Adsorption Of Extracellular Polymeric Substances Research Articles

Extracellular polymeric substances altered the physicochemical properties of molybdenum disulfide nanomaterials to mitigate its toxicity to Chlorella vulgaris

Although the toxic effects of two-dimensional nanomaterials (2D-NMs) have been widely reported, the influence of extracellular polymeric substances (EPS) on the environmental fate and risk of 2D-NMs in aquatic environments is largely unknown, and the processes and mechanisms involved remain to be revealed. Herein, we investigated the impact of EPS secreted by microalgae (Chlorella vulgaris (C. vulgaris)) on the environmental transformation and risk of molybdenum disulfide (MoS2). We found that the attachment of EPS increased the thickness of MoS2 (from 2 nm to 5 nm), changed it from a monolayer sheet to a fuzzy multilayer structure, and promoted the formation of defects on MoS2. The blue-shift of the peak associated with the plasmon resonances in the 1 T phase and the generation of electron-hole pairs suggested that EPS altered the surface electronic structure of MoS2. EPS interacted mainly with the S atoms on the 1 T phase, and the attachment of EPS promoted the oxidation of MoS2. The reduction in hydrodynamic diameter (Dh) and the decrease in zeta potential indicated that EPS inhibited the agglomeration behavior of MoS2 and enhanced its dispersion and stability in aqueous media. Notably, EPS reduced the generation of free radicals (superoxide anion (•O2−), singlet oxygen (1O2), and hydroxyl radicals (•OH−)). Furthermore, EPS mitigated the toxicity of MoS2 to C. vulgaris, such as attenuated reduction in biomass and chlorophyll content. Compared to pristine MoS2, MoS2 + BG11 + EPS exhibited weaker oxidative stress, membrane damage and lipid peroxidation. The adsorption of EPS on MoS2 surface reduced the attachment sites of MoS2, making MoS2 less likely to be enriched on the cell surface. The findings have significant contribution for understanding the interactions between EPS and MoS2 in aquatic ecosystems, providing scientific guidance for risk assessment of 2D-NMs.

Pitting corrosion behavior and mechanism of 316L stainless steel induced by marine fungal extracellular polymeric substances

In this study, effect of extracellular polymeric substances (EPS) secreted by fungus Aspergillus terreus on the pitting corrosion of 316L stainless steels (SS) was deeply investigated by electrochemical measurements and surface analysis. Results demonstrated that adsorption of EPS can change surface wettability of 316L SS leading to a much more hydrophilic steel–water interface. EPS not only accelerates uniform corrosion but enhances pitting corrosion of 316L SS. EPS can promote the formation of metastable pitting corrosion and the subsequent growth of corrosion pits. The density of corrosion pits (>2 µm) reach (5.6 ± 0.5)× 103 pits/cm2 when EPS is 400 mg/L.

Unravelling the complex adsorption behavior of extracellular polymeric substances onto pristine and UV-aged microplastics using two-dimensional correlation spectroscopy

In this study, we examined the preferential adsorption behavior of extracellular polymeric substances (EPS) on two commonly used microplastics (MPs), including polyethylene (PE) and polypropylene (PP), through adsorption kinetics and isotherm experiments. The effects of UV aging on EPS adsorption were also explored. The results showed that EPS adsorption was greater on UV-aged MPs than on pristine MPs, with an adsorption capacity of approximately 27.0 mg-C/m2 for aged PP-MPs and 23.5 mg-C/m2 for pristine PP-MPs, and 16.4 mg-C/m2 for aged PE-MPs and 12.5 mg-C/m2 for pristine PE-MPs. Fourier transform infrared (FTIR) spectra revealed that EPS adsorption was governed by hydrogen bonds between EPS molecules and methylene groups in pristine MPs and CO, C–O groups in UV-aged MPs, as evidenced by the addition and the reduction of the related peaks shown in MP surfaces and residual EPS after adsorption, respectively. Fluorescence spectroscopy revealed that protein-like components exhibited higher Freundlich adsorption affinity (i.e., Kf), ranging from 0.34 to 1.29 (RU⋅L m−2) (RU⋅L−1)n than humic-like components (0.01 to 0.12 (RU⋅L m−2) (RU⋅L−1)n). The EPS molecular distribution was consistent with the FTIR results, showing preferable adsorption of biopolymer versus humic substances fraction. Two-dimensional correlation spectroscopy combined with FTIR (2D-COS-IR) revealed that polysaccharides in EPS were more preferentially adsorbed onto MPs and the order of the sequence was polysaccharides > proteins > humic-like substances for all MPs tested. This study provides new insight into the complex adsorption behavior of heterogeneous EPS on MPs and the associated alterations in the potential environmental fate of MPs.

