Twenty-one plant leaf materials were screened for benzene adsorption efficiency in the static system, and the leaf material from Dieffenbachia picta, Acrostichum aureum, Ficus religiosa, Lagerstroemia macrocarpa, Alstonia scholaris, and Dracaena sanderiana were found to have high potential for benzene removal. The relation between quantity and composition of wax to benzene removal efficiency was studied. Although high quantities of wax occurred in some leaf materials, low benzene removal was clearly found if compared with other plant materials with the same wax quantity. Alpha-linoleic acid and dodecyl cyclohexane were found to be the main composition in plant leaf materials with high benzene adsorption, and it might be a key factor for benzene removal.

Measurements of solute dispersion in porous media is generally much more time consuming than gas dispersion measurements performed under equivalent conditions. Significant time savings may therefore, be achieved if solute dispersion coefficients can be estimated based on measured gas dispersion data. This paper evaluates the possibility for estimating solute dispersion based on gas dispersion measurements. Breakthrough measurements were carried out at different fluid velocities (covering the same range in Reynolds number), using O₂ and NaCl as gas and solute tracers, respectively. Three different, granular porous materials were used: (1) crushed granite (very angular particles), (2) gravel (particles of intermediate roundness) and (3) Leca® (almost spherical particles). For each material, 21 different particle size fractions were used. Gas and solute dispersion coefficients were determined by fitting the advection–dispersion equation to the measured breakthrough curves and in turn used to calculate gas and solute dispersivities as a function of mean particle size (D ₘ) and particle size range (R) for the 63 particle size fractions considered. The results show that solute and gas dispersivities are related and that their ratio depends on both R and D ₘ. Based on these observations a simple model for predicting the dispersivity ratio from D ₘ and R, was proposed.

In Asturias (north of Spain), mercury mining has been identified as a potential source of trace elements such as As, Sb, Pb, and Hg. In particular, at Los Rueldos mine site, some of these contaminants are dissolved in acidic mine drainage (AMD). Here we treated this leachate by means of nanofiltration to remove some of its pollutants. In order to improve our understanding of the geochemical factors involved in nanofiltration, we analyzed sediment geochemistry and the origin of acidic waters. In coherence with the observation of similar behaviors of As, Fe, and Al in the nanofiltration tests, a clear geochemical association between As, Sb, S, and Fe both in sediments and in the occurrence of AMD was detected. The FILMTEC™ NF-2540 membrane used in this study proved to be highly suitable for the treatment and concentration of the metallic and semimetallic contaminants in the acidic water, even at low pH and moderate pressures.

The comparative and competitive adsorption of Cr(VI) and Ni(II) in single and binary systems using coconut shell activated carbon (CSAC) was investigated. The CSAC was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM). The effects of pH, initial metal concentration, and temperature on the adsorption of metal ions were studied. Cr(VI) removal was found to be maximum (94.5 %) at pH = 2.0. While, Ni(II) removal was found to be maximum at pH = 9.0 (58.92 %). The adsorption capacity of Cr(VI) was greater than that of Ni(II) in single component system. Parameters of adsorption isotherm model, kinetics, and thermodynamics were calculated. The single ion equilibrium adsorption data were fitted to the Langmuir, Freundlich and Dubinin-Radushkevich (D-R) isotherm models. The Langmuir and Freundlich models represented the equilibrium data better than the D-R model. The result of the fitting of D-R isotherm model indicated a physical adsorption process. The adsorption kinetic data of Cr(VI) and Ni(II) were found fitting well in pseudo second-order equation both in single and binary system (r 2 > 0.99) and intraparticle diffusion was the rate controlling step. The negative ΔG and the positive ΔH indicated the spontaneous and endothermic nature of the adsorption process. The extended Langmuir isotherm model fitted well with the competitive adsorption data of Cr(VI) and Ni(II). For the desorption experiments, EDTA showed the maximum desorption efficiency of 69 % for Cr(VI) and 81 % for Ni(II). © 2013 Springer Science+Business Media Dordrecht.

