Quenching residual H2O2 from UV/H2O2 with granular activated carbon: A significant impact of bicarbonate.

UV/H2O2 has been used as an advanced oxidation process to remove organic micropollutants from drinking water. It is essential to quench residual H2O2 to prevent increased chlorine demand during chlorination/chloramination and within distribution systems. Granular activated carbon (GAC) filter can quench the residual oxidant and eliminate some of the dissolved organic matter. However, knowledge on the kinetics and governing factors of GAC quenching of residual H2O2 from UV/H2O2 and the mechanism underlying the enhancement of the process by HCO3- is limited. Therefore, this study aimed to analyse the kinetics and influential factors, particularly the significant impact of bicarbonate (HCO3-). H2O2 decomposition by GAC followed first-order kinetics, and the rate constants normalised by the GAC dosage (kn) were steady (1.6 × 10-3 L g-1 min-1) with variations in the GAC dosage and initial H2O2 concentration. Alkaline conditions favour H2O2 quenching. The content of basic groups exhibited a stronger correlation with the efficiency of GAC in quenching H2O2 than did the acidic groups， with their specific kn values being 8.9 and 2.4 min-1 M-1, respectively. The presence of chloride, sulfate, nitrate, and dissolved organic matter inhibited H2O2 quenching, while HCO3- promoted it. The interfacial hydroxyl radical (HO•) zones were visualised on the GAC surface, and HCO3- addition increased the HO• concentration. HCO3- increased the concentration of persistent free radicals (PFRs) on the GAC surface, which mainly contributed to HO• generation. A significant enhancement of HCO3- on H2O2 quenching by GAC was also verified in real water. This study revealed the synergistic mechanism of HCO3- and GAC on H2O2 quenching and presents the potential applications of residual H2O2 in the H2O2-based oxidation processes.

Effects of simulated acid rain on hydrochemical factors and microbial community structure in red soil aquifers.

Acid rain can lower the pH of groundwater and affect its hydrogeochemistry and microbial ecology. However, the effects of acid rain on the hydrogeochemistry and microbial ecology of red soil groundwater systems in southern China are poorly understood. Previous research had mainly investigated the sources and patterns of groundwater acidification, but not the microbial mechanisms that contribute to this process and their associations with hydrochemical factors. To address this knowledge gap, we conducted a soil column experiment to simulate the infiltration of acid rain through various filter materials (coarse, medium, and fine sand) and to examine the hydrochemical and microbial features of the infiltrate, which can reveal how simulated acid rain (pH 3.5-7.0) alters the hydrochemistry and microbial community composition in red soil aquifers. The results showed that the pH of the leachate decreased due to simulated acid rain, and that the leaching efficiency of nitrogen and metal ions was influenced by the particle size of the filter media. Illumina 16S rRNA gene sequencing revealed that the leachate was dominated by Proteobacteria, Patescibacteria, Actinobacteria, and Acidobacteria, with Proteobacteria accounting for 67.04-74.69% of the bacterial community and containing a high proportion of nitrifying and denitrifying bacteria. Additionally, several genera with heavy metal tolerance, such as Burkholderia-Caballeronia-Paraburkholderia, Delftia, Methylversatilis, Aquicella, and Ralstonia, were widely distributed in the leachate, indicating the strong adaptive capacity of the microbial population. A correlation analysis between the hydrochemical factors and the microbial community structure revealed that pH was the most influential factor, followed by NO2--N, Fe, Al, Cu, Mn, and others. These results indicate that acidification modifies the hydrochemical conditions of the aquifer, creating an environment that is unfavorable for microbial growth and survival. However, some microorganisms may acquire resistance genes to cope with environmental changes.

Ethanol-diluted turbidimetry method for rapid and accurate quantification of low-density microplastics in synthetic samples.

