Simultaneous removal of ammonia nitrogen, phosphate, zinc, and phenol by degradation of cellulose in composite mycelial pellet bioreactor: Enhanced performance and community co-assembly mechanism.

In this experiment, the prepared tea biochar-cellulose@LDH material (TB-CL@LDH) was combined with mycelium pellets to form the composite mycelial pellets (CMP), then assembled and immobilized with strains Pseudomonas sp. Y1 and Cupriavidus sp. ZY7 to construct a bioreactor. At the best operating parameters, the initial concentrations of phosphate (PO43--P), ammonia nitrogen (NH4+-N), chemical oxygen demand (COD), zinc (Zn2+), and phenol were 22.3, 25.0, 763.8, 1.0, and 1.0 mg L-1, the corresponding removal efficiencies were 80.4, 87.0, 83.4, 91.8, and 96.6%, respectively. Various characterization analyses demonstrated that the strain Y1 used the additional carbon source produced by the strain ZY7 degradation of cellulose to enhance the removal of composite pollutants and clarified the principle of Zn2+ and PO43--P removal by adsorption, co-precipitation and biomineralization. Pseudomonas and Cupriavidus were the dominant genera according to the high-throughput sequencing. As shown by KEGG results, nitrification and denitrification genes were affected by phenol. The study offers prospects for the simultaneous removal of complex pollutants consisting of NH4+-N, PO43--P, Zn2+, and phenol.

Anthraquinone (AQS)/polyaniline (PANI) modified carbon felt (CF) cathode for selective H2O2 generation and efficient pollutant removal in electro-Fenton.

A novel binder-free anthraquinone (AQS)/polyaniline (PANI) modified carbon felt (CF) cathode for selective H2O2 generation and efficient pollutant removal in electro-Fenton was fabricated by CV electro-deposition method. AQS, the oxygen reduction reaction (ORR) catalyst, was immobilized by the PANI film, which contributed to the obtained high stability of the AQS/PANI@CF cathode. The concentration of the electro-generated H2O2 on AQS/PANI@CF cathode (83.3 µmol L-1) was about 10 times higher than that of the bare CF cathode. And the high yield of H2O2 was attributed to the catalytic reduction of O2 by AQS to generate more superoxide radical (O2•-), which combined with H+ to form H2O2. Additionally, the rhodamine B (RhB) degradation efficiency reached 98.8% within 60 min with the AQS/PANI@CF served as the cathode with high stability and good repeatability. The main generated reactive radicals were determined by the quenching experiments and the electron paramagnetic resonance (EPR) tests. Besides, a plausible mechanism of the AQS/PANI@CF cathode applied electro-Fenton process was proposed. This work provided a reliable reference for the subsequent investigations of the binder-free cathode with high performance and stability.

Aging of PVDF and PES ultrafiltration membranes by sodium hypochlorite: Effect of solution pH.

Sodium hypochlorite (NaClO) is a commonly applied cleaning agent for ultrafiltration membranes in water and wastewater treatment. Long-term exposure to NaClO might change the properties and performance of polymeric membranes, and ultimately shorten membrane lifespan. Active species in NaClO solution vary with solution pH, and the aging effects can change depending on the membrane material. In this study, the aging of polyvinylidene fluoride (PVDF) and polyethersulfone (PES) membranes by NaClO at pH 3-11 was investigated by examining variations in chemical composition, surface charge, surface morphology, mechanical strength, permeability, and retention ability. Polyvinyl pyrrolidone (PVP), which was blended in both membranes, was oxidized and dislodged due to NaClO aging at all investigated pH values, but the oxidation products and dislodgement ratio of PVP varied with solution pH. For the PVDF membrane, NaClO aging at pH 3-11 caused a moderate increase in permeability and decreased retention due to the oxidation and release of PVP. The tensile strength decreased only at pH 11 because of the defluorination of PVDF molecules. For the PES membrane, NaClO aging at all investigated pH resulted in chain scission of PES molecules, which was favored at pH 7 and 9, potentially due to the formation of free radicals. Therefore, a decrease in tensile strength and retention ability, as well as an increase in permeability, occurred in the PES membrane for NaClO aging at pH 3-11. Overall, the results can provide a basis for selecting chemical cleaning conditions for PVDF and PES membranes.

