There is a pollution risk when disposing of post-remediation biomass from chelate-assisted metal phytoremediation. To assess this risk, we measured water extractable lead (Pb) in Brassica rapa tissues with ICP-MS, determined if chelated Pb was present with HPLC-MS, and identified Pb storage locations using electron microscopy with x-ray microanalysis. Ethylenediaminetetraacetic acid (EDTA) and ethylenediaminedisuccinic acid (EDDS) were used to enhance Pb movement from contaminated soil to above ground B. rapa tissues. With Pb-EDTA, 92 % (5) of Pb was water extractable from dried tissues and complexed as Pb-EDTA. Electron microscopy and x-ray microanalysis showed Pb stored in xylem vessels. After composting of plant tissues, 79 % (2) of Pb was water extractable and complexed as Pb-EDTA. Total plant Pb accumulation was lower from soils amended with EDDS, but only 6.7 % (0.3) of Pb was water extractable from dried tissues and 55 % (25) from wet tissues of plants grown in EDDS-amended soils. Pb-EDDS was detected in tissues but not at quantifiable levels. This work emphasizes the need for proper treatment and disposal of contaminated post-remediation plant tissues, especially when using EDTA. Composting of plant tissues containing Pb-EDTA was shown to significantly reduce waste material volume and slightly reduce the water extractable fraction, but further immobilization of Pb would be necessary to minimize transport risk. Amending Pb-contaminated soils with EDDS can result in plant biomass with a lower potential to leach Pb into groundwater, but the lower Pb accumulation with EDDS would require longer phytoremediation time compared with EDTA. © 2013 Springer Science Media Dordrecht.

Chemical reagents used by the textile industry are very diverse in their composition, ranging from inorganic compounds to polymeric compounds. Strong color is the most notable characteristic of textile effluents, and a large number of processes have been employed for color removal. In recent years, attention has been directed toward various natural solid materials that are able to remove pollutants from contaminated water at low cost, such as sugarcane bagasse. Cell immobilization has emerged as an alternative that offers many advantages in the biodegradation process, including the reuse of immobilized cells and high mechanical strength, which enables metabolic processes to occur under adverse conditions of pH, sterility, and agitation. Support treatment also increases the number of charges on the surface, thereby facilitating cell immobilization processes through adsorption and ionic bonds. Polyethyleneimine (PEI) is a polycationic compound known to have a positive effect on enzyme activity and stability. The aim of the present study was to investigate a low-cost alternative for the biodegradation and bioremediation of textile dyes, analyzing Saccharomyces cerevisiae immobilization in activated bagasse for the promotion of Acid Black 48 dye biodegradation in an aqueous solution. A 1 % concentration of a S. cerevisiae suspension was evaluated to determine cell immobilization rates. Once immobilization was established, biodegradation assays with free and immobilized yeast in PEI-treated sugarcane bagasse were evaluated for 240 h using UV–vis spectrophotometry. The analysis revealed significant relative absorbance values, indicating the occurrence of biodegradation in both treatments. Therefore, S. cerevisiae immobilized in sugarcane bagasse is very attractive for use in biodegradation processes for the treatment of textile effluents.

The accumulation of Ag by the marine herbivorous gastropod, Littorina littorea, has been studied in a series of exposures in which the metal was added in aqueous form and as nanoparticles, both in the presence and absence of contaminated algal food (Ulva lactuca). Significant accumulation occurred in the gill, kidney, stomach and visceral mass when the snail was exposed to aqueous Ag in the absence of food. Despite the consumption of U. lactuca that had been previously contaminated by Ag, no accumulation was observed from the dietary route. When added as nanoparticles, accumulation of Ag was only measured in the head and gill and only in the absence of contaminated food. These observations suggest that Ag is most bioavailable to L. littorina when in true solution and that Ag measured in external tissues of the snail following exposure to nanoparticles arises from some physical association that does not result in significant transfer of the metal to internal organs.

The recovery of Tween 80 from a liquid residue, obtained after washing of a contaminated soil with p-Cresol, was studied by selective adsorption of p-Cresol with activated carbons. A modified expression of the Langmuir equation was succesfully used to predict the adsorption isotherms of p-Cresol in the absence and presence of different surfactant concentrations. The presence of surfactant seems to modify the adsorption equilibrium, but it does not produce any significant influence on the adsorption kinetic of p-Cresol. A mathematical model was developed to predict the optimum activated carbon dosage demanded to reduce the p-Cresol concentration as a function of the surfactant concentration, also obtaining the corresponding surfactant loss. The regenerated solution was favorably used as washing solution in a new contaminated soil. These results indicate that this technique can be adequate to recover the surfactant solution, with a relatively minimal loss, for a subsequent application.

The present work explores the sorption capacity of an inexpensive and highly available agricultural waste, rice husk, to remove mercury using realistic concentrations of this metal. The efficiency of the process was evaluated for two initial Hg(II) concentrations, one representing the maximum value for Hg discharges from industrial sectors (0.05 mg L-1), and the other ten times higher. A very small amount of rice husk (0.25 and 0.50 g L-1) was able to reduce the Hg(II) levels in more than 80 % for an initial concentration of 0.05 mg L-1 and in more than 90 % for 0.50 mg L-1, corresponding to residual concentrations of Hg(II) of 0.048 and 0.009 mg L-1, respectively. The biosorvent was reused in further cleaning treatments, maintaining the efficiency and high performance. The sorption kinetics of the Hg-rice husk system is well fitted by the Elovich model and the diffusion models suggested that, depending on the initial Hg(II) concentrations, the sorption process can be controlled by intraparticle diffusion or by both film and intraparticle diffusion. The equilibrium data are well described by the linear isotherm and the distribution coefficient found was 36.1 L g-1. © 2013 Springer Science+Business Media Dordrecht.