Retention and transport behaviours of microplastics (MPs) and their associated pollutants in porous media are of great concern. The homogeneity of the studied MPs in artificially controlled lab-scale studies makes rapid and accurate MP quantification feasible. In this study, an economical ethanol-diluted turbidimetry method for polypropylene (PP) and polyethylene (PE) MPs was developed. With ethanol dilution, the MP dispersion system exhibited an excellent suspension performance. Strong linear relationships were observed between MP concentrations and turbidities in both low (<1.3 mg L-1) and high (<170 mg L-1) MP concentration ranges. Solution density and MP agglomeration governed the MP suspension performance. For low surface tension and high molecular mass, the addition of ethanol decreased the contact angles of PP-MPs with solutions from 81.73 to 15.5°, and consequently improved the MP suspension performance. The suspension system was optimised to an ethanol/water (v/v) ratio of 3:2 and 4:1 for PP- and PE-MPs, when the slopes of standard curves were determined to be 1.252 and 0.471 with the recovery of 100.54 ± 3.09% and 103.19 ± 1.66%, and the limit of detection and quantification values of 0.025 and 0.082 mg L-1, and 0.060 and 0.201 mg L-1, respectively. Solution pH, salinity, and dissolved organic matter in the selected range induced acceptable fluctuations in the MP recovery and matrix effect values. The Derjaguin-Landau-Verwey-Overbeek (DLVO) energy barriers were calculated to be > 20 kT, indicating excellent tolerance to the solution matrix. Additionally, applications in real water samples were validated to demonstrate the potential of the developed method.

Rapid start-up of PN/A process and efficient enrichment of functional bacteria: A novel aerobic-biofilm/anaerobic-granular nitrogen removal system (OANRS).

Reactor configuration, control strategy and inoculation method were key factors affecting the rapid start-up of partial nitrification/anammox (PN/A) process and the efficient enrichment of functional bacteria (anammox and ammonia oxidizing bacteria). At present, PN/A process was generally operated through single factor rather than forming a system. In this study, a novel aerobic-biofilm/anaerobic-granular nitrogen removal system (OANRS) was constructed, which consisted of a multi-stage aerobic-biofilm/anaerobic-granular baffle reactor (MOABR) and a control strategy on pH/aeration time. PN process was started within 10d, and PN/A process was started on the basis of stable PN process within 41d. The simultaneous enrichment of functional bacteria was achieved by combining the advantages of single-stage and two-stage PN/A process. The results of high-throughput sequencing showed that Candidatus Kuenenia (20.42 ± 15.88%) was highly enriched in each compartment at day 98, and the relative abundance of Candidatus Kuenenia in the anaerobic compartment R4 was as high as 43.13%.

Interactions between H2O2 and dissolved organic matter during granular activated carbon-based residual H2O2 quenching from the upstream UV/H2O2 process.

Granular activated carbon (GAC) filtration can be employed to synchronously quench residual H2O2 from the upstream UV/H2O2 process and further degrade dissolved organic matter (DOM). In this study, rapid small-scale column tests (RSSCTs) were performed to clarify the mechanisms underlying the interactions between H2O2 and DOM during the GAC-based H2O2 quenching process. It was observed that GAC can catalytically decompose H2O2, with a long-lasting high efficiency (>80% for approximately 50,000 empty-bed volumes). DOM inhibited GAC-based H2O2 quenching via a pore-blocking effect, especially at high concentrations (10 mg/L), with the adsorbed DOM molecules being oxidized by the continuously generated ·OH; this further deteriorated the H2O2 quenching efficiency. In batch experiments, H2O2 could enhance DOM adsorption by GAC; however, in RSSCTs, it deteriorated DOM removal. This observation could be attributed to the different ·OH exposure in these two systems. It was also observed that aging with H2O2 and DOM altered the morphology, specific surface area, pore volume, and the surface functional groups of GAC, owing to the oxidation effect of H2O2 and ·OH on the GAC surface as well as the effect of DOM. Additionally, the changes in the content of persistent free radicals in the GAC samples were insignificant following different aging processes. This work contributes to enhancing understanding regarding the UV/H2O2-GAC filtration scheme, and promoting the application in drinking water treatment.

Design a flower-like magnetic graphite carbon microsphere for enhanced adsorption of 2,4-dichlorophenol.

