Photocatalysis is one of environment-friendly and efficient methods for municipal wastewater disinfection. In this research, two pathogens, Staphylococcus aureus and fecal coliform, were chosen to investigate the disinfection effects of several TiO₂ photocatalysts on sewage plant secondary treatment effluent, compared with UV disinfection. The results show that TiO₂ species and concentrations, light intensity, light time, and pH all have significant influences on the pathogen deactivation. It was found that the optimum operation parameters were as follows: the P25 commercial TiO₂ powder at the concentration of 0.5 g/L, the light intensity of 40 W, and the radiation duration of 20 min. The photocatalyst performed better at either acid or alkaline condition than neutral. The TiO₂ photocatalytic deactivation to S. aureus was more effective than the UV.

A significant amount of artificial radionuclides has been introduced into the environment in the last century during atmospheric nuclear weapons tests and the Chernobyl accident. In this study, we investigated the temporal changes of concentrations and amounts of these radionuclides (⁹⁰Sr and ¹³⁷Cs) in surface water and river bed sediments. In order to evaluate the artificial radionuclide contamination diminution, we used and compared two different approaches: using a kinetic equation of the first order and, if needed, dividing the monitored period into two intervals, and in addition expressing the whole process in one equation with a series of exponential functions. Effective ecological half-lives were estimated as rates of decrease. In most cases, the ecological processes were proven to affect the radionuclide removal from the hydrosphere besides their radioactive decay. Furthermore, based on the assessment made, the ⁹⁰Sr and ¹³⁷Cs data were extrapolated and the radionuclide concentrations, which occurred in the hydrosphere after the fallout deposition in 1986, were estimated.

Eutrophication related to excess phosphorus (P) loadings continues to be an important issue for watersheds in North Carolina and other regions. Identifying the contributing sources of P in nutrient-sensitive waters is important for improving water quality. Prior studies have indicated that onsite wastewater treatment systems (OWS) can be a contributing source of P to surface waters, but more information is needed regarding their contribution relative to other wastewater treatment technologies. The goal of this study was to determine if P concentrations in groundwater and surface water were significantly different in a coastal plain watershed served by OWS in comparison to a watershed served by a municipal sewer system (MWS). Groundwater P concentrations were monitored at ten residential sites (five5 OWS and five MWS) once during each season (four times), and stream P concentrations and watershed exports were monitored monthly for 1 year (August 2011–August 2012). Groundwater in the OWS watershed had higher P concentrations than the MWS watershed. Stream P concentrations and P exports were also elevated in the OWS watersheds. However, the OWS were more efficient at reducing P prior to surface water discharge than the wastewater treatment plant that served the MWS watershed. The site-scale and watershed-scale P treatment efficiencies of OWS were between 73 and 99 %, whereas P treatment efficiency for the wastewater treatment plant was 54 %. While the OWS were efficient at reducing P concentrations and loads, OWS were still significant sources of P exports from the studied watershed. Potential contributions of P from OWS should be included in watershed nutrient management strategies along with other known sources such as agriculture and urban runoff if the strategies are to be considered comprehensive.

The elimination of five selected emerging contaminants (1-H-benzotriazole, N,N-diethyl-m-toluamide (DEET), chlorophene, 3-methylindole, and nortriptyline HCl) dissolved in different water matrices (surface water and secondary effluents) was carried out by sequential membrane filtration and chemical oxidation processes. First, a membrane filtration (ultrafiltration (UF) or nanofiltration(NF)) pre-treatment was conducted, and both permeate and retentate were afterwards treated by chemical oxidation, using ozone or chlorine. The application of UF and especially of NF provided a large volume of permeate, whose quality can be improved by a chemical treatment to completely remove residual contaminants except 1-H-benzotriazole. Chlorination and especially ozonation have demonstrated to be effective for the reduction of emerging contaminants in the concentrated stream, thus generating an effluent that might be recycled to the activated sludge treatment in the wastewater treatment plants (WWTP). In a second group of experiments, a chemical oxidation pre-treatment (by using ozone, chlorine, O₃/H₂O₂, ultraviolet (UV) radiation, or UV/H₂O₂) was applied followed by a nanofiltration process. Results of removals and rejection coefficients for the emerging contaminants showed that the chemical pre-treatment exerted a positive influence on the subsequent NF process, not only in terms of ECs removal but also of dissolved organic carbon content (DOC) reduction. While global removals higher than 97 % were reached for DEET, chlorophene, 3-methylindole, and nortriptyline HCl, lower values were obtained for 1-H-benzotriazole, especially for chlorine pre-treatment and in those water matrices with high content of natural organic matter. Therefore, both sequential treatments are promising to remove the selected micropollutants while reducing the chlorine doses needed to achieve final water disinfection.

