Microcystins are cyanobacterial hepatotoxins capable of accumulation into animal tissues. The toxins act by inhibiting specific protein phosphatases and both non-covalent and covalent interactions occur. The 2-methyl-3-methoxy-4-phenylbutyric acid (MMPB) method determines the total, i.e. the sum of free and protein-bound microcystin in tissues. The aim of the method development in this paper was to tackle the problems with the MMPB methodology: the rather laborious workflow and the loss of material during different steps of the method. In the optimised workflow the oxidation recovery was of acceptable level (29–40%), the extraction efficiency good (62–97%), but the signal suppression effect from the matrix remained severe in our system (16–37% signal left). The extraction efficiency for the determination of the free, extractable microcystins, was found to be good, 52–100%, depending on the sample and the toxin variant and concentration. The study concerns method development for the LC–MS–MS analysis of both free and protein-bound microcystin in tissue materials.

In the context of the European Water Framework Directive, controlled flooding of lowlands is considered as a potential water management strategy to minimise the risk of flooding of inhabited areas. However, due to historical pollution and overbank sedimentation, metal levels are elevated in most wetlands, which can cause adverse effects on the ecosystem's dynamics. Additionally, salinity affects the bioavailability of metals present or imported into these systems. The effect of different flooding regimes and salinity exposure scenarios (fresh- and brackish water conditions) on Cu and Zn accumulation in the oligochaete Tubifex tubifex (Müller, 1774) was examined. Metal mobility was closely linked to redox potential, which is directly related to the prevalent hydrological regime. Flooded, and thus more reduced, conditions minimized the availability of metals, while oxidation of the substrates during a drier period was associated with a rapid increase of metal availability and accumulation in the oligochaetes.

Polyfluoroalkyl compounds (PFCs) are widely used in industry and consumer products. These products could end up finally in landfills where their leachates are a potential source for PFCs into the aqueous environment. In this study, samples of untreated and treated leachate from 22 landfill sites in Germany were analysed for 43 PFCs. ΣPFC concentrations ranged from 31 to 12,819 ng/L in untreated leachate and 4-8060 ng/L in treated leachate. The dominating compounds in untreated leachate were perfluorobutanoic acid (PFBA) (mean contribution 27%) and perfluorobutane sulfonate (PFBS) (24%). The discharge of PFCs into the aqueous environment depended on the cleaning treatment systems. Membrane treatments (reverse osmosis and nanofiltrations) and activated carbon released lower concentrations of PFCs into the environment than cleaning systems using wet air oxidation or only biological treatment. The mass flows of ∑PFCs into the aqueous environment ranged between 0.08 and 956 mg/day.

Composting municipal wastewater sludge may generate composting wastewater (acid washer water and tunnel wastewater) with high ammonium-nitrogen (NH₄-N) concentration; this kind of wastewater is usually generated in a rather small daily amount. A procedure of air stripping with catalytic oxidation was developed and tested with pilot-scale and full-scale units for synthetic disposal of the high NH₄-N wastewaters from composting facilities. In air stripping, around 90% NH₄-N removal efficiency was reliably achieved with a maximum of 98%. A model to describe the stripping process efficiency was constructed, which can be used for process optimization. After catalytic oxidation, the concentrations in the outlet gas were acceptable for NH₃, NOX, NO₂, and N₂O, but the NH₃ and N₂O concentrations limited the feasible loading range. The treatment costs were estimated in detail. The results indicate that air stripping with the catalytic oxidation process can be applied for wastewater treatment in composting facilities.

Stable isotope analyses were performed on gas samples collected within two instrumented biocovers, with the goal of evaluating CH₄ oxidation efficiencies (f ₀). In each of the biocovers, gas probes were installed at four locations and at several depths. One of the biocovers was fed with biogas directly from the waste mass, whereas the other was fed through a gas distribution system that allowed monitoring of biogas fluxes. While the f ₀ values obtained at a depth of 0.1 m were low (between 0.0% and 25.2%) for profiles with poor aeration, they were high for profiles with better aeration, reaching 89.7%. Several interrelated factors affecting aeration seem to be influencing f ₀, including the degree of water saturation, the magnitude of the biogas flux and the temperature within the substrate. Low f ₀ values do not mean necessarily that little CH₄ was oxidized. In fact, in certain cases where the CH₄ loading was high, the absolute amount of CH₄ oxidized was quite high and comparable to the rate of CH₄ oxidation for cases with low CH₄ loading and high f ₀. For the experimental biocover for which the CH₄ loading was known, the oxidation efficiency obtained using stable isotopes (f ₀ = 55.67% for samples taken inside flux chambers) was compared to the value obtained by mass balance (f ₀ = 70.0%). Several factors can explain this discrepancy, including the high sensitivity of f ₀ to slight changes in the isotopic fractionation factor for bacterial oxidation, α ox, uncertainties related to mass flow metre readings and to the static chamber method.

