Wastewater Treatment for Carbon Dioxide Removal.

Wastewater treatment is notorious for its hefty carbon footprint, accounting for 1-2% of global greenhouse gas (GHG) emissions. Nonetheless, the treatment process itself could also present an innovative carbon dioxide removal (CDR) approach. Here, the calcium (Ca)-rich effluent of a phosphorus (P) recovery system from municipal wastewater (P recovered as calcium phosphate) was used for CDR. The effluent was bubbled with concentrated CO2, leading to its mineralization, i.e., CO2 stored as stable carbonate minerals. The chemical and microstructural properties of the newly formed minerals were ascertained by using state-of-the-art analytical techniques. FTIR identified CO3 bonds and carbonate stretching, XRF and SEM-EDX measured a high Ca concentration, and SEM imaging showed that Ca is well distributed, suggesting homogeneous formation. Furthermore, FIB-SEM revealed rhombohedral and needle-like structures and TEM revealed rod-like structures, indicating that calcium carbonate (CaCO3) was formed, while XRD suggested that this material mainly comprises aragonite and calcite. Results imply that high-quality CaCO3 was synthesized, which could be stored or valorized, while if atmospheric air is used for bubbling, a partial direct air capture (DAC) system could be achieved. The quality of the bubbled effluent was also improved, thus creating water reclamation and circular economy opportunities. Results are indicative of other alkaline Ca-rich wastewaters such as effluents or leachates from legacy iron and steel wastes (steel slags) that can possibly be used for CDR. Overall, it was identified that wastewater can be used for carbon mineralization and can greatly reduce the carbon footprint of the treatment process, thus establishing sustainable paradigms for the introduction of CDR in this sector.

Response behavior of antibiotic resistance genes and human pathogens to slope gradient and position: An environmental risk analysis in sloping cultivated land.

Soils, especially in farmlands, are key media for the transmission of antibiotic resistance genes (ARGs) and their hosts from the environment to humans. Sloping farmland is an important agricultural resource, but there lack of studies on the fate and risk of ARGs in sloping land. Also, the behavior and drivers of ARGs in response to slope gradient and position are unclear. Here, metagenomics was used to investigate the profiles of ARGs, mobile genetic elements, and microbial communities in soils from lands of five slope gradients (5°, 10°, 15°, 20°, and 25°) with two slope positions (uphill and downhill). Results showed that while the abundance (except 15°) and diversity (except 20°) of ARGs increased as the slope gradient increased, the diversity of ARGs with health risk, especially the high-risk ones, decreased. For slope positions, abundant and diverse ARGs were more likely to accumulate at downhill. Furthermore, 52 bacterial genera and 12 human pathogenic bacteria (HPB) species were identified as the potential hosts for ARGs with high risk, and abundant HPB species were also detected in the soils with low gradients at downhill. Moreover, the structural equation model analysis revealed that the slope gradient and the slope position have both direct and indirect effects on the abundance of ARGs. Further correlation analysis revealed that the slope gradient has a positive effect (p < 0.05) on nitrite nitrogen in the soils. Also, the slope position has a negative effect (p < 0.05) on total phosphorus and microbial nitrogen, while positively affected (p < 0.05) on particulate nitrogen and microbial carbon, which were the key factors driving the behavior of ARGs. Overall, this study provided comprehensive information on ARGs with health risks and their potential pathogenic hosts in sloping farmland. It can be important for controlling antibiotic resistance transmission and be consistent with the One Health framework.

Copper in different forms and tetracycline affect behavior and risk of antibiotic resistome in thermophilic anaerobic digestion of cattle manure.

The metagenomics-based behavior and risk of antibiotic resistance genes (ARGs) were investigated during cattle manure thermophilic anaerobic digestion with tetracycline and copper, namely, bulk-copper oxide, nano-copper oxide, and copper sulfate, which are common feed additives. Although bulk-copper oxide reduced ARGs' diversity, it enriched high-risk ARGs the most than the other two copper species, while copper sulfate could strongly mitigate the ARG risk by decreasing their abundances. Compared to corresponding individual effects, copper and tetracycline combinations may decrease ARGs' co-occurrence potential by 22.0%, and particularly, tetracycline combined separately with copper sulfate and nano-copper oxide reduces the ARGs' risk in abundance (by 7.2%) and human health (by 4.0%). These were mainly driven by bioavailable copper, volatile fatty acids, and pH, as well as the main potential hosts in phyla Firmicutes, Coprothermobacterota, and Euryarchaeota. Notably, the twin risks of pathogenicity and ARGs should be emphasized due to the ARGs' positive correlation with human pathogens of Clostridioides difficile and Arcobacter peruensis. These findings are important for understanding the potential ARGs' risk in treatments of livestock wastes containing feed additives of different sizes and speciation.

