Visible light-induced photocatalytic and antibacterial adhesion properties of superhydrophilic TiO2 nanoparticles.

Bacterial infections triggered by patient or healthcare worker contact with surfaces are a major cause of medically acquired infections. By controlling the kinetics of tetrabutyl titanate hydrolysis and condensation during the sol-gel process, it is possible to regulate the content of Ti3+ and oxygen vacancies (OVs) in TiO2, and adjust the associated visible light-induced photocatalytic performance and anti-bacterial adhesion properties. The results have shown that the Ti3+ content in TiO2 was 9.87% at the calcination temperature of the reaction system was 300 °C and pH was 1.0, corresponding to optimal photocatalytic and hydrophilic properties. The formation of a hydrated layer on the superhydrophilic surface provided resistance to bacterial adhesion, preventing cross-contamination on high-touch surfaces. The excellent photocatalytic self-cleaning performance and anti-bacterial adhesion properties can be attributed to synergistic effects associated with the high specific surface area of TiO2 nanoparticles, the mesoporous structure, and the presence of Ti3+ and OVs. The formation of superhydrophilic self-cleaning surfaces under visible light can serve as the basis for the development of a new class of anti-bacterial adhesion materials.

Eddy Current Identification Methods and Applications in the Chemical Industry: A Mini-Review.

As one of the most common fluid patterns in the fluid flow process of chemical production, a vortex has been successfully demonstrated to be a structure that promotes interphase mixing and enhances heat and mass transfer. Therefore, it is essential to reveal the vortex evolution laws in order to realize more efficient and less energy-consuming chemical production. In this Mini-Review, the vortex identification criteria are introduced in detail and categorized according to their development history. The application of vortex identification technology and its application in the chemical industry are explored with a large number of examples. This review enhances our understanding of vortex structures and provides plenty of innovative ideas for the study of chemical industry production.

Preparation of a Molecularly Imprinted Silica Nanoparticles Embedded Microfiltration Membrane for Selective Separation of Tetrabromobisphenol A from Water.

The ubiquitous presence of tetrabromobisphenol A (TBBPA) in aquatic environments has caused severe environmental and public health concerns; it is therefore of great significance to develop effective techniques to remove this compound from contaminated waters. Herein, a TBBPA imprinted membrane was successfully fabricated via incorporating imprinted silica nanoparticles (SiO2 NPs). The TBBPA imprinted layer was synthesized on the 3-(methacryloyloxy) propyltrimethoxysilane (KH-570) modified SiO2 NPs via surface imprinting. Eluted TBBPA molecularly imprinted nanoparticles (E-TBBPA-MINs) were incorporated onto a polyvinylidene difluoride (PVDF) microfiltration membrane via vacuum-assisted filtration. The obtained E-TBBPA-MINs embedded membrane (E-TBBPA-MIM) showed appreciable permeation selectivity toward the structurally analogous to TBBPA (i.e., 6.74, 5.24 and 6.31 of the permselectivity factors for p-tert-butylphenol (BP), bisphenol A (BPA) and 4,4'-dihydroxybiphenyl (DDBP), respectively), far superior to the non-imprinted membrane (i.e., 1.47, 1.17 and 1.56 for BP, BPA and DDBP, respectively). The permselectivity mechanism of E-TBBPA-MIM could be attributed to the specific chemical adsorption and spatial complementation of TBBPA molecules by the imprinted cavities. The resulting E-TBBPA-MIM exhibited good stability after five adsorption/desorption cycles. The findings of this study validated the feasibility of developing nanoparticles embedded molecularly imprinted membrane for efficient separation and removal of TBBPA from water.

Mineralogical characteristics of root iron plaque and its functional mechanism for regulating Cr phytoextraction of hyperaccumulator Leersia hexandra Swartz.