Sediment pollution characteristics and in situ control in a deep drinking water reservoir.

Sediment pollution characteristics, in situ sediment release potential, and in situ inhibition of sediment release were investigated in a drinking water reservoir. Results showed that organic carbon (OC), total nitrogen (TN), and total phosphorus (TP) in sediments increased from the reservoir mouth to the main reservoir. Fraction analysis indicated that nitrogen in ion exchangeable form and NaOH-extractable P (Fe/Al-P) accounted for 43% and 26% of TN and TP in sediments of the main reservoir. The Risk Assessment Code for metal elements showed that Fe and Mn posed high to very high risk. The results of the in situ reactor experiment in the main reservoir showed the same trends as those observed in the natural state of the reservoir in 2011 and 2012; the maximum concentrations of total OC, TN, TP, Fe, and Mn reached 4.42mg/L, 3.33mg/L, 0.22mg/L, 2.56mg/L, and 0.61mg/L, respectively. An in situ sediment release inhibition technology, the water-lifting aerator, was utilized in the reservoir. The results of operating the water-lifting aerator indicated that sediment release was successfully inhibited and that OC, TN, TP, Fe, and Mn in surface sediment could be reduced by 13.25%, 15.23%, 14.10%, 5.32%, and 3.94%, respectively.

Inorganic/organic doped carbon aerogels as biosensing materials for the detection of hydrogen peroxide.

In this article, three different inorganic/organic doped carbon aerogel (CA) materials (Ni-CA, Pd-CA, and Ppy-CA) were, respectively, mixed with ionic liquid (IL) to form three stable composite films, which were used as enhanced elements for an integrated sensing platform to increase the surface area and to improve the electronic transmission rate. Subsequently, the effect of the materials performances such as adsorption, specific surface area and conductivity on electrochemistry for myoglobin (Mb) was discussed using N2 adsorption-desorption isotherm measurements, scanning electron microscopy (SEM), and electrochemical impedance spectroscopy (EIS). Moreover, they could act as sensors toward the detection of hydrogen peroxide (H2O2) with lower detection limits (1.68 µM, 1.02 µM, and 0.85 µM, for Ni-CA/IL/Mb-CPE, Pd-CA/IL/Mb-CPE, and Ppy-CA/IL/Mb-CPE, respectively) and smaller apparent Michaelis-Menten constants KM. The results indicated that the electroconductibility of the doped CA materials would become dominant, thus playing an important role in facilitating the electron transfer. Meanwhile, the synergetic effect with [BMIm]BF4 IL improved the capability of the composite inorganic/organic doped CA/IL matrix for protein immobilization. This work demonstrates the feasibility and the potential of a series of CA-based hybrid materials as biosensors, and further research and development are required to prepare other functional CAs and make them valuable for more extensive application in biosensing.

Synergistic removal of nitrate by a cellulose-degrading and denitrifying strain through iron loaded corn cobs filled biofilm reactor at low C/N ratio: Capability, enhancement and microbiome analysis.

Optimization of nitrate removal rate under low carbon-to-nitrogen ratio has always been one of the research hotspots. Biofilm reactor based on functional carrier and using interspecific synergic effect of strains provides an insight. In this study, iron-loaded corn cob was used as a functional carrier that can contribute to the cellulose degradation, iron cycling, and collaborative denitrification process of microorganisms. During biofilm reactor operation, the maximum nitrate removal efficiency was 99.30% and could reach 81.73% at no carbon source. Dissolved organic carbon and carrier characterization showed that strain ZY7 promoted the release of carbon source. The crystallinity of cellulose I and II in carrier of experimental group increased by 31.26% and decreased by 21.83%, respectively, in comparison to the control group. Microbial community showed the synergistic effect among different strains. The vitality and metabolic activity of the target microorganisms in bioreactor were increased through interspecific bacterial cooperation.

