Thermally Induced Reaction of Potato Starch with Thiourea

Thermally induced reaction of thiourea with potato starch was carried out with involvement of either conventional or microwave heating. Under applied reaction conditions conventional heating provided a higher degree of transformation. The course of reaction was complex. Thiourea reacted with starch but the reaction products underwent further decompositions. Dextrins contaminated with isothiocyanates were obtained. Not necessarily they underwent alpha-amylolysis more readily than original starch.     

Modelling deposition and air concentration of reduced nitrogen in Poland and sensitivity to variability in annual meteorology

The relative contribution of reduced nitrogen to acid and eutrophic deposition in Europe has increased recently as a result of European policies which have been successful in reducing SO(2) and NO(x) emissions but have had smaller impacts on ammonia (NH(3)) emissions. In this paper the Fine Resolution Atmospheric Multi-pollutant Exchange (FRAME) model was used to calculate the spatial patterns of annual average ammonia and ammonium (NH(4)(+)) air concentrations and reduced nitrogen (NH(x)) dry and wet deposition with a 5 km × 5 km grid for years 2002-2005. The modelled air concentrations of NH(3) and dry deposition of NH(x) show similar spatial patterns for all years considered. The largest year to year changes were found for wet deposition, which vary considerably with precipitation amount. The FRAME modelled air concentrations and wet deposition are in reasonable agreement with available measurements (Pearson's correlation coefficients above 0.6 for years 2002-2005), and with spatial patterns of concentrations and deposition of NH(x) reported with the EMEP results, but show larger spatial gradients. The error statistics show that the FRAME model results are in better agreement with measurements if compared with EMEP estimates. The differences in deposition budgets calculated with FRAME and EMEP do not exceed 17% for wet and 6% for dry deposition, with FRAME estimates higher than for EMEP wet deposition for modelled period and lower or equal for dry deposition. The FRAME estimates of wet deposition budget are lower than the measurement-based values reported by the Chief Inspectorate of Environmental Protection of Poland, with the differences by approximately 3%. Up to 93% of dry and 53% of wet deposition of NH(x) in Poland originates from national sources. Over the western part of Poland and mountainous areas in the south, transboundary transport can contribute over 80% of total (dry + wet) NH(x) deposition. The spatial pattern of the relative contribution of national sources to total deposition of NH(x) may change significantly due to the general circulation of air.     

Determination of EC 50 toxicity data of selected heavy metals toward Heterocypris incongruens and their comparison to ��direct-contact�� and microbiotests

The sensitivity of Heterocypris incongruens to selected heavy metal ions is discussed. Although the Ostracodtoxkit ${\textregistered}$ has been present on the market for a few years, data on its selectivity and sensitivity to toxicants is scarce; such data is indispensable when interpreting the results of sediment toxicity. The LC₅₀ and EC₅₀ results with the Ostracodtoxkit ${\textregistered}$ are compared with those obtained with other commercially available ??direct-contact?? tests (utilizing Hyalella azteca and Chironomus riparius) and microbiotests for assessing the toxicity of aqueous samples (Vibrio fischeri, Daphnia magna, and Selenastrum capricornatum). The sensitivity of H. incongruens to metal ions (Cd^2?+?>?>Hg^2?+?> Cu^2?+?>Cr^6?+?>Ni^2?+???Mn^7?+?>Zn^2?+?>Pb^2?+?>Li^1?+?> Fe^3?+?) was found to be similar to that of H. azteca and of C. riparius. The Ostracodtoxkit ${\textregistered}$ has shown itself to be an efficient and reliable element of test batteries for toxicity determination.     

The Relationship Between the Difference in Prismatic Refractive Power of an Eye-and-Face Protector and Its Thickness,Radius of Curvature,and Material

With the help of the research results presented here and on the basis of a graphic analysis we aim to prove the existence of a relationship between the difference in prismatic refractive power and the thickness, curvature radius, and type of material used for panoramic oculars in protective spectacles, goggles, and face shields. The difference in the prismatic refractive power is a fundamental optical characteristic of a protective ocular without corrective effect. According to Standard No. EN 165:1995 (European Committee for Standardization, 1995) the difference in the prismatic refractive power is a difference in the prismatic effect at 2 observation points of an eye-protector.     

Multiplicative sensitivity analysis and its role in development of simulation models

A procedure of extended sensitivity analysis for simulation models is developed which is applicable to the situation in which input uncertainties are specified in a multiplicative (rather than an additive) way. This type of specification usually occurs when error estimates are large relative to the parameter values. The input parameter errors are assumed to have log-normal distributions and the basis for this assumption is explained along with the advantages it provides. The new procedure, multiplicative sensitivity analysis, is developed for the purposes of internal model validation and identification of priorities for specific experimental and theoretical studies needed for a particular system being modelled. The applicability of the procedure in the very early stages of a research program is its main advantage and further expands the rôle of simulation models.     

