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Wastewater recycling helps address the challenge of microalgae biomass commercialization by allowing for efficient resource recovery. In this study, three conventional harvesting methods, including centrifugation, microfiltration, and flocculation sedimentation, were investigated to explore the effects of harvesting methods on the characteristics of recycled wastewater and the growth of microalgae to select a suitable harvesting method for the microalgal wastewater recycling system. During the wastewater recycling process, the least amount of accumulated substances was exhibited in the wastewater recycled by microfiltration, followed by centrifugation, and the most by flocculation sedimentation. After 4 batches of cultivation, microalgal biomass harvested from centrifugation wastewater and microfiltration wastewater was 21.26 % and 13.54 % higher than that from flocculation wastewater, respectively. Lipids, carbohydrates and pigments were all increased by varying degrees. Additionally, flocculation sedimentation was not suitable for the microalgal wastewater recycling process since the low residual nutrients, high salinity, and excessive algal organic matter severely inhibited the growth of microalgae. Under the regulation of phytohormones, microalgae increased their energy reserves, enhanced photosynthesis, and improved their defense capability to resist the increasing abiotic stress. This study provides scientific support for the selection of suitable harvesting technology during the microalgal wastewater recycling process.

Activation of peracetic acid (PAA) to generate powerful oxidizing species has become a promising advanced oxidation processes (AOPs) in wastewater treatment, yet the development of low-cost and high-performance activators is still a primary challenge. Herein, a range of Co-Mn spinel oxides (Co

Thiosulfate (S

Acrylonitrile wastewater is a kind of highly toxic industrial wastewater, but it contains a lot of valuable chemical materials. In this study, by using the most promising hydrothermal technology, we investigated the best reaction conditions and possible reaction pathways for the conversion of the three nitriles (acrylonitrile, acetonitrile, and succinonitrile) to organic acids under alkaline hydrothermal conditions. Then, the reaction conditions for the conversion of actual acrylonitrile wastewater to organic acids were further optimized. The actual wastewater of acrylonitrile was converted into 1.33 × 104 mg/L acrylic acid, 1.98 × 104 mg/L formic acid and 9.40 × 103 mg/L acetic acid at optimal reaction conditions (reaction temperature 300 °C, reaction time 90 s, and initial NaOH concentration 1.0 mol/L). It is the theoretical basis of the application of the hydrothermal alkali-catalyzed method in the acrylonitrile wastewater resource engineering.

Biochar and hydrochar, as valuable and eco-friendly soil remediation materials from greenwaste, have potential to enhance methane oxidation in paddy soil. But the mechanism of biomass carbon on the improvement of methane-oxidizing bacteria communities in paddy soil has not been adequately elucidated. In the present study, the effect of different-temperature rice straw-based biomass carbon (RB400, RB600, RH250 and RH300) on methane oxidation were investigated by analyzing the soil dissolved organic matter (DOM), physicochemical properties and changes in microbial community structure. The results of the 17-day incubation experiment showed that the methane oxidation rate increased under all types of biomass carbon in the first 6 days. The enhancement of methane oxidation rate was more pronounced for biochar compared to hydrochar, with RB600 being the most effective treatment. The result of excitation-emission matrix (EEM) fluorescence spectroscopy showed that less DOM were released from the soil in the biochar treatments compared to the hydrochar treatments and protein-like were detected only in the hydrochar group. Microbial analysis further showed that hydrochar inhibited the growth of Bacillus, Methylobacter, and Methylocystis, while RB600 significantly increased the relative abundance of methanotrophs (responsible for methane oxidation), such as Methylocystis and Methylobacter, which was consistent with their different effects on the methane oxidation rate. Moreover, from the analysis of principal component analysis (PCA) and canonical correspondence analysis (CCA), Methylobacter and Methylocystis were negatively respond to H/C of biomass carbon. The present study provides a deeper understanding of the effect of biomass carbon obtained by different processes on methane oxidation when applied to soil from the perspective of organic matter and microbial communities.

Carbon-based materials activated peracetic acid (PAA) to repair groundwater is an environmentally friendly and low-cost technology to overcome secondary pollution problems. In this study, thermally modified activated carbon (AC600) was applied to activate PAA to degrade sulfamethoxazole (SMX). And the effect of groundwater pH, chloride ion (Cl

Graphene oxide quantum dots (GOQDs) can convert the ultraviolet (200- 380 nm) into available wavelength (400- 700 nm) for microalgae cultivation. However, it has not been applied in large-scale microalgae culture due to its high cost and difficulties in recovery. This study proposed a new strategy for the sustainable use of GOQDs, namely, GOQDs solution was added to the outer sandwich of the reactor. Herein, the effects of direct and indirect exposure of different GOQDs concentrations (0, 100, and 1000 mg/L) on the microalgae culture were compared. When microalgae were directly exposed to the GOQDs, 100 mg/L of GOQDs increased the biomass production of microalgae by 24.0 %, while 1000 mg/L of GOQDs decreased biomass production by 31 %. High concentration of GOQDs (direct exposure) could cause extra oxidative stress in the microalgae cells and result in a significant reduction of pigment content. When microalgae were indirectly exposed to the GOQDs, the increased concentration of GOQDs enhanced the growth of microalgae. Compared to the blank group, 1000 mg/L of GOQDs increased the microalgae biomass production and bioenergy by 14.1 % and 40.17 %, respectively. The indirect exposure of GOQDs can effectively avoid photo-oxidation and organelle damage to the microalgae cells. Overall, the indirect exposure of GOQDs is a sustainable way for effectively promoting microalgae growth and reducing the application cost.

