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Architecture and management of a geological repository - Andra

Architecture and management of a geological repository - Andra

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3 – High Level Long-Lived Wastesupport systemGuide thimblescontaining cluster rodsFigure 3.2.1PWR fuel assembly with its rodsThe neutronic poison rods are used during reactor start-up (first operating cycle) to control excessreactivity due to the use <strong>of</strong> entirely new fuel; they are removed during the following cycles <strong>and</strong>therefore become waste. The control rods are used to control the reactor power level <strong>and</strong> its immediateshut-down if necessary. They are replaced after several cycles in the reactor <strong>and</strong> also become waste.Some rods contain neutron-absorbing materials: boron, in the form <strong>of</strong> PYREX glass for the neutronicpoison rods, boron carbide (B 4 C) <strong>and</strong>/or an alloy <strong>of</strong> silver, indium <strong>and</strong> cadmium (SIC) for control rods.The number <strong>of</strong> rods containing these materials depends on the reactor.Other activated wastes from PWRs include metal waste, mainly dead-end tubes, known as coreinstrumentation system (CIS) thimbles fitted on the underside <strong>of</strong> the reactor vessel. These tubes areused to insert the neutron probes required to control the nuclear reaction. They are replaced, ifnecessary, after a certain period <strong>of</strong> use <strong>and</strong> then become waste.These various types <strong>of</strong> reactor operation waste have specific chemical <strong>and</strong> radiological characteristicsdistinguishing them from other types <strong>of</strong> B waste. Their specific chemical nature is due to the nature <strong>of</strong>the materials making up some <strong>of</strong> the waste. More specifically, control rods add significant quantities<strong>of</strong> SIC alloys <strong>and</strong> B 4 C, whereas other types <strong>of</strong> B waste generally contain none <strong>of</strong> these. Theradiological activity is due solely to activation products formed by neutronic activation <strong>of</strong> the elements<strong>and</strong> impurities contained in the waste materials during their time in the reactor. These activationproducts are located inside the materials <strong>and</strong> are therefore unlikely to be dispersed. Among them, theactivation products that contribute most to the radioactivity <strong>of</strong> the waste are, in decreasing order,nickel 63 ( 63 Ni) which is a long-lived isotope (half-life 100 years), then iron 55 ( 55 Fe) <strong>and</strong> cobalt 60( 60 Co) which are short-lived isotopes.The high radioactivity <strong>of</strong> 60 Co has thermal consequences. This waste therefore belongs to category B,with the highest heat rating in relative terms (roughly 20 Watts per package when the packages areproduced, taking the conditioning hypotheses set out below). Since this is largely due to cobalt, theresidual heat rating <strong>of</strong> the package drops rapidly as the cobalt decays. As an illustration, the heat ratingis divided by 2 after 5 years <strong>of</strong> cooling, by 3.5 after 10 years <strong>of</strong> cooling <strong>and</strong> by 6 after 15 years <strong>of</strong>cooling. Another consequence <strong>of</strong> this radiological inventory is the high level <strong>of</strong> radiation <strong>of</strong> thepackages. Thus, the equivalent ß-γ dose rate in pseudo-contact with the package (i.e. at a distance <strong>of</strong>5 centimetres) is roughly 50 sieverts per hour (Sv/h), at the time <strong>of</strong> its production. This is mainlyattributable to 60 Co, but also to silver-108m ( 108m Ag) whose half-life is 420 years, <strong>and</strong> remains at arelatively high level even after 10 years' cooling (around 15 Sv/h).DOSSIER 2005 ARGILE -ARCHITECTURE AND MANAGEMENT OF A GEOLOGICAL DISPOSAL SYSTEM77/495

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