A systematic review of antibiotics and antibiotic resistance genes (ARGs) in mariculture wastewater: Antibiotics removal by microalgal-bacterial symbiotic system (MBSS), ARGs characterization on the metagenomic.

Antibiotic residues in mariculture wastewater seriously affect the aquatic environment. Antibiotic Resistance Genes (ARGs) produced under antibiotic stress flow through the environment and eventually enter the human body, seriously affecting human health. Microalgal-bacterial symbiotic system (MBSS) can remove antibiotics from mariculture and reduce the flow of ARGs into the environment. This review encapsulates the present scenario of mariculture wastewater, the removal mechanism of MBSS for antibiotics, and the biomolecular information under metagenomic assay. When confronted with antibiotics, there was a notable augmentation in the extracellular polymeric substances (EPS) content within MBSS, along with a concurrent elevation in the proportion of protein (PN) constituents within the EPS, which limits the entry of antibiotics into the cellular interior. Quorum sensing stimulates the microorganisms to produce biological responses (DNA synthesis - for adhesion) through signaling. Oxidative stress promotes gene expression (coupling, conjugation) to enhance horizontal gene transfer (HGT) in MBSS. The microbial community under metagenomic detection is dominated by aerobic bacteria in the bacterial-microalgal system. Compared to aerobic bacteria, anaerobic bacteria had the significant advantage of decreasing the distribution of ARGs. Overall, MBSS exhibits remarkable efficacy in mitigating the challenges posed by antibiotics and resistant genes from mariculture wastewater.

Mechanistic insights into different illumination positions control algae production in anaerobic dynamic membrane filtration (AnDM) during decentralized wastewater treatment.

Sunlight illumination has the potential to control the stability and sustainability of dynamic membrane (DM) systems. In this study, an up-flow anaerobic sludge blanket (UASB) reactor was combined with DM under different illumination positions (direct, indirect and no illumination) to treat wastewater. Results indicated that the UASB achieved a COD removal up to 87.05 % with an average methane production of 0.28 L/d. Following treatment by the UASB, it was found that under illumination, the removal of organic substances by DM exhibited poor performance due to algal proliferation. However, the DM systems demonstrated efficient removal of ammonia nitrogen, ranging from 96.21 % to 97.67 % after stabilization. Total phosphorus removal was 45.72 %, and membrane flux remained stable when directly illuminated. Conversely, the DM system subjected to indirect illumination showed unstable membrane flux and severe fouling resistance. These findings offer valuable insights into optimizing illumination positions in DM systems under anaerobic conditions.

Biochar induces different responses of intracellular and extracellular antibiotic resistance genes and suppresses horizontal transfer during lincomycin fermentation dregs composting.

This study aims to indicate the influence of biochar on extracellular and intracellular ARGs (e/iARGs) variation and proliferation during lincomycin fermentation dregs (LFDs) compost. Biochar addition made iARGs keep reducing but eARGs increase to the maximum at the middle thermophilic phase and reduce at the end of the compost. Compared to control 3.15-log and 5.42-log reduction of iARGs and eARGs were observed, respectively. Biochar addition, bacterial community, and MGEs were the major contributors to iARGs and eARGs removal, with the contribution percentages of 38.4%, 31.0%, 23.7%, and 27.2%, 29.1%, and 34.9%, respectively. Moreover, biochar significantly inhibited eARGs transformation and RP4 plasmid conjugative transfer among E. coli DH5α and Pseudomonas aeruginosa HLS-6. The underlying mechanism involved in broken cell membranes of bacteria, and altered expression of oxidative stress genes and save our souls (SOS) response-related genes. The results indicated that biochar addition in composting could limit the dissemination of ARGs.

[Ultrasonic Composite Iron-carbon Activated Persulfate for Treating Organic Wastewater].

A coupling system of ultrasonic composite iron-carbon activated persulfate (US/PS/Fe-C) was built to treat a triphenylmethane derivative, crystal violet (CV). The results revealed that US/PS/Fe-C ternary system had a good coupling effect. The structure and surface morphology of commercial Fe-C and self-made Fe-C catalysts were analyzed using an X-ray diffractometer (XRD) and scanning electron microscope (SEM), respectively. Finally, commercial Fe-C was used to study the effects of different factors on the CV of US/PS/Fe-C ternary coupling degradation, and the optimum conditions were as follows:PDS concentration 2 mmol·L-1, iron-carbon catalyst 1 g·L-1, pH without adjustment, and the removal rate of 15 mg·L-1 CV reached 90% after 30 min. To explore the effects of anions and cations on the system, it was observed that Mg2+ and NO3- had almost no effect on the treatment of the system, and Mn2+, Cl-, and CO32- had a certain effect on the treatment of the system, whereas Fe2+ could promote the reaction at low concentration and inhibit the reaction at high concentration. By adding different quenchants, it was concluded that there were four types of active substances:1O2, SO4-·,·O2-, and·OH.

