Particulate Sulfates in Pittsburgh Air

Atmospheric dustfall was qualitatively examined for sulfate content by the techniques of chemical micrurgy. Quantitative assessment of suspended sulfate particulate according to size was by cascade impactor sampling and turbidimetric analysis of stage washings as BaSO₄. Sulfate particles less than 1.9 micron mass median diameter in size contributed approximately 43% by weight and 90% by number to total particulate sulfate in Pittsburgh air. The mechanics of particulate sulfate formation in the atmosphere are discussed on the basis of these findings.     

Odor concentration decay and stability in gas sampling bags

This paper presents results of an experimental study into factors contributing to decay of odor samples during storage, between 4 and 40 hr after sample collection. The odor studied was sampled from a tobacco processing plant as part of collaborative research with a view to establishing a manual outlining methods for odor annoyance management, specifically for the tobacco industry. In August and September 1997, an experimental program was carried out in which two types of tobacco odor were sampled: Burley Toaster and Mix. The dependent variable was odor concentration in the bag, measured by dynamic olfactometry in accordance with the draft Comité Européen de Normalisation (CEN) standard EN13725 "Air Quality-Determination of Odor Concentration by Dynamic Olfactometry." The independent variables were sampling bag material, degree of dilution during sampling, dilution gas used, particle removal during sampling, and age of sample in hours. In the first phase, 94 odor analyses were carried out. In a second test, 32 samples were analyzed for odor concentration. In addition, 16 samples were analyzed using gas chromatography-mass spectrometry (GC-MS). Analysis of the results (analysis of variance) led to the unexpected conclusion that Nalophan film bags performed significantly better than metalized Cali-Bond layered film as a bag material. The odor concentration of samples in Nalophan bags remained relatively stable between 4 and 12 hr after sampling. After 30 hr, decay to about half the initial concentration, as measured at 4 hr, was observed. Particle removal during sampling caused the odor concentration in the bags to be reduced by approximately 20%. For practical reasons, particle removal remains useful, to avoid contamination of equipment. Using air or nitrogen as the neutral gas for pre-dilution during sampling or the dilution factor used (between factor 2 and 6) did not appear to have an effect on the decay characteristic of odor samples. The following recommendations are suggested for the practice of collecting odor samples and apply specifically to tobacco processing emissions: Analyze samples as soon as possible, preferably within 12 hr; When samples age for more than 12 hr, decay is likely to cause a reduction in odor concentration to half the original concentration at age 30 hr; Use sampling bags made of Nalophan NA or benchmark performance of other materials against Nalophan NA before using alternative materials; Use pre-dilution when sampling only for the purpose of avoiding condensation during sample storage. Use an appropriate minimum dilution factor to avoid condensation; Both nitrogen and high-purity (synthetic) air are suitable to use as neutral gas for pre-dilution; and When sampling tobacco odors, use an odorless filter to remove particles. This practice removes a source of variation and avoids contamination of equipment. The effect on results, despite being consistently lower in odor concentration, is not meaningful in terms of perceived intensity or annoyance potential.     

The integrated project AquaTerra of the EU sixth framework lays foundations for better understanding of river-sediment-soil-groundwater systems

The integrated project "AquaTerra" with the full title "integrated modeling of the river-sediment-soil-groundwater system; advanced tools for the management of catchment areas and river basins in the context of global change" is among the first environmental projects within the sixth Framework Program of the European Union. Commencing in June 2004, it brought together a multidisciplinary team of 45 partner organizations from 12 EU countries, Romania, Switzerland, Serbia and Montenegro. AquaTerra is an ambitious project with the primary objective of laying the foundations for a better understanding of the behavior of environmental pollutants and their fluxes in the soil-sediment-water system with respect to climate and land use changes. The project performs research as well as modeling on river-sediment-soil-groundwater systems through quantification of deposition, sorption and turnover rates and the development of numerical models to reveal fluxes and trends in soil and sediment functioning. Scales ranging from the laboratory to river basins are addressed with the potential to provide improved river basin management, enhanced soil and groundwater monitoring as well as the early identification and forecasting of impacts on water quantity and quality. Study areas are the catchments of the Ebro, Meuse, Elbe and Danube Rivers and the Brévilles Spring. Here we outline the general structure of the project and the activities conducted within eleven existing sub-projects of AquaTerra.     