Microplastics (MPs) are susceptible to aging in the environment, and aged MPs are highly migratory in soil due to their smaller particle size and more negative surface charge, but the effects of soil environmental factors on the fate and transport of aged MPs are still unclear. In this study, the transport behavior of pristine/aged MPs in unsaturated sandy porous media was examined under different ionic strength (IS), cationic type (Na

The microalgal wastewater cyclic cultivation technology (AWC

In this study, the removal of Cr (VI) was examined in the presence of bio-produced Fe (II) from hematite, sulfate and dissolved organic matter by Geobacter sulfurreducens. The adaptation results of G. sulfurreducens showed that cells growth was stimulated up to 576 μM of Cr (VI) concentration. The first-order rate and electron transfer rate in each step during Cr (VI) reduction by G. sulfurreducens in the presence of hematite was clearly modeled and calculated. For Cr (VI) reduction rate, both separately dissolved and adsorbed bio-produced Fe (II) were faster than G. sulfurreducens although bio-produced Fe (II) contributed only 20% to total Cr (VI) removal in a combined system containing Cr (VI), hematite and G. sulfurreducens. The electron transfer rate from G. sulfurreducens to hematite (R2) to produce Fe (II) was a limited step and electron transfer rate from acetate to Cr (VI) (1.8 μeq L−1 h−1) by G. sulfurreducens was much higher than that to hematite (0.272 μeq L−1 h−1, producing Fe (II)). Cr (VI) reduction was enhanced in the presence of SO42− due to sulfate boost cells growth. AQDS enhanced Cr (VI) reduction by serving as an electron shuttle thus accelerating the electron transfer rate.

Cu(II) enhanced the oxygen activation by Fe(II) to increase the yield of oxidants. However the factors controlling the catalytic performance and indeed the underlying influencing mechanisms remained unclear. Here, we presented the detailed study of Cu(II)-Fe(II) reactions for a range of pH and Cu(II)/Fe(II) ratios. From the results obtained, we provided insight into the factors controlling the redox reactions of Fe-Cu and the catalytic behaviours of active species. A reaction scheme for the Fe(II)/Cu(II) system was developed in which the in-situ formed Cu(I) mainly contributed to producing H2O2 and Fe(II) dominantly decomposed H2O2 to hydroxyl radical (HO ) [see companion article] (Yufan Chen). Circumneutral conditions facilitated the catalytic processes; under acidic conditions, the reverse reaction between Fe(III) and Cu(I) was strongly favoured; alkaline conditions improved the reducing capacity, which subsequently enhanced the generation of Cu(0) instead of Cu(I). There was a saturated Cu(II)/Fe(II) ratio above which further addition of Cu(II) could not be reduced, and then excessive Cu(I) and Cu(II) consumed HO and O2 –, respectively. Therefore, the highest removal efficiency of organic pollutants was achieved when the stoichiometric Cu(II)/Fe(II) ratio was 60% at circumneutral pH. The new findings have implications for the treatment of mixed wastewater where copper and organic pollutants coexist.

In this study, nanosized ordered magnetic mesoporous Fe-Ce bimetal oxides (Nanosized-MMIC) with highly well-ordered inner-connected mesostructure were successfully synthesized through the KIT-6 template method. This Nanosized-MMIC displayed excellent adsorption capacities for As(V), Cr(VI) and AO7, and the corresponding calculated maximum adsorption capacities of material were 111.17, 125.28 and 156.52 mg/g, respectively. As(V) and Cr(VI) removal by Nanosized-MMIC were slightly dependent on the ionic strength but highly solution pH-dependent, the coexistent silicate and phosphate ions competed remarkably with both As(V) and Cr(VI) for the adsorption active site. Mechanisms indicated As(V) and Cr(VI) formed inner-sphere complexes on Nanosized-MMIC interface via the electrostatic interaction and surface complexation, while the total organic carbon (TOC) change demonstrated that AO7 could be removed completely and no organic intermediates formed through the adsorption process. In addition, Nanosized-MMIC also possessed superior adsorption performance in As(V)/Cr(VI)-AO7 binary systems, and the reusable and regeneration properties indicated that the obtained nanomaterials could maintain at a comparatively high level after several recycling. Finally, fixed-bed experiments suggested the Nanosized-MMIC was expected to have a promising excellent nano-adsorbent with high application potential for co-existed toxic heavy metals and organic dyes removal in practical wastewater treatment.

Hydrated electron (e

Polylactic acid (PLA) is biodegraded rapidly under composting or thermophilic temperature but slowly under natural conditions with substantial microplastics generated. In this study, we examined the feasibility of PLA biodegradation and developed a novel approach for PLA waste management using yellow mealworms (Tenebrio molitor larvae) to achieve biodegradation and resource recovery simultaneously. Results confirmed PLA biodegradation in mealworms as sole PLA and PLA-bran mixtures (10%, 20%, 30% and 50% PLA, wt/wt). Feeding PLA-bran mixtures supported the larval development with higher survival rates and lower cannibal rates than feeding PLA only at ambient temperature. The PLA conversion efficiency was 90.9% with 100% PLA diet and was around 81.5–86.9% with PLA-bran mixtures. A peak insect biomass yield was achieved at a PLA ratio of 20%. PLA biodegradation was verified via detection of chemical and thermal modifications. Gut microbial community analysis indicated that intestinal communities shifted with PLA biodegradation, resulting in clusters with OTUs unique to the PLA diet. Based on these findings, we propose a circular approach for PLA waste management via resource recovery of used PLA as the feedstock for insect biomass production, management of mealworm excrement waste as fertilizer, and utilization of agricultural products for PLA production.

