Optimization of a Novel Engineered Ecosystem Integrating Carbon, Nitrogen, Phosphorus, and Sulfur Biotransformation for Saline Wastewater Treatment Using an Interpretable Machine Learning Approach.

The denitrifying sulfur (S) conversion-associated enhanced biological phosphorus removal (DS-EBPR) process for treating saline wastewater is characterized by its unique microbial ecology that integrates carbon (C), nitrogen (N), phosphorus (P), and S biotransformation. However, operational instability arises due to the numerous parameters and intricates bacterial interactions. This study introduces a two-stage interpretable machine learning approach to predict S conversion-driven P removal efficiency and optimize DS-EBPR process. Stage one utilized the XGBoost regression model, achieving an R2 value of 0.948 for predicting sulfate reduction (SR) intensity from anaerobic parameters with feature engineering. Stage two involved the CatBoost classification and regression model integrating anoxic parameters with the predicted SR values for predicting P removal, reaching an accuracy of 94% and an R2 value of 0.93, respectively. This study identified key environmental factors, including SR intensity (20-45 mg S/L), influent P concentration (<9.0 mg P/L), mixed liquor volatile suspended solids (MLVSS)/mixed liquor suspended solids (MLSS) ratio (0.55-0.72), influent C/S ratio (0.5-1.0), anoxic reaction time (5-6 h), and MLSS concentration (>6.50 g/L). A user-friendly graphic interface was developed to facilitate easier optimization and control. This approach streamlines the determination of optimal conditions for enhancing P removal in the DS-EBPR process.

Synergistic effects of chemical additives and mature compost on reducing H2S emission during kitchen waste composting.

Additives could improve composting performance and reduce gaseous emission, but few studies have explored the synergistic of additives on H2S emission and compost maturity. This research aims to make an investigation about the effects of chemical additives and mature compost on H2S emission and compost maturity of kitchen waste composting. The results showed that additives increased the germination index value and H2S emission reduction over 15 days and the treatment with both chemical additives and mature compost achieved highest germination index value and H2S emission reduction (85%). Except for the treatment with only chemical additives, the total sulfur content increased during the kitchen waste composting. The proportion of effective sulfur was higher with the addition of chemical additives, compared with other groups. The relative abundance of H2S-formation bacterial (Desulfovibrio) was reduced and the relative abundance of bacterial (Pseudomonas and Paracoccus), which could convert sulfur-containing substances and H2S to sulfate was improved with additives. In the composting process with both chemical additives and mature compost, the relative abundance of Desulfovibrio was lowest, while the relative abundance of Pseudomonas and Paracoccus was highest. Taken together, the chemical additives and mature compost achieved H2S emission reduction by regulating the dynamics of microbial community.

Fence-type Molecular Electrocatalysts for High-Performance Lithium-Sulfur Batteries.

Improving the slow redox kinetics of sulfur species and shuttling issues of soluble intermediates induced from the multiphase sulfur redox reactions are crucial factors for developing the next-generation high-energy-density lithium-sulfur (Li-S) batteries. In this study, we successfully constructed a novel molecular electrocatalyst through in situ polymerization of bis(3,4-dibromobenzene)-18-crown-6 (BD18C6) with polysulfide anions on the cathode interface. The crown ether (CE)-based polymer acts as a spatial "fence" to precisely control the unique redox characteristics of sulfur species, which could confine sulfur substance within its interior and interact with lithium polysulfides (LiPSs) to optimize the reaction barrier of sulfur species. The "fence" structure and the double-sided Li+ penetrability of the CE molecule may also prevent the CE catalytic sites from being covered by sulfur during cycling. This new fence-type electrocatalyst mitigates the "shuttle effect", enhances the redox activity of sulfur species, and promotes the formation of three-dimensional stacked lithium sulfide (Li2S) simultaneously. It thus enables lithium-sulfur batteries to exhibit superior rate performance and cycle stability, which may also inspire development facing analogous multiphase electrochemical energy-efficient conversion process.