Ammonia emission from broiler houses is a major concern because of its impacts on the environment. To reduce ammonia emissions, it is necessary to understand the fate of ammonia/um in the broiler waste. In broiler waste, uric acid and urea hydrolyze to ammonia (NH₃) and a fraction of NH₃ converts to ammonium (NH₄ ⁺) depending on pH and temperature. Further, NH₄ ⁺ undergoes solid–liquid partitioning and the ammonia fraction is partitioned among the solid, liquid, and gas phases in the waste. Ammonium partitioning between solid and liquid phases in broiler cake and litter were measured at pH of 4, 6, and 7. Ammonium adsorption increased with pH in both broiler litter and cake. Adsorption capacity of the litter was much lower than broiler cake. Six NH₄ ⁺ adsorption/desorption isotherms (linear, Langmuir, Freundlich, Temkin, Redlich–Peterson, and Toth) were evaluated. The isotherm that provided the best fit for partitioning NH₄ ⁺ in litter or cake for each pH value was selected by comparing up to six sets of parameters modeled using linear and nonlinear (with five error functions) regressions. Despite high R ² values obtained using linear regression, linearizing the models introduced an offset into the model reducing their accuracy. The sum of normalized error was used to select the most suitable parameter set for each isotherm. While the nonlinear error functions were the more suitable for developing parameter sets in broiler litter, for cake, linear regression generally provided the most optimum parameter sets. Whereas the Freundlich, linear, and Temkin isotherms were the most suitable for broiler litter for pH of 4, 6, and 7, respectively, for the cake, the linear isotherm was the most suitable for the entire range of pH evaluated. Overall, due to its simplicity, the linear isotherm seems suitable for partitioning NH₄ ⁺ in the adsorbed and dissolved phases for simulating nitrogen fate and dynamics in broiler waste more accurately.

The processes of wind erosion of fertile soil, dune movement in sand deserts, dust storms in arid and semi-arid regions, as well as the emission and dispersion of agricultural or industrial dusts create a lot of problems and dangers for human life, environment, and infrastructure. Conventional ways to suppress dust emission to the atmosphere are agricultural fixation in the case of fertile soil surface and application of chemical agents to immobilize dust particulates onto the surface of soil, desert sand, country roads, or mining areas. However, these methods are often too expensive to be applied for large-scale suppression of sand dust. Chemical methods of dust suppression are often environmentally unfriendly due to the release of toxic reagents in water, air, and soil. This paper examines, for the first time, the microbially mediated aggregation of fine sand particles to suppress the emission of sand dust and its chemical and bacteriological pollutants. The bioaggregation reagent was a solution of calcium chloride and urea sprayed over the sand surface, which was preliminarily treated with the suspension of urease-producing bacteria. Quantity of calcium used for sand dust suppression was 15.6 g of Ca/m2. After the biotreatment of fine sand, the release of sand dust and its artificial pollutants to the atmosphere decreased in comparison with control by 99.8 % for dust, 92.7 % for phenantherene, 94.4 % for led nitrate, and 99.8 % for bacterial cells of Bacillus megaterium. This immobilization of dust and dust pollutants was due to the bioaggregation of fine sand particles. The sizes of 90 % of the sand dust particles increased from 29 μm in control to 181 μm after bioaggregation. Bioaggregation treatment of the soil surface could be a useful method to prevent the dispersion of dust and dust-associated chemical and bacteriological pollutants in water, air, and soil. © 2013 Springer Science+Business Media Dordrecht.

The characterisation of plant responses to metal exposure represents a basic step to select a plant species for phytoremediation. In the present work, 3-week-old Amaranthus paniculatus L. plants were subjected to nickel chloride concentrations of 0 (control), 25, 50, 100 and 150 μM in hydroponic solution for 1 week to evaluate morphophysiological responses, such as biomass production and partitioning, nickel accumulation in plants and nickel removal ability from the polluted solutions. The results showed a progressive decrease in plant organ dry mass with the enhancement of nickel (Ni) concentration in the solution, suggesting a good metal tolerance at 25 μM Ni and a marked sensitivity at 150 μM Ni. The modification of biomass partitioning was particularly appreciated in leaves, analysing the organ mass ratio, the total leaf area and the specific leaf area. Amaranthus plants accumulated a significant amount of Ni in roots exposed to the highest Ni concentrations, while lower metal contents were observed in the aerial organs. The Ni uptake ratio was progressively reduced in plants exposed to increased Ni concentrations. The metal translocation from root to shoots, appreciated by the Ni translocation index, showed a far lower value in Ni-exposed plants than in controls. Moreover, by measuring the daily Ni content of the solutions, a lower Ni removal ability was found in Amaranthus plants at increasing Ni concentrations. Remarkably, plants exposed to 25 μM Ni succeeded in removing almost 60 % of the initial Ni content of the solution showing no stress symptoms. The potential of A. paniculatus for phytoremediation was discussed.

