Emission Characteristics of Aerosols Generated during the Micro-Nano Bubble Aeration Process in Wastewater.

Micro-nano bubble (MNB) aeration is an emerging technology that considerably enhances the aeration efficiency of wastewater. This study evaluates, for the first time, aerosolization at the water-air interface during MNB aeration. Our results show that the concentration of culturable mixed microorganisms (i.e., bacteria, fungi, and intestinal bacteria) in the in situ MNB generation (MNBs-G) phase is 2170 CFU/m3, 1.38 and 1.58-fold higher than those in medium-bubble aeration (MBA; 1568 CFU/m3) and small-bubble aeration (SBA; 1376 CFU/m3) aerosols, respectively. Conversely, the concentration of culturable mixed microorganisms in the MNB persistent dissolved oxygen (MNBs-O) phase is only 914 CFU/m3. Microbiological analysis shows a lower abundance of bacterial pathogens in MNBs-G (34.12%) and MNBs-O (34.02%) phases than in MBA (39.63%) and SBA (38.87%) aerosols. Acinetobacter is prevalent in MNBs-G (14.76%) and MNBs-O (8.22%) aerosols, whereas Bacillus and Arcobacter are prevalent in MBA (23.96%) and SBA (6.92%) aerosols, respectively. The total concentrations of chemicals [i.e., total organic carbon, water-soluble ions, and metal(loid)s] in aerosols formed via MNB aeration (205.98-373.74 µg/m3) are lower than those in MBA and SBA (398.69-594.92 µg/m3). Compared to MBA and SBA, the MNBs-G phase exhibits higher emissions of 12 elements in aerosols (i.e., NO3-, NO2-, Ca2+, Na+, K+, Mg2+, Zn, Cd, Fe, Mn, As, and Cr), whereas the MNBs-O phase generally shows lower emissions. These findings highlight the potential of optimized MNB aeration technology in considerably mitigating aerosol emissions and thereby advancing environmental sustainability in wastewater treatment.

Determining priority control factors for heavy metal management in urban road dust based on source-oriented probabilistic ecological-health risk assessment: A study in Xi'an during peak pollution season.

Urban road dust (URD) is essential for transporting heavy metals (HMs), which can be a major danger to both the environment and human health. Moreover, URD has the potential to be carried into bodies of water, leading to contamination of the aquatic ecosystem. A study was conducted in Xi'an, a city in northwestern China known for high air pollution levels, during January 2024 - a period characterized by peak pollution due to frequent low wind speeds and temperature inversions. The research investigated the presence of 10 types of HMs (Cu, Zn, Cd, Cr, Pb, As, Ni, Hg, Co, and Mn) in URD. Findings revealed elevated levels of Cu, Zn, Cd, Cr, Pb, As, and Hg in URD compared to background levels. Hg showed the most significant contamination (moderate to heavy), followed by moderate contamination of Cd, and lower levels of As, Zn, and Cu. The main sources of HMs were traffic (58.2%), mixed natural and industrial (30.3%), and industrial (11.5%). The ecological risk in the area was deemed to be very high, primarily because of Hg and Cd. Based on probabilistic health risk assessments, it was determined that non-carcinogenic risks were deemed acceptable for all groups. Nevertheless, the possibility of carcinogenic risks should not be disregarded. Strategies for controlling ecological-health risks prioritize mixed natural and industrial sources, with a focus on Hg, Cd, and As in URD. The results offer a foundation for policymakers to create specific control strategies.

Study on the mechanism and reaction characteristics of metal-supported phosphogypsum as oxygen carrier in a chemical looping gasification application.