Effects of micron-scale zero valent iron on behaviors of antibiotic resistance genes and pathogens in thermophilic anaerobic digestion of waste activated sludge.

This work investigated the metagenomics-based behavior and risk of antibiotic resistance genes (ARGs), and their potential hosts during thermophilic anaerobic digestion (TAD) of waste activated sludge, enhanced by micron-scale zero valent iron (mZVI). Tests were conducted with 0, 25, 100, and 250 mg mZVI/g total solids (TS). Results showed that up to 7.3% and 4.8% decrease in ARGs' abundance and diversity, respectively, were achieved with 100 mg mZVI/g TS. At these conditions, ARGs with health risk in abundance and human pathogenic bacteria (HPB) diversity were also decreased by 8.3% and 3.6%, respectively. Additionally, mZVI reduced abundance of 72 potential pathogenic supercarriers for ARGs with high health risk by 2.5%, 5.0%, and 6.1%, as its dosage increased. Overall, mZVI, especially at 100 mg/g TS, can mitigate antibiotic resistance risk in TAD. These findings are important for better understanding risks of ARGs and their pathogenic hosts in ZVI-enhanced TAD of solid wastes.

Insights into the shift of microbial community related to nitrogen cycle, especially N2O in vanadium-polluted soil.

Soil is a vital contributor to the production of nitrous oxide (N2O), a potent greenhouse gas, through the nitrogen cycle, which can be influenced by accumulated vanadium (V) in soil but it is less pronounced. This work investigated the response of soil N2O fluxes along with major nitrogen cycle products (ammonium, nitrate, and nitrite) to different vanadium contents (0, 200, 500, 800, and 1100 mg V/kg), and the underlying microbial mechanisms. N2O fluxes was significantly influenced at high V content (1100 mg V/kg) due to its corresponding high water-soluble V content. Microbial composition and their correlations with nitrogen cycle products showed that microbes in dominant phyla (Actinobacteriota and Proteobacteria) and genus (Nocardioides, Lysobacter, Sphingomonas, and Marmoricola) might be the important contributor to N2O fluxes regardless of the V content. Moreover, high V contents (800, and 1100 mg V/kg) could enrich microbes involved in nitrogen cycle, but weaken their correlations with nitrogen-related products, such as in genus Bacillus, and change microbial correlation with N2O from associated with nitrate and nitrite to ammonium. Meanwhile, functional gene predication results showed that denitrifying genes nirKS and nosZ were negatively and positively correlated with V contents, respectively. These all further suggested that the shift of possible N2O metabolic pathways induced mainly by water-soluble V might be the underlying reason for N2O fluxes. These findings promote an understanding of the potential effect of metal pollution on N2O fluxes in soil.

Microplastics in aquatic systems, a comprehensive review: origination, accumulation, impact, and removal technologies.

Although the discovery of plastic in the last century has brought enormous benefits to daily activities, it must be said that its use produces countless environmental problems that are difficult to solve. The indiscriminate use and the increase in industrial production of cleaning, cosmetic, packaging, fertilizer, automotive, construction and pharmaceutical products have introduced tons of plastics and microplastics into the environment. The latter are of greatest concern due to their size and their omnipresence in the various environmental sectors. Today, they represent a contaminant of increasing ecotoxicological interest especially in aquatic environments due to their high stability and diffusion. In this regard, this critical review aims to describe the different sources of microplastics, emphasizing their effects in aquatic ecosystems and the danger to the health of living beings, while examining, at the same time, those few modelling studies conducted to estimate the future impact of plastic towards the marine ecosystem. Furthermore, this review summarizes the latest scientific advances related to removal techniques, evaluating their advantages and disadvantages. The final purpose is to highlight the great environmental problem that we are going to face in the coming decades, and the need to develop appropriate strategies to invert the current scenario as well as better performing removal techniques to minimize the environmental impacts of microplastics.