Synergy effects of Methylomonas koyamae and Hyphomicrobium methylovorum under methanethiol stress.

Methanotrophs are able to metabolize volatile organic sulfur compounds (VOSCs), excrete organic carbon during CH4 oxidation, and influence microbial community structure and function of the ecosystem. In return, microbial community structure and environmental factors can affect the growth metabolism of methanotrophs. In this study, Methylomonas koyamae and Hyphomicrobium methylovorum were used for model organisms, and methanethiol (MT) was chosen for a typical VOSC to investigate the synergy effects under VOSC stress. The results showed that when Hyphomicrobium methylovorum was co-cultured with Methylomonas koyamae in the medium with CH4 used as the carbon source, the co-culture had better MT tolerance relative to Methylomonas koyamae and oxidized all CH4 within 120 h, even at the initial MT concentration of 2000 mg m-3. The optimal co-culture ratios of Methylomonas koyamae to Hyphomicrobium methylovorum were 4:1-12:1. Although MT could be converted spontaneously to dimethyl disulfide (DMDS), H2S, and CS2 in air, faster losses of MT, DMDS, H2S, and CS2 were observed in each strain mono-culture and the co-culture. Compared with Hyphomicrobium methylovorum, MT was degraded more quickly in the Methylomonas koyamae culture. During the co-culture, the CH4 oxidation process of Methylomonas koyamae could provide carbon and energy sources for the growth of Hyphomicrobium methylovorum, while Hyphomicrobium methylovorum oxidized MT to help Methylomonas koyamae detoxify. These findings are helpful to understand the synergy effects of Methylomonas koyamae and Hyphomicrobium methylovorum under MT stress and enrich the role of methanotrophs in the sulfur biogeochemical cycle. KEY POINTS: • The co-culture of Methylomonas and Hyphomicrobium has better tolerance to CH3SH. • Methylomonas can provide carbon sources for the growth of Hyphomicrobium. • The co-culture of Methylomonas and Hyphomicrobium enhances the removal of CH4 and CH3SH.

An Endogenous Prompting Mechanism for Sulfur Conversions Via Coupling with Polysulfides in Li-S Batteries.

The sluggish kinetics process and shuttling of soluble intermediates present in complex conversion between sulfur and lithium sulfide severely limit the practical application of lithium-sulfur batteries. Herein, by introducing a designated functional organic molecule to couple with polysulfide intermediators, an endogenous prompting mechanism of sulfur conversions has thus been created leading to an alternative sulfur-electrode process, in another words, to build a fast "internal cycle" of promotors that can promote the slow "external cycle" of sulfur conversions. The coupling-intermediators between the functional organic molecule and polysulfides, organophosphorus polysulfides, to be the "promotors" for sulfur conversions, are not only insoluble in the electrolyte but also with higher redox-activity. So the sulfur-electrode process kinetics is greatly improved and the shuttle effect is eliminated simultaneously by this strategy. Meanwhile, with the endogenous prompting mechanism, the morphology of the final discharge product can be modified into a uniform covering film, which is more conducive to its decomposition when charging. Benefiting from the effective mediation of reaction kinetics and control of intermediates solubility, the lithium-sulfur batteries can act out excellent rate performance and cycling stability.

Co4 N-Decorated 3D Wood-Derived Carbon Host Enables Enhanced Cathodic Electrocatalysis and Homogeneous Lithium Deposition for Lithium-Sulfur Full Cells.