Phototransformation of extracellular polymeric substances in activated sludge and their interaction with microplastics.

Substantial amounts of extracellular polymeric substances (EPS) are present in sludge from wastewater treatment plants (WWTP), and EPS can significantly affect the fate, bioavailability, and toxicity of microplastics (MPs) that coexist in the effluent, however, the mechanism of action between EPS and microplastics remains unclear. In addition, ultraviolet (UV) disinfection is indispensable in the wastewater treatment process in WWTP, which can significantly affect the characteristics of EPS. Therefore, it is of great significance to study the photochemical characteristics of EPS and the effect on binding MPs. In this study, using multispectral technology and two-dimensional correlation spectroscopy analysis, indicates that the molecular weight and aromaticity of EPS after phototransformation were reduced. The results showed that the adsorption of EPS on PSMPs was in the order of TB-EPS > LB-EPS > S-EPS, which was positively correlated with the SUVA254, but negatively correlated with O/C of EPS. This indicates that the main adsorption mechanisms of PSMPs on EPS were π-π and hydrophobicity. The adsorption capacity of S-EPS, LB-EPS and TB-EPS to PSMPs decreased with the increasing of illumination time. After phototransformation, the adsorption sensitivity and reaction sequence of EPS and PSMPs did not change much. This research provides a theoretical basis for understanding the photochemical transformation of extracellular polymers and the morphology and migration of microplastics in sewage treatment, and evaluating the impact of microplastics on ecosystems.

Application of aerobic denitrifier for simultaneous removal of nitrogen, zinc, and bisphenol A from wastewater

High concentrations of heavy metals and other pollutants affect microbial activity in the wastewater treatment system and impede biological denitrification process. In this study, a novel Zn(II)-resistant aerobic denitrifier (Pseudomonas stutzeri KY-37) was isolated with potential in Bisphenol A (BPA) biodegradation and removal. The capability of this denitrifier in removing nitrogen, zinc, and BPA was tested. Using 56 mg/L nitrate as the sole nitrogen source, its removal efficiency achieved 98.5% in 12 h. This novel denitrifier had a strong auto-aggregation (maximum 65.8%), a high hydrophobicity rate (maximum 88.2%), and a massive amount (maximum 41.1 mg/g cell dry weight) of extracellular polymeric substances (EPS) production. Moreover, Zn(II) removal efficiency reached more than 95% with the initial high concentrations of 200 mg/L. The maximum BPA removal efficiency reached 88.8% with initial 10 mg/L. The removal mechanism of BPA was further explored in terms of microbial degradation, EPS adsorption, and intermediate degradation products.

