Ambient aerosol concentrations have been implicated in human health effects, in visibility reduction in urban and regional areas, in acid deposition and in perturbing the Earth’s radiation balance. The main concern of the air quality managers is to achieve compliance to the established air quality standards (AQS). As AQS are exceeded in numerous sites worldwide, it is essential to reduce the emissions. Having decided which statistical distribution fits well to the PM10 parent distribution, it is feasible to estimate the reduction in emissions that is required in order to meet AQS. In this study, it is verified that the PM10 concentration distribution can be adequately simulated by lognormal distribution, a conclusion drawn by the calculation of several statistical indexes. The study area is the city of Volos in central Greece, which is experiencing an unpleasant situation concerning the levels of PM10 pollution. The probability density function of lognormal distribution is capable to predict the number of days when the European Union (EU) AQS for PM10 concentration are exceeded in Volos area. Furthermore, the minimum reduction in current emission sources of PM10 required in order to meet the air quality regulations that are established by the EU is calculated for the study area and is found to be ~33%. The results could be utilized as reference for air pollution control strategy.

Two varieties of Bechmeria nivea (L.) Gaud. (Ramie), namely, triploid Tri-2 and diploid Xiangzhu-3, were potted with soils from Guangdong for 15 weeks and treated with 10 mmol kg⁻¹ EDTA or EGTA before harvest at 17th week. Lead, Zn, and Cd in plant and soil materials were analyzed, and their potential ecological risk in soils was simultaneously evaluated. These three metals in soils was found to be above 14.4, 3.0, and 29.9 times higher than the national (China) background value, 10.9, 6.19, and 96.7 times higher than the local (Guangdong) background value, and 1.25, 1.20, and 9.67 times higher than the maximum permissible concentration for soils, respectively. An ecological risk analysis of metals using Häkanson's method indicated an extremely high contamination and a significantly high potential ecological risk by these three metals in soils. The both ramie varieties contained respective concentration exceeding the concentration of <10, <80, and <0.27 mg kg⁻¹, respectively, for Pb, Zn, and Cd in normal plants, suggesting they were multimetal tolerant. Tri-2 generally contained higher Pb, Zn, and Cd than Xiangzhu-3. Treatment with EDTA or EGTA applied at 10 mmol kg⁻¹ generally promoted Pb or Cd concentration in both plants while the uptake of Zn was depressed. The ramie variety of Tri-2 and Xiangzhu-3 could extract 0.161 and 0.147 t ha⁻¹ of Cd, respectively, equaling to the 0.17 t Cd per hectare by Cd-hyperaccumulating species Viola baoshanensis. Therefore, two ramie varieties in this study had a higher extracting potential for removal of Cd from contaminated soils.

The primary purpose of water aeration is to increase the oxygen saturation of the water. This can be achieved by using hydraulic structures because of substantial air bubble entrainment at these structures. This paper reviewed the literature on hydraulic structures used in water aeration processes. The hydraulic structures were divided into two groups as the high-head flow systems and the free-surface flow systems. The high-head flow systems were circular and venturi nozzles, pipe with venturi tube, and high-head conduit, and the free-surface flow systems were weir, stepped cascade, and free-surface conduit. Air/water flow ratio and aeration efficiency in circular nozzles with air holes and venturi nozzles were significantly high. Pipes with venturi tubes showed high aeration efficiency although they had low air/water flow ratio. In high-head and free-surface conduits, almost full oxygen transfer, up to the saturation value, occurred. Forty-five degrees triangular sharp-crested weir had significantly better air/water flow ratio and aeration efficiency than other sharp-crested weir shapes. Stepped cascades, in particular nappe flow regime, were very efficient means of aeration.

The objective of the investigations of the Cetina River, located in southern Croatia, was to record specific characteristics and properties of the Cetina waters at nine stations. In addition to measurements undertaken in the Cetina River, the water quality of its most significant springs and tributaries, such as Kosinac, Šilovka, Studenci and Mala Ruda, Velika Ruda and Grab, has also been measured. The water quality in the Cetina watershed has been evaluated in the following storage reservoirs: Peruča, Buško Blato and Prančevići. The nitrogen compounds and phosphorus concentrations have been estimated at all these sampling sites over a 3-year period (2005-2008). Concentration levels at the Cetina-Vinalić sampling site for total N (from August 2005 to December 2008) ranged from 0 to 1.759 mg/L, for NH₃-N from 0 to 0.374 mg/L, for NO₃-N from 0.063 to 0.916 mg/L and for PO₄-P from 0 to 0.099 mg/L. The results prove that the Cetina-Vinalić sampling site is not polluted by nitrogen and phosphorus compounds. The river section from Trilj to the Prančevići dam, where the water is used for the water supply of Omiš, Makarska and Dalmatian islands, has been polluted by wastewater because the majority of agricultural area, roads, industry and settlements are located upstream of it. The highest concentration for total N of 1.128 mg/L and of 1,527 total coliforms in 100 mL, expressed as a mean value for a 3-year period of investigations, was found at the sampling site Trilj. The results of concentration changes at the Čikotina Lađa and Cetina Radmanove Mlinice sampling sites show no regularities. The highest concentration for total N of 0.941 mg/L was measured at the Cetina Radmanove Mlinice during 2007. The highest concentration for NO₃-N of 0.916 mg/L was measured at the same sampling site. According to the investigations of the water quality of the Cetina springs and tributaries, the bacteriological most polluted river spring is Kosinac, and the bacteriological most polluted river tributary is Grab. With reference to the water quality in the Cetina storage reservoirs, it may be concluded that the lowest quality standard has been found within the Prančevići storage reservoir regarding nitrogen compounds and phosphorus concentration levels.