Leersia hexandra Swartz (L. hexandra) is a promising hyperaccumulator for Cr pollution remediation, but whether its Cr phytoextraction is subject to the root surface-attached iron plaque (IP) remains unclear. In this research, the natural and artificial IPs were proven to be comprised of small amounts of exchangeable Fe as well as carbonate Fe, and dominantly Fe minerals involving amorphous two-line ferrihydrite (Fh), poorly crystalline lepidocrocite (Le) and highly crystalline goethite (Go). The Fe content in the artificial IPs augmented with increasing induced Fe(II) concentration, and the 50 mg/L Fe(II) led to the identical Fe content and different component proportions of artificial IP (Fe50) and natural IP. Fh was consisted of highly aggregated nanoparticles, and the aging of Fh caused its phase conversion to rod-like Le and Go. The Cr(VI) adsorption results of Fe minerals corroborated the coordination of Cr(VI) onto the Fh surface and the significantly greater equilibrium Cr(VI) adsorption amount of Fh over Le and Go. The greatest Cr(VI) reduction capacity of Fh among three Fe minerals was found to be related to its most abundant surface-adsorbed Fe(II) content. The results of hydroponic experiment of L. hexandra showed that the presence of IP facilitated the Cr(VI) removal by L. hexandra during the cultivation period of 10-45 days, and consequently, compared to the Fe0 group (without IP), around 60% of increase in the Cr accumulation of shoots was achieved by Fe50 group. The findings of this work are conductive to furthering our understanding of IP-regulated Cr phytoextraction of L. hexandra.

Synthesis of CuO x /TiO2 Photocatalysts with Enhanced Photocatalytic Performance.

CuO x /TiO2 co-photocatalysts with various Cu loading contents were synthesized by an impregnation method, and their photocatalytic activities were evaluated by photodegradation of organic pollutants under visible light illumination. The as-prepared CuO x /TiO2 composites exhibited a unique structure, in which CuO x clusters with about 2-3 nm nanocrystals were uniformly distributed on the TiO2 cube. The mesoporous Ti3+/TiO2 substrate with a uniform pore structure greatly improved the uniformity of the loaded Cu, wherein Ti3+ acted as a reducing agent for reducing Cu2+ to Cu+ and Cu0. The reversible process of the Cu species between Cu+ and Cu0 markedly enhanced the photocatalytic activity of the CuO x /TiO2 co-photocatalyst, by promoting the transfer of photogenerated electrons and suppressing the recombination of photogenerated electron and hole pairs. The synergistic effect between CuO x and TiO2 also played an important role in enhancing the photocatalytic activity of the CuO x /TiO2 co-photocatalyst. The results indicated that CuO x /TiO2-1 had the highest photocatalytic efficiency, which was 1.5 times higher than that of the commercial nano-TiO2 P25 under visible light, and demonstrated a good stability even after five recycles. This structural design and the valence control strategy for the Cu atom provide an idea that facilitates the utilization of visible light and the improvement of the photocatalytic activity of TiO2, promoting the practical application of the TiO2 photocatalyst.

Induced mazEF-mediated programmed cell death contributes to antibiofouling properties of quaternary ammonium compounds modified membranes.

Functionalized antibiofouling membranes have attracted increasing attention in water and wastewater treatment. Among them, contact-killing antibiofouling membranes deliver a long-lasting effect with no leaching or release, thus providing distinctive advantages. However, the antibiofouling mechanism especially in the vicinity of the membrane surface remains unclear. Herein, we demonstrate that mazEF-mediated programmed cell death (PCD) is critical for the antibiofouling behaviors of quaternary ammonium compounds modified membranes (QM). The viability of wild type Escherichia coli (WT E. coli) upon exposure to QM for 1 h was decreased dramatically (31.5 ± 1.4% of the control). In contrast, the bacterial activity of E. coli with the knockout of mazEF gene (KO E. coli) largely remained (85.8 ± 5.2%). Through addition of quorum sensing factor, i.e., extracellular death factor (EDF), the antibacterial activity was significantly enhanced in a dilute culture, indicating that the density-dependent bacterial communication played an important role in the mazEF-mediated PCD system in biofouling control. Long-term study further showed that QM exhibited a better antibiofouling performance to treat feedwater containing WT E. coli, especially when EDF was dosed. Results of this study suggested that the bacteria on the membrane surface subject to contact killing could modulate the population growth in the vicinity via quorum-sensing mazEF-mediated PCD, paving a way to develop efficient antibiofouling materials based on contact-killing scenarios.

