antibiotic wastewater treatment due to its unique electronic structure and corresponding to visible light. In this study, a series of Bi/Ce/g-C3N4 photocatalysts with different doping amount were developed by direct calcination method for Rhodamine B and sulfamethoxazole photocatalytic degradation. The experiment result shows that the photocatalytic performance of Bi/Ce/g-C3N4 catalysts were better than that of single component samples. Under the optimal experimental conditions, the degradation rates of RhB (20 min) and SMX (120 min) by 3Bi/Ce/g-C3N4 reached 98.3% and 70.5%, respectively. The theoretical calculation results of DFT show that after Bi and Ce doping modification, the band-gap width of g-C3N4 is reduced to 1.215 eV and carrier migration rate is greatly improved. The enhanced photocatalytic activity was mainly attributed to the capture of electrons after doping modification, which inhibition of photogenerated carriers recombination and reduced the gap width. The cyclic treatment experiment of sulfamethoxazole showed that Bi/Ce/g-C3N4 catalysts had good stability. Ecosar evaluation and leaching toxicity test showed that Bi/Ce/g-C3N4 can be safely used for wastewater treatment. This study provides a perfect strategy for modifying g-C3N4 and a new way to improve the photocatalytic performance.

Catalytic ozonation mechanisms of Norfloxacin using Cu-CuFe2O4.

As an easily recoverable, environmentally friendly and cost-effective catalyst, CuFe2O4 is a promising candidate for the catalytic ozonation of antibiotics in wastewater. However, its catalytic activity is restricted due to its limited active sites and low electron transfer efficiency. In this study, cetyl trimethyl ammonium bromide (CTAB) and Cu0 were doped with CuFe2O4 to introduce more OV, providing more active sites and improving electron transfer efficiency. Experimental results show that the optimum removal efficiency of the catalytic ozonation of Norfloxacin (NOR, a widely used antibiotic) using CTAB doped with Cu-CuFe2O4 as the catalyst is 81.58% with a first-order reaction kinetics constant of 0.03967 min-1. The associated O3 and catalyst dosages are 2.72 mg·L-1 and 0.1 g·L-1, respectively, which are 1.63 times and 2.22 times higher than those in an equivalent O3 system. OV can provide generation sites for surface hydroxyl groups and trigger ·O2- and 1O2 as the main active oxygen species. The synergistic redox cycles of Fe2+/Fe3+ and Cu0/Cu2+ accelerate electron transfer efficiency. The possible degradation pathways of NOR are identified as defluorination, naphthyridine ring-opening and piperazine ring-opening. In summary, this work proposes a new strategy for the modification of CuFe2O4 catalysts and provides new insights into the catalytic ozonation mechanisms for NOR removal.

Diatomite Composited with a Zeolitic Imidazolate Framework for Removing Phosphate from Water.

Adsorption technology based on various adsorbents has been widely applied in wastewater treatment containing phosphate. A novel diatomite adsorbent composited with ZIF-8 (CZD) was developed for removing phosphate from water in this work. The chitosan was used to pre-modify the diatomite so that ZIF-8 could be anchored on the surface of the diatomite solidly and uniformly. The diatomite composited with ZIF-8 was then used to remove phosphate in water by an adsorption process, the process variables such as adsorption time, temperature, pH, and competitive ions were investigated. The electrostatic attraction was the primary mechanism of phosphate removal. The adsorption reached equilibrium within 90 min, and its sorption capacity increased when adsorption time and temperature increased. Especially, CZD had a rapid adsorption rate and 85% of the phosphate in the solution can be adsorbed within the first 10 min. The maximum phosphate adsorption capacities of the modified diatomite reached 13.46, 13.55, and 13.95 mg/g at 25, 35, and 45 °C, respectively. The removal efficiencies of CZD for phosphate were more than 98% and even came up to 100% at 45 °C. The adsorption isotherms fit well with the Langmuir isotherm model. The Freundlich isotherm and Temkin isotherm showed that the adsorption process is physical in nature. The kinetic data of the adsorption process were fitted by the pseudo-second-order kinetics. Thermodynamic parameters indicated that the adsorption process was endothermic. This adsorbent provided an alternative for phosphate removal on account of the high adsorption efficiency in a short time. Therefore, CZD could be a promising and eco-friendly phosphate adsorbent for wastewater treatment.

