Chemical properties of transactinides

Abstract.: First investigations of chemical properties of bohrium (Z = 107) and hassium (Z = 108) showed an expected behaviour as ordinary members of groups 7 and 8 of the periodic table. Two attempts to study element 112 yielded some indication for a behaviour like a very volatile noble metal. However, a very recent experiment to confirm this preliminary observation failed. Two examples are described how chemical studies may help to support element discovery claims from purely physics experiments. The two examples are the discovery claims of the elements 112 and 115, respectively, where the progenies hassium and dubnium were chemically identifie

Dating of ice cores from Vernagtferner (Austria) with fission products and lead-210

Fission product (90Sr_ 90y, I37CS, total beta) and 2tOPb_210pO activities were measured in core samples from the temperate vernagtferner (3150 m altitude, Oetztal Alps, Austria). The results show that the investigated fission products are transported with water resulting from melting processes, and are sorbed on dust or dirt horizons. These products are, therefore, not suited for dating temperate glaciers. 210Pb is also transported with water and displaced from its original deposition. However, despite large fluctuations, the specific activity of 210Pb decreases with depth, and can be used to estimate accumulation rates and the age of the ice. The average annual accumulation rate amounts to about 80 cm water equivalent, and the deepest sample (81 m i. e. "" 65 m w. e.) was deposited in the beginning of this century. These results agree with data obtained from other observations on this glacier and show that the 210Pb_method is suitable to date temperate glaciers, if the ice cores cover a time interval of about 100 years (i. e. "" 4 half-lives of 210Pb). The surface activity of 210Pb was found to be 5 ± I dpm per kg of ice in agreement with other locations in the Alps and with measurements of fresh snow

Accommodation coefficient of HOBr on deliquescent sodium bromide aerosol particles

Uptake of HOBr on sea salt aerosol, sea salt brine or ice is believed to be a key process providing a source of photolabile bromine (Br₂) and sustaining ozone depletion cycles in the Arctic troposphere. In the present study, uptake of HOBr on sodium bromide (NaBr) aerosol particles was investigated at an extremely low HOBr concentration of 300 cm^-3 using the short-lived radioactive isotopes ^83-86Br. Under these conditions, at maximum one HOBr molecule was taken up per particle. The rate of uptake was clearly limited by the mass accommodation coefficient, which was calculated to be 0.6 ± 0.2. This value is a factor of 10 larger than estimates used in earlier models. The atmospheric implications are discussed using the box model "MOCCA'', showing that the increase of the accommodation coefficient of HOBr by a factor of 10 only slightly affects net ozone loss, but significantly increases chlorine release

Sources and distribution of trace species in Alpine precipitation inferred from two 60-year ice core paleorecords

International audienceThe Alps represent the largest barrier to meridional air flow in Europe, strongly influencing the weather and hence the distribution of atmospheric trace components. Here for the first time, chemical records from two ice cores retrieved from glaciers located in the northern and southern Swiss Alps were compared in conjunction with an analysis of "weather type", in order to assess geographical and seasonal trends in the deposition of trace species and to identify source regions and transport patterns. Using a correlation analysis, investigated trace species (NH4+, NO3?, SO42?, Ca2+, Mg2+, Na+, K+, and Cl? were grouped into classes of different origin (anthropogenic, sea salt, or Saharan dust). Over the last 60 years, precipitation chemistry at both sites was dominated by NH4+, NO4?, and SO42?, all of anthropogenic origin and deposited mainly in summer by way of convective precipitation. The similarity of the SO42? profiles with historical records of SO4 emissions from France and Italy indicated these two countries as key source areas for the anthropogenic species. In contrast, sea salt and Saharan dust showed major differences in transport pattern and deposition across the Alps. Currently, the sea-salt constituents Na+, K+, and Cl? are transported to the northern site during advective westerly-wind situations, independent of Saharan dust events. At the southern site, sea salt and Saharan dust are deposited simultaneously, indicating a coupled transport active mainly in summer during south-westerly wind situations

Isotope records from Mongolian and Alpine ice cores as climate indicators

The link between long term changes in the isotopic composition of precipitation and surface air temperature at a given location is of exceptional importance for paleoclimatic studies, as ahs been demonstrated by many recent publications based on the isotope records from polar ice cores. By means of direct comparison with instrumental data, this paper evaluates the potential of the deuterium and oxygen-18 records from two continental glaciers for monitoring climatic trends. The isotopic data presented characterize climatically contrasted enviroments. The records from the Swiss glacier show distinct seasonal variations. Oxygen-18 is fairly well correlated with the instrumental record of atmospheric temperature; the seasonal differences in deuterium excess reflect nearness to the oceanic moisture source. By contrast, the isotope data from the Mongolian site show poor correlation with atmospheric temperature. The seasonal variations in deuterium excess, with higher values during summer time, indicate that precipitation largely originates from re-evaporated continental moisture sources. In both cases however, the correlation with temperature is significantly improved by the elimination of values derived from years where major changes in seasonal distribution and/or snow loss obviously have occurred, thereby distoring the isotopic ratios for that particular year. Depending on the site selected for study, the stable isotope composition of ice cores should therefore be viewed not only as a proxy for atmospheric temperature, but also as an additional hydrometeorological parameter and source indicator for atmospheric moisture

Prediction of the thermal release of transactinide elements (112 ≤ Z ≤ 116) from metals

Metallic catcher foils have been investigated on their thermal release capabilities for future superheavy element studies. These catcher materials shall serve as connection between production and chemical investigation of superheavy elements (SHE) at vacuum conditions. The diffusion constants and activation energies of diffusion have been extrapolated for various catcher materials using an atomic volume based model. Release rates can now be estimated for predefined experimental conditions using the determined diffusion values. The potential release behavior of the volatile SHE Cn (E112), E113, Fl (E114), E115, and Lv (E116) from polycrystalline, metallic foils of Ni, Y, Zr, Nb, Mo, Hf, Ta, and W is predicted. Example calculations showed that Zr is the best suited material in terms of on-line release efficiency and long-term operation stability. If higher temperatures up to 2773K are applicable, tungsten is suggested to be the material of choice for such experiment