A novel reduced graphene oxide/polypyrrole conductive ceramic membrane enhanced electric field membrane bioreactor: Mariculture wastewater treatment performance and membrane fouling mitigation.

A novel electric field membrane bioreactor (EMBR) for mariculture wastewater treatment utilizing reduced graphene oxide/polypyrrole ceramic membrane (rGO/PPy CM) was constructed and compared with MBRs using CM support and rGO/PPy CM. EMBR (rGO/PPy) obtained the highest pollutant removal rates (84.99% for TOC, 85.98% for NH4+-N), the lowest average membrane fouling rate (2.42 kPa/d) and pollutant adhesion performance by characterization. Meanwhile, the specific fluxes of characteristic foulants in EMBR were enhanced, and the total resistances were reduced by 8.12% to 62.46%. The underlying mechanisms included reduced attraction energy and improved electrostatic repulsion between contaminants in EMBR and membrane by the extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory, DLVO model and force analysis. Therefore, this study complemented the understanding of antifouling effect and mechanism in EMBR by interaction energy and force analysis of characteristic pollutants. These findings also provided new insights into the application of EMBR for mariculture wastewater treatment.

Iron species activating chlorite: Neglected selective oxidation for water treatment.

Chlorite (ClO2 -) is the by-product of the water treatment process carried out using chlorine dioxide (ClO2) as an effective disinfectant and oxidant; however, the reactivation of ClO2 - has commonly been overlooked. Herein, it was unprecedentedly found that ClO2 - could be activated by iron species (Feb: Fe0, FeII, or FeIII), which contributed to the synchronous removal of ClO2 - and selective oxidative treatment of organic contaminants. However, the above-mentioned activation process presented intensive H+-dependent reactivity. The introduction of Feb significantly shortened the autocatalysis process via the accumulation of Cl- or ClO- during the protonation of ClO2 - driven by ultrasonic field. Furthermore, it was found that the interdependent high-valent-Fe-oxo and ClO2, after identification, were the dominant active species for accelerating the oxidation process. Accordingly, the unified mechanisms based on coordination catalysis ([Fe N (H2O) a (ClO x m-) b ] n +-P) were putative, and this process was thus used to account for the pollutant removal by the Feb-activated protonated ClO2 -. This study pioneers the activation of ClO2 - for water treatment and provides a novel strategy for "waste treating waste". Derivatively, this activation process further provides the preparation methods for sulfones and ClO2, including the oriented oxidation of sulfoxides to sulfones and the production of ClO2 for on-site use.

Impacts of bio-carriers on the characteristics of cake layer and membrane fouling in a novel hybrid membrane bioreactor for treating mariculture wastewater.

Membrane fouling is generally considered as a major bottleneck to the wide application of membrane bioreactor (MBR) for high saline mariculture wastewater treatment. Though numerous researches have investigated the membrane fouling of MBR combined with bio-carriers, few studies reveal the impacts of bio-carriers on the characteristics of cake layer and the mechanism of bio-carriers alleviating membrane fouling. In this study, two systems, namely carriers-enhanced MBR (R1) and conventional MBR (R2) were parallel operated, drawing a conclusion that bio-carriers effectively improved the characteristics of cake layer, thus mitigating membrane fouling. Fluorescence excitation emission matrix (EEM) analysis indicated that bio-carriers reduced the adhesion of proteins and humic acid-like materials on membrane surface. Molecular weight (Mw) distribution suggested that soluble microbial products (SMP) with small Mw (6-20 kDa) and biopolymers in extracellular polymeric substances (EPS) (50-300 kDa) was easier to accumulate on membrane surface in R2. The above results indicated that the presence of bio-carriers could effectively reduce the attachment of these organics on membrane surface, contributing to a larger porosity of cake layer and thus mitigating membrane fouling. Meanwhile, gas chromatography-mass spectrometry (GC-MS) clarified that more components were present in R2 than R1. Moreover, the majority of compounds in the SMP were present in both systems, while only 14 compounds in the EPS were the same between R1 and R2. Noticeably, certain aromatics only existed in R2, suggesting that bio-carriers effectively reduced the accumulation of recalcitrant materials, especially aromatics. These results revealed that bio-carriers shifted the precise composition of cake layers.

