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Tuning proton transfer and catalytic properties in triple junction nanostructured catalyts
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The performance of magnetic lens for focusing VCN-SANS.
We have developed a prototype rotating-permanent magnet sextupole lens (named rot-PMSx) for more efficient experiments with neutron beams in time of flight (ToF) mode. This lens can modulate the focusing strength over range 1.5 x 10{sup 4} T/m{sup 2} {le} g' {le} 5.9 x 10{sup 4} T/m{sup 2}. Synchronization between the modulation and the beam pulse produces a focused beam without significant chromatic aberration. We anticipate that this lens could be utilized in focusing small angle neutron scattering (SANS) instruments for novel approach to high resolution SANS. We carried out experiments testing the principle of this lens at the very cold neutron (VCN) beamline (PF2) at Institut Laue-Langevin (ILL), France. The focused beam image size at the detector was kept constant at the same beam size as the source ({approx} 3 mm) over a wavelength range of 30 {angstrom} {le} {lambda} {le} 48 {angstrom} in focal length of {approx} 1.14 m. The flux gain was about 12 relative to a beam without focusing, and the depth of focus was quite large. These results show the good performance of this lens and the system. Thereupon we have demonstrated the performance of this test bed for high resolution focusing of VCN-SANS for a well-studied softmatter sample; a deuterium oxide solution of Pluronic F127, an (PEO){sub 100}(PPO){sub 65}(PEO){sub 100} tri-block copolymer in deuterium oxide. The results of the focusing experiment and the focusing VCN-SANS are presented.
Time-of-Flight Mass Measurements of Exotic Nuclei
Atomic masses play an important role in nuclear physics and astrophysics. The need of experimental mass values for unstable nuclides has triggered the development of a wide range of mass measurement techniques, with devices installed at many laboratories around the world. We have implemented a time-of-flight magnetic-rigidity (TOF-B ) technique at the National Superconducting Cyclotron Laboratory (NSCL) that includes a position measurement for magnetic rigidity corrections and uses the A1900 separator and the S800 spectrograph. We performed a successful first experiment measuring masses of neutron-rich isotopes in the region of Z 20 30, important for calculations of processes occurring in the crust of accreting neutron stars. The masses of 16 nuclei were determined, for 61V, 63Cr, 66Mn, and 74Ni for the first time, with atomic mass excesses of 30.510(890) MeV, 35.280(650) MeV, 36.900(790) MeV, and 49.210(990) MeV, respectively. The mass resolution achieved was 1.8 10 4.
An algorithm for charge-integration, pulse-shape discrimination and estimation of neutron/photon misclassification in organic scintillators
Organic scintillators are frequently used for measurements that require sensitivity to both photons and fast neutrons because of their pulse shape discrimination capabilities. In these measurement scenarios, particle identification is commonly handled using the charge-integration pulse shape discrimination method. This method works particularly well for high-energy depositions, but is prone to misclassification for relatively low-energy depositions. A novel algorithm has been developed for automatically performing charge-integration pulse shape discrimination in a consistent and repeatable manner. The algorithm is able to estimate the photon and neutron misclassification corresponding to the calculated discrimination parameters, and is capable of doing so using only the information measured by a single organic scintillator. This paper describes the algorithm and assesses its performance by comparing algorithm-estimated misclassification to values computed via a more traditional time-of-flight estimation. A single data set was processed using four different low-energy thresholds: 40, 60, 90, and 120 keVee. Overall, the results compared well between the two methods; in most cases, the algorithm-estimated values fell within the uncertainties of the TOF-estimated values.
High time-resolution photodetectors for PET applications
This paper describes recent developments aiming at the improvement of the time resolution of photodetectors used in positron emission tomography (PET). Promising photodetector candidates for future PET-time-of-flight (TOF) applications are also discussed.
A new measurement of the 6 Li(n,α)t cross section at MeV energies using a 252 Cf fission chamber and 6 Li scintillators
We present a new measurement of the 6 Li(n,α)t cross section from 245 keV to 10 MeV using a 252 Cf fission chamber with 6 LiI(Eu) and Cs 2 LiYCl 6 :Ce (CLYC) scintillators which act as both target and detector. Neutron energies are determined from the time of flight (TOF) method using the signals from spontaneous fission and reaction product recoil. Simulations of neutron downscatter in the crystals and fission chamber bring 6 Li(n,α)t cross section values measured with the 6 LiI(Eu) into agreement with previous experiments and evaluations, except for two resonances at 4.2 and 6.5 MeV introduced by ENDF/B-VII.1. Suspected neutron transport modeling issues cause the cross section values obtained with CLYC to be discrepant above 2 MeV.
