In this work, photocatalytic degradation of two reactive dyes, Reactive Yellow 84 (RY 84) and Reactive Black 5 (RB 5), on FeTiO₃/TiO₂ heterojunction in the presence of UV–visible radiation and H₂O₂ has been reported. FeTiO₃/TiO₂ heterojunction has been prepared from ilmenite FeTiO₃ and anatase TiO₂ by employing oxalic acid as an organic linker. FeTiO₃/TiO₂ ratios have been varied from 1 to 5 wt.%, and the materials were characterized by X-ray diffraction, scanning electron microscope and diffused reflectance UV–visible spectroscopic analysis. The photocatalytic activity of FeTiO₃/TiO₂ heterojunction for the degradation of the organic dyes RY 84 and RB 5 in the presence of UV–visible light was found to be higher than that of pure TiO₂. The addition of H₂O₂ increases the rate of degradation of both dyes on FeTiO₃/TiO₂ heterojunction. It facilitates the fast degradation of dye solutions even when their concentration was above 100 mg/l, which is otherwise very slow due to the low transmittance of light by the dye solution. The extent of mineralisation of the reactive dye during photocatalytic degradation was estimated from chemical oxygen demand analysis. FeTiO₃/TiO₂ heterojunction photocatalyst was also found to have good photostability; the material retains almost 97 % of its initial activity even in the fifth cycle.

The presence of macrolide antibiotics in aquatic environments causes serious antibiotic resistance propagation in microorganisms. In this study, the use of porous resins as adsorbents for the removal of tylosin from aqueous solutions was evaluated. The effectiveness of the resins (macroporous resin XAD-4, hypercross-linked resin MN-202, and aminated polystyrene resin MN-150) was compared with commercial hydroxylated multiwall carbon nanotubes (H-MWCNTs). Similar patterns of pH-dependent adsorption were observed despite the different surface properties and pore structures of the three resins, implying the importance of the tylosin molecular form in the adsorption process. Tylosin adsorption onto the four adsorbents showed different ionic strengths and temperature dependence consistent with the tylosin speciation and corresponding adsorption mechanism. The adsorption of tylosin onto the XAD-4 and MN-202 is mainly controlled by the intermolecular interactions between the matrix of the adsorbents and the tylosin molecule, whereas specific bonds among multiple surface functional groups are the predominant contributors to MN-150 and H-MWCNTs. The pore size is the key parameter in tylosin adsorption onto the surface of the adsorbents. The adsorption kinetics of the four adsorbents followed the pseudo-second-order model. The adsorption isotherm data well fit the Langmuir models, indicating surface coverage by a monomolecular layer.

Colistin is a peptide antibiotic widely used as a food additive in animal farming, specially swine and poultry, and also has recently been applied in human medicine to treat infections caused by multiresistant gram-negative bacteria strains. When orally administered, colistin is eliminated in feces virtually unaltered; thus, it may reach water bodies and wastewater treatment facilities in its active form. Apart from the risks associated with development of antimicrobial resistance and environmental toxicity issues, the presence of antimicrobials in wastewater can, additionally, interfere in biological processes commonly used to treat them. Nitrifying bacteria are among the most sensitive microorganisms to inhibitory compounds, including pharmaceuticals, and are useful as biosensors to access contaminant toxicity information in wastewater treatment plants. Therefore, in order to assess the colistin acute toxicity to the microorganisms involved in the nitrification processes, the nitritation and nitratation kinetics were monitored under different colistin concentrations. The results showed that only ammonia-oxidizing bacteria are sensitive to the antibiotic, presenting an IC50 of 10.8 mg L⁻¹ of colistin when used as a commercial formulation and 67.0 mg L⁻¹ when used as raw colistin sulfate. For nitrite-oxidizing bacteria, even the highest colistin concentration used in the assays (316 mg L⁻¹) was not sufficient to inhibit the process. According to these results, the colistin concentrations expected in animal farming wastewater, when its dosage is used as a growth promoter, would not be enough to keep nitrification from taking place. Nevertheless, when used in higher concentrations, such as for therapeutic purposes, it could endanger the maintenance of the process.