Molecular level insight into the different interaction intensity between microplastics and aromatic hydrocarbon in pure water and seawater.

The interaction of MPs and aromatic hydrocarbons in seawater and pure water was examined using experimental measurements, molecular dynamics (MD) simulations, and density functional theory (DFT) calculations in light of the potential health risks posed by microplastic (MPs)-associated aromatic hydrocarbon pollutants. Isothermal studies and MD simulations suggested that MPs have a stronger affinity for aromatic hydrocarbons in seawater. To uncover the mechanism, MPs' surface characteristics and their intermolecular interactions with aromatic hydrocarbons were examined. According to the research, MPs in seawater have less compact structure, bigger pores, and a higher specific surface area, all of which contribute to more sorption sites. Analysis of the intermolecular interaction indicated that MPs have a greater ability for molecular interactions in seawater and the interaction energy between MPs and aromatic hydrocarbons in seawater is higher. Additionally, seawater cations may act as bridges, which also accelerate sorption in seawater. In summary, this study provides a molecular-level understanding of MPs-aromatic hydrocarbons interaction and demonstrates that the interaction is stronger in seawater.

Aging of polyvinylidene fluoride (PVDF) ultrafiltration membrane due to ozone exposure in water treatment: Evolution of membrane properties and performance.

Pre-ozonation is an effective pretreatment tactic for mitigating fouling of ultrafiltration (UF) membrane in water and wastewater treatment, but the compatibility of polymeric UF membranes with residual ozone remains unclear. In this study, effects of long-term ozone exposure on properties and performance of polyvinylidene fluoride (PVDF) UF membrane reinforced by polyethylene terephthalate (PET) layer were systematically investigated. The exposure intensities were designed to simulate ozone exposure at 0.1 mg/L for 0.5-5 years. Chemical composition analysis suggested that the hydrophilic additives, such as possibly polyvinyl pyrrolidone (PVP), was gradually degraded and released from the membrane, whereas the PVDF matrix exhibited fairly good ozone resistance. Ozonation resulted in increase of pore size and decrease of surface hydrophilicity, which can be attributed to oxidation and dislodgement of hydrophilic additives. Accordingly, long-term ozonation led to moderate changes in performance factors, including increase of membrane permeability by 34%, decrease of retention ability by 21.8%, increase of organic fouling propensity. It is worth noting that membrane tensile strength suffered substantial decrease after ozonation, probably due to ozonation of the PET support layer. Overall, it seems that the PVDF functional layer exhibited good ozone resistance, but the PET support layer was the Achilles' heel of the reinforced PVDF membrane for integrating with pre-ozonation.

Hydrophilic spongy biochar crosslinked with starch and polyvinyl alcohol biocarrier for nitrate, phosphorus, and cadmium removal in low carbon wastewater: Enhanced performance mechanism and detoxification.

This study aims to develop a functional biocarrier with hydrophilic spongy biochar crosslinked with starch and polyvinyl alcohol (WSB/starch-PVA) for simultaneous removal of NO3--N, total phosphorus (TP) and Cd2+ in low carbon wastewater. Results showed that the WSB/starch-PVA bioreactor achieved the maximum NO3--N removal efficiency in subphase 1.2 with 98.07 % (3.64 mg L-1h-1) versus control (75.30 %, 2.81 mg L-1h-1), and removed 54.84 % and 73.97 % of TP and Cd2+. Material characterization suggested that functional groups (related to C, N and O) on biocarrier and biofilm, and biogenic co-precipitation facilitated TP and Cd2+ removal. The WSB made the biocarrier pores larger and regular, and decreased fluorescent soluble microbial products. The predicted metagenome further suggested that central citrate cycle, oxidative phosphorylation of bio-community, and NO3--N removal were enhanced. Functions for microbial induced co-precipitation, Cd2+ transport/efflux, antioxidants, and enhanced biofilm formation favored the NO3--N/TP removal and Cd2+ detoxification.

Pilot scale evaluation on ferric floc sludge concentration with pelleting flocculation blanket process.