Diatomite Modified with an Alkyl Ketene Dimer for Hydrophobicity of Cellulosic Paper.

Multifunctionalization of papermaking chemicals is one of the main developing strategies. Fillers and internal sizing agents are often mutually restricted in practice. Therefore, it is feasible to prepare a new papermaking chemical by combining the functions of both. A process of diatomite modified with an alkyl ketene dimer (AKD) was developed in this study. The modified diatomite (AD) can concurrently play the role of a mineral filler and sizing agent in the papermaking process. With the equal dosage of AKD, the AD showed better sizing and retention performance than the commercial AKD emulsion in the case of cationic polyacrylamide (CPAM) and the CPAM/bentonite retention system. The sizing mechanism of the AD can be interpreted to be due to numerous hydrophobic sites and the microsurface structure of the paper sheet caused by the AD. Since ketones were not detected in Fourier-transform infrared spectra of the paper sheet filled by the AD, the chemical reaction may not be indispensable for its sizing performance. What is more, an interesting "sticky" hydrophobicity phenomenon was observed when filling with AD. The approach in this study to prepare the "sticky" hydrophobic paper sheet can find its applications in some nontraditional application fields of cellulosic paper.

The performance of electrode ultrafiltration membrane bioreactor in treating cosmetics wastewater and its anti-fouling properties.

The membrane fouling problem of the membrane bioreactor (MBR) for wastewater treatment reduces the membrane flux and the pollutants removal efficiencies, which is the major obstacle limiting its application and should be properly solved. The combination of membrane and electricity can effectively slow down the membrane fouling rate due to electric repulsion between the pollutants and the membrane. In this study, the performance and the membrane fouling features of an electrode ultrafiltration membrane bioreactor (EMBR) fed with cosmetics wastewater were compared with a conventional ultrafiltration membrane bioreactor (UMBR). The results showed the COD removal efficiency increased by 4.43% and the transmembrane pressure (TMP) reduced by 50% in the EMBR as compared with the UMBR. The specific surface areas of electrode ultrafiltration membrane and conventional ultrafiltration membrane declined by 56.9% and 78.8% after 90 days of operation, respectively. The Protein (PN), polysaccharide (PS) and humic acids (HA) in the cake layer of EMBR were only 61.27%, 78.37% and 34.85% of that of UMBR, which contributed to its loose and porous structure and thus decreased the growth rate of TMP and extended the operation cycle. Extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory calculation proved that the energy barrier between the electrode ultrafiltration membrane and the pollutants was 50% higher than that between the conventional ultrafiltration membrane and the pollutants. Therefore, the strong anti-fouling property of the electrode ultrafiltration membrane could reduce the chemicals dosage and manpower consumption for membrane cleaning and could be preferred for the treatment of cosmetics or alike wastewater containing high concentrations of surfactants and fatty acids.

Effect of Mn2+ on the phosphorus removal and bioflocculation under anoxic condition.

Manganese ion (Mn2+) generated from metallurgical, steel making and chemical industries enters sewage treatment plants and affects the sludge activity and flocculation. The effect of Mn2+ on the removal of chemical oxygen demand (COD) and total phosphorus (TP) and sludge activity were investigated in anoxic zone of an anaerobic/anoxic/oxic (A2O) process. The compositions and structures of extracellular polymeric substances (EPS) were characterized using three-dimensional excitation emission matrix fluorescence spectroscopy (3D-EEM), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) to reveal the relationship among Mn2+, EPS and sludge flocculation. The results showed that low concentration of Mn2+ (<5 mg/L) improved removal efficiencies of COD and TP and increased the activity of alkaline phosphatase, acid phosphatase and dehydrogenase. Meanwhile, the addition of Mn2+ increased total EPS, sludge contact angle, Zeta potential and sludge particle size, and thus enhanced sludge flocculation. However, high concentration of Mn2+ (>10 mg/L) hindered microbial flocculation and reduced removal efficiencies of the pollutants. When Mn2+was 5 mg/L, removal efficiencies of COD and TP reached 65% and 90%, respectively. Sludge flocculation was the best and SVI was 70.56 mL/g. The changes of Mn2+ concentration caused deviation of groups' compositions in LB-EPS and TB-EPS, where the main components were always protein (PN) and polysaccharide (PS). The addition of Mn2+ resulted in the degradation of humic acids. However, it did not give rise to significant morphology changes of EPS.

