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TUTORIAL ON HEAT TRANSFER and CORROSION TESTING UNDER ITS INFLUENCE
David C. Silverman
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Table of Contents
Laboratory Corrosion Testing Under Heat Transfer Conditions – a Critique
The transfer of heat through a surface can affect corrosion through a combination
of increased surface temperature and, especially in the case of natural convection,
by inducing fluid motion where it otherwise might not exist.
The Tutorial on CYLEXPERTTM and the Rotating Cylinder Electrode
discussed using the rotating cylinder electrode for corrosion prediction in
the presence of single phase fluid motion but in the absence of heat transfer (under
isothermal conditions). Increasing the temperature of the fluid and using
the rotating cylinder electrode or equivalent to assess corrosion under
dynamic conditions does not duplicate the effect of heat transfer through
a wall. The thermal boundary layer disappears when the
specimen reaches the fluid temperature. The wall temperature is different
than when heat transfer occurs to maintain the same temperature.
Thermal effects on mass transfer are also absent when the temperature differential
disappears. Proper testing of heat transfer effects on a corroding surface
through which heat transfer occurs requires that heat transfer through that
surface be included in the testing.
The relative values of the
Prandtl number
and Schmidt number
provide a good illustration of the relative effects. This figure
shows how the three boundary layers might develop for liquids in which
the Prandtl number is greater than 1, the Schmidt number is much
greater than one, and heat and mass transfer both begin at the beginning of a
horizontal surface. The kinematic viscosity (diffusivity
of momentum) is greater than both the thermal diffusivity and the
mass diffusivity in this fluid. The result is that both the thermal
and mass transfer boundary layers lie within the momentum boundary layer.
In this picture, the mass transfer boundary layer lies within the thermal boundary
indicating that the free stream concentration is reached at other than
the free stream temperature. The free stream concentration is reached
at a distance shorter than that needed for the free stream temperature to
be reached. This complex relationship might be some of the reason
that controversy has existed on whether heat flux or wall temperature
is the important corrosion variable for some systems.
Unfortunately for the corrosion practitioner, routine laboratory tools
for predicting the effect of fluid motion on corrosion in the presence of heat
transfer are far less developed than for prediction of the effect of fluid
motion on corrosion under isothermal conditions. See
Tutorial on CYLEXPERTTM
and the Rotating Cylinder Electrode
for more information on the latter case. This portion of the tutorial briefly
reviews some of the methods that have been reported. Pilot plant sized equipment
such as a simulated heat exchanger is mentioned but not emphasized.
Heat Flux Apparatus (sometimes with stirring)
One of the earliest laboratory methods to be adopted for routine use
was a heat flux apparatus sometimes equipped with an agitator
(A. O. Fisher and F. L. Whitney, Jr., Corrosion, Vol. 15, p. 257t, 1959
and A. O. Fisher, Corrosion, Vol. 17, p. 215t, 1961). In a later adaptation,
the test rig was outfitted for electrochemical measurements (R. J. L. Andon, et al., Br. Corrosion J., Vol. 29, p. 119, 1986).
This figure
shows an illustration of the important parts of the apparatus. Detailed drawings are provided
in the cited literature. This type of apparatus has the following characteristics:
- One liter or so container (possible ability to withstand pressure) which
narrows to an open bottom. Size dictates "capacitance".
- Internal agitator, internal condenser or "cold finger", thermocouple
for fluid temperature measurement and control of fluid.
- The open bottom rests on a flat test specimen fitted with one or more
internal thermocouples for temperature measurement. Several thermocouples
at various distances may enable extrapolation of the wall temperature.
- A soldering iron with special flat head mounted below the specimen or
a block fit flush to surface and externally heated to provide heat to the specimen.
- Heat controlled by an external source such as a Variac or similar device with
manual or automatic regulation.
- Heat generated by the soldering iron or block flows through the test specimen
into the fluid.
- Heat flux is adjusted so that the fluid temperature is that expected under
operating conditions.
This laboratory technique is still used. It can be relatively simple to construct,
but a bit more difficult to operate. Specimens are fairly easy to manufacture. To
its credit, it can provide a qualitative estimate of the effect of a hot wall on
corrosion. Rankings of alloys have been reported to be in agreement with field
observations for some environments. But, this apparatus has limited ability
to predict corrosion on a more routine basis for a variety of situations.
