Continental-scale distribution and inter-continental transport of four polychlorinated biphenyl (PCB) congeners (28, 101, 153, 180) from 1950 to 2010 were studied using the global multicompartment chemistry transport model MPI-MCTM. Following identical primary emissions for all PCB congeners into air, most of the burden is stored in terrestrial (soil and vegetation) compartments. Thereby, PCB-28, PCB-101 and PCB-153 show a shift of the soil burden maxima from source to remote regions. This shift is downwind with regard to the westerlies for Eurasia and upwind for North America and more prominent for the lighter PCBs than for PCB-153 or PCB-180. In meridional direction, all congeners’ distributions underwent a northward migration in Eurasia and North America since the 1950s. Inter-continental transport from Eurasian sources accounts largely for contamination of Alaska and British Columbia and determines the migration of the PCB distribution in soil in North America. Trans-Pacific transport occurs mainly in the gas phase in boreal winter (December–January–February) at 3–4 km altitude and is on a multi-year time scale strongly linked to the atmospheric pressure systems over the Pacific. Inter-continental transport of the lighter, more volatile PCBs is more efficient than for the heavier PCBs.

This study evaluates the effect of integrated solar-assisted advanced oxidation process (AOP) and biological treatment on the extent of degradation of effluents from chlorination (C) and first alkaline extraction (E1) stages of soda pulp bleaching in agro-residue-based pulp and paper mill. Biodegradation of the effluents was attempted in suspended mode using activated sludge from the functional pulp and paper industry effluent treatment plant acclimatized to effluents in question. The photocatalytic treatment was employed using zinc oxide (ZnO) in slurry mode for decontamination of effluents in a batch manner and the degradation was evaluated in terms of reduction in chemical oxygen demand. The biological treatment (24 h) of C and E1 effluent resulted in 30 and 57 % of degradation, respectively. Solar-induced AOP of C and E1 effluents resulted in 53 and 43 % degradation under optimized conditions (2.5 g L−1 ZnO at pH 8.0) after 6 h of exposure. For C effluent, a short duration of solar/ZnO (1 h) prior to biological treatment reduced the time required at biological step from 24 to 12 h for almost same extent (92 %) of degradation. However, sequential biological treatment (24 h) followed by solar/ZnO (2 h) resulted in 85.5 % degradation. In contrast, in the case of E1 effluent, sequential biological (24 h)–solar/ZnO (2 h) system effectively degrades effluent to 95.4 % as compared to 84.8 % degradation achieved in solar/ZnO (2 h)–biological treatment (24 h) system. In the present study, the sequencing of photocatalysis with the biological treatment is observably efficient and technically viable process for the complete mineralization of the effluents.

PURPOSE: Exploratory data analysis (EDA) is applied in this research to study the behavior of radioactive aerosols present in the surface atmosphere of Granada, using 7Be as radiotracer. The reason for this study is to reduce the large number of parameters involved in understanding their behavior, given the complexity of the atmosphere. METHODS: Aerosol particles were collected weekly in Granada (Spain) over a 5-year period. Low-background gamma spectrometry was used to determine concentrations of 7Be-aerosol activity. The variables studied were: 7Be concentration, cosmic ray intensity, temperature, temperature interval, rainfall, relative humidity, and Saharan intrusions. Least significant difference test (LSD), hierarchical cluster analysis (HCA), and principal component analysis (PCA) with varimax rotation have been applied to study the datasets. RESULTS AND DISCUSSION: The results of our study reveal that aerosol behavior is represented by two principal components which explain 86.23 % of total variance. Components PC1 and PC2 respectively explain 74.61 and 11.62 % of total variance. PC1 explains the cyclical and seasonal pattern of the samples, while PC2 is related to the production of 7Be. In addition, PCA and HCA show good distribution of the samples by families with two groups, summer and winter, at the extremes and spring–autumn in the middle. This result corroborates that there are no differences between spring and autumn in the climate of Granada. CONCLUSIONS: EDA has been found to be quite useful in studying the behavior of radioactive aerosols in the surface atmosphere of a city with the climate and geographical characteristics of Granada.

