An airlift biofilm reactor was employed to study phenol biodegradation by Pseudomonas putida. Hydrodynamic tests were also conducted in a conventional column to facilitate the comparison of the dynamic behavior in different types of columns. The three-phase airlift column offered better aeration than the conventional column as liquid and solid circulation in the downcomer favored bubble breakup, increasing oxygen dissolved in the liquid phase and favoring the phenol biodegradation process. Kinetic parameters of phenol biodegradation by P. putida were obtained in an agitated batch reactor, with the initial phenol concentration varying from 10 to 750 mg/L. Experimental data were fitted using different microbial growth models found in literature. The Yano and Koga model, which considers the formation of multiple inactive enzyme–substrate complexes, fitted well with our experimental data, with a correlation coefficient, R ² = 0.952. An internal loop airlift bioreactor was used for aerobic phenol biodegradation in which polystyrene particles were utilized to support biomass immobilization. Several tests were performed by varying the influent phenol concentration, hydraulic retention time, upstream flow, and superficial air velocity. It was concluded that until an influent phenol concentration of approximately 300 mg/L, phenol acted as the limiting substrate. For higher phenol concentrations, oxygen became the limiting substrate. An increase in the oxygen concentration resulted in the complete consumption of phenol under high phenol concentration of 500 mg/L.

The removal of copper, nickel, and cobalt ions from synthetic mining wastewater was investigated in this study using micellar-enhanced ultrafiltration (MEUF). The effect of surfactant-to-metal (S/M) ratio and pH on metal rejection and permeate flux were examined. A Monte Carlo-based artificial neural network (ANN) modeling approach was proposed to predict the MEUF performance and to reveal the importance of process parameters. The results showed that model-predicted values were in agreement with experimental data (R > 0.99). S/M ratio and pH had relatively greater contributions (30–50%) to the metal rejection rate and permeate flux, whereas sampling time contributed less (10%), which indicated high MEUF efficiency. An S/M ratio of 8.5 with a pH of 8–10 was found to be the optimal condition for MEUF, under which the rejection rates of all three metals exceeded 99% and were in compliance with Canadian environmental standards. Flux decrease and concentration polarization effect were observed during the experimental procedure. Statistical analysis showed that the type of metal examined in this study did not affect MEUF performance.

The purpose of this study was to determine the different kinds and concentrations of intermediates, and investigate on the effects of contact time and ozone (O₃) doses on the removal of humic acid (HA), which is served as the main disinfection by-product (DBP) precursor. Based on that, the knowledge gap of DBPs generated was made up. The results showed that HA was the major precursor material for aldehydes and carboxylic acids. The concentrations of aldehydes increased as contact time and O₃ doses, and reached up maximum at 2~10 min but approached a plateau at the higher O₃ doses. The concentrations of formic and acetic acids increased as contact time and O₃ doses. However, aromatic acids, including protocatechuic, 3-hydroxybenzoic, and benzoic acids, declined rapidly at longer reaction time and higher O₃ doses. It was worth mentioning that aromatic acids had been rarely reported. Besides, a possible formation pathway was proposed: (a) HA was degraded into fulvic acid (FA)-like compounds; (b) FA-like compounds were further converted into aromatic acids; (c) aromatic acids were transformed into low-molecular-weight organic matters; (d) chlorine reacted with aldehydes and/or carboxylic acids by addition, hydrolysis, and decarbonylation reactions, leading to DBP formation. Furthermore, not only HA were the main DBPs precursors, but also the oxidation intermediates of HA could be the DBPs precursors, and they gave a certain amount of DBPs. Consequently, aldehydes and carboxylic acids should be under control in drinking water treatment plants.