Distribution of mercury in di erent environmental compartments in the aquatic ecosystem of the coastal zone of the Southern Baltic Sea

The aim of this study was to characterize mercury (Hg) contamination in the coastal waters of the Southern Baltic Sea, and to investigate transformations of Hg in the initial links of the marine food chain. Concentrations of Hg in water, particulate matter, plankton and macrophytes at various stations in the coastal zone (a bay with restricted water exchange, near an industrial city, river mouths, and the open sea) were measured in 2006–2008. Hg concentrations observed in the Southern Baltic varied greatly, showing the highest average values in all environmental compartments near the river mouths. In shallow, sheltered parts of the gulf, where water exchange is restricted, Hg concentrations in the water and in macrophytes were elevated relative to those in the coastal zone of the deeper part of the bay and in the open Baltic. Distance to the river mouth, terrestrial runo , and quantity and quality of organic matter were more important than seasonal variations in controlling Hg and HgSPM concentrations in water samples. Mercury concentrations in the surface microlayer at the air/sea interface were over 10 times higher than those in the bulk surface water. Concentrations of Hg in macrophytes in the winter were significantly higher than those in the warm seasons (spring, summer, autumn). This was probably the combined e ect of higher availability of Hg in porewaters and leaf growth inhibition.     

Relationships between volatile organic compounds with an emphasis on terpene compounds and genetic matrix in inoculated and non-inoculated winter wheat cultivars

In the present study, we focus on the analysis of the volatile organic compound (VOC) contents in the grain of a representative set of winter wheat cultivars grown in Central Europe. The cultivars were grown in control conditions or were inoculated with the fungus Fusarium culmorum. In the analysed samples, hydrocarbons, alcohols, aldehydes and ketones, aromatics, terpenes and others were found. Among them, results for terpenes seem particularly important. The discriminant analysis allowed complete separation of the quality groups of wheat based on VOCs. Simultaneously, a genetic matrix was created based on the genetic distance between the wheat cultivars and the Mantel test was used to compare it with the VOC matrix. The analysis revealed relationships between the genetic matrix and the overall VOCs, as well as terpenes. The obtained results indicate a significant relationship between microorganisms that exist in the environment, genetic features of plants and VOCs formed in the grain.     

Do evergreen and deciduous trees have different effects on net N mineralization in soil?

Evergreen and deciduous plants are widely expected to have different impacts on soil nitrogen (N) availability because of differences in leaf litter chemistry and ensuing effects on net N mineralization (N(min)). We evaluated this hypothesis by compiling published data on net N(min) rates beneath co-occurring stands of evergreen and deciduous trees. The compiled data included 35 sets of co-occurring stands in temperate and boreal forests. Evergreen and deciduous stands did not have consistently divergent effects on net N(min) rates; net N(min) beneath deciduous trees was higher when comparing natural stands (19 contrasts), but equivalent to evergreens in plantations (16 contrasts). We also compared net N(min) rates beneath pairs of co-occurring genera. Most pairs of genera did not differ consistently, i.e., tree species from one genus had higher net N(min) at some sites and lower net N(min) at other sites. Moreover, several common deciduous genera (Acer, Betula, Populus) and deciduous Quercus spp. did not typically have higher net N(min) rates than common evergreen genera (Pinus, Picea). There are several reasons why tree effects on net N(min) are poorly predicted by leaf habit and phylogeny. For example, the amount of N mineralized from decomposing leaves might be less than the amount of N mineralized from organic matter pools that are less affected by leaf litter traits, such as dead roots and soil organic matter. Also, effects of plant traits and plant groups on net N(min) probably depend on site-specific factors such as stand age and soil type.     

Arsenic,cadmium, lead and thallium in coal ash from individual household furnaces

52 coal ash samples from individual households were analyzed to determine the pH and the concentrations of four toxic elements: arsenic, cadmium, lead and thallium. The method used was atomic absorption spectrometry with graphite-furnace atomization. The ash samples originated from various coal grades and statistical analysis showed existing correlations between the concentrations of studied elements, pH and the coal grades. The maximum concentrations of arsenic, cadmium, lead and thallium were 50,900, 43,500, 128,900, and 6660 µg/kg, respectively. The results were compared with the published data for the ash of industrial origin.

     

Management of hazardous fly-ash energy waste in the adsorptive removal of diclofenac by the use of synthetic zeolitic materials

Zeolite-carbon composites (Na-P1(C), Na-X(C)) and pure zeolites (Na-P1, Na-X) were synthesized from hazardous high-carbon fly ash waste (HC FA) via hydrothermal reaction with sodium hydroxide (NaOH). These solids were applied in the removal of diclofenac (DCF) from aqueous solution, with and without poly(acrylic acid) (PAA). The experiments included adsorption–desorption measurements, as well as electrokinetic and stability analyses. The obtained results showed that HC FA and Na-P1(C) had the greatest adsorption capacity towards DCF, i.e., 26.51 and 21.19 mg/g, respectively. PAA caused considerable decrease in the DCF adsorption due to the competition of both adsorbates of anionic character for active sites. For example, the adsorbed amount of DCF on Na-P1 without PAA was 14.11 mg/g, whereas the one measured with PAA was 5.08 mg/g. Most of prepared solids were effectively regenerated by the use of NaOH. Desorption degree reached even 73.65% in the single systems (with one adsorbate) and 97.24% in the mixed ones (with two adsorbates). Zeolitic materials formed suspensions of rather low stability, which underwent further deterioration in the organic molecules presence. All the results obtained in this study indicated that HC FA can be successfully managed in the removal of organic substances.