In this study, a novel rotating anode-based reactor (RAR) was designed to investigate its effectiveness in removing dissolved salts (i.e., Br⁻, Cl⁻, TDS, and SO₄²⁻) from saline water samples. Two configurations of an impeller’s rotating anode with various operation factors, such as operating time (min), rotating speed (rpm), current density (mA/cm²), temperature (°C), pH, and inter-electrode space (cm), were used in the desalination process. The total cost consumed was calculated on the basis of the energy consumption and aluminum (Al) used in the desalination. In this respect, operating costs were calculated using optimal operating conditions. Salinity was removed electrochemically from saline water through electrocoagulation (EC). Results showed that the optimal adjustments for treating saline water were carried out at the following conditions: 150 and 75 rpm rotating speeds for the impeller’s rod anode and plate anode designs, respectively; 2 mA/cm² current density (I), 1 cm² inter-electrode space, 25 °C temperature, 10 min operation time, and pH 8. The results indicated that EC technology with impeller plates of rotating anode can be considered a very cost-effective technique for treating saline water.

Accumulation and oral bioavailability of nickel (Ni) were rarely assessed for staple crops grown in high geogenic Ni soils. To assess exposure risk of geogenic Ni, soil, wheat, and rice samples were collected from a naturally high background Ni area and measured for Ni oral relative bioavailability (RBA, relative to NiSO₄) using a newly developed mouse urinary Ni excretion bioassay. Results showed that soils were enriched with Ni (80.5 ± 23.0 mg kg⁻¹, n = 58), while high Ni contents were observed in rice (2.66 ± 1.46 mg kg⁻¹) and wheat (1.32 ± 0.78 mg kg⁻¹) grains, with rice containing ∼2-fold higher Ni content than wheat. Ni-RBA was low in soil (14.8 ± 7.79%, n = 18), but high in wheat and rice with rice Ni-RBA (85.9 ± 19.1%, n = 9) being ∼2-fold higher than wheat (46.1 ± 21.2%, n = 16). A negative correlation (r = 0.61) was observed between Ni-RBA and iron content in rice and wheat, suggesting the low iron status of rice drives its high Ni bioavailability. The higher Ni accumulation and bioavailability for rice highlights that rice consumption was a more important contributor to daily Ni intake compared to wheat, while Ni intake from direct soil ingestion was negligible. This study suggests a potential health risk of staple crops especially rice when grown in high geogenic Ni areas.

Destructive development of suburban areas in some metropolises has exposed suburban soils to high risk of potentially toxic trace elements (PTEs) enrichment, which also threatens human and ecosystem health. This study investigated the pollution status, sources and spatial patterns of four PTEs (Pb, Cd, Cr and As) in 1805 soil samples collected from the suburbs of Shanghai in 2015. Nineteen potential sources, including: 6 soil property factors, 10 proximity factors and 3 topography factors, were selected to help explain the PTEs aggregation using logistic regression models from global and local perspectives. The statistical results of PTEs concentration revealed that Cd showed the highest pollution risk in local soils, which was followed by As. Soil property was the primary factor affecting the PTEs (except Cr) enrichment, both identified by global models and local models. The local model particularly emphasized the significant correlation between soil property and PTEs in most parts of the outer suburbs and southeastern inner suburbs. Some proximity factors such as distance to district center and water were negatively correlated with Cd pollution and some topography factors such as elevation and slope were closely related to As pollution. It is worth noting that in the coastal areas, especially Chongming Island, there were obvious PTEs depositions in the soil near the estuary. This study helps to identify the sources of anthropogenic contamination and geogenic enrichment of the four PTEs and their spatial patterns, playing an essential role in formulating regional environmental policies for coastal cities.

We conducted the first comprehensive assessment of the presence, source, and ecotoxicological implication of 13 banned and restricted organochlorine pesticides (OCPs) in the surface water along the Ganga River for two different seasons. Surface water samples were collected along the 2525 km stretch of the Ganga through 43 sites representing five zones of diverse land-use pattern, pesticide consumption rate, and varied flow. The mean concentrations of ΣOCPs were significantly higher (∼2–5 times) in the post-monsoon or wet season [range: 0.126 to 10.402 μg/L (mean: 2.482 μg/L ± 3.589 and median: 1.433)] than in the post-winter or dry season [range: 0.053 to 3.010 μg/L (mean: 0.765 μg/L±1.033 and median: 0.399)]. Lindane (γ-HCH) was the dominant and most frequently detected pesticide at all the sites, indicating possible continued use of this banned pesticide in agricultural practices. The spatial distribution of OCPs revealed non-significant difference amongst different zones and indicate that point source pollution from the open drains along the Ganga could be responsible for observed trend. Ratio diagnostic analysis highlighted the fresh inputs and potential illegal use of lindane and chlordane at all the zones whereas, historical use of DDT was revealed at the majority of sites. Interestingly, fresh inputs of DDT were observed in the relatively pristine high altitude Upper zone (UZ) suggesting long-range atmospheric transfer and its continued use in the zone. Risk quotient (RQ) analysis revealed high ecotoxicological risks (>1), at all the studied sites for p, p’ DDE. The lower zone (LZ) emerged as a high ecological risk zone. The study highlights that though the OCPs analysed in this study are banned/restricted in India, still the implementation of the ban is poor and delayed and the country requires stricter adherence to its National Implementation Plan (NIP) on pesticides.