Recyclable self-floating A-GUN-coated foam as effective visible-light-driven photocatalyst for inactivation of Microcystis aeruginosa.

In this work, a recyclable self-floating A-GUN-coated (Ag/AgCl@g-C3N4@UIO-66(NH2)-coated) foam was fabricated for effective inactivation of Microcystis aeruginosa (M. aeruginosa) under visible light. The floating photocatalyst was able to inactivate 98% of M. aeruginosa within 180 min under the visible-light irrigation, and the floating photocatalyst exhibited a stable performance in various conditions. Moreover, the inactivation efficiency can still maintain nearly 92% after five times recycle experiments, showing excellent photocatalytic stability. Furthermore, effects of A-GUN/SMF floating catalyst on the physiological properties, cellular organics, and algal functional groups of M. aeruginosa were studied. The floating photocatalyst can not only make full use of excellent photocatalytic activities of A-GUN nanocomposite, but also promote contact between catalyst and algae, and realize the effective recovery of the photocatalyst. Finally, possible photocatalytic inactivation mechanisms of algae were obtained, which provides references for removing cyanobacteria blooms in real water bodies.

Microbial community dynamic shifts associated with sulfamethoxazole degradation in microbial fuel cells.

Though sulfamethoxazole (SMX) degradation at the low or medium concentration (SMX< 30 mg/L) has been reported in the microbial fuel cell (MFC), further exploration is still urgently required to investigate how the high concentration of SMX affect the anode biofilm formation. In this study, the degradation mechanism of SMX and the response of microbial community to SMX at different initial concentrations (0, 0.5, 5 and 50 mg/L) were investigated in MFCs. The highest SMX removal efficiency of 98.4% was obtained in MFC (5 mg/L). SMX at optimal concentration (5 mg/L) could serve as substrate accelerating the extracellular electron transfer. However, high concentration of SMX (50 mg/L) conferred significant inhibition on the electron transfer with SMX removal decline to 84.4%. The 16S rRNA high-throughput sequencing revealed the significant shift of the anode biofilms communities with different initial SMX concentrations were observed in MFCs. Thauera and Geobacter were the predominant genus, with relative abundance of 31.9% in MFC (50 mg/L SMX) and 52.7% in MFC (5 mg/L SMX). Methylophilus exhibited a huge increase with the highest percentage of 16.4% in MFC (50 mg/L). Hence, the functional bacteria of Thauera, Geobacter and Methylophilus endowed significant tolerance to the selection pressure from high concentration of SMX in MFCs. Meanwhile, some bacteria including Ornatilinea, Dechloromonas and Longilinea exhibited a decrease or even disappeared in MFCs. Therefore, initial concentrations of SMX played a fundamental role in modifying the relative abundance of predominant populations. This finding would promote theories support for understanding the evolution of anode biofilm formation related to the different initial concentrations of SMX in MFCs.

Can ultrafiltration singly treat the iron- and manganese-containing groundwater?

The presence of Fe2+ and Mn2+ would cause severe ultrafiltration (UF) membrane fouling and limited its extensive application in treating the groundwater. A pilot-scale gravity-driven membrane (GDM) process which coupled the dual roles of biocake layer and UF membrane was introduced to treat the groundwater under high Mn2+concentrations and low temperature conditions. The results indicated that flux stabilization was observed during long-term GDM filtration with average stabilized fluxes of 3.6-5.7 L m-2 h-1. GDM process conferred efficient removals of Fe2+ and Mn2+ with both average removals > 95%. Pre-adding manganese oxides (MnOx) could effectively shorten the ripening period of manganese removal from 50 to 30 days, and simultaneously contribute to the Mn2+ removal and flux improvements. The presence of Mn2+ facilitated the formation of heterogeneous structures of biocake layer to primarily determine the flux stabilization of GDM, while the influence of extracellular polymeric substances (EPS) concentrations was nearly negligible. Besides, the Mn2+ removal was primarily attributed to the biocake layer other than UF membrane itself, and the chemically auto-catalytic oxidation by MnOx particles played the pivotal role. Therefore, these findings provide relevance for establishing new strategies in treating the iron-and manganese-containing groundwater.