Effect of Fe3+ on the sludge properties and microbial community structure in a lab-scale A2O process.

During biological wastewater treatment, ferric salt (Fe3+) usually serves as an inorganic flocculant to improve the agglomeration and sedimentation of suspended solids, and thus the removal efficiency of pollutants to meet the increasing strictly regulated wastewater discharge standards. In this study, we investigated the effects of Fe3+ on the removal efficiencies of pollutants, sludge properties, dominant flora and metabolic pathways of bacterial community in a classical anaerobic-anoxic-oxic (A2O) process. The results showed that a Fe3+ concentration lower than 10 mg·L-1 could improve the removal efficiencies of chemical oxygen demand (COD) and total nitrogen (TN), while an inhibition effect was exerted at concentration higher than 10 mg·L-1. The maximum removal efficiencies of COD and TN were 97% and 89%, respectively, under the critical Fe3+ concentration of 10 mg·L-1. Total phosphorous (TP) removal was constantly positively correlated with Fe3+ concentration, due to the enhanced adsorption of phosphorus on activated sludge with the increase of surface roughness. Thauera displayed the highest relative abundance, and certain bacteria in Proteobacteria, Dehloromonas and Candidatus-Competibacter exhibited good adaptability to high concentration of Fe3+. In the context of metabolic collaterals, the most abundant functional gene families were identified to be Carbohydrate Metabolism, Amino Acid Metabolism, Cell Motility, Membrane Transport, and Replication and Repair. This study provides an extensive mechanistic insight into the impact of Fe3+ on the A2O process, which is of fundamental significance to exploit the contributions of inorganic salts to biological wastewater treatment.

Nitrous oxide emission in a laboratory anoxic-oxic process at different influent pHs: Generation pathways and the composition and function of bacterial community.

This study focused on the nitrous oxide (N2O) generation from the biological nitrogen removal process under different pH levels. To explore a pH optimum, the online N2O emission and the bacterial composition and function in the anoxic-oxic process were investigated. The mean gaseous N2O emission accounted for 0.329%, 0.103%, 0.085%, and 0.793% of the influent total nitrogen at pH of 5, 6, 8, and 9, respectively. Incomplete oxidation in oxic tanks was the primary source of N2O, while N2O in the anoxic tank was mainly generated by nitrifier denitrification. No direct correlations were observed between N2O emission and potential nitrifiers and denitrifiers. The impacts of pH on N2O generation were more likely related to the response of bacterial enzymes and nitrogen compounds, rather than the feedback of bacterial community structure itself. Above all, an influent pH range of 6-8 is recommended for nitrogen removal and N2O mitigation in anoxic-oxic process.

Degradation of an Organic Dye by Bisulfite Catalytically Activated with Iron Manganese Oxides: The Role of Superoxide Radicals.

Metal-activated bisulfite systems have been widely used to treat recalcitrant wastewater. However, due to the disadvantages of their narrow effective pH range and difficulty in recovering metal ions, homogeneous systems are severely limited in practical applications. To overcome these problems, Fe/Mn bimetallic catalysts with different molar ratios were prepared using a simple sol-gel method to activate bisulfite. Influential factors, such as catalyst and system types, catalyst dosage, bisulfite concentration, pH value, and bisulfite addition modes, were investigated. The new system exhibited a wide effective pH range and high degradation efficiency, and it was found that the dissolved oxygen content played an important role in the activation system. The radical quenching test showed that a superoxide radical (O2 •-), instead of a hydroxyl radical (HO•) or a sulfate radical (SO4 •-), was the main oxide species for the degradation of rhodamine B (RhB).

Effects of graphite particles/Fe3+ on the properties of anoxic activated sludge.

In order to improve the sludge flocculation, the combination of graphite particles/Fe3+ was used to change the sludge properties and accelerate the electron transfer rate. The effects of Fe3+ on the properties of graphite particles were investigated and the synergistic effects of graphite particles/Fe3+ on the sludge properties were analyzed using N2-adsorption/desorption, scanning electron microscopy-X-ray energy dispersive analysis (SEM-EDX), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The results showed that the operation time affected the specific surface area and pore size of graphite particles. The addition of Fe3+ reduced the specific surface area and increased the pore size of graphite particles, but it did not change the crystal structure of the graphite particles and the group structure of the sludge. Under the function of graphite particles/Fe3+, Zeta potential were improved and the relative hydrophobicity of the sludge was weakened. The contact angle was slightly lowered and flocculation ability (FA) was increased. Therefore, graphite particles/Fe3+ played an important role in the charge transfer and bioflocculation improvement.