EPS for bacterial anti-adhesive properties investigated on a model metal surface

Understanding Extracellular Polymeric Substances (EPS) interaction on a well-defined chromium surface is of importance especially for biocorrosion processes. Adsorption of EPS extracted from Pseudoalteromonas NCIMB 2021 on Cr surfaces was investigated using in situ quartz crystal microbalance (QCM) and X-ray photoelectron spectroscopy (XPS). We show that EPS adsorption is an irreversible process. The amount of adsorbed EPS increases with increasing EPS concentration in solution. For low EPS concentration, the surface is only partially covered by EPS, whereas a continuous organic film of around 15 nm is formed at the surface for high EPS concentrations. An in-depth structuration of this organic layer is evidenced with a strong enrichment of proteins in the inner part and of polysaccharides in the outer part. Adhesion of Pseudoalteromonas NCIMB 2021 has been tested on Cr surfaces covered or not by EPS extracted from Pseudoalteromonas NCIMB 2021. EPS conditioning with a 15 nm film inhibits bacterial adhesion on Cr, showing that this organic film has efficient anti-adhesive properties.

Red Yeast Improves the Potential Safe Utilization of Solid Waste (Phosphogypsum and Titanogypsum) Through Bioleaching.

Phosphogypsum (PG) and titanium gypsum (TG), as a by-product (solid waste) in phosphate fertilizer and titanium dioxide industry, are causing serious environmental hazards. The resource/harmless application of PG and TG is the development trend in the future. The biological function of red yeast (Rho: Rhodotorula mucilaginosa) can effectively reduce the concentration of pollutants in the environment and has the potential of biological flotation/purification of mineral solid waste. In this study, the bioremediation mechanism and safe utilization efficiency of Rho for different contents of PG and TG were explored by using its biological flotation function. The X-ray fluorescence spectrometry (XRF) results showed that F was the main toxic element in PG and TG, and Pb and Cd did not reach the detection limit. The processing capacity of Rho for PG (>10 g/ml) is higher than that of TG (<5 g/ml). After bioleaching by Rho, the proportion of F in PG and TG solid decreased by 61.45–63.79% and 49.45–59.19%, respectively. The results of three-dimensional fluorescence, extracellular polymeric substance (EPS) extraction, X-ray diffraction (XRD), and scanning electron microscopy (SEM) confirmed that Rho could accelerate the release of harmful elements (F) in PG and TG. SEM showed that Rho cells and secretions adhered and wrapped on PG/TG, causing PG/TG decomposition and fragmentation. In addition, the adsorption of EPS and the formation of Ca5(PO4)3F are two main ways for Rho to remove F. Furthermore, under the condition of high concentration bioleaching, Rho can accelerate the release and utilization of P in PG, which is not only for the re-precipitation of Ca5(PO4)3F but also conducive to the reproduction and utilization of microorganisms. Meanwhile, the purification/safe reuse of PG by Rho is easier than that of TG. Therefore, the toxicity of PG and TG bioleaching by Rho can be greatly reduced, suggesting the huge potential of Rho in soil improvement and remediation.

Selective retention of extracellular polymeric substances induced by adsorption to and coprecipitation with ferrihydrite