In this work, we evaluated the effect of harmful ecotoxins, 4,5,6-trichloroguaicol (4,5,6-TCG) and tetrachloroguaiacol (TeCG), on the oxidation of the fluorescent probe dihydrorhodamine 123, the content of free phenols and the level of the total, oxidized and reduced glutathione in the leaves of reed canary grass (Phalaris arudinacea). Furthermore, the effect on the activity of guaiacol peroxidase and glutathione S-transferase was investigated. Both 4,5,6-TCG and TeCG increased the activity of guaiacol peroxidase and glutathione S-transferase, they also elevated the content of free phenols and the level of the total glutathione. A stronger effect was exerted by tetrachloroguaiacol, which strongly increased the level of the total glutathione and the content of free phenols on the 3rd and 6th day of the experiment. The activity of glutathione S-transferase was more intensively induced by trichloroguaiacol. Both 4,5,6-TCG and TeCG oxidized dihydrorodamine 123 and the effect was stronger in the presence of magnesium ions.

The main objective of this study was to find out a cost-effective treatment methodology for the treatment of palm oil effluent (POE) obtained from a food processing industry. An electro-Fenton pretreatment and biological oxidation has been suggested for the removal of recalcitrant contaminants present in POE. An initial COD of about 6,700 mg/L of POE was subjected to electrolytic degradation for 2 h and subsequently by biological oxidation. The biological oxidation was carried out using Aspergillus niger and Pseudomonas putida in anaerobic condition. Electro-Fenton process removed 48.35% of the COD. Biological oxidation subsequently decreased the COD to 86.12% and BOD to 85.23%. In the combined process, a high reduction in TOC and TN were achieved. Experimental conditions have been optimized and performances of these techniques have been discussed. The treated water can be reused for general and agricultural purposes.

Reaction behaviors and kinetics of catalytic oxidation of benzene, toluene, and ethyl acetate with feed concentrations in the range of 700-5,000 ppm over Pd/ZSM-5 catalyst were investigated. Results for single components show that ethyl acetate (T ₅₀ = 190-200°C) is more easily oxidized than benzene (T ₅₀ = 215-225°C) and toluene (T ₅₀ = 225-235°C). The conversion of ethyl acetate was increased with the increase of its feeding concentration, while the opposite behaviors were observed for benzene and toluene as their conversion rates were decreased with the increase of the inlet concentration. Different behaviors were observed in catalytic oxidation of volatile organic compound (VOC) multi-components, the presence of benzene or toluene inhibits the conversion of ethyl acetate, and the aromatic hydrocarbons inhibit each other in all cases. Ethyl acetate possesses obvious inhibitory effect on benzene oxidation, while it is interesting to note that ethyl acetate has a promotion effect on toluene conversion. The kinetic data were fitted by the Power-law and Mars-van Krevelen kinetic models. The fitting result shows that the Power-law model is more suitable for predicting the conversion of benzene than the other VOCs, and the Mars-van Krevelen model can accurately express the reaction rate of all investigated VOCs.

The arsenic contamination of Bangladesh groundwater involves heavy arsenic inputs to irrigated rice fields. Beside adsorption on soil colloids, iron-arsenic co-precipitation phenomena can affect arsenic retention in soils. In paddy fields of Satkhira District, Bangladesh, the study of the arsenic and iron forms in the irrigation waters and in soils at different times and distances from the irrigation well evidenced that a higher Fe/As ratio in the well water was related to a faster oxidation of Fe(II) and As(III) in water and to a close Fe-As association in soils, together with a greater accumulation of arsenic and poorly ordered iron oxides. The concentration of arsenic and of labile iron forms decreased with the distance from the well and with the depth, as well as the reversibility of arsenic binding. The fate of the arsenic added to the soils by irrigation hence resulted strongly influenced by iron-arsenic co-precipitation, depending on the Fe/As ratio in water. Irrigation systems favouring the sedimentation of the Fe-As flocks could help in protecting the rice from the adverse effects of dissolved arsenic.

Reductive dechlorination of tetrachloroethylene (PCE) by green rust modified with copper (GR(Cu)) was investigated using a batch reactor system. Four different forms of GRs (GR-Cl, GR-SO₄, GR-CO₃, and GR-F) were synthesized by partial air oxidation of Fe(OH)₂ and used in reductive dechlorination. The addition of Cu(II) into GRs produced 100-nm particles on the surface of GRs, which were considered to be metallic Cu and transformed a portion of GR to magnetite. Concentration of Fe(II) in the liquid phase increased and concentration of Fe(II) in the solid phase decreased during the modification process and the extent of these changes was dependent on the amount of Cu(II) added. The most reactive of the modified GRs was GR-F(Cu), which reacted with PCE at a rate that was 80 times faster than that of GR-Cl(Cu). The rate of PCE degradation by GR-F(Cu) was strongly dependent on pH with higher rates at higher pH over the range of pH 7.5-11. Increasing concentrations of Cu(II) over the range of 0 to 5 mM increased rate constants. The rate of dechlorination of PCE by GR-F(Cu) showed surface saturation behavior with respect to PCE concentration.