Application of iron [Fe(0)]-rich substrate as a novel capping material for efficient simultaneous remediation of contaminated sediments and the overlying water body.

Release of contaminants from sediments has been one of the main pollution sources causing eutrophication and malodorous black of ponds. In this study, an iron-rich substrate (IRS) was developed based on iron­carbon micro-electrolysis and applied for simultaneous sediments and overlying water remediation. IRS obtained high ammonia and phosphate adsorption capacities (Langmuir isotherm) of 13.02 and 18.12 mg·kg-1, respectively. In the 90-day long-term remediation, IRS reduced NH4+-N, PO43--P, organic-N, organic-P, TN and TP in overlying water by 48.6%, 97.9%, 34.2%, 67.1%, 53.2% and 90.4%, respectively. In sediments, IRS reduced NO3--N, NH4+-N and organic-N by 98.5%, 26.5% and 6.3%, respectively. The unstable P-compounds (i.e., organic-P, Ca-bounded-P and labile-P) were effectively transferred (20.1%, 54.3% and 98.2%, respectively) into inert P-compounds (i.e., Fe-bounded-P and residual-P). Meanwhile, flux rates of nitrogen and phosphorus from sediments to overlying water were reduced from 7.02 to 4.92 mg·m-2·d-1 (by 29.9%) and from 7.42 to 2.21 mg·m-2·d-1 (by 70.2%), respectively. Due to micro-electrolysis, Fe2+/Fe3+/[H] were in-situ generated from IRS and NO3--N was effectively reduced. Additionally, the generation of O2· was promoted by Fe2+/[H] and strengthened the NH4+-N, organic-N/P oxidation. Fe3+ enhanced the immobilization of PO43- (e.g., as FePO4·H2O and FenPO4(OH)3n-3). The released Fe2+/Fe3+ from IRS were finally stabilized as poorly reactive sheet silicate (PRS)-Fe and magnetite-Fe in the sediments and hardly showed side effect to sediments and water body. The developed IRS obtained advantages of high efficiency, ecologically safe and cost-effective in contaminated sediments and overlying water remediation.

An oxic/anoxic-integrated and Fe/C micro-electrolysis-mediated vertical constructed wetland for decentralized low-carbon greywater treatment.

The treatment of decentralized low-carbon greywater in rural area, particularly in cold weather, remains a challenge. Oxic/anoxic process and Fe/C micro-electrolysis were incorporated into vertical constructed wetland to develop ME-(O/A)CW for practical decentralized low-carbon greywater treatment. ME-(O/A)CW provided NH4+-N, TN, TP and COD removal of 94.3%, 86.2%, 98.0% and 92.7%, respectively, at hydraulic loading rate of 0.9 m3/(m2·d) under low ambient temperature of -11.5 to 8.0 °C. Effective nitrification, phosphorus-accumulating and organic-degradation were proceeded in the aerobic layers and efficient H2-/Fe2+-mediated autotrophic denitrification and Fe3+-based phosphorus immobilization were developed in the anaerobic layers through in-situ H2-/Fe2+-supply by Fe/C micro-electrolysis. AOB (e.g. Nitrosomonadales), NOB/PAOs (e.g. Nitrospira), autotrophic denitrificans (e.g. Thiobacillus, Hydrogenophaga and Sulfurimonas), heterotrophic denitrificans (e.g. Denitratisoma) and Fe(II)-oxidizing bacteria (e.g. Ferritrophicum) dominated ME-(O/A)CW and confirmed the reaction mechanisms. The developed ME-(O/A)CW presented significant potential in the practical application for decentralized low-carbon greywater treatment under low ambient temperature.

Application of heat-activated peroxydisulfate pre-oxidation for degrading contaminants and mitigating ultrafiltration membrane fouling in the natural surface water treatment.