This study aimed to explore the chemical looping gasification (CLG) reaction characteristics of the metal-supported composite phosphogypsum (PG) oxygen carriers (OCs) and the thermodynamic mechanism. The FactSage 7.1 thermodynamic simulation was used to explore the oxygen release and H2S removal mechanisms. The experimental results showed that the syngas yield of CLG with PG-CuFe2O4 was more than that with PG-Fe2O320/CuO40 or PG-Fe2O330/CuO30 OC at 1023 K when the water vapor content was 0.3. Furthermore, the maximum syngas yield of the CO selectivity was 70.3% and of the CO2 selectivity was 23.8%. The H2/CO value was 0.78, and the highest carbon conversion efficiency was 91.9% in PG-CuFe2O4 at the gasification temperature of 1073 K. The metal-supported PG composite oxygen carrier was proved not only as an oxygen carrier to participate in the preparation of syngas but also as a catalyst to catalyze coal gasification reactions. Furthermore, both the experimental results and FactSage 7.1 thermodynamic analysis revealed that the trapping mechanism of H2S by composite OCs was as follows: CuO first lost lattice oxygen as an oxygen carrier to generate Cu2O, which, in turn, reacted with H2S to generate Cu2S. This study provided efficient guidance and reference for OC design in CLG.

Resource utilization of drinking water treatment aluminum sludge in green cementing materials: Hydration characteristics and hydration kinetics.

As a byproduct of water treatment, drinking water treatment aluminum sludge (DWTAS) has challenges related to imperfect treatment and disposal, which has caused potential harm to human health and the environment. In this paper, heat treatment DWTAS as a supplement cementitious material was used to prepare a green cementing material. The results show that the 800°C is considered as the optimum heat treatment temperature for DWTAS. DWTAS-800°C is fully activated after thermal decomposition to form incompletely crystallized highly active γ-Al2O3 and active SiO2. The addition of DWTAS promoted the formation of ettringite and C-(A)-S-H gel, which could make up for the low early compressive strength of cementing materials to a certain extent. When cured for 90 days, the compressive strength of the mortar with 30% DWTAS-800°C reached 44.86 MPa. The dynamic process was well simulated by Krstulovic-Dabic hydration kinetics model. This study provided a methodology for the fabrication of environmentally friendly and cost-effective compound cementitious materials and proposed a "waste-to-resource" strategy for the sustainable management of typical solid wastes.

New insight into scale inhibition during tea brewing: Ca2+/Mg2+ complexing and alkalinity consumption.

Scale not only affects the taste and color of water, but also increases the risks of osteoporosis and cardiovascular diseases associated with drinking it. As a popular beverage, tea is rich many substances that have considerable potential for scale inhibition, including protein, tea polyphenols and organic acids. In this study, the effect of tea brewing on scale formation was explored. It was found that the proteins, catechins and organic acids in tea leaves could be released when the green tea was brewed in water with sufficient hardness and alkalinity. The tea-released protein was able to provide carboxyl groups to chelate with calcium ions (Ca2+), preventing the Ca2+ from reacting with the carbonate ions (CO32-). The B rings of catechins were another important structure in the complexation of Ca2+ and magnesium ions (Mg2+). The carboxyl and hydroxyl groups on the organic acids was able to form five-membered chelating rings with Ca2+ and Mg2+, resulting in a significant decrease in Ca2+ from 100.0 to 60.0 mg/L. Additionally, the hydrogen ions (H+) provided by the organic acids consumed and decreased the alkalinity of the water from 250.0 to 131.4 mg/L, leading to a remarkable reduction in pH from 8.93 to 7.73. It further prevented the bicarbonate (HCO3-) from producing CO32- when the water was heated. The reaction of the tea constituents with the hardness and alkalinity inhibited the formation of scale, leading to a significant decrease in turbidity from 10.6 to 1.4 NTU. Overall, this study provides information to help build towards an understanding of the scale inhibition properties of tea and the prospects of tea for anti-scaling in industrial applications.

Inactivation and subsequent reactivation of Aspergillus species by the combination of UV and monochloramine: Comparisons with UV/chlorine.