Anaerobic digestion of pharmaceutical wastewater is challenged by its contained toxic compounds which limits the stability and efficiency of methane production and organic degradation. In this study, zero valent iron (ZVI) and granular activated carbon (GAC) were added with different strategies to improve anaerobic digestion of pharmaceutical wastewater. The results confirmed synergy effects of ZVI + GAC for both COD removal (increased by 13.4%) and methane production (increased by 11.0%). Furthermore, ZVI + GAC improved the removal of pharmaceutical intermediates, in particular, the residues (%) of dehydroepiandrosterone (DHEA) and 2,2'-methylenebis(6-tert-butyl-4-methylphenol) were only 30.48 ± 6.53 and 39.92 ± 4.50, and effectively reduced biotoxicity. The promoted results were attributed to the establishment of direct interspecies electron transfer (DIET). Microbial community analysis revealed that ZVI + GAC decreased species evenness and richness in bacterial whereas increased in archaeal. The relative abundance of acetotrophic methanogens decreased but hydrogenotrophic and methylotrophic methanogens increased, which broadening the pathway of methane production.

The application of phenylurea herbicides (PUHs) may lead to the extensive distribution in soils, while the role of straw biochar as a soil amendment on the transport and sorption of PUHs are still unclear. Thus, the transport and sorption behavior of three typical PUHs with rice straw biochar (RSB) was studied in both adsorption simulation experiments of aqueous solution and packed column experiments. The sorption mechanism of RSB to herbicides was investigated through batch sorption studies with three influencing factors including dosage of RSB, pH, and ionic strength (IS) with orthogonal test. The sorption coefficients were improved significantly by increasing the dosage of RSB, while there was no obvious influence by enhancing the pH and IS value. The optimal sorption conditions (pH value at 3, IS at 0.1 M, and RSB dosage at 60 mg) of three herbicides were set and the maximum removal rates of Monuron, Diuron, and Linuron were 41.9%, 25%, and 56.8%, respectively. The co-transport process of RSB and PUHs were investigated under different RSB dosage, pH value, and IS value. The retention effect increased greatly with enhancing the RSB dosage and pH value. However, IS did not have a significant influence on the retention of RSB, and therefore it had little effect on the adsorption capacity, which was consistent with the results of sorption experiments. The breakthrough curves (BTCs) for co-transport were well simulated by the two-site non-equilibrium convection–dispersion equation (CDE). Most of the regression coefficients (R2) were above 0.99, which uncovered the co-transport in packed column were affected by physical absorption and chemical forces. According to the fitting parameters analysis, the RSB particles and PUHs were subjected to a greater resistance and a stronger stability by reducing pH value in porous media. The presence of RSB increased the amount of dynamic sorption sites in the entire co-transport system, which led to a significant promotion of the PUHs' sorption and interception.

A series of ordered mesoporous Fe Mn bimetal oxides (OMFMs) were fabricated by using a novel inverse micelle method, and the texture, nanostructure and interface chemistry properties of OMFMs were closely correlated to the calcination temperature. Due to the amorphous regular inner-connected nanostructure and bimetallic synergistic effect, the obtained OMFMs exhibited superior arsenic sequestration performance than pure mesoporous Fe oxides (PMF) and Mn oxides (PMM). The optimum ratio of Fe/Mn and calcination temperature for arsenic removal was 3/1 and 350 °C (OMFM-3), and the maximum As(III) and As(V) adsorption capacities of OMFM-3 were 174.59 and 134.58 mg/g, respectively. Solution pH value negligibly affected the uptake of arsenic (ranged from 3.0 to 7.0), while SiO32−/PO43− ions and humic acid (HA) displayed significant inhibitory effect on arsenic removal by OMFM-3. According to the mechanism of arsenic removal, which simultaneously analyzed the arsenic redox transformation in aqueous phase and on solid phase interface, it was concluded that manganese oxides in OMFM-3 mainly played the role as a remarkable As(III) oxidant in water, whereas iron oxides dominantly acted as an excellent arsenic species adsorbent. Finally, the prominent arsenic sequestration behavior and performance in surface water suggested that OMFM-3 could be a promising and hopeful candidate for arsenic-contaminated (especially As(III)) surface water and groundwater remediation and treatment.

Magnetite is known to exhibit high catalytic reactivity in Fenton-like reactions merely at low pH conditions. Here we report the association of Cu2+ ion can significantly enhance peroxydisulfate (PDS) activation with magnetite under environmental aquatic conditions (near neutral pH). Cu2+ is able to synergistically activate PDS with magnetite to generate radicals, e.g., SO4·−, at neutral or slightly alkaline pH, and such synergistic activation of PDS is promising to degrade various contaminants in groundwater. In-depth study reveals Cu2+ ion adsorbed on magnetite plays a crucial role in PDS activation. The adsorbed Cu2+ is labile to be reduced by the structural Fe(II) on magnetite to generate Cu+, which is relatively stable in the presence of magnetite at neutral or alkaline pH, but extremely unstable at acidic pH. The generated Cu+ on magnetite surface, rather than Cu2+, contributes to PDS activation in the reaction system, and the recycling of Cu+/Cu2+ sustains continuous activation of PDS. This study is among the first to report the synergistic activation of PDS by magnetite and Cu2+ ion at neutral pH, and unambiguously discern the role of Cu+ in PDS activation. The new mechanistic knowledge provides a more accurate understanding of PDS activation by natural minerals in environmental remediation.