2,4-Dichlorophenol (2,4-DCP) is a hazardous chlorinated organic chemical, so its removal is an important task to protect the whole ecosystem and human health. During the material preparation, the magnetic graphitic carbon adsorbent (HFMCM) with a sparse sheet-like stacking structure was formed by interlayer assembly of nickel hydroxide nanosheets and hydrothermal glucose carbon. The conditions for optimal performance of the adsorbent are 45 °C and pH 5. The maximum adsorption capacity of HFMCM-180 for 2,4-DCP is 147.06 mg·g-1. Adsorption behavior in accordance with Langmuir isothermal model and pseudo-second-order kinetic models. The adsorbent remains selective for 2,4-DCP in metal ion solutions. More than 75% of the adsorption capacity is maintained after five cycles of adsorption. Electrostatic interaction, hydrogen bonding, and π-π bonding play a major role in the adsorption of 2,4-DCP by HFMCM. The adsorbent was glucose as the carbon source, nickel sulfate as the magnetic source, and hexamethylenetetramine as the precipitant. Its carbonization after pretreatment with different hydrothermal temperatures resulted in the synthesis of flower-like graphitic carbon spheres with magnetic properties. The interconnected pore channels on the adsorbent surface conferred large specific surface area to the material. 2,4-DCP was efficiently adsorbed by π-π stacking, hydrogen bonding, and electrostatic attraction within the pore channels with low spatial potential resistance.

The Removal of Pb2+ from Aqueous Solution by Using Navel Orange Peel Biochar Supported Graphene Oxide: Characteristics, Response Surface Methodology, and Mechanism.

The value-added utilization of waste resources to synthesize functional materials is important to achieve the environmentally sustainable development. In this paper, the biochar supported graphene oxide (BGO) materials were prepared by using navel orange peel and natural graphite. The optimal adsorption parameters were analyzed by response surface methodology under the conditions of solution pH, adsorbent dosage, and rotating speed. The adsorption isotherm and kinetic model fitting experiments were carried out according to the optimal adsorption parameters, and the mechanism of BGO adsorption of Pb2+ was explained using Scanning Electron Microscope (SEM-EDS), X-ray Photoelectron Spectroscopy (XPS), X-ray Diffraction (XRD), and Fourier Transform Infrared Spectroscopy (FTIR). Compared with virgin biochar, the adsorption capacity of Pb2+ on biochar supported graphene oxide was significantly increased. The results of response surface methodology optimization design showed that the order of influence on adsorption of Pb2+ was solution pH > adsorbent dosage > rotating speed. The optimal conditions were as follows: solution pH was 4.97, rotating speed was 172.97 rpm, and adsorbent dosage was 0.086 g. In the adsorption−desorption experiment, the desorption efficiency ranged from 54.3 to 63.3%. The process of Pb2+ adsorption by BGO is spontaneous and endothermic, mainly through electrostatic interaction and surface complexation. It is a heterogeneous adsorption process with heterogeneous surface, including surface adsorption, external liquid film diffusion, and intra-particle diffusion.

[Effect of Controlling Heavy Metals in Soil of Rare Earth Mining Area by Biochar Supported Graphene Oxide].

Using navel orange peels and natural graphite as raw materials, biochar-supported graphene oxide (BGO) material was prepared using an improved hummer and co-pyrolysis method. The effects of BGO on the forms of heavy metals in the soil of a rare earth mining area were investigated via a soil passivation experiment. The soil column leaching experiment was carried out to explore the change characteristics of heavy metal content in leaching filtrate and the vertical migration law of heavy metals in soil, and the accumulation and release model of heavy metals under leaching conditions was determined. The results showed that pH value and organic matter content of soil with BGO composite increased, and acid-extractable Pb of raw ore and tailings soil decreased by 17% and 8.6%, respectively. The content of Mn form in the raw ore soil did not change significantly, whereas the content of acid-extractable, reducible, and oxidizable state in tailings soil decreased. The accumulation and release characteristics of heavy metals in soil could be divided into two stages:rapid release stage and slow stage. The release rate of heavy metals in soil with BGO composite was lower than that without addition, and the Pb and Mn removed from the tailings soil decreased by 2.5% and 28.4%, respectively, compared with that of the control group, whereas the raw ore soil decreased by 5.7% and 1.1%, respectively. The release of heavy metals in soil is a complex reaction process controlled by a variety of diffusion mechanisms. BGO composites can effectively inhibit the migration of heavy metals by increasing soil pH, surface complexation, and precipitation.

