The synthesis, characterization, and photocatalytic evaluation of titania-loaded MCM-41 with and without Au doping are reported in the present study. The samples were characterized by powder XRD, TEM, low temperature N₂adsorption/desorption, UV–Vis, and FTIR. UV-induced vapor-phase photo-oxidation of acetone was used as a probe reaction to study the role of Au in mineralization of volatile organic compounds (VOCs), viz. acetone at different concentrations. The doping of Au in titania-loaded MCM-41 resulted in the decrease of BET surface area, total pore volume, and average pore size. UV–Vis diffuse reflectance spectra of Au-doped titania-loaded MCM-41 showed the red shift in their absorption bands compared to titania-loaded MCM-41. The activity of mineralization of acetone by photocatalysis for 2 % Au-doped titania-loaded MCM-41 was found to be ∼1.6 times higher than titania-loaded MCM-41. The presence of cocatalytic nanosized gold might be responsible for their enhanced activity on account of the delayed recombination of electron/hole pair. Although, almost complete mineralization of acetone was observed irrespective of the initial concentration of acetone in air (up to 3.72 mol%) by all the catalysts, 2 wt.% Au-doped titania-loaded MCM-41 has shown the most enhanced activity.

Different cases of bioremediation technique were experimentally investigated here for decontaminating light non-aqueous phase liquid (LNAPL)-polluted groundwater collected from Panipat oil refinery situated in Haryana, India. Natural biodegradation of toluene, the selected LNAPL, was studied first under different varying substrate concentrations at room temperature (21.6 ± 0.3 °C). Biostimulation was then studied by mixing the polluted groundwater with a primary treated domestic wastewater for providing nutrients and other supplementary components to the native microbial population. For studying the remaining cases, small-scale wetland having plants of Canna generalis was developed in the laboratory with and without the presence of toluene in the rhizosphere. The wetland system in the presence of toluene was used here for developing the pre-grown microbial cultures to enhance the degradation rate of the LNAPL (bioaugmentation). The plant-assisted biostimulation was studied in the third case by adding the polluted groundwater with the root zone water of the wetland system developed without the presence of toluene. In the fourth case, the biostimulation was coupled with the bioaugmentation strategy by mixing the groundwater with the root zone water of the wetland system developed in the presence of toluene. A comparative account of these four different bioremediation techniques was prepared for their respective rates of biodegradation, duration of lag phases, and the total time of degradation. It was observed that the plant-assisted bioremediation techniques had better performance over the natural biodegradation and biostimulation methods of the considered LNAPL. The plant-assisted biostimulation coupled with the bioaugmentation technique needed almost no acclimatization time and accelerated the rate of degradation almost twofold compared to the natural bioremediation and, hence, is proved to be the best one among the other bioremediation techniques for decontaminating the LNAPL-polluted groundwater. The results of the conducted experiments can be used to obtain vital information on framing the engineered bioremediation planning for LNAPL-contaminated sites.

Textile industry is responsible for a large amount of polluted water released daily, mainly due to the dyes used. This article has aimed to study and improve methodologies for degrading textile effluents containing the dyes Acid Red 151 and Acid Blue 40 using an electrolytic reactor. Different solutions were prepared for the experiments in the electrolytic reactor with a 70 % TiO₂/30 % RuO₂anode. The textile effluents underwent 0 (control), 3, and 30 min treatment intervals. A suspension of Saccharomyces cerevisiae cells was used for toxicity tests and performed at the same day that samples were collected. The same test was applied to the samples after 15 days resting in order to verify changes in toxicity. The electrolytic treatment successfully removed the color in all effluents. However, the process efficiency varies according to the dye used and the experimental conditions, such as current and NaCl concentration. Also, it was observed that treatments longer than 30 min are very toxic to S. cerevisiae cells because of the high concentration of Cl₂.