Ultraviolet (UV)/monochloramine (NH2Cl) as an advanced oxidation process was firstly applied for Aspergillus spores inactivation. This study aims to: i) clarify the inactivation and photoreactivation characteristics of UV/NH2Cl process, ii) compared with UV/Cl2 in inactivation efficiency, photoreactivation and energy consumption. The results illustrated that UV/NH2Cl showed better inactivation efficiency than that of UV alone and UV/Cl2, and could effectively control the photoreactivation. For instance, the inactivation rates for Aspergillus flavus, Aspergillus niger and Aspergillus fumigatus in the processes of UV/NH2Cl (2.0 mg/L) was 0.034, 0.030 and 0.061 cm2/mJ, respectively, which were higher than that of UV alone (0.027, 0.026 and 0.024 cm2/mJ) and UV/Cl2 (0.023, 0.026 and 0.031 cm2/mJ). However, there was no synergistic effect for Aspergillus flavus and Aspergillus fumigatus. As for Aspergillus niger, the best synergistic effect can reach 1.86-log10. This may be due to their different resistance to disinfectants, which were related to the size, an outer layer of rodlets (hydrophobins) and pigments. After UV/NH2Cl inactivation, the degree of cell membrane damage and intracellular reactive oxygen species were higher than that of UV alone. UV/NH2Cl had the advantages of high inactivation efficiency and inhibition of photoreactivation, which provides a new entry point for the disinfection of waterborne fungi.

Algae functional group characteristics in reservoirs and lakes with different trophic levels in northwestern semi-humid and semi-arid regions in China.

In order to study the differences in algae species and their biomass in water bodies in a region, three reservoirs and two lakes at the center of Guanzhong Plain were chosen to identify algae functional groups, measure biomass, and assess water quality, from January 2013 to December 2014. The water bodies represented different trophic levels: one oligotrophic, three mesotrophic, and one eutrophic. Based on the Reynolds' functional groups, they had 10 groups in common-B, P, D, X1, M, MP, F, S1, J, and G, but the algae biomasses and proportions were different. In the oligotrophic reservoir, functional group B reached a peak biomass of 576×104L-1, which accounted for 31.27%. In the eutrophic lake, functional group D reached a peak biomass of 3227×104L-1, which accounted for only 13.38%. When samples collected from other water bodies with similar trophic levels were compared, we found differences in the algae species functional groups. The potential reasons for the differences in algae functional group characteristics in the different water bodies in the region were water temperature and nutritional states.

Effect of nitrate concentration, pH, and hydraulic retention time on autotrophic denitrification efficiency with Fe(II) and Mn(II) as electron donors.

The role of electron donors (Fe(2+) and Mn(2+)) in the autotrophic denitrification of contaminated groundwater by bacterial strain SY6 was characterized based on empirical laboratory-scale analysis. Strain SY6 can utilize Fe(2+) more efficiently than Mn(2+) as an electron donor. This study has shown that the highest nitrate removal ratio, observed with Fe(2+) as the electron donor, was approximately 88.89%. An immobilized biological filter reactor was tested by using three levels of influent nitrate (10, 30, and 50 mg/L), three pH levels (6, 7, and 8), and three levels of hydraulic retention time (HRT; 6, 8, and 12 h), respectively. An optimal nitrate removal ratio of about 95% was achieved at pH 6.0 using a nitrate concentration of 50 mg/L and HRT of 12 h with Fe(2+) as an electron donor. The study showed that 90% of Fe(2+) and 75.52% removal of Mn(2+) were achieved at pH 8.0 with a nitrate concentration of 50 mg/L and a HRT of 12 h. Removal ratio of Fe(2+) and Mn(2+) is higher with higher influent nitrate and HRT. A weakly alkaline environment assisted the removal of Fe(2+) and Mn(2+).

Determination of fungicides in sediments using a dispersive liquid-liquid microextraction procedure based on solidification of floating organic drop.

A dispersive liquid-liquid microextraction procedure based on solidification of floating organic droplet has been investigated for the determination of fungicides (cyprodinil, difenoconazole, myclobutanil, and spiroxamine) in sediments by HPLC with diode array detection. In the overall extraction process, the extraction solvents can be separated easily from the sample solution, and the experiment time was shortened. Moreover, several parameters such as the type and volume of the extraction solvent and dispersive solvent, centrifugal speed, extraction time, and salt effect that affect the extraction efficiencies of the target fungicides were studied and optimized. Under the optimized conditions, the LOD for the target analytes were in the range of 0.1-0.5 µg/g. Satisfactory recoveries of the target analytes in the sediment samples were 81.00-99.00%, with RSDs (n = 5) that ranged from 1.8 to 6.5%. Finally, the simple, sensitive, and environmentally friendly method was successfully applied to determine the target fungicides in actual sediment samples.

