PURPOSE: Biodegradation and biodecolorization of Drimarene blue K2RL (anthraquinone) dye by a fungal isolate Aspergillus flavus SA2 was studied in lab-scale immobilized fluidized bed bioreactor (FBR) system. METHOD: Fungus was immobilized on 0.2-mm sand particles. The reactor operation was carried out at room temperature and pH 5.0 in continuous flow mode with increasing concentrations (50, 100, 150, 200, 300, 500 mg l−1) of dye in simulated textile effluent on the 1st, 2nd, 5th, 8th, 11th, and 14th days. The reactors were run on fill, react, settle, and draw mode, with hydraulic retention time (HRT) of 24–72 h. Total run time for reactor operation was 17 days. RESULTS: The average overall biological oxygen demand (BOD), chemical oxygen demand (COD), and color removal in the FBR system were up to 85.57%, 84.70%, and 71.3%, respectively, with 50-mg l−1 initial dye concentration and HRT of 24 h. Reductions in BOD and COD levels along with color removal proved that the mechanism of biodecolorization and biodegradation occurred simultaneously. HPLC and LC–MS analysis identified phthalic acid, benzoic acid, 1, 4-dihydroxyanthraquinone, 2,3-dihydro-9,10-dihydroxy-1,4-anthracenedione, and catechol as degradation products of Drimarene blue K2RL dye. Phytotoxicity analysis of bioreactor treatments provided evidence for the production of less toxic metabolites in comparison to the parent dye. CONCLUSION: The present fluidized bed bioreactor setup with indigenously isolated fungal strain in its immobilized form is efficiently able to convert the parent toxic dye into less toxic by-products.

PURPOSE: We used a sequential extraction to investigate the effects of compost amendment on Cd fractionation in soil during different incubation periods in order to assess Cd stabilization in soil over time. METHODS: Pot experiments using rice plants growing on Cd-spiked soils were carried out to evaluate the influence of compost amendment on plant growth and Cd accumulation by rice. Two agricultural soils (Pinchen and Lukang) of Taiwan were used for the experiments. The relationship between the redistribution of Cd fractions and the reduction of plant Cd concentration due to compost amendment was then investigated. RESULTS AND DISCUSSION: Compost amendment in Pinchen soil (lower pH) could transform exchangeable Cd into the Fe- and Mn-oxide-bound forms. With increasing incubation time, exchangeable Cd tended to transform into carbonate- and Fe- and Mn-oxide-bound fractions. In Lukang soil (higher pH), carbonate- and Fe- and Mn-oxide-bonded Cd were the main fractions. Exchangeable Cd was low. Compost amendment transformed the carbonate-bound form into the Fe and Mn oxide form. Pot experiments of rice plants showed that compost amendment enhanced plant growth more in Pinchen soil than in Lukang soil. Compost amendment could significantly reduce Cd accumulation in rice roots in both Pinchen and Lukang soils and restrict internal transport of Cd from the roots to the shoots. Because exchangeable Cd can be transformed into the stronger bonded fractions quickly in Pinchen soil, a reduction of Cd accumulation in rice due to compost amendment of Pinchen soil was significant by 45 days of growth. However, carbonate-bonded fractions in Lukang soil may provide a source of available Cd to rice plants, and exchangeable and carbonate-bonded fractions are transformed into the other fractions slowly. Thus, reduction of Cd accumulation by rice due to compost amendment in Lukang soil was significant by 75 days of growth. CONCLUSIONS: The results of the study suggest that the effectiveness of compost amendment used for stabilization of Cd and to decrease the phytoavailability of Cd for rice plants is different in acidic and alkaline soils. In acidic soil, Cd fractionation redistributes quickly after compost amendment and shows a significant reduction of Cd accumulation by the plant within a few weeks. In alkaline soil, due to the strongly bound fractions of Cd being in greater quantity than the weakly bound ones, a longer period (a few months) to redistribute Cd fractions is needed.