Particle size effects in microbial characteristics in thermophilic anaerobic digestion of cattle manure containing copper oxide.

Roles of bulk-, micron-, and nano-copper oxide (CuO) on methane production, microbial diversity, functions during thermophilic anaerobic digestion (AD) were investigated in this study. Results showed that bulk-, micron-, and nano-CuO promoted methane production by 27.8%, 47.6%. and 83.1% compared to the control group, respectively. Microbial community analysis demonstrated that different particle sizes could cause various shifts on bacteria community, while had little effect on archaeal diversity. Thereinto, bacteria belonging to phylum Firmicutes and Coprothermobacterota dominated in enhanced hydrolysis process in groups with nano-CuO and bulk-CuO, respectively, while micron-CuO had stronger promotion on the abundances of hydrolytic and fermentative bacteria belonging to families Peptostreptococcaceae, Caloramatoraceae, Erysipelotrichaceae, and Clostridiaceae, than other two CuO sizes. Metabolic pathways revealed that energy-related metabolism and material transformation in bacteria were only boosted by micron-CuO, and nano-CuO and bulk-CuO were important to methanogenic activity, stimulating energy consumption and methane metabolism, respectively.

Response behavior of antibiotic resistance genes to zinc oxide nanoparticles in cattle manure thermophilic anaerobic digestion process: A metagenomic analysis.

This work investigated the metagenomics-based behavior of antibiotic resistance genes (ARGs) during cattle manure anaerobic digestion with zinc oxide nanoparticles (ZnO NPs) that are commonly used as animal feed additives. The 6.6% decrease in total ARGs abundance while remained unchanged ARGs diversity with ZnO NPs (5 mg/g total solid), suggested ZnO NPs may mitigate ARGs risk by abundance. Also, ZnO NPs affected ARGs with mechanisms specifically of antibiotic inactivation and antibiotic target change, and declined potential hosts' abundance (bacterial genus Ruminiclostridium, Riminococcus, and Paenibacillus) which mainly contributed to the decreased ARGs' abundance. Besides, microbial chemotaxis decreased by 17% with ZnO NPs compared to that without nanoparticles indicated a depression on potential hosts, who could develop the mechanism to adapt to altered digestion conditions, which probably inhibited the ARGs' propagation. These findings are important to promote understanding of the potential ARGs risks in treatments of livestock wastes containing animal feed additives.

Photocatalytic inactivation of Escherichia coli bacteria in water using low pressure plasma deposited TiO2 cellulose fabric.

Fabrics obtained from cellulose spinning, extracted from Spanish broom, were coated with TiO2 film, through the low pressure plasma sputtering technique, in order to get antibacterial activity. The obtained fabrics were used for the photocatalytic degradation of Escherichia coli, by irradiation with UV-light emitting diodes (UV-LED), in a batch photocatalytic reactor. Before and after functionalization treatments, cellulosic substrates were chemically characterized by X-ray photoelectron spectroscopy (XPS) analyses. Water Contact Angle (WCA) measurements allowed obtaining information about the hydrophilicity of the materials, while their antibacterial efficiency was determined at several initial concentrations (from 103 up to 108 CFU mL-1) of bacteria in distilled water, bottled water and synthetic wastewater. It was found that photocatalytic reactions were capable of achieving up to 100% bacterial inactivation in 1 h of treatment, following a pseudo-first order kinetic model. No bacterial regrowth was observed after photocatalytic treatments in almost all experimental conditions. In contrast, during photolytic treatment (i.e. in the absence of the TiO2 coated fabrics) bacteria recovered their initial concentration after 3 h in the dark. Finally, the reusability of the plasma modified fibers to inactivate bacteria was studied.

The relationship between microstructure and photocatalytic behavior in lanthanum-modified 2D TiO2 nanosheets upon annealing of a freeze-cast precursor.