Vibration membrane filtration has been confirmed as an effective method to improve algae separation from water. However, the fouling evolution process and the antifouling mechanism are not well understood. In this study, a novel hybrid method based on a dynamics model was proposed, a comprehensive evaluation was conducted, and the critical vibration frequency for accurate analysis and prediction of membrane fouling was developed. The dynamics model was studied with an improved collision-attachment model by considering all the concurrent and synergistic effects of the hydrodynamic interactions acting on algae. From the perspective of potential energy, the improved model systematically elucidated the reason why the antifouling performance was enhanced when the vibration frequency varied from 1 Hz to 5 Hz. In addition, the Technique for Order Preference by Similarity to Ideal Solution-grey relational analysis (TOPSIS-GRA) method with combined weights was incorporated for the first time to provide direct comprehensive evaluation evidence to determine the effect of the vibration frequency on membrane fouling. It was found that increasing the vibration frequency could not alleviate membrane fouling caused by extracellular organic matter. Moreover, the concept of a critical vibration frequency was proposed using genetic algorithm optimized back propagation neural network, and the energy consumption was analyzed. This combination could provide an effective means to choose the most appropriate vibration frequency, thereby improving the efficiency of the vibration membrane system in the algae separation process.

The indoor environments of severely polluted toilets are associated with an increased risk of transmission of severe diseases. Enhancing the ventilation effectiveness can improve the indoor air quality (IAQ). The characteristics of pollutant transmission in a public toilet model were analyzed using a computational fluid dynamic program and were further validated based on experimental measurements using a tracer gas (SF6). This study investigated the typical pollutant (ammonia and hydrogen sulfide) diffusion characteristics, relationship between the number of air changes per hour and concentration of pollutants, and personal exposure under two types of typical ventilation systems—mixing ventilation (MV) and personalized ventilation (PV)—in public toilets. The results show that MV can reduce the concentration of pollutants in the toilet, but the IAQ cannot reach the desired level. Under a constant total ventilation rate, PV can effectively remove pollutants in the toilet and reduce the concentration of pollutants in the breathing area. The results of this study can contribute to improving the IAQ of public toilets.

Post-hydrothermal liquefaction wastewater (PHWW), which contains approximately 80% of original feedstock resources, shows great potential to achieve sustainable development of an environment-enhancing energy system. A combination of anaerobic digestion and algae cultivation was proposed for methane recovery and nutrient supply from PHWW. Granular activated carbon (GAC) and ozone were used to enhance energy recovery from the PHWW. The results indicated that with GAC addition, the maximum methane yield increased by 67.7%–228 mL/g CODremoval. In addition, Chlorella vulgaris displayed optimal growth in a 5-fold diluted digestate with a 2.32 g/L maximum biomass content and 180 mg/(L·d) biomass production rate. The total energy yield was 565 kJ/g COD, which was 27.4 times higher than that without GAC. Integration of anaerobic digestion and algae cultivation, particularly with GAC addition during fermentation, is a feasible and advantageous process for energy recovery from PHWW.

Nanoscale zerovalent iron (nZVI) has been proposed to remediate heavy metal ions in the subsurface. However, the fate of metal-nZVI hybrid has not been fully investigated. In this study, we investigated (1) the long-term removal performance of nZVI for molybdate (Mo(VI)); (2) the relationship between the ageing of Mo-nZVI hybrid in specific solution chemistries and the remobilization of Mo(VI) from the hybrid; and (3) the effects of Mo-nZVI hybrid on cyanobacteria (Microcystis aeruginosa). Results showed that although common ions have limited influence on the removal ratio of Mo(VI) by nZVI, they do impact the structure evolution and transformation of the Mo-nZVI nanohybrid formed thereafter. Ageing time was crucial for the chemical stabilization of Mo-nZVI hybrid, but common groundwater ions retarded the stabilizing process, which may lead to a significant remobilization of Mo(VI) from the hybrid after exposure to water bodies. While low levels of Mo(VI) ions could stimulate the growth of M. aeruginosa, aged Mo-nZVI hybrid inhibited the growth of M. aeruginosa, except when ageing occurred in the presence of HPO42−/CO32− (which also retarded hybrid stabilization). This study shows that nZVI can immobilize Mo(VI) ions in groundwater, and the derived metal-nZVI hybrid can effectively suppress the potential growth of M. aeruginosa in river water.

The widely used carbamazepine (CBZ) is one of the most persistent pharmaceuticals and suffers insufficient removal efficiency by conventional wastewater treatment. A synthesized Co-based perovskite (LaCoO3) was used to activate peroxymonosulfate (PMS) in order to degrade CBZ. Results showed that LaCoO3 exhibited an excellent performance in PMS activation and CBZ degradation at neutral pH, with low cobalt leaching. The results of FT-IR and XPS verified the high structurally and chemically stability of LaCoO3 in PMS activation. Electron spin resonance (ESR) analysis suggested the generation of radical species, such as sulfate radicals (SO4 -) and hydroxyl radicals ( OH). Radical quenching experiments further revealed the responsibility of SO4 - as the dominant oxidant for CBZ oxidation. Ten products were detected via the oxidation of CBZ, with the olefinic double bond attacked by SO4 - as the initial step. Hydroxylation, hydrolysis, cyclization and dehydration were involved along the transformation of CBZ. The toxicity of CBZ solution was significantly reduced after treating by PMS/LaCoO3.

Microalgae residue was efficiently converted into lactic acid with a high yield (33.9%) under mild reaction conditions (210 °C, 2 h) over a Fe-Sn-Beta catalyst. Under the action of homogeneous H3O+ and distinct Lewis acid sites on the catalyst, the production of lactic acid from microalgae residue underwent three main reaction steps: hydrolysis, isomerization, and retro-aldol condensation. Results demonstrated that the lipid component had a strong inhibitory effect on the production of lactic acid due to the formation of aromatics, esters, and complex nitrogenous heterocyclic compounds, which covered or poisoned the Lewis acid sites of the catalyst. The protein component acted as a chemical buffer that enhanced the production of lactic acid by controlling the release of monosaccharides from the carbohydrate fraction of microalgae and maintaining the catalytic activity of the catalyst. Thus, microalgae residue demonstrated great promise for the production of value-added chemicals.