UV-assisted nitrogen-doped reduced graphene oxide/Fe3O4 composite activated peroxodisulfate degradation of norfloxacin.

We reported the preparation of NGO-Fe3O4 by simple hydrothermal-co-precipitation. The catalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). It was demonstrated that norfloxacin (NOR) could be effectively degraded by the UV/NGO-Fe3O4/PDS system. The degradation efficiency reached 100% within 13 min (the concentration of NOR and S2O82- were 100 mg L-1 and 1 mM, respectively; m(NGO-Fe3O4): m(PDS) = 4: 1; pH: 3.0). In addition, NGO-Fe3O4 showed stable catalytic activity in recycling. The analysis found that the in-situ generated ·OH was the main active free radicals but SO4-⋅ also participated in the NOR degradation. Based on the identified intermediates, the NOR degradation pathways were proposed with UV/NGO-Fe3O4/PDS system.

Thermal treatment's enhancement on high solid anaerobic digestion: effects of temperature and reaction time.

The methane production rate of high solid anaerobic digestion (HSAD) was poor although it was a promising technology with the advantages of small reactor, low energy consumption, and less digestate. In our research before, thermal treatment was proved to enhance HSAD's methane production rate via both batch experiments and continuous experiments of swine manure. However, the effect or investigation of thermal treatment's temperature-time combinations was not yet reported. In this study, swine manure was firstly thermally treated in 500-mL glass bottles with 400-mL work volume at 45-65 °C for 1-4 days. HSAD experiment of 10% solid content was then set up. The VS ratio of substrate to inoculum was 1:1. Thermal treatment at 45 °C (3 days), 55 °C (1 day), and 65 °C (3 days) could obtain the highest methane production rate, which was around 40% higher. Kinetics analysis suggested that the degradation of swine manure was quite different at different temperatures. Furthermore, energy assessment indicated that "thermal treatment + HSAD" had significant advantages in improving HSAD economic feasibility, because the improved methane production rate could compensate for the extra energy utilized for thermal treatment. Heat treatment at 45 °C (4 days) was preferred when the heating equipment was limited. Heat treatment at 55 °C (1 day) was preferred when the floor space and reactor volume were restricted. Heat treatment at 65°C (3 days) was preferred when the requirement of the digestate's sanitary condition is strict.

Computational fluid dynamics modelling of quasi-collimated beam apparatus - a typical bench scale UV apparatus for water treatment.

Quasi-collimated beam apparatus (QCBA), a typical bench scale UV apparatus, is crucial for the biodosimetry determination of UV dose in target reactors. However, the key parameters for the QCBA construction are usually estimated via rule-of-thumb calculations. Computational fluid dynamics models are applied in this study to simulate the UV fluence rate (FR) distributions in QCBAs. QCBAs with either a cylindrical tube or successive apertures irradiate quasi parallel light into selected dishes. The simulated Petri factors (PF) in the target QCBAs with a single aperture were all >0.84, and increased with the extended distance (L1) from the UV lamp to the upper aperture. QCBAs with two successive apertures are recommended compared with those with three apertures or cylindrical tube. A trend of FR distribution from dispersed to concentrated is observed when L1 or the interval distance between each aperture increases in a dual-aperture QCBA. QCBAs with multiple lamps were favorable to increase the UV output power, while having a nearly negligible loss of parallelism. An actual QCBA was constructed, and the maximal and average FR and PF values in a 60-mm dish were 0.159 and 0.164 W/m2, and 0.967, respectively, in accordance with the simulated results.

Effect of low-intensity ultrasound on partial nitrification: Performance, sludge characteristics, and properties of extracellular polymeric substances.