The sluggish kinetics of sulfur conversion in the cathode and the nonuniform deposition of lithium metal at the anode result in severe capacity decay and poor cycle life for lithium-sulfur (Li-S) batteries. Resolving these deficiencies is the most direct route toward achieving practical cells of this chemistry. Herein, a vertically aligned wood-derived carbon plate decorated with Co4 N nanoparticles host (Co4 N/WCP) is proposed that can serve as a host for both the sulfur cathode and the metallic lithium anode. This Co4 N/WCP electrode host drastically enhances the reaction kinetics in the sulfur cathode and homogenizes the electric field at the anode for the uniform lithium plating. Density functional theory calculations confirm the experimental observations that Co4 N/WCP provides a lower energy barrier for the polysulfide redox reaction in the cathode and a low adsorption energy for lithium deposition at the anode. Employing the Co4 N/WCP host at both electrodes in a S@Co4 N/WCP||Li@Co4 N/WCP full cell delivers a specific capacity of 807.9 mAh g-1 after 500 cycles at a 1 C rate. Additional experiments are performed with high areal sulfur loading of 4 mg cm-2 to demonstrate the viability of this strategy for producing practical Li-S cells.

Microbial behaviours inside alternating anaerobic-anoxic environment of a sulfur cycle-driven EBPR system: A metagenomic investigation.

Denitrifying sulfur conversion-assisted enhanced biological phosphorus removal (DS-EBPR) was recently developed for saline wastewater treatment. However, the main functional bacteria and the interrelationship of functional bacteria of the DS-EBPR have not been defined and identified so far. This study used metagenomics and multivariate statistics to deduce the functional microbial community and distribution of functional genes associated with the critical metabolic pathways of carbon (C), nitrogen (N), phosphorus (P) and sulfur (S), particularly regarding how they would behave under the alternating anaerobic-anoxic conditions inside a long-term DS-EBPR system. An analysis of the metagenomics and metabolic functions identified 11 major microbial species which were classifiable into four groups: sulfate reducing bacteria (SRB, 0.8-2.2%), sulfur oxidizing bacteria (SOB, 31.9-37.7%), denitrifying phosphate accumulating organisms (DPAOs, 10.0-15.8%) and glycogen accumulating organisms (GAOs, 3.7-7.7%). The four groups of microorganisms performed their respective metabolisms synergistically. In terms of distribution of functional genes, SRB (Desulfococcus and Desulfobacter) and SOB (Chromatiaceae and Thiobacillus) are not only encoded by the related sulfur conversion genes (sqr, dsrAB, aprAB and sat), but also encoded by the necessary ppx and ppk1 gene for P removal that they can be considered as the potential S-related PAOs. Between the anaerobic and anoxic conditions, the metagenome-based microbial community remained structurally similar, but the functional genes, which encode various key enzymes for the P, N, and S pathways, changed in abundance. This study contributes to our understanding on the interactions and competition between the SRB, SOB, DPAOs, and GAOs in a DS-EBPR system.

Long-term stable and efficient degradation of ornidazole with minimized by-product formation by a biological sulfidogenic process based on elemental sulfur.

Conventional biological treatment processes cannot efficiently and completely degrade nitroimidazole antibiotics, due to the formation of highly antibacterial and carcinogenic nitroreduction by-products. This study investigated the removal of a typical nitroimidazole antibiotic (ornidazole) during wastewater treatment by a biological sulfidogenic process based on elemental sulfur (S0-BSP). Efficient and stable ornidazole degradation and organic carbon mineralization were simultaneously achieved by the S0-BSP in a 798-day bench-scale trial. Over 99.8 % of ornidazole (200‒500 µg/L) was removed with the removal rates of up to 0.59 g/(m3·d). Meanwhile, the efficiencies of organic carbon mineralization and sulfide production were hardly impacted by the dosed ornidazole, and their rates were maintained at 0.15 kg C/(m3·d) and 0.49 kg S/(m3·d), respectively. The genera associated with ornidazole degradation were identified (e.g., Sedimentibacter, Trichococcus, and Longilinea), and their abundances increased significantly. Microbial degradation of ornidazole proceeded by several functional genes, such as dehalogenases, cysteine synthase, and dioxygenases, mainly through dechlorination, denitration, N-heterocyclic ring cleavage, and oxidation. More importantly, the nucleophilic substitution of nitro group mediated by in-situ formed reducing sulfur species (e.g., sulfide, polysulfides, and cysteine hydropolysulfides), instead of nitroreduction, enhanced the complete ornidazole degradation and minimized the formation of carcinogenic and antibacterial nitroreduction by-products. The findings suggest that S0-BSP can be a promising approach to treat wastewater containing multiple contaminants, such as emerging organic pollutants, organic carbon, nitrate, and heavy metals.