Despite the strong ability for complexation of heavy metals, a high amount of humic substances (HS) is always contained in membrane retentate from municipal solid waste landfill leachates treatment processes. Submerged Combustion Evaporation (SCE) can be used to effectively concentrate the membrane retentate. However, the impact of the SCE treatment on HS complexation capacity is still unclear. Since cadmium (Cd) plays a vital role in the pollution of soil and food, this study investigated the influence of the SCE treatment on the Cd complexation potential of leachate HS. Specific effects and complexation properties on Cd complexation of leachate HS before and after the SCE treatment were demonstrated using the Non-Ideal Competitive Adsorption model. The results showed that the Cd complexation capacity of carboxyl sites increased from 3.76 to 4.65 mol/kg-Total Organic Carbon (TOC) after the SCE treatment, which agreed with the stoichiometric number of proton binding sites. Moreover, characterization results indicated that SCE increased the affinity of HS for Cd by enhancing the overall aromaticity of HS (E₂:E₄ from 9.8 to 9.3), dominantly due to the humic acid contribution. By modeling the practical Cd remediation scenarios, the enhanced Cd complexation performance of HS after SCE treatment was observed even at low pH values (pH = 5) or insufficient TOC content (TOC = 50 mg/L).

Sludge from a groundwater treatment plant was used to prepare biochar by pyrolysis. The Fe–Mn rich biochar was used to activate percarbonate for the remediation of polycyclic aromatic hydrocarbons (PAHs) contaminated aquatic sediments. Results showed that the sludge–derived biochar (SBC) produced at a pyrolysis temperature of 700 °C was the most effective in activating percarbonate, which exhibited significant oxidative removal of PAHs. PAHs degradation took place via a Fenton-like oxidation manners, contributed from the Fe³⁺/Fe²⁺ and Mn³⁺/Mn²⁺ redox pairs, and achieved the highest degradation efficiency of 87% at pH₀ 6.0. Reactions between oxygenated functional groups of biochar and H₂O₂ generated of O₂•– and HO• radicals in abundance under neutral and alkaline pH was responsible for the catalytic degradation of PAHs. Our results provided new insights into the environmental applications of SBC for the green sustainable remediation of organics-contaminated sediments and aided in reduction of associated environmental and health risk.

The stability of community functioning in anaerobic ammonia oxidation (anammox) sludge adaptation to various salinity changes are concerned but not fully explored. In this study, two anammox reactors were designed in response to different salt levels and salt-adding methods. The reactor PI, run with small stepwise salt increments (0.5%–1.0%), removed >90% of nitrite and ammonium in the influent over the range of 0%–4% salt. By contrast, the reactor SI, run with a sharp salt increment (>2.5%), exhibited a reduced performance (by up to 44%) over the same salt range with a new steady state. The observed resilience times after salt perturbations indicated that the PI reactor recovered substantially and rapidly at all imposed salt levels. Principal coordinates analysis of 16S rRNA gene amplicon sequences revealed that bacterial community structures of the anammox sludge altered conspicuously in response to the salinity changes. However, quantitative PCR analysis showed that the shift in copy number of studied nitrogen-converting genes encoding hydrazine synthase (hzsA), bacterial and archaeal ammonia monooxygenases (amoA), nitrite oxidoreductase (nxrB), nitrite reductase (nirK), and nitrous oxide reductase (nosZ) was not significant (p > 0.05) in anammox sludge across the salt levels of 0.5%–4%, which suggests the stability of microbial community functioning in the osmoadaptation processes. The freshwater anammox Ca. Kuenenia showed high osmoadaptation by potentially adopting both high-salt-in and low-salt-in strategies to dominate in both reactors. The quantitative transcript analysis showed that the active anammox bacteria represented by hzsA transcripts in the SI reactor were approximately two orders of magnitude lower than those in the PI reactor during the long-term exposure to 4% salinity, manifesting the influence by the salt-increasing methods. These results provided new insight into osmo-adaptation of the anammox microbiome and will be useful for managing salinity effects on nitrogen removal processes.