Artificial adamite [Zn₂(AsO₄)(OH)] is a convenient structural model because it is isostructural with other rock-forming minerals in secondary ore deposits formed in cementation zones. Microbial activity in these zones accelerates mineral biogeochemical deterioration and metal release, and our results confirmed that Pseudomonas, Rhodococcus and Cupriavidus strains accelerate adamite leaching by 10 to 465 times compared to controls. Here, the Pseudomonas chlororaphis ZK-1 bacterial strain in a static 42-day cultivation proved more effective than Rhodococcus and Cupriavidus by leaching over 90% arsenic and 10% zinc from adamite in one-step in vitro. We evaluated adamite with the VESTA visualization system for electronic and structural analysis, and our results enhance understanding of zinc and arsenic biogeochemical cycles and mobilization, and highlight bacteria’s beneficial natural and biotechnological application in environmental geochemistry and biohydrometallurgy.

As a newly emerging persistent environmental contaminant, perchlorate (ClO₄⁻) has adverse effects on thyroid function by inhibiting iodide uptake and could result in neurodevelopment deficits. Our study was performed to investigate the concentration of perchlorate in size-segregated airborne particulate matter (APM) and evaluate its human exposure for children and adults. In this study, 45 size-segregated APM samples were collected from Changsha, China, during July 20 to July 31, 2016. The total APM concentrations ranged from 93.367 to 253.271 μg/m³ (mean 154.651 ± 59.175 μg/m³), and a bimodal size distribution was observed during the sampling period. The concentrations of perchlorate in size-segregated APM were in the range of 0.05–4.99 ng/m³ (mean 2.03 ng/m³). Exposure evaluation indicated that the ingestion was the predominant exposure pathway for daily intake of perchlorate via size-segregated APM, and children are more likely to intake more perchlorate via APM than adults. We suggested that the risk of exposure to perchlorate for children is worthy of attention, and a further study is required, especially for seasonal variations.

The operation variables and electro-kinetic field (EKF) were investigated to enhance the remediation of arsenic (As)- and cesium (Cs)-contaminated soils with soil washing. Extractant types, concentrations, liquid/solid (L/S) ratios, solution pH values, washing temperatures, and agitation modes were important criteria to determine the efficiency of soil washing. The KH₂PO₄ was proved to be a suitable alternative to Na₂EDTA in extracting As and Cs from contaminated soils. A 2-h washing with KH₂PO₄ at concentration of 0.01 M and L/S ratio of 20 mL g⁻¹ showed the most efficient washing performance. In addition, the lower solution pH, higher temperature, and ultrasound also favored soil washing of As and Cs with KH₂PO₄. The EKF greatly enhanced metals extraction with soil washing. It offered acidic soil environment around the anode areas for the release of soluble Cs from its soil solid-phase components before soil washing. Moreover, the alkalization around the cathode areas also benefited the desorption of stable As since labile As were mainly presented in anionic forms. The effect of CA for neutralizing OH⁻ was proved to be limited, while the reversed subsequent EKF process effectively alleviated Cs precipitation generated during the initial EKF process. It also effectively restored soil pH altered by the initial EKF. The overall EKF (4 V cm⁻¹) enhanced removal efficiency of As and Cs with soil washing from the anode area was 37 and 31%, respectively. Higher removal of As (52%) was obtained in the cathode area. Moreover, the reversed EKF resulted in another 28% removal of Cs in the initial cathode area which showed the capacity of EKF on continuous soil metal remediation.

Effects of ethanol and nitrate on linear alkyl benzene sulfonate (LAS) degradation were investigated using central composite design. At experimental design, removal of 99.9% was observed in batch reactors (1 L) with 9.8 to 41.2 mg L⁻¹ of LAS. The batch reactors were kept under agitation at 120 rpm and 30 °C. Ethanol (co-substrate) and nitrate (electron acceptor) were statistically significant factors (p < 0.05) in surfactant removal. Optimal values were 97.5 and 88 mg L⁻¹ for ethanol and nitrate, respectively. LAS removal was kinetically investigated by varying surfactant concentration while using optimal values. Batch I (27 mg L⁻¹ LAS) exhibited greater degradation rate (KᴸᴬS) (0.054 h⁻¹) in the presence of ethanol and nitrate. Nonetheless, in Batch II (60 mg L⁻¹ LAS), the KᴸᴬS values decreased in those reactors probably due to inhibition by excess substrate for same concentrations of nitrate and ethanol added in reactors. As LAS concentration increased, the dominance of bacterial populations also increased, whereas diversity index decreased from 2.8 (inoculum) to 2.4 and 2.5 for reactors with both added nitrate and ethanol and those with only added ethanol, respectively. Probably, a selection of microbial populations occurred in relation to LAS concentration. The nitrate and ethanol, at able concentration, made it possible the induction of denitrifying microrganisms foward to LAS removal.

