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A recent experimental campaign performed at the LOHENGRIN spectrometer at ILL aimed at measuring the independent fission yield of 136Cs in the 239Pu(nth,f) reaction. This nuclide can have an important contribution to the total dose rate coming from spent light water reactor UOX and MOX fuels. Moreover, its impact is of first order on the uncertainty of the total dose rate calculated in specific areas of Nuclear Power Plants within accidental conditions. One of the most important sources of uncertainty is its independent fission yield. Therefore, a new measurement of its independent yield along with a rigorous uncertainty analysis was performed. Due to its low independent yield, a new measurement technique has been applied. Ions recoiling from neutron-irradiated 239Pu target were collected by implantation into an Al foil placed inside a vacuum chamber. This foil was then transferred to a low γ-ray background setup located at nearby laboratory (LPSC). The procedure was then repeated for different LOHENGRIN settings. Compared to the JEFF-3.1.1 library, a decrease of the fission yield of 136Cs with a reduced uncertainty is obtained.

An apparatus for the Detection of Internal Conversion Electrons (DICE) has been built and commissioned at Johannes Gutenberg University Mainz (JGU) for the study of recoil ion sources of 239Pu, which emit 235mU nuclei that deexcite to the ground state by emitting low-energy internal conversion (IC) electrons. We present an overview of DICE and its commissioning with 207Bi and 235mU electron sources, demonstrating that DICE allows the detection and counting of IC electrons from 235mU deexcitation. Our preliminary 235mU half-life of ≈ 26 min agrees with literature. DICE is thus an interesting tool to broaden analytical capabilities for recoil ion source characterization via studies of the peculiar decay of 235mU.

Molecular plating is a well-established and widely used method for producing thin films of various elements, which are used in variety of nuclear physics applications. Sixty years have passed since the method was established, and some insights into the chemical process underlying the method and the composition of the thin films have been gained. A brief overview of what has been learned about molecular plating since its introduction and the methods applied in the characterization of molecular plated thin films is given here. Through various spectroscopic and microscopic methods, the process of molecular plating and the chemical composition are gradually being elucidated, albeit we still do not understand all aspects.

Actinide and lanthanide thin layers with specific requirements regarding thickness, homogeneity, chemical purity, mechanical stability, and backing properties are applied in a multitude of physics and chemistry experiments. A novel target preparation method, the so-called “Drop-on-Demand” (DoD) technique, based on a commercial nanoliter (nL) dispenser is applied since a few years in the Nuclear Chemistry unit at Johannes Gutenberg University Mainz. The wetting behaviour of the nL droplets on the substrate’s surface is a key parameter determining the spatial distribution of the deposited material after evaporation. By switching from aqueous to organic solvents as well as by substrate surface modifications, the wetting behaviour can be influenced. Recent investigations on this influence and applications of the DoD method are presented. The produced actinide deposits were characterized by optical and scanning electron microscopy, by α spectroscopy as well as by radiographic imaging.

The first ionization potential (IP1) of element 103, lawrencium (Lr), has been successfully determined for the first time by using a newly developed method based on a surface ionization process. The measured IP1 value is 4.9630.080.07 eV. This value is the smallest among those of actinide elements and is in excellent agreement with the value of 4.963(15) eV predicted by state-of-the-art relativistic calculations also performed in this work. Our results strongly support that the Lr atom has an electronic configuration of [Rn]7s25f147p11/2, which is influenced by strong relativistic effects. The present work provides a reliable benchmark for theoretical calculations and also opens the way for studies on atomic properties of heavy elements with atomic number Z > 100. Moreover, the present achievement has triggered a controversy on the position of lutetium (Lu) and Lr in the Periodic Table of Elements.

Four different techniques were applied for the production of 233U alpha recoil ion sources, providing 229Th ions. They were compared with respect to a minimum energy spread of the 229Th recoil ions, using the emitted alpha particles as an indicator. The techniques of Molecular Plating, Drop-on-Demand inkjet printing, chelation from dilute nitric acid solution on chemically functionalized silicon surfaces, and self-adsorption on passivated titanium surfaces were used. All fabricated sources were characterized by using alpha spectrometry, radiographic imaging, and scanning electron microscopy. A direct validation for the estimated recoil ion rate was obtained by collecting 228Th recoil ions from 232U recoil ion sources prepared by self-adsorption and Molecular Plating. The chelation and the self-adsorption based approaches appear most promising for the preparation of recoil ion sources delivering monochromatic recoil ions. [ABSTRACT FROM AUTHOR]

The masses of the lightest atomic nuclei and the electron mass1 are interlinked, and their values affect observables in atomic2, molecular3–5 and neutrino physics6, as well as metrology. The most precise values for these fundamental parameters come from Penning trap mass spectrometry, which achieves relative mass uncertainties of the order of 10−11. However, redundancy checks using data from different experiments reveal considerable inconsistencies in the masses of the proton, the deuteron and the helion (the nucleus of helium-3), suggesting that the uncertainty of these values may have been underestimated. Here we present results from absolute mass measurements of the deuteron and the HD+ molecular ion using 12C as a mass reference. Our value for the deuteron mass, 2.013553212535(17) atomic mass units, has better precision than the CODATA value7 by a factor of 2.4 and differs from it by 4.8 standard deviations. With a relative uncertainty of eight parts per trillion, this is the most precise mass value measured directly in atomic mass units. Furthermore, our measurement of the mass of the HD+ molecular ion, 3.021378241561(61) atomic mass units, not only allows a rigorous consistency check of our results for the masses of the deuteron (this work) and the proton8, but also establishes an additional link for the masses of tritium9 and helium-3 (ref. 10) to the atomic mass unit. Combined with a recent measurement of the deuteron-to-proton mass ratio11, the uncertainty of the reference value of the proton mass7 can be reduced by a factor of three. Penning trap mass spectrometry is used to measure the masses of the deuteron and the HD+ ion with unprecedented precision, reducing the uncertainty of the proton mass reference value. [ABSTRACT FROM AUTHOR]

The Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) is a powerful, highly reliable and selective reaction which allows for a rapid synthesis in high yields and under mild conditions (pH, temperature). However, the cytotoxicity of copper requires its complete removal prior to an application in vivo. This is an issue especially when it comes to CuAAC reactions on macromolecular structures or drug delivery systems, as copper might be retained by these systems. Thus, a quantification of the final copper content of these systems is inevitable, which we exemplified for a CuAAC reaction on liposomes using 64Cu-spiked Cu(I). In this respect, a Cu(II) nitrate solution was irradiated at the TRIGA Mark II research reactor Mainz to obtain c.a. [64Cu]Cu(II). The irradiated solution was directly used for a CuAAC on liposomes. After purification, their copper content was calculated utilizing γ-ray spectrometry. Only 0.018% of the added 64Cu-activity was still present in the liposome containing fractions after purification. This refers to a total amount of copper of 0.17 ng. The amount of retained copper is so low, that an in vivo application of the liposomes is absolutely reasonable. Besides this particular study, the experimental methodology may be applied to study many other CuAAC reactions, used for the synthesis of radiolabeled or non-radioactive species, which are intended for human applications. [ABSTRACT FROM AUTHOR]

Thorium ions exhibit unique nuclear properties with high relevance for testing symmetries of nature, and Paul traps feature an ideal experimental platform for performing high precision quantum logic spectroscopy. Loading of stable or long-lived isotopes is well-established and relies on ionization from an atomic beam. A different approach allows trapping short-lived isotopes available as alpha-decay daughters, which recoil from a thin sample of the precursor nuclide. A prominent example is the short-lived 229mTh, populated in a decay of long-lived 233U. Here, ions are provided by an external source and are decelerated to be available for trapping. Such setups offer the option to trap various isotopes and charge states of thorium. Investigating this complex procedure, we demonstrate the observation of single 232Th+ ions trapped, embedded into and sympathetically cooled via Coulomb interactions by co-trapped 40Ca+ ions. Furthermore, we discuss different options for a non-destructive identification of the sympathetically cooled thorium ions in the trap, and describe in detail our chosen experimental method, identifying mass and charge of thorium ions from the positions of calcium ions, as their fluorescence is imaged on a CCD camera. These findings are verified by means of a time-of-flight signal when extracting ions of different mass-to-charge ratio from the Paul trap and steering them into a detector. [ABSTRACT FROM AUTHOR]

229Th is the only nucleus currently under investigation for the development of a nuclear optical clock (NOC) of ultra-high accuracy. The insufficient knowledge of the first nuclear excitation energy of 229Th has so far hindered direct nuclear laser spectroscopy of thorium ions and thus the development of a NOC. Here, a nuclear laser excitation scheme is detailed, which makes use of thorium atoms instead of ions. This concept, besides potentially leading to the first nuclear laser spectroscopy, would determine the isomeric energy to 40 μeV resolution, corresponding to 10 GHz, which is a 104 times improvement compared to the current best energy constraint. This would determine the nuclear isomeric energy to a sufficient accuracy to allow for nuclear laser spectroscopy of individual thorium ions in a Paul trap and thus the development of a single-ion nuclear optical clock. [ABSTRACT FROM AUTHOR]

Sodium induces and amplifies human TH2 cell responses, potentially shaping the atopic skin microenvironment. Salting T cells' game: Sodium chloride can encourage TH17 differentiation in CD4 T cells. Matthias et al. now show that sodium chloride can also promote TH2 responses, which are central in allergic diseases. They measured effects of different concentrations of sodium chloride on memory and naïve human T cells as well as mouse cells. Collectively, higher sodium chloride enforced a TH2 transcriptional and phenotypic program. Interestingly, lesional skin from atopic dermatitis patients, but not psoriasis patients, had elevated sodium. These findings suggest that sodium chloride could be a potential player in the progression of allergy in the skin. The incidence of allergic diseases has increased over the past 50 years, likely due to environmental factors. However, the nature of these factors and the mode of action by which they induce the type 2 immune deviation characteristic of atopic diseases remain unclear. It has previously been reported that dietary sodium chloride promotes the polarization of T helper 17 (TH17) cells with implications for autoimmune diseases such as multiple sclerosis. Here, we demonstrate that sodium chloride also potently promotes TH2 cell responses on multiple regulatory levels. Sodium chloride enhanced interleukin-4 (IL-4) and IL-13 production while suppressing interferon-γ (IFN-γ) production in memory T cells. It diverted alternative T cell fates into the TH2 cell phenotype and also induced de novo TH2 cell polarization from naïve T cell precursors. Mechanistically, sodium chloride exerted its effects via the osmosensitive transcription factor NFAT5 and the kinase SGK-1, which regulated TH2 signature cytokines and master transcription factors in hyperosmolar salt conditions. The skin of patients suffering from atopic dermatitis contained elevated sodium compared to nonlesional atopic and healthy skin. These results suggest that sodium chloride represents a so far overlooked cutaneous microenvironmental checkpoint in atopic dermatitis that can induce TH2 cell responses, the orchestrators of atopic diseases. [ABSTRACT FROM AUTHOR]