MESIP∗: Modelling environmental scenarios in ponds

MESIP is a fugacity model which can predict the fate of organic hydrophobic chemicals in aquatic ecosystems. In this paper a short introduction to the mathematical model is presented together with a more detailed listing of the required input data. Comparison of the calculated and measured fate of a fluorescent whitening compound in an artificial outdoor pond is shown     

The effect of limiting nutrient on metal toxicity to selenastrum capricornutum

Metal toxicity on selenastrum capricornutum were examined by batch culture and chemostat culture system. EC₅₀ values under nutrient‐limited condition and saturated condition were compared. The two EC_5Os differed by a factor of 10.6 for Cd in batch test, and differed by a factor of 6.5 in continuous test. Both batch and continuous test results indicate that inhibition on algal growth is more severe under nutrient‐limited conditions compared to that under near saturation conditions.

Strong correlation, as characterized by the correlation coefficient ρ, were found between the activation level (nutrient requirement) and the tolerance of microorganisms to the toxicant. ρ is equal to 0.9 for the case of Cd in batch test and 0.6 in continuous test. The theory in this study provides generally good estimations to the dose‐response relationship at limiting nutrient conditions. The study indicate that nutrient conditions constitute an important factor in algal toxicity tests.     

Arsenic species in the well water and sediments of the blackfoot disease area in Taiwan

The blackfoot disease (BFD) observed in southwestern Taiwan is due to drinking high arsenic concentrations in well water. This paper presents some results concerning the distributions of arsenic species in water and sediments collected in the BFD (well, river and coastal) area and the background (lake and ocean) area for comparison. The results show that the concentrations of arsenate (870 ± 26 ug/L) and arsenite (70.2 ± 2.6 ug/ L) in well waters, and the contents of arsenic (1640 ug/g) with high percentage of easily reducible (Fe and Mn oxides, 91.7%) and exchangeable and carbonate (4.6%) phases in well sediments were much higher than those in river, lake and coastal samples. Low arsenic (3.46–31.8 ug/g) with high percentages (73.8–97.3%) of detritus and minerals phase with low percentages (0.4–9.8%) of total carbonate and exchangeable phases were found in the river and coastal samples in the BFD area as well as the lake and ocean samples in background area. It might suggest that the higher concentrations of toxic As(III) in well water and arsenic with higher values of easily reducible, carbonate and exchangeable phases in the well sediments, combined with the higher values of dissolved organic carbon, humic and fulvic acids and aromatic carbon as well as the higher fluorescence indensity in the well water are the key factors to cause the BFD in Taiwan.     

The estimation of bioconcentration factors of aromatic hydrocarbons by high‐performance liquid chromatography

The determination of Bioconcentration Factors (BCF) via HPLC capacity factors (k') has been studied, including the effect of column type and mobile phase composition on the correlation between log BCF and log k’. Values of BCF correlate well with the phenylsilica column capacity factors. The phenylsilica column followed by C18 column give better correlations than either C8 or C2 column. The use of HPLC with phenylsilica as stationary phase and methanol‐water as mobile phase in the prediction of BCF can be at least as good or better than the use of n‐octanol/water partitioning system. There are no significant differences in the correlations between log k’ and log BCF with the changes of methanol concentration in the mobile phase, and it seems that a high proportion of methanol in the eluent is required to obtain good results.     

Fate of organo‐heavy metal complexes of sludges from domestic wastes in soils: A simplified modelization

Simplified models provided information on the binding ability of organic acids with trace elements, the distribution of the formed organo‐heavy metal complexes at different pH, and the biological stability (biodegradation ability) of these complexes.     

Pah characteristics in ambient air within a steel industrial complex

Ambient air samples at ten sites in an iron and steel industrial complex were collected from June to December for analyzing polycyclic aromatic hydrocarbons (PAHs). Sixteen species of PAH components in air samples were identified. The results indicate that both gaseous phase and particle‐bound PAHs at the top of the cokemaking plants are unusually high. The profiles of particle‐bound PAHs indicate that the predominant species at the top of, the coke oven batteries are those of high molecular weight components. The major components of particle‐bound PAHs at sampling sites near the fenceline, however, include the medium molecular weight components. The PAH profiles of air samples within the industrial complex show a strong similarity to those of cokemaking plant samples. The concentrations and the specific content of benzo(a)pyrene in the iron and steel industrial complex are higher than those values measured in urban area, petrochemical industry park, and open‐air burning area.     