Mechanistic insights into CO2 pressure regulating microbial competition in a hydrogen-based membrane biofilm reactor for denitrification.

CO2 is a proven pH regulator in hydrogen-based membrane biofilm reactor (H2-MBfR) but how its pressure regulates microbial competition in this system remains unclear. This work evaluates the CO2 pressure dependent system performance, CO2 allocation, microbial structure and activity of CO2 source H2-MBfR. The optimum system performance was reached at the CO2 pressure of 0.008 MPa, and this pressure enabled 0.18 g C/(m2·d) of dissolved inorganic carbon (DIC) allocated to denitrifying bacteria (DNB) for carbon source anabolism and denitrification-related proton compensation, while inducing a bulk liquid pH (pH 7.4) in favor of DNB activity by remaining 0.21 g C/(m2·d) of DIC as pH buffer. Increasing CO2 pressure from 0.008 to 0.016 MPa caused the markedly changed DNB composition, and the diminished DNB population was accompanied by the enrichment of sulfate-reducing bacteria (SRB). A high CO2 pressure of 0.016 MPa was estimated to induce the enhanced SRB activity and weakened DNB activity.

Metal-Coordinated Nanofiltration Membranes Constructed on Metal Ions Blended Support toward Enhanced Dye/Salt Separation and Antifouling Performances.

Metal-phenol coordination is a widely used method to prepare nanofiltration membrane. However, the facile, controllable and scaled fabrication remains a great challenge. Herein, a novel strategy was developed to fabricate a loose nanofiltration membrane via integrating blending and interfacial coordination strategy. Specifically, iron acetylacetonate was firstly blended in Polyether sulfone (PES) substrate via non-solvent induced phase separation (NIPS), and then the loose selective layer was formed on the membrane surface with tannic acid (TA) crosslinking reaction with Fe3+. The surface properties, morphologies, permeability and selectivity of the membranes were carefully investigated. The introduction of TA improved the surface hydrophilicity and negative charge. Moreover, the thickness of top layer increased about from ~30 nm to 119 nm with the increase of TA assembly time. Under the optimum preparation condition, the membrane with assembly 3 h (PES/Fe-TA3h) showed pure water flux of 175.8 L·m−2·h−1, dye rejections of 97.7%, 97.1% and 95.0% for Congo red (CR), Methyl blue (MB) and Eriochrome Black T (EBT), along with a salt penetration rate of 93.8%, 95.1%, 97.4% and 98.1% for Na2SO4, MgSO4, NaCl and MgCl2 at 0.2 MPa, respectively. Both static adhesion tests and dynamic fouling experiments implied that the TA modified membranes showed significantly reduced adsorption and high FRR for the dye solutions separation. The PES/Fe-TA3h membrane exhibited high FRR of 90.3%, 87.5% and 81.6% for CR, EBT and MB in the fouling test, stable CR rejection (>97.2%) and NaCl permeation (>94.6%) in 24 h continuous filtration test. The combination of blending and interfacial coordination assembly method could be expected to be a universal way to fabricate the loose nanofiltration membrane for effective fractionation of dyes and salts in the saline textile wastewater.

Metal-organic framework enables ultraselective polyamide membrane for desalination and water reuse.

While reverse osmosis (RO) is the leading technology to address the global challenge of water scarcity through desalination and potable reuse of wastewater, current RO membranes fall short in rejecting certain harmful constituents from seawater (e.g., boron) and wastewater [e.g., N-nitrosodimethylamine (NDMA)]. In this study, we develop an ultraselective polyamide (PA) membrane by enhancing interfacial polymerization with amphiphilic metal-organic framework (MOF) nanoflakes. These MOF nanoflakes horizontally align at the water/hexane interface to accelerate the transport of diamine monomers across the interface and retain gas bubbles and heat of the reaction in the interfacial reaction zone. These mechanisms synergistically lead to the formation of a crumpled and ultrathin PA nanofilm with an intrinsic thickness of ~5 nm and a high cross-linking degree of ~98%. The resulting PA membrane delivers exceptional desalination performance that is beyond the existing upper bound of permselectivity and exhibited very high rejection (>90%) of boron and NDMA unmatched by state-of-the-art RO membranes.