Recent work shows that microbially-derived compounds constitute a significant fraction of the soil organic matter (OM) pool. These compounds include extracellular polymeric substances (EPS) whose mass can far exceed total microbial cell biomass. Sorption of EPS to soil minerals occurs via adsorption and coprecipitation and contributes to the preservation of OM in the soil environment. Little is known, however, about the sorption mechanisms of EPS and selective retention of different EPS constituents on iron (oxyhydr)oxides, especially during EPS adsorption versus coprecipitation with these reactive soil phases. This study examines how EPS interacts with the ubiquitous soil iron (oxyhydr)oxide ferrihydrite during EPS adsorption and coprecipitation and whether these different EPS-mineral association pathways affect EPS sorption and selective retention, and thus the mobility and fate of microbially-derived OM in the soil environment. We use several complimentary techniques to i) examine EPS-carbon, EPS-nitrogen and EPS-phosphorus sorption and fractionation, ii) visualize spatial relationships between EPS biomolecular classes and ferrihydrite using confocal laser scanning microscopy (CLSM), iii) determine EPS-C speciation and chemical fractionation with ferrihydrite using X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure spectroscopy (NEXAFS), and iv) determine functional group interactions with ferrihydrite using Fourier transform infrared spectroscopy (FTIR) combined with two-dimensional correlation spectroscopy (2D-COS) analysis. Results show that the coprecipitation of EPS does not change the ferrihydrite mineralogy, as the main mineral phase for EPS association, but it substantially increases the particle size of EPS-ferrihydrite. A substantial difference in the EPS mass fraction associated with the ferrihydrite is observed between the adsorption and coprecipitation experiments at an initial molar C/Fe ratio >1. The EPS-N is relatively enriched during the adsorption process, while more EPS-C and near-complete EPS-P are fixed in the coprecipitation process. XPS results show that the surface of the ferrihydrite formed through EPS adsorption is preferentially enriched with protein-like components, whereas, the surface of the ferrihydrite formed through EPS coprecipitation is enriched with polysaccharide-like components, which is visually confirmed with CLSM images. NEXAFS results reveal that the carboxylic/amide C-containing components are selectively retained during adsorption, with the aliphatic and O-alkyl C-containing components relatively enriched during coprecipitation. 2D-FTIR-COS results indicate that during EPS adsorption on ferrihydrite the PO functional groups are adsorbed faster than the amide and carboxylate functional groups, while during EPS coprecipitation with ferrihydrite the opposite trend is observed. The findings from this study indicate that the formation pathway of EPS-ferrihydrite associations substantially effects the sorption mechanisms and selective retention of EPS and may thus affect the mobility and fate of microbially-derived carbon (C), nitrogen (N) and phosphorus (P) in soils. These new insights on EPS behaviour at the mineral–water interface might be used to evaluate how microbially-derived compounds like EPS are stabilized by iron (oxyhydr)oxides and how EPS-iron (oxyhydr)oxide couplings might affect the reactivity and cycling of OM in natural environments.

The roles of extracellular polymeric substances of Pandoraea sp. XY-2 in the removal of tetracycline.

In this study, the roles of extracellular polymeric substances (EPSs) excreted by Pandoraea sp. XY-2 in the removal of tetracycline (TC) were investigated. In the early stage, TC in the solution was mainly removed by the adsorption of EPSs, which accounted for 20% of TC. Thereafter, large amount of TC was transported into the intracellular and biodegraded. EPSs was extracted and the contents of polyprotein and polysaccharides reached their maximum values (30.84mg/g and 11.15mg/g) in the first four days. Fourier transform infrared spectroscopy analysis revealed that hydroxyl, methylidyne, methylene and amide I groups in EPSs participated in the adsorption of TC. Furthermore, three-dimensional excitation-emission matrix fluorescence spectroscopy analysis revealed that TC caused the quenching of EPSs fluorescent groups. The quenching mechanism was attributed to static quenching and protein-like substances in EPSs from Pandoraea sp. XY-2 dominated the TC adsorption process. Bioinformatic analysis of Pandoraea sp. XY-2 genome identified multiple genes involved in exopolysaccharide synthesis and EPSs formation. The insights gained in this study might provide a better understanding about the adsorption process of EPSs in tetracycline-contaminated environment.

Constructing zwitterionic polymer brush layer to enhance gravity-driven membrane performance by governing biofilm formation

In this study, zwitterionic polymer brushes with controlled architecture were grafted on the surface of gravity-driven membrane (GDM) via surface-initiated reaction to impart antifouling property. A variety of membrane characterization techniques were conducted to demonstrate the successful functionalization of zwitterionic polymers on PVDF hollow fiber membrane. The membrane underwent 90 min of reaction time possessing strong hydrophilicity and high permeability was determined as the optimal modified membrane. Long-term GDM dynamic fouling experiments operated for 30 days using sewage wastewater as feed solution indicated zwitterionic polymer modified membrane exhibit excellent membrane fouling resistance thus enhanced stable flux. Confocal laser scanning microscopy (CLSM) imaging implied that zwitterionic polymer modification significantly inhibit the adsorption of extracellular polymeric substances (EPS) which dominates fouling propensity, resulting in the formation of a thin biofilm with high porosity under synthetic functions of foulants deposition and microbial activities. Interfacial free energy prediction affirmed the presence of zwitterionic functional layer on membrane surface could substantially decrease the interactions (e.g., electrostatic attractions and hydrophobic effects) between membrane and foulants, thereby reduced flux decline and high stable flux. Our study suggests surface hydrophilic functionalization shows promising potential for improving the performance of ultra-low pressure filtration.