Membrane fouling is posing a critical obstacle limiting the widespread application of ultrafiltration (UF). Among the numerous membrane foulants, natural organic matter (NOM) is one of the most problematic since it exists ubiquitously in natural waters and can cause severe membrane fouling. This study investigated the removal of NOM in surface water and the mitigation of membrane fouling using heat-activated peroxydisulfate (PDS) as a pretreatment for UF process. The results demonstrated that the NOM was efficiently removed, with ultraviolet absorbance (UV254) and dissolved organic carbon (DOC) decreasing by approximately 71% and 52%, respectively, at a PDS dose of 0.8 mM within 60 min (80 °C). The chromatograms of high performance size exclusion chromatography (HPSEC) indicated that some high molecular weight humic substances with a peak at approximately 10 kDa were oxidized to low molecular weight organic matters distributed in the range of < 100 Da during the pretreatment process. Moreover, three-dimensional fluorescence parallel factor analysis (PARAFAC) indicated that humic-like substances were much more easily degraded by heat-activated PDS pretreatment than protein-like substances. These results indicated that some unsaturated NOM fractions were first degraded and then mineralized to carbon dioxide during pretreatment. Meanwhile, the destroyed structure of humic substances might hinder its binding with high valence cations to reduce the possibility of high valence cations deposited on the membrane surface, thereby reducing membrane fouling. Therefore, membrane fouling could be significantly mitigated due to the shifts of NOM concentration and structure by heat-activated PDS pretreatment in the surface water treatment.

Iron-carbon galvanic cells strengthened anaerobic/anoxic/oxic process (Fe/C-A2O) for high-nitrogen/phosphorus and low-carbon sewage treatment.

The treatment of sewage with high-nitrogen/-phosphorus and low-carbon remains a challenge. A novel iron-carbon galvanic cells strengthened anaerobic/anoxic/oxic process (Fe/C-A2O) was developed for high-nitrogen/-phosphorus and low-carbon sewage treatment. The cost-effective iron-scraps (ISs) was recycled as Fe(0)-source under the mediation of Fe/C galvanic cell reaction to develop effective Fe(0)-oxidizing autotrophic-denitrification and -dephosphorization. Utilizing practical high-nitrogen/-phosphorus and low-carbon sewage as target wastewater, the performance, impact factors, contribution of Fe/C galvanic cell reactions, microbial characteristics, strengthening mechanisms, and application potential of Fe/C-A2O process were investigated. The Fe/C-A2O process achieved high TN and TP removal efficiencies of 92.0 ± 1.3% and 97.2 ± 0.9% with removal loads of 0.176 ± 0.002 kg TN/(m3·d) and 0.017 ± 0.002 kg TP/(m3·d), respectively. Optimal HRT of 12 h, DO of 4.0-4.5 mg/L, and reflux-ratio of 4:1 were obtained, and no sludge-reflux was required. Autotrophic-denitrification and -dephosphorization supported by the Fe/C galvanic cell reactions contributed 63.1% and 75.3% of TN and TP removal, respectively. Microbial characterization revealed the dominance of autotrophic denitrifiers (e.g., Thiobacillus), AOB (e.g., Nitrosomonas), NOB (e.g., Nitrospira), and heterotrophic denitrifiers (e.g., Zoogloea). The mechanism analysis demonstrated that Fe/C galvanic cells strengthened nitrogen removal by raising Fe2+/H2-supported autotrophic denitrification; and strengthened dephosphorization by introducing Fe3+-based PO43--precipitation and enhancing the denitrifying phosphate-accumulation by denitrifying phosphate-accumulating organisms (DPAOs). Based on the efficiency and cost evaluation, the ISs-based Fe/C-A2O process showed significant application potential as an upgrade strategy for traditional A2O process in advanced high-nitrogen/phosphorus and low-carbon sewage treatment.

Application potential of simultaneous nitrification/Fe0-supported autotrophic denitrification (SNAD) based on iron-scraps and micro-electrolysis.

Oxygen has not been purposely introduced to the autotrophic denitrification systems and simultaneous nitrification/autotrophic denitrification (SNAD) has not been proposed. In this study, oxygen was introduced into a micro-electrolysis-enhanced Fe0-supported autotrophic denitrification (mFe0AD) system. The nitrogen removal performance was investigated and the application potential of iron-scraps-supported simultaneous nitrification/mFe0AD was evaluated. The results showed that Fe0AD was surprisingly enhanced by oxygen together with nitrification at average dissolved oxygen (DO) of 0.08-1.56 mg/L. The ammonia oxidizing bacterial, nitrite oxidizing bacteria, facultative autotrophic denitrificans, and iron compounds transformation bacteria were markedly enriched. Average denitrification rate shifted from 0.116 to 0.340 kg N/(m3·d) with increase of average total nitrogen removal efficiency from 31.4% to 90.5%. Oxygen could enhance the biological conversion and storage of iron compounds, which was capable of reducing the coating of Fe0 surface.The accelerating of oxygen on  Fe0 passivation appeared when increasing the average DO from 1.56 to 2.17 mg/L. Therefore, the SNAD was recommended to be operated at the DO range of 0.08-1.56 mg/L. ME significantly enhanced Fe0AD, and the utilization of iron-scraps reduced its cost. The denitrification rate is comparable with methanol supported heterotrophic denitrification with 58.9% reduction on the cost. The iron-scraps supported SNAD is competitive in both denitrification rate and costs in the ammonia contaminated low-carbon water treatment.