Anion-Regulated Sulfur Conversion in High-Content Carbon Layer Confined Sulfur Cathode Maximizes Voltage and Rate Capability of K-S Batteries.

Potassium-sulfur (K-S) batteries have attracted attention in large-scale energy storage systems. Small-molecule/covalent sulfur (SMCS) can help to avoid the shuttle effect of polysulfide ions via solid-solid sulfur conversion. However, the content of SMCS is relatively low (≤40%), and solid-solid reactions cause sluggish kinetics and low discharge potentials. Herein, SMCS is confined in turbo carbon layers with a content of ≈74.1 wt% via a C/S co-deposition process. In the K-S battery assembled by using as-fabricated SMCS@C as cathode and KFSI-EC/DEC as an electrolyte, anion-regulated two-plateau solid-state S conversion chemistry and a novel high discharge potential plateau at 2.5-2.0 V with a remarkable reversible capacity of 384 mAh g-1 at 3 A g-1 after 1000 cycles are found. The SMCS@C||K full cell showed energy and power density of 72.8 Wh kg-1 and 873.2 W kg-1, respectively, at 3 A g-1. Mechanism studies reveal that the enlarged carbon layer space enables the diffusion of K+-FSI- ion pairs, and the coulombic attraction between them accelerates their diffusion in SMCS@C. In addition, FSI- regulates sulfur conversion in situ inside the carbon layers along a two-plateau solid-state reaction pathway, which lowers the free energy and weakens the S─S bond of intermediates, leading to faster and more efficient S conversion.

Anaerobic biotransformation of sulfonated anthraquinones by Pseudomonas nitroreducens WA and the fate of the sulfonic acid group in the presence of nitrate.

The presence of the sulfonic acid group in sulfonated anthraquinones (SAs) resulted in the difficulty in the mineralization of anthraquinone ring. Little information is available on the removal pathway of the sulfonic acid group of SAs under aerobic/anaerobic conditions. Herein, sodium 1-aminoanthraquinone-2-sulfonate (ASA-2) was used as an important intermediate of SAs. A novel Pseudomonas nitroreducens WA capable of ASA-2 desulfonation was isolated from the Reactive Blue 19-degrading consortium WRB. Anaerobic desulfonation efficiency of 0.165 mM ASA-2 by strain WA reached 99% in 36 h at pH 7.5 and 35 â„ƒ using glucose as an electron donor. Further analysis showed that ASA-2 as an electron acceptor could be anaerobically transformed into 1-aminoanthraquinone and sulfite via the cleavage of C-S bond. Strain WA could also desulfonate sodium 1-amino-4-bromoanthraquinone-2-sulfonate and sodium anthraquinone-2-sulfonate. Under denitrification conditions, the formed sulfite could be oxidized to sulfate by nitrite via a chemical reaction, which was beneficial for nitrite removal. This phenomenon was observed in consortium WRB-amended system. Moreover, the consortium WRB could reduce the formed sulfite to sulfide due to the presence of Desulfovibrio. These results provide a theoretical basis for the anaerobic biodesulfonation of SAs along with nitrate removal and support for the development of sulfite-based biotechnology.

Thiosulfate enhanced Cu(II)-catalyzed Fenton-like reaction at neutral condition: Critical role of sulfidation in copper cycle and Cu(III) production.

