This paper points out the role and significance of civil engineering in dealing with the problems related to the water environment. Examples presented consider hydraulic structures and their impact on the aeration level in the watercourse. Aeration and reaeration have the most important effect on the oxygen water quality parameters and therefore on the entire living world in the particular ecosystem.

Constructed wetlands integrated with microbial fuel cells (MFC-CWs) have been recently developed and tested for removing antibiotics. However, the effects of carbon source availability, electron transfer flux and cathode conditions on antibiotics removal in MFC-CWs through co-metabolism remained unclear. In this study, four experiments were conducted in MFC-CW microcosms to investigate the influence of carbon source species and concentrations, external resistance and aeration duration on sulfamethoxazole (SMX) and tetracycline (TC) removal and bioelectricity generation performance. MFC-CWs supplied with glucose as carbon source outperformed other carbon sources, and moderate influent glucose concentration (200 mg L⁻¹) resulted in the best removal of both SMX and TC. Highest removal percentages of SMX (99.4%) and TC (97.8%) were obtained in MFC-CWs with the external resistance of 700 Ω compared to other external resistance treatments. SMX and TC removal percentages in MFC-CWs were improved by 4.98% and 4.34%, respectively, by increasing the aeration duration to 12 h compared to no aeration. For bioelectricity generation performance, glucose outperformed sodium acetate, sucrose and starch, with the highest voltages of 386 ± 20 mV, maximum power density (MPD) of 123.43 mW m⁻³, and coulombic efficiency (CE) of 0.273%. Increasing carbon source concentrations from 100 to 400 mg L⁻¹, significantly (p < 0.05) increased the voltage and MPD, but decreased the internal resistance and CE. The highest MPD was obtained when the external resistance (700 Ω) was close to the internal resistance (600.11 Ω). Aeration not only improved the voltage and MPD, but also reduced the internal resistance. This study demonstrates that carbon source species and concentrations, external resistances and aeration duration, all play vital roles in regulating SMX and TC removal in MFC-CWs.

Landfill mining and reclamation is a new strategy for addressing the lack of space available for new landfills and realizing the sustainable development of landfills. A gas-water joint bioreactor landfill is regulated by injecting water and/or recirculating leachate, and a blasting aeration system to optimize waste stabilization. In this study, four landfill reactors were constructed to investigate the effects of ventilation methods, including continuous (20 h d⁻¹) and intermittent aeration (4 h d⁻¹ in continuous or 2-h aeration per 12 h, twice a day), on the degradation of organic matter and volatile organic compound (VOC) emissions in comparison with traditional landfills. A total of 62 VOCs were detected in the landfill reactors. Among them, halogenated compounds had the highest abundance (39.8–65.4 %), followed by oxygenated compounds, alkanes and alkenes, and aromatic compounds. Both intermittent and continuous aeration could accelerate the degradation of landfilled waste and increase the volatilization rate of VOCs. Compared with intermittent aeration, the degradation of landfilled waste was more quickly in the landfill reactor with continuous aeration. However, intermittent aeration could create anaerobic-anoxic-aerobic conditions, which were conducive to the growth and metabolism of anaerobic and aerobic microorganisms in landfills and thereby reduced more than 63.4 % of total VOC emissions from the landfill reactor with continuous aeration. Moreover, intermittent aeration could reduce the ventilation rate and decrease the cost of aeration by 80 % relative to continuous aeration. Firmicutes, Bacteroidetes, Proteobacteria and Tenericutes predominated in the landfill reactors. The environmental variables including organic matter and VOCs concentrations had significant influences on microbial community structure in the landfilled waste. These findings indicated that intermittent aeration was an effective way to accelerate the stabilization of landfilled waste and reduce the cost and environmental risks in bioreactor landfills with gas-water joint regulation.

Given that studies on actual sewage treatment plants are often affected by environmental conditions, it is challenging to clearly understand the associated bioaerosol generation and diffusion characteristics during the aeration process. Therefore, to enhance understanding in this regard, in this study, bioaerosol generator was used to simulate bioaerosol generation and diffusion under two aeration modes, i.e., bubble bottom aeration and brush surface aeration. The total concentration range of culturable bacteria in the bioaerosol produced by bubble bottom aeration and that produced by brush surface aeration were 300–3000 CFU/m³. Under bubble bottom aeration, the generated bioaerosol was symmetrically distributed around the source point, whereas under brush surface aeration, it was primarily distributed in the forward direction of the rotating brush surface. These bioaerosols from bubble bottom aeration predominantly consisted of particles with sizes below 3.3 μm, particularly those with sizes in the range 1.1–2.1 μm. On the contrary, the bioaerosols produced via brush surface aeration predominantly consisted of particles with sizes above 3.3 μm. The distribution characteristics of population structure in the two aeration modes were consistent with the distribution characteristics of concentration in the corresponding models. Additionally, the results showed that when the aeration process is unaffected by environmental conditions (particle matters, wind direct, wind speed, etc.), the bioaerosol components originate primarily from the parent sewage or sludge, and do not diffuse far from the source point. Therefore, source reduction (capping or sealing) can be recommended as the primary control strategy for bioaerosols in sewage treatment plants. The adoption of such measures will significantly limit the diffusion of bioaerosols, thereby reducing the potential risks associated with human exposure.