Sewer sediment adhesion degeneration and gelatinous biopolymer deconstruction by structural cation chelation and alkaline macromolecule hydrolysis for improving hydraulic erosion.

Sediment siltation has been regarded as the serious challenge in sewer system, which dominantly root in the gelatinous extracellular polymeric substance (EPS) structure and cohesive ability. Considering the crucial roles of divalent cation bridging and macromolecular biopolymer winding in sediment EPS formation and adhesive behavior, an innovative combination strategy of sodium pyrophosphate (SP)-mediated divalent cation chelation and alkaline biopolymer hydrolysis was developed to degenerate sediment adhesion. At the SP dosage of 0.25 g/g TS and the alkaline pH 12, the SP + pH 12 treatment triggered structural transformation of aromatic proteins (α-helix to ß-turn) and functional group shifts of macromolecular biopolymers. In this case, the deconstruction and outward dissolution of gelatinous biopolymers were achievable, including proteins (tyrosine-like proteins, tryptophan-like proteins), humic acids, fulvic acids, polysaccharides and various soluble microbial products. These were identified as the major driving forces for sediment EPS matrix disintegration and bio-aggregation deflocculation. The extraction EPS content was obviously increased by 18.88 mg COD/g TS. The sediment adhesion was sensitive to EPS matrix damage and gelatinous biopolymer deconstruction, leading to considerable average adhesion degeneration to 0.98 nN with reduction rate of 78.32%. As such, the sediments could be disrupted into dispersive fragments with increased surface electronegativity and electric repulsion (up to -45.6 mV), thereby the sediment resistance to hydraulic erosion was impaired, providing feasibility for in-situ sediment floating and removal by gravity sewage flow in sewer.

Application of high-dose UV irradiation as nanofiltration pretreatment for drinking water production: Organic fouling mitigation and micropollutant removal.

Nanofiltration (NF) is being increasingly applied to produce high-quality drinking water; however, its cost-effective operation remains challenging due to the perennial membrane fouling. On account of the low tolerance of common NF membranes to chemical oxidants, this study proposed high-dose UV irradiation as a pretreatment strategy for organic fouling mitigation. Results showed that the permeate flux decline of the membrane with UV-treated feedwater (with a dose of 750 mJ cm-2) was less drastic than that with raw feedwater, but slightly faster as compared to that with UV/Cl2 pretreatment. The final normalized fluxes were 0.69, 0.79, and 0.82, respectively, after 10 h of operation with raw, UV- and UV/Cl2-treated feedwaters. With the characterization of feedwaters and membranes, the fouling was found to be initiated by the adsorption of hydrophilic biopolymers onto the membrane, followed by the deposition of hydrophobic humic substances. Reduction of the "glue" biopolymers was crucial to membrane fouling mitigation. The applicability of UV pretreatment in practice was testified with a pilot-scale UV-NF system where permeate flux of the NF module decreased by 37% after six-week continuous operation. Moreover, UV pretreatment could remove most of the identified pesticides in the feedwater with a removal efficiency over 80% for metolachlor and imidacloprid, but had no or even a negative effect on perfluorinated compounds. This work discloses the efficacy and mechanism of high-dose UV irradiation for NF membrane fouling control, which facilitates future research and application of NF technology.

Effects of chloride on corrosion scale compositions and heavy metal release in drinking water distribution systems.