Lead contamination remains a persistent global environmental problem, the hazards of which are often difficult to identify without specific and targeted research. This study examines environmental contamination arising from the widespread use of lead solder in the joints of large gravity water supply pipelines. Contamination of adjacent grazing lands and subsequent poisoning of domestic livestock are evaluated. In particular, the study demonstrates that replacement of lead joints along an above ground 70 km water supply pipeline in central New South Wales (NSW), Australia, has caused soil lead contamination of up to 20,600 mg/kg. Contamination either side of the pipeline corridor extends to ∼10 m before surface soil lead values correspond more closely to natural background concentrations of 26 mg/kg. The estimated total volume of contaminated soil requiring remediation is 21,000 m³. Contamination is linked to toxicity and mortality in several farm animals and to elevated contamination of grass fodder (up to 50 mg/kg of lead) close to the pipeline. Other similar large-scale above ground reticulation systems in the Sydney (NSW) Metropolitan region and adjacent to the 560 km long Kalgoorlie (Western Australia) Golden Pipeline are shown to present similar environmental hazards. The use of lead solder joints in other international large scale reticulation networks are also identified, demonstrating that this specific anthropogenic hazard is likely to be a more global problem, which has not has been detailed in the research literature to any significant extent.

A study has been conducted to enhance fluoranthene degradation by combining biodegradation with hydrogen peroxide oxidation, as a chemical oxidant calcium peroxide has been used. The impacts of addition of calcium peroxide on microbial activity (phenol oxidase and acid phosphatase) as well as fluoranthene removal efficiency were investigated. It was observed that in the presence of calcium peroxide, the removal efficiency of fluoranthene on day 30 of the experiment was threefold higher as compared to a reference sample. It was found that the activity of phenol oxidase was stimulated on days 1, 7, and 14, by the presence of fluoranthene, whereas stimulation of the acid phosphatase activity in the samples of soil contaminated by fluoranthene was observed only after 14 days of the experiment. This may indicate that the induction period for this enzyme is longer compared with the induction period for phenol oxidase. The inhibition of the activity of both enzymes was observed in the presence of calcium peroxide.

Solar Photo-Fenton reaction, using FeSO₄ and H₂O₂, is an effective and energy-efficient advanced oxidation process (AOP) for degradation of pesticides. However, a major environmental concern is whether the net toxicity after the photo-Fenton process is within the tolerance limit of the aquatic plants and animals, since the unreacted pesticide and Fenton’s reagent may impart additional toxicity to the treated water. Here, we report the oxidative removal of dichlorvos pesticide in wastewater by solar photo-Fenton reaction along with the residual toxicity analysis of the treated water on an aquatic alga. It was found that at pH 3, dichlorvos, with an initial concentration of 6.9 × 10⁻⁵ mol L⁻¹, was observed to be fully degraded within a batch time of 120 min, though the corresponding reduction of chemical oxygen demand (COD) was about 53 % signifying incomplete mineralisation. In order to predict the transient concentration profiles of dichlorvos under different initial concentrations, a four-parameter mathematical model was formulated. Additionally, the resultant toxicity was also examined using a model blue-green alga Nostoc sp. Compared to the raw wastewater, the net biomass of chlorophyll-a was found to increase significantly. Respective estimate of the protein concentration also indicated the same trend. Therefore, sunlight-assisted photo-Fenton process may be regarded as an effective and safe technique for the treatment of pesticide-contaminated agricultural wastewater.