Immobilizing Microcystis aeruginosa and powdered activated carbon for the anaerobic digestate effluent treatment.

The environment pollution caused by livestock anaerobic digestate effluent (ADE) is becoming increasingly severe recently. In this study, immobilized technology, embedding Microcystis aeruginosa (MA) and powdered activated carbon (PAC) with sodium alginate (SA), was employed to investigate the removal performance of nitrogen (N), phosphorus (P) and dissolved organic matter (DOM) in the treatment of ADE solution. Initially, orthogonal experiment was carried out to achieve the optimal conditions of the beads fabrication with the concentration of imbedding agents (PAC-SA) of 5% (w/w) and the ratio of microalgae and imbedding agents was 1:1 (v/v). The results indicated that the total nitrogen (TN), total phosphorus (TP) and total organic carbon (TOC) can be efficiently removed under the optimal operation conditions, with average removals of 91.88 ± 2.91% in TN, 98.24 ± 0.12 in TP and 78.31 ± 1.57% in TOC, respectively. Moreover, the fluorescence excitation-mission matrix (EEM) results illustrated that IMA-PAC beads joined system can efficiently diminish the concentrations of protein-like compounds and humic substances. Therefore, the organic contaminants and nutrients (i.e. N and P) can be efficiently removed in IMA-PAC beads joined system, which would contribute to developing new strategies for the treatment of ADE solution and nutrient recycle.

Scaling behavior of iron in capacitive deionization (CDI) system.

This study investigated the fouling and scaling behaviors in a capacitive deionization (CDI) system in the presence of iron and natural organic matter (NOM). It was found that the salt adsorption capacity (SAC) significantly decreased when treating Fe-containing brackish water, with higher Fe concentrations leading to severer SAC reduction. Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) analysis demonstrated that Fe2O3 appeared to be the predominant foulant attached on the electrode surface, which was difficult to be removed via backwashing, indicating the irreversible property of the foulant. Further characterizations (e.g., N2 sorption-desorption isotherms, electrochemical impedance spectroscopy and cyclic voltammetry) revealed that the CDI electrodes suffered from obvious deterioration such as specific surface area loss, resistance increase and capacitance decline with the occurrence of Fe scaling. While the presence of NOM alleviated the Fe scaling through NOM-Fe complexing effects, NOM itself was found to have negative impacts on CDI desalination performance due to their strong interactions with the carbon electrodes.

Ordered Mesoporous Cobalt Containing Perovskite as a High-Performance Heterogeneous Catalyst in Activation of Peroxymonosulfate.

An ordered mesoporous perovskite, La2CoMnO6-δ (MLCMO), was synthesized for the first time using a facile method of evaporation-induced self-assembly. The N2-sorption, scanning electron microscopy, and transmission electron microscopy measurements indicated that the optimized MLCMO possessed a high specific surface area (58.7 m2/g) and was uniformly mesoporous (11.6 nm). The MLCMO exhibited superior catalytic performance in peroxymonosulfate (PMS) activation for atrazine (ATZ) degradation. From a comparison view, the catalytic activity of the mesoporous MLCMO outperformed that of the bulk La2CoMnO6-δ (LCMO) and other common PMS activators, including α-MnO2, Co3O4, and CoFe2O4. The mechanisms of PMS activation by the MLCMO were investigated by X-ray photoelectron spectroscopy, electron spin resonance, and quenching tests. SO4•-, •OH, 1O2, and O2•- were identified as main reactive oxygen species generated from PMS activation. The Co and Mn in MLCMO were the active sites responsible for active radical generation. The lattice oxygen reversible redox sites (OL-/OL2-), which were involved in the electron transfer of the MnIII/MnIV cycle, were demonstrated as redox partners to the cation active sites. In addition, the SO4•-/•OH radical conversion was promoted at pH 11, which accelerated the consumption of PMS and seriously inhibited the degradation of ATZ.

