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- Author or Editor: A.C. de Oliveira x
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Abstract
The standard molar enthalpy of formation of crystalline di-isobutyldithiocarbamate complexes of P, As, Sb and Bi(III) has been derived by solution calorimetry at 298.15 K. The corresponding standard molar enthalpies of sublimation were estimated by means of differential scanning calorimetry. From the standard molar enthalpies of formation of the gaseous chelates the homolytic and heterolytic mean metal-sulphur bond-dissociation enthalpies were calculated.
Abstract
Sulfated molecular sieves were synthesized and characterized by XRD, FTIR, chemical analyses, acidity measurements and N2 adsorption–desorption isotherms. Sulfatation led to structural changes in the solid framework by increasing the acidity and accessibility of the acid sites. Br⊘nsted and Lewis acid sites of mild to high strength improved the conversion of alcohols, but the selectivity was modest over sulfated FAU type Y, ZSM-5 and γ-Al2O3 solids at temperatures lower than 200 °C. The characteristics of the sulfated AlSBA-15 molecular sieve in terms of acidity, textural properties and accessibility possibly make this solid useful for catalytic reactions involving bulky organic compounds.
Abstract
Sediments from the Admiralty Bay, King George Island, Antarctica, were investigated by 57Fe Mössbauer spectroscopy, X-ray diffractometry, and radiometry. Quartz, feldspar, chlorite, calcite, dolomite, mica, kaolinite, hematite and magnetite were identified as constituent minerals in the sediment samples. The phase composition and the iron distribution among the crystallographic sites of iron-bearing minerals (silicates, magnetite and hematite) of samples from different location have been derived from the complex Mössbauer spectra. At different locations sediments had significant characteristic differences in the mineral composition, in the iron distribution among the crystallographic site of silicates, and in the specific radioactivity of Cs radionuclides. These results indicate differences in the rock formation and alteration by the sediments in this maritime part of Antarctica. There is a much higher amount of iron oxides in the sediments from south part of the geological fault across the Admiralty Bay than in the north part. This can be associated with much more alteration in the rocks in the south part compared to the northern one. This finding can contribute to the question of the history of the formation and alteration of volcanic rocks in the border of Antarctica.
Abstract
In the present work, results from a survey on mercury concentration in sediments and soils from a gold mining area along the Vila Nova river, in Amapá State, Brazil, are presented. These values were compared with those from the Igarapé Pedra Preta basin, an area unaffected by mining activities. Total mercury contents were determined in the muddy (silt+clay) fraction of the sediments and in the <2 mm fraction of the soils using radiochemical neutron activation analysis (RNAA). The detection limit of the method was 54 µg·kg–1 for soils and 14 µg·kg–1 for sediments when 200 mg of sample were analysed. The Hg results obtained from a comparison between our current method (RNAA) and CV AAS are also presented. Mercury levels showed to be very high in the soils and sediments collected in the Vila Nova river (up to 2 mg·kg–1) when compared to background values (0.3 mg·kg–1) for this region. An enrichment factor was calculated, using Al as a normalizing factor. It showed values up to 8 in sediments of the Vila Nova river basin, indicating a relatively high degree of pollution as compared to the values of about 1 for the samples of the Igarapé Pedra Pretra basin.