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.

A set of ten heavy metals (Al, As, Cd, Cr, Cu, Hg, Ni, Pb, V, and Zn) was investigated in surface sediments (0-5 cm) collected in 21 sites of the Gulf of Trieste, Northern Adriatic Sea (Italy). The aim of this work was to obtain a preliminary assessment about the levels and spatial distribution of these selected elements. Ancillary parameters such as grain size, total organic carbon, and total nitrogen were also determined. The enrichment factor was calculated to discriminate if a natural condition or a status of anthropogenic contamination occurs. In addition, a set of sediment quality guidelines, mean effect low range and effect medium range quotients, was also applied in order to predict the probability of adverse biological effects on the benthic community.

Many soils derived from pyrite mines spoils are acidic, poor in organic matter and plant nutrients, contaminated with trace elements, and support only sparse vegetation. The establishment of a plant cover is essential to decrease erosion and the contamination of water bodies with acid drainage containing large concentrations of trace elements. We tested the application of compost and polyacrylate polymers to promote the growth of indigenous plant species present in the mine area. Soil treatments consisted of unamended soil (control), soil with mineral fertilizers only, soil with fertilizer plus compost, soil with fertilizer plus polyacrylate polymers, and soil with fertilizer plus both amendments. Half of the soil was grown with Briza maxima L. (greater quaking grass), Chaetopogon fasciculatus (Link) Hayek (chaetopogon), and Spergularia purpurea (Persoon) G. Don fil. (purple sandspurry), while the remainder was left bare. In the absence of plants, the greatest improvements in soil conditions were obtained by the application of both amendments, which was associated with the greatest values of protease, acid phosphatase, and β-glucosidase, whereas the activity of cellulase and microbial respiration were similar in soil amended with compost or polymer. Dehydrogenase activity was greatest in soil with compost (with or without polymer), whereas urease activity was impaired by both amendments. In the presence of plants, the application of both amendments led to the greatest activities of protease, urease, β-glucosidase, cellulase, and microbial respiration, but acid phosphatase was mainly enhanced by polymer and dehydrogenase was increased by compost. Plant growth was stimulated in all treatments compared with unamended soil, but the greatest value for total accumulated biomass was obtained in fertilized soil receiving both amendments. However, species responded differently to treatment: while the growth of B. maxima was greatest in soil with compost and polymer, the growth of C. fasciculatus responded better to soil with compost, and S. purpurea grew better in polymer-amended soil. The amendments tested improved the quality of a mine soil and stimulated plant growth. However, botanical composition likely changes over time with amendments, and this needs to be considered when a large scale application of amendments is projected.

The degradation of diethyl phthalate (DEP) in aqueous solution by titanium dioxide (TiO2) photocatalysis has been investigated in our research. DEP was completely removed in the solution by 50-min irradiation. Results show that DEP degradation rate was affected by initial DEP concentration, photocatalyst amount, light intensity, and pH. Photocatalytic degradation intermediates were identified by gas chromatography-mass spectrometry intermediates were identified by gas chromatography-mass spectrometry. The major intermediates are methyl benzoate, ethyl benzoate, and carboxylic derivatives. The photocatalytic degradation process was found to obey first-order reaction. Consequently, the result of photocatalytic degradation could be an efficient method of DEP removal from wastewater.

Three organic wastes (banana skin (BS), brewery spent grain (BSG), and spent mushroom compost (SMC)) were used for bioremediation of soil spiked with used engine oil to determine the potential of these organic wastes in enhancing biodegradation of used oil in soil. The rates of biodegradation of the oil were studied for a period of 84 days under laboratory conditions. Hydrocarbon-utilizing bacterial counts were high in all the organic waste-amended soil ranging between 10.2 × 10⁶ and 80.5 × 10⁶ CFU/g compared to unamended control soil throughout the 84 days of study. Oil-contaminated soil amended with BSG showed the highest reduction in total petroleum hydrocarbon with net loss of 26.76% in 84 days compared to other treatments. First-order kinetic model revealed that BSG was the best of the three organic wastes used with biodegradation rate constant of 0.3163 day⁻¹ and half-life of 2.19 days. The results obtained demonstrated the potential of organic wastes for oil bioremediation in the order BSG > BS > SMC.