Thiosulfate (S2O32-) has been proven to be an effective promoter of Fenton-like reactions by accelerating the metal ions cycle. However, up to now, little is known about the role of sulfur transformation and intermediate sulfur in the regulation of metal chemical cycle and reactive species production. Herein, free Cu(II) was selected as catalyst for the activation of H2O2. The introduction of S2O32- significantly enhanced the degradation of benzoic acid, and the degradation rate (kobs) was 5.8 times that of Cu(II)/H2O2 system. The kinetic model revealed the transformation of sulfur species and demonstrated that sulfides (i.e., HS-/S2-, S2O32-) and S0 were the dominant electron donor for the reduction of Cu(II) into Cu(I). Consequently, the reduction and complexation roles of S2O32- significantly resolve the rate-limiting step and broaden the pH range of in Fenton-like reactions. Evidence for the critical role of high-valent copper (Cu(III)) and HO• on BA degradation was obtained by scavengers experiments, electron paramagnetic resonance and fluorescent probes. Meanwhile, the Cu(II)/H2O2/S2O32- system also exhibited satisfactory anti-interference ability of the various matrix. Overall, this study offers mechanistic insight into sulfidation in Cu chemical cycle and Cu(III) generation, and highlights the potential of S2O32- for Fenton-like reactions to control pollutants.

Synergetic Anion Vacancies and Dense Heterointerfaces into Bimetal Chalcogenide Nanosheet Arrays for Boosting Electrocatalysis Sulfur Conversion.

Vacancy and interface engineering are regarded as effective strategies to modulate the electronic structure and enhance the activity of metal chalcogenides. However, the practical application of metal chalcogenides in lithium-sulfur (Li-S) batteries is limited by their low conductivity, rapid decline in catalytic activity, and large volume variation during the discharging/charging process. Herein, bimetal sulfide (CoZn-S) nanosheet arrays with sulfur vacancies and dense heterointerfaces are proposed to accelerate sulfur conversion and improve the performance of Li-S batteries. Systematic investigations reveal that sulfur-vacancy and build-in interfacial field in CoZn-S facilitate the electron transfer and regulate the electronic structure. The well-designed 3D nanosheet array structures shorten the ion-transport pathway and inhibit the volume fluctuation of CoZn-S during the electrocatalysis process. Density functional theory studies confirm that the built-in interfacial field and sulfur vacancy can promote the thermodynamic formation and decomposition of Li2 S, thus improving their intrinsic activity.

Electrocatalysis in Room Temperature Sodium-Sulfur Batteries: Tunable Pathway of Sulfur Speciation.

Benefiting from the merits of natural abundance, low cost, and ultrahigh theoretical energy density, the room temperature sodium-sulfur (RT NaS) batteries are regarded as one of the promising candidates for the next-generation scalable energy storage devices. However, the uncontrollable sulfur speciation pathways severely hinder its practical applications. Recently, various strategies have been employed to tune the conversion pathways of sulfur, such as physical confinement, chemical inhibition, and electrocatalysis. Herein, the recent advances in electrocatalytic effects manipulate sulfur speciation pathways in advanced RT NaS electrochemistry are reviewed, including the promotion of the nearly full conversion of long-chain polysulfides, short-chain polysulfides, and small sulfur molecules. The underlying catalytic modulation mechanism that fundamentally tunes the electrochemical pathway of sulfur species is comprehensively summarized along with the design strategies for catalytic active centers. Furthermore, the challenge and potential solutions to realize the quasi-solid conversion of sulfur are proposed to accelerate the real application of RT NaS batteries.

Engineering Catalytic CoSe-ZnSe Heterojunctions Anchored on Graphene Aerogels for Bidirectional Sulfur Conversion Reactions.