Thifluzamide fungicide is widely used to protect rice (Oryza sativa) against the sheath blight fungus (Rhizoctonia solani). The continuous application of thifluzamide may lead to accumulation in soil and contaminate rice crop. To sustain the environment, it is necessary to assess its accumulation and degradation in field. The method limit of detection (LOD) was 0.022 ng. The limits of quantitation detection (LOQ) were 5.0 μg L⁻¹in water and 4.0 μg kg⁻¹in paddy soil and rice crop. In this study, a 2-year (2011–2012) field study was performed to monitor thifluzamide degradation in the rice production areas of Nanjing, Xiaoxian, and Changsha. The degradation dynamics of thifluzamide in paddy water, paddy soil, and rice crop were well described by the first-order kinetics equation. The 2-year average half-lives of thifluzamide in paddy water, paddy soil, and rice crop were 26.19, 17.92, 14.61 days (Nanjing), 15.63, 20.71, 9.10 days (Xiaoxian), and 9.47, 13.92, 10.08 days (Changsha), respectively. Thifluzamide degraded more rapidly in rice crop than in soil and paddy water. The variation in thifluzamide degradation was attributed to the difference in rainfall during the period of rice cultivation. The maximum residue of thifluzamide in brown rice was 0.0303 mg kg⁻¹in Nanjing and the residue of thifluzamide in brown rice was not detected in other two sites before thifluzamide was applied at pre-harvest. The experimental data demonstrated that thifluzamide recommended dosage of 72 g a.i.ha⁻¹can be used in rice fields with less than three times within a 30-day time interval.

Bioindicators are useful in monitoring air pollution. This study assessed the efficacy of various tree leaf morphological, physiological and biochemical biomarkers in reflecting different intensities of air pollution. Leaves from Brachylaena discolor trees growing 0, 2.5, 6 and 11 km from an industrial hub (pollution source) in eThekwini, South Africa, were analysed for leaf area, chlorophyll (Chl) content, superoxide and hydrogen peroxide (H₂O₂) production, electrolyte leakage, total antioxidant activity and concentration of selected minerals. B. discolor saplings grown under greenhouse conditions served as an ex situ control. Surface SO₂ and NOₓ levels which were measured at the in situ and control sites declined significantly with increasing distance from the source but were below detectable limits at the control site. At the site closest to the source, leaf area was significantly lower and Chl, electrolyte leakage, and copper (Cu) and phosphorous (P) levels were significantly higher than the control. Leaf area was significantly positively, and Chl content significantly negatively, correlated with distance from the source, while H₂O₂ production, electrolyte leakage and Cu and P concentrations were all significantly negatively correlated with distance from the source. The aforementioned parameters represent potential biomarkers of air pollution in B. discolor and in some cases (e.g., H₂O₂ and electrolyte leakage; leaf area and leaf Chl content) should be measured in conjunction with each other to accommodate for interactive effects. Using B. discolor leaves as bioindicators of air pollution may represent a more viable option for monitoring air pollution than monitoring stations.

Disposing of nitrate-containing effluents from seawater-fed intensive aquacultural applications is a major environmental problem. A possible solution is to mix nitrate-rich effluents from marine recirculating aquaculture systems (RASs) with citrate-rich liquid wastes (CLW), a common by-product of the food industry. Where possible, such strategy can alleviate two environmental problems simultaneously, in a cost-effective fashion. However, concerns are often raised regarding secondary pollution stemming from the use of CLW, particularly related to phosphorus and heavy metals. This work showed that both phosphorus and heavy metal were completely absorbed by the bacterial sludge generated in the process, indicating low environmental risk associated with the disposal of the treated effluent to the environment. Operation of continuous stirred-tank reactor (CSTR) single-sludge denitrification reactor with CLW as electron and carbon donor resulted in high nitrate removal efficiency (>95 %) and denitrification rate of up to 1.6 g NO₃-N L⁻¹reactor day⁻¹along with low bacterial biomass yield [0.23 g chemical oxygen demand (COD) new cells g⁻¹COD citrate]. Moreover, the use of CLW was found to be environmentally safe and equally efficient to the use of traditional, costly carbon sources such as methanol and acetic acid, rendering this alternative attractive for treatment of nitrate-rich saline effluents.