Plastic scintillation detectors for time-of-flight mass measurements
Fast timing detectors are an essential element in the experimental setup for time-of-flight (ToF) mass measurements of unstable nuclei. We have upgraded the scintillator detectors used in experiments at the National Superconducting Cyclotron Laboratory (NSCL) by increasing the number of photomultiplier tubes that read out their light signals to four per detector, and characterized them in a test experiment with 48 Ca beam at the NSCL. The new detectors achieved a time resolution (σ) of 7.5 ps. We systematically investigated different factors that affect their timing performance. In addition, we evaluated the ability of positioning the hitting points on the scintillator using the timing information and obtained a resolution (σ) below 1 mm for well-defined beam spots.
Characterization and description of a spectrum unfolding method for the $\mathrm{CATRiNA}$ neutron detector array
We report the CATRiNA deuterated neutron detector array at Florida State University consists of 16 2" x 2" and 16 $" x 2" EJ-315 detectors with characteristic light output and pulse-shape discrimination capabilities. The unique properties of the detectors, in part due to the anisotropic nature of (d,n) scattering, are used to extract the energy of neutrons via pulse-height spectrum unfolding. The unfolding method uses the light output and response matrix of the detectors to extract neutron energies, independent of the traditional time-of-flight (ToF) technique. Detailed response matrices of the CATRiNA detectors were measured at the Edwards Accelerator Laboratory at Ohio University via the 9 Be(d,n) and 27 Al(d,n) reactions. Full characterization of the detectors using digital electronics, as well as a description of the unfolding method are reported.
Automated integration gate selection for Gaussian mixture model pulse shape discrimination
Pulse shapes differ between neutron and gamma particles when measured with detector devices employing pulse shape discriminating (PSD) scintillators. Digitized waveforms can be used in detection systems to perform pulse shape discrimination for this application. Prior Gaussian Mixture Model (GMM) methods require access to the pulse full-waveform. Reducing the waveform to a smaller set of combined samples reduces computational cost while affecting PSD performance. In this work, we develop a method for selecting the best performing combination of integration gates, or contiguous summed segments of the digitized pulse for PSD. The method uses a discrimination score based on the GMM PSD approach. Furthermore, the final selection is performed using Bayesian Optimization. PSD detection results are compared with varying numbers of selected gates on time-of-flight (TOF) data. This method can be used to fully automate the selection of gates in an unsupervised (without ground truth labels) setting.
Neutron resonance transmission analysis prototype system for thorium fuel cycle safeguards
Emerging thorium-based reactor designs and fuel cycles present challenges to traditional non-destructive assay techniques used in international safeguards. Specifically, assaying the masses of 233 U and 235 U when they are present together in samples with high gamma ray backgrounds is difficult because of similar passive neutron signatures and relatively weak gamma-ray emissions of 233 U. The Pacific Northwest National Laboratory (PNNL) and the Massachusetts Institute of Technology (MIT) are developing a compact neutron resonance transmission analysis (NRTA) system as one potential solution to these challenges. The NRTA technique provides isotopic information for a sample via neutron time-of-flight (TOF) measurements that exploit a sample’s epithermal neutron resonance cross-sections. A recently developed portable NRTA system uses a commercially available, pulsed deuterium-tritium neutron generator with a ~2 m flight path and a GS20 lithium glass scintillator detector. Finally, this paper describes the prototype NRTA system design, a refined radiation transport model of the system, preliminary measurements with thorium and uranium sources, and demonstration of a quantitative isotopic estimation algorithm.