INTRODUCTION: The paper analyses the environment pollution state in different case studies of economic activities (i.e. co-generation electric and thermal power production, iron profile manufacturing, cement processing, waste landfilling, and wood furniture manufacturing), evaluating mainly the environmental cumulative impacts (e.g. cumulative impact against the health of the environment and different life forms). MATERIALS AND METHODS: The status of the environment (air, water resources, soil, and noise) is analysed with respect to discharges such as gaseous discharges in the air, final effluents discharged in natural receiving basins or sewerage system, and discharges onto the soil together with the principal pollutants expressed by different environmental indicators corresponding to each specific productive activity. The alternative methodology of global pollution index (I GP * ) for quantification of environmental impacts is applied. RESULTS AND DISCUSSION: Environmental data analysis permits the identification of potential impact, prediction of significant impact, and evaluation of cumulative impact on a commensurate scale by evaluation scores (ESi) for discharge quality, and global effect to the environment pollution state by calculation of the global pollution index (I GP * ). CONCLUSIONS: The I GP * values for each productive unit (i.e. 1.664–2.414) correspond to an ‘environment modified by industrial/economic activity within admissible limits, having potential of generating discomfort effects’. The evaluation results are significant in view of future development of each productive unit and sustain the economic production in terms of environment protection with respect to a preventive environment protection scheme and continuous measures of pollution control.

INTRODUCTION: Titanium dioxide (TiO2) nanoparticle powders have been extensively studied to quickly photodegrade some organic pollutants; however, the effect of the particle size of TiO2 nanoparticle aggregates on degradation remains unclear because microscale aggregates form once the nanoparticle powders enter into water. METHODS: The degradation of azo dye by different particle sizes of TiO2 nanoparticle aggregates controlled by NaCl concentrations was investigated to evaluate the particle size effect. Removal reactions of reactive black 5 (RB5) with TiO2 nanoparticles followed pseudo-first-order kinetics. RESULTS: The increase of TiO2 dosage from 40 to 70 mg/L enhanced the degradation. At doses around 100 mg/L TiO2, degradation rates decreased which could be the result of poor UV light transmittance at high-particle concentrations. At average particle sizes of TiO2 nanopowders less than around 500 nm, the degradation rates increased with decreasing particle size. As the average particle size exceeded 500 nm, the degradation rates were not significantly changed. CONCLUSIONS: For the complete degradation experiments, the mineralization rates of total organic carbon disappearance are generally following the RB5 decolorization kinetic trend. These findings can facilitate the application of TiO2 nanoparticles to the design of photodegradation treatments for wastewater.

PURPOSE: Increases in dissolved organic carbon (DOC) concentrations have been reported in surface waters worldwide in the last 10 to 20 years. The causes behind these increases have been attributed to many factors, including climate change and decreasing depositions of atmospheric sulphate ([Formula: see text]). Trends in DOC concentrations and their potential causal factors were examined in a network of 30 lakes lying in undisturbed temperate and boreal catchments in the province of Quebec, Canada. METHODS: Temporal trends in lake DOC concentrations were analysed with the seasonal Kendall test. For each lake, the variation in DOC concentration over time was assessed in light of the variation in [Formula: see text] concentration in precipitation, air temperature, precipitation and solar radiation using the forward stepwise multiple regression. RESULTS: Between 1989 and 2006, significant increases in DOC were observed in most of the lakes, the mean rate of change being 0.05 mg L−1 year−1. Lake DOC concentrations were significantly explained by different models that yielded a variance explanation ranging from 13% to 77%. The models included long-term temperature variables (i.e. averaged over intervals of 10 years), short-term precipitation variables (i.e. summed over intervals 6 months), radiation (i.e. ice-free period prior to the DOC observation) and precipitation [Formula: see text] concentration as explanatory variables. CONCLUSION: Temporal changes in DOC concentrations seem more consistent with the evolution of climate parameters rather than [Formula: see text] concentrations despite the fact that most lakes were in the process of recovery, showing increases in pH.

PURPOSE: Ciprofloxacin (CIP), a broad-spectrum, second-generation fluoroquinolone, has frequently been found in hospital wastewaters and effluents of sewage treatment plants. CIP is scarcely biodegradable, has toxic effects on microorganisms and is photosensitive. The aim of this study was to assess the genotoxic potential of CIP in human HepG2 liver cells during photolysis. METHODS: Photolysis of CIP was performed in aqueous solution by irradiation with an Hg lamp, and transformation products were monitored by HPLC-MS/MS and by the determination of dissolved organic carbon (DOC). The cytotoxicity and genotoxicity of CIP and of the irradiated samples were determined after 24 h of exposure using the WST-1 assay and the in vitro micronucleus (MN) test in HepG2 cells. RESULTS: The concentration of CIP decreased during photolysis, whereas the content of DOC remained unchanged. CIP and its transformation products were not cytotoxic towards HepG2 cells. A concentration-dependent increase of MN frequencies was observed for the parent compound CIP (lowest observed effect level, 1.2 μmol L−1). Furthermore, CIP and the irradiated samples were found to be genotoxic with a significant increase relative to the parent compound after 32 min (P < 0.05). A significant reduction of genotoxicity was found after 2 h of irradiation (P < 0.05). CONCLUSIONS: Photolytic decomposition of aqueous CIP leads to genotoxic transformation products. This proves that irradiated samples of CIP are able to exert heritable genotoxic effects on human liver cells in vitro. Therefore, photolysis as a technique for wastewater treatment needs to be evaluated in detail in further studies, not only for CIP but in general.

