Resonance Escape Probability

Resonance Escape Probability

The fast fission factor determined the number of fast neutrons produced by fissions at all energies, but in thermal reactors the bulk of fissions occurs at thermal energies and it is obvious these fission neutrons have to be thermalized. But during this thermalisation neutrons may collide not only with moderator nuclei, but also with fuel nuclei. Unfortunately, especially 238U exhibits resonance behaviour between the fast region and the thermal region. While the neutrons are slowing down through the resonance region of 238U, which extends from about 6 eV to 200 eV, there is a chance that some neutrons will be captured. The probability that a neutron will not be captured in entire resonance region is called the resonance escape probability.

See also: Nuclear Resonance

979

↓

p ~ 0.75

↓

734

The resonance escape probability, symbolized by p, is the probability that a neutron will be slowed to thermal energy and will escape resonance capture. This probability is defined as the ratio of the number of neutrons that reach thermal energies to the number of fast neutrons that start to slow down.

resonance escape probability

 
Neutron Life Cycle
Nuclear Fission Chain Reaction
Radiative Capture Reaction
The neutron capture is one of the possible absorption reactions that may occur. In fact, for non-fissionable nuclei it is the only possible absorption reaction. Capture reactions result in the loss of a neutron coupled with the production of one or more gamma rays. This capture reaction is also referred to as a radiative capture or (n, γ) reaction, and its cross-section is denoted by σγ.

The radiative capture is a reaction, in which the incident neutron is completely absorbed and compound nucleus is formed. The compound nucleus then decays to its ground state by gamma emission. This process can occur at all incident neutron energies, but the probability of the interaction strongly depends on the incident neutron energy and also on the target energy (temperature). In fact the energy in the center-of-mass system determines this probability.

See also: Radiative Capture

What is Nuclear Resonance?
Compound state - resonance
Energy levels of compound state. For neutron absorption reaction on 238U the first resonance E1 corresponds to the excitation energy of 6.67eV. E0 is a base state of 239U.

The compound nucleus is the intermediate state formed in a compound nucleus reaction. It is normally one of the excited states of the nucleus formed by the combination of the incident particle and target nucleus. If a target nucleus X is bombarded with particles a, it is sometimes observed that the ensuing nuclear reaction takes place with appreciable probability only if the energy of the particle a is in the neighborhood of certain definite energy values. These energy values are referred to as resonance energies. The compound nuclei of these certain energies are reffered to as nuclear resonances. Resonances are usually found only at relatively low energies of the projectile. The widths of the resonances increase in general with increasing energies. At higher energies the widths may reach the order of the distances between resonances and then no resonances can be observed. The narrowest resonances are usually the compound states of heavy nuclei (such as fissionable nuclei) and thermal neutrons (usually in (n,γ) capture reactions). The observation of resonances is by no means restricted to neutron nuclear reactions.

See also: Compound Nucleus Reactions

From the definition p is always less than 1.0 when there is any amount of 238U or 240Pu present in the core, which means that resonance capture by these isotopes always removes some of the neutrons from the neutron flux.

It is obvious the resonance escape probability is strongly influenced by the arrangement and the geometry of the reactor core. In a homogenous reactor core, where fuel nuclei are surrounded by many of moderator nuclei, there is a significantly higher probability, that the resonance neutron will collide with the fuel nucleus. Therefore in homogenous reactor cores, the resonance escape probability is lower than in heterogeneous cores.

On the other hand, in a heterogeneous reactor core, all the fuel nuclei are in fuel pellets that are encapsulated within a fuel rod. This arrangement increases the probability, that the fast neutron will escape the fuel matrix. The neutron slows down in the moderator where there are no atoms of 238U and 240Pu present. Therefore in heterogeneous reactor cores, the resonance escape probability is significantly higher than in homogenous cores.

Resonance region - Compound Nucleus
Doppler coefficient - fuel burnup
Region of resonances of 238U and 240Pu nuclei.
Source: JANIS (Java-based Nuclear Data Information Software); The JEFF-3.1.1 Nuclear Data Library
 
Table of average logarithmic energy decrement for some elements.
Example: Determine the number of collisions required for thermalization for the 2 MeV neutron in the carbon.

ξCARBON = 0.158N(2MeV → 1eV) = ln 2⋅106/ξ =14.5/0.158 = 92

Table of average logarithmic energy decrement for some elements
Table of average logarithmic energy decrement for some elements.
Table of moderation lengths, diffusion lengths for various moderators
Neutron Moderators - Parameters
The resonance escape probability is for heterogeneous reactor cores about 0.75. But more than its own value, the ways, how can be this value changed during reactor operation, are crucial. The resonance capture, is the main phenomenon, which contributes to the reactor stability and makes the reactor core inherently safe and resistant to prompt power changes as in case of reactivity initiated accidents (RIA). This feature depends strongly on certain reactor design and also on certain fuel loading pattern. Therefore it must be verified during the reload safety assessment.