Adsorption of extracellular polymeric substances from two microbes by TiO2 nanoparticles

Extracellular polymeric substance (EPS) secreted by microbes can interact with nanoparticles (NPs) and thus influence environmental behavior and toxicity of NPs. The adsorption of EPSs from two species of microbes (Escherichia coli and Chlorella pyrenoidosa) by four types of titanium dioxide nanoparticles (nTiO2) (5, 10, and 40 nm anatase nTiO2 and 25 nm rutile nTiO2) were therefore specifically investigated. Results show that the adsorption kinetics and thermodynamics were dependent on sources and chemical properties of EPSs. EPS (20 mg C/L) from Escherichia coli mainly composed of protein (86%) with relatively higher molecular weight and aromaticity and more active functional groups (i.e., NH and –COOH) was effectively removed (>90%) by adsorption on nTiO2 (100 mg and more), while much less (<40%) EPS from Chlorella pyrenoidosa with a main component of polysaccharide (68%) was adsorptively removed. The Fourier transform ion cyclotron resonance mass spectrometry analysis revealed the selective adsorption of aromatic components of EPSs by nTiO2. The EPS adsorption capacity of nTiO2 linearly increased with the specific surface area of the NPs. The rutile nTiO2 with the smallest specific surface area had the highest EPS adsorption per unit surface area. These findings promote a deeper understanding of the interaction between EPS and NPs.

Nitrogen aeration alters the spatial distribution and metal adsorption of extracellular polymeric substances in waste-activated sludge.

Extracellular polymeric substances (EPS) extracted from waste-activated sludge (WAS) have the potential to remove heavy metal ions from wastewater; both the spatial distribution and metal adsorption of EPS from WAS after nitrogen aeration were systematically investigated in this study. Compared with air aeration, nitrogen aeration significantly improved the contents of proteins (PN) and polysaccharides (PS) in the Slime-EPS (S-EPS) and loosely-bound EPS (LB-EPS), significantly increased the PS content, and slightly increased the PN content in the tightly-bound EPS (TB-EPS). The variations in the fluorescence intensities (FI) of the peaks I and II for the S-EPS, LB-EPS and TB-EPS were basically consistent with the abovementioned variations in the concentrations of these EPS. Notably, nitrogen aeration dramatically improved the content of protein-like substances in the LB-EPS. For the same aeration time, the Pb2+ reclamation rates obtained by the LB-EPS extracted from the nitrogen-aerated WAS were much higher than those achieved by the LB-EPS extracted from the air-aerated WAS. The FTIR analyses further indicated that nitrogen aeration improved the contents of the functional groups, especially –OH, –COOH and –NH2, responsible for binding heavy metals, in both the LB-EPS and TB-EPS. The SEM analyses verified that the nitrogen scours contributed to the EPS release, and Pb2+ reclamation was achieved via the attachment of Pb2+ onto the edge of the EPS. The influences of the nitrogen aeration on the spatial distribution and metal adsorption of the EPS in WAS were revealed for the first time in this study. Thus, this study lays the foundation for the application of nitrogen aeration in the resource utilization of WAS.