The role of humic substances in chromium sorption onto natural organic matter (peat)

To elucidate mechanisms of Cr³⁺ sorption onto the unaltered solid natural organic matter, the comparative studies of this ion binding from a solution at pH 4.0 onto three selected particle size fractions: 2000–1000 μm, 630–200 μm and 63–20 μm of markedly different HS content and structure, separated by a wet sieving from an overall sample of peat (Brushwood Peat Humus) were carried out. Comparable patterns of COOH groups and CEC_t confirmed that for cation exchange capacity were responsible mainly cations connected with COO⁻ functional groups. It was though found that aliphatic acids in the solid state did not take part in Cr³⁺ binding, thus the finest studied fraction 63–20 μm of the highest contents of functional groups showed the lowest sorption capacity for Cr³⁺, while similar patterns of sorbed Cr³⁺, soluble HS content and base CEC₀ indicated that these parameters were directly interrelated. The base ion exchange processes determined by CEC₀ (with Ca²⁺ as a predominant exchangeable cation) appeared to be not the major mechanisms responsible for Cr³⁺ sorption. For this metal, strong binding to insoluble large molecular weight organic pool two- to threefold prevailed over the ion exchange processes. Very low acid desorption indicated generally low mobility of Cr³⁺-organic compounds.     

Resource development,rural communities and rapid growth: Managing social change in the modern boomtown

Resource development in the western United States of America offers the prospect of rapid population and economic growth which may dramatically alter the traditional social bases of these rural communities. Reports from other western boomtowns suggests that such rapid growth can lead to substantial community disruption with a disproportionate increase in social problems and an eventual lowered productivity in the synthetic fuels industry. Changes related to population growth need not produce such disruptive results. Cooperation among industry, government, and community and well planned and coordinated human services and programs designed to relieve the stresses of change, to provide a sense of community, and to integrate newcomers into the community can reduce or prevent many of the negative impacts as well as reduce overall costs by building on existing resources.     

Early prenatal diagnosis of congenital hypophosphatasia: Case report

Congenital hypophosphatasia is an autosomal recessive disorder, which usually has a fatal outcome during the neonatal period. This report presents the prenatal diagnosis of hypophosphatasia at 16 weeks of gestation. The characteristic ultrasonic findings in this abnormality demonstrate the superiority of ultrasound as compared with radiography.     

Maternal serum alfa-fetoprotein levels in the pregnancy complicated by hypertension

Maternal serum alpha-fetoprotein (MSAFP) was determined in patients 33 to 40 weeks pregnant, and the results were analysed with consideration of the presence and quality of hypertensive disease that complicated many of the pregnancies. Patients with incompletely controlled hypertension had significantly higher MSAFP levels than control patients with pregnancies uncomplicated by any risk factor. MSAFP elevation was greatest in pre-eclampsia (301·6 ± 147·6 kU/L, n = 35) > chronic hypertension with superimposed pre-eclampsia (240·4±74.7 kU/L, n = 30) > chronic hypertension (204·1± 105·3 kU/L, n=141). Each was significantly increased (P< 0·0001) over control pregnant patients' levels (104·3 ± 38·8, n= 187). At each gestational week from 33 weeks to term, MSAFP of combined hypertensive women was significantly greater than corresponding control levels (P< 0·003 to < 0·000l). The magnitude and time of onset of MSAFP increase may indicate severe fetal distress.     

A new approach for modelling potential effects in cation adsorption onto binary (hydr) oxides

The current approach for modelling ion adsorption onto binary (hydr)oxides using homogeneous surface complexation models involves the assumption of either an ideal mixture of the two surfaces (i.e. two surface sites on one surface) or a patchwise surface (i.e. two surfaces with one surface site on each surface). As the physical truth should be between these two limiting cases, a model which assumes a patchwise surface constituted of three patches is proposed. Two patches represent the distinct (hydr)oxides, and the third one a mixture of these distinct (hydr)oxides. Using the diffuse layer model, the three approaches are applied to literature data for Cd adsorption onto binary mixtures of alumina-coated silica at total constant Cd concentration and varying amounts of alumina coatings. For Cd adsorption onto these binary (hydr)oxide systems, the new approach explains the observed potential effects. The proposed model, which contains two additional adjustable parameters in terms of site concentrations or one adjustable parameter in terms of specific surface area, is more successful than the two limiting cases. The new model is then validated by predicting Ca and Zn behaviour on the same binary (hydr)oxide system.