Variations in water chemistry may lead to the release of harmful heavy metals in drinking water distribution systems (DWDSs). In this study, the effects of chloride on the release of heavy metals such as Fe, Mn, As, Cr, Mo, V, Sr, and Co were examined using steel and cast iron pipe loops. After chloride was added, the relative contents of goethite (α-FeOOH), lepidocrocite (γ-FeOOH), and siderite (FeCO3) in pipe scales increased, but the contents of magnetite (Fe3O4) decreased. The most prevalent compounds were α-FeOOH and γ-FeOOH. When the chloride levels were increased, the effluent concentrations of Fe, Mn, As, Cr, Mo, V, Sr, and Co significantly increased. These heavy metals were released presumably because of the destabilization and dissolution of corrosion scales induced by chloride and adsorption site competition. Strong positive correlations were also observed between Fe&Mn, Fe/Mn&As, Fe/Mn&Cr, Fe/Mn&Mo, Fe/Mn&V, Fe/Mn&Sr, and Fe/Mn&Co, indicating the co-release of Fe, Mn, and other metals. This study may be helpful for the potential strategies on avoidance of heavy metal release and improvement of water supply security.

Continuation of a cleaning process: Application of MNBs-coagulation process to mitigate ultrafiltration membrane fouling.

The MNBs-coagulation process as a novel and cleaning enhanced coagulation process has been demonstrated to enhance the removal efficiency of hydrophilic organics. In this study, while continuing the concept of cleaning production, the MNBs-coagulation process was first applied to the ultrafiltration process and was expected to alleviate the ultrafiltration membrane fouling. This study investigated the effect of the involvement of MNBs in coagulation-ultrafiltration process (the MC-UF process) on the fouling behaviour of ultrafiltration membrane based on the calculation of membrane resistance distribution and the fitting of membrane fouling model. In addition, the NOM removal efficiency, floc characteristics analysis and membrane hydrophilicity analysis were used to illustrate the mechanism of mitigating ultrafiltration mebrane fouling by the MC-UF process. The experimental results showed that the involvement of MNBs in the coagulation-ultrafiltration process was able to reduce the irreversible fouling and TMP by 43.1 % and 41.6 % respectively. This phenomenon could be attributed to the involvement of MNBs in the coagulation process to improve the removal efficiency of hydrophilic organics and to enhance the characteristics of flocs, thus reducing the possibility of hydrophilic organics and broken flocs entering and blocking the membrane pores. In addition, the FT-IR spectral changes before and after the floc breakage were analyzed by 2D-COS technique in this study, and it was found for the first time that the participation of MNBs in the coagulation process could change the sequence of functional group transformation within the floc, and promote the generation of hydrogen bonds between flocs by hindering the generation of hydroxyl groups (-OH), and improve the shear resistance and regrowth capacity of flocs while reducing the possibility of broken flocs entering and blocking membrane pores. In summary, the MC-UF process proposed in this study can significantly mitigate ultrafiltration membrane fouling while meeting cleaning production, providing theoretical support for the application of the process to practical engineering.

The fate of pharmaceuticals and personal care products (PPCPs) in sewer sediments:Adsorption triggering resistance gene proliferation.

In recent years, large quantities of pharmaceuticals and personal care products (PPCPs) have been discharged into sewers, while the mechanisms of PPCPs enrichment in sewer sediments have rarely been revealed. In this study, three PPCPs (tetracycline, sulfamethoxazole, and triclocarban) were added consecutively over a 90-day experimental period to reveal the mechanisms of PPCPs enrichment and the transmission of resistance genes in sewer sediments. The results showed that tetracycline (TC) and triclocarban (TCC) have higher adsorption concentration in sediments compared to sulfamethoxazole (SMX). The absolute abundance of Tets and suls genes increased in sediments under PPCPs pressure. The increase in secretion of extracellular polymeric substances (EPS) and the loosening of the structure exposed a large number of hydrophobic functional groups, which promoted the adsorption of PPCPs. The absolute abundance of antibiotic resistance genes (ARGs), EPS and the content of PPCPs in sediments exhibited significant correlations. The enrichment of PPCPs in sediments was attributed to the accumulation of EPS, which led to the proliferation of ARGs. These findings contributed to further understanding of the fate of PPCPs in sewer sediments and opened a new perspective for consideration of controlling the proliferation of resistance genes.

Sewer sediment adhesion reduction and hydraulic floating promotion by alkaline treatment.