EPS adsorption to goethite: Molecular level adsorption mechanisms using 2D correlation spectroscopy

The adsorption of extracellular polymeric substances (EPS) onto soil minerals is an important process for understanding bacterial adhesion to mineral surfaces and environmental cycling of nutrients and contaminants. To clarify the molecular level mechanisms and processes of EPS adsorption, the interaction mechanisms between EPS and goethite was explored using two-dimensional (2D) Fourier transformation infrared (FTIR) correlation spectroscopy (CoS) assisted by C 1s near edge X-ray absorption fine structure spectroscopy (NEXAFS). Results show that the amide functional groups of EPS play an important role in its adsorption on goethite, and the adsorption of EPS-proteins on goethite is a function of electrolyte concentration, with increasing adsorption at a higher electrolyte concentration. Results also show that the order in which the EPS functional groups interact and bind with goethite is dependent on electrolyte concentration, where carboxyl and phosphoryl functional groups are the first to adsorb at low electrolyte concentration, while amide groups are the first to adsorb at higher electrolyte concentration. Deconvolution and curve fitting of the amide I band at the end of the adsorption process (~300 min) shows that the secondary structure of proteins is converted from a random coil conformation to aggregated strands, α-helices and turns. This conversion leads to increased adsorption of EPS-proteins and explains the overall adsorption increase of EPS on goethite surfaces with an increasing concentration of electrolyte. Furthermore, the adsorption of the carboxyl functional groups of EPS decreases with increasing electrolyte concentration, likely due to more effective screening of the goethite surface charge with increasing concentration of electrolyte. The integrated results from ATR-FTIR and 2D-CoS allow us to construct a comprehensive overview of EPS-goethite interaction processes at the molecular level, which can be used to improve our understanding of EPS-mineral interactions in the natural environment. These results also provide fundamental information for a better understanding of bacterial biofilm formation on soil and sediment minerals, and facilitate research on the subsequent interaction of nutrients and contaminants with the reactive constituents of biofilms in natural and contaminated environments.

Exopolysaccharide produced by Vibrio neocaledonicus sp. as a green corrosion inhibitor: Production and structural characterization

An exopolysaccharide substances produced by Vibrio neocaledonicus sp. was introduced as a novel green inhibitor against the corrosion of carbon steel in artificial seawater and acidic media. The produced extracellular polymeric substance (EPS) is heterogeneous with composition of polysaccharides, nucleic acids and protein and average molecular weight of 29,572Da. Adsorption of EPS on the metal surfaces and formation of Fe-EPS complexes acted as a barrier to prevent the oxygen penetration and hindered anodic and cathodic reactions. The inhibitory effect increases with increasing EPS concentration and exposure time. The highest corrosion inhibitory effect (95.1%) was observed for 10g/L of EPS after 5 days of exposure in seawater. This is the highest inhibitory effect ever been reported by EPSs. While, the optimum concentration of EPS with the highest inhibition efficiency in 1 N H2SO4 was 1000ppm. The influence of different parameters, such as initial pH, growth phase, various nitrogen and carbon sources on the production of EPS and its corrosion inhibitory effect were also investigated. According to results, the optimum culture medium for EPS production is contained artificial seawater including 5% mannitol as carbon source and 0.1% (NH4)2SO4 as nitrogen source at pH=8. This medium could produce 22.24g/L EPS during 3 days’ incubation at 30°C. The corrosion inhibitory efficiency of obtained EPS was 95.97%.

Adsorption of Extracellular Polymeric Substances Derived from S. cerevisiae to Ceria Nanoparticles and the Effects on Their Colloidal Stability

