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Safety and Security of Commercial Spent Nuclear Fuel Storage: Public Report
These oxidation reactions can become locally self-sustaining (i.e., autocatalytic3) at high temperatures (i.e., about a factor of 10 higher than the boiling point of water) if a supply of oxygen and/or steam is available to sustain the reactions. (These reactions will not occur when the spent fuel is under water because heat removal prevents such high temperatures from being reached). The result could be a runaway oxidation reaction—referred to in this report as a zirconium cladding fire—that proceeds as a burn front (e.g., as seen in a forest fire or a fireworks sparkler) along the axis of the fuel rod toward the source of oxidant (i.e., air or steam). The heat released from such fires can be even greater than the decay heat produced in newly discharged spent fuel.
As fuel rod temperatures increase, the gas pressure inside the fuel rod increases and eventually can cause the cladding to balloon out and rupture. At higher temperatures (around 1800°C [approximately 3300°F]), zirconium cladding reacts with the uranium oxide fuel to form a complex molten phase containing zirconium-uranium oxide. Beginning with the cladding rupture, these events would result in the release of radioactive fission gases and some of the fuel’s radioactive material in the form of aerosols into the building that houses the spent fuel pool and possibly into the environment. If the heat from one burning assembly is not dissipated, the fire could spread to other spent fuel assemblies in the pool, producing a propagating zirconium cladding fire.
The high-temperature reaction of zirconium and steam has been described quantitatively since at least the early 1960s (e.g., Baker and Just, 1962), The accident at the Three Mile Island Unit 2 reactor and a set of experiments (e.g., CORA, FPT 1–6, CODEX, ORNL-VI, VERCORS) have provided a basis for understanding the phenomena of zirconium cladding fires and fission-product releases from irradiated fuel in a reactor core accident. This understanding and data from the experiments form the foundation for computer simulations of severe accidents involving nuclear fuel. These experiments and computer simulations are for inside-reactor vessel events rather than events in an open-air spent fuel pool array.
This chapter examines possible initiating factors for such loss-of-pool-coolant events and the potential consequences of such events. It is organized into the following four main sections:
Background on spent fuel pool storage.
Previous studies on safety and security of pool storage.
Evaluation of the potential risks of pool storage.
Findings and recommendations.
That is, the reaction heat will increase temperatures in adjacent areas of the fuel rod, which in turn will accelerate oxidation and release even more heat. Autocatalytic oxidation leading to a “runaway” reaction requires a complex balance of heat and mass transfer, so assigning a specific ignition temperature is not possible. Empirical equations have been developed to predict the reaction rate as a function of temperature when steam and oxygen supply are not limited (see, e.g., Tong and Weisman, 1996, p. 223). Numerous scaled experiments have found that the oxidation reaction proceeds very slowly below approximately 900°C (1700°F).