The resonance escape probability for all resonances can be calculated according to following equation:

resonance escape probability - equationflux of resonance neutronsThe integral in this expression is called the effective resonance integral Ιeff. In practical situations, this integral strongly depends on the geometry of the unit cell. The geometry of the core strongly influences the spatial and energy self-shielding, that take place primarily in heterogeneous reactor cores. This phenomenon causes a significant increase in the resonance escape probability (“p” from four factor formula) in comparison with homogeneous cores. Without the spatial self-shielding provided by the separation of fuel and moderator, values of keff = 1 are possible with natural uranium fuel only if heavy water is used as the moderator. In the literature empirical relations have been developed for the effective resonance integral of the following form:

resonance escape probability - heterogeneous cores

where the resonance integrals are in barns, rho is the material density in g/cm3, and D is the fuel rod diameter in cm. This equation is valid for isolated rods with diameter higher than 0.2cm.

For tightly packed lattice in the fuel assembly self-shielding increases somewhat through what is called a Dancoff correction.

 
Dancoff Correction
In reactor criticality calculations the most usual approach is to start with an elementary cell of the fuel lattice (this cell contains fuel and moderator separated). In this elementary cell the neutron slowing down and thermalization problems can be treated with optical reflecting or isotropic reflecting (white boundary condition). However, even this is too complicated in the resonance energy range. In a closely packed lattice the in-current of resonance neutrons into the fuel is reduced, as compared to the in-current into a single fuel rod in an infinite moderator, because of the shadowing effect of adjacent rods.

As a first approximation in the resonance self-shielding calculations, a single fuel lump (usually a fuel rod) in an infinite moderator is considered, and the presence of other fuel rods is taken into account by applying a certain correction, generally called the Dancoff correction.

moderator-to-fuel ratioFrom the equation it is obvious, the resonance escape probability is dependent also on the moderator-to-fuel ratio – NM / NF (the term before Ieff). With the change of the moderator-to-fuel ratio changes also the neutron flux spectrum in the reactor core. Most of light water reactors are designed as so called undermoderated and the neutron flux spectrum is slightly harder (the moderation is slightly insufficient) than in an optimum case. But this design provides important safety feature. This feature will be discussed in following section.

Main operational changes, that affect this factor:

  • Change in the moderator temperature. It is known, the resonance escape probability is dependent also on the moderator-to-fuel ratio. As the moderator temperature increases the ratio of the moderating atoms (molecules of water) decreases as a result of the thermal expansion of water. Its density simply decreases. This, in turn, causes a hardening of neutron spectrum in the reactor core resulting in higher resonance absorption (lower p). Decreasing density of the moderator causes that neutrons stay at a higher energy for a longer period, which increases the probability of non-fission capture of these neutrons. This process is one of two processes, which determine the moderator temperature coefficient (MTC). The second process is connected with the leakage probability of the neutrons. The moderator temperature coefficient must be for most PWRs negative, which improves the reactor stability, because a reactor core heating causes a negative reactivity insertion.
  • Change in the fuel temperature. The second operational change, which affects the resonance escape probability, is connected with the phenomenon usually known as the Doppler broadening. The effect of the Doppler broadening is generally considered to be even more important than a negative moderator temperature coefficient. Especially in case of reactivity initiated accidents (RIA), the Doppler coefficient of reactivity would be the first and most important effect in the compensation of the inserted positive reactivity. The time for heat to be transferred to the moderator is usually measured in seconds, while the Doppler coefficient is effective almost instantaneously. The Doppler broadening with the process of self-shielding causes, that the Doppler coefficient (or the fuel temperature coefficient) is for all power reactors always negative. Therefore an increase in the fuel temperature promptly causes an increase in the resonance integral (Ieff), which, in turn, causes a negative reactivity insertion. It is of the highest importance in the reactor safety.

See also: Doppler Broadening
See also: Self-shielding

 
References:
Nuclear and Reactor Physics:
  1. J. R. Lamarsh, Introduction to Nuclear Reactor Theory, 2nd ed., Addison-Wesley, Reading, MA (1983).
  2. J. R. Lamarsh, A. J. Baratta, Introduction to Nuclear Engineering, 3d ed., Prentice-Hall, 2001, ISBN: 0-201-82498-1.
  3. W. M. Stacey, Nuclear Reactor Physics, John Wiley & Sons, 2001, ISBN: 0- 471-39127-1.
  4. Glasstone, Sesonske. Nuclear Reactor Engineering: Reactor Systems Engineering, Springer; 4th edition, 1994, ISBN: 978-0412985317
  5. W.S.C. Williams. Nuclear and Particle Physics. Clarendon Press; 1 edition, 1991, ISBN: 978-0198520467
  6. G.R.Keepin. Physics of Nuclear Kinetics. Addison-Wesley Pub. Co; 1st edition, 1965
  7. Robert Reed Burn, Introduction to Nuclear Reactor Operation, 1988.
  8. U.S. Department of Energy, Nuclear Physics and Reactor Theory. DOE Fundamentals Handbook, Volume 1 and 2. January 1993.

Advanced Reactor Physics:

  1. K. O. Ott, W. A. Bezella, Introductory Nuclear Reactor Statics, American Nuclear Society, Revised edition (1989), 1989, ISBN: 0-894-48033-2.
  2. K. O. Ott, R. J. Neuhold, Introductory Nuclear Reactor Dynamics, American Nuclear Society, 1985, ISBN: 0-894-48029-4.
  3. D. L. Hetrick, Dynamics of Nuclear Reactors, American Nuclear Society, 1993, ISBN: 0-894-48453-2. 
  4. E. E. Lewis, W. F. Miller, Computational Methods of Neutron Transport, American Nuclear Society, 1993, ISBN: 0-894-48452-4.

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See above:

Chain Reaction

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