Effects of Al3+ on the microstructure and bioflocculation of anoxic sludge.

The aluminum ions generated from mining aluminum, electrolytic aluminum and the industrial production of aluminum-based coagulants (such as AlCl3 and Al2(SO4)3) enter sewage treatment plants and interact with activated sludges. An anaerobic/anoxic/oxic (A2O) process was used to reveal the effects of Al3+ on the pollutant removal efficiencies, bioflocculation and the microstructure of sludge. The results showed that a low concentration of Al3+ improved the pollutant removal efficiencies and increased the sludge particle size. However, a high concentration of Al3+ hindered microbial flocculation and reduced the pollutant removal efficiencies. With a 10 mg/L Al3+ addition, the chemical oxygen demand (COD), total nitrogen (TN) and NH4+-N increased by 3%, 16% and 27%, and reached as high as 68%, 60% and 87%, respectively. At the same time, the dehydrogenase activity, flocculation ability (FA) and contact angle of the sludge reached their maximum levels at 41.3 mg/L/hr, 45% and 79.63°, respectively. The specific surface area of the sludge decreased to 7.084 m2/g and the sludge pore size distribution shifted to concentrate in the mesoporous range. Most of Al3+ was adsorbed on the surface of sludge, changing the physicochemical properties and physical structure of the sludge.

Risk of penicillin fermentation dreg: Increase of antibiotic resistance genes after soil discharge.

Penicillin fermentation dreg (PFD) is a solid waste discharged by pharmaceutical enterprises in the fermentation production process. Due to the residual antibiotic of PFD, the risk of antibiotic resistance bacteria (ARB) generation should be considered in the disposal process. High-throughput quantitative PCR (HT-qPCR) and 16S rRNA gene sequencing were performed to investigate the effect of PFD on the dynamics of antibiotic resistance genes (ARGs) and bacterial community during a lab-scale soil experiment. After the application of PFD, the bacterial number and diversity showed an obvious decrease in the initial days. The abundances of Streptomyces and Bacillus, which are the most widespread predicted source phyla of ARGs, increased remarkably from 4.42% to 2.59%-22.97% and 21.35%. The increase of ARGs was observed during the PFD application and the ARGs carried by PFD itself contributed to the initiation of soil ARGs. The results of redundancy analysis (RDA) show that the shift in bacterial community induced by variation of penicillin content is the primary driver shaping ARGs compositions.

Preparation of Pd/GO/Cu Electrode and Its Electrochemical Degradation for 2,4-Dichlorophenol.

Chlorinated aromatic compounds (CACs) are a class of persistent organic pollutants, which have serious damage to water environment due to their own stable structure. But a good many of CACs were abandoned because of their tremendous yields and wide applications, so it is urgent to find the effective degradation methods for CACs. The electrochemical method is supposed to be a simple, environmentally friendly and effective pathway to degrade CACs. In this paper, a Pd/GO/Cu composite electrode was prepared by a combination of impregnation method and constant current electrodeposition method, which showed good electrochemical degradation efficiency for the 2,4-dichlorophenol. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) were used to characterize the surface structure, functional group composition, crystal structure and surface element valence of the electrode. Moreover, the stability of the electrode was investigated, and the preparation conditions of the electrode were optimized.

[Effect of Ca2+ on the Nitrification Activity and the Flocculation and Sedimentation Performances of the Activated Sludge].