Coal mine methane is a significant greenhouse gas source as well as a potential lost energy resource if not effectively used. In recent years, mine ventilation air (MVA) capture and use has become a key element of research and development due to comparatively larger methane emissions by MVA than other coal mine sources. Technologies have been evaluated to treat the low methane concentrations in MVA such as thermal-based technologies or processing by biofiltration. This review initially considers the techniques available for treating the low methane concentrations encountered in MVA, after which it focuses on developments in biofiltration systems. Biofiltration represents a simple, energy-efficient, and cheap alternative to oxidize methane from MVA. Major factors influencing biofilter performance along with knowledge gaps in relation to its application to MVA are identified and discussed.

Robust and cheap, biofiltration is one of the most used methods for the biological treatment of industrial gaseous odours and VOCs emissions. The chemical, physical and microbial properties, as well as the economical impact of 11 organic and inorganic packing materials potentially suitable for biofiltration, have been investigated in order to select the most relevant for the treatment of rendering gaseous emissions. Fibrous materials such as peat and coconut fibres are predisposed to compaction. Moreover, according to their low expected running period, their implementation remains expensive, such as activated carbon which induce overweening costs (>100,000€ an -1 for the treatment of 40,000 m3 h-1 with a 60-s empty bed gas residence time). Considering economical aspects, physico-chemical and biological properties, pines barks, composted wood mulch and expanded schist seem fit for this application. The performance of these materials was therefore investigated in a pilot-scale study conducted on a rendering site. According to its appropriate pH (8.62) and water-holding capacity (1.41 g g-1) and its highest nutrients content and colonization at the biofilter start-up (93 g of ATP m-3, 29.10 13 CFU m-3), composted would mulch show the best odour removal efficiency during the 134 days of operation. Performances ranged between 75 and 93 % for the treatment of odourous inlet load between 1.16 and 10.10·106 ouE m-3 h-1 with an empty bed gas residence time of 47 s. However, the pressure drop of the compost bed decreased, suggesting structural changes which may impact the performances in the long term. © 2013 Springer Science+Business Media Dordrecht.

The use of Cu-based fungicide can pose a risk to nearby surface water bodies due to the run-off of accumulated Cu from agricultural soils. In 2008, we conducted a reconnaissance survey of the presence and concentration of copper in sediments at 18 sites within the Yarra River Catchment, an important horticultural production system in south-eastern Australia. Observed Cu concentrations in sediment samples from the study sites (mean (95 % confidence interval) 12.0 (10.6-13.6) mg/kg dry weight) were similar to the concentrations present in the samples from the reference sites (mean (95 % confidence interval) 12.0 (6.7-16.8) mg/kg dry weight). The data on Cu and other metals in the sediments suggest that that there is unlikely to have been wide spread, diffuse, off-site transport of Cu from the soils of horticultural properties to nearby surface waterways in the Yarra River Catchment and that that observed sediment metal concentrations are unlikely to pose an ecological risk to sediment-dwelling organisms at the study sites. © 2013 Springer Science+Business Media Dordrecht.

The effects of six phosphate (P) fertilizers in mobilizing and immobilizing water-soluble lead (Pb) were determined in a contaminated soil (Alfisol from Shaoxing) from China and four Australian soils (an Oxisol from Twonsville Queensland and three South Australian soils from Cooke Plains (Typic Palexeralf)), Inman Valley (Vertisol), and Two Wells (Natric Palexeralf). The fertilizers tested were single superphosphate (SSP), triple superphosphate (TSP), monoammonium phosphate (MAP), diammonium phosphate (DAP), monocalcium phosphate (MCP), and dicalcium phosphate (DCP) to produce an initial P concentration of 1,000 mg/L. The Chinese soil contained 16,397 mg/kg total Pb, but the Australian soils were uncontaminated. The four Australian soils were each spiked with 1,000 mg Pb/kg soil (as Pb(NO3)2) and incubated for a month. Single superphosphate treatments decreased total soluble Pb in soil solution to 2-14 % of those of the nil-P (0P) treatment in the four Pb-spiked soils and to 48 % in the Chinese Pb-contaminated soil. The DAP treatment followed by the MAP treatment greatly increased the total soluble Pb in soil solution up to 135-500 % of the 0P treatment, except in the Two Wells soil. MCP could decrease the total soluble Pb in Cooke Plains, Inman Valley, Shaoxing, and Two Wells soils while increase it in the Queensland soil; DCP decreased the total soluble Pb in Cooke Plains and Queensland soils while increased it in the Shaoxing and Inman Valley soils. There were close relationships between the total soluble Pb, total soluble Al, and total soluble Fe in the water extracts of each. Soluble Al and Fe ions in soil solution increased soluble Pb concentrations. We conclude that not all phosphate fertilizers immobilize Pb in soils equally well. SSP and TSP are excellent Pb-immobilizing fertilizers, while MAP and DAP are strong Pb-mobilizing fertilizers. MCP and DCP are either Pb-immobilizing fertilizers or Pb-mobilizing fertilizers depending on their reactions with individual soils. © 2013 Springer Science+Business Media Dordrecht.

