Effect of cycle time on biodegradation of azo dye in sequencing batch reactor

The effects of cycle time on the biodegradation of the azo dye remazol brilliant violet 5R (RBV-5R) were investigated in an anaerobic–aerobic sequencing batch reactor (SBR). System performance was determined by monitoring chemical oxygen demand (COD), color, anaerobic enzyme (azo reductase) and aerobic enzyme (catechol 2,3-dioxygenase), and aromatic amine concentration. SBR was operated in three different total cycle times (48 h, 24 h and 12 h), fed with a synthetic textile wastewater. In this study, the anaerobic period of SBR was found to allow the reductive decolorization of azo dye and the aerobic period was found to be effective on further COD removal after the anaerobic period. The percentage reductions in color by the anaerobic stage of the SBR were at 72%, 89% and 86% for the 24-h, 12-h and 6-h cycle times, respectively. Total COD removal efficiencies were over 75% for all operational conditions and about 70% of the COD removal was achieved in the first 3 h of anaerobic stages. During the decolorization of RBV-5R, two sulfonated aromatic amines (benzene-based and naphthalene-based) were formed and detected by HPLC. Aerobic phases of SBR with total cycle times of 48 h, 24 h and 12 h were able to remove benzene-based aromatic amines with removal efficiency of 64%, 92% and 89%, respectively. The results indicated that the best SBR performance in terms of color removal and aromatic amine degradation was achieved from total cycle time of 24 h.     

Leachability of Cr(VI) and other metals from asphalt composites with addition of filter dust

The potential use of filter dust in asphalt composites for road construction was investigated. Filter dust contains high concentrations of metals, of which Cr(VI) and Pb are leached with water. Compact and ground asphalt composites with addition of 2% of filter dust by mass were studied. In order to evaluate their environmental impact, leachability tests were performed using water and salt water as leaching agents. The concentrations of Cr(VI) and Pb were determined in leachates over a time period of 182 days. The results indicated that Pb was not leached with leaching agents from asphalt composites. Cr(VI) was also not leached with leaching agents from compact asphalt composites. However, in ground asphalt composites, Cr(VI) was leached with water in concentrations up to 220 microg L(-1) and in salt water up to 150 microg L(-1). From the physico-mechanical and environmental aspects, filter dust can be used as a component in asphalt mixtures.     

A high-resolution reverse-phase liquid chromatography method for the analysis of mycosporine-like amino acids (MAAs) in marine organisms

Mycosporine-like amino acids (MAAs) are a group of about 20 structurally related water-soluble compounds, widely distributed among freshwater and marine organisms. To provide a better assessment of the diversity and concentration of MAAs in aquatic environments a high-performance liquid chromatography (HPLC) method of analysis based on reverse-phase C₁₈ column and trifluoroacetic acid and an ammonium-containing mobile phase was developed. The improvements with respect to previous methods and the extraction and clean-up procedures are described here. With this method the clean-up recovery of MAAs of high polarity (shinorine), medium polarity (palythinol), and low polarity (palythene) is greater than 99% (±1%). The method is selective enough to resolve in a single run most of the characterized MAAs found in marine organisms, including the critical and highly polar compounds shinorine, mycosporine-2-glycine, and palythine-serine, the medium polarity pair palythenic acid and shinorine methyl ester (M-333), and the low polarity isomeric pair usujirene and palythene. A chromatogram of a mixture of over 20 MAAs such as might be found in complex samples of marine organisms is given. Good precision was obtained in the separations. The relative standard deviation for retention times was below 1% and the mean relative standard deviation for integrated area estimations was below 2%. A mean column recovery of standards was 99% (±1%) whereas limits of detection (signal-to-noise, S/N=2) for different MAAs varied between 0.08 and 0.47 pmol injected. The applicability of the method was tested using extracts of three microalgae cultures, three natural phytoplankton populations, two scleractinian corals, and one species of sea anemone. Results reveal the occurrence of several unknown MAAs not previously reported in the literature. The selectivity of the method toward some recently discovered MAAs makes it especially suitable not only for studying new field samples, but also for re-examining the MAA composition of previously studied organisms.Communicated by O. Kinne, Oldendorf/Luhe     

Determining the heavy metal pollution in Denizli (Turkey) by using Robinio pseudo-acacia L

The leaves of Robinia pseudo-acacia L. (Fabaceae) were evaluated as a biomonitors of heavy metal contamination in Denizli city, Turkey. Concentrations of Fe, Zn, Pb, Cu, Mn and Cd were determined in washed and unwashed leaves and soils collected from a wide range of sites with different degrees of metal pollution (industry, urban roadside, suburban) and from a rural (control) site by atomic absorption spectrometry. All the elements that measured were found to be at high levels in samples collected at industrial sites, except for lead and copper which were found at high levels in samples collected from urban roadsides that associated with the road traffic. The strong correlation between the degree of contamination and concentrations in all plant leaves assessed display that the leaves of R. pseudo-acacia reflect the environmental changes accurately, and that they seem as an effective biomonitor of environmental quality in areas subjected to industrial and traffic pollutions.     

Distribution of Redox-sensitive Elements in Bottom Waters,Porewaters and Sediments of Rogoznica Lake (Croatia) in Both Oxic and Anoxic Conditions

Geochemical, mineralogical and sedimentological analyses were carried out to contrast two different sites (respectively characterized by permanently oxic and anoxic conditions) in a small, meromictic, seawater lake. In fact, due to relatively high organic matter content, and reduced water exchange, the Rogoznica Lake has almost permanent anoxic conditions below the depth of 12 m, where sediment can be considered an anoxic–sulphidic sedimentary environment. Different water column and sediments redox conditions affect the distribution and speciation of major redox-sensitive metals (Fe, Mn, Mo), reduced sulphur species (RSS) and dissolved organic C (DOC). Trace metals, especially those that accumulate in anoxic–sulphidic environments (Fe, Mo) showed a marked enrichment in the solid phase, whereas the low solubility of sulphides leads to low porewater concentrations. The relatively high sedimentary enrichment of Mo (up to 81 mg/kg) also confirms highly anoxic conditions within the Rogoznica Lake sediments. Results clearly show that chemical species within the sediments will tend towards equilibrium between porewater and solid phase according the prevailing environment conditions such as redox, pH, salinity, DOC.