Ca2+ is an important microbial growth factor that can affect the activity, flocculation, and sedimentation of activated sludge. In order to study the roles of Ca2+ in the activated sludge system, the activity changes of ammonium oxidizing bacteria (AOB) and nitrite oxidizing bacteria (NOB) were analyzed using the specific oxygen uptake rates (SOURAOB and SOURNOB). The changes in composition and structure of extracellular polymeric substances (EPS) were analyzed using Fourier transform infrared spectroscopy (FTIR) and three-dimensional excitation emission fluorescence spectroscopy (3D-EEM). The effects of Ca2+on the nitrification activity and microbial metabolites were investigated. The results showed that when the Ca2+concentration increased from 0.45 mmol·L-1 to 3 mmol·L-1, SOURAOB and SOURNOB increased from 6.3 mg·(g·h)-1 to 10.4 mg·(g·h)-1 and from 2.3 mg·(g·h)-1 to 3.7 mg·(g·h)-1, respectively. The EPS concentrations increased from 68 mg·g-1 to 93 mg·g-1, and the flocculation ability (FA) of the sludge was improved. When the Ca2+ concentration was higher than 3 mmol·L-1, SOURAOB and SOURNOBboth decreased. The FA was maintained at about 30%, and the particle size of the sludge continued to increase. Based on FTIR analysis, the main components of EPS were always amino, amide Ⅰ, and carboxyl with an increase in Ca2+ concentration. Based on EEM analysis, the composition of loosely-bound (LB)-EPS did not change, and humic acid substances appeared in the tightly-bound (TB)-EPS at low nitrification rates. Low concentrations of Ca2+ promoted nitrification activity and flocculation of the sludge. However, high concentrations of Ca2+ led to a decline in the sludge nitrification activity.

Characterization of activated sludge flocs in membrane bioreactor: stable and unstable flocs.

In this study, the properties of unstable and stable flocs were investigated under the steady operation of a membrane bioreactor (MBR). The extracellular polymeric substances (EPS) composition, surface charge, and hydrophobicity of unstable and stable flocs were examined and compared. Interfacial interactions of the membrane with unstable flocs, unstable flocs themselves, and unstable and stable flocs were assessed using the extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) models. Cake layer resistance was found to contribute more than 80% of total resistance under steady operating conditions. Compared with stable flocs, unstable flocs possessed a higher level of EPS, more diverse protein, more negative charge, weaker hydrophobicity, and higher fouling potential. Thermodynamic analyses showed that unstable flocs had a higher adhesive strength (- 63.4 mJ/m2) with the membrane, lower self-cohesive strength (- 18.3 mJ/m2), and higher cohesive strength (- 54.3 mJ/m2) with stable flocs. Therefore, some unstable flocs remained on the membrane surface to form the cake layer due to their poor cohesion strength.

Characterization of the Initial Fouling Layer on the Membrane Surface in a Membrane Bioreactor: Effects of Permeation Drag.

In this study, the properties of the initial fouling layer on the membrane surface of a bioreactor were investigated under different operating modes (with or without permeate flux) to improve the understanding of the effect of permeation drag on the formation of the initial fouling layer. It was found that protein was the major component in the two types of initial fouling layers, and that the permeation drag enhanced the tryptophan protein-like substances. The attraction of the initial foulants to the polyvinylidene fluoride (PVDF) membrane was ascribed to the high zeta potential and electron donor component (γ-) of the membrane. Thermodynamic analyses showed that the permeation drag-induced fouling layer possessed high hydrophobicity and low γ-. Due to permeation drag, a portion of the foulants overcame an energy barrier before they contacted the membrane surface, which itself possessed a higher fouling propensity. A declining trend of the cohesive strength among the foulants was found with the increasing development of both fouling layers.

Effects of K+ salinity on the sludge activity and the microbial community structure of an A2O process.

Salt ions are ubiquitous in wastewater and have significant impacts on the microbial activity and nitrogen and phosphorus removal in biological wastewater treatment processes. The effects of KCl salinity on the removal of COD, TN and PO43--P were investigated in a lab-scale A2O process. Meanwhile, the effects of K+ concentration on the composition of extracellular polymeric substances (EPS) and the microbial community structure were demonstrated. The results showed that the pollutant removal efficiencies and the bioactivity of the activated sludge decreased and the EPS content enhanced under high concentration of K+, which resulted in the deterioration of sludge compactness and settleability. The microbial diversity reduced after K+ addition and the microbial community structure was distinct between the system with (10 g L-1 and 40 g L-1) and without K+ addition. The relative abundance of Candidatus-Competibacter, Acinetobacter and Azoarcus decreased in the anoxic zone with the increase of K+ concentration, which might led to the decrease in denitrifying phosphorus removal capacity. However, the relative abundance of some genera of Firmicutes (such as Fusibacter, Acetoanaerobium, Planococcus and Exiguobacterium) increased, which was coincident with the enhanced microbial salt-tolerance capacity. Proteobacteria, Bacteroides, Chloroflexi and Firmicutes were the dominant phyla irrespective of the salinity changed, which guaranteed the removal of organic compounds, nitrogen and phosphorus in salty environment.