Up to now, carbon gas fluxes from urban lakes in the boreal zone have seldom been studied. In summer 2005 we investigated fluxes from an urban boreal lake basin in southern Finland with long history of eutrophication and anoxia. Hypolimnetic CO₂ and CH₄ concentrations were high compared to other boreal lakes. During the open-water period, the lake basin acted as a source of CO₂ and CH₄ with fluxes of 2.10 mol m⁻² and 0.04 mol m⁻², respectively. Despite the high oxidation rate (83%), CH₄ flux was higher than in other lakes and CH₄ contributed 60% to Global Warming Potential. The ratio of carbon emission to accumulation was 4, i.e. emissions were an important route for carbon departure but less so than in rural lakes. Since the lake oxygen conditions affected nutrient availability, there was a positive feedback from hypolimnion to carbon uptake, which was reflected in gas concentrations.

Bisphenol F (BPF), an environmental estrogen, is used as a monomer in plastic industry and its environmental fate and decontamination are emerging concern. This study focused on the kinetics, influencing factors and pathways of its oxidation by MnO₂. At pH 5.5, about 90% of BPF was oxidized in 20min in a solution containing 100μM MnO₂ and 4.4μM BPF. The reaction was pH-dependent, following an order of pH 4.5>pH 5.5>pH 8.6>pH 7.5>pH 6.5>pH 9.6. Humic acids inhibited the reaction at low (≤pH 5.5) and high pH (≥pH 8.6) at high concentrations. In addition, metal ions and anions also suppressed the reaction, following the order Mn²⁺>Ca²⁺>Mg²⁺>Na⁺ and HPO₄ ²⁻>Cl⁻>NO₃ ⁻≈SO₄ ²⁻, respectively. A total of 5 products were identified, from which a tentative pathway was proposed.

Methane biofiltration (MBF) is a novel low-cost technique for reducing low volume point source emissions of methane (CH₄). MBF uses a granular medium, such as soil or compost, to support the growth of methanotrophic bacteria responsible for converting CH₄ to carbon dioxide (CO₂) and water (H₂O). A field research program was undertaken to evaluate the potential to treat low volume point source engineered CH₄ emissions using an MBF at a natural gas monitoring station. A new comprehensive three-dimensional numerical model was developed incorporating advection-diffusive flow of gas, biological reactions and heat and moisture flow. The one-dimensional version of this model was used as a guiding tool for designing and operating the MBF. The long-term monitoring results of the field MBF are also presented. The field MBF operated with no control of precipitation, evaporation, and temperature, provided more than 80% of CH₄ oxidation throughout spring, summer, and fall seasons. The numerical model was able to predict the CH₄ oxidation behavior of the field MBF with high accuracy. The numerical model simulations are presented for estimating CH₄ oxidation efficiencies under various operating conditions, including different filter bed depths and CH₄ flux rates. The field observations as well as numerical model simulations indicated that the long-term performance of MBFs is strongly dependent on environmental factors, such as ambient temperature and precipitation.

We tested the resistance of five different fullerenes (C₆₀, C₇₀, C₇₆/₇₈ mix, and C₈₄) to chemothermal oxidation at 375 °C (CTO-375), a method that has been used and tested for quantifying black carbon (BC) and CNTs in soils and sediments. C₆₀ survived CTO-375 the most (50%), while C₇₀ was the fullerene with the lowest survival rate (<1%). Standard additions of C₆₀ to soil and sediment reference materials yielded recoveries between 18 and 36%. Although lower than recoveries previously observed for soot and CNTs, these results demonstrate the capability of CTO-375 to partially isolate C₆₀ from solid environmental matrices. Standard additions of C₇₀, C₇₆/₇₈, and C₈₄ yielded slightly higher survival rates when added to soil and sediment than in their pure form. These results indicate that the mineral matrices of these samples probably had a catalytic effect towards C₆₀ and a protective effect towards C₇₀, C₇₆/₇₈, and C₈₄ during CTO-375.

Iron-based nanotechnologies are increasingly used for environmental remediation; however, toxicologic impacts of iron nanoparticles on the aquatic ecosystem remain poorly understood. We treated larvae of medaka fish (Oryzias latipes) with thoroughly characterized solutions containing carboxymethyl cellulose (CMC)-stabilized nanoscale zerovalent iron (nZVI), aged nanoscale iron oxides (nFe-oxides) or ferrous ion (Fe[II]) for 12–14days’ aqueous exposure to assess the causal toxic effect(s) of iron NPs on the fish. With the CMC-nZVI solution, the dissolved oxygen level decreased, and a burst of reactive oxygen species (ROS) was generated as Fe(II) oxidized to ferric ion (Fe[III]); with the other two iron solutions, these parameters did not significantly change. CMC-nZVI and Fe(II) solutions caused acute lethally and sublethally toxic effects in medaka larvae, with nFe-oxide-containing solutions causing the least toxic effects. We discuss modes of toxic action of iron NPs and chronic toxic effects in terms of hypoxia, Fe(II) toxicity and ROS-mediated oxidative damage.