Titanium dioxide modified with 3 wt% La was prepared via a green freeze-casting method, and its photocatalytic activity was tested in terms of its ability to degrade 4-chlorophenol (4-CP) and remove total organic carbon (TOC). Under annealing conditions, the freeze-cast precursor was transformed into an La-modified anatase with a well-defined 2D TiO2 nanosheet morphology. Rietveld refinement of the X-ray diffraction patterns confirmed the substitutional nature of the La cation that induced local structural variations and involved subtle ion displacement in the TiO2 lattice due to the ionic size effect. Despite nearly identical tetragonal structures, replacement of Ti with La alters the photocatalytic activity through a reduction in band gap energies and an increase in charge carrier mobility. Material annealed at 650 °C exhibited the highest photocatalytic performance and achieved efficient TOC removal. Upon annealing at 800 °C, nanoscale lanthanum-enriched regions were generated due to the diffusive migration of La cations and phase transition from anatase to rutile. The La3+ cation, acting as a structural promoter, supported 2D TiO2 growth with well controlled crystallite size, surface area and porosity. La3+ could be regarded as a potential electronic promoter that can reduce the band gap of 2D TiO2 nanosheets and can provide a signature of the electron transfer and carrier charge separation. Both methods, kinetics of degradation of 4-CP and TOC, provided similar results, revealing that the photocatalytic activity under UV light irradiation increased in the order 950C < 500 °C < 800 °C < 650 °C < TiO2-P25.

Solid-state polymer membranes for simple, sensitive, and low-cost monitoring of mercury in water.

Solid-state Hg(II) selective membranes were produced and assessed by means of X-ray absorption near edge structure in the total reflection X-ray fluorescence (TXRF-XANES) setup and by the energy dispersive X-ray fluorescence (EDXRF) technique. Membranes were functionalized using four promising ligands for mercury complexation, i.e.: i) 4-(2-Pyridylazo) resorcinol (PAR), ii) thiourea, iii) calconcarboxylic acid (CCS), and iv) dithizone. A simple analytical procedure was followed, using miniscule reagent quantities, thus suggesting the process is also cost-effective. TXRF-XANES revealed that mercury complexes with the ligands, and is not simply adsorbed onto the PVC matrix, while the complexation was found to not be affected by the matrix existence. Mercury exhibited an increased oxidation grade and was covalently bound to the ligand functional groups, via a strong chemical bond. EDXRF revealed that the solid-state membranes can be used for mercury speciation and trace analysis from environmentally relevant matrices, such as tap water. The membranes could be a promising alternative to polymer inclusion membranes (PIMs), due to their simple configuration and high Hg (II) selectivity in aqueous media, but more research is needed. PAR appears to be the most promising ligand, followed by dithizone and thiourea. CCS had a minuscule preconcentration efficiency since it was preferably bound with Cu in tap water, indicating limited usefulness for mercury preconcentration. However, results suggest that, depending on the ligand, the solid-state membranes could be also possibly used for multi-elemental heavy metals analysis in water.

Removal of Endocrine Disrupting Chemicals from Water: Adsorption of Bisphenol-A by Biobased Hydrophobic Functionalized Cellulose.

The aim of this study is to examine the efficiency of biobased Spanish broom (SB) surface modified cellulose fibers to remove bisphenol A (BPA), a well-known endocrine disruptor, from water. Spanish brooms are flowering plants, which are native and abundant to Mediterranean regions. The functionalized fibers (FF) were found to have the best adsorption efficiency at pH 5, due to the optimal hydrophobic interaction between the FF fiber and BPA. Adsorption kinetics of BPA was found to fit well a pseudo-second order reaction. Equilibrium isotherm data were fitted by Langmuir and Freundlich models. A very fast and simple regeneration method was developed and it was observed that adsorption capacity of the fibers was kept almost unchanged after 3 consecutive uses. Bottled water and synthetic wastewater were also tested to assess the efficiency of the process under more realistic water and wastewater treatment conditions. It was found that BPA removal was slightly decreased from 77% in ultrapure water to 64% in synthetic wastewater matrix, indicating that FF has a high selectivity toward BPA, even in the presence of other organic compounds. Overall, it was observed that SB-modified fibers can be a new promising green biotechnology for water purification.

Assessing the sustainability of acid mine drainage (AMD) treatment in South Africa.