HO ‐ initiated oxidation of acridine and aminacrine in aqueous media: Kinetic model

The photodecomposition of diluted aqueous solutions of acridine and aminacrine in the presence of hydrogen peroxide was studied. Irradiation was carried out with a low pressure mercury vapour lamp. The kinetic model describes the photodegradation rate of the organic compound with respect to the technological parameters of the reactor and provides the reaction rate constants of hydroxyl radicals towards these two molecules. This model was extented to high hydrogen peroxide concentrations ([H₂O₂] > 200 μmol/l) by considering the reactivity of hydroxyl radicals towards hydrogen peroxide. This assumption allows us to define an optimal hydrogen peroxide concentration.     

Diazinon leaching through a sandy soil amended with different humic materials

The water leaching of diazinon (O,O‐diethyl‐O‐2‐isopropyl‐6‐methylpyrirnidin‐4‐yl phosphoroth‐ioate) through soil columns, was studied after column amendments with two well characterized humic acids (HA), in both liquid and solid state, and with the original raw organic materials, an oxidized coal and a leonardite, from which the HA were extracted. The percolation curves and the pesticide distribution over the soil columns showed that the addition of the raw organic materials and the solid HAs reduced significantly the mobility of the pesticide along the soil column. The oxidized coal was more effective than the leonardite original material; the different origin of the two carbon‐rich materials had an influence on the diazinon movement along the soil columns and such difference was enhanced with increasing addition rates. Moreover, incubation at field capacity for two months of the soil columns treated with raw oxidized coal and leonardite, largely enhanced the described effects on pesticide behaviour. A complete adsorption of diazinon on columns and a practical absence of leaching was observed when the HA from both materials were added in dissolved form. These results were explained with the swelling of the humic micelles in water and the enhanced availability of inner hydrophobic surfaces for the strong adsorption of diazinon. The water diffusion into the solid humic materials after two months incubation, also explains their high pesticide retention capacity. This work indicates the usefulness of either solid o dissolved humic substances, with the proper hydrophobic character, in preventing the vertical leaching of non‐polar organic pesticides in soils.     

Evaluation of linear alkylbenzenesulfonate (LAS) biodegradability in sediment by solid‐phase extraction and HPLC analysis

The linear alkylbenzenesulfonate (LAS) sorption on environmental sediments has been known long ago. Their high concentrations reflect the massive input of these chemicals from household and industrial uses. However few attempts were made to identify biodegradation metabolites of LAS in sediment. In this report, a method for the determination of these compounds in sediment samples by high‐performance liquid chromatography (HPLC) is described. The first step of our work was performed by solid‐phase extraction with octadecyl‐bonded silica (C18) mini‐columns and provided a suitable recovery of LAS (90 ± 5%) and most metabolites. Furthermore, laboratory investigations led to study the behaviour of LAS in sediment. The environmental samples used for this purpose were collected from a pond (named étang de Bolmon) located in the French Mediterranean coast. Our results were in agreement with an aerobic biodegradation process of LAS that occurred only with high values of sediment redox potential and needed the samples to be vigorously shaken to ensure adequate mixing and suspension of particulate material. In a stagnant sediment or under anaerobic conditions, LAS is not degraded. p‐Sulfophenylacetic acid and p‐sulfocinnamic acid were evidenced as predominant metabolites and were found not to be persistent.     

Determination and QSPR analysis of log Kow and log Koc for fluorine containing benzene derivatives

Octanol‐water partition coefficients (Kow) and soil organic carbon sorption coefficients (Koc) were determined for 14 fluorinated benzene derivatives. Quantitative structure‐property relationships were developed using molecular connectivity indices and quantum chemical parameters to analyze the most significant factors influencing these physico‐chemical properties of the compounds. The substitution by F in benzene derivatives has greater influence on Koc than on Kow.