The scope of this study was to investigate the uptake of chromium and nickel by onions (Allium cepa) and potatoes (Solanum tuberosum) and their impact on plant enzymes catalase (CAT, E.C. 1.11.1.6) and peroxidase (POX, E.C. 1.11.1.7). A greenhouse experiment was conducted, simulating the irrigating conditions existing in the two biggest tuber-producing regions of Greece (Asopos and Messapia). Plants were cultivated for 4 months in six irrigation lines, each one supplied by an aqueous solution, containing levels of Cr(VI) and Ni(II) ranging from 0 μg/L (control) to 1,000 μg/L. Significant statistical correlations were observed between (i) the levels of heavy metals in plants, (ii) the levels of heavy metals in plants and in irrigation water, and (iii) the levels of heavy metals and the enzymatic activities in plants. The existing EU legislation has no legal limits for Ni and Cr in food, and the nutritional implications of this study are discussed.

Filtration can be a convenient technique for removing phosphorus (P) at on-site wastewater treatment facilities to recycle this non-renewable element. When testing potentially suitable materials for these filters, the properties of the influent and the method used to analyse measured effluent concentrations both affect the P binding capacity determined in filter tests and therewith filter longevity predictions. At present, there is a lack of robust methods for material investigation and filter test interpretation. This study was conducted to investigate the effect of inflow PO₄–P concentrations (concentration) and hydraulic surface load (load) on P binding capacity and to analyse possible interpretations of laboratory filter tests. A 2²factorial experiment with replicates was performed on the calcium-based filter material Filtra P. The investigated concentrations ranged from 12 to 50 mg L⁻¹and loads from 419 to 1,023 L m⁻² day⁻¹. P binding capacity (calculated by mass balance including data until PO₄–P breakthrough point) was negatively affected by concentration and positively affected by load, with the effect of concentration being slightly greater. Depending on the factors' settings and on the method of evaluation (i.e. analysing all pre-saturation data or considering only pre-breakthrough results), the total measured P binding capacity varied between 2.2 and 9.0 g kg⁻¹. The part of the breakthrough curve between the breakthrough point and saturation contributed significantly to the measured P binding capacity, and it took about three times longer for the filters to become saturated than to reach breakthrough. Furthermore, a considerable amount of P that had reacted with the filter material was washed out of the filters as particle-bound P. This indicates that it is important to determine both the PO₄–P and the particle-bound P phases in the filter effluent.

The majority of consumer products used today are comprised of some form of plastic. Worldwide, almost 280 million t of plastic materials are produced annually, much of which ends up in landfills or the oceans (Shaw and Sahni Journal of Mechanical and Civil Engineering 46–48, 2014). While plastics are lightweight, inexpensive, and durable, these same qualities can make them very harmful to wildlife, especially once they become waterborne. Once seaborne, plastics are most likely found circulating in one of five major ocean gyres: two in the Pacific, one in the Indian, and two in the Atlantic. These ocean garbage patches are not solid islands of plastic; instead, they are a turbid mix of plastics (Kostigen 2008; Livingeco 2011). Recent research conducted on the surfaces of the Great Lakes has identified similar problems (Erikson et al. Marine Pollution Bulletin, 77(1), 177–182, 2013). A growing concern is that once plastics reach the wild, they may cause entanglement, death from ingestion, and carry invasive species. Several cutting edge technologies have been piloted to monitor or gather the plastics already in our environments and convert them back into oil with hopes to reduce the damage plastics are causing to our ecosystems.