Ultrasound technology, which is environment-friendly and economical, has emerged as a novel strategy that can be used to enhance the partial nitrification process. However, its effect on this process remains unclear. Therefore, in this study, partial nitrification sludge was subjected to low-intensity (0.15 W/mL) ultrasound treatment for 10 min, and the effect of ultrasonic treatment on the partial nitrification process was evaluated based on changes in reactor performance, sludge characteristics, and the properties of extracellular polymeric substances (EPS). The results obtained showed that the ultrasonic treatment enhanced nitrite accumulation performance as well as the activity of ammonia-oxidizing bacteria from 3.3 to 16.6 mg O2/g VSS,⋅while inhibiting the activity of nitrite-oxidizing bacteria. Further analysis showed that owing to the ultrasonic treatment, there was an increase in EPS contents. Particularly, there was a significant increase in loosely bound polysaccharide (PS) contents, indicating the occurrence of intracellular PS anabolics as well as PS secretion. Additionally, ultrasonic treatment induced a significant increase in carbonyl, hydroxyl, and amine functional group contents, and EPS analysis results revealed that it had a positive effect on mass transfer efficiency; thus, it enhanced the partial nitrification process. Overall, this study describes the effect of intermittent low-intensity ultrasound on the partial nitrification process as well as the associated enhancement mechanism.

Adaptation, restoration and collapse of anammox process to La(III) stress: Performance, microbial community, metabolic function and network analysis.

During the mining of rare earth mineral, the use of lanthanum-containing fertilizers, and the disposal of lanthanum-containing electronic products, the content of lanthanum (La(III)) in typical ammonia wastewater with low carbon to nitrogen ratio is increasing day by day. Here, effects of La(III) on anammox process in performance, microbial community structure, metabolic function, and microbial co-occurrence network were investigated. The results shown that the nitrogen removal efficiency was declines briefly and then gradually recovers after low dosage (1-5 mg/L) La(III) treatment and the decrease to low level (24.25 ± 1.74%) under high La(III) dosage (10 mg/L). La(III) in the range of 1-5 mg/L significantly promoted the relative abundance of Anammoxoglobus (0.024% to 9.762%). The blocking of key metabolic pathways was confirmed to cause the breakdown of anammox by PICRUSt. Furthermore, network analysis revealed that lack of cooperation bacteria limits the activity of Anammoxoglobus.

Exploring potential impact(s) of cerium in mining wastewater on the performance of partial-nitrification process and nitrogen conversion microflora.

Cerium Ce(III) is one of the major pollutants contained in wastewater generated during Ce(III) mining. However, the effect(s) of Ce(III) on the functional genera responsible for removing nitrogen biologically from wastewater has not been studied and reported. In this study, the effects of Ce(III) on aspects of partial-nitritation-(PN) process including ammonia oxidation rate (AOR), process kinetics, and microbial activities were investigated. It was found that the effect of dosing Ce(III) in the PN system correlated strongly with the AOR. Compared to the control, batch assays dosed with 5 mg/L Ce(III) showed elevated PN efficiency of about 121%, an indication that maximum biological response was feasible upon Ce(III) dose. It was also found that, PN performance was not adversely affected, given that Ce(III) dose was ≤20 mg/L. Process kinetics investigated also suggested that the maximum Ce(III) dose without any visible inhibition to the activities of ammonium oxidizing bacteria was 1.37 mg/L, but demonstrated otherwise when Ce(III) dose exceeded 5.63 mg/L. Compared to the control, microbes conducted efficient Ce(III) removal (averaged 98.66%) via biosorption using extracellular polymeric substances (EPS). Notably, significant deposits of Ce(III) was found within the EPS produced as revealed by SEM, EDX, CLSM and FTIR. 2-dimensional correlation infrared-(2DCOS-IR) revealed ester group (uronic acid) as a major organic functional group that promoted Ce(III) removal. Excitation-emission matrix-(EEM) spectrum and 2DCOS-IR suggested the dominance of Fulvic acid, hypothesized to have promoted the performance of the PN process under Ce(III) dosage.

"Umbrella" Structure Trisiloxane Surfactant: Synthesis and Application for Reverse Flotation of Phosphorite Ore in Phosphate Fertilizer Production.

