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Film Boiling

In film boiling, heat flux causes a film of vapor to cover the surface fully. This significantly reduces the convection coefficient.

Film boiling occurs when the pressure of a system drops or the flow decreases. In this case, the bubbles cannot escape as quickly from the heat transfer surface. Likewise, if the temperature of the heat transfer surface is increased, more bubbles are created. As the temperature increases, more bubbles are formed than can be efficiently carried away. The bubbles grow and group together, covering small areas of the heat transfer surface with a film of steam.

The nucleate boiling heat flux cannot be increased indefinitely. We call it the “critical heat flux” (CHF) at some value. The steam produced can form an insulating layer over the surface, which in turn deteriorates the heat transfer coefficient. This is because a large fraction of the surface is covered by a vapor film, which acts as thermal insulation due to the low thermal conductivity of the vapor relative to that of the liquid. Immediately after the critical heat flux has been reached, boiling becomes unstable, and transition boiling occurs. The transition from nucleate boiling to film boiling is known as the “boiling crisis”. Since the heat transfer coefficient decreases beyond the CHF point, the transition to film boiling is usually inevitable.

Film Boiling - Boiling Modes

A further increase in the heat flux causes a film of vapor to cover the surface fully. This significantly reduces the convection coefficient since the vapor layer has significantly lower heat transfer ability. As a result, the excess temperature shoots up to a very high value. Beyond the Leidenfrost point, a continuous vapor film blankets the surface, and there is no contact between the liquid phase and the surface. In this situation, the heat transfer is both by radiation and conduction to the vapor.

Boiling Curve - Boiling Modes

If the material is not strong enough for withstanding this temperature, the equipment will fail by damage to the material. This phenomenon is also known as burnout. In pressurized water reactors, one of the key safety requirements (maybe the most important) is that a departure from nucleate boiling (DNB)  will not occur during steady-state operation, normal operational transients, and anticipated operational occurrences (AOOs). Fuel cladding integrity will be maintained if the minimum DNBR remains above the 95/95 DNBR limit for PWRs ( a 95% probability at a 95% confidence level). Since this phenomenon deteriorates the heat transfer coefficient and the heat flux remains, heat accumulates in the fuel rod, causing the dramatic rise of cladding and fuel temperature. Simply, a very high-temperature difference is required to transfer the critical heat flux produced from the fuel rod’s surface to the reactor coolant (through the vapor layer).

Film boiling occurs when the pressure of a system drops or the flow decreases. In this case, the bubbles cannot escape as quickly from the heat transfer surface. Likewise, if the temperature of the heat transfer surface is increased, more bubbles are created. As the temperature increases, more bubbles are formed than can be efficiently carried away. The bubbles grow and group together, covering small areas of the heat transfer surface with a film of steam. This is known as partial film boiling.

The following sections describe:

Boiling and Condensation
Phase diagram of water
Phase diagram of water.
Source: wikipedia.org CC BY-SA

In the preceding chapters, we have discussed convective heat transfer with a very important assumption, and we have assumed a single-phase convective heat transfer without any phase change. This chapter focuses on convective heat transfer associated with the change in phase of a fluid. In particular, we consider processes that can occur at a solid-liquid or solid–vapor interface, namely, boiling (liquid-to-vapor phase change) and condensation (vapor-to-liquid phase change).

Latent heat effects associated with the phase change are significant for these cases. Latent heat, also known as the enthalpy of vaporization, is the amount of heat added to or removed from a substance to produce a phase change. This energy breaks down the intermolecular attractive forces and must provide the energy necessary to expand the gas (the pΔV work). When latent heat is added, no temperature change occurs.

Latent heat of vaporization - water at 0.1 MPa, 3 MPa, 16 MPa
The heat of vaporization diminishes with increasing pressure while the boiling point increases, and it vanishes completely at a certain point called the critical point.

The enthalpy of vaporization is a function of the pressure at which that transformation takes place.