Application of Machine Learning in a Mineral Leaching Process-Taking Pyrolusite Leaching as an Example.

In this study, several machine learning models were used to analyze the process variables of electric-field-enhanced pyrolusite leaching and predict the leaching rate of manganese, and the applicability of those models in the leaching process of hydrometallurgy was compared. It showed that there was no correlation between the six leaching conditions; in addition to the leaching time, the concentrations of sulfuric acid and ferrous sulfate had great influences on the leaching of pyrolusite. The results of the prediction models showed that the support vector regression model has the best prediction performance, with regression index (R 2) = 0.92 and mean square error = 25.04, followed by the gradient boosting regression model (R 2 > 0.85). In this research, machine learning models were applied to the optimization of the manganese leaching process, and the research process and methods were also applicable to other hydrometallurgical processes for majorization and result prediction.

Novel Technology for Vanadium and Chromium Extraction with KMnO4 in an Alkaline Medium.

This paper focused on the oxidation-alkaline extraction process of vanadium-chromium-reducing residue. The affected parameters including reaction temperature, KMnO4 dosage, reaction time, NaOH dosage, and liquid-to-solid ratio on the extraction process were investigated. The E-pH diagram and the thermodynamic analysis indicated that KMnO4 was suitable for the oxidation of low-valence vanadium and chromium. Vanadium (97.24%) and chromium (56.20%) were extracted under the following optimal reaction conditions: reaction temperature of 90 °C, reaction time of 90 min, dosage of KMnO4 at m(KMnO4)/m(residue) = 0.40, dosage of NaOH at m(NaOH)/m(residue) = 0.30, and liquid-to-solid ratio at 5:1 mL/g. The extraction process of vanadium was controlled by the reactant through the solid product layer and the extraction kinetics behavior fitted well with the shrink core model with an E a of 15.37 kJ/mol. At the same time, the surface chemical reaction was the controlling step for chromium extraction, which was difficult with an E a of 39.78 kJ/mol.

Membrane Biofouling Control by Surface Modification of Quaternary Ammonium Compound Using Atom-Transfer Radical-Polymerization Method with Silica Nanoparticle as Interlayer.

A facile approach to fabricate antibiofouling membrane was developed by grafting quaternary ammonium compounds (QACs) onto polyvinylidene fluoride (PVDF) membrane via surface-initiated activators regenerated by electron transfer atom-transfer radical-polymerization (ARGET ATRP) method. During the modification process, a hydrophilic silica nanoparticle layer was also immobilized onto the membrane surface as an interlayer through silicification reaction for QAC grafting, which imparted the membrane with favorable surface properties (e.g., hydrophilic and negatively charged surface). The QAC-modified membrane (MQ) showed significantly improved hydrophilicity and permeability mainly due to the introduction of silica nanoparticles and exposure of hydrophilic quaternary ammonium groups instead of long alkyl chains. Furthermore, the coverage of QAC onto membrane surface enabled MQ membrane to have clear antibacterial effect, with an inhibition rate ~99.9% of Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive), respectively. According to the batch filtration test, MQ had better antibiofouling performance compared to the control membrane, which was ascribed to enhanced hydrophilicity and antibacterial activity. Furthermore, the MQ membrane also exhibited impressive stability of QAC upon suffering repeated fouling-cleaning tests. The modification protocols provide a new robust way to fabricate high-performance antibiofouling QAC-based membranes for wastewater treatment.

A low cost of phosphate-based binder for Mn2+ and NH4+-N simultaneous stabilization in electrolytic manganese residue.