A tropical soil Actinomycete, Gordonia amicalis HS-11, has been previously demonstrated to degrade unsaturated and saturated hydrocarbons (squalene and n-hexadecane, respectively) in an effective manner. In present study, G. amicalis HS-11 degraded 92.85 ± 3.42% of the provided diesel oil [1% (v/v)] after 16 days of aerobic incubation. The effect of different culture conditions such as carbon source, nitrogen source, pH, temperature, and aeration on degradation was studied. During degradation, this Actinomycete synthesized surface active compounds (SACs) in an extracellular manner that brought about a reduction in surface tension from 69 ± 2.1 to 30 ± 1.1 mN m⁻¹ after 16 days. The morphology of cells grown on diesel was monitored by using a Field Emission Scanning Electron Microscope. Diesel-grown cells were longer and clumped with smooth surfaces, possibly due to the secretion of SACs. The interaction between the cells and diesel oil was studied by Confocal Laser Scanning Microscope. Some cells were adherent on small diesel droplets and others were present in the non-attached form thus confirming the emulsification ability of this organism. The fatty acid profiles of the organism grown on diesel oil for 48 h were different from those on Luria Bertani Broth. The genotoxicity and cytotoxicity of diesel oil before and after degradation were determined. Cytogenetic parameters such as mitotic index (MI); mitosis distribution and chromosomal aberration (type and frequency) were assessed. Oxidative stress was evaluated by measuring levels of catalase, superoxide dismutase and concentration of malondialdehyde. On the basis of these studies it was deduced that the degradation metabolites were relatively non-toxic.

Rice fields significantly contribute to the global N₂O and NH₃ emissions. Nitrification inhibitors (NIs) show promise in decreasing N₂O emission, but they can increase NH₃ volatilization under traditional broadcasting. Root zone fertilization (RZF) can mitigate NH₃ volatilization, but it may pose a high risk to N₂O emission. Additionally, most chemical NIs have limited availability and potential for environmental contamination, in contrast, biological NIs, such as methyl 3-(4-hydroxyphenyl) propionate (MHPP), are easily available and eco-friendly. However, the effects of RZF combined with MHPP on N₂O and NH₃ emissions are unknown. Therefore, a field experiment was conducted in a Chinese rice field with five treatments at 210 kg urea-N ha⁻¹ (BC: 3-split surface broadcasting; BC + MHPP: BC with MHPP; RZ, root zone fertilization; RZ + MHPP, RZF with MHPP; RZ + MHPP + NBPT, RZF with MHPP and NBPT). The results showed that although RZ eliminated NH₃ volatilization, it significantly increased total N₂O emission by 761% compared with BC due to the stimulation of nitrification by mid-season aeration (MSA) and the trigger of denitrification by a large amount of NO₃⁻. Nearly 90% N₂O was emitted at MSA stage for RZF treatments, and their N₂O fluxes were exponentially related to the soil NO₃⁻-N concentrations in the 7–20 cm deep soil layer. RZ + MHPP greatly reduced the peak values of N₂O flux due to the suppression of nitrification by MHPP and then less production of NO₃⁻ for denitrification, its total N₂O emission was 79% lower compared with that of RZ. However, RZ + MHPP + NBPT further increased the total N₂O emission by 1044% compared with that of BC. Compared to BC, the RZF practice reduced total NH₃ volatilization by 88–92% regardless use of NIs. RZF had no influence on CH₄ emissions and enhanced the rice yields. In conclusion, RZF + MHPP is a promising strategy for simultaneously reducing N₂O and NH₃ emissions in rice fields.