Latent heat of vaporization – water at 0.1 MPa (atmospheric pressure)

hlg = 2257 kJ/kg

Latent heat of vaporization – water at 3 MPa

hlg = 1795 kJ/kg

Latent heat of vaporization – water at 16 MPa (pressure inside a pressurizer)

hlg = 931 kJ/kg

The heat of vaporization diminishes with increasing pressure while the boiling point increases, and it vanishes completely at a certain point called the critical point. Above the critical point, the liquid and vapor phases are indistinguishable, and the substance is called a supercritical fluid.

supercritical-phase-critical-point-minThe change from the liquid to the vapor state due to boiling is sustained by heat transfer from the solid surface; conversely, condensation of a vapor to the liquid state results in heat transfer to the solid surface. Boiling and condensation differ from other forms of convection in that they depend on the latent heat of vaporization, which is very high for common pressures. Therefore large amounts of heat can be transferred during boiling and condensation essentially at a constant temperature. Heat transfer coefficients, h, associated with boiling and condensation are typically much higher than those encountered in other forms of convection processes that involve a single phase.

This is due to the fact even in a turbulent flow. There is a stagnant fluid film layer (laminar sublayer) that isolates the surface of the heat exchanger. This stagnant fluid film layer plays a crucial role in the convective heat transfer coefficient. It is observed that the fluid comes to a complete stop at the surface and assumes a zero velocity relative to the surface. This phenomenon is known as the no-slip condition, and therefore, at the surface, energy flow occurs purely by conduction. But in the next layers, both conduction and diffusion-mass movement occur at the molecular or macroscopic levels. Due to the mass movement, the rate of energy transfer is higher. As was written, nucleate boiling at the surface effectively disrupts this stagnant layer. Therefore, nucleate boiling significantly increases the ability of a surface to transfer thermal energy to the bulk fluid.

Boiling Crisis – Critical Heat Flux

Dryout vs. DNBAs was written, in nuclear reactors, limitations of the local heat flux are of the highest importance for reactor safety. For pressurized water reactors and boiling water reactors, there are thermal-hydraulic phenomena, which cause a sudden decrease in heat transfer efficiency (more precisely in the heat transfer coefficient). These phenomena occur at a certain value of heat flux, known as the “critical heat flux”. The phenomena that cause heat transfer deterioration are different for PWRs and BWRs.

In both types of reactors, the problem is more or less associated with departure from nucleate boiling. The nucleate boiling heat flux cannot be increased indefinitely, and we call it the “critical heat flux” (CHF) at some value. The steam produced can form an insulating layer over the surface, which in turn deteriorates the heat transfer coefficient. Immediately after the critical heat flux has been reached, boiling becomes unstable, and film boiling occurs. The transition from nucleate boiling to film boiling is known as the “boiling crisis”. As was written, the phenomena that cause heat transfer deterioration are different for PWRs and BWRs.

Departure From Nucleate Boiling – DNB

DNBR - Departure from Nucleate Boiling RatioIn the case of PWRs, the critical safety issue is named DNB (departure from nucleate boiling), which causes the formation of a local vapor layer, causing a dramatic reduction in heat transfer capability. This phenomenon occurs in the subcooled or low-quality region. The behavior of the boiling crisis depends on many flow conditions (pressure, temperature, flow rate). Still, the boiling crisis occurs at relatively high heat fluxes and appears to be associated with the cloud of bubbles adjacent to the surface. These bubbles or films of vapor reduce the amount of incoming water. Since this phenomenon deteriorates the heat transfer coefficient and the heat flux remains, heat accumulates in the fuel rod, causing the dramatic rise of cladding and fuel temperature. Simply, a very high-temperature difference is required to transfer the critical heat flux being produced from the surface of the fuel rod to the reactor coolant (through the vapor layer).

In the case of PWRs, the critical flow is inverted annular flow, while in BWRs, the critical flow is usually annular flow. The difference in flow regime between post-dry-out flow and post-DNB flow is depicted in the figure. In PWRs at normal operation, the flow is considered to be single-phase. But a great deal of study has been performed on the nature of two-phase flow in case of transients and accidents (such as the loss-of-coolant accident – LOCA or trip of RCPs), which are of importance in reactor safety and in must be proved and declared in the Safety Analysis Report (SAR).

