Modeling Air Flow Dynamics in Radon Mitigation Systems: A Simplified Approach

Subslab air flow dynamics provide important diagnostic information for designing optimal radon mitigation systems based on the subslab depressurization technique. In this paper, it is suggested that subslab air flow induced by a central suction point be treated as radial air flow through a porous bed contained between two impermeable disks. Next, we show that subslab air flow is most likely to be turbulent under actual field situations in houses with subslab gravel beds, while remaining laminar when soil is present under the slab. The physical significance of this model is discussed and simplified closedform equations are derived to predict pressure and flows at various distances from a single central depressurization point. A laboratory apparatus was built in order to verify our model and experimentally determine the model coefficients of the pressure drop versus flow for commonly encountered subslab gravel materials. These pressure drop coefficients can be used in conjunction with our simplified model as a rational means of assessing subslab connectivity in actual houses, which is an important aspect of the pre-mitigation diagnostic phase. Preliminary field verification results in a house with gravel under the basement slab are presented and discussed.     

Modeling the energy content of combustible ship-scrapping waste at Alang-Sosiya, India, using multiple regression analysis

Alang-Sosiya is the largest ship-scrapping yard in the world, established in 1982. Every year an average of 171 ships having a mean weight of 2.10 x 10(6)(+/-7.82 x 10(5)) of light dead weight tonnage (LDT) being scrapped. Apart from scrapped metals, this yard generates a massive amount of combustible solid waste in the form of waste wood, plastic, insulation material, paper, glass wool, thermocol pieces (polyurethane foam material), sponge, oiled rope, cotton waste, rubber, etc. In this study multiple regression analysis was used to develop predictive models for energy content of combustible ship-scrapping solid wastes. The scope of work comprised qualitative and quantitative estimation of solid waste samples and performing a sequential selection procedure for isolating variables. Three regression models were developed to correlate the energy content (net calorific values (LHV)) with variables derived from material composition, proximate and ultimate analyses. The performance of these models for this particular waste complies well with the equations developed by other researchers (Dulong, Steuer, Scheurer-Kestner and Bento's) for estimating energy content of municipal solid waste.     

Elemental uptake and distribution of nutrients in avocado mesocarp and the impact of soil quality

The distribution of 14 elements (both essential and non-essential) in the Hass and Fuerte cultivars of avocados grown at six different sites in KwaZulu-Natal, South Africa, was investigated. Soils from the different sites were concurrently analysed for elemental concentration (both total and exchangeable), pH, organic matter and cation exchange capacity. In both varieties of the fruit, concentrations of the elements Cd, Co, Cr, Pb and Se were extremely low with the other elements being in decreasing order of Mg > Ca > Fe > Al > Zn > Mn > Cu > Ni > As. Nutritionally, avocados were found to be a good dietary source of the micronutrients Cu and Mn. In soil, Pb concentrations indicated enrichment (positive geoaccumuluation indices) but this did not influence uptake of the metal by the plant. Statistical analysis was done to evaluate the impact of soil quality parameters on the nutrient composition of the fruits. This analysis indicated the prevalence of complex metal interactions at the soil–plant interface that influenced their uptake by the plant. However, the plant invariably controlled metal uptake according to metabolic needs as evidenced by their accumulation and exclusion.     

Phosphorus sorbing materials: sorption dynamics and physicochemical characteristics

The effectiveness of various management practices to reduce phosphorus (P) loss from soil to water can potentially be improved by using by-product materials that have the capacity to sorb phosphorus. This study evaluated the P sorption and desorption potential, and the physicochemical characteristics of various phosphorus sorbing materials. Twelve materials were selected and P sorption potentials ranged between 66 and 990 mg kg(-1). Iron, and calcium drinking water treatment residuals (DWTRs), a magnesium fertilizer by-product, aluminum, and humate materials all removed substantial amounts of P from solution and desorbed little. Humate had the highest maximum P sorption capacity (S(max)). Materials which had a low equilibrium P concentration (EPC(0)) and a high S(max) included aluminum and humate by-products. In a kinetic study, the Fe-DWTR, Ca-DWTR, aluminum, and magnesium by-product materials all removed P (to relatively low levels) from solution within 4 h. Phosphorus fractionation suggests that most materials contained little or no P that was readily available to water. Sand materials contained the greatest P fraction associated with fulvic and humic acids. In general, materials (not Ca-DWTR) and magnesium by-product were composed of sand-sized particles. There were no relationships between particle size distributions and P sorption in materials other than sands. The Ca- and Fe-DWTR, and magnesium by-product also contained plant nutrients and thus, may be desirable as soil amendments after being used to sorb P. Further, using Ca-DWTRs and Fe-DWTRs as soil amendments may also increase soil cation exchange and water holding capacity.     

Assessment of bioavailable nitrogen and phosphorus content in the sediments of Indian mangroves

Environmental Science and Pollution Research - Efficient nutrient cycling and adequate sediment bioavailable nutrient supply are considered to be the two most important factors regulating the high...     

