The FuTure oF nuclear Fuel cycle - MIT Energy Initiative
The FuTure oF nuclear Fuel cycle - MIT Energy Initiative
The FuTure oF nuclear Fuel cycle - MIT Energy Initiative
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Table 6.3 HLW in the <strong>Fuel</strong> Cycle Options<br />
hlW<br />
onCe-throuGh<br />
CyCle<br />
tWiCe-throuGh<br />
SCheme (lWr-mox)<br />
SCenario<br />
FaSt reaCtorS<br />
SCheme (lWr-Fr)<br />
tWo-tier SCheme<br />
(mox Fr)<br />
Spent uo 2 fuel na na na<br />
FP in spent uo 2 fuel<br />
na<br />
Ma in spent uo 2 fuel na na na<br />
MoX fuel fabrication losses na na<br />
Spent uo 2 /MoX fuel reprocessing losses<br />
na<br />
Spent MoX fuel na na na<br />
Fr fuel fabrication losses na na<br />
FP in spent Fr fuel na na<br />
Fr spent fuel reprocessing losses na na<br />
Spent Fr fuel na na na na<br />
As high-level wastes have various levels of decay heat and radiotoxicity, both varying over<br />
time, one cannot simply aggregate their masses to make comparisons among the scenarios.<br />
However, “Densification factors” may be used to aggregate the different types of wastes in<br />
order to compare the total repository requirements. A densification factor can be defined as<br />
[BCG, 2006]: “the quantity of HLW or used fuel that can be disposed per unit length of (disposal<br />
drift in) Yucca Mountain is … referred to as the “drift loading factor” and is expressed<br />
in MTHM/m YM . …<strong>The</strong> densification factor is the ratio of the drift loading factor of HLW to<br />
the drift loading factor of used fuel 4 ”.<br />
Two potential constraints are considered: volume and heat (taking the waste package into<br />
account). In all studies, a total cooling time of 25 years prior to disposal in repository is assumed,<br />
and the repository is assumed to be ventilated for 75 years after it is fully loaded. <strong>The</strong><br />
values of the densification factors are also sensitive to the assumptions about the burnup,<br />
the cooling time before reprocessing (e.g the build-up of 241 Am from 241 Pu decay drives up<br />
long-term heat) and above all to the amounts of TRU, cesium and strontium remaining in<br />
the spent fuel, as shown by Figure 6.4 [Wigeland, 2006]. In this figure, the impact on the<br />
repository capacity for waste storage of removal of Cs and Sr as well as transuranic elements<br />
(Pu, Am and Cm) is shown. <strong>The</strong> cumulative densification factor is somewhat correlated<br />
with repository costs, as discussed in Chapter 7. 5<br />
In CAFCA, it is assumed that 99.9% w of the Pu or TRU (depending on the scenario) is removed<br />
from spent fuel during the reprocessing process 6 . <strong>The</strong> fission products are assumed<br />
to remain in the waste. However, various densification factors can be found in the literature,<br />
for both the Pu (or TRu) and fissions Products (FP):<br />
1. <strong>The</strong> densification factor found in [BCG, 2006] for the FP/MA mix resulting from spent<br />
UO 2 fuel reprocessing in the TTC scenario is ~ 4.<br />
2. <strong>The</strong> [Shropshire et al., 2009] study suggested densification factors from 2 to 10 for the<br />
FPs alone (separated from spent UO 2 fuel), with an effective value of 2.5. This value is<br />
more pessimistic about the benefit of separations than the [BCG, 2006] estimation. In<br />
chapter 6: analysis of <strong>Fuel</strong> <strong>cycle</strong> options 79