Deposition of sediment in sewers decreased flow capacity, with harmful gases and pipe erosion. Sediment floating and removal remained challenges due to its gelatinous structure, which induced strong erosion resistance. This study proposed an innovative alkaline treatment for destructuring gelatinous organic matters and improving hydraulic flushing capacity of sediments. At the optimal pH 11.0 condition, the gelatinous extracellular polymeric substance (EPS) and microbial cells were disrupted, with numerous outward migration and solubilization of proteins, polysaccharides and humus. The aromatic protein solubilization (tryptophan-like and tyrosine-like proteins) and humic acid-like substance deconstruction were the major driving factors for sediment cohesion reduction, which disintegrated the bio-aggregation and increased the surface electronegativity. Meanwhile, the variations of functional groups (CC, CO, COO-, CN, NH, C-O-C, C-OH, OH) also contributed to the interaction breakage and glutinous structure disruption of sediment particles. It was found that the rising pH conditions reduced sediment adhesion and promoted particle floating. Solubilizations of total suspended solids and volatile suspended solids were increased by 12.8 and 9.4 times, respectively, while the sediment adhesion was reduced by 3.8 fold. The alkaline treatment greatly improved sediment erosion and flushing capacities under shear stress of gravity sewage flow. Such sustainable strategy only cost 36.4 CNY per sewer meter length, which was 29.5-55.0 % of the high-pressure water jet flushing and perforated tube flushing approaches.

Kinetics and mechanism of sulfate radical-and hydroxyl radical-induced disinfection of bacteria and fungal spores by transition metal ions-activated peroxymonosulfate.

Peroxymonosulfate(PMS)-based advanced oxidation process have been recognized as efficient disinfection processes. This study comprehensively investigated the role of sulfate radical (SO4•-) and hydroxyl radical (•OH)-driven disinfection of bacteria and fungal spores by the PMS/metals ions (Me(II)) systems and modeled the CT value based on the relationship between survival and ∫[Radical]dt, with the aim to provide an accurate and quantitative kinetic data of inactivation processes. The results indicated that •OH played a more central role than SO4•- in the inactivation process, and bacteria were more vulnerable to radical attack than fungal spores due to the differences in antioxidant mechanisms and external structures. The k value of •OH -induced inactivation of E. coli was approximately 3-fold higher than that of A. niger, and the shoulder length of •OH -induced inactivation of E. coli was closely 52-fold shorter than that of A. niger after treated with the PMS/Co(II) system. The morphological and biochemical changes revealed that PMS/Me(II) treatment caused membrane damage, intracellular ROS accumulation and esterase activity loss in microorganisms. This study significantly improved the understanding of the contribution of radicals in the process of microbial inactivation by PMS/Me(II) and would provide important implications for the further development of technologies to cope with the highly resistant fungal spores in drinking water.

Endogenous biopolymer hydrolysis for enhancing short-chain fatty acids recovery from excess sludge: Combination of lysozyme-catalyzing and cation exchange resin-mediated metal regulation.

In decades, anaerobic fermentation with short-chain fatty acids (SCFAs) recovery from excess sludge have attained rising attention. However, rigid particulate organic matter (POMs) structure with slow hydrolysis limited anaerobic fermentation performance of excess sludge. Remarkable sludge hydrolysis performance was supposed to be achievable by the synchronous EPS repture and microbial cell lysis. This study clarified the improvement of overall anaerobic fermentation performance by combination treatment of lysozyme (Lyso) catalysis and metal regulation (MR). The Lyso + MR treatment triggered EPS rupture by protein structure deflocculation while catalyzing microbial cell lysis, which promoted massive extracellular and intracellular POMs hydrolysis. As a result, a significant amount of SCOD (5646.67 mg/L) was produced. Such endogenous organic matters hydrolysis led to considerable SCFAs accumulation (3651.14 mg COD/L) through 48-h anaerobic fermentation at 1.75 g/g SS cation-exchange resin and Lyso dosage of 10% (w/w), which was 5.945 times higher than that in the control. Additionally, it suggested that most of the recovered SCFAs remained in fermentative liquid after chemical conditioning and mechanical dewatering towards solid-liquid separation, which provided considerable economic benefit of 363.6-1059.1 CNY/ton SS.