Electrolytic manganese residue (EMR) is a solid waste remained in filters after using sulfuric acid to leaching manganese carbonate ore. EMR contains high concentration of soluble manganese (Mn2+) and ammonia nitrogen (NH4+-N), which seriously pollutes the environment. In this study, a low cost of phosphate based binder for Mn2+ and NH4+-N stabilization in EMR by low grade-MgO (LG-MgO) and superphosphate was studied. The effects of different types of stabilizing agent on the concentrations of NH4+-N and Mn2+, the pH of the EMR leaching solution, stabilizing mechanisms of NH4+-N and Mn2+, leaching test and economic analysis were investigated. The results shown that the pH of the EMR leaching solution was 8.07, and the concentration of Mn2+ was 1.58 mg/L, both of which met the integrated wastewater discharge standard (GB8978-1996), as well as the concentration of NH4+-N decreased from 523.46 mg/L to 32 mg/L, when 4.5 wt.% LG-MgO and 8 wt.% superphosphate dosage were simultaneously used for the stabilization of EMR for 50 d Mn2+ and NH4+-N were mainly stabilized by Mn3(PO4)2·2H2O, MnOOH, Mn3O4, Mn(H2PO4)2·2H2O and NH4MgPO4·6H2O. Economic evaluation revealed that the treatment cost of EMR was $ 11.89/t. This study provides a low-cost materials for NH4+-N and Mn2+ stabilization in EMR.

Leaching of Valuable Elements from the Waste Chromite Ore Processing Residue: A Kinetic Analysis.

The efficacious treatment and resource utilization of the chromite ore processing residue (COPR) is important for chromate salt production. In this study, the leaching of valuable elements from the waste COPR was investigated. X-ray diffraction (XRD) analysis showed that the COPR mainly contained periclase (MgCr2O4), magnesiochromite ((Fe, Mg) (Cr, Fe)2O4), Fe (Cr, Al)2O4, and MgFeAlO4. The optimum parameters for COPR leaching were as follows: mechanical ball-milling time of 120 min, sulfuric acid concentration (w/w % H2SO4) of 60%, reaction temperature (T) of 403 K, liquid-solid ratio (L/S) of 8 mL/g, and reaction time (t) of 6 h. Under these conditions, the valuable components such as Fe, Al, and Cr were extracted with an ideal leaching efficiency of 94.8, 75.1, and 76%, respectively. The results of the leaching kinetics analysis indicated that the leaching of Fe and Cr from the COPR was controlled by a surface chemical reaction, and the leaching of Al was controlled by diffusion through a product layer. The apparent activation energy of the leaching of Fe, Cr, and Al was calculated to be 23.03, 44.15, and 17.54 kJ/mol, respectively. It is believed that this approach has potential applications for the chromate salt industry because of its advantage of ideal leaching efficiency.

Leaching Kinetics of Vanadium from Calcium-Roasting High-Chromium Vanadium Slag Enhanced by Electric Field.

Vanadium exists as multivalent valences in high-chromium vanadium slag, and it is hard to leach out in low valence. Electro-oxidation technology has been applied to enhance the leaching process of calcium-roasting high-chromium vanadium slag. The effect of parameters that affect the leaching efficiency of vanadium including concentration of sulfur acid, current density, reaction temperature, and liquid-to-solid ratio was investigated. The results showed that vanadium in low valence could be oxidized and efficiently leached out enhanced with electricity. The leaching kinetics was analyzed, which indicates that the leaching rate was controlled by the surface chemical reaction with an apparent activation energy of 40.11 kJ/mol. On the basis of this process, vanadium could be efficiently leached out with a leaching efficiency of 92.14% under optimal conditions: concentration of sulfur acid of 40 vol %, current density of 750 A/m2, reaction temperature of 90 °C, reaction time of 180 min, particle size under 75 µm, liquid-to-solid ratio of 4:1 mL/g, and stirring rate of 500 rpm. The relationship between the leaching efficiency and the parameters affecting the leaching process could be described as 1 - (1 - x)1/3 = K 0 × [H2SO4]0.1390 × [J]0.03354 × [T]2.8247 × [L/S]-0.2598 × exp40.11/T × t.

