A study of the exposure of various population groups to platinum in Vienna (Austria) through urine analysis by inductively coupled plasma-mass spectrometry

Platinum is emitted to environment by automobile catalytic converters (ACCs), hospitals, noble metal refineries, and other industries. Due to abrasion of ACCs platinum leaves the cars with the exhaust fumes and can thus be found in urban and rural atmospheres. To study the exposure to this element its concentration in urine is determined. Urine represents an often used specimen for monitoring studies, as it plays an important role in the elimination of various substances from the body and in addition it can be collected easily. It is supposed that the Pt-intake depends on the physical activity of a person, i.e. the amount of air inhaled and food consumed. Therefore subjects without and with one or two hip-endoprostheses were selected for this monitoring study. The medians obtained for the Pt-concentration of the urine-samples of these three groups were 3.7 µg/g, 3.3 µg/g and 1.9 µg/g for persons with no, one and two prostheses, respectively. Applying a Mann-Whitney-U-test on these data leads to a p-value of 0.051 comparing the groups with n = 0 and n = 2, and a p-value of 0.052 for n = 1 and n = 2 (n = number of prostheses).     

Computational study of the thermal decomposition of 2-methylbutyraldehyde and 2-pentanone through retro-ene reactions

In this work, a theoretical study at the MP2/6-31G(d) level of the thermal decomposition retro-ene reaction of 2-methylbutyraldehyde was carried out at a pressure of 1.5 atm. and temperatures ranging from 1110 to 1190 K. The progress of the reaction has been followed by means of the Wiberg bond indices which in turn allowed the calculation of the reaction synchronicity. Transition state theory was used to calculate the theoretical rate constant at 1150 K which was compared with the previously reported experimental value at the same conditions. We found that both values show a close agreement. The obtained computational evidence allowed us to support a reaction mechanism which proceeds in two steps: the first one with the formation of ethylene and 1-propenol via a six-membered cyclic transition state and the second one involving keto-enol equilibrium of 1-propenol to propionaldehyde via a four-membered cyclic transition state. It was found that the reaction is a highly synchronous and concerted process. The results obtained for the thermolysis of 2-methylbutyraldehyde were compared with those obtained for the thermolysis of 2-pentanone. A comparison of our results with those reported for their corresponding β-hydroxy counterparts, 3-hydroxy-2-methylpropionaldehyde and 4-hydroxy-2-butanone has also been made. A study of the thermochemistry of the compounds involved in the reactions studied has been carried out at the G3 level.     

Comparison of methods for the determination of vanadium in sea-water

Procedures for the determination of vanadium in sea-water have been independently developed at two laboratories. The separation and concentration steps were distinctly different and quantification was by neutron activation or atomic absorption. Both methods provide a reliable measurement of vanadium concentration at natural levels in sea-water.     

Equivalance de marita relative

We define a relative Morita equivalence and we extend the Morita—invariance of cyclic and Hochschild homology to the relative'case.     

Re-entrant-Groove-Assisted VLS Growth of Boron Carbide Five-Fold Twinned Nanowires

We report a preferential growth of boron carbide nanowires with a five-fold twinned internal structure. The nanowires are found to grow catalytically via iron boron nanoparticles, but unusually the catalytic particle is in contact with the low-energy surfaces of boron carbide with V-shaped contact lines. We propose that this catalytical growth may be caused by preferential nucleation at the re-entrant grooves due to the twinning planes, followed by rapid spreading of atomic steps. This is consistent with the observed temperature dependence of the five-fold twinned nanowire growth.     

ETAAS method for the determination of Cd, Cr, Cu, Mn and Se in blood fractions and whole blood

An electrothermal atomic absorption method (ETAAS) for the direct determination of trace elements (Cd, Cr, Cu, Mn, Se) both in blood fractions (erythrocytes, plasma and lymphocytes) and whole blood was developed. Zeeman background correction and graphite tubes with L'vov platforms were used. Samples were diluted with HNO3/Triton X-100 and pipetted directly into the graphite tube. Ashing, pretreatment and atomization steps were optimized carefully for the different fractions and elements applying different matrix modifiers for each element. For the lymphocyte fraction a multi-fold injection technique was applied. Low detection limits of the ETAAS method (Cd 0.13 microgram/L, Cr 0.11 microgram/L, Cu 0.52 microgram/L, Mn 0.13 microgram/L, Se 0.7 microgram/L of whole blood) combined with small quantities of sample necessary for analysis allow determination of trace elements in this matrix. Verification of possible differences in the trace element status of humans was performed with statistical significance (P < 0.05). In addition, a contribution to the determination of normal values of essential elements was achieved. The method was applied for determination of trace elements in human blood and blood fractions of two groups (n = 50) different in health status.     

The promoting effect of a dicyanamide based ionic liquid in the selective hydrogenation of citral

Conventional supported heterogeneous palladium catalysts in combination with a dicyanamide based ionic liquid are highly active with excellent selectivity in enabling the one-pot synthesis of citronellal through citral hydrogenation.