Visible-UVC upconversion polymer films for prevention of microbial infection.

Bacterial infections caused by the growth and reproduction of pathogenic bacteria on wounds are one of the main reasons that hinder wound healing. Antibacterial wound dressings protect wounds from bacterial infections. Herein, we developed a polymeric antibacterial composite film using polyvinyl alcohol (PVA) and sodium alginate (SA) as the substrate. The film used praseodymium-doped yttrium orthosilicate (Y2SiO5: Pr3+, YSO-Pr) to convert visible light into short-wavelength ultraviolet light (UVC) to kill bacteria. The YSO-Pr/PVA/SA showed upconversion luminescence in photoluminescence spectrometry tests, and the emitted UVC inhibited Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli and Pseudomonas aeruginosa) bacteria in antibacterial tests. In vivo animal tests showed that YSO-Pr/PVA/SA is effective and safe for inhibiting bacteria in real wounds. The in vitro cytotoxicity test further confirmed the good biocompatibility of the antibacterial film. In addition, YSO-Pr/PVA/SA exhibited sufficient tensile strength. Overall, this study demonstrates the potential of upconversion materials for use in medical dressings.

A novel colorimetric method for field arsenic speciation analysis.

Accurate on-site determination of arsenic (As) concentration as well as its speciation presents a great environmental challenge especially to developing countries. To meet the need of routine field monitoring, we developed a rapid colorimetric method with a wide dynamic detection range and high precision. The novel application of KMnO4 and CH4N2S as effective As(III) oxidant and As(V) reductant, respectively, in the formation of molybdenum blue complexes enabled the differentiation of As(III) and As(V). The detection limit of the method was 8 microg/L with a linear range (R2 = 0.998) of four orders of magnitude in total As concentrations. The As speciation in groundwater samples determined with the colorimetric method in the field were consistent with the results using the high performance liquid chromatography atomic fluorescence spectrometry, as evidenced by a linear correlation in paired analysis with a slope of 0.9990-0.9997 (p < 0.0001, n = 28). The recovery of 96%-116% for total As, 85%-122% for As(III), and 88%-127% for As(V) were achieved for groundwater samples with a total As concentration range 100-800 microg/L. The colorimetric result showed that 3.61 g/L As(III) existed as the only As species in a real industrial wastewater, which was in good agreement with the HPLC-AFS result of 3.56 g/L As(III). No interference with the color development was observed in the presence of sulfate, phosphate, silicate, humic acid, and heavy metals from complex water matrix. This accurate, sensitive, and easy-to-use method is especially suitable for field As determination.

[Investigation on Oxygen Gas-liquid Mass Transfer in Sewage Pipelines Under Enhanced Ventilation].

The anaerobic environment of sewers is the main cause of the production of toxic and harmful gases such as hydrogen sulfide and methane. The installation of septic-tanks between the drainage standpipes and municipal sewage pipes has aggravated the current situation of poor ventilation in sewage pipes. A system of enhanced ventilation has been formed. By connecting the drainage standpipes and sewage pipes, the system of enhanced ventilation can ameliorate the ventilation of sewage pipes and improve the gas-phase space environment. The experimental and computational fluid dynamics (CFD) simulation methods were established to explore the law of oxygen gas-liquid mass transfer under the different sewage flow rates or wind speeds. This study aimed to seek a method to enhance the oxygen mass transfer, suppress the anaerobic environment, and achieve the purpose of long-term control of harmful gases. The results showed that increasing the gas-liquid flow rates can accelerate the oxygen mass transfer, and the volumetric mass transfer coefficient increased by 3.5×10-4 min-1 for every increase of 0.1 m·s-1. However, the faster sewage reduced hydraulic retention time. The mass transfer time of oxygen was also shortened, and the promotion effect was not as good as that by enhancing the gas velocity in the pipelines. At the same time, when the average gas velocity increased by 0.1 m·s-1, the lengths of pipes where dissolved oxygen could effectively inhibit H2S increased by 25 m.