Towards a new generation of solid total-energy detectors for neutron-capture time-of-flight experiments with intense neutron beams
Challenging neutron-capture cross-section measurements of small cross sections and samples with a very limited number of atoms require high-flux time-of-flight facilities. In turn, such facilities need innovative detection setups that are fast, have low sensitivity to neutrons, can quickly recover from the so-called γ-flash, and offer the highest possible detection sensitivity. In this paper, we present several steps towards such advanced systems. Specifically, we describe the performance of a high-sensitivity experimental setup at CERN n_TOF EAR2. It consists of nine sTED detector modules in a compact cylindrical configuration, two conventional used large-volume C 6 D 6 detectors, and one LaCl 3 (Ce) detector. The performance of these detection systems is compared using 93 Nb(n, γ) data. We also developed a detailed G EANT small4 Monte Carlo model of the experimental EAR2 setup, which allows for a better understanding of the detector features, including their efficiency determination. This Monte Carlo model has been used for further optimization, thus leading to a new conceptual design of a γ detector array, STAR, based on a deuterated-stilbene crystal array. Finally, the suitability of deuterated-stilbene crystals for the future STAR array is investigated experimentally utilizing a small stilbene-d12 prototype. The results suggest a similar or superior performance of STAR with respect to other setups based on liquid-scintillators, and allow for additional features such as neutron-gamma discrimination and a higher level of customization capability.
Combination of imaging mass spectrometry and electron microscopy for quasi nondestructive surface analysis
We report on a combination of imaging mass spectrometry (MS) and scanning electron microscopy (SEM) developed in a custom designed time-of-flight (TOF) MS instrument with laser post-ionization of sputtered atoms. Elemental (by MS) and topographical (by SEM) mapping of surfaces of heavily contaminated Si collectors from the NASA Genesis sample return mission enabled obtaining much more accurate and detailed depth distribution of the Solar Wind Mg and Ca implanted in these collectors. This is because the cleanest areas were identified by the SEM/MS mapping, and high resolution sputter depth profiling at these locations revealed near-surface (0-15 nm) depth distribution of Mg and Ca, that were used for more accurate fluence calculations of these Solar Wind species. MS imaging was virtually nondestructive at primary ion fluence 10(12) cm(-2), causing no effect on accuracy and precision of quantitative depth profiling that followed the imaging. We also demonstrate importance of such an approach by directly comparing high resolution depth profiles measured on clean areas versus arbitrarily selected areas.
The N = 126 factory: A new facility to produce very heavy neutron-rich isotopes
A new facility, the N = 126 factory, is currently under construction at Argonne National Laboratory. It will use multi-nucleon transfer reactions to create neutron-rich isotopes of very heavy elements for studies of interest to the formation of the A similar to 195 abundance peak in the r-process. This region of the nuclear chart is difficult to access by standard fragmentation or spallation reactions and as a result has remained mostly unexplored. The nuclei of interest, very neutron-rich isotopes around Z = 70-95, will be produced by multi-nucleon exchange of a high intensity 10 MeV/u heavy-ion beam on the most neutron-rich stable isotopes of heavy elements such as 198 Pt and 238 U. This reaction mechanism can transfer a large number of neutrons and create very neutron-rich isotopes with larger than mb cross-section. The reaction mechanism is a nuclear surface process and the reaction products come out close to the grazing angle, which makes them very difficult to collect. The N = 126 factory circumvents this difficulty by using a unique large high-intensity RF gas catcher, similar to the one currently in operation at CARIBU, to collect the target-like reaction products and transform them into a low-energy beam that will then be mass separated with a medium resolution electromagnetic separator (Delta M/M similar or equal to 1/1500), followed by an RFQ buncher and an MR-TOF (Delta M/M similar or equal to 1/100,000) system. The extracted radioactive beams will be essentially pure and available at low-energy for mass measurements with the CPT mass spectrometer or decay study with the X-array.
Plasma exposures of a high-conductivity graphitic foam for plasma facing components
The plasma-surface interactions from samples of high-conductivity graphitic foam biased to 120 V and placed in 6–8 eV deuterium plasmas with densities as high as 10 19 m -3 were investigated at the PSI-2 linear plasma device in Jülich. Graphitic foam-plasma interactions were also studied at the Wendelstein 7-X (W7-X) stellarator in Greifswald by exposure to hydrogen and helium plasmas using the Jülich multi-purpose manipulator. The purpose was to explore the possibility of using the material in a plasma facing component, and initial results were encouraging. In W7-X, no measurable erosion or cracking was observed. The PSI-2 samples received a deuterium fluence of 5 × 10 25 m -2 resulting in an average erosion of 43 µm or about 5 mg per sample. Residual gas analysis (RGA) data were acquired to monitor sample outgassing. Laser-induced Breakdown Spectroscopy (LIBS) was used to measure deuterium retention in the porous foam. After exposure, the surfaces were characterized with scanning electron microscopy, energy dispersive x-ray analysis and time-of-flight secondary ion mass spectrometry (ToF-SIMS). The graphitic foam has a thermal conductivity as high as 287 W/mK and is considered as a replacement to more exotic carbon fiber composites such as SepCarb NB31 or isotropic graphites like ATJ that are no longer produced but used in present-day tokamak experiments. Actively cooled monoblocks were made from the foam and underwent extensive materials characterization including infrared response studies at Oak Ridge National Laboratory. This material is under consideration for the proposed actively-cooled W7-X divertor scraper element.