Arsenic (As) adsorption onto metal oxide-precipitated clinoptilolite was investigated by using response surface methodology (RSM). Box-Behnken experimental design combined with RSM was used to examine and to optimize major process parameters. The quadratic statistical model was defined by three independent variables namely, pH (3-7), temperature (25-65 C), and initial arsenate (As(V)) concentration (0.5-9.5 mg L-1) while adsorption capacities of modified zeolites were designated as dependent variables. The iron oxide-precipitated zeolite (ZNa-Fe) was found to be more effective adsorbent when compared with aluminum oxide-modified one (ZNa-Al). The maximum As(V) adsorption capacities for ZNa-Fe and ZNa-Al were observed at pH 3.0 and pH 4.96, respectively. In the chosen range, higher adsorption capacities were achieved with increasing temperature, indicating the endothermic behavior of process for both samples. Initial As(V) concentration had a marked favorable effect on the amount of As(V) adsorbed onto adsorbents in the selected field. The constructed polynomial model was found significant, as was evident from the model F values (FZNa-Fe = 414.95 and F ZNa-Al = 167.17). The coefficients of determination values of second-order polynomial regression models were found as 0.9981 and 0.9953 for ZNa-Fe and ZNa-Al, respectively, indicating the accuracy and general availability of the model. © 2013 Springer Science+Business Media Dordrecht.

Normative regulations on benzene in fuels and urban management strategies are expected to improve air quality. The present study deals with the application of self-organizing maps (SOMs) in order to explore the spatiotemporal variations of benzene, toluene, ethylbenzene, and xylene levels in an urban atmosphere. Temperature, wind speed, and concentration values of these four volatile organic compounds were measured after passive sampling at 21 different sampling sites located in the city of Trieste (Italy) in the framework of a multi-year long-term monitoring program. SOM helps in defining pollution patterns and changes in the urban context, showing clear improvements for what concerns benzene, toluene, ethylbenzene, and xylene concentrations in air for the 2001–2008 timeframe.

In recent years, much attention has been devoted in developing inexpensive or alternative systems for treating acid mine drainage (AMD). Manganese is a common component of AMD, and it is traditionally removed by precipitation. However, in order to meet the standard limits for discharging, usually <1 mg L, it is necessary to raise the pH above 10 which implies in high consumption of reagents and a final pH that does not meet the required value for discharging. This study investigated the removal of manganese from an acid mine effluent and laboratory solutions by using an industrial residue consisted of manganese dioxide (MnO). The pH of the acid effluent is around 2.7, and the manganese concentration is approximately 140 mg L. Batch experiments assessed the influence of pH and the efficiency of manganese dioxide (MnO) in the Mn removal. In the presence of MnO, the metal concentration meets the discharging limit at pH range of 6.8 to 7.2. Experiments carried out with columns packed with MnO assessed the influence of the flow rate on the process. Best results were obtained for columns fed with mine water neutralized with limestone at pH 7.0 and a residence time of 3.3 h. The maximum manganese loading capacity for MnO was around 14 mg g. RAMAN spectroscopy showed that the MnO is essentially constituted of pyrolusite. In addition, the solid hausmannite (MnO) was observed on the surface of the MnO residue after its contact with the Mn solution.

The objective of this study is to investigate the potential impact of future climate change on ozone air quality in Europe. To provide a full assessment, simulations with the global chemical transport model GEOS-CHEM driven by the NASA Goddard Institute for Space Studies general circulation model (NASA/GISS GCM) are conducted. To isolate the effects from changes in climate and anthropogenic emissions four types of simulations are performed: (1) present-day climate and emissions (2) future climate following the IPCC Special Report on Emission Scenarios (SRES) A1B scenario and present-day anthropogenic emissions of ozone precursors (3) present-day climate and future emissions and (4) future climate and future emissions. Results indicate that climate change impact on its own leads to an increase of less than 3 ppb in western and central Europe whereas decreases are evident for the rest of the areas with the highest (about 2.5 ppb) in southeastern Europe (Italy, Greece). Increases are attributed to the increases of isoprene biogenic emissions due to increasing temperatures whereas decreases are associated with the increase of water vapor over sea which tends to decrease the lifetime of ozone as well as the increased wind speeds in the 2050 climate. When future emissions are implemented in the future climate simulations, the greatest increases are seen in the southwest and southeast Mediterranean (about 16 ppb) due to the increased isoprene biogenic emissions under higher levels of NO ₓ in the model. Decreases up to 2 ppb of ozone are shown for France, Switzerland, Northern Italy and northern Europe.

The use of aqueous suspension of nanoparticles of titanium dioxide for photocatalytic removal of pollutants is not suitable for industrial applications due to the inconvenient and expensive separation of nanoparticles of titanium dioxide for reuse. The nanosized titanium dioxide needs to be immobilized on the support for improving the efficiency and economics of the photocatalytic process. In the present paper, nanoparticles of titanium dioxide have been immobilized on the surface of the support using three different techniques. The immobilized films of titanium dioxide have been characterized using X-ray diffraction and scanning electron microscopy to notice any change in the phase composition and photocatalytic properties of the titanium dioxide after immobilization on the support. A photocatalytic test has been performed under similar reaction conditions to compare the photocatalytic performance of the films of immobilized titanium dioxide prepared using different techniques.