Antibiofouling performance and mechanisms of a modified polyvinylidene fluoride membrane in an MBR for wastewater treatment: Role of silver@silica nanopollens.

Biofouling remains to be one of major obstacles in membrane bioreactors (MBRs), calling for the development of antibiofouling membranes. Silver nanoparticles (AgNPs), being a kind of broad spectrum bactericidal agent, have been widely used for modifying membrane; however, uncontrollable release of AgNPs and thus a short lifetime of modified membranes are thorny issues for the AgNPs-modified membranes. In this study, silica nanopollens were used as AgNPs nanocarriers for membrane modification (ASNP-M), which could improve silver delivery efficacy, avoid agglomeration and control Ag+ release towards bacteria. At a silver loading of 107.7 ± 10.9 µg Ag/cm2, ASNP-M effectively inhibited growth of Escherichia coli and Staphylococcus aureus, with an Ag+ release rate of 0.5 µg/(cm2 d). Long-term MBR tests showed that ASNP-M exhibited a significantly reduced transmembrane pressure increase rate of 0.88 ± 0.34 kPa/d which was much lower than that of two control membranes, i.e., pristine membrane (M0) (2.32 ± 0.86 kPa/d) and Ag@silica nanospheres (without spikes) modified membrane (ASNS-M) (2.25 ± 1.28 kPa/d). No significant adverse influences on the pollutant removal were also observed in the reactor. Foulants analysis revealed that biofilm of ASNP-M was thinner and comprised of mainly dead cells, and only organic matter with strong adhesion properties was allowed to attach onto the membrane surface. Bacterial community analysis suggested that the incorporation of Ag@silica nanopollens inhibited colonization of bacteria which are capable of causing membrane biofouling (e.g., Proteobacteria and Actinobacteria). These findings highlight the potential of the antibiofouling membrane to be used in MBRs for wastewater treatment and reclamation.

Microbial responses to transient shock loads of quaternary ammonium compounds with different length of alkyl chain in a membrane bioreactor.

Extensive applications of quaternary ammonium compounds (QACs) in household and industrial products inevitably lead to their release into wastewaters; however, little attention has been paid to the acute effects on activated sludge. In this work, we investigated the responses of microorganisms in a membrane bioreactor (MBR) to transient shock loads of QACs with different alkyl chain length and their impacts on MBR performance. Results showed that QACs affected microbial viability and caused damage to key enzymes (e.g., ammonium monooxygenase and nitrite oxidoreductase), inhibiting organic matter degradation and nitrogen removal. The presence of QACs also caused negative influences on dehydrogenase activity, catalase and superoxide dismutase, thus increasing the production of reactive oxygen species. Moreover, QACs with longer alkyl chains and/or benzyl groups bonded to the nitrogen atom could induce a more severe damage to cell integrity and microbial viability. The interaction with QACs also induced the release of organic matters and the changes of adhesion properties of microbial products, resulting in aggravated membrane fouling in MBRs. Our results demonstrate the acute negative effects of QACs on activated sludge, and special attention should be paid to the performance of biological wastewater treatment processes subject to the shock loads of QAC-bearing industrial streams.

Impacts of quaternary ammonium compounds on membrane bioreactor performance: Acute and chronic responses of microorganisms.