To solve the problem of organic and inorganic arsenic species contamination in drinking water and/or wastewater, porous biochar-supported MnFe2O4 magnetic nanocomposite (BC-MF) was successfully fabricated and used as an excellent adsorbent for simultaneous removal of p-ASA and As(V) from water environment. This obtained BC-MF displayed remarkable adsorption performance for both p-ASA and As(V) removal at acidic and neutral pH (3−7), and di-anionic and mono-anionic species of p-ASA and As(V) facilitated the adsorption process. Specifically, BC-MF exceeded some reported adsorbents, and the adsorption capacities of p-ASA and As(V) were approximately 105 and 90 mg/g at a 10 μg/L equilibrium concentration. Satisfactory adsorption behavior including adsorption isotherms, competitive ions, humic acid (HA), and regeneration/reusability property in single and binary systems demonstrated the BC-MF can improve the potential application for arsenic-containing wastewater remediation. Proposed adsorption mechanism indicated that electrostatic interaction and surface complexation were involved the p-ASA and As(V) immobilization, whereas hydrogen bonding and π-π interactions may also contribute to the p-ASA removal. Additionally, the prominent sequestration p-ASA and As(V) performance in different water matrix and fixed-bed column studies indicated that BC-MF was a promising nanocomposite for simultaneously removal of organic and inorganic arsenic species in practical wastewater treatment.

Miscanthus is a promising source of bioenergy with high lignocellulose content. This paper studied the effect of hydrothermal pretreatment on Miscanthus biogas production. Different pretreatment temperature from 125 to 200°C was tested. After pretreatment, hemicellulose was partially removed and this led to a change in cellulose accessibility. Enzymatic hydrolysis was used to examine the digestibility of different samples. There was no obvious enhancement in low temperature (125 and 150°C) conditions. According to the results, 200°C hydrothermal pretreatment was the optimal condition saving 50% on the digestion time and increasing glucose production 13.2 times compared with the raw material. Although the cellulose crystallinity increased after the pretreatment, its effect on biogas production and enzymatic hydrolysis was limited.

Inspired by iron fertilization experiments in HNLC (high-nitrate, low-chlorophyll) sea areas, we proposed the use of iron-rich engineered microalgae for microbial contaminant control in iron-free culture media. Based on the genome sequence and natural transformation system of Synechocystis sp. PCC6803, ftnA (encoding ferritin) was selected as our target gene and was cloned into wild-type Synechocystis sp. PCC6803. Tests at the molecular level confirmed the successful construction of the engineered Synechocystis sp. PCC6803-ftnA. After Fe(3+)-EDTA pulsing, the intracellular iron content of Synechocystis sp. PCC6803-ftnA was significantly enhanced, and the algae was used in the microbial contamination control system. In the coupled Synechocystis sp. PCC6803-ftnA production and municipal wastewater (MW, including Scenedesmus obliquus and Bacillus) treatment, Synechocystis sp. PCC6803-ftnA accounted for all of the microbial activity and significantly increased from 70% of the microbial community to 95%. These results revealed that while the stored iron in the Synechocystis sp. PCC6803-ftnA cells was used for growth and reproduction of this microalga in the MW, the growth of other microbes was inhibited because of the iron limitation, and these results provide a new method for microbial contamination control during a coupling process.

Membrane fouling by algae and extracellular organic matter (EOM) is a major problem in algae harvesting. In this study, the axial vibration ultrafiltration-membrane (AVM) is able to limit membrane fouling during filtration effectively. A membrane can achieve high critical flux at a high shear rate. During filtration, AVM is capable of operating with less fouling at a constant flux. The result from “extended Derjaguin, Landau, Verwey, Overbeek” (XDLVO) calculation indicates that with the increase of shear rate, it is more difficult for algae to foul the membrane. At a frequency of 5 Hz, the average inertial lift force is 0.024 nN, and the interaction force becomes a long-range attractive force that draws algae to the membrane; there are still certain smaller algae, algae debris and EOM that deposit on the membrane; leading to many algae depositing on the membrane. At a frequency of 10 Hz, the average inertial lift force is 0.12 nN, and there is a long-range repulsive region preventing algae from depositing on the membrane; however, the result shows that the mechanism of fouling mitigation by vibration is preventing algae from approaching the membrane, which reduces the deposition of algae on the membrane.

Chelated coppers, such as Cu(II)-EDTA, are characteristically refractory and difficult to break down because of their high stability and solubility. Cu(II)-EDTA sequestration by structural Fe(II) (Fe(II)) was investigated intensively in this study. Up to 101.21mgCu(II)/gFe(II) was obtained by Fe(II) in chelated copper sequestration under near neutral pH condition (pH 7.70). The mechanism of Cu(II)-EDTA sequestration by Fe(II) was concluded as follows: 3Cu(II)-EDTA+7Fe(II)+9H2O → Cu(0)↓+ Cu2O↓(the major product)+2Fe2O3·H2O↓+3Fe(II)-EDTA +14H(+) Novel results strongly indicate that Cu(II) reductive transformation induced by surface Fe(II) was mainly responsible for chelated copper sequestration. Cu(0) generation was initially facilitated, and subsequent reduction of Cu(II) into Cu(I) was closely combined with the gradual increase of ORP (Oxidation-Reduction Potential). Cu-containing products were inherently stable, but Cu2O would be reoxidized to Cu(II) with extra-aeration, resulting in the release of copper, which was beneficial to Cu reclamation. Concentration diminution of Cu(II)-EDTA within the electric double layer and competitive adsorption were responsible for the negative effects of Ca(2+), Mg(2+). By generating vivianite, PO4(3-) was found to decrease surface Fe(II) content. This study is among the first ones to identify the indispensible role of reductive decomplexation in chelated copper sequestration. Given the high feasibility and reactivity, Fe(II) may provide a potential alternative in chelated metals pollution controlling.