In order to understand the adsorption preferences of extracellular polymeric substances (EPS) components derived from fungus Saccharomyces cerevisiae on sparingly soluble CeO2 nanoparticles (CeNPs), the adsorption experiments of the EPS including organic matter with low molecular weight have been performed at pH 6.0 at room temperature (25 ± 1 °C). The subsequent effects of the coating on the dispersibility of CeNPs was systematically measured as a function of time and ionic strength ranging from 1 to 1000 mmol L−1. Among the EPS and other components, orthophosphate and saccharides preferentially adsorb onto CeNPs, and proteins are the only major N-compounds adsorbing onto the CeNP surfaces. Adsorption of orthophosphate resulted in a dramatic decrease in ζ potential to −40 mV at pH &gt; 5, whereas the EPS adsorption suppressed the deviation of ζ potential within a narrow range (−20–+20 mV) at pHs ranging from 3 to 11. Critical aggregation concentrations (CAC) of an electrolyte (NaCl), inorganic orthophosphate, and EPS solutions are 0.01, 0.14, and 0.25 mol L−1, respectively, indicating that the EPS adsorption suppresses aggregation of CeNPs by the electrostatic repulsive forces derived from the adsorbed orthophosphate and the steric barrier formed by organic matter on the nanoparticle surfaces. Therefore, the EPS derived from fungus S. cerevisiae can potentially enhance colloidal dispersibility of CeNPs at circumneutral pH.

Robust biochar-assisted alleviation of membrane fouling in MBRs by indirect mechanism

Abstract Biochar is a low-cost by-product of biomass pyrolysis to obtain renewable energy, and is composed of carbon skeleton, oxygen-containing functional groups, and minerals. Herein a new environmental application of biochar is detailed, namely, alleviating membrane fouling in a membrane bioreactor (MBR) process by dosing the bioreactor with quantities of various modified biochars (alkali washed (AW-BC), hydrophobic (HB-BC), hydrophilic (HL-BC), and activated biochars (AC-BC)). Results of trans-membrane pressure (TMP) tests showed that with the exception of HB-BC, all the other modified biochars exhibited robust antifouling capability and the TMP was decreased by as much as 36.8% and 31.4% at 24 h and 10 d respectively for AW-BC (most easily prepared) compared to a control. This was comparable to the results obtained in the use of expensive activated carbon (AC). Instead of dealing with the large surface area and scouring effects of AC, it was found that the indirect effects of biochar on sludge may be the basis for the antifouling mechanism, where the hydrophilicity of the biochar improved the settling of sludge. In addition, it was speculated that the abundant functional groups of the biochar increased the adsorption of Extracellular polymeric substance (EPS) based on the characterizations of N 2 -adsorption-desorption, fourier transform infrared spectroscopy (FTIR), X–ray photoelectron spectroscopy (XPS), Raman, scanning electron microscopy (SEM), and confocal laser scanning microscopy (CLSM). Compared to traditional antifouling materials, the results of this study may offer a low-cost alternate for alleviating membrane fouling in MBRs.

Interactions of EPS with soil minerals: A combination study by ITC and CLSM

The adsorption of extracellular polymeric substances (EPS) from Pseudomonas putida on montmorillonite, kaolinite and goethite was investigated as a function of pH using batch studies coupled with confocal laser scanning microscopy (CLSM) and isothermal titration calorimetry (ITC). Characterization by Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) spectroscopy showed that the extracted EPS contained carboxyl, phosphoryl, amino, and hydroxyl on functional groups as well as polysaccharides, protein and nucleic acid on components. The mass fraction of EPS adsorption on minerals decreased with the final pH increased from 3.0 to 9.0. The mass fraction of EPS-N adsorption varied with pH values and was higher than that of EPS-C or EPS-P on montmorillonite and kaolinite, while the mass fraction of EPS-P adsorption was the highest on goethite. CLSM results further demonstrated that proteins were predominantly distributed on the montmorillonite and kaolinite surfaces, while nucleic acids were mainly on the goethite surface. ITC results revealed that the adsorption process in all mineral systems was exothermic, and pH altered the heat effect of EPS-mineral reactions. The data obtained in this study would facilitate a better understanding of the adsorption mechanisms of EPS on minerals.