Phosphorite is generally used in the manufacture of phosphate fertilizer and plays a vital role in the development of agricultural and food production. Nonetheless, how to obtain phosphorite concentrates efficiently and sustainably has become an urgent problem. In this study, a newly designed trisiloxane surfactant, N-(2-Aminoethyl)-3-aminopropyltrisiloxane (AATS), has been prepared and utilized as an emerging collector for reverse flotation of phosphorite ore. Its collecting ability was compared with the conventional surfactant 1-dodecamine (DDA). In the collector concentration tests, AATS with lower concentrations showed stronger collecting ability for quartz. In the pH tests, AATS always performed better than DDA in the acidic or alkaline condition. In bench-scale flotation experiments, the P2O5 recovery of phosphorite concentrates with 150 g/t AATS was 10.77% higher than that with 300 g/t DDA, which proved that AATS can be applied to the sustainable production of phosphorite concentrates. For a 4000 t/d phosphorite ore processing plant, the profit could be increased 7,014,702.07 USD every year by using AATS as the collector. Therefore, this work provides a promising approach to enhance the production efficiency of phosphate fertilizer and to promote the sustainable development of agriculture.

Visible light-assisted NGO-Fe3O4 composite activated peroxydisulfate for degradation of oxytetracycline.

A nitrogen-doped reduced graphene oxide/Fe3O4 composite (NGO-Fe3O4) was prepared through the simplified hydrothermal and deposition-precipitation method and characterized by X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectroscopy. The degradation efficiency of oxytetracycline (OTC) by NGO-Fe3O4 activated peroxodisulfate (PDS) under visible light irradiation was studied. The degradation efficiency reached 100% within 32.5 min (the initial OTC concentration 50 mg L-1 and PDS 1 mM; [NGO-Fe3O4]:[ PDS] = 4:1; pH = 3.0). No apparent decrease in degradation efficiency was observed after five cycles. SO4 -· and ·OH were the main active oxides for OTC degradation in this system. Moreover, four degradation pathways were proposed, namely hydroxylation, dehydration, decarbonylation and demethylation according to the analysis results of high-performance liquid chromatography mass spectrometry.

Enhanced adsorption of perfluorooctanoic acid (PFOA) from water by granular activated carbon supported magnetite nanoparticles.

A new composite material (Fe3O4@GAC, Fe3O4 nanoparticles loaded on a commercial granular activated carbon (GAC)) was prepared through a facile hydrothermal process at controlled Fe2+:Fe3+ molar ratios in air. Fe3O4@GAC was thoroughly characterized and tested for adsorption of perfluorooctanoic acid (PFOA) in water. Fe3O4@GAC(2:1), prepared at an Fe2+:Fe3+ molar ratio of 2:1, showed the best PFOA removal and offered 28.8% higher adsorption capacity than the parent GAC at final pH 4.0. The enhanced adsorption of PFOA was attributed to concurrent hydrophobic, electrostatic and complexation interactions between PFOA, GAC and Fe3O4. GAC in the composite played an important role for PFOA adsorption. The presence of Ca2+ ions (10 mM) at final pH 5.0-10.0 more than doubled the PFOA equilibrium uptake of PFOA by Fe3O4@GAC(2:1) due to the calcium bridging effect between PFOA and the Si-OH or Fe-OH groups in Fe3O4@GAC(2:1), and because of the Ca2+-modification induced formation of PFOA hemi-micelles on the surface or in the relatively large pores (2.27 nm) of Fe3O4@GAC(2:1). Fe3O4@GAC(2:1) was amenable to efficient regeneration using a mixture of NaOH solution and methanol. Fe3O4@GAC holds the potential to be used as a simple and low-cost adsorbent for enhanced adsorption of PFOA, especially in waters of high hardness and alkalinity.

Effects of heavy rare earth element (yttrium) on partial-nitritation process, bacterial activity and structure of responsible microbial communities.