Some of these limitations are outlined below.
- The wall temperature in the test may or may not be the same as the wall
temperature in practice. Field corrosion rates may be significantly different
from those estimated in this apparatus especially if wall temperatures cannot
be simulated.
- The agitator provides a poorly defined flow regime. Since the
thermal boundary layer
and mass boundary layer (if mass transfer is important) lie within
the hydrodynamic boundary layer for most liquids, these latter boundary layers
may be ill-defined. The result would likely be an inability to translate the
results between geometries.
- If the agitator is turned off, natural convection from the horizontal
specimen could induce significant fluid motion. Translating the effect to
other geometries that may or may not have a significant natural convection
contribution could be difficult
- The wall temperature could be different from the wall-environment interface
temperature because of the temperature gradient through the wall. Multiple
thermocouples placed inside of the specimens may help to estimate wall
temperature by extrapolation but such mounting may be difficult. Machining
costs of specimens could become an impediment routine testing with these
thermocouples.
- Maintaining fluid temperatures identical to the process could result in both
heat flux and wall temperature being different from those found in the process
- The horizontal arrangement may not simulate vertical surfaces and pipes.
Simulation of nucleate boiling (or condensation) or where
natural convection plays role may not be possible.
- Equipping the apparatus for electrochemical measurements could be difficult though
as mentioned above, such an alteration has been reported.
Rotating Disk Electrode
The next generation heat transfer apparatus that has been reported is the rotating
disk or rotating ring disk electrode with internal heat transfer capability.
This device was developed in the 1940’s but applied to corrosion in the 1960’s
(P. I. Zarubin, L. A. Poluboyartseva, and V. M. Novakovskii,
Zashchita Metallov, Vol. 1, p297, 1965, among others ).
It was investigated further in the 1980’s (S. H. Alwash, V. Ashworth,
M. Schirkhanzadeh, and G. E. Thompson, Corrosion Science, Vol. 27, p. 383, 1987,
among others). It was further developed as a ring-disk electrode.
This figure
shows an illustration of the important parts of the apparatus. The heater has
appeared as a cartridge in the shaft and as a heat transfer medium closer to
the disk surface. More detailed drawings can be found in the above references.
The rotating disk electrode is a step closer to being able to simulate heat
transfer effects on corrosion under convective conditions because it, in theory,
operates under well-defined hydrodynamics. In fact, data in the first of the
above citations showed that heat transfer versus the square root of the rotation
velocity was a straight line until higher velocities were reached. Unfortunately,
the few studies reported in the 1960’s through the 1980’s do not fully explore the
rotating disk electrode for routine corrosion evaluation and simulation under
heat transfer conditions. An early paper (P. I. Zarubin,
L. A. Poluboyartseva, and V. M. Novakovskii, Zashchita Metallov, Vol. 1, p297,
1965, among others ) attempted to develop equations to relate heat transfer
in the rotating disk to that in a pipe. The methodology was to equate the
Nusselt numbers
in the two geometries by a somewhat circuitous route. The approach may
be too simplistic in view of the results found with respect to relating mass
transfer between geometries where flow regimes are not the same (e.g. laminar
versus turbulent).
The rotating disk electrode has not been adopted for routine laboratory evaluation
of the effect of heat transfer on corrosion. It may be an alternative for
ranking conditions or alloys but validation for such a use is lacking. The ability
to add electrochemistry fairly easily could enable additional mechanistic
information to be obtained. But, the ability of this apparatus to predict
corrosion on a more routine basis may have the limitations outlined below.
- The wall temperature in the test may or may not be the same as the wall
temperature in practice. Field corrosion rates may be significantly different
from those estimated in this apparatus especially if wall temperatures cannot
be simulated.
- Thermocouples are placed inside of the electrode housing and, possibly,
the specimen itself. The measured temperature of each thermocouple could
be different from the surface temperature because of the temperature gradient.
Multiple thermocouples placed
inside of the specimens could provide a profile that may aid in extrapolating the
wall temperature but such extrapolation is not guaranteed.