PURPOSE: Lack of focus on the treatment of wastewaters bearing potentially hazardous pollutants like 1,1,2 trichloroethane and 1,1,2,2 tetrachloroethane in anaerobic reactors has provided an impetus to undertake this study. The objective of this exercise was to quantify the behavior of upflow anaerobic sludge blanket reactors and predict their performance based on the overall organic substrate removal. METHODS: The reactors (wastewater-bearing TCA (R2), and wastewater-bearing TeCA (R3)) were operated at different hydraulic retention times (HRTs), i.e., 36, 30, 24, 18, and 12 h corresponding to food-to-mass ratios varying in the range of 0.2–0.7 mg chemical oxygen demand (COD) mg−1 volatile suspended solids day−1. The process kinetics of substrate utilization was evaluated on the basis of experimental results, by applying three mathematical models namely first order, Grau second order, and Michaelis-Menten type kinetics. RESULTS: The results showed that the lowering of HRT below 24 h resulted in reduced COD removal efficiencies and higher effluent pollutant concentrations in the reactors. The Grau second-order model was successfully applied to obtain the substrate utilization kinetics with high value of R 2 (>0.95). The Grau second-order substrate removal constant (K 2) was calculated as 1.12 and 7.53 day−1 for reactors R2 and R3, respectively. CONCLUSION: This study demonstrated the suitability of Grau second-order kinetic model over other models, for predicting the performance of reactors R2 and R3, in treating wastewaters containing chlorinated ethanes under different organic and hydraulic loading conditions.

PURPOSE: Prevalence of organic pollutants or their natural analogs in soil is often assumed to lead to adaptation in the bacterial community, which results in enhanced bioremediation if the soil is later contaminated. In this study, the effects of soil type and contamination history on diesel oil degradation and bacterial adaptation were studied. METHODS: Mesocosms of mineral and organic forest soil (humus) were artificially treated with diesel oil, and oil hydrocarbon concentrations (GC-FID), bacterial community composition (denaturing gradient gel electrophoresis, DGGE), and oil hydrocarbon degraders (DGGE + sequencing of 16S rRNA genes) were monitored for 20 weeks at 16°C. RESULTS: Degradation was advanced in previously contaminated soils as compared with pristine soils and in coniferous organic forest soil as compared with mineral soil. Contamination affected bacterial community composition especially in the pristine mineral soil, where diesel addition increased the number of strong bands in the DGGE gel. Sequencing of cloned 16S rRNA gene fragments and DGGE bands showed that potential oil-degrading bacteria were found in mineral and organic soils and in both pristine and previously contaminated mesocosms. Fast oil degradation was not associated with the presence of any particular bacterial strain in soil. CONCLUSIONS: We demonstrate at the mesocosm scale that previously contaminated and coniferous organic soils are superior environments for fast oil degradation as compared with pristine and mineral soil environments. These results may be utilized in preventing soil pollution and planning soil remediation.

PURPOSE: An online cloud-point extraction (CPE) coupled with flow injection method is developed for the separation and preconcentration of palladium and lead from various matrices using flame atomic absorption spectrometry (FAAS). METHOD: The method employs the formation of complexes of the metallic species with dimethylglyoxime, which are subsequently entrapped in the micelles of the surfactant Triton X-114, upon increase of the solution temperature to 60°C and loaded into the flow injection system at a flow rate of 4.6 mL min−1. The surfactant rich-phase was retained in a minicolumn packed with animal wool at pH 6 and eluted with 1.0 mol L−1 nitric acid in methanol at a flow rate of 1.1 mL min−1 directly into the nebulizer of the FAAS. The CPE variables and flow injection conditions affecting the analytical performance of the combined methodology was studied and optimized. RESULTS: Under the optimized conditions for 25 mL of preconcentrated solution, the enrichment factors were 51 and 44, and the limit of detections were 1.0 and 1.4 ng mL−1 for palladium and lead, respectively. Finally, the developed method was applied for the determination of palladium and lead in street dust, soil, radiology waste, catalytic converter, and urban aerosol samples. CONCLUSIONS: Cloud-point extraction coupled with flow injection-FAAS was proposed as an effective preconcentration and separation method for Pd and Pb determination in radiology waste, road dust, soil, and urban aerosol samples. The most favorable feature of this method is its much higher selectivity, sensitivity, rapidity, good extraction efficiency, and employs the green chemistry concept, as it does not require the addition of toxic chemicals. In addition, this proposed method gives very low detection limits and good relative standard.