Neglected Effects of Inoculum Preservation on the Start-Up of Psychrophilic Bioelectrochemical Systems and Shaping Bacterial Communities at Low Temperature.

Bioelectrochemical systems (BESs) are capable of simultaneous wastewater treatment and resource recovery at low temperatures. However, the direct enrichment of psychrophilic and electroactive biofilms in BESs at 4°C is difficult due to the lack of understanding in the physioecology of psychrophilic exoelectrogens. Here, we report the start-up and operation of microbial fuel cells (MFCs) at 4°C with pre-acclimated inocula at different temperatures (4°C, 10°C, 25°C, and -20°C) for 7 days and 14 days. MFCs with 7-day-pretreated inocula reached higher peak voltages than did those with 14-day-pretreated inocula. The highest power densities were obtained by MFCs with 25°C - 7-day-, 25°C - 14-day-, and 4°C - 7-day-pretreated inocula (650-700 mW/m2). In contrast, the control MFCs with untreated inocula were stable at 450 mW/m2. The power densities of MFCs with 7-day-pretreated inocula were higher than those obtained by MFCs with 14-day-pretreated inocula. The MFCs with 10°C - 7-day-pretreated inocula and the control MFCs showed higher chemical oxygen demand (COD) removal (90-91%) than other MFCs. Illumina HiSeq sequencing based on 16S rRNA gene amplicons indicated that bacterial communities of the anode biofilms were shaped by pretreated inocula at different temperatures. Compared with the control MFCs with untreated inocula, MFCs with temperature-pretreated inocula demonstrated higher microbial diversity, but did not do so with -20°C-pretreated inocula. Principal components analysis (PCA) revealed an obvious separation between the inocula pretreated at 4°C and those pretreated at 10°C, implying that bacterial community structures could be shaped by pretreated inocula at low temperatures. The pretreatment period also had a diverse impact on the abundance of exoelectrogens and non-exoelectrogens in MFCs with inocula pretreated at different temperatures. The majority of the predominant population was affiliated with Geobacter with a relative abundance of 17-70% at different pre-acclimated temperatures, suggesting that the exoelectrogenic Geobacter could be effectively enriched at 4°C even with inocula pretreated at different temperatures. This study provides a strategy that was previously neglected for fast enrichment of psychrophilic exoelectrogens in BESs at low temperatures.

Enhancement of anaerobic digestion effluent treatment by microalgae immobilization: Characterized by fluorescence excitation-emission matrix coupled with parallel factor analysis in the photobioreactor.

The bacterial-microalgal consortium has been investigated to anaerobic digestion effluent (ADE) treatment in the photobioreactor (PBR). However, the high concentrations of nutrients reduced the ADE treatment efficiency and the transformation of organic pollutants in PBR was still unclear. In this study, two-sequencing batch PBRs were operated with suspended Microcystis aeruginosa (M. aeruginosa, SMA) and immobilized M. aeruginosa (IMA) to compare the ADE treatment performance. Fluorescence excitation-emission matrix coupled with parallel factor analysis (EEM-PARAFAC) was conducted to identify organics degradations. The results showed that the proportion of living M. aeruginosa cell (86.4%) in PBR (IMA) was highly significant (p < 0.05) higher than that in PBR (SMA) (75.2%). This indicated immobilized microalgae beads enhanced the resistance to the high concentration of nutrients in PBR (IMA). EEM-PARAFAC analysis displayed the biodegradation order in the bacterial-microalgal consortium system was humic-like substances > tyrosine-like substances > tryptophan-like substances. The removals of humic-like matters (94.05 ±â€¯0.92%) and tyrosine-like matters (91.13 ±â€¯2.49%) in PBR (IMA) were significantly (p < 0.01) higher than those in PBR (SMA). Notably, the average removals of nutrients in PBR (IMA) were significantly (p < 0.05) higher than those in PBR (SMA). This result verified that microalgae immobilization benefitted nutrients removals with 93.05 ±â€¯1.45% of NH4+-N and complete PO43--P removal in PBR (IMA). Moreover, the enrichment of functional genera Flavobacterium and Opitutus contributed to decreasing the organics loadings and strengthening the ADE treatment performance. Therefore, this study verified microalgae immobilization enhanced the actual ADE treatment. Additionally, fluorescent organic pollutants degradations were further evaluated by EEM-PARAFAC analysis in the bacterial-microalgal consortium.