Quaternary ammonium compounds (QACs) are emerging contaminants with the extensive applications in a variety of fields. However, little is known about their potential impacts on activated sludge and performance of biological wastewater treatment processes. In this work, the effects of benzalkonium chloride (BAC, a kind of QACs) on acute and chronic responses of microorganisms and on MBR performance were systematically investigated. The results showed that a low concentration (0.5-2.0 mg BAC/g SS) caused no significant effects on activated sludge property. In contrast, an elevated concentration of BAC led to severer inhibition on activated sludge and key enzyme activity (e.g., dehydrogenase activity) in both short-term and long-term exposure, thus deteriorating the pollutant removal efficiency. Compared with the control MBR (R1) and the reactor with 0.5 mg/L BAC (R2), the removal efficiency of ammonia in R3 with 5.0 mg/L BAC at identical hydraulic retention time (4.3 h) and sludge retention time (30 d) was decreased, i.e., ammonium removal efficiency in R1∼R3 was 95.4 ±â€¯6.1, 93.4 ±â€¯8.1 and 89.3 ±â€¯17.6%, respectively. Moreover, MBR tests showed that membrane fouling was aggravated in the presence of high-concentration BAC. Long-term exposure to BAC reduced microbial community diversity and enriched the BAC-resistant microbes. For instance, the abundance of Pseudomonas genus in R3 was increased from 0.02% to 14.9% with the increase of operation time. Microbial community structure was changed to resist the environmental stress induced by BAC during long-term exposure, thus decreasing the inhibition effects.

QAC modified PVDF membranes: Antibiofouling performance, mechanisms, and effects on microbial communities in an MBR treating municipal wastewater.

Biofouling remains as a critical issue limiting the widespread applications of membrane bioreactors (MBRs). The use of antibiofouling membranes is an emerging method to tackle this issue. In this study, a polyvinylidene fluoride (PVDF) membrane was modified using a quaternary ammonium compound (QAC) to create an antibiofouling membrane. The membrane was used in an MBR and the performance, mechanisms, and effects on microbial communities of this membrane were compared to a control operated in parallel. Results showed that the membrane exhibited a significantly reduced transmembrane pressure increase rate of 0.29 kPa/d compared with 0.91 kPa/d of the control. Analysis using a confocal laser scanning microscope (CLSM) revealed almost complete lack of living microbes on the antibiofouling membrane in contrast to the control. However, specific oxygen uptake rate and dehydrogenase activity analyses demonstrated no adverse impacts on microbial viability of the bulk activated sludge. Bacterial population analysis using the Illumina Miseq platform added further evidence that the use of antibiofouling membrane did not exert negative influences on richness, diversity and structure of the bacterial community. Effluent quality of the test MBR also exhibited minimal difference from that of the control reactor. The amount of polysaccharides and proteins in the biofouling layer was also significantly reduced. Quartz crystal microbalance with dissipation monitoring suggested that the antibiofouling membrane only allowed organic matter with strong adhesion properties to attach onto the membrane surfaces. These findings highlight the potential of the antibiofouling membrane to be used in MBRs for wastewater treatment and reclamation.

Acute Responses of Microorganisms from Membrane Bioreactors in the Presence of NaOCl: Protective Mechanisms of Extracellular Polymeric Substances.

Extracellular polymeric substances (EPS) are key foulants in membrane bioreactors (MBRs). However, their positive functions of protecting microorganisms from environmental stresses, e.g., during in situ hypochlorite chemical cleaning of membranes, have not been adequately elucidated. In this work, we investigated the response of microorganisms in an MBR to various dosages of NaOCl, with a particular emphasis on the mechanistic roles of EPS. Results showed that functional groups in EPS such as the hydroxyl and amino groups were attacked by NaOCl, causing the oxidation of polysaccharides, denaturation of amino acids, damage to protein secondary structure, and transformation of tryptophan protein-like substances to condensed aromatic ring substances. The presence of EPS alleviated the negative impacts on catalase and superoxide dismutase, which in turn reduced the concentration of reactive oxygen species (ROS) in microbial cells. The direct extracellular reaction and the mitigated intracellular oxidative responses facilitated the maintenance of microbial metabolism, as indicated by the quantity of adenosine triphosphate and the activity of dehydrogenase. The reaction with NaOCl also led to the changes of cell integrity and adhesion properties of EPS, which promoted the release of organic matter into bulk solution. Our results systematically demonstrate the protective roles of EPS and the underlying mechanisms in resisting the environmental stress caused by NaOCl, which provides important implications for in situ chemical cleaning in MBRs.