The oxidation of di-(2-ethylhexyl) phthalate (DEHP) in solution using UV/H₂O₂ and direct UV photolysis are analyzed in this study. It was found that DEHP was 100% removal in the solution by 180-min UV/H₂O₂ treatment and 73.5% removal by 180-min direct UV photolysis. The effect of different factors, such as DEHP concentration, H₂O₂ concentration, and UV light intensity, on photochemical degradation was investigated. The degradation mechanism of DEHP and the acute toxicity of intermediates were also studied. The photochemical degradation process was found to follow pseudo-first-order kinetics. The results of our study suggested that the concentration with 40 mg/L H₂O₂ and 5 μg/mL DEHP in the solution at pH 7 with 10.0 × 10⁻⁶ Einstein l⁻¹ s⁻¹ UV was the optimal condition for the photochemical degradation of DEHP. The photochemical degradation with UV/H₂O₂ can be an efficient method to remove DEHP in wastewater.

Prairie grasslands are very species rich but have declined in their extent considerably due to land-use change and exploitation. Many remaining prairie fragments are situated within an agricultural matrix and can be subjected to high levels of atmospheric ammonia deposition from animal units. Three prairie fragments in Minnesota that were located in close proximity to feedlots were selected, and 500-m transects were studied at an increasing distance from the feedlot. Changes in soil pH, soil nitrate concentration, and soil ammonium concentration with increasing distance from the source were variable between the sites, possibly due to differences in the processing of nitrogen in the soil and the degree of nitrogen limitation. Species richness showed significant negative relationships with ammonia deposition and soil nitrate concentration, whereas aboveground biomass showed a positive relationship with ammonia deposition. Both the richness and biomass of nongraminoid species declined with increasing soil nitrate concentration, whereas graminoid biomass was positively related to ammonia deposition and was negatively associated to richness. Bromus inermis, a non-native perennial grass, was the main species that increased at high deposition. The results of this study have important implications for the conservation and restoration of prairie grasslands.

This study aimed to understand the seasonal and spatial variations of N₂O emissions from newly created littoral marshes in the drawdown area of the Three Gorges Reservoir (TGR), China. We measured N₂O emissions at 10-day intervals during the growing season (early July to late September) in 2008. N₂O emissions were measured with static chambers in four typical vegetation stands. The results showed great spatial variations of N₂O emissions among the four stands. The greatest N₂O emissions (0.052 ± 0.063 mg N₂O m⁻² h⁻¹) were from Scirpus triqueter stand, while the lowest N₂O emissions (0.020 ± 0.020 mg N₂O m⁻² h⁻¹) were from Typha angustifolia stand. To such spatial variations in N₂O emissions, standing water depths and soil water content may be important explaining factors. Besides spatial variations, we also found significant temporal variations of N₂O emissions in this area. The temporal variation of N₂O emissions in the growing season was not found significantly related to any measured factor in the study. However, based on principal component analysis, we consider it partly caused by thermal conditions and the marked temporal variation of the standing water depth in the growing season, which to some degree influenced the process of denitrification and N₂O emissions. These results about TGR enable us to make a more reasonable estimate of N₂O emissions from large dam reservoirs, particularly those with a large drawdown area in the growing season in an agricultural landscape.

The use of two new ligands, (1Z)-1-(4-aminophenyl) ethan-1-one semicarbazone (L¹) and (1Z)-1-(4-nitrophenyl)ethan-1-one semicarbazone (L²), was evaluated for their potential use as chelators in increasing phytoremediation effectiveness. The uptake of heavy metals by Teddy Bear sunflowers increased when L¹ added at 0.1 and 0.3 g/kg. Metal uptake selectivity was Cr > Ni ≫ Cd for each treatment. The 0.1-g/kg L¹ ligands produced a significant uptake of metals in Sundance sunflowers. The 0.3-g/kg L¹ level increased the metal uptake, but it was lower than 0.1-g/kg L¹ treatment. The uptake selectivity with L² ligand was Cr > Ni > Cd, with the majority of metals retained in the roots. L¹ ligand was better compared in comparison to L² ligand for enhancing uptake of metals.

The increasing number of degraded soil areas caused by open cast mining activities has brought about a critical damage to the environment. The mine spoil must be ameliorated with anthropogenic interferences which consist of revegetating soils after organic matter amendment and provision of microbial diversity, to guarantee basic conditions for a sustainable soil biological activity. Five woody species, Acacia mangium Willd., Inga edulis Mart., Mimosa caesalpiniaefolia Benth, Parkia multijuga Benth., and Schinus terebinthifolia Schlecht. & Cham were cultivated under greenhouse conditions to evaluate the potential of plant establishment on cassiterite mining waste, considering the contribution of mycorrhizal fungi inoculation, organic compost, and thermophosphate amendment. The shoot height, dry weight, and nitrogen and phosphorus shoot contents were determined. Three species of nodulating legumes, A. mangium, M. caesalpiniaefolia, and S. terebinthifolia showed a great positive response to organic compost, termophosphate, and mycorrhizal inoculation, increasing the plant height and the shoot dry weight. Plants inoculated with arbuscular mycorrhizal fungi and fertilized with organic compost also increased their nitrogen and phosphorus shoot contents. The addition of organic compost and mycorrhizal fungi were essential for plant development and the reforestation of mining areas should be initiated with mycotrophic and nodulating legumes.