Pathogens are the leading cause of water quality impairments as defined by the US Environmental Protection Agency and their transport within water bodies is poorly understood. Because of this, watershed-scale, water quality models often have poor bacterial prediction capabilities. To improve the understanding of in-stream bacterial transport, a cow pie was deposited in a recirculating flume with flows ranging from 0.0102 to 0.0176 m³ s⁻¹. Water samples were collected and analyzed for Escherichia coli concentration, E. coli attached fraction, and turbidity. E. coli concentrations ranged from 4.72 × 10³ to 1.70 × 10⁵ CFU 100 mL⁻¹ and turbidity ranged from 1.93 to 369 NTU over both locations and all times. The percentage of E. coli attached to particles ranged from an average of 2.9 to 31 % downstream of the fecal deposition point. Spearman correlation analysis demonstrated that bacteria concentrations were significantly related with water depth (ρ = 0.128, p = 0.018), and the concentration of attached bacteria was significantly correlated with both the total concentration of E. coli (ρ = 0.4081, p = 0.009) and turbidity (ρ = 0.3627, p = 0.0214). This analysis is useful to indicate parameters that should be considered when monitoring or predicting bacteria transport in streams.

A special sequential extraction (SE) procedure for mercury (Hg) was conducted to determine biogeochemical fractions of Hg and their controlling factors in four contaminated soil profiles located in two distinct floodplain ecosystems which differ in their industrial histories and thus in their Hg loads. The first study area is located at the Wupper River (Western Germany) and the soil profiles reveal sum of Hg (Hgₛᵤₘ) concentrations up to 48 ppm. The second study area is located at the Saale River (Eastern Germany) and the soil profiles have Hgₛᵤₘ concentrations up to 4.3 ppm. The majority of Hg was found in fraction IV (FIV, Hg⁰) for both study areas, indicating its anthropogenic origin. Moreover, we have detected Hg in fraction V (FV) and in fraction III (FIII). As Hg in FV is mostly associated with Hg sulfides being formed under reducing conditions, it indicates reduction processes which usually occurred during flooding. Mercury in FIII (organo-chelated Hg) exhibits a moderate mobility and a high methylation potential. Between Hg in FIII and hot-water-extractable carbon (CHWE) as a measure of easy degradable, labile soil organic matter, we found a significant correlation. Sum of Hg seem to have a high affinity to organic carbon (Cₒᵣg). The concentrations of Hg in the mobile and exchangeable fractions FI and FII were low. Moreover, the significant positive correlation between iron (Fe) and Hg in FIV indicate an interaction between Hg and Fe. The majority of the Hg in our soils is considered to be relatively immobile. However, since the formation of more mobile Hg species via oxidation or methylation might occur in floodplain soils, the low Hg concentrations in mobile fractions should not be underestimated due to their high mobility and potential plant availability.

Many airborne and soil-borne nanoparticles (NPs) can enter plants, which are the primary producers in the food chain; recently, studies on the genotoxic effects of NPs on plants are emerging. In the present study, the phytotoxic and genotoxic effects of ZnO and CuO NPs on buckwheat (Fagopyrum esculentum) seedlings were estimated. The inhibition of root growth and biomass at the tested concentrations of NP suspensions and dissolved free ion suspensions were compared. Changes in root morphological features and localization of NPs inside the root epidermis cells were observed. Growth of root treated with ZnO NPs (84.9 and 89.6 %) and CuO NPs (75.4 and 80.1 %) at 2,000 and 4,000 mg L -1, respectively, was decreased significantly than control. The root morphological features and NP incorporation into the root epidermal cells at a high dose of NP showed completely different patterns compared to those for the controls. Through random amplified polymorphic DNA assays for comparison of the effect of ZnO and CuO NPs on DNA stability, it was shown as different DNA polymorphisms at 2,000 and 4,000 mg L-1 of ZnO and CuO NPs, compared to those for controls. Our results provide the first clue to the genotoxic effects of ZnO and CuO NPs on early growth of edible plants such as buckwheat. © 2013 Springer Science+Business Media Dordrecht.