The environmental sustainability of acid mine drainage (AMD) treatment at semi-industrial scale is examined by means of the life cycle assessment (LCA) methodology. An integrated process which includes magnesite, lime, soda ash and CO2 bubbling treatment was employed to effectively treat, at semi-industrial scale, AMD originating from a coal mine in South Africa. Economic aspects are also discussed. AMD is a growing problem of emerging concern that cause detrimental effects to the environment and living organisms, including humans, and impose on development, health, access to clean water, thus also affect economic growth and cause social instability. Therefore, sustainable and cost effective treatment methods are required. A life cycle cost analysis (LCCA) revealed the viability of the system, since the levelized cost of AMD treatment can be as low as R112.78/m3 (€7.60/m3 or $9.35/m3). Moreover, due to its versatility, the system can be used both at remote locales, at stand-alone mode (e.g. using solar energy), or can treat AMD at industrial scale, thus substantially improving community resilience at local and national level. In terms of environmental sustainability, 29.6 kg CO2eq are emitted per treated m3 AMD or its environmental footprint amount to 2.96 Pt/m3. South Africa's fossil-fuel depended energy mix and liquid CO2 consumption were the main environmental hotspots. The total environmental footprint is reduced by 45% and 36% by using solar energy and gaseous CO2, respectively. Finally, AMD sludge valorisation, i.e. mineral recovery, can reduce the total environmental footprint by up to 12%.

Environmental sustainability of the solar photo-Fenton process for wastewater treatment and pharmaceuticals mineralization at semi-industrial scale.

The environmental sustainability of a semi-industrial solar photo-Fenton reactor, treating real effluents emanating from a pharmaceutical laboratory, is assessed herein. The life cycle assessment/analysis (LCA) methodology was employed and real life cycle inventory (LCI) data was collected from a ferrioxalate-assisted homogeneous solar photo-Fenton wastewater treatment plant (WWTP), at Ciudad Real, Spain. Electricity was provided by photovoltaic (PV) panels in tandem with a battery bank, making the plant autonomous from the local grid. The effective treatment of 1m3 of secondary-treated pharmaceutical wastewater, containing antipyrine, was used as a functional unit. The main environmental hotspot was identified to be the chemical reagents used to enhance treatment efficiency, mainly hydrogen peroxide (H2O2) and to a smaller degree oxalic acid. On the other hand, land use, PV panels, battery units, compound parabolic collectors (CPC), tanks, pipes and pumps, as materials, had a low contribution, ranging from as little as 0.06% up to about 2% on the total CO2eq emissions. Overall, the solar photo-Fenton process was found to be a sustainable technology for treating wastewater containing micropollutants at semi-industrial level, since the total environmental footprint was found to be 2.71kgCO2m-3 or 272mPtm-3, using IPCC 2013 and ReCiPe impact assessment methods, respectively. A sensitivity analysis revealed that if the excess of solar power is fed back into the grid then the total environmental footprint is reduced. Depending on the amount of solar power fed back into the grid the process could have a near zero total environmental footprint.

A novel use of the caesium-137 technique to estimate human interference and historical water level in a Mediterranean Temporary Pond.

The sustainability of, and the effects of human pressures on, Omalos Mediterranean Temporary Pond (MTP), Chanea, Greece was assessed. The (137)Cs technique was used to identify alleged anthropogenic interference (excavation) in the studied area. It was found that about one third of the ponds bed surface material had been removed and disposed of on the northeast edge, confirming unplanned excavations that took place in the MTP area some years ago. Nonetheless, five years after the excavation, the MTP's ecosystem (flora and fauna) had recovered, which indicates that these small ecosystems are resilient to direct human pressures, like excavations. Moreover, with the (137)Cs technique it was possible to identify the historical water level of Omalos MTP, when the fallout from the Chernobyl accident reached this area, in May of 1986. Therefore, the (137)Cs technique can be useful in the identification of the historical water level of small MTPs and other ephemeral water bodies. Applications include the verification and validation of hydrological models.

Recovery of antioxidants from olive mill wastewaters: a viable solution that promotes their overall sustainable management.