Carbamazepine (CBZ), a widely detected pharmaceutical in wastewaters, cannot currently be treated by conventional activated sludge technologies, as it is highly resistant to biodegradation. In this study, the degradation kinetics and reaction mechanisms of CBZ by hydroxyl radical (OH) and sulfate radical (▪)–based advanced oxidation processes (AOPs) were investigated with a combined experimental/theoretical approach. We first measured the UV absorption spectrum of CBZ and compared it to the theoretical spectrum. The agreement of two spectra reveals an extended π–conjugation system on CBZ molecular structure. The second–order rate constants of OH and ▪ with CBZ, measured by competition kinetics method, were (4.63 ± 0.01) × 10⁹ M⁻¹ s⁻¹ and (8.27 ± 0.01) × 10⁸ M⁻¹ s⁻¹, respectively at pH 3. The energetics of the initial steps of CBZ reaction with OH and ▪ were also calculated by density functional theory (DFT) at SMD/M05–2X/6–311++G**//M05–2X/6–31 + G**level. Our results reveal that radical addition is the dominant pathway for both OH and ▪. Further, compared to the positive ΔGR0 value for the single electron transfer (SET) reaction pathway between CBZ and OH, the ΔGR0 value for SET reaction between CBZ and ▪ is negative, showing that this reaction route is thermodynamically favorable. Our results demonstrated the remarkable advantages of AOPs for the removal of refractory organic contaminants during wastewater treatment processes. The elucidation of the pathways for the reaction of OH and ▪ with CBZ are beneficial to predict byproducts formation and assess associated ecotoxicity, providing an evaluation mean for the feasibility of AOPs application.

The existence of micropollutants (MPs) including pathogens in waters poses great risks to ecological safety and human health. Sulfate radical (SO4•−)‒based advanced oxidation processes (AOPs) have attracted considerable attention in water treatment for both disinfection and removal of emerging MPs. Here, we investigated the SO4•−‒mediated kinetic and mechanistic aspects of simultaneous inactivation of Enterococcus faecalis (E. faecalis) and degradation of carbamazepine (CBZ), a typical MP with high occurrence in wastewater. In the absence of CBZ, (73.8 ± 2.3) % E. faecalis were inactivated after 12 min of treatment, while in the presence of CBZ, (68 ± 1.6) % of E. faecalis were inactivated, exhibiting similar inactivation efficiency with or without MP. The second‒order rate constant (k) of E. faecalis reacting with SO4•− was determined to be (5.42 ± 0.64) × 10⁹ M⁻¹ s⁻¹. In addition, two distinct types of disinfection models, one based on the quenching ratio (Q model) and the other on steady‒state concentration of SO4•− (R model), were developed to predict the inactivation kinetics of E. faecalis. Both models exhibited good performance for describing the disinfection of E. faecalis with RMSE of 0.065 and 0.048, respectively. Our kinetic experimental and modelling results on bacterial disinfection and degradation of CBZ were projected to offer valuable insight into future developments for typical wastewater scenarios where microorganisms and MPs coexist.

Traffic-generated ultrafine particles (UFPs) in the urban atmosphere have a high proportion of their composition comprised of semi-volatile compounds (SVOCs). The evaporation/condensation processes of these SVOCs can alter UFP number size distributions and play an important role in determining the fate of UFPs in urban areas. The neighbourhood-scale dispersion (over distances < 1 km) and evolution of traffic-generated UFPs for a real-world street network in central London was simulated by using the WRF-LES model (the large eddy simulation mode of the Weather Research and Forecasting modelling system) coupled with multicomponent microphysics. The neighbourhood scale dispersion of UFPs was significantly influenced by the spatial pattern of the real-world street emissions. Model output indicated the shrinkage of the peak diameter from the emitted profile to the downwind profile, due to an evaporation process during neighbourhood-scale dispersion. The dilution process and the aerosol microphysics interact with each other during the neighbourhood dispersion of UFPs, yielding model output that compares well with measurements made at a location downwind of an intense roadside source. The model captured the total SVOC concentrations well, with overestimations for gas concentrations and underestimations for particle concentrations, particularly of the lighter SVOCs. The contribution of the intense source, Marylebone Road (MR) in London, to concentrations at the downwind location (as estimated by a model scenario with emissions from MR only) is comparable with that of the rest of the street network (a scenario without emissions from MR), implying that both are important. An appreciable level of non-linearity is demonstrated for nucleation mode UFPs and medium range carbon SVOCs at the downwind receptor site.