Mature landfill leachate contains some macromolecular organic substances that are resistant to biodegradation. The photocatalytic process helps to enhance biodegradability of landfill leachate. Batch experiments were employed to determine the optimum conditions for removal of organic matter by UV-TiO2 photocatalysis. Under optimum conditions, the removal of chemical oxygen demand (COD), dissolved organic carbon (DOC), biological oxygen demand (BOD), and color was determined. Moreover, gas chromatography coupled with mass spectrometry (GC/MS) was used to analyze the organic matter in the treated leachate before and after treatment by the photocatalysis. The experimental results indicated that the removal of COD, DOC, and color by UV-TiO2 photocatalysis could reach above 60%, 70% and 97%, respectively. Under optimal conditions, the ratio of biological oxygen demand (BOD)/chemical oxygen demand (COD) was elevated from 0.09 to 0.39, representing substantial improvement in biodegradability. GC/MS analysis revealed that 37 out of 72 kinds of organic pollutants in the leachate remained after 72 h treatment. Esters were produced during photocatalytic process and ketones, hydrocarbons, aromatic hydrocarbons, hydroxybenzenes, and acids were easier to be degraded during photocatalytic oxidation processes. The UV-TiO2 photocatalysis systems proposed may be a cost-effective approach for pre-treatment of landfill leachate.

This study was conducted to evaluate the contribution of environmental factors such as solar radiation and dissolved organic matter (DOM) on the photo-induced dissolved gaseous mercury (DGM) production through laboratory experiments using field water samples collected from wetlands. DGM production was more significantly influenced by UVB intensity than UVA. DGM formation was also significantly affected by DOM chemical structure/composition rather than its concentration. Increasing NO3 − concentration limited DGM production, but photo-induced Hg oxidation stimulated by NO3 − would possibly occur when the NO3 − level is more than twice the DOC level. The addition of phosphorus into the field water samples induced a slight increase of DGM production; however, the addition of nitrogen decreased DGM formation, suggesting that an increase of limiting nutrients in water may promote biotic DGM production. Experiments using a Selenastrum capricornutum monoculture solution showed that cell density had a positive effect on DGM production. Moreover, the difference in DGM production between filtered and unfiltered samples showed that S. capricornutum significantly produced biotic DGM under UVA irradiation. Finally, our results imply that environmental factors such as light intensity, DOM sources, and site-specific microorganisms can significantly affect photo-induced Hg transformation.

Cyanide is found as free cyanide and metal–cyanide complexes in metal finishing rinse wastewaters. Experiments were performed to seek removal of cyanide in Ni(II)–cyanide and Ni(II)–cyanide–ethylenediaminetetraacetate (EDTA) solutions by the environmentally friendly oxidant, ferrate(VI) (FeO4 2−, Fe(VI)) as a function of pH (8.0–11.0). Incomplete removal of cyanide in Ni(II)–cyanide solutions (≤60%) was observed at the studied pH range. However, cyanide removal efficiency approached to 100% in Ni(II)–cyanide–EDTA solutions. Formation of Ni(II)–cyanide and Ni(II)–EDTA complexes and relative rates of the reactions of Fe(VI) with various species (water, cyanide, Ni(II)–cyanide, and EDTA) present in solutions were responsible for the variation in removal efficiencies in mixtures at various pH. The oxidation of cyanide by Fe(VI) produced cyanate. Tests using electroplating rinse wastewaters demonstrated that Fe(VI) was highly effective in removing cyanide.

Sediment and porewater samples from an enclosed bay receiving stormwater discharge (Skutviken) near the centre of Luleå, northern Sweden were analysed for major and trace elements and 16 polycyclic aromatic hydrocarbons (PAHs). Among the studied metals Cd, Cu, Pb and Zn were enriched at Skutviken. Also, the PAH content was enriched, in particular for phenantrene, anthracene, fluoranthene and pyrene which are regarded as common constituents in stormwater. The use of trace metal ratios provided indications about pollutant sources for the sediment. Cs-137 dating was used to determine historical changes in metal and PAH fixation in the sediment. The bay Skutviken is enclosed through the construction of a road bank since 1962. The enclosure led to reduced water circulation in the bay that promotes the occurrence of anoxic conditions with sulphate reduction within the bay. As a consequence of these conditions, metals are trapped in the sediments as sulphides. This study suggests that enclosed bays with restricted water circulation may be efficient traps for urban pollutants, reducing the present-day input of pollutants to the sea. In areas with postglacial land uplift, where such bays are common, bay sediments are a potential future source of pollutants when uplift results in erosion and oxidation of the sediments.

The presence of endocrine-disrupting chemicals (EDCs) in wastewater effluent is a major concern to the scientific community. This research effort was aimed at investigating Fenton-like degradation of two EDCs 17β-estradiol (E2) and 17α-ethinylestradiol (EE2). The results of the study showed that E2 and EE2 were effectively removed by the Fenton-like oxidation process. Removal efficiencies of 95% and 98% at ferric concentration of 1 × 10−3 M (58.6 mg l−1) were achieved for E2 and EE2, respectively. The kinetics of Fenton-like degradation of E2 and EE2 were adequately described by the pseudo second order kinetic model. Values of 27.8 and 22.5 kJ mol−1 were obtained for the activation energy for E2 and EE2, respectively, from the Arrhenius-type plot, showing that the process does not just involve radical reactions but also intermediate reaction steps involving radical–molecule or ion–molecule reactions. The presence of high dissolved organics in wastewater significantly reduced the removal efficiencies. The reaction by-products for E2 and EE2 were more stable to the oxidation process and more readily biodegradable. Fenton-like oxidations therefore offers a promising alternative for the removal of these EDCs in wastewater treatment applications at the tertiary treatment stage.