Pyrite, FeS₂, is the most common sulfide mineral. The aim of this work was to assess the oxidative ability of H₂O₂ in presence of natural pyrite by employing reactive black 5, acid red GR, and cationic red X-GRL as model pollutants. The effects of H₂O₂ dosage, pyrite loading, and initial pH on reaction were investigated. The results reveal that natural pyrite-promoted H₂O₂ has a great activity in the decoloration of azo dyes. About 85 % of reactive black 5 and acid red GR can be removed within 10 min when 0.3 mM H₂O₂ and 0.3 g/L pyrite are used with initial pH values ranging from 6.32 to 6.96. The discoloration efficiencies are demonstrated to be less sensitive to the initial solution pH value. Approximately 90 % of discoloration for reactive black 5 and acid red GR can be achieved when initial pH value ranges from 2 to 10. Ion leaching experiments show that high levels of ferrous iron and sulfate can be detected when natural pyrite is added to dye solution alone. To gain an understanding of the reaction mechanism and the role of natural pyrite takes in these processes, techniques including scanning electron microscope, X-ray diffraction, and X-ray photoelectron were employed to characterize the solid sample and ion leaching experiments were also carried out. Results indicate that the determined high levels of ions have resulted from the dissolution of FeSO₄·H₂O formed on the surface of pyrite and the homogeneous Fenton reaction initiated by ferrous iron in presence of H₂O₂ is mainly responsible for the observed fast color removal rate.

Persistence and dissipation kinetics of clothianidin were studied in sandy loam soil of sugarcane ecosystem by adopting a rapid and sensitive analytical method. This single-step analytical method was observed to be superior to multi-step conventional method reported to quantify the residues of clothianidin in soil, in terms of recovery, sensitivity and rapidity besides cost-effectiveness. The recoveries of clothianidin were in the range of 93.19 ± 3.07-95.43 ± 2.09 % at 0.01-0.1 μg/g level of fortification in soil. The limit of quantification of the method was 0.01 μg/g. Dissipation pattern of clothianidin followed first-order kinetics with a good fit (R 2 > 0.96). Half-life of clothianidin was 17.2 and 17.4 days at the single (50 g a.i./ha) and double doses (100 g a.i./ha), respectively. Clothianidin was observed to be more persistent than imidacloprid and thiamethoxam in the soil of tropical sugarcane ecosystem. © 2013 Springer Science+Business Media Dordrecht.

Development of aminopolycarboxylate chelants (APCs) having enhanced biodegradability is gaining increasing focus to replace the EDTA and its homologs with those used widely for the ex situ treatment of contaminated soils and are potential eco-threats. The paper reports the chelant-assisted extraction of the toxic metals (Cd, Cu, Pb, and Zn) from the metal-spiked European reference soils (Eurosoil 1 and Eurosoil 4) using biodegradable APCs, namely EDDS, GLDA, and HIDS. The effects of chelant-to-metal molar ratio, solution pH, and metal/chelant stability constants were evaluated, and compared with that of EDTA. The selectivity aptitude of the biodegradable chelants towards the toxic metals was assumed from the speciation calculations, and a proportionate correlation was observed at neutral pH. Pre- and post-extractive solid phase distributions of the target metals were defined using the sequential extraction procedure and dissolution of metals from the theoretically immobilized fraction was witnessed. The effect of competing species (Al, Ca, Fe, Mg, and Mn) concentrations was proven to be minimized with an excess of chelant in solution. The highlight of the outcomes is the superior decontamination ability of GLDA, a biodegradable APC, at minimum chelant concentration in solution and applicability at a wide range of pH environments.