The submerged aeration membrane (SAM) system and axial vibration membrane (AVM) system can mitigate membrane fouling. In this study, both systems were investigated to compare the performance of filtration and the membrane fouling in algae filtration. In 5-h filtration, the transmembrane pressure (TMP) of SAM reached to 70.0 kPa, while there was almost no increase in TMP for AVM. After continuous filtration, it could be found that there was hardly any algae cells on the membrane of AVM (0.11 g/m2), which was about 32.4 times less than that of SAM (3.56 g/m2). Compared with the SAM system, AVM had a lesser membrane fouling, regardless of the reversible fouling or irreversible fouling. By SEM, FTIR and EEM, it could be found there was less irreversible extracellular organic matter (EOM) on the membrane of AVM. By MW distribution, it could be observed that less EOM with high-MW adhered to membrane of AVM.

Immobilized pellets obtained by means of entrapping activated sludge in waterborne polyurethane were successfully adapted in ammonium (NH4(+)-N) synthetic wastewater. Its physicochemical characteristics were determined using scanning electron microscope, pyrosequencing, and microelectrodes, and its influence on the nitrification process in sequencing batch reactors (SBRs) at low temperatures was evaluated. A large number of rod-shaped bacteria were observed on the surface of the immobilized pellet, in which Rudaea spp. (Xanthomonadaceae family) was an important bacterial component (23.44% of the total bacteria). The oxygen uptake rate of immobilized pellets reached 240.83±15.59 mgO2/(L·hr), and the oxygen was primarily consumed by the bacteria on the pellet surfaces (0-600 μm). The dosing of the pellets (30 mL/L) into an SBR significantly improved the nitrification efficiency at low temperatures of 7-11°C, achieving an average NH4(+)-N removal of 84.09%, which is higher than the removal of 67.46% observed for the control group.

Microalgae-based technology is an environmental-friendly and cost-effective method for biofuel production and pollutants removal. In this study, Scenedesmus obliquus (S. obliquus) was cultured with varying concentrations of ofloxacin (OFL) in BG11 medium. In the algae-antibiotics culture system, S. obliquus could effectively remove OFL with a concentration of 10 mg/L; however, the removal efficiency was restricted under higher doses (20–320 mg/L). Meanwhile, the lipid content significantly increased by 21.10–49.63%, which was caused by carbon being converted from carbohydrate to lipid. The greatest lipid productivity (7.53 mg/L/d) occurred at an OFL concentration of 10 mg/L, which was approximately 1.5-fold greater than the control. Moreover, S. obliquus cultured with OFL was able to improve the biodiesel quality due to an increase of saturated fatty acids and a decrease of unsaturated fatty acids. This study demonstrates that an algae-antibiotics system is a promising solution to simultaneously achieve antibiotics removal and biofuel production.

Peroxymonosulfate (PMS) is an appealing oxidant for organic contaminant destruction relying on radical generation after activation. Herein, we report PMS-promoted rapid degradation of histamine H2-receptor antagonists (HRAs) through non-radical process for the first time. Five commonly used HRAs, i.e., ranitidine (RNTD), cimetidine (CMTD), famotidine (FMTD), nizatidine (NZTD) and roxatidine (RXTD), were examined their reactivity towards PMS. Results show that HRAs (except RXTD) exhibit high reactivity towards PMS, with apparent second-order rate constants from 403 to 872 M−1s−1 at pH 7.0. Radical scavenging experiments excluded the contribution of radicals to PMS-promoted degradation of HRAs, and this non-radical process was unaffected by the real water matrices. Structure-activity assessment and theoretical calculation indicated that the thioether sulfur in HRAs (except RXTD) was the main reactive site for PMS oxidation. Transformation product analysis further elucidated oxidation of the thioether sulfur to sulfoxide product through an oxygen atom transfer process. Moreover, the thioether sulfur on the straight chain was more susceptible to oxygen transfer with PMS than that on the thiazole ring of HRAs. Toxicity evaluation indicated the ecotoxicity of HRAs could be remarkably reduced after PMS oxidation. Hence, this work provides a promising strategy to rapidly remove HRAs and significantly reduce their toxicity in water treatment.

There is growing pressure for wastewater treatment plants to mitigate the discharge of antibiotic resistant bacteria (ARB) and extracellular resistance genes (eARGs), which requires technological innovation. Here, hierarchical Bi2O2CO3 microspheres were wrapped with nitrogen-doped, reduced graphene oxide (NRGO) for enhanced inactivation of multidrug-resistant E. coli NDM-1 and degradation of the plasmid-encoded ARG (blaNDM-1) in secondary effluent. The NRGO shell enhanced reactive oxygen species (ROS) generation (•OH and H2O2) by about three-fold, which was ascribed to broadened light absorption region (red-shifted up to 459 nm) and decreased electron-transfer time (from 55.3 to 19.8 ns). Wrapping enhanced E. coli adsorption near photocatalytic sites to minimize ROS scavenging by background constituents, which contributed to the NRGO-wrapped microspheres significantly outperforming commercial TiO2 photocatalyst. ROS scavenger tests indicated that wrapping also changed the primary inactivation pathway, with photogenerated electron holes and surface-attached hydroxyl radicals becoming the predominant oxidizing species with wrapped microspheres, versus free ROS (e.g., •OH, H2O2 and •O2−) for bare microspheres. Formation of resistance plasmid-composited microsphere complexes, primary due to the π-π stacking and hydrogen bonding between the shell and nucleotides, also minimized ROS scavenging and kept free plasmid concentrations below 102 copies/mL. As proof-of-concept, this work offers promising insight into the utilization of NRGO-wrapped microspheres for mitigating antibiotic resistance propagation in the environment.