Fungus Pleurotus ostreatus HAAS can tolerate and remove heavy metals from water. Among three heavy metals tested, the removal of Pb was the most efficient (99.9–100.0%), followed by Cd (45.9–61.1%), and Cr (29.4–64.5%). The uptake of heavy metals by the fungus varied and was dependent on the element. Pb was found to be transported primarily into the fungal cell wall (68.2–91.2% of the total), which was much higher than the insoluble form (20.1–32.7%), and the maximum intracellular concentration of Pb was found to be 119,830.4 mg kg⁻¹. In the cases of Cd and Cr, their insoluble forms were the main products of the reaction with the fungus, which accounted for 30.0–39.1 and 19.6–37.4% of the total. P. ostreatus HAAS produces oxalic acid, and this production is stimulated by Pb and Cr but inhibited by Cd. Parallel experimental results indicated that the concentration of the soluble metals in solution decreased with the increase of oxalic acid, which further suggested that oxalic acid played a partial role in the removal of the soluble heavy metals by chelation. These results revealed that this species of fungus has a variety of response mechanisms to the presence of heavy metals in solution.

Petroleum products which are used in a wide variety of industries as energy sources and raw materials have become a major concern in pollution of terrestrial and marine environments. The purpose of this study was to assess the potential of indigenous microbial isolates for degradation of diesel fuel. Two most proficient bacterial strains among five isolated strains from polluted soil of an industrial refinery were studied. The isolates then were identified as Pseudomonas aeruginosa and Bacillus subtilis using biochemical tests and 16S rRNA gene sequence analyses. P. aeruginosa showed higher biodegradation efficiency than B. subtilis in shaking flask containing diesel-contaminated water. P. aeruginosa and B. subtilis degraded about 87 and 75% of total hydrocarbons, respectively, in flasks containing 2% diesel and 98% water. The biodegradation efficiency of the isolates decreased as diesel contamination increased from 2 to 5%. The isolates showed significantly higher efficiency on degradation of short-chain hydrocarbons in 20 days, i.e., by using P. aeruginosa, removal efficiency of C₁₀ hydrocarbons was near 90%, while about 69% of C₂₀₊ hydrocarbons and 47% of aromatic hydrocarbons were removed. Therefore, the isolates showed high capability in biodegradation of diesel contamination of the refinery.

Nitrogen recovery and valorization is gaining interest due to the current need for nitrogen removal, so it is of great interest that ammonium-selective sorbents be evaluated. In this study, a zeolitic material synthesized from coal fly ash (Ze–Na) in sodium form as well as its modification to potassium form (Ze–K) were evaluated as sorbent materials for the recovery of ammonium from wastewater effluents. The sorption performance was assessed through three consecutive sorption-desorption cycles reporting opposite behavior in terms of ammonium sorption capacity. Decreasing in the case of Ze–Na and to slightly increase for Ze–K due to alkaline activation of zeolite surface. The maximum sorption capacities obtained were 109 ± 4 mg NH₄/g and 33 ± 1 mg NH₄/g for Ze–Na and Ze–K, respectively. It is important to point out that in the case of Ze–Na, the maximum sorbent capacity was obtained during the first sorption cycle whereas in the case of Ze–K, it was obtained during the last working cycle due to the alkaline regeneration. Kinetic studies showed that after every regeneration step, the sorption kinetics turn faster as alkaline desorption increased the zeolite-specific surface, thus increasing the size of porous and enhancing the diffusion through the particle. Results obtained indicate that sorption capacity decreased significantly after every working cycle using Ze–Na whereas Ze–K followed the opposite behavior despite its initial lower sorption capacity.