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1. Introduction<br />

New reactors using the uranium-thorium fuel cycle are under studies in order to provide safer and<br />

cleaner nuclear energy as highly radiotoxic actinide waste (Pu, Am and Cm isotopes) will be produced<br />

in lower quantities than the currently used uranium fuelled reactors. Moreover, further developments<br />

of this thorium based cycle rely on nuclear data libraries of the quality achieved for the uranium ones.<br />

The primary reaction of importance using the thorium cycle is the one producing 233 U from<br />

neutron capture on 232 Th, the net production of 233 U is controlled by the 27 days half-life of 233 Pa: a<br />

fertile nucleus ( 232 Th) is transformed into a fissile nucleus ( 233 U) after neutron capture and 2 successive<br />

β decays.<br />

+n β β<br />

232 Th<br />

233 Th<br />

233 Pa<br />

(22 min) (27 days)<br />

233 Pa as a precursor of 233 U may capture neutrons and could lead to a reactivity decrease of the<br />

reactor, conversely and after a shut down, the build up of 233 U increases this reactivity; this so called<br />

Protactinium effect should add severe requests on the 233 Pa and 233 U inventories for reactivity control.<br />

There is no equivalent effect in the well studied 238 U- 239 Pu fuel cycle as the equivalent intermediate<br />

isotope 239 Np has a relatively shorter half-life (2.35 days).<br />

Furthermore, neither the neutron capture cross-section nor the neutron induced fission<br />

cross-section have been measured for 233 Pa up to now. The reason of this absence is the short decay<br />

half life of the 233 Pa nucleus (27 days) that leads to an extreme activity of 7.10 8 bq µg -1 s-1. Due to this<br />

high radioactivity, there is no technique presently available to measure directly the 233 Pa(n,f) reaction<br />

cross-section.<br />

The particular aim of this work is to provide data for the neutron induced fission of 233 Pa in the<br />

fast neutron energy range from 0.5 to 10 MeV. To overcome the problem of the induced radioactive<br />

233 Pa, we have used the transfer reaction 232 Th( 3 He,p) 234 Pa that leads to the desired 234 Pa nucleus as it<br />

should be observed in the 233 Pa(n,f) reaction. Several years ago, this method has been used<br />

successfully to estimate the neutron-induced fission of short-lived targets like 231 Th (25.6 h), 233 Th<br />

(22.1 min) etc.<br />

233 U<br />

2. Theory<br />

Transfer reaction measurements give access to the fission probability Pf(E * ) as a function of<br />

excitation energy. The equation relating the two quantities can be written as:<br />

Pf(E<br />

exc<br />

where α(E exc<br />

,J,π) is the relative population of spin states (J, π).<br />

⎛<br />

⎞<br />

⎜<br />

Γ (E<br />

* π ⎟<br />

⎜<br />

⎟<br />

∑ α π F<br />

,J, )<br />

)= ( E<br />

⎜ exc<br />

, J, )<br />

⎟<br />

(1)<br />

Jπ<br />

⎜<br />

∑Γ<br />

i<br />

(E<br />

*<br />

,J, π)<br />

⎟<br />

⎝<br />

i<br />

⎠<br />

Neutron induced fission measurements give access to the fission cross-section σ F (En) as a<br />

function of the incident neutron energy that is relating to the excitation energy as:<br />

E exc<br />

≈ Sn + En (2)<br />

752

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