Olive mill wastewaters (OMW) are rich in water-soluble polyphenolic compounds that show remarkable antioxidant properties. In this work, the recovery yield of compounds, such as hydroxytyrosol and tyrosol, as well as total phenols (TPh) from real OMW was investigated. Antioxidants were recovered by means of liquid-liquid solvent extraction. For this purpose, a laboratory-scale pilot unit was established and the effect of various organic solvents, namely ethyl acetate, diethyl ether and a mixture of chloroform/isopropyl alcohol, on process efficiency was investigated. It was found that the performance of the three extraction systems decreased in the order: ethyl acetate > chloroform/isopropanol > diethyl ether, in terms of their antioxidant recovery yield. It was estimated that treatment of 1 m(3) OMW with ethyl acetate could provide 0.247 kg hydroxytyrosol, 0.062 kg tyrosol and 3.44 kg of TPh. Furthermore, the environmental footprint of the whole liquid-liquid extraction system was estimated by means of the life cycle assessment (LCA) methodology to provide the best available and most sustainable extraction technique. From an environmental perspective, it was found that ethyl acetate and diethyl ether had similar environmental impacts. Specifically, for the production of 1 g hydroxytyrosol, tyrosol or TPh, 13.3, 53.1 or 0.949 kg CO2 equivalent would be released to the atmosphere, respectively. On the other hand, the chloroform/isopropyl alcohol mixture had detrimental effects onto ecosystems, human health and fossil fuels resources. In total, ethyl acetate yields low environmental impacts and high antioxidant recovery yield and thus it can be considered as the best solution, both from the environmental and technical point of view. Three alternative scenarios to improve the recovery performance and boost the sustainability of the ethyl acetate extraction system were also investigated and their total environmental impacts were estimated. It was found that with small process modifications the environmental impacts could be reduced by 29%, thus achieving a more sustainable antioxidants recovery process.

Photoelectrocatalytic disinfection of water and wastewater: performance evaluation by qPCR and culture techniques.

Photoelectrocatalytic oxidation (PEC) was evaluated as a disinfection technique using water and secondary treated wastewater spiked with Escherichia coli and Enterococcus faecalis. PEC experiments were carried out using a TiO(2)/Ti-film anode and a zirconium cathode under simulated solar radiation. Bacterial inactivation was monitored by culture and quantitative polymerase chain reaction (qPCR). Inactivation rates were enhanced when the duration of the treatment was prolonged and when the bacterial density and the complexity of the water matrix were decreased. E. coli cells were reduced by approximately 6 orders of magnitude after 15 min of PEC treatment in water at 2V of applied potential and an initial concentration of 10(7) CFU/mL; pure photocatalysis (PC) led to about 5 log reduction, while electrochemical oxidation alone resulted in negligible inactivation. The superiority of PEC relative to PC can be attributed to a more efficient separation of the photogenerated charge carriers. Regarding disinfection in mixed bacterial suspensions, E. coli was more susceptible than E. faecalis at a potential of 2V. The complex composition of wastewater affected disinfection efficiency, yielding lower inactivation rates compared to water treatment. qPCR yielded lower inactivation rates at longer treatment times than culture techniques, presumably due to the fact that the latter do not take into account the viable but not culturable state of microorganisms.

Inactivation of Bacillus anthracis in water by photocatalytic, photolytic and sonochemical treatment.

Bacillus anthracis is one of the most dangerous and pathogenic bacterial species and its intrusion in aquatic environments is a serious threat to public health. The aim of the present study was to investigate inactivation rates of B. anthracis in water by means of photocatalytic (UVA/TiO2), photolytic (UVC) and sonochemical treatment. The effect of various operating conditions such as bacterial concentration, TiO2 loading, UV irradiation source, ultrasound power and treatment time was examined. The reference strain of B. anthracis proved to be highly resistant during photocatalytic and sonochemical treatment of aquatic samples, even in the presence of hydrogen peroxide solution, which is considered among the chemical disinfectants recommended for B. anthracis removal from aqueous suspensions. UVC irradiation was far more effective, as it achieved total inactivation in short treatment time (10 min) and at high initial concentrations (10(6) CFU mL(-1)). The effectiveness of UVC irradiation is also reinforced by the fact that no photoreactivation occurred even after 72 h of exposure under sunlight after the end of the treatment. Furthermore, the virulence of residual cells was investigated, targeting two genes carried in the plasmids pXO1 and pXO2, respectively, which are required for a fully virulent type. Interestingly, the plasmid pXO2 seems to be lost from the host after photocatalytic and photolytic disinfection, resulting in apathogenic residual strains contained in the treated sample. Overall, our results highlight the importance of B. anthracis efficient inactivation in water, as it shows considerable resistance towards effective and reliable disinfection techniques.