Exploration of Sn 70 Li 30 alloy as possible material for flowing liquid metal plasma facing components
As an advanced alternative to solid materials, Liquid Metals (LM) may offer more resilient and feasible Plasma Facing Components (PFCs). Particularly, regarding the unavoidable material erosion/degradation produced by particle/heat fluxes in future fusion devices where much longer duty cycles are expected. Furthermore, configurations that propose a flowing LM surface can add the advantage of a continuously fresh and clean layer facing the plasma. Although lithium is the most widely tested option, tin-lithium (SnLi) alloys have been proposed to attempt to combine the positive characteristics of both pure elements and ameliorate the specific issues of lithium. In this work, the potential use of Sn70Li30 alloy in such flowing concepts has been explored by addressing several preliminary and mandatory aspects for its utilization. Key issues such as wettability and compatibility of the alloy with relevant substrates have been studied in a multidisciplinary approach. The data obtained from deposited liquid tin-lithium droplets indicates approximate wetting temperatures of 360 °C, 390 °C and 405 °C for the fresh alloy on 316 stainless steel, molybdenum, and tungsten, respectively. However, the alloy contamination appeared to strongly affect the wetting characteristics of materials, increasing their wetting temperature by ~130 °C in the worst observed cases. Interestingly, in some instances, the instability of the liquid alloy surface was observed in the form of sudden gaseous ejection. The deposited droplets were posteriorly characterized in terms of absolute composition and depth profile by Inductively Coupled PlasmaOptical Emission Spectroscopy (ICP-OES) and Secondary Ion Mass Spectrometry (SIMS-ToF). Additionally, the nature and composition of the boundaries between the substrates and alloy microparticles was investigated by Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Spectroscopy (EDS), and 3D Laser microscopy. The overall results of this post-mortem characterization revealed that first signs of corrosion induced by both alloy elements (lithium-chromium association and iron-tin intermetallic mixing) were present on 316 stainless steel after short exposures (≤3 h) at temperatures lower than 550 °C. Conversely, molybdenum and tungsten showed good compatibility with the alloy in equivalent conditions. The global implications of these results are finally addressed, focusing on the future perspectives and the more viable scenarios for the eventual utilization of these alloys in flowing liquid metal configurations.
The STAR BES-II and Forward Rapidity Physics and Upgrades
The second phase of the Beam Energy Scan at RHIC, BES-II, is scheduled to start in 2019 and will explore with precision measurements the high baryon density region of the QCD phase diagram. The detector upgrades will enhance some of the key measurements by extending STAR’s kinematical reach. Examples are the kurtosis of net-protons, which could pinpoint the position of a critical point. The upgrades currently under way comprise: the replacement of the inner TPC sectors, the Event Plane Detector and the end-cap TOF. Building on these upgrades STAR is planning to further enhance its detector capabilities by installing a Forward Calorimeter System integrating an electromagnetic and hadronic calorimeter and a Forward Tracking System combining 3 Silicon mini-strip disks and 4 Small-Strip Thin Gap Chamber (sTGC) wheels. The forward upgrade is motivated by studying the initial state of nucleons and nuclei and the exploration of cold QCD physics in the very high and low regions of x. This proceeding will highlight these upgrades and some of their selected physics opportunities.
Improved high-precision mass measurements of mid-shell neon isotopes
New mass values measured with the TITAN MR-TOF-MS are reported for the short-lived isotopes 24-26 Ne, produced at TRIUMF's ISAC facility using a uranium carbide target and cold FEBIAD ion source. A least-squares adjustment within the framework of the Atomic Mass Evaluation was performed and the improved precision of the new mass values is highlighted. The improved mass accuracy in this N = 14mid-shell region can also point to the refinement in values of the charge radii. By reducing the mass uncertainty of isotopes, their contribution of the mass shift uncertainty in laser spectroscopy can be negated. The work is part of developments for reaching the N = 20 Island of Inversion, where high molecular contamination hinders mass measurements of the neon isotopes.