Sluggish sulfur reduction and lithium sulfide (Li2 S) oxidation prevent the widespread use of lithium-sulfur (Li-S) batteries, which are attractive alternatives to Li-ion batteries. The authors propose that a transition metal selenide heterojunction (CoSe-ZnSe) catalytically accelerates bidirectional sulfur conversion reactions. A combination of synchrotron X-ray absorption spectroscopy and density functional theory calculations show that a highly active heterointerface with charge redistribution and structure distortion effectively immobilizes sulfur species, facilitates Li ion diffusion, and decreases the sulfur reduction and Li2 S oxidation energy barriers. The CoSe-ZnSe catalytic cathode exhibits high areal capacities, good rate capability, and superior cycling stability with capacity fading rate of 0.027% per cycle over 1700 cycles. Furthermore, CoSe-ZnSe heterojunctions anchored on graphene aerogels (CoSe-ZnSe@G) enhance ionic transport and catalytic activity under high sulfur loading and lean electrolyte conditions. A high areal capacity of 8.0 mAh cm-2 is achieved at an electrolyte/sulfur ratio of 3 µL mg-1 . This study demonstrates the importance of bidirectional catalytic heterojunctions and structure engineering in boosting Li-S battery performances.

Progress and Prospect of Organic Electrocatalysts in Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries featured by ultra-high energy density and cost-efficiency are considered the most promising candidate for the next-generation energy storage system. However, their pragmatic applications confront several non-negligible drawbacks that mainly originate from the reaction and transformation of sulfur intermediates. Grasping and catalyzing these sulfur species motivated the research topics in this field. In this regard, carbon dopants with metal/metal-free atoms together with transition-metal complex, as traditional lithium polysulfide (LiPS) propellers, exhibited significant electrochemical performance promotions. Nevertheless, only the surface atoms of these host-accelerators can possibly be used as active sites. In sharp contrast, organic materials with a tunable structure and composition can be dispersed as individual molecules on the surface of substrates that may be more efficient electrocatalysts. The well-defined molecular structures also contribute to elucidate the involved surface-binding mechanisms. Inspired by these perceptions, organic electrocatalysts have achieved a great progress in recent decades. This review focuses on the organic electrocatalysts used in each part of Li-S batteries and discusses the structure-activity relationship between the introduced organic molecules and LiPSs. Ultimately, the future developments and prospects of organic electrocatalysts in Li-S batteries are also discussed.

Organic carbon coupling with sulfur reducer boosts sulfur based denitrification by Thiobacillus denitrificans.

Sulfur autotrophic denitrification utilizes elemental sulfur as the electron donor for nitrate removal from aquatic environments. Organic carbon could stimulate the conversion of sulfur and facilitates the S0-based denitrification process in the mix-trophic. In this study, the co-cultured system of sulfur reducer (Geobacter sulfurreducens) and Thiobacillus denitrificans was used to investigate that how organic carbon could boost the S0-based denitrification. The results showed that the rate of S0-based denitrification was improved with C/N ratio of 0.13 and this improvement continued even after the acetate was exhausted. Sulfur probe test and Raman analysis suggested that reduced sulfur species (Sx2-) were formed with the addition of organic carbon. The Sx2- could recombine with element sulfur and the bioavailability of S0 would be improved, as a result, the rate of S0-based denitrification increased as well. Nitrate reduction rate could further increase with the C/N ratio of 0.88, but it would decrease significantly when the C/N ratio increased to 1.50 as the high concentration of generated S2-. Our results provided explanations that why organic carbon addition would improve the bioavailability of S0 which could further promote the S0-dominant denitrification process.

Enhancement of Sulfur Conversion Rate in the Production of l-Cysteine by Engineered Escherichia coli.