Removal of faecal indicator pathogens from waters and wastewaters by photoelectrocatalytic oxidation on TiO(2)/Ti films under simulated solar radiation.

PURPOSE: The disinfection efficiency of water and secondary treated wastewater by means of photoelectrocatalytic oxidation (PEC) using reference strains of Enterococcus faecalis and Escherichia coli as faecal indicators was evaluated. Operating parameters such as applied potential (2-10 V), initial bacterial concentration (10(3)-10(7) CFU/mL), treatment time (up to 90 min) and aqueous matrix (pure water and treated effluent) were assessed concerning their impact on disinfection. METHODS: PEC experiments were carried out using a TiO(2)/Ti film anode and a zirconium cathode in the presence of simulated solar radiation. Bacterial inactivation was monitored by the culture method and real-time SYBR green PCR. RESULTS: A 6.2 log reduction in E. faecalis population was achieved after 15 min of PEC treatment in water at 10 V of applied potential and an initial concentration of 10(7) CFU/mL; pure photocatalysis (PC) led to only about 4.3 log reduction, whilst negligible inactivation was recorded when the respective electrochemical oxidation process was applied (i.e. without radiation). PEC efficiency was generally improved increasing the applied potential and decreasing initial bacterial concentration. Regarding real wastewater, E. coli was more susceptible than E. faecalis during treatment at a potential of 5 V. Wastewater disinfection was affected by its complex composition and the contained mixed bacterial populations, yielding lower inactivation rates compared to water treatment. Screening the results obtained from both applied techniques (culture method and real-time PCR), there was a discrepancy regarding the recorded time periods of total bacterial inactivation, with qPCR revealing longer periods for complete bacterial reduction. CONCLUSIONS: PEC is superior to PC in terms of E. faecalis inactivation presumably due to a more efficient separation and utilization of the photogenerated charge carriers, and it is mainly affected by the applied potential, initial bacterial concentration and the aqueous matrix.

Inactivation of Enterococcus faecalis by TiO2-mediated UV and solar irradiation in water and wastewater: culture techniques never say the whole truth.

In this work, the disinfection efficiency of water and secondary treated wastewater by means of UV-A, UV-C and solar irradiation in the presence or absence of TiO(2), using a reference strain of Enterococcus faecalis as faecal indicator, was evaluated. Operating parameters such as TiO(2) loading (0-1500 mg L(-1)), initial bacterial concentration (2 × 10(2)-10(8) CFU mL(-1)) and treatment time (up to 120 min) were assessed concerning their impact on disinfection. E. faecalis inactivation was monitored by the conventional culture method and real-time PCR. Regarding photocatalytic treatment, disinfection efficiency was improved by increasing TiO(2) concentration and bacterial inactivation took place in relatively short treatment times. Comparing the three disinfection methods, it was observed that UV-C irradiation yielded a better efficiency during water treatment than UV-A and solar irradiation. Furthermore, UV-A was more efficient than solar irradiation in the presence of the same loading of TiO(2). Regarding real wastewater, it was observed that only UV-C irradiation was capable of totally inactivating E. faecalis population in a short time. Screening the results obtained from both applied techniques (culture method and real-time PCR), there was a discrepancy, regarding the recorded time periods of total bacterial inactivation. Real-time PCR data revealed that longer periods are needed for 100% bacterial reduction during the treatments tested compared to the estimated time by culture method. This is probably attributed to the phenomenon of "viable but not culturable bacteria", caused by stressed conditions induced during disinfection experiments. Taking into account the contrast of results and in order to perform a thorough evaluation of disinfection techniques, conventional culture method should be accompanied by a DNA-based method. According to our findings, real-time PCR proved to be a reliable and accurate molecular tool for the identification and quantification of bacterial indicators, like E. faecalis, in aquatic samples after disinfection treatment.