Direct measurements of neutron capture on radioactive isotopes

We simulated the response of a 4p calorimetric g-detector array to decays of radioactive isotopes on the s-process path. The GEANT 3.21 simulation package was used. The main table contains estimates on the maximum sample size and required neutron flux based on the latest available neutron capture cross section at 30 keV. The results are intended to be used to estimate the feasibility of neutron capture measurements with 4p arrays using the time of flight technique

Opportunities for Nuclear Astrophysics at FRANZ

The "Frankfurter Neutronenquelle am Stern-Gerlach-Zentrum" (FRANZ), which is currently under development, will be the strongest neutron source in the astrophysically interesting energy region in the world. It will be about three orders of magnitude more intense than the well-established neutron source at the Research Center Karlsruhe (FZK)

Neutron activation of natural zinc samples at kT = 25 keV

The neutron-capture cross sections of 64Zn, 68Zn, and 70Zn have been measured with the activation technique in a quasistellar neutron spectrum corresponding to a thermal energy of kT = 25 keV. By a series of repeated irradiations with different experimental conditions, an uncertainty of 3% could be achieved for the 64Zn(n,g)65Zn cross section and for the partial cross section 68Zn(n,g)69Zn-m feeding the isomeric state in 69Zn. For the partial cross sections 70Zn(n,g)71Zn-m and 70Zn(n,g)71Zn-g, which had not been measured so far, uncertainties of only 16% and 6% could be reached because of limited counting statistics and decay intensities. Compared to previous measurements on 64,68Zn, the uncertainties could be significantly improved, while the 70Zn cross section was found to be two times smaller than existing model calculations. From these results Maxwellian average cross sections were determined between 5 and 100 keV. Additionally, the beta-decay half-life of 71Zn-m could be determined with significantly improved accuracy. The consequences of these data have been studied by network calculations for convective core He burning and convective shell C burning in massive stars

Measurements of neutron-induced reactions in inverse kinematics and applications to nuclear astrophysics

Neutron capture cross sections of unstable isotopes are important for neutron-induced nucleosynthesis as well as for technological applications. A combination of a radioactive beam facility, an ion storage ring and a high flux reactor would allow a direct measurement of neutron induced reactions over a wide energy range on isotopes with half lives down to minutes. The idea is to measure neutron-induced reactions on radioactive ions in inverse kinematics. This means, the radioactive ions will pass through a neutron target. In order to efficiently use the rare nuclides as well as to enhance the luminosity, the exotic nuclides can be stored in an ion storage ring. The neutron target can be the core of a research reactor, where one of the central fuel elements is replaced by the evacuated beam pipe of the storage ring. Using particle detectors and Schottky spectroscopy, most of the important neutron-induced reactions, such as (n,$\gamma$), (n,p), (n,$\alpha$), (n,2n), or (n,f), could be investigated.Comment: 5 pages, 7 figures, Invited Talk given at the Fifteenth International Symposium on Capture Gamma-Ray Spectroscopy and Related Topics (CGS15), Dresden, Germany, 201

Uptake and intracellular fate of polymeric nanoparticles studied by light and electron microscopy: from labeling strategies for polymers towards a correlative microscopy approach

In nanomedicine, synthetic nanoscale objects are utilized as vectors to transfer pharmaceutically active compounds into partiular cell types, where they are released in a controlled manner to address intracellular organelles selectively. Polymeric nanomaterials, which represent a material class of tremendous interest for drug delivery, are in focus of this present thesis. In order to study their mode-of-action and deduce comprehensive concepts of particle-cell interactions, high-performance imaging techniques represent a particularly valuable investigation platform, since they provide a direct insight into cellular uptake mechanisms as well as their intracellular distribution. For this reason, the present thesis pursues the implementation of two suitable imaging techniques providing information on a high-resolution level, i.e. fluorescence microscopy (FM) as well as transmission electron microscopy (TEM). In this context, the utilization of carefully selected labeling strategies renders FM a powerful technique, which enables the unambiguous identification of the particles within their intracellular environment with an appropriate image contrast. Nonetheless, this method suffers from a poor resolution, so that individual particles cannot be sufficiently visualized. TEM, on the contrary, exhibits a resolution far beyond the particle size; however, polymeric nanomaterials do not show an appropriate image contrast alongside the cellular interior, which is a direct result of their similar electron contrasts. In this thesis, the implementation of both microscopy approaches into uptake studies is in focus, and the informative value of both methods is discussed. The advantages and drawbacks of both methods are pointed out, and it is illustrated that a comparison or even a correlation of both methods is highly beneficial to obtain a more complete insight. This discussion comprises as well different labeling strategies and experimental challenges

Photosystem II: Thermodynamics and Kinetics of Electron Transport from QA- to QB(QB- ) and Deleterious Effects of Copper(II)

Studies on thermodynamics and kinetics of electron transfer from QA- to QB(QB-) were performed by monitoring laser flash induced changes of the relative fluorescence emission as a function of temperature (220 K < T < 310 K) in isolated thylakoids and PS II membrane fragments. In addition, effects of bivalent metal ions on PS II were investigated by measuring conventional fluorescence induction curves, oxygen evolution, manganese content and atrazine binding mostly in PS II membrane fragments. It was found: a) the normalized level of the fluorescence remaining 10 s after the actinic flash (Ft/F0) steeply increases at temperatures below -10 to - 20 °C, b) the fast phase of the transient fluorescence change becomes markedly retarded with decreasing temperatures, c) among different cations (Cu2+, Zn2+, Cd2+, Ni2+, Co2+) only Cu2+ exhibits marked effects in the concentration range below 100 μᴍ and d) Cu2+ decreases the normalized variable fluorescence, inhibits oxygen evolution and diminishes the affinity to atrazine binding without affecting the number of binding sites. The content of about four manganeses per functionally competent oxygen evolving complex is not changed by [Cu2+] < 70 μᴍ. Based on these findings it is concluded: i) a temperature dependent equilibrium between an inactive (I) and active (A) state of QA- reoxidation by QB(QB- ) is characterized by standard enthalpies ΔH° of 95 kJ mol-1 and 60 kJ mol-1 and standard entropies ΔS° of 370 kJ K-1 mol-1 and 240 kJ K-1 mol-1 in isolated thylakoids and PS II membrane fragments, respectively, ii) the activation energies of QA- reoxidation by plastoquinone bound to the QB site are about 30 kJ mol-1 (thylakoids) and 40 kJ mol-1 (PS II membrane fragments) in 220 K < T < 300 K, and iii) Cu2+ causes at least a two-fold effect on PS II by modifying the atrazine binding affinity at lower concentrations ( ~ 5 μᴍ) and interference with the redox active tyrosine Yz at slightly higher concentration ( ~ 10 μᴍ) leading to blockage of oxygen evolution