Yttrium (Y(III)) is mined commercially for industrial purposes due to its excellent physical properties. However, the effects of Y(III) in mining-wastewater on the performance of partial-nitritation process and ammonia-oxidizing bacteria (AOB) have not been explored. To elucidate Y(III) effects on biological mechanisms, kinetics was conducted to establish a correlation between Y(III) dosage and specific-oxygen-uptake-rate (SOUR). The mechanism(s) demonstrated by bacterial population to resist against toxic effects from Y(III) dose was also investigated using scanning electron microscopy-(SEM), energy-dispersive X-ray spectroscopy-(EDS), confocal laser scanning microscopy-(CLSM)，Fourier transform infrared-(FTIR) spectroscopy, and 2-dimensional correlation infrared-(2DCOS-IR) approach. The study revealed a strong correlation between ammonium oxidation rate (AOR) and Y(III) dosage. AOR promotion was more pronounced when Y(III) concentration was ≤20 mg/L (maximum AOR of 12.39 mgN/L/h, at 5 mg/L), whereas inhibition when Y(III) in influent was >20 mg/L (minimum AOR of 7.34 mgN/L/h, at 500 mg/L). Aiba model demonstrated high-performance (R2 = 0.962) when Y(III) concentration ranged 0-20 mg/L, whereas linear model fitted well (R2 of 0.984) to experimental data when Y(III) dose ranged 20-500 mg/L. The maximum change in SOUR (Vmax), half-rate constant (Km), and inhibition constant (Ki) reached 1.04 d-1, 20.12 mg/L, and 4.87 mg/L, respectively, an indication that dosage of Y(III) could affect the partial-nitritation process. SEM-EDS showed that the content of extracellular polymeric substances (EPS) increased along with increasing Y(III) dosage. When 20 mg/L of Y(III) was dosed, the fraction of Y(III) within the surface elemental composition of the sludge increased gradually whereas that of calcium decreased. To further comprehend the EPS production, CLSM results further revealed ß-polysaccharide as the dominant component in the EPS. FTIR/2DCOD-IR showed that the chelation of polyguluronic sections within ß-polysaccharide, together with hydrazine might be the main pathways of cell resistance, but ß- glucan, may have caused the hormesis.

Effects of low-intensity ultrasound on nitrite accumulation and microbial characteristics during partial nitrification.

Ultrasound technology has attracted increasing attention in the field of sewage sludge treatment. This study investigated the nitrite accumulation ratio (NAR) and microbial characteristics of the partial nitrification (PN) process in a sequencing batch reactor employing ultrasonic treatment (ultrasound density = 0.25 W/mL, irradiation time = 10 min). PN was achieved over 73 days with a NAR above 85% under ambient temperatures. A low dissolved oxygen (DO) environment was generated in the reactor by enhancing the oxygen utilization rate of ammonia-oxidizing bacteria (AOB). Additionally, the application of long-term ultrasonic treatment led to the enhancement of the dominance of the Nitrosomonas genus of AOB, while populations of the Nitrospira genus of nitrite-oxidizing bacteria (NOB) were eradicated. At the same time, the activities of the aerobic denitrifying bacteria Thauera, Terrimonas, Defluviimonas, and Thermomonas were enhanced and their relative abundance was increased. Overall, the results suggest that ultrasonic treatment can enhance AOB activity and generate a low DO environment that facilitates effective PN.

Enhancement in the partial nitrification of wastewater sludge via low-intensity ultrasound: Effects on rapid start-up and temperature resilience.

The partial nitrification process can reduce the aeration energy consumption in bioreactors by 25%. Low-intensity ultrasound (0.25 W·mL-1) was applied during the partial nitrification process to evaluate its effects on start-up and temperature resilience. Ultrasound application led to rapid start-up of the partial nitrification process (within 18 d) with a nitrite accumulation ratio of above 80% at 18 °C. Moreover, when the temperature was increased to 28 °C, the partial nitrification process was effectively maintained with a nitrite accumulation ratio of above 80%. Ultrasonic treatment for a long duration had a positive effect on ammonia oxidizing bacteria of the genus Nitrososphaera, whereas the population of nitrite oxidizing bacteria, Nitrospira, decreased. The temperature resilience of Nitrososphaera was also enhanced. These findings indicate that ultrasound induces rapid start-up of the partial nitrification process and enhances the temperature resilience of Nitrososphaera.