The potential competitive effect of background electrolytes (Na₂HPO₄ ·2H₂O, NaHCO₃, Na₂SO₄ and NaCl solutions) on arsenate adsorption onto synthetic 2-line ferrihydrite has been studied by means of kinetic batch experiments conducted at pH values from 4.0 to 10.0 and at anionic concentrations of 0.01 and 0.1 M. The results indicate that the adsorptive capacity of ferrihydrite for arsenate decreases strongly in the presence of phosphate species at pH in the range of 4-10 and in the presence of bicarbonate at pH 8.3 as a consequence of their competitive effect. Analogously to phosphate, a surface interaction of inner-sphere type between ferrihydrite and bicarbonate is suggested. Chloride has negligible effects on arsenate adsorption processes, confirming it as an outer-sphere ion that does not compete with the inner-sphere binding peculiar to arsenate onto ferrihydrite. Sulphate exhibits an intermediate behaviour; at 0.01 M concentration, the competitive effect of sulphate is similar to that of chloride, whereas at 0.1 M concentration sulphate shows a moderate influence on arsenate adsorption. The results of the kinetic studies can be summarised by the following order of competitive capacity: phosphate > carbonate > sulphate > chloride. The process of arsenate adsorption follows pseudo-second order kinetics and the reaction half-time notably increases in the presence of strong competitor anions such as phosphate and carbonate with respect to an ineffective competitor anion such as chloride. Modelling of arsenate adsorption with PHREEQC, according to the Generalized Two-Layer Model, confirms that the pH effect is notably less important than the competitive effect of carbonate species in determining the amount of arsenate adsorbed onto ferrihydrite at pH 8.3 in 0.1 M NaHCO₃ solution, whereas the model greatly underestimates the competitive effect of carbonate species at pH 8.3 in 0.01 M NaHCO₃ solution. The results of the batch experiments in 0.1 M NaHCO₃ solution are substantiated by XPS analyses of ferrihydrite after immersion in the same solution, both with and without dissolved arsenate. XPS confirms the interaction between ferrihydrite surface and arsenate; the binding energy of As3d shifts towards higher binding energies after adsorption with respect to the pure compound Na₂HAsO₄·7H₂O taken as reference standard. In presence of carbonate species, the As3d binding energy is found at intermediate values. XPS quantitative analysis shows a depletion of arsenate on ferrihydrite surface, providing further evidence of the competition of the two species (i.e. arsenate and bicarbonate) for the ferrihydrite adsorption sites. Important environmental implications concerning arsenic mobility, as well as possible application in various fields (e.g. irrigation agriculture, soil decontamination, water treatment), might derive from these findings.

Investigations were made on living strains of fungi in a bioremediation process of three metal (lead) contaminated soils. Three saprotrophic fungi (Aspergillus niger, Penicillium bilaiae, and a Penicillium sp.) were exposed to poor and rich nutrient conditions (no carbon availability or 0.11 M d-glucose, respectively) and metal stress (25 µM lead or contaminated soils) for 5 days. Exudation of low molecular weight organic acids was investigated as a response to the metal and nutrient conditions. Main organic acids identified were oxalic acid (A. niger) and citric acid (P. bilaiae). Exudation rates of oxalate decreased in response to lead exposure, while exudation rates of citrate were less affected. Total production under poor nutrient conditions was low, except for A. niger, for which no significant difference was found between the poor and rich control. Maximum exudation rates were 20 µmol oxalic acid g⁻¹ biomass h⁻¹ (A. niger) and 20 µmol citric acid g⁻¹ biomass h⁻¹ (P. bilaiae), in the presence of the contaminated soil, but only 5 µmol organic acids g⁻¹ biomass h⁻¹, in total, for the Penicillium sp. There was a significant mobilization of metals from the soils in the carbon rich treatments and maximum release of Pb was 12% from the soils after 5 days. This was not sufficient to bring down the remaining concentration to the target level 300 mg kg⁻¹ from initial levels of 3,800, 1,600, and 370 mg kg⁻¹in the three soils. Target levels for Ni, Zn, and Cu, were 120, 500, and 200 mg kg⁻¹, respectively, and were prior to the bioremediation already below these concentrations (except for Cu Soil 1). However, maximum release of Ni, Zn, and Cu was 28%, 35%, and 90%, respectively. The release of metals was related to the production of chelating acids, but also to the pH-decrease. This illustrates the potential to use fungi exudates in bioremediation of contaminated soil. Nonetheless, the extent of the generation of organic acids is depending on several processes and mechanisms that need to be further investigated.