Petroleum hydrocarbons are among the most important contaminants in aquatic ecosystems, but the effects of different petroleum components on the archaeal communities in these environments are still poorly investigated. Therefore, the effects of representative alkanes, polycyclic aromatic hydrocarbons and crude oil on archaeal communities from marine (Massambaba Beach) and hypersaline waters (Vermelha Lagoon) from the Massambaba Environmental Protection Area, Rio de Janeiro, Brazil, were examined in this study. Hydrocarbon contamination was simulated in vitro, and the resulting microcosms were temporally analyzed (4, 12 and 32 days after contamination) using molecular methods. DNA and RNA extractions were followed by polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) analyses and by the further molecular identification of selected DGGE bands. Archaeal communities could not be detected in the marine microcosms after contamination with the different hydrocarbons. In contrast, they were detected by DNA- and RNA-based methods in hypersaline water. Dendrogram analyses of PCR-DGGE showed that the archaeal communities in the hypersaline water-derived microcosms selected for by the addition of heptadecane, naphthalene or crude oil differed from the natural ones observed before the hydrocarbon contaminations. Principal coordinate analysis of the DGGE patterns showed an important effect of incubation time on the archaeal communities. A total of 103 DGGE bands were identified, and phylogenetic analysis showed that 84.4 % and 15.5 % of these sequences were associated with the Euryarchaeota and Crenarchaeota groups, respectively. Most of the sequences obtained were related to uncultivated archaea. Using redundancy analysis, the response of archaeal communities to the type of hydrocarbon contamination used could also be observed in the hypersaline water-derived microcosms.

Sorption–desorption behavior of the antibiotic tetracycline (TET) and the synthetic estrogen hormone 17α-ethinylestradiol (EE2) with wastewater sludge and sludge-derived humic substances [humic acid (HA) and humin] was investigated. From acidic functional group capacity and elemental analyses, HA had higher polarity, aromaticity, and acidity than humin; humin contained aliphatic chains with high mineral content. The different physicochemical properties of the pharmaceuticals and sludge components yielded different kinds of sorption–desorption interactions. Partitioning coefficients (Kd) of TET to sludge were higher (1,552 ± 41–4,667 ± 41 L/kg) than EE2 (534 ± 52–609 ± 47 L/kg). TET sorption was highly pH-dependent and maximal at pH 9. Ca²⁺ions enhanced sorption, emphasizing the role of polyvalent metal ions in forming TET–sludge complexes. Humin was the dominant component for TET sorption due to its high inorganic matter content. In contrast, EE2 sorption was independent of solution pH, forming mostly hydrophobic interactions with sludge organic matter. EE2 had a high affinity for HA due to its chemical structure. Desorption of the two pharmaceuticals differed as well. The amount of desorbed TET (18.7 ± 1.3–29.8 ± 2 %) was lower than that of EE2 (60.6 ± 3–62.3 ± 2 %), and the hysteresis index was higher for TET than EE2. While TET desorption tended to be delayed in the solid matrix, EE2 desorbed easily and in accordance with the aqueous equilibrium concentration. The conclusions emphasize the need for further research into frequently used pharmaceuticals with different physicochemical properties and the recognition of sludge application as an important source of distribution for these contaminants in the environment.

This is the first study that investigates in detail the effect of different sulfate concentrations on trichloroethene-dechlorinating microbial communities, both in terms of dechlorinating performance and microbial composition. The study used a series of Dehalococcoides-containing trichloroethene-dechlorinating microbial communities, which operated for more than 800 days in the presence of different sulfate concentrations and limiting-electron donor conditions. This study proves the ability of Dehalococcoides spp., the only genus able to completely dechlorinate trichloroethene, to predominate in mixed anaerobic microbial communities regardless of the magnitude of sulfate concentration, even under limiting-electron donor conditions. Although other microorganisms, such as the Sulfurospirillum spp. bacteria and members of the sulfate-reducing bacteria group were able to thrive, they were not able to predominate in such a competitive environment. However, this picture was not reflected in reductive dechlorination, which demonstrated a much better performance under methanogenic conditions or in the presence of low sulfate concentration (30 mg/l) than in the presence of higher sulfate concentrations (>400 mg/l). Therefore, different species of Dehalococcoides or other dechlorinating bacteria, which are not able to thrive in the presence of high sulfate concentrations (>400 mg/l), are possibly responsible for the higher dechlorination efficiency that was observed under methanogenic conditions.