The article presents results of a case study in northeastern Germany, where magnetic susceptibility assessment was carried out at grid-wise field measurements. The measurements were clustered into three different depth levels, which represent the humus layer, the transition zone between humus layer and mineral horizon, and the mineral horizon. Taking these three depth levels, a multiple regression-based regionalization approach was applied, testing and using additional environmental parameters derived from geology, topography, and stand type with the aim to develop a comprehensive model for spatial variability of magnetic susceptibility. Spatial variation of magnetic susceptibility was predicted with a high precision by the multiple linear regression models. A slightly differing set of model parameters was selected for the single depth levels. In tendency, magnetic susceptibility values in depth level 6-10 cm were best explained by the distance to Bitterfeld and by soil properties. In depth level 11-15 cm, variables which describe the orographic conditions and stand properties gain in importance. In depth level 21-25 cm, variables indicating soil and site properties disappear completely. Here, aspect and land surface characteristics play a major role together with stand properties. A spatial stratification of the model for a distance of up to 25 km to the former emitters provided a further improvement of the model quality considering the prediction of small-scale variations of magnetic susceptibility.

Amine-functionalized SiO₂/TiO₂ photocatalytic films have been synthesized using the peroxo titanic acid (PTA) approach coupled with the sol-gel dip-coating method. The 3-aminopropyl-trimethoxysilane (APTMS) and methyltrimethoxysilane (MTMOS) were employed as the amine functional groups and silica precursor. The effects of the ratio of APTMS/MTMOS, PTA refluxed time, and pH of prepared sol on the characteristics and the formaldehyde degradation efficiency were investigated. Physicochemical properties of prepared photocatalysts were characterized with nitrogen adsorption-desorption isotherm measurement, SEM, X-ray diffraction (XRD), UV-vis spectrophotometer, and Fourier transform infrared (FTIR) spectroscopy. The XRD and FTIR results indicated that the obtained photocatalysts consisted of -NH₂ groups, SiO₂, and anatase TiO₂. The photocatalytic films showed high transmittance of 80-90% in the visible light region. The obtained film prepared with the APTMS/MTMOS ratio of 0.03, pH of 1.8, and 10 h of refluxed time possessed high specific surface area (604.0 m² g⁻¹) and 85% formaldehyde degradation efficiency. The enhancement of formaldehyde degradation efficiency was observed when increasing the PTA refluxed time. The repeatability of photocatalytic film was also tested, and the degradation efficiency was 92.0% of initial efficiency after seven cycles.

The adsorption and photocatalytic degradation of methyl orange (MO) aqueous solution under visible light illumination by polythiophene/titanium dioxide (PTh/TiO₂) composite particles were studied. The experimental observations from UV-vis spectrophotometer indicate that MO molecules were degraded in a different degree during the visible light-induced photocatalysis reaction. We propose a new degradation mechanism of MO during the photocatalytic reaction, based on blue shift of UV-vis absorption spectra of MO solution and other researches. The data from total organic carbon analyzer definitely prove that MO can be mineralized to CO₂ and H₂O, and some intermediate products are generated during the photocatalysis degradation of MO.

Polycyclic aromatic hydrocarbons (PAHs); their derivatives nitro, and methyl-PAHs; n-alkanes; and organic acids were investigated in the aerosol samples collected during two field campaigns conducted at three sampling stations in an industrialized city in southern Italy. The main sources affecting the atmosphere and its toxicity were investigated by means of the diagnostic ratios of: specific particulate-phase PAHs, marker compounds among nitro-PAHs, alkanes, and acids, the dominant wind direction, daily and seasonal abundance of carcinogenic organic substances. The potential importance of the non-regulated pollutants to assess the air quality was confirmed; in fact the carcinogenic organic compounds showed to have scarce correlation with particulate matter (PM) concentration. An exceptionally high variability of toxic compounds at a daily scale was due to meteorological condition causing periods of extremely high pollution levels.

The removal of chlorinated benzenes (CBs) from the compartments and from polluted industrial sites is of great public interest for the decontamination of polluted water and for the protection of the environment. Biological degradation could be considered as a feasible process to eliminate these compounds from the environment as soil or groundwater. A research program in progress since the year 2007 was initiated to investigate the capacity of eco-remediation of CB-contaminated groundwater using a pilot-scale subsurface flow constructed wetland. In order to assess the removal efficiency of these compounds and to evaluate the biological activities, column experiments were performed. The fate of three CBs was investigated by feeding spiked tap water through laboratory columns filled with two different solid-state materials: peat and pozzolana. In order to stimulate biological activity, organic matter coming from aged vertical flow constructed wetland was added to the media. Concentrations of CBs in water effluent and in air and biological activities were monitored during 4 months. At the end of the experimental period, CB concentrations in the depth of columns were determined and a mass balance was calculated for the CBs. Removal efficiencies of the laboratory columns were >98% in the peat columns and situated around 87% to 95% in the pozzolana columns, indicating the suitability of the experimental systems for the removal of CBs. Higher effluent CB concentrations from the pozzolana columns were detected. Concentration of CBs in ambient air indicates that volatilization was low. ATP monitoring, reduction of tetrazolium violet, and exopolysaccharide determination indicated considerable biological activity with variations according to column depth and carrier material.