Sorption of strontium on bentonite

Sorption of Sr on bentonite was studied using the batch technique. Distribution coefficients (K_d) were determined as a function of contact time, pH, sorbent and sorbate concentration and temperature. The data were interpreted in terms of Freundlich, Langmuir and Dubinin-Radushkevich isotherms. Thermodynamic parameters for the sorption system were determined at three different temperatures. The positive value of the heat of sorption, ΔH° = 30.62 kJ/mol at 298 K, shows that the sorption of strontium on bentonite is endothermic. The negative value of the free energy of sorption, ΔG° = −10.69 kJ/mol at 298 K, shows the spontaneity of the reaction. ΔG° becomes more negative with increasing temperature, which shows that the sorption process is more favorable at higher temperatures. The mean free energy for sorption, E 9 kJ/mol, suggests that ion exchange is the predominant mode of sorption in the Sr concentration range studied, i.e. 0.01 – 0.3 mol/dm³. The presence of complementary cations depresses the sorption of strontium on bentonite in the order Ca²⁺>Mg²⁺>K⁺>Na⁺. Some organic complexing agents and natural ligands also affect the sorption of strontium. The desorption studies with ground water at low strontium loadings on bentonite show that about 90% of Sr is irreversibly sorbed on the bentonite.     

Smoldering combustion of dust layer on hot surface

The critical temperature as well as the critical flux for ignition of a dust layer of cornflour and a mixture of wheatflour and cornflour (80% wheatflour+20% cornflour) on a hot plate have been determined. The moulded sample was cylindrical in shape and of different heights and diameters. The particle size of dusts ranged between 63 μm to 150 μm. The temperature–time histories for self-heating without ignition and with ignition are offered, showing the critical boundaries between them. Also the times to ignition for each dust, showing the effect of sample size on their values, are determined. Certain experimental correlations which relate to times to ignition, as well as the critical temperature for ignition and thermal and geometrical dimensions of sample are presented.     

The assessment of water quality in the Lower Luján River (Buenos Aires,Argentina): phytoplankton and algal bioassays

The monitoring of river phytoplankton and several hydrological, physical and chemical variables, in combination with bioassays using Selenastrum capricornutum Printz, allowed the characterisation of three distinct reaches of the Lower River Luján. The upstream stretch, characterised by the lowest depth and discharge, registered the highest nutrient, dissolved heavy metal and chlorophyll a concentrations in accordance with low phytoplankton diversity and the occurrence of several species typical of organically polluted lowland rivers. A downstream improvement, concomitant to increasing river discharge, is revealed by a progressive decrease of organic pollution parameters even though algal toxicity is registered through bioassays. The water input from the Parana River through the G. Arias Channel plays an important role in the regulation of the limnology of the Lower Luján River. As a result of marked increasing discharge, depth and width, there is a decrease in nutrient concentration and phytoplankton density and an increase in dissolved oxygen concentration. Likewise, algal growth rates in the bioassays showed less toxic effect.     

Molecular Detection of Human Salivirus in Italy Through Monitoring of Urban Sewages

Food and Environmental Virology - Salivirus (SalV) is a newly discovered virus associated to acute gastroenteritis in humans. In Italy, its prevalence and genetic diversity is unknown. To reduce...     

Releases of phosphate fertilizer industry in the surrounding environment: Investigation on heavy metals and polonium-210 in soil

Distribution of Cu,Zn,Pb,Cr,Ni,Mn concentrations and the activity of polonium-210 in the surrounding area of a phosphate fertilizer industry located on the eastern coast of the Mediterranean Sea has been determined.Nineteen sampling sites were distributed around the industrial zone on a surface area of about 100,000 m2.Atomic absorption spectroscopy and Alpha spectroscopy were used to quantify the heavy elements and polonium-210,respectively.Investigation on a particle scale was conducted by TEM and SEM coupled to EDX and X-ray cartography to determine the nature of heavy elements carriers and their distribution.Heavy elements were mainly concentrated inside the particle size fraction 50 μm.Their levels decreased with distance increasing from the industry.According to the reference soil,enrichment factors were about 10,15,32 and 100 times for Zn,Pb,Cu,and Cr,respectively inside the particle size fraction 50 μm on the closest sites to the industry.The main contaminant sources were transport and storage of row materials and the free release of phosphogypsum waste.Heavy elements were entrapped inside agglomerates of sulfates,phosphates and iron oxihydroxides in a di used shape.Polonium-210 with an enrichment factor of about 56,showed the same behavior of the spatial distribution of the trace elements.