After elevated concentrations of perfluorooctanoate (PFO) were found in river and groundwater in the vicinity of a fluoropolymer manufacturing facility, numerous soils at adjacent sites were sampled in 2007. Within a 5-km northeast-oriented sector around a probable point source, 20 forest sites were investigated and compared to deposition and groundwater data. PFO concentrations up to 600 µg/kg were detected in the soils, and PFO concentrations typically decreased toward deeper soil depths. In mixed or deciduous forests, maximum concentrations of PFO occurred in the topsoil, pointing to the favorable decomposition and incorporation of deciduous litter. PFO concentrations of the organic layer over the 20 sampling sites were interpolated using ordinary kriging. Highest PFO content in the organic layer was located about 500 m away from the point source in the regional wind direction, decreasing asymptotically outwards. Long-term monitoring data pointed to an accumulation of PFO over time in the organic layer. The data suggest that PFO might be released in the course of litter decomposition and transported toward deeper soil regions only gradually. The soils' PFO concentrations reflect the deposition data. The transport link toward groundwater is currently established in lysimeter studies.

An experimental approach for estimating the parameters for an extended biokinetic model (Peev et al. 2004) of micropollutant removal in wastewater treatment is presented and exemplarily performed with 2,6-naphthalene disulfonate (2,6-NDSA) and benzothiazole sulfonate (BTSA) as model compounds. In particular, a set of short-term batch experiments, consisting of a micropollutant degradation experiment and a biomass decay experiment, were carried out. Both experiments comprise only the chemical analysis of micropollutant substrate concentrations over time. The experimental data were used to determine the biokinetic parameters by applying and verifying the methodology introduced in a previous publication (Schoenerklee and Peev, 2008). The results suggest that the model assumption of competent heterotrophic biomass utilizing the target micropollutant as growth substrate, gives a satisfactory description of the micropollutant biodegradation process by mixed bacterial cultures.

The chemical dynamics at Meio Stream Basin, São Paulo State, Brazil were evaluated using major elements as natural tracers. The surface water samples from Meio Stream were collected near the mouth of Meio Stream at the confluence with the Mogi-Guaçu River on February 25, 2005, April 20, 2005, and July 8, 2005. Rainwater samples were collected (using a “bulk” collector) for 1 year at one sampling point located about 4 km from downtown Leme city and other possible sources of contamination. The analyses were performed by pH, temperature, dissolved oxygen, electrical conductivity, total solids, sulfate, nitrate, phosphate, alkalinity, chloride, sodium, calcium, potassium, and magnesium. This basin has serious environmental problems in terms of rainwater and surface water quality, which result in the negative annual flux of cations and anions at Meio Stream Basin, with the exception of chlorine. The Meio Stream, downstream from Leme city, receives several elements/compounds through anthropogenic activities, mainly related to the discharge of domestic effluents. Anthropogenic inputs (mining, fossil fuel burning, and agricultural activities) are responsible for the higher concentrations of cations and anions in the rainwater from this basin.

The concentration of Al, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Sb, Se, V and Zn was measured in the aquatic bryophyte Rhynchostegium riparioides after a 4-week transplantation at 83 stations in seven main watercourses and three smaller tributaries of the basin of the River Bacchiglione (NE Italy). The study, carried out in 9 months, aimed at establishing a database for statistical analyses to define a novel index of water quality, specifically calibrated for moss bags, and suitable for bio-monitoring purposes where autochthonous bryophytes are not available. The background level was estimated for each element, the ratio between sample and background concentration was adopted as measure of environmental alteration and a five-class interpretation scale was defined. The 73.8% of measured concentrations reflected a condition of naturality, 16.6% suspect of alteration, 7.6% sure alteration, 1.6% severe alteration and <0.5% extreme alteration. The condition of global environmental alteration (all contaminants) at each station was also defined. Forty-four stations presented absence or suspect of alteration, 39 sure alteration for one or more elements. Bivariate and multivariate analyses revealed (1) highly significant correlations (p < 0.001) between the concentrations of Co-Mn, Sb-Zn, and Fe-V, depending on both natural and human factors, (2) chemical patterns leading to galvanic industries, metallurgy or urban sewages, in some case with a geographical distribution and (3) a gradient of environmental alteration from the Pre-Alps to the lowland. Coloured maps indicate both point sources and widespread environmental alteration, highlighting not only industrial-urban areas but also some apparently undisturbed sites.

Mercury concentrations in largemouth bass and mercury accumulation rates in age-dated sediment cores were examined at Lake Ozette and Lake Dickey in Washington State. Goals of the study were to compare concentrations in fish tissues at the two lakes with a larger statewide dataset and examine mercury pathways to the lakes. After accounting for fish length, tissue concentrations at the lakes were significantly higher than other Washington State lakes. Wet deposition and historical atmospheric monitoring from the area show no indication of enhanced local or regional deposition. Sediment core records from the lakes indicate rising sedimentation rates coinciding with logging in the lakes' drainages has greatly increased the net flux of mercury to the waterbodies.