It is well known that mass transfer of a solid compound into a liquid phase is characterized by mutual properties of both sides. Solubilization capacity of the liquid phase is primary affected by its composition in inorganic species inducing salting in/out effect evaluated by Setschenow constant, generally defined at 298.15 K. On the other hand, the equilibrium process is highly influenced by polar compatibility issue. Therefore, the study of such transfer is essential in order to set the role of each party participating in the solid-liquid equilibrium. Thus, a comparison of transfer magnitude and feasibility of carbaryl from pure water, to seawater, and lab-made seawater was held. To do so, solubility of the compound was experimented at different temperature in multiple media. Solubility determination is based on the saturation of a specific heated fluid passing through a saturation cell. The solute transported is subsequently trapped in a specific extraction column. Back flashing method is then applied to dissolve the compound. After validation, aqueous solubility of carbaryl was studied as function of temperature ranging from (273.15 to 318.15 K) at atmospheric pressure. In addition, solubility was determined in pure, seawater, and corresponding lab-made water, thus solubility values ranged from 3.57E-06 to 3.49E-05 in pure water, from 3.04E-06 to 2.53E-05 in seawater and from 6.51E-06 to 3.61E-05 in lab-made water. As a result, thermophysical properties of transfer and usage of lab-made water on the mass transfer properties divergence was spotted. The Salting out phenomenon observed for carbaryl was interpreted by the internal pressure theory that suggests the reduction of internal cavities in the presence of salt, making solubilization process more difficult to achieve. Thus, showing an overall endogenic process with a positive Gibbs free energy of transfer that is highly affected by the magnitude of salting out effect and the temperature. The molar entropy of transfer increases versus temperature caused by the disorder of solvent molecules due to the dissolution process.

Present research has delineated the biosorption potential of three different nonliving biomasses namely eucalyptus bark saw dust, mango bark saw dust, and pineapple fruit peel with respect to Zn (II) ion removal from liquid phase through batch experiments. The efficacy of Zn (II) ion biosorption onto surface of biosorbents was judged and correlated with biosorbent particle size, surface chemistry, and surface texture. Maximum metal ion uptake capacity, percentage removal, and minimum equilibrium concentration as 1.688 mg/g, 84.4%, and 1.56 mg/l, respectively, was obtained using eucalyptus bark saw dust mediated biosorption followed by mango bark saw dust as 1.028 mg/g, 51.4%, and 4.867 mg/l and pineapple fruit peel as 0.45 mg/g, 22.9%, and 7.71 mg/l, respectively, at a particle size of 0.5 mm. Additionally, present investigation also proved that biosorption efficiency and metal ion interaction with adsorbent surface also depends upon presence of functional groups involved in metal ion adsorption and surface porosity.

Actually, there is a growing interest in finding efficient low-cost materials that allow the removal of chemical substances from water in order to decrease the environmental impact. The use of nanoscale systems is a new area of investigation for the elimination of polluting agents from water among other useful applications in science and technology. In this work, removal of indigo blue in water solutions has been evaluated using Fe/Cu nanoparticles and composites of C/Fe–Cu nanoalloy. The first composite was using carbon obtained by pyrolysis of sewage sludge with Fe/Cu nanoparticles (MCL-NP); the second one was made with commercial activated carbon and Fe–Cu nanoparticles (CAC-NP). Synthesis of materials were carried out by the sodium borohydride reduction of FeSO4[Symbol: see text]7H2O and CuSO4[Symbol: see text]5H2O aqueous mixture. Batch adsorption and isotherm experiments were carried out in order to know the behavior of each adsorbent material employed. The experimental data were adjusted to Langmuir, Freundlich, and BET models.

Nonpoint source pollution management initiated by the Ministry of Environment (MOE) in Korea resulted to the construction of 25 pilot facilities termed Best Management Practices (BMPs) until 2005. The national nonpoint sources control projects were employed to fulfill the Total Maximum Daily Load programs. The long-term monitoring being conducted at the sites which began in 2006 is providing detailed insight into the performance of the BMPs. The experience and performance data will be used to better understand and implement similar structural BMPs in the future as well as to assist the MOE in developing the design and maintenance guidelines of BMPs. This study presents the results gathered from the monitoring field tests and experiments over 22 rainfall events between the June 2006 and September 2008 period investigating the pollutant removal efficiency of the infiltration trench BMP that is one of the 25 pilot projects of the MOE. In addition, it includes the development of simple linear regression models to estimate constituent event mean concentration. The results reveal high treatment efficiencies for total suspended solids (89%); biochemical oxygen demand, chemical oxygen demand, and dissolved organic carbon (89-93%); oil and grease (100%); cadmium, lead, and zinc (89-93%); total nitrogen (84%); and total phosphorus (82%). The monitoring data and results will represent a step forward to a better prediction of impacts in the environment and to the national development of BMPs for sustainable watershed management in the country.