One of the key safety requirements of pressurized water reactors is that a departure from nucleate boiling (DNB) will not occur during steady-state operation, normal operational transients, and anticipated operational occurrences (AOOs). Fuel cladding integrity will be maintained if the minimum DNBR remains above the 95/95 DNBR limit for PWRs ( a 95% probability at a 95% confidence level). DNB criterion is one of the acceptance criteria in safety analyses as well as it constitutes one of the safety limits in technical specifications.

Heat Flux Limitations in Nuclear Reactors
Nuclear reactors produce enormous amount of heat (energy) in a small volume. The density of the energy generation is very large, which puts demands on its heat transfer system (reactor coolant system). For a reactor to operate in a steady-state, all of the heat released in the system must be removed as fast as it is produced. This is accomplished by passing a liquid or gaseous coolant through the core and through other regions where heat is generated. The heat transfer must be equal to or greater than the heat generation rate or overheating, and possible damage to the fuel may occur.

The temperature in an operating reactor varies from point to point within the system. Consequently, there is always one fuel rod and one local volume hotter than all the rest. Peak power limits must be introduced to limit these hot places. The peak power limits are associated with such phenomena as the departure from nucleate boiling and the conditions that could cause fuel pellet melt.

Therefore power distribution within the core must be properly limited. These limitations are usually divided into two basic categories:

Dryout – BWRs

Flow Boiling - DryoutIn BWRs, a similar phenomenon is known as “dry out,” and it is directly associated with changes in flow pattern during evaporation in the high-quality region. At given combinations of flow rate through a channel, pressure, flow quality, and linear heat rate, the liquid wall film may exhaust, and the wall may be dried out. At normal, the fuel surface is effectively cooled by boiling coolant. However, when the heat flux exceeds a critical value (CHF – critical heat flux), the flow pattern may reach the dry-out conditions (the thin film of liquid disappears). The heat transfer from the fuel surface into the coolant is deteriorated due to a drastically increased fuel surface temperature. In the high-quality region, the crisis occurs at a lower heat flux. Since the flow velocity in the vapor core is high, post-CHF heat transfer is much better than low-quality critical flux (i.e., for PWRs, temperature rises are higher and more rapid).

Departure from Film Boiling – Leidefrost Point

Leidenfrost PointThe Leidenfrost point, which corresponds to the minimal heat flux, is of practical interest since it represents the lower limit for the heat flux in the film boiling regime. If the heat flux drops below this minimum, the film will collapse, causing the surface to cool and nucleate boiling to be reestablished. Therefore, return to nucleate boiling (RNB) occurs at this point. The terms quenching, minimum heat flux, return to nucleate boiling, departure from film boiling, film boiling collapse, and Leidenfrost point have been used interchangeably to refer to various forms of rewetting, but they are not exactly synonymous.

Using the stability theory, Zuber derived the following expression for the minimum heat flux (and corresponding Leidenfrost point) for a large horizontal plate:

leidenfrost point - equation

where

  • qmin – minimal heat flux [W/m2]
  • hfg  – enthalpy of vaporization, J/kg
  • g – gravitational acceleration m/s2
  • ρl — density of the liquid kg/m3
  • ρv — density of vapor kg/m3
  • σ — surface tension-liquid-vapor interface N/m
 
References:
Heat Transfer:
  1. Fundamentals of Heat and Mass Transfer, 7th Edition. Theodore L. Bergman, Adrienne S. Lavine, Frank P. Incropera. John Wiley & Sons, Incorporated, 2011. ISBN: 9781118137253.
  2. Heat and Mass Transfer. Yunus A. Cengel. McGraw-Hill Education, 2011. ISBN: 9780071077866.
  3. U.S. Department of Energy, Thermodynamics, Heat Transfer and Fluid Flow. DOE Fundamentals Handbook, Volume 2 of 3. May 2016.

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.
  9. Paul Reuss, Neutron Physics. EDP Sciences, 2008. ISBN: 978-2759800414.

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.

See above:

Boiling and Condensation