Cysteine is a commercially important sulfur-containing amino acid widely used as a supplement in the agricultural and food industries. It is extremely desirable to achieve a high sulfur conversion rate in the fermentation-based cysteine production. Here, the metabolic engineering of Escherichia coli was performed to enhance the sulfur conversion rate in cysteine biosynthesis. Accordingly, the reduction of sulfur loss by the regulator decR and its yhaOM operons were deleted. serACB was integrated into chromosome with constitutive promoter to coordinately increase sulfur utilization. The sulfur assimilation pathways and sulfur transcriptional regulator cysB were overexpressed to regulate sulfur metabolism and enhance sulfur conversion significantly. After the process optimization in fed-batch fermentation, LH16 [SLH02 ΔyhaM Ptrc1-serACB-cysM-nrdH-(pLH03, pTrc99a-cysB)] produced 7.5 g/L of cysteine with a sulfur conversion rate of 90.11%. These results indicate that cysteine production by LH16 is a valuable process in the agricultural and food industries.

Denitrifying sulfur conversion-EBPR (DS-EBPR) process for treatment of seawater-based highly saline wastewater: Evaluation on performance, kinetics and microbial community structure.

DS-EBPR is an alternative to the conventional activated sludge process which face great challenge for treatment of seawater-based highly saline wastewater. This study aims to investigate the impacts of long-term (248 days) 20% and 30% seawater fractions and short-term shock of 30%, 40%, 70% and 100% seawater fractions (corresponding to 1.0, 1.4, 2.5 and 3.5% of salinity) on the DS-EBPR performance, kinetics and microbial community structure. Long-term operation with high fraction (30%) of seawater marginally decreased the sulfur conversion and phosphorus uptake, which correlated well with the microbial dynamics. Temporal salinity shock from 1.0% (30% seawater) to 3.5% (100% seawater) remarkably reduced the phosphorus release/uptake by 36-44%, which was partly due to the decrease in the abundance of functional bacteria and chlorapatite (Ca5[PO4]3Cl) forming as P precipitates with 70-100% seawater addition. The formed chlorapatite contributed to approximately 8-26% of total P removal estimated by X-ray photoelectron spectroscopy analysis.

Formation and characterization of the micro-size granular sludge in denitrifying sulfur-conversion associated enhanced biological phosphorus removal (DS-EBPR) process.

Denitrifying Sulfur conversion-associated Enhanced Biological Phosphorus Removal (DS-EBPR) bioprocess has been recently developed for saline sewage treatment. This study investigated the applicability of granulation technology in DS-EBPR by long-term operation (272 days) of a lab-scale reactor to cultivate sludge granules, then analyzed important physicochemical and biological properties. The findings of this research showed that the net P removal and denitrification efficiencies in DS-EBPR were 80% and 98%, respectively. The average particle size was about 100 µm, and the ratio of SVI5 and SVI30 was <1.3, indicating the activated sludge was well aggregated as micro-granules. The dry density was between 32 and 56 mg/mL, and the specific surface area was 28 m2/g, demonstrating good microporous structure. FISH reveals absence of PAOs, but enriched with SRB (predominant) and denitrifying bacteria in the DS-EBPR granular sludge. Overall, this study provided essential characterization information of DS-EBPR granular sludge which can be used for future development.

Advances in sulfur conversion-associated enhanced biological phosphorus removal in sulfate-rich wastewater treatment: A review.

Recently an innovative sulfur conversion-associated enhanced biological phosphorus removal (S-EBPR) process has been developed for treating sulfate-rich wastewater. This process has successfully integrated sulfur (S), carbon (C), nitrogen (N) and P cycles for simultaneous metabolism or removal of C, N and P; moreover this new process relies on the synergy among the slow-growing sulfate-reducing bacteria and sulfur-oxidizing bacteria, hence generating little excess sludge. To elucidate this new process, researchers have investigated the microorganisms proliferated in the system, identified the biochemical pathways and assessed the impact of operational and environmental factors on process performance as well as trials on process optimization. This paper for the first time reviews the recent advances that have been achieved, particularly relating to the areas of S-EBPR microbiology and biochemistry, as well as the effects of environmental factors (e.g., electron donors/acceptors, pH, temperature, etc.). Moreover, future directions for researches and applications are proposed.