Nanoscale zerovalent iron (nZVI) and sulfidated nanoscale zerovalent iron (S-nZVI) have been increasingly studied for heavy metal removal in the subsurface. However, a comprehensive comparison of the effectiveness of the technologies and the stability of derived metal-adsorbed composites is lacking. In this study, we evaluated the colloidal stability and transport of nZVI, S-nZVI and S-nZVI modified with nanosized silica (FeSSi). Furthermore, we monitored the metal immobilization performance of the three nanoparticles (NPs) under anoxic conditions in synthetic groundwater for 30 days. The NP-metal composites were thereafter discharged into a river water and metal remobilization was monitored for 20 days. Sulfidation improved the colloidal stability of nZVI in both simple media and in natural waters, although a lower initial agglomeration rate constant (ka) was observed in unmodified nZVI at acidic pH. The transport of nZVI in saturated soil column was enhanced with sulfidation due to decreased electrostatic attraction between the NPs and sand. The three NPs sequestered more than 80 % of Cu2+, Zn2+, Cd2+ and Cr2O72- from groundwater. Among the three NPs tested, S-nZVI had a slightly higher removal capacity for metals than nZVI in synthetic groundwater and the chemical stability of metal-S-nZVI composites upon discharge into river water was the highest.

Tetracyclines (TCs) discharged from livestock wastewater have received worldwide concerns owing to their potential threats to the ecosystem and human health. Advanced oxidation processes always exhibit low efficiency to remove TCs in livestock wastewater due to the radical scavenging by water matrices. Herein, we report selective elimination of TCs by peroxymonosulfate (PMS) in livestock wastewater. A kinetic model was developed to describe the rapid degradation of TCs by PMS in the real livestock wastewater. The radical scavenging study and electron paramagnetic resonance (EPR) technique excluded the contribution of radical species (e.g., SO4 −) in the PMS-promoted oxidation of TCs. Theoretical calculations revealed the electrophilic attacks of PMS most likely located on the B-ring of TCs. Transformation product analysis further elucidated that hydroxylation dominated in the PMS-promoted oxidation of TCs, and N-demethylation also significantly contributed to chlorotetracycline (CTC) oxidation by PMS. These results demonstrate a promising strategy to eliminate TCs in livestock wastewater, because PMS shows specific reactivity towards TCs, and thus suffers less interference from the complicated water matrices.

Hydrothermal liquefaction is a promising technology to convert wet biomass into bio-oil. However, post-hydrothermal liquefaction wastewater (PHWW) is also produced during the process. This wastewater contains a high concentration of organic compounds, including phenols and N-heterocyclic compounds which are two main inhibitors for biological treatment. Thus, proper treatment is required. In this work, ozone was used to convert phenols and N-heterocyclic compounds with a dosage range of 0–4.64 mg O3/mL PHWW. After ozone treatment, the phenols were fully converted, and acids were produced. However, N-heterocyclic compounds were found to have a low conversion rate (21.7%). The kinetic analysis for the degradation of phenols and N-heterocyclic compounds showed that the substitute played an important role in determining the priority of ozone reactions. The OH moiety in the ring compounds (phenols and pyridinol) may form hydroxyl radical, which lead to an efficient reaction. A substantial improved biodegradability of PHWW was observed after ozone treatment. The ratio of BOD5/COD was increased by about 32.36%, and reached a maximum of 0.41. The improved biodegradability of PHWW was justified by the conversion of phenols and N-heterocyclic compounds.

In this study, we investigated the destruction and by-product formation of perfluorooctanoic acid (PFOA) using ultraviolet light and persulfate (UV-PS). Additionally, we developed a first-principles kinetic model to simulate both PFOA destruction and by-product and chlorate (ClO3(-)) formation in ultrapure water (UW), surface water (SW), and wastewater (WW). PFOA degradation was significantly suppressed in the presence of chloride and carbonate species and did not occur until all the chloride was converted to ClO3(-) in UW and for low DOC concentrations in SW. The model was able to simulate the PS decay, pH changes, radical concentrations, and ClO3(-) formation for UW and SW. However, our model was unable to simulate PFOA degradation well in WW, possibly from PS activation by NOM, which in turn produced sulfate radicals.

It has been proven that extrusion can change the structure of rice straw and increase biogas production, but the effect of a single pretreatment is limited. Ca(OH)2 pretreatment was used to enhance the enzyme hydrolysis and biogas production of extruded rice straw. After Ca(OH)2 pretreatment, the glucose and xylose conversion rates in enzymatic hydrolysis increased from 36.0% and 22.4% to 66.8% and 50.2%, respectively. The highest biogas production observed in 8% and 10% Ca(OH)2 pretreated rice straw reached 564.7mL/g VS and 574.5mL/g VS, respectively, which are 34.3% and 36.7% higher than the non-Ca(OH)2-loaded sample. The Ca(OH)2 pretreatment can effectively remove the lignin and increase the fermentable sugar content. The structural changes in the extruded rice straw have also been analyzed by XRD, FTIR, and SEM. Considering all of the results, an 8% Ca(OH)2 loading rate is the best option for the pretreatment of extruded rice straw.