Pelleting flocculation blanket (PFB) process has been successfully applied to high turbidity suspensions for high efficient solid/liquid separation. In this paper, by using the PFB process, a dynamic experimental study was carried out on concentrating ferric flocs sludge with a scale of 1.3-5.4 m(3)/h. The pilot experiment aimed to optimize the conditioning system and determine the operational parameters. Under the raw sludge concentrations of 103-1,154 mg/L, the system could achieve ideal conditioning effect with polyacrylamide (PAM) dosages of 0.3-2.7 mg/L, agitation speed of 10 rpm, and water up-flow rates of 18-48 m/h. Under the experimental conditions, the increase of polymer dosage would improve effluent turbidity and pellets settling behaviour, the moderate up-flow rate had no marked effect on treatment results, while too large surface loading could worsen effluent turbidity. The experimental results also revealed that there existed an approximately linear relationship between the raw sludge concentration and optimum PAM dosage, that is, the optimum dosage of PAM increased synchronously as the raw sludge concentration increased. While the relationship between the raw sludge concentration and maximum up-flow rate reflected another linear dependence, namely, the maximum up-flow rate would decreased linearly as the raw sludge concentration increased.

Modified PVA (polyvinyl alcohol) biomaterials as carriers for simultaneous removal of nitrate, Cd (II), and Mn (II): performance and microbial community.

The ecological toxicity and potential risks of heavy metals that coexist with nitrates in wastewater have aroused public attention. This study developed an immobilized Fe3O4@Cu/PVA mixotrophic reactor (Fe3O4@Cu/PVA-IMR) to investigate the effect of different Mn (II) concentrations (10 mg L-1, 50 mg L-1, and 90 mg L-1), Cd (II) concentrations (10 mg L-1, 20 mg L-1, and 30 mg L-1), and hydraulic retention time (HRT) (6 h, 8 h, and 10 h) on simultaneous nitrate, Cd (II), and Mn (II) removal. Using the advanced modified biomaterial Fe3O4@Cu/PVA as carrier to embed bacteria, the performance of the reactor was further improved. The surface morphology of Fe3O4@Cu/PVA was characterized by SEM as a rough surface three-dimensional skeleton structure. When the HRT was 10 h, Mn (II) and Cd (II) concentrations were 40 mg L-1 and 10 mg L-1, respectively, indicating that the immobilized Pseudomonas sp. H117 with Fe3O4@Cu/PVA achieved the highest nitrate, Cd (II), and Mn (II) removal efficiencies of 100% (1.64 mg L-1 h-1), 98.90% (0.92 mg L-1 h-1), and 92.26% (3.58 mg L-1 h-1), respectively. Compared with a reactor without Fe3O4@Cu/PVA addition, the corresponding removal ratio increased by 22.63%, 7.09%, and 15.96%. Gas chromatography (GC) identified nitrogen as the main gaseous product. Moreover, high-throughput sequencing showed that Pseudomonas sp. H117 plays a primary role in the denitrification process.

Removal of tetracycline by denitrifying Mn(II)-oxidizing bacterium Pseudomonas sp. H117 and biomaterials (BMO and MBMO): Efficiency and mechanisms.

Coexistence of multiple pollutants such as antibiotic, nitrate and heavy metal has received increasing attention resently. In this study, the functions of Pseudomonas sp.H117 on the removal of tetracycline(TC), nitrate and Mn(II), and biological materials (BMO(biogenic manganese oxides), MBMO(magnetic BMO)) on the removal of TC were investigated. Strain H117 showed higher TC removal efficiency of 68.86% (0.071 mg·L-1·h-1) within 96 h. Meanwhile, NO3-N and Mn(II) achieved high removal efficiency of 100% (0.211 mg·L-1·h-1) and 64.64% (0.265 mg·L-1·h-1), respectively. Furthermore, trapping experiments testified that Mn(III) intermediate formed during the biological manganese oxidation process, which contribute to the TC degradation. 91.29% and 96.63% of TC removal efficiency within 12 h were achieved by BMO and MBMO. Moreover, XPS, FTIR spectra, kinetics analysis and adsorption isotherms elucidated Mn(III) oxidation, chemical adsorption and ligand exchange reactions contribute to the removal of TC by biomaterials.

