This paper presents some of the challenges ahead of us even after 75 years of the discovery of the fission process and large progress made since then. The focus is on application orientation, which requires improved measurements on fission cross-sections and neutron and -ray multiplicities. Experimental possibilities have vastly improved the past decade leading to developments of highly sophisticated detector systems and the use of digital data acquisition and signal processing. The development of innovative fast nuclear reactor technology needs improved respective nuclear data. Advancements in theoretical modelling also require better experimental data. Theory has made progress in calculating fission fragment distributions (i.e. GEF code) as well as prompt neutron and -ray emission to catch up with the improved experiments. This is an Open Access article distributed under the terms of the Creative Commons Attribution License 2.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract. The VERDI time-of-flight spectrometer is dedicated to measurements of fission product yields and of prompt neutron emission data. Pre-neutron fission-fragment masses will be determined by the double time-of-flight (TOF) technique. For this purpose an excellent time resolution is required. The time of flight of the fragments will be measured by electrostatic mirrors located near the target and the time signal coming from silicon detectors located at 50 cm on both sides of the target. This configuration, where the stop detector will provide us simultaneously with the kinetic energy of the fragment and timing information, significantly limits energy straggling in comparison to legacy experimental setup where a thin foil was usually used as a stop detector. In order to improve timing resolution, neutron transmutation doped silicon will be used. The high resistivity homogeneity of this material should significantly improve resolution in comparison to standard silicon detectors. Post-neutron fission fragment masses are obtained form the timeof-flight and the energy signal in the silicon detector. As an intermediary step a diamond detector will also be used as start detector located very close to the target. Previous tests have shown that poly-crystalline chemical vapour deposition (pCVD) diamonds provides a coincidence time resolution of 150 ps not allowing complete separation between very low-energy fission fragments, alpha particles and noise. New results from using artificial single-crystal diamonds (sCVD) show similar time resolution as from pCVD diamonds but also sufficiently good energy resolution.
Prompt neutron multiplicities and mass distributionsThe last years have seen the development of many nuclear applications, such as nuclear reactors of 4 th generation, spallation source etc. requiring precise nuclear data for reactions induced by neutrons with energy going up to 20 MeV. Pre-neutron mass and total kinetic energy (TKE) of fragments produced in neutron-induced fission are routinely measured at the European Commission Joint Research Center (EC JRC-IRMM) by means of twin Frisch-grid ionization chambers, where the energy of both fragments is measured. Thanks to the momentum conservation it is possible to infer the pre-neutron mass, but it is necessary to correct for prompt neutron emission. To do this correction, it is assumed that fragments are a
The Van de Graaff accelerator at IRMM works since many years providing proton, deuteron, and helium beams for nuclear data measurements. The original ion source was of RF type with quartz bottle. This kind of source, as well known, needs regular maintenance for which the accelerator tank must be completely opened. The heavy usage at high currents of the IRMM accelerator necessitated an opening about once every month. In 2010, the full permanent magnet Microgan electron cyclotron resonance (ECR) ion source from PANTECHNIK was installed into a new terminal platform together with a solid state amplifier of 50 W, a dedicated dosing system for 4 gases (with respective gas bottles H(2), D(2), He, and Ar), and a set of dedicated power supplies and electronic devices for the remote tuning of the source. The new system shows a very stable behaviour of the produced beam allowing running the Van de Graaf without maintenance for several months. This contribution will describe the full installed system in details (working at high pressure in the terminal, spark effects, and optic of the extraction), as well as beam results in dc or pulsed mode.
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