Low-cost but high-efficiency composites of iron-containing porous carbons were prepared using sewage sludge and ferric salts as raw materials. Unlike previous time- and energy-consuming manufacturing procedures, this study shows that pyrolyzing a mixture of sludge and ferric salt can produce suitable composites for lead adsorption. The specific surface area, the total pore volume and the average pore width of the optimal composite were 321m(2)/g, 0.25cm(3)/g, and 3.17nm, respectively. X-ray diffraction analysis indicated that ferric salt favored the formation of metallic iron, while Fourier transform infrared spectroscopy revealed the formation of hydroxyl and carboxylic groups. The result of batch tests indicated that the adsorption capacity of carbons activated with ferric salt could be as high as 128.9mg/g, while that of carbons without activation was 79.1mg/g. The new manufacturing procedure used in this study could save at least 19.5kJ of energy per gram of activated carbon.

Microalgae harvesting has been a primary problem encountered during microalgae utilization because of the low biomass concentration of microalgae and the severe membrane fouling caused by extracellular organic matters (EOM). Our previous study verified the applicability of dynamic membrane technology for algae dewatering. The aims of this study are to investigate the performances of both the diatomite dynamic membrane (DDM) technology, used for algae dewatering during a long-term (96 h) operation period, and the membrane fouling mechanisms, as well as their relationship with algae growth phases. The stable filtration flux reached 12.8 L/m 2 h, and the ultimate biomass concentration reached 49 g/L. The DDM continued to have advantages in cost, energy consumption and ultimate algae concentration. However, the stability of the DDM was questionable for long-term operations. Algae growth phases had distinct impacts on the EOM concentrations and composition and, therefore, on the membrane fouling mechanisms. The osmotic pressure originating from the EOM might exist during the DDM filtration process and could be largely responsible for the high cake resistance. As the algae growth phase advanced from the logarithmic phase to the decline phase, membrane fouling became much more severe.

The catalytic reduction of nitrate is a promising technology for groundwater purification because it transforms nitrate into nitrogen and water. Recent studies have mainly focused on new catalysts with higher activities for the reduction of nitrate. Consequently, metal nanoparticles supported on mesoporous metal oxides have become a major research direction. However, the complex surface chemistry and porous structures of mesoporous metal oxides lead to a non-uniform distribution of metal nanoparticles, thereby resulting in a low catalytic efficiency. In this paper, a method for synthesizing the sustainable nitrate reduction catalyst Pd-In/Al2O3 with a dimensional structure is introduced. The TEM results indicated that Pd and In nanoparticles could efficiently disperse into the mesopores of the alumina. At room temperature in CO2-buffered water and under continuous H2 as the electron donor, the synthesized material (4.9 wt% Pd) was the most active at a Pd-In ratio of 4, with a first-order rate constant (k(obs) = 0.241 L min(-1) g(cata)(-1)) that was 1.3× higher than that of conventional Pd-In/Al2O3 (5 wt% Pd; 0.19 L min(-1) g(cata)(-1)). The Pd-In/mesoporous alumina is a promising catalyst for improving the catalytic reduction of nitrate.

Magnetic mesoporous iron cerium bimetal oxides (MMIC) with large surface area and pore volume was synthesized via the hard template approach. This obtained MMIC was easily separated from aqueous solution with an external magnetic field and was proposed as a heterogeneous Fenton-like catalyst for oxidation of As(III). The MMIC presented excellent catalytic activity for the oxidation of As(III), achieving almost complete oxidation of 1000 ppb As(III) after 60 min and complete removal of arsenic species after 180 min with reaction conditions of 0.4 g/L catalyst, pH of 3.0 and 0.4 mM H 2 O 2 . Kinetics analysis showed that arsenic removal followed the pseudo-first order, and the pseudo-first-order rate constants increased from 0.0014 min −1 to 0.0548 min −1 as the H 2 O 2 concentration increased from 0.04 mM to 0.4 mM. On the basis of the effects of XPS analysis and reactive oxidizing species, As(III) in aqueous solution was mainly oxidized by OH radicals, including the surface-bound OH ads generated on the MMIC surface which were involved in Fe 2+ and Ce 3+ , and free OH free generation by soluble iron ions which were released from the MMIC into the bulk solution, and the generated As(V) was finally removed by MMIC through adsorption.

The present study proposed and demonstrated a novel process for the bioconversion of syngas (mainly CO and H2) to valuable volatile fatty acids (VFA) by integrating with mesophilic alkaline fermentation of waste activated sludge (WAS). The results showed that although pH 9 was suitable for VFA production from WAS, 62.5% of the consumed CO was converted to methane due to the presence of hydrogenogenic pathway for CO conversion. The increase of pH from 9 to 9.5 inhibited the methane production from CO because of the possible presence of only acetogenic pathway for CO conversion. However, methane was still produced from H2 contained in syngas through hydrogenotrophic methanogenesis, and around 32–34% of the consumed syngas was converted to methane. At both pH 9 and 9.5, methane was produced by hydrogenotrophic methanogens Methanobacteriales. Further increase of pH to 10 effectively inhibited methane production from syngas, and efficient VFA (mainly acetate with the concentration of around 135 mM) production by simultaneous conversion of syngas and WAS was achieved. High acetate concentrations (>150 mM) were shown to have serious negative effects on the conversion of syngas. The addition of syngas to the mesophilic alkaline fermentation of WAS at pH 10 not only resulted in the enrichment of some known bacteria related with syngas conversion, but also changed the microbial community compositions for the fermentation of WAS.