Feasibility study of the separation of chlorinated films from plastic packaging wastes

This study describes the possible separation of chlorinated plastic films (PVC and PVDC) from other heavy plastic packaging waste (PPW) by selective twist formation and gravity separation. Twists formation was mechanically induced in chlorinated plastic films, whereas twist formation did not occur in PS and PET films. After twist formation, all the films had the apparent density of less than 1.0 g/cm³ and floated in water even though the true density was more than 1.0 g/cm³. However, the apparent density of the PS and the PET films increased with agitation to more than 1.0 g/cm³, whereas that of chlorinated plastic films was kept less than 1.0 g/cm³. The main reason would be the air being held inside the chlorinated plastic films which was difficult to be removed by agitation. Simple gravity separation after twist formation was applied for artificial film with 10 wt.% of the chlorinated films and real PPW films with 9 wt.% of the chlorinated films. About 76 wt.% of the artificial PPW films and 75 wt.% of real PPW films after the removal of PP and PE were recovered as settling fraction with 4.7 wt.% and 3.0 wt.% of chlorinated plastic films, respectively. These results indicate that simple gravity separation process after twist formation can be used to reduce the chlorinated plastic concentration from mixed heavy PPW films.     

Organohalogen contaminants and metabolites in cerebrospinal fluid and cerebellum gray matter in short-beaked common dolphins and Atlantic white-sided dolphins from the western North Atlantic

Concentrations of several congeners and classes of organohalogen contaminants (OHCs) and/or their metabolites, namely organochlorine pesticides (OCs), polychlorinated biphenyls (PCBs), hydroxylated-PCBs (OH-PCBs), methylsulfonyl-PCBs (MeSO₂-PCBs), polybrominated diphenyl ether (PBDE) flame retardants, and OH-PBDEs, were measured in cerebrospinal fluid (CSF) of short-beaked common dolphins (n = 2), Atlantic white-sided dolphins (n = 8), and gray seal (n = 1) from the western North Atlantic. In three Atlantic white-sided dolphins, cerebellum gray matter (GM) was also analyzed. The levels of OCs, PCBs, MeSO₂-PCBs, PBDEs, and OH-PBDEs in cerebellum GM were higher than the concentrations in CSF. 4-OH-2,3,3′,4′,5-pentachlorobiphenyl (4-OH-CB107) was the only detectable OH-PCB congener present in CSF. The sum (Σ) OH-PCBs/Σ PCB concentration ratio in CSF was approximately two to three orders of magnitude greater than the ratio in cerebellum GM for dolphins.     

Air Quality Status of Visakhapatnam (India) – Indices Basis

Industrial development in Visakhapatnam is conspicuous to urban agglomeration and the city is located in a topographical bowl formed by two-hill ranges. A major portion of the city is within the bowl area wherein most of the industrial and commercial activities are existing and lies within a distance of 10 km from the shore of the Bay of Bengal. Due to the peculiar geographic location of city, wind movement is either eastern or western and is engulfed within the hill ranges. Hence, there is a possibility of buildup of air pollution levels within the city. Due to gravity of prevailing situation, air quality status of Visakhapatnam on indices basis is analyzed using a non-linear equation for variable parameters i.e. Suspended particulate matter (SPM). Sulfur dioxide (SO2) and Oxides of nitrogen (NO(x)), which are main criteria pollutants in India. For current analysis seasonal air quality data is used, which indicates SPM values in winter at most of the sites and in summer at few sites are exceeding the prescribed standards. Calculated indices reveal that, in winter as well as in summer, most of the locations experienced poor or bad air quality, which is mainly due to higher concentration of SPM and certain extent of SO2 values. Application of Oak Ridge Air Quality Index (ORAQI) type equations (non-linear) are helpful for air quality management plan in the region on long-term basis and it has been also observed that there are certain lapses of weightage assignment for individual pollutant in application.     

Hydrogeochemical characterization of contaminated groundwater in Patancheru industrial area,southern India

The groundwater is one of the most contaminated natural resources in Patancheru industrial area due to unplanned and haphazard industrial growth and urbanization without following basic pollution control norms. The rapid industrialization initiated in early 1970 has started showing up its after effects few years later in the form of physiochemical contamination of the both surface and groundwater bodies of the area. It has resulted in local people being deprived of safe drinking water, plant and aquatic life has severely affected, and situation is deteriorating over the years in the area in spite of some preventive and remedial measures being initiated. The focus of the present study is to understand the chemical characteristics of groundwater and geochemical processes the contaminant water is undergoing which are normally imprinted in its ionic assemblages. The water samples collected in pre- and post-monsoon seasons from forty two groundwater and four surface water sources were analyzed for major constituents such as Ca²⁺, Mg²⁺, Na⁺, K⁺, CO₃⁻, HCO₃⁻, Cl⁻, SO₄²⁻, NO₃⁻, and F⁻, and selected samples were tested for ten important trace metals like Fe, Pb, Bi, Mn, Cr, Co, Ni, Cu, Zn, and Cd. Na⁺ among cations and Cl⁻ among anions dominate the water in both the seasons where as Ca²⁺, HCO₃⁻, and Cl⁻ show significant reduction in their ionic strength in post-monsoon. The groundwater in general is of mixed type, but most of it belong to Na⁺–Cl⁻, Na⁺–HCO₃⁻, Ca²⁺–Mg²⁺–HCO₃⁻, and Ca²⁺–Mg²⁺–Cl⁻ facies. The Na⁺ and Ca²⁺ are in the transitional state with Na⁺ replacing Ca²⁺ and HCO₃⁻–Cl⁻ due to physiochemical changes in the aquifer system. The evaluation of hydrochemistry through various ionic indices, ratios, and plots suggest that silicate–carbonate weathering, ion exchange, dissolution, and evaporation processes are responsible for origin of the present chemical status of the groundwater which is also controlled by the contamination from extraneous sources that could have accelerated the dissolution processes. Gibbs plots authenticate that the evolution of water chemistry is influenced by interaction of percolating water with aquifer matrix apart from anthropogenic enrichment of elements which get over concentrated due to evaporation.