Using hybrid packing materials in biofiltration systems takes advantage of both the inorganic and organic properties offered by the medium including structural stability and a source of available nutrients, respectively. In this study, hybrid mixtures of compost with either lava rock or biochar in four different mixture ratios were compared against 100% compost in a methane biofilter with active aeration at two ports along the height of the biofilter. Biochar outperformed lava rock as a packing material by providing the added benefit of participating in sorption reactions with CH4. This study provides evidence that a 7:1 volumetric mixture of biochar and compost can successfully remove up to 877 g CH4/m3·d with empty-bed residence times of 82.8 min. Low-affinity methanotrophs were responsible for the CH4 removal in these systems (KM(app) ranging from 5.7 to 42.7 µM CH4). Sequencing of 16S rRNA gene amplicons indicated that Gammaproteobacteria methanotrophs, especially members of the genus Methylobacter, were responsible for most of the CH4 removal. However, as the compost medium was replaced with more inert medium, there was a decline in CH4 removal efficiency coinciding with an increased dominance of Alphaproteobacteria methanotrophs like Methylocystis and Methylocella. As a biologically-active material, compost served as the sole source of nutrients and inoculum for the biofilters which greatly simplified the operation of the system. Higher elimination capacities may be possible with higher compost content such as a 1:1 ratio of either biochar or lava rock, while maintaining the empty-bed residence time at 82.8 min.

This study investigated the treatment performance and nitrogen removal mechanism of highly alkaline ammonia-stripped digestate effluent in horizontal subsurface flow constructed wetlands (CWs). A promising nitrogen removal performance (up to 91%) was observed in CWs coupled with intensified configurations, i.e., aeration and effluent recirculation. The results clearly supported that the higher aeration ratio and presence of effluent recirculation are important to improve the alkalinity and pollutant removal in CWs. The influent pH (>10) was significantly decreased to 8.2–8.8 under the volumetric hydraulic loading rates of 0.105 and 0.21 d−1 in the CWs. Simultaneously, up to 91% of NH4+-N removal was achieved under the operation of a higher aeration ratio and effluent recirculation. Biological nitrogen transformations accounted for 94% of the consumption of alkalinity in the CWs. The significant enrichment of δ15N-NH4+ in the effluent (47–58‰) strongly supports the occurrence of microbial transformations for NH4+-N removal. However, relatively lower enrichment factors of δ15N-NH4+ (−1.8‰ to −11.6‰) compared to the values reported in previous studies reflected the inhibition effect of the high pH alkaline environment on nitrifiers in these CWs.

Paddy soil plays an essential role in contributing to the emission of methane (CH₄), a potent greenhouse gas, to the atmosphere. This study aimed to demonstrate the effects of straw incorporation and straw-derived biochar amendment on CH₄ emissions from double-rice cropping fields and to explore their potential mechanisms based on in-situ field measurements conducted for a period of three years (2012–2014) and model analysis. The results showed that the improved soil aeration due to biochar amendment resulted in low CH₄ emissions and that sufficient substrate carbon availability in straw amendment treatments caused high CH₄ emissions. The newly developed CH₄ emission module for the water and nitrogen management model (WNMM), a process-based biophysical model, performed well when simulating both daily CH₄ fluxes and the annual cumulative CH₄ emissions under straw incorporation and biochar amendment. Results of our study indicate that the model has a great potential for upscaling and could benefit mechanism analyses about the factors regulating CH₄ emissions. Application of biochar into paddy fields provides a great opportunity to reduce CH₄ emissions, and the decrease in CH₄ emissions following biochar amendment with repeated crop cycles would sustain for a prolonged period.

Per- and polyfluoroalkyl substances (PFASs) were detected in the atmosphere of a source region in Tianjin, China. Fluorotelomer alcohols (FTOHs) were the dominant neutral PFASs in the atmosphere with total concentrations of 93.6-131 pg/m3 and 8:2 FTOH contributing the most, whereas perfluorooctane sulfonamide derivatives (PFOSAs) were two magnitudes lower or undetected. In comparison, ionic PFASs (perfluoroalkyl carboxyl acids (PFCAs)) in the atmosphere were detected at similar or even higher levels. At wastewater treatment plants (WWTPs), the air over influent was found with higher levels of FTOHs than over aeration tank and effluent; whereas in the air over the aeration tank, the concentrations of PFOSAs and nonvolatile ionic PFASs substantially increased, suggesting a possible direct release of ionic PFASs to the atmosphere besides the atmospheric conversion from volatile precursors. In the air phase, a low proportion (1-5%) of PFCAs was subjected to dry deposition in the source region. Interestingly, the dry-deposition-to-bulk-air ratios of PFCA analogues were the lowest at medium chain lengths (C8 and C9) and increased with either shorter or longer chain length. The extraordinary affinity of shorter-chain PFCAs (C6-C7) to particles was presumed to be due to their smaller molecular size favoring the interactions between the carboxyl head groups and specific sorption sites on particulate matter.