As a polycyclic aromatic hydrocarbon (PAH), pyrene is one of hazardous persistent organic pollutants in the aquatic environment. The aim of this study was to investigate the influence of denitrifying conditions on pyrene degradation in a pure culture. With a strain isolated from petrol-contaminated river sediment, treatments of pyrene biodegradations were set up using various ratios of nitrate to nitrite (NO₃ ⁻/NO₂ ⁻). Results showed that various NO₃ ⁻/NO₂ ⁻ conditions significantly influenced the anaerobic pyrene degradation efficiency. Nitrite could induce the complete denitrification process so that NO₂ ⁻ acted as a key factor to promote high degradation efficiency. The low N treatment of NO₃ ⁻ and NO₂ ⁻ concentrations made the denitrifying-pyrene-degradation process more effective. Additionally, high C/N value stimulated high degradation rates. High concentrations of NO₃ ⁻ and NO₂ ⁻ as well as toxic intermediate product accumulation might inhibit the bacterial growth and biodegradation process. The information from this study should be useful to design bioremediation strategies of PAH.

Application of an agricultural residue (rice husk, RH) as a raw material for catalyst support for advanced oxidative processes (AOPs) was evaluated. The supported catalyst was produced by the calcination of TiCl₄ impregnated in RH, thereby providing a composite TiO₂/Si-C, which was characterized by elemental analysis (CHN), scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM–EDX), X-ray photoelectron spectroscopy (XPS), UV/VIS diffuse reflectance spectroscopic (DRS), diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), atomic force microscopy (AFM), SEM, and nitrogen adsorption–desorption isotherms (BET and BJH). Catalytic photodecomposition of methylene blue (MB), naphthalene, phenol, and abamectin and acid drainage of a mine by a titania-based catalyst composite were investigated. For comparative purposes, a commercial photocatalyst (TiO₂) was also employed. Photocatalytic degradation of MB, phenol, naphthalene, abamectin, and from coal mining effluent ranged from 8 to 93 % of the initial concentration. Performances of both catalysts were comparable. Additionally, in these evaluated systems, the toxicity of the effluent decreased after photocatalysis, either for Daphnia magna or for Scenedesmus subspicatus (employed as bioindicators).

A chitosan-graft-poly(N-allyl maleamic acid) hydrogel membrane was prepared by radical polymerization in the absence of a cross-linker. The product was characterized by Fourier transform infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA), and scanning electron microscopy (SEM) to confirm the formation of hydrogels. Transparent hydrogels have been observed to exhibit as much as 223.4 % swelling capacity, following pseudo-second-order kinetic models. The synthesized hydrogel membrane was subsequently utilized for removal of copper ions from an aqueous solution in the presence of several different functional groups. The effects on adsorption efficiency of various parameters such as time, temperature, pH, initial concentration of copper (II) solution, and amount of hydrogel were also investigated. The maximum adsorption capacity and efficiency were found to be 50.75 mg g-1 and 99.91 %, respectively, by the 0.004 mg adsorbent after 12 h of immersion in copper solution. Finally, the result showed that hydrogel membrane is pH sensitive to copper (II) adsorption and has maximum adsorption efficiency near to the pH of ground water. © 2013 Springer Science+Business Media Dordrecht.

Rhizoremediation is a complex type of green clean-up technology that involves both plants and the rhizosphere-associated microorganisms to decompose hazardous compounds. The success of the strategy strongly depends on plant tolerance towards the pollutant, as well as plant's interactions with the rhizospheric microbes. The microorganisms may be stimulated by the secreted root exudates, which results in an increased breakdown of contaminants in the rhizosphere. The main goal of this study was to establish a potential rhizoremediation combination for a diesel-polluted site. Inoculation of plant roots or seeds with indigenous rhizospheric populations is a common approach in the rhizoremediation. However, we introduced hydrocarbon-degrading consortia (M10, R3, and K52) that were previously isolated from crude oil-contaminated soil instead of indigenous microbes. Bioaugmentation with these petroleum degraders was applied to screen four high biomass crop species (Indian mustard, alfalfa, high erucic acid rapeseed, HEAR, and low erucic acid rapeseed, LEAR) for their tolerance towards diesel oil. At no pollution, a promoting effect of M10 bacteria could be observed on germination and root elongation of all plant species. Moreover, M10 consortiums increased the germination index at 6,000 mg diesel oil per kilogram dry soil in the case of Indian mustard, alfalfa, and HEAR. The latter species was found to increment its dry weight upon bioaugmentation with M10 bacteria and all diesel oil treatments (6,000 and 24,000 mg diesel oil per kilogram dry soil). The initial results indicate HEAR and the M10 bacterial consortium as a promising plant-microbe tandem for a long-term rhizoremediation process. © 2013 The Author(s).

The subalpine and alpine areas in North-Western Italy and Southern Switzerland (Canton Ticino) receive high deposition of atmospheric pollutants transported from emission sources in the Po Valley. Long-term studies on high-altitude lakes in these areas indicate widespread recovery from acidification, even though most of them are still substantially affected, especially by deposition of nitrogen compounds. We analysed long-term trends of the major chemical compounds in a sample (n = 41) of high-altitude lakes, both at the site and regional levels, with the aim to assess the response of water chemistry to changes in atmospheric deposition and climate. These lakes have been studied since the early 1980s in the context of research programmes on acidification and atmospheric pollution. The significant decrease of sulfate and acidity in atmospheric deposition led to acidification recovery in the majority of the lakes. However, some lakes are still acidic or show a high sensitivity to acidification. This sensitivity is particularly evident at the snowmelt, when alkalinity is still fully depleted in some lakes. At present, nitrate is the dominant acidifying agent in the studied lakes, due to the high input of nitrogen compounds from atmospheric deposition. Our study also demonstrated that climatic factors interact with atmospheric deposition affecting the long-term changes in lake water.