Effects of Hydrogen Peroxide and Sodium Hypochlorite Aging on Properties and Performance of Polyethersulfone Ultrafiltration Membrane.

Chemical reaction of main polymer and additive with oxidative cleaning agents plays an important role in aging of polymeric membrane for water and wastewater treatment. As a green and powerful oxidant, hydrogen peroxide (H2O2) can achieve good cleaning efficacy under alkaline condition, but its influence on membrane aging was poorly understood. In this study, degradation of polyethersulfone (PES) membrane due to H2O2 exposure under alkaline condition (pH 9 and 11) was holistically investigated by humic acid (HA) filtration experiments and multiple membrane characterization techniques, with sodium hypochlorite (NaClO) aging examined as a comparison. Membrane permeability and HA retention rate was hardly changed by H2O2 aging at an exposure dose of 500 g·h/L, whereas NaClO aging led to substantial increase of membrane permeability and significant decrease of retention ability. Meanwhile, H2O2 aging slightly increased fouling propensity with HA filtration, while NaClO aging resulted in more serious fouling. ATR-FTIR and XPS analysis revealed much less degradation of PES and hydrophilic additive by H2O2 than that by NaClO, and membrane morphology and surface properties were characterized to explain the variation of filtration performance. Overall, compared with cleaning with NaClO, membrane degradation can be minimized by cleaning with H2O2.

Chemical Cleaning of Ultrafiltration Membrane Fouled by Humic Substances: Comparison between Hydrogen Peroxide and Sodium Hypochlorite.

Chemical cleaning is indispensable for the sustainable operation of ultrafiltration (UF) system in water and wastewater treatment. Sodium hypochlorite (NaClO) is an established cleaning agent for membranes subject to organic and microbial fouling, but concerns have been raised about the generation of toxic halogenated by-products during NaClO cleaning. Hydrogen peroxide (H2O2) is a potential "green" cleaning agent that can avoid the formation of halogenated by-products. In this work, cleaning efficacy of H2O2 and NaClO for UF membrane fouled by humic substances (HS) was evaluated under a wide pH range, and change of HS's properties due to reaction with cleaning agents was examined. The cleaning efficacy of H2O2 was lower than that of NaClO at pH 3-9, but it increased to a level (91.4%) comparable with that of NaClO at pH 11. The extents of changes in properties and fouling potential of HS due to reacting with cleaning agents were consistent with their cleaning efficacy. H2O2 treatment at pH 11 significantly increased negative charge of HS molecules, decomposed high-MW molecules, and reduced its fouling potential. Therefore, considering treatment/disposal of cleaning waste and cleaning efficacy, H2O2 cleaning under strong alkaline condition can be a good choice for HS-fouled membrane.

Effect of pre-oxidation on low pressure membrane (LPM) for water and wastewater treatment: A review.

Low pressure membrane (LPM) filtration is a promising technology for drinking water production, wastewater reclamation as well as pretreatment for seawater desalination. However, wider implementation of LPM is restricted by their inherent drawbacks, i.e., membrane fouling and insufficient rejection for dissolved contaminants. Pretreatment of feed water is a major method to improve the performance of LPM, and pre-oxidation has gained extensive attention because it can significantly alter compositions and properties of feed water through chemical reactions. This paper attempts to systematically review efficiency and mechanisms of pre-oxidation in membrane fouling control and permeate water quality improvement. On the basis of briefly discussing major foulants and fouling mechanisms of LPM, advantages and disadvantages of pre-oxidation in mitigating organic fouling, inorganic fouling and biofouling are discussed in detail. Impacts of pre-oxidation on removal of micropollutants, bulk organic matter and inorganic pollutants are summarized, and potential by-products of different oxidants are presented. As a prerequisite for the integration of chemical oxidation with LPM filtration, compatibility of membrane with oxidants at low concentration and long exposure time are highlighted. Finally, the existing challenges and future research needs in practical application of chemical oxidation to improve performance of LPM are also discussed.