INTRODUCTION: The copper bioaccumulation by the floating Lemna minor and by the completely submerged Ranunculus tricophyllus as a function of exposure time and copper concentration was studied, with the aim of proposing these species as environmental biosensors of the water pollution. RESULTS: The results show that both these aquatic angiosperms are good indicators of copper pollution because the copper uptake is the only function of metal concentration (water pollution). CONCLUSION: Uptake behavior is reported as a function of the time and concentration, based on the results of a 3-year study. Kinetic evaluations are proposed.

INTRODUCTION: The kinetics of the transformation of ammonia and acid gases into components of PM2.5 has been examined. The interactions of existing aerosols and meteorology with the transformation mechanism have also been investigated. The specific objective was to discern the kinetics for the gas-to-particle conversion processes where the reactions of NH3 with H2SO4, HNO3, and HCl take place to form (NH4)2SO4, NH4NO3, and NH4Cl, respectively, in PM2.5. MATERIALS AND METHODS: A Teflon-based outdoor environmental chamber facility (volume of 12.5 m3) with state-of-the-art instrumentation to monitor the concentration–time profiles of precursor gases, ozone, and aerosol and meteorological parameters was built to simulate photochemical reactions. RESULTS AND DISCUSSION: The reaction rate constants of NH3 with H2SO4, HNO3, and HCl (i.e., k S, k N, and k Cl) were estimated as (1) k S = 2.68 × 10−4 (±1.38 × 10−4) m3/μmol/s, (2) k N = 1.59 × 10−4 (±8.97 × 10−5) m3/μmol/s, and (3) k Cl = 5.16 × 10−5 (±3.50 × 10−5) m3/μmol/s. The rate constants k S and k N showed significant day–night variations, whereas k Cl did not show any significant variation. The D/N (i.e., daytime/nighttime values) ratio was 1.3 for k S and 0.33 for k N. The significant role of temperature, solar radiation, and O3 concentration in the formation of (NH4)2SO4 was recognized from the correlation analysis of k S with these factors. The negative correlations of temperature with k N and k Cl indicate that the reactions for the formation of NH4NO3 and NH4Cl seem to be reversible under higher temperature due to their semivolatile nature. It was observed that the rate constants (k S, k N, and k Cl) showed a positive correlation with the initial PM2.5 levels in the chamber, suggesting that the existing surface of the aerosol could play a significant role in the formation of (NH4)2SO4, NH4NO3, and NH4Cl. CONCLUSIONS: Therefore, this study recommends an intelligent control of primary aerosols and precursor gases (NO x , SO2, and NH3) for achieving reduction in PM2.5 levels.

BACKGROUND, AIM: The aims of the NORMACAT project are: to develop tools and unbiased standardized methods to measure the performance and to validate the safety of new materials and systems integrating photocatalysis, to develop new photocatalytic media with higher efficiency and to give recommendations aimed at improving the tested materials and systems. METHOD: To achieve this objective, it was necessary to design standardized test benches and protocols to assess photocatalytic efficiency of materials or systems used in the treatment of volatile organic compounds (VOCs) and odour under conditions close to applications. The tests are based on the validation of robust analytical methods at the parts per billion by volume level that not only follow the disappearance of the initial VOCs but also identify the secondary species and calculate the mineralization rates. RESULTS: The first results of inter-laboratory closed chamber tests, according to XP B44-013 AFNOR standard, are described. The photocatalytic degradation of mixtures of several defined pollutants under controlled conditions (temperature, relative humidity, initial concentration) was carried out in two independent laboratories with the same photocatalytic device and with various analytical procedures. Comparison of the degradation rate and of the mineralization efficiency allowed the determination of the clean air delivery rate in both cases. Formaldehyde was the only by-product detected during photocatalytic test under standardized experimental conditions. The concentration of transient formaldehyde varied according to the initial VOC concentration. Moreover the photocatalytic reaction rate of formaldehyde in mixture with other pollutants was analysed. It was concluded that formaldehyde concentration did not increase with time. CONCLUSION—PERSPECTIVE: This type of experiment should allow the comparison of the performances of different photoreactors and of photocatalytic media under controlled and reproducible conditions against mixtures of pollutants including formaldehyde.