Volatile organic compounds (VOCs) are ubiquitous in marine areas in many parts of the world. Effect of environmental factors (light intensity, temperature, oxygen levels, and presence of sensitizer) on photodegradation of VOCs present in water-soluble fraction of Kuwait crude oil was investigated in laboratory conditions. The results showed that all factors investigated had significant effects on photo degradation rates. Higher temperatures produced faster degradation rates. At 15 °C, most of the volatile optimally degraded when light intensity was set at 750 W/m². Oxygen level of 7 ppm and presence of sensitizer was also required. Oxygen level of 4 ppm and light intensity of 500 W/m² and presence of a sensitizer produced optimal degradation rates for most of the compounds at 30 °C. At 40 °C, deoxygenated water-soluble fraction and light intensity of 500 W/m² produced the fastest degradation for many of the volatile compounds. Linear regression indicated that for most of the compounds temperature had the greatest effect on degradation rates.

The present paper examines the phosphate adsorption from aqueous solutions onto goethite, bentonite, and bentonite–goethite system. The properties of the materials were studied by X-ray diffraction (XRD), attenuated total reflectance (ATR), and NMR spectra and by the measurement of the specific surface area, the point of zero charge (p.z.c.) and the pore-specific volume. ATR and NMR spectra of bentonite and bentonite–goethite system show peaks which correspond to tetrahedrally and octahedrally coordinated Al. The specific surface area of the system differs according to the appropriate method used, while system’s p.z.c. is higher than bentonite and lower than goethite. The pore-specific volume of bentonite–goethite system is higher than that of bentonite or goethite. According to XRD spectrum of bentonite–goethite system, goethite coats the (001) spacing of bentonite while the coating of (010) plane of bentonite is limited. The crystallinity of the system decreases and the negative permanent charge increases. Phosphate adsorption experiments took place at different pH (3.8–9.0) and concentrations (40.3–443.5 μmol L⁻¹) and constant capacitance model was applied to describe adsorption. A ligand exchange mechanism characterizes the model because the charge is divided among adsorbate and adsorbent. The constant capacitance model describes the adsorption mechanism in all examined pH. This model can be utilized in such systems using the surface protonation-dissociation constant of goethite and showing the exact shape of the adsorption isotherms for different pH values. Τhe produced low-cost bentonite–goethite system presents the highest adsorption of P per kilogram of goethite.

Adsorption potentials of native and amine-modified plant biomass of Alyssum caricum for the removal of Reactive Green 19 (RG-19) and Reactive Red 2 (RR-2) dyes from aqueous solutions were studied. The adsorbents were characterized before and after modification process using Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET) and potentiometric titration analysis. Modification of the surface of A. caricum biomass with hexamethylenediamine (HMDA) showed an increase of 1.18-fold in its surface area. Batch studies illustrated that dye adsorption were highly dependent on different process variables, pH, initial dye concentration of solution, adsorbent dosage, and temperature. The maximum adsorption capacities of the native and amine-modified adsorbents were 27.6 and 63.4 mg/g adsorbent for RG-19 dye and 16.5 and 36.8 mg/g adsorbent for RR-2 dye, respectively. The adsorption of both dyes on the native and amine-modified plant biomass correlated well with the Langmuir and Temkin isotherm equations as compared to Freundlich and D-R equations. The calculated thermodynamic parameters for both native and amine-modified adsorbents showed that the adsorption was feasible, spontaneous, and exothermic. The information gained from these studies was expected to indicate whether native and amine-modified adsorbents can have potential to be used for the removal of other dyes from wastewaters. © 2013 Springer Science+Business Media Dordrecht.

In this study, we evaluated the needle anatomy of Norway spruce trees growing on a territory that was exposed to different alkaline dust pollution. The anatomy of the needles of spruce growing on a polluted site in the vicinity of the Kunda cement plant (Northeast Estonia) was compared with the anatomy and physiological state of the needles from an unpolluted site. The needles from polluted sites had a significantly larger average mesophyll area and thicker epidermis. These needles also had significantly smaller average vascular bundles and xylem areas than needles from the unpolluted site. Although in the alkalised growth conditions, the mesophyll area enlarged, the number of damaged mesophyll cells increased, and as a result, the concentration of chlorophylls decreased reducing the photosynthetic potential of trees. Our study indicates that even though cement dust pollution has practically ceased in the area, the alkalised soil is affecting physiological processes in trees for a long time.

The release of heavy oil from laboratory-contaminated sediments was studied in a series of kinetic and equilibrium experiments. The kinetic curves could be interpreted by a two-compartment first-order equation including rapid and slow release steps. The slow step was dominant and the rate constant was 3 orders of magnitude smaller than for the rapid step. Equilibrium experiments for the slow step revealed that the isotherms could be described by the Freundlich equation. The release of heavy oil was found to correlate with higher contamination level, larger particle size, lower salinity, and higher temperature. The effect of coexisting surfactant on the release was also investigated and the results showed that the presence of Tween-20 promoted the process. The oil release process was endothermic and the randomness at the solid–liquid interface increased during the desorption process. The values of activation energy and standard enthalpy change indicated that this process was a physical one.