INTRODUCTION: In this study, UV/Oxone/Co2+ oxidation process was applied to degradation of ofloxacin (OFL) in the presence of Co2+ as the catalytic and Oxone as the oxidant. The operation parameters including pH, temperature, dosages of reagents, and reaction time were studied in detail. RESULTS: The results showed that the optimum conditions for the UV/Oxone/Co2+ processes were determined as follows: temperature = 25°C, pH = 5.0, [Oxone] = 0.6 mmol/L, [Oxone]/[Co2+] = 1,000, and reaction time = 60 min. Under these conditions, 100% of the OFL degraded. The kinetics was also studied, and degradation of OFL by the UV/Oxone/Co2+ process could be described by first-order kinetics. CONCLUSIONS: Mineralization of the process was investigated by measuring the total organic carbon (TOC), and the TOC decreased by 87.0% after 60 min. This process could be used as a pretreatment method for wastewater containing ofloxacin.

BACKGROUND AND AIM: The biosorption of Basic Violet 5BN (BV) and Basic Green (BG) by waste brewery’s yeast (WBY) from single and binary systems was investigated. RESULTS AND DISCUSSION: For the single system, the adsorption of both dyes is pH-dependent and the optimum value is 5.0. At a lower initial concentration, the kinetic data agree well with both pseudo-first-order and pseudo-second-order models, while at a higher initial concentration the data fit better with the pseudo-second-order model. External diffusion is the rate-controlling step at initial fast adsorption, and then the intraparticle diffusion dominated the mass transfer process. Equilibrium data for BV and BG fit better with the Langmuir model. The maximum biosorption capacities of WBY onto BV and BG obtained at 303 K are 114.65 and 141.89 mg/g, respectively. Thermodynamic analysis reveals that the adsorption process for the two dyes is spontaneous and exothermic. CONCLUSIONS: The hydroxyl, amino, amide, carboxyl, and phosphate groups are responsible for the biosorption based on Fourier transform infrared analysis. The presence of BV significantly affects the biosorption of BG, but not vice versa. The P-factor model and Sheindrof–Rebhun–Sheintuch equation gave a good description of the equilibrium adsorption data at the multicomponent system.

PURPOSE: This paper presents a novel approach to interpret ground-level O3 with the measured atmospheric stability index (ASI). METHODS: O3 concentrations were monitored by automatic analysers at three types of stations: traffic site, residential site and regional background site in 2005, and the ASI was simultaneously measured by observing radon and its short-lived decay products. RESULTS: The observed results showed a clear annual variation of O3 concentrations with a maximum in spring, relatively high at the regional background site over 120 ppb, and lower at the residential and traffic sites at about 70 ppb. ASI gives information about the dilution properties of the lower boundary layer and allows to highlight the relevant role of the dilution factor in determining atmospheric pollution events. We demonstrated the analysis of O3 night peak episodes with vertical wind and ASI. CONCLUSIONS: With the advantage of ASI and vertical wind profiles, it was possible to isolate particular photochemical pollution phenomena of O3 peaks from the free troposphere reservoir or formed by local reactions. This shows that the index constitutes a powerful and valuable tool for describing O3 night-peak episodes at background station.

PURPOSE: In this study, we investigated the effects of maternal transfer of bisphenol A (BPA) and di(2-ethylhexyl) phthalate (DEHP) during gestational and weaning periods on gonadal development of male offspring. METHODS: Pregnant CD-1 mice were administered by gavages in corn oil with 0.1, 1, or 10 mg/kg/day of BPA and DEHP from gestational days (GD1–21) to the weaning period (postnatal days (PND) 1–21). RESULTS: Our data indicated that the exposure significantly reduced the male-to-female sex ratio and the sizes of the gonads of male pups as recorded at PND15. The testes of the perinatally exposed male pups were developed less and the expression levels of testicular anti-mullerian hormone, androgen receptor, cyclin A, and StAR were significantly lesser than the control male pups. The less developed testes were accompanied with significant reductions in the expression levels of Gnrh and Fsh at the hypothalamic–pituitary levels. The negative effects were found to be persistent in the sexually mature pups at PND42. CONCLUSION: Our data reveal that the maternal transfer of BPA and DEHP may impose negative influence on the development and functions of the reproductive system of male pups.