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Register a new userMeasurement of Ac227 Impurity in Ac225 using Decay Energy Spectroscopy
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225Ac is a valuable medical radionuclide for targeted alpha therapy, but 227Ac is an undesirable byproduct of an accelerator-based synthesis method under investigation. Sufficient detector sensitivity is critical for quantifying the trace impurity of 227Ac, with the 227Ac/225Ac activity ratio predicted to be approximately 0.15% by end-of-bombardment (EOB). Superconducting transition edge sensor (TES) microcalorimeters offer high resolution energy spectroscopy using the normal-to-superconducting phase transition to measure small change in temperature. By embedding 225Ac production samples in a gold foil thermally coupled to a TES microcalorimeter we can measure the decay energies of the radionuclides embedded with high resolution and efficiency. This technique, known as decay energy spectroscopy (DES), collapses several peaks from alpha decays into single Q-value peaks. In practice there are more complex factors in the interpretation of data using DES, which we will discuss herein. Using this technique we measured the EOB 227Ac impurity to be (0.142 +/- 0.005)% for a single production sample. This demonstration has shown that DES can distinguish closely related isotopic features and is a useful tool for quantitative measures.
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The photoneutron source (PNS, phase 1), an electron linear accelerator (linac)-based pulsed neutron facility that uses the time-of-flight (TOF) technique, was constructed for the acquisition of nuclear data from the thorium molten salt reactor(TMSR) at the Shanghai Institute of Applied Physics (SINAP). The neutron detector signal, with the information on the pulse arrival time, pulse shape, and pulse height, was recorded by using a waveform digitizer (WFD). By using the pulse height and pulse-shape discrimination (PSD) analysis to identify neutrons and $gamma$-rays, the neutron TOF spectrum was obtained by employing a simple electronic design, and a new WFD-based DAQ system was developed and tested in this commissioning experiment. The developed DAQ system is characterized by a very high efficiency with respect to millisecond neutron TOF spectroscopy
The study of nuclei farther from the valley of $beta$-stability goes hand-in-hand with shorter-lived nuclei produced in smaller abundances than their more stable counterparts. The measurement, to high precision, of nuclear masses therefore requires innovations in technique in order to keep up. TRIUMFs Ion Trap for Atomic and Nuclear science (TITAN) facility deploys three ion traps, with a fourth in the commissioning phase, to perform and support Penning trap mass spectrometry and in-trap decay spectroscopy on some of the shortest-lived nuclei ever studied. We report on recent advances and updates to the TITAN facility since the 2012 EMIS Conference. TITANs charge breeding capabilities have been improved and in-trap decay spectroscopy can be performed in TITANs electron beam ion trap (EBIT). Higher charge states can improve the precision of mass measurements, reduce the beam-time requirements for a given measurement, improve beam purity and opens the door to access, via in-trap decay and recapture, isotopes not available from the ISOL method. This was recently demonstrated during TITANs mass measurement of $^{30}$Al. The EBITs decay spectroscopy setup was commissioned with a successful branching ratio and half-life measurement of $^{124}$Cs. Charge breeding in the EBIT increases the energy spread of the ion bunch sent to the Penning trap for mass measurement so a new Cooler Penning Trap (CPET), which aims to cool highly charge ions with an electron plasma, is undergoing online commissioning. Already, CPET has demonstrated the trapping and self-cooling of a room-temperature electron plasma which was stored for several minutes. A new detector has been installed inside the CPET magnetic field which will allow for in-magnet charged particle detection.
This paper presents an absolute X-ray photon energy measurement method that uses a Bond diffractometer. The proposed system enables the prompt and rapid in-situ measurement of photon energies in a wide energy range. The diffractometer uses a reference silicon single crystal plate and a highly accurate angle encoder called SelfA. We evaluate the performance of the system by repeatedly measuring the energy of the first excited state of the potassium-40 nuclide. The excitation energy is determined as 29829.39(6) eV. It is one order of magnitude more precise than the previous measurement. The estimated uncertainty of the photon energy measurement was 0.7 ppm as a standard deviation and the maximum observed deviation was 2 ppm.
This article presents an upgraded in-trap decay spectroscopy apparatus which has been developed and constructed for use with TRIUMFs Ion Trap for Atomic and Nuclear science (TITAN). This device consists of an open-access electron-beam ion-trap (EBIT), which is surrounded radially by seven low-energy planar Si(Li) detectors. The environment of the EBIT allows for the detection of low-energy photons by providing backing-free storage of the radioactive ions, while guiding charged decay particles away from the trap centre via the strong (up to 6 T) magnetic field. In addition to excellent ion confinement and storage, the EBIT also provides a venue for performing decay spectroscopy on highly-charged radioactive ions. Recent technical advancements have been able to provide a significant increase in sensitivity for low-energy photon detection, towards the goal of measuring weak electron-capture branching ratios of the intermediate nuclei in the two-neutrino double beta ($2 ubetabeta$) decay process. The design, development, and commissioning of this apparatus are presented together with the main physics objectives. The future of the device and experimental technique are discussed.
A study of identification properties of a Si-Si DE-E telescope exploiting an underdepleted residual-energy detector has been performed. Five different bias voltages have been used, one corresponding to full depletion, the others associated with a depleted layer ranging from 90% to 60% of the detector thickness. Fragment identification has been performed using either the DE-E technique or Pulse Shape Analysis (PSA). Both detectors are reverse mounted: particles enter from the low field side, to enhance the PSA performance. The achieved charge and mass resolution has been quantitatively expressed using a Figure of Merit (FoM). Charge collection efficiency has been evaluated and the possibility of energy calibration corrections has been considered. We find that the DE-E performance is not affected by incomplete depletion even when only 60% of the wafer is depleted. Isotopic separation capability improves at lower bias voltages with respect to full depletion, though charge identification thresholds are higher than at full depletion. Good isotopic identification via PSA has been obtained from a partially depleted detector whose doping uniformity is not good enough for isotopic identification at full depletion.
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