- Machining costs of the body and specimens could become an impediment to
routine testing.
- The flow regime is laminar until the rotation rate becomes very large.
The flow regime varies across the electrode surface. Simulation of turbulent
flow conditions in the field combined with heat transfer (e.g. in a pipe or
along a flat surface) would be difficult at best and could lead to incorrect
conclusions.
- The thermal boundary layer
in the rotating disk may not simulate the thermal boundary layer in the system being
simulated because of the variation in flow across the disk surface.
- Maintaining fluid temperatures identical to the process could result in
both heat flux and wall temperature being different from those found in the
process.
- The horizontal (upside-down) arrangement may not simulate vertical surfaces
and pipes. Simulation of nucleate boiling or where
natural convection may play
a role may not be possible.
Rotating Cylinder Electrode
An alternative to the rotating disk electrode is the rotating cylinder electrode.
As discussed in the Tutorial on
CYLEXPERTTM and the Rotating Cylinder Electrode
this apparatus is extremely useful for examining velocity sensitive corrosion under
isothermal conditions and single phase flow. Two positive attributes are that
the flow regime is turbulent at low rotation rates as is often encountered in the
field and the
flow field is uniform across the surface. Unfortunately, studies have not
been reported of such an apparatus for examination of corrosion under heat
transfer conditions though a recent patent application for such a device has
appeared (A. Jaralla, "Corrosion Testing Apparatus", US Patent Application
20060162432).
The design of the heat transfer portion in that application
is derived directly from the rotating disk apparatus discussed above. This figure
illustrates the components of this type of apparatus.
Application of the rotating cylinder electrode to predicting velocity sensitive
corrosion has been discussed in detail in D. C. Silverman, "The Rotating Cylinder
Electrode for Examining Velocity-Sensitive Corrosion - A Review", Corrosion,
Vol.60, No.11, p. 1003, 2004. 1 (1560k).
As discussed in a subsequent paper (D. C. Silverman, "Conditions for Similarity of Mass-Transfer Coefficients and Fluid Shear Stresses Between the Rotating Cylinder Electrode and Pipe", Corrosion, Vol.61, No.6, p. 515, 2005 1 (403k)),
a procedure might be established to use the rotating cylinder electrode to
estimate the effect of velocity on corrosion in other geometries. The procedure
involves a simultaneous equating of shear stress and mass transfer coefficient in the
two geometries. The question is if this type of analysis can be used with respect to heat
transfer. One of the issues is that the
Prandtl number is not as large as
the Schmidt number .
The ratio of the thermal boundary layer thickness to momentum boundary layerthickness may not
be the same as the mass transfer boundary layer thickness to momentum boundary layer thickness.
Certain assumptions used to relate geometries in the case of mass transfer may
not be valid for all cases involving heat transfer.
The following concept on relating geometries in the presence of fluid flow and heat
transfer is hypothesis since corroborating data are not available. The implicit
assumption is that the uniformity of flow and thermal boundary layers in the
rotating cylinder electrode translates to other geometries also exhibiting similar
uniformity.
Assuming that a working rotating cylinder electrode with heat transfer capability
can be built, the next step is to establish the correlation of the
Nusselt number  and
Reynolds number.
in the form
(25)
There are two approaches. The first is to make the measurements of the heat
transfer coefficient versus Reynolds number.
That approach might be difficult
experimentally. The exponents might also be functions of the
Prandtl number .
The second is to assume the the Reynolds analogy for the
relationship between heat and momentum transfer to establish the heat transfer correlation. It is similar
to using the Chilton-Colburn modification of the Reynolds number for
the mass transfer correlations already developed.
These correlations are in the form of equation (25) and are a linearization of
a more general correlation. The Reynolds analogy (originally developed
for gases in which the Prandtl number is approximately 1) is
(26a)
and
(26b)
where St is the Stanton number as defined in equation (26a),
Re is the Reynolds number, Nu is the Nusselt number, Pr is the Prandtl number,
and f is the friction factor. The exponent "b" is approximately 0.25 to 0.3
depending on correlation.