Dynamic fouling behavior and cake layer structure changes in nonwoven membrane bioreactor for bath wastewater treatment

A nonwoven fabric module was used as a solid–liquid medium in a membrane bioreactor for bath wastewater treatment. The flux-step method was performed to define the maximum allowable flux and then was verified over a long period operation under six different imposed fluxes ranging from 8L/(m2h) to 18L/(m2h). During the long-term tests, the treatment performance and filtration characteristics of the nonwoven membrane bioreactor (NWMBR) were investigated. The membrane fouling mechanisms under the different operating phases of the NWMBR were also discussed. Results show that the NWMBR operated in two stages during the six tests. In the early stage, the filling up of the internal structure of the membrane caused the rapid formation of a dense cake layer. In the late stage, the increasing imposed flux changed the morphology of the cake layer and affected the membrane fouling differently. When the flux exceeded the critical flux of 15L/(m2h), a thin but dense cake layer formed rapidly and decreased the membrane permeability. When the flux was lower than the critical flux, a loose filamentous biomass layer formed on the nonwoven membrane surface, which acted as a secondary membrane that prevented the adsorption of extracellular polymeric substances, soluble microbial products, and particles onto the membrane surfaces.

Effects of cyanobacterial extracellular polymeric substances on the stability of ZnO nanoparticles in eutrophic shallow lakes

Extracellular polymeric substances (EPS) from bloom-forming cyanobacteria exist ubiquitously in eutrophic waters, while their effects on the aggregation/stabilization of nanoparticles remain unknown. In this study, the stability of ZnO nanoparticles (ZNPs) upon adsorption of cyanobacterial EPS was investigated by using two dimensional ATR-FTIR correlation spectroscopy, XPS and DLVO theory. Results showed that the adsorption process followed the Langmuir isotherm and pseudo-second-order kinetics both for the total organic contents as well as the individual parallel factor-derived components. The physicochemical and spectroscopic techniques revealed the mechanism of both electrostatic attraction and surface complexation in EPS adsorption. Further analysis showed increased absorbance and turbidity of ZNPs solutions with EPS addition, demonstrating the enhanced colloidal stability. The DLVO theory explained that the increased energy barriers and values of second energy maximum were responsible for the stability enhancement. This study facilitates a deeper insight into the environmental behavior of nanoparticles in eutrophic algae-rich waters.

Long-term impact of anaerobic reaction time on the performance and granular characteristics of granular denitrifying biological phosphorus removal systems

Removal of nitrogen and phosphorus (P) from wastewater is successfully and widely practiced in systems employing both granular sludge technology and enhanced biological P removal (EBPR) processes; however, the key parameter, anaerobic reaction time (AnRT), has not been thoroughly investigated. Successful EBPR is highly dependent on an appropriate AnRT, which induces carbon and polyphosphate metabolism by phosphorus accumulating organisms (PAOs). Therefore, the long-term impact of AnRT on denitrifying P removal performance and granular characteristics was investigated in three identical granular sludge sequencing batch reactors with AnRTs of 90 (R1), 120 (R2) and 150 min (R3). The microbial community structures and anaerobic stoichiometric parameters related to various AnRTs were monitored over time. Free nitrite acid (FNA) accumulation (e.g., 0.0008–0.0016 mg HNO2–N/L) occurred frequently owing to incomplete denitrification in the adaptation period, especially in R3, which influenced the anaerobic/anoxic intracellular intermediate metabolites and activities of intracellular enzymes negatively, resulting in lower levels of poly-P and reduced activity of polyphosphate kinase. As a result, the Accumulibacter-PAOs population decreased from 51 ± 2.5% to 43 ± 2.1% when AnRT was extended from 90 to 150 min, leading to decreased denitrifying P removal performance. Additionally, frequent exposure of microorganisms to the FNA accumulation and anaerobic endogenous conditions in excess AnRT cases (e.g., 150 min) stimulated increased extracellular polymeric substances (EPS) production by microorganisms, resulting in enhanced granular formation and larger granules (size of 0.6–1.2 mm), but decreasing anaerobic PHA synthesis and glycogen hydrolysis. Phosphorus removal capacity was mediated to some extent by EPS adsorption in granular sludge systems that possessed more EPS, longer AnRT and relatively higher GAOs.