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A Review of Criticality Accidents A Review of Criticality Accidents

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Figure 64. Energy model computation <strong>of</strong> power vs time. The initial reactivity is 1.0 $ above delayed critical. Neutron<br />

lifetime values are 10 -8 , 10 -6 , and 10 -4 seconds. The bottom panel shows the corresponding curves <strong>of</strong> reactivity vs<br />

time.<br />

t 1/2 = 3.52 l / ∆k p<br />

(3)<br />

where l = the neutron lifetime and the maximum power<br />

is<br />

dE/dt max ≈ 2 ∆k p 2 / 3.5 bl (4)<br />

The experimental systems that have been intensively<br />

studied and that exemplify the data in Figures 63<br />

and 64 are the Godiva, KEWB, and SPERT reactors,<br />

and the CRAC experiments.<br />

Godiva I and II were near solid uranium (93% 235 U)<br />

metal critical assemblies, pressed into service as<br />

irradiation facilities. At a few cents above prompt<br />

criticality, controlled prompt excursions provide an<br />

excellent experimental picture to complement the<br />

curves <strong>of</strong> Figures 63 and 64. The prompt negative<br />

temperature coefficient <strong>of</strong> reactivity <strong>of</strong> about<br />

4.3 × 10 3 $/°C (depending on the model) arises from<br />

thermal expansion and is directly related to the<br />

deposition <strong>of</strong> fission energy. The transient proceeds so<br />

rapidly that no heat is lost from the system. When the<br />

step change <strong>of</strong> reactivity is increased to 4 or 5 ¢ above<br />

prompt criticality, a new effect sets in. The power rises<br />

to such high values that the thermal expansion lags the<br />

energy deposition and the simple ratio <strong>of</strong> E and ∆k p in<br />

Eq. (2) is no longer true. At still higher step changes,<br />

the energy release becomes proportional to the square<br />

and eventually to the cube <strong>of</strong> the initial excess reactivity.<br />

Structural damage from shocks commences at 10<br />

or 11 ¢, thus providing a limit for planned repetitive<br />

bursts.<br />

The transient behavior <strong>of</strong> solution systems has been<br />

studied with the two KEWB reactors. The KEWB–A<br />

core was a 13.6 l stainless steel sphere containing<br />

11.5 l <strong>of</strong> highly enriched UO 2 SO 4 solution; the<br />

reflector was thick graphite. This reactor provided a<br />

means <strong>of</strong> studying transients in solution systems during<br />

which the period was as short as 2 milliseconds. The<br />

109

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