The exponent c is most likely between about 0.3 and 0.4. Note that the exponent "n"
on the friction factor is usually assumed to be 1. That may be an
overestimate depending on system. For example, an exponent closer to 0.5 has been suggested
for some types of fluids with respect to mass transfer. Once the correlation is developed, how to relate it
to pipe flow or other geometries becomes another issue. Such relationships for
mass transfer under isothermal conditions have been discussed in the
tutorial on CYLEXPERTTM
and the rotating cylinder electrodeand in the literature
(D. C. Silverman, "The Rotating Cylinder Electrode for Examining
Velocity-Sensitive Corrosion - A Review", Corrosion, Vol.60, No.11,
p. 1003, 2004. 1
(1560k)).
In that case, equating shear stress and mass transfer coefficient or determining conditions
under which both are equal in the two geometries was concluded to be a reasonable approach
(D. C. Silverman, "Conditions for Similarity of Mass-Transfer Coefficients and Fluid Shear Stresses Between the Rotating Cylinder Electrode and Pipe", Corrosion, Vol.61, No.6, p. 515, 2005 1 (403k)),.
But, there is no reason to believe a priori that equating shear stress and heat transfer coefficients
is appropriate without experimental corroboration.
Though the rotating cylinder electrode is a promising technology, its
use for examining corrosion under heat transfer has not been demonstrated
and theoretical underpinnings are required to make it a routine tool.
Some additional possible shortcomings are as follows.
- The wall temperature in the test may or may not be the same as the wall
temperature in practice. Field corrosion rates may be significantly different
from those estimated in this apparatus especially if wall temperatures cannot
be simulated.
- The equations on how to choose rotation rates to duplicate conditions in
the plant geometry have not been developed and verified.
- In the one patent application, thermocouples are placed inside of the
electrode housing and, possibly, the specimen itself. The measured temperature
of each thermocouple
could be different from the surface temperature because of the temperature gradient.
Multiple thermocouples placed inside of the specimens could provide a profile that
may aid in extrapolating the wall temperature but such extrapolation is not
guaranteed.
- Machining costs for both the apparatus and specimens could become an
impediment to routine testing.
- Maintaining fluid temperatures identical to the process could result in both
heat flux and wall temperature being different from those found in the process.
- The vertical wall arrangement may not simulate horizontal surfaces
(plates and pipes). Simulation of nucleate boiling or where
natural convection
may play a role may not be possible.
Heat Exchanger Simulation
Reports have surfaced periodically on attempts to simulate corrosion in a
heat exchanger
in a laboratory scale apparatus. But, to date, no laboratory device has
been developed for routine use that can fit multiple situations. Equipment
has tended to be "pilot plant" sized. Some of the issues that can impact such
development of a laboratory scale apparatus are as follows.
- Many heat exchanger arrangements have multiple rows of tubes across
which one fluid flows. Flow external to the tubes results in fairly
complex hydrodynamics. For example, tubes can have flow separation at
some point on their surface. The fluid boundary layer set up by the cross
flow can separate from the surface. The result is a flow near the surface
that is counter to the external fluid flow. The relationship among the Nusselt,
Reynolds, and Prandtl numbers is different than for flow inside of the tube.
- Tube banks have different geometries. For example tube banks can be
in-line or staggered. The flow pattern and resulting heat transfer coefficient
for the external flow is a function of the tube layout.
- Tube banks for two different exchangers can have different spacing even
if the tube layouts are the same. The empirical friction factor and heat
transfer coefficients are a function of this spacing
- Fouling
is a complex function of hydrodynamics, fluid chemistry,
and wall temperature. While having the potential of being somewhat
predictable for flow inside tubes, such functionality is far more
complex for external flow.
Previous Page: Natural Convection
Return to Table of Contents
1 © NACE International publication and year shown in citation above. All rights reserved. Displayed with permission from NACE International, Houston, TX (http://www.nace.org). Published in Corrosion, in the month and year shown in the citation above.
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David C. Silverman, Ph.D. - Primary Consultant
E-Mail: dcsilverman@argentumsolutions.com
Phone: 314-576-3586
Fax: 314-754-9825
Address: The Argentum House
14314 Strawbridge Ct.
Chesterfield, MO 63017
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