Annual Report 2005 - Institute of Radiochemistry

The Institute of Radiochemistry (IRC), one of the six institutes of the Forschungszentrum Rossendorf (FZR), performs application-oriented research in the fields of radiochemistry and radioecology. Motivation and background of our research are environmental processes relevant for the installation of nuclear waste repositories, for remediation of uranium mining and milling sites, and for radioactive contaminations caused by nuclear accidents and fallout. Due to their high radiotoxicity and long half-life the actinides are of special interest. Hence our research focuses on the chemical behavior of actinides at the molecular level in order to predict the relevant macroscopic processes in the environment. Within this framework, special emphasis is on the interface between geological and biological systems. In the last year our research topics were as follows: # Aquatic chemistry of actinides # Actinides in bio-systems # Interaction of actinides with solid phases # Reactive transport of actinides About 60 scientists, technicians and PhD students are employed in the Institute of Radiochemistry. We have achieved a wide range of new scientific results in the past year, which are presented in this Annual Report. Among them only a few can be highlighted here in this preface. For the first time it was possible to determine uranium speciation in situ in drinking and mineral waters e.g. by a dedicated fluorescence spectrometer at lowest µg/L concentrations. This methodical progress is an important prerequisite to study the uranium toxicity and its dependence on chemical speciation. We were very successful in the determination of formation pathways and structure of various actinide complexes, e.g., the surface complexes of uranium (VI) onto mica and iron hydroxides over a wide range of pH and carbonate concentration. These results contribute to a better understanding of actinide speciation in geo- and bio-systems, especially with respect to the chemical processes on the interfaces. Studies to the interaction of uranium with biofilms, green algae and bacteria coming from extreme habitats extended our research on the field of bio-systems. Major progress in the structural analysis of multiple uranium species has been achieved by applying Monte Carlo simulations and iterative transformation factor analysis to EXAFS spectroscopy. Furthermore, our new radiochemical experimental station at the Free Electron Laser of the Rossendorf accelerator ELBE is now in full operation. We have started first experiments on the uranium and neptunium complexation on selected mineral surfaces

Co-Transport of Polycyclic Aromatic Hydrocarbons by Motile Microorganisms Leads to Enhanced Mass Transfer under Diffusive Conditions.

The environmental chemodynamics of hydrophobic organic chemicals (HOCs) are often rate-limited by diffusion in stagnant boundary layers. This study investigated whether motile microorganisms can act as microbial carriers that enhance mass transfer of HOCs through diffusive boundary layers. A new experimental system was developed that allows (1) generation of concentration gradients of HOCs under the microscope, (2) exposure and direct observation of microorganisms in such gradients, and (3) quantification of HOC mass transfer. Silicone O-rings were integrated into a Dunn chemotaxis chamber to serve as sink and source for polycyclic aromatic hydrocarbons (PAHs). This resulted in stable concentration gradients in water (>24 h). Adding the model organism <i>Tetrahymena pyriformis</i> to the experimental system enhanced PAH mass transfer up to hundred-fold (benzo­[a]­pyrene). Increasing mass transfer enhancement with hydrophobicity indicated PAH co-transport with the motile organisms. Fluorescence microscopy confirmed such transport. The effective diffusivity of <i>T. pyriformis</i>, determined by video imaging microscopy, was found to exceed molecular diffusivities of the PAHs up to four-fold. Cell-bound PAH fractions were determined to range from 28% (naphthalene) to 92% (pyrene). Motile microorganisms can therefore function as effective carriers for HOCs under diffusive conditions and might significantly enhance mobility and availability of HOCs

Investigation of the complexation and the migration of actinides and non-radioactive substances with humic acids under geogenic conditions : complexation of humic acids with actinides in the oxidation state IV Th, U, Np ; final report

[no abstract available

Joint project: Migration of actinides in the system clay, humic substance, aquifer - migration behavior of actinides (Uranium, Neptunium) in clays: Characterization and quantification of the influence of humic substances : final report

[no abstract available

Annual Report 2005 - Institute of Radiochemistry

The Institute of Radiochemistry (IRC), one of the six institutes of the Forschungszentrum Rossendorf (FZR), performs application-oriented research in the fields of radiochemistry and radioecology. Motivation and background of our research are environmental processes relevant for the installation of nuclear waste repositories, for remediation of uranium mining and milling sites, and for radioactive contaminations caused by nuclear accidents and fallout. Due to their high radiotoxicity and long half-life the actinides are of special interest. Hence our research focuses on the chemical behavior of actinides at the molecular level in order to predict the relevant macroscopic processes in the environment. Within this framework, special emphasis is on the interface between geological and biological systems. In the last year our research topics were as follows: # Aquatic chemistry of actinides # Actinides in bio-systems # Interaction of actinides with solid phases # Reactive transport of actinides About 60 scientists, technicians and PhD students are employed in the Institute of Radiochemistry. We have achieved a wide range of new scientific results in the past year, which are presented in this Annual Report. Among them only a few can be highlighted here in this preface. For the first time it was possible to determine uranium speciation in situ in drinking and mineral waters e.g. by a dedicated fluorescence spectrometer at lowest µg/L concentrations. This methodical progress is an important prerequisite to study the uranium toxicity and its dependence on chemical speciation. We were very successful in the determination of formation pathways and structure of various actinide complexes, e.g., the surface complexes of uranium (VI) onto mica and iron hydroxides over a wide range of pH and carbonate concentration. These results contribute to a better understanding of actinide speciation in geo- and bio-systems, especially with respect to the chemical processes on the interfaces. Studies to the interaction of uranium with biofilms, green algae and bacteria coming from extreme habitats extended our research on the field of bio-systems. Major progress in the structural analysis of multiple uranium species has been achieved by applying Monte Carlo simulations and iterative transformation factor analysis to EXAFS spectroscopy. Furthermore, our new radiochemical experimental station at the Free Electron Laser of the Rossendorf accelerator ELBE is now in full operation. We have started first experiments on the uranium and neptunium complexation on selected mineral surfaces