9.6 Transition boiling and system influences Many system features influence the pool boiling behavior we have dis-cussed thus far.. It makes it clear that a change in the surface chemistry
Trang 1§9.6 Transition boiling and system influences 489
or
qmin= 18, 990 W/m2From Fig 9.2 we read 20,000 W/m2, which is the same, within the
accuracy of the graph
9.6 Transition boiling and system influences
Many system features influence the pool boiling behavior we have
dis-cussed thus far These include forced convection, subcooling, gravity,
surface roughness and surface chemistry, and the heater configuration,
among others To understand one of the most serious of these—the
influ-ence of surface roughness and surface chemistry—we begin by thinking
about transition boiling, which is extremely sensitive to both
Surface condition and transition boiling
Less is known about transition boiling than about any other mode of
boiling Data are limited, and there is no comprehensive body of theory
The first systematic sets of accurate measurements of transition boiling
were reported by Berenson [9.30] in 1960 Figure9.14shows two sets of
his data
The upper set of curves shows the typical influence of surface
chem-istry on transition boiling It makes it clear that a change in the surface
chemistry has little effect on the boiling curve except in the transition
boiling region and the low heat flux film boiling region The oxidation of
the surface has the effect of changing the contact angle dramatically—
making it far easier for the liquid to wet the surface when it touches it
Transition boiling is more susceptible than any other mode to such a
change
The bottom set of curves shows the influence of surface roughness on
boiling In this case, nucleate boiling is far more susceptible to roughness
than any other mode of boiling except, perhaps, the very lowest end of the
film boiling range That is because as roughness increases the number
of active nucleation sites, the heat transfer rises in accordance with the
Yamagata relation, eqn (9.3)
It is important to recognize that neither roughness nor surface
chem-istry affects film boiling, because the liquid does not touch the heater
Trang 2490
Trang 3§9.6 Transition boiling and system influences 491
Figure 9.15 The transition boiling regime.
The fact that both effects appear to influence the lower film boiling range
means that they actually cause film boiling to break down by initiating
liquid–solid contact at low heat fluxes
Figure9.15shows what an actual boiling curve looks like under the
influence of a wetting (or even slightly wetting) contact angle This figure
is based on the work of Witte and Lienhard ([9.32] and [9.33]) On it are
identified a nucleate-transition and a film-transition boiling region These
are continuations of nucleate boiling behavior with decreasing liquid–
solid contact (as shown in Fig 9.3c) and of film boiling behavior with
increasing liquid–solid contact, respectively
These two regions of transition boiling are often connected by abrupt
jumps However, no one has yet seen how to predict where such jumps
take place Reference [9.33] is a full discussion of the hydrodynamic
theory of boiling, which includes an extended discussion of the transition
boiling problem and a correlation for the transition-film boiling heat flux
by Ramilison and Lienhard [9.34]
Trang 4Figure9.14also indicates fairly accurately the influence of roughness
and surface chemistry on qmax It suggests that these influences mally can cause significant variations in qmax that are not predicted inthe hydrodynamic theory Ramilison et al [9.35] correlated these effects
nor-for large flat-plate heaters using the rms surface roughness, r in µm, and the receding contact angle for the liquid on the heater material, β r
in radians:
qmax
qmaxZ = 0.0336 (π − β r ) 3.0 r 0.0125 (9.36)This correlation collapses the data to±6% Uncorrected, variations from
the predictions of hydrodynamic theory reached 40% as a result of ness and finish Equivalent results are needed for other geometries
rough-Subcooling
A stationary pool will normally not remain below its saturation ature over an extended period of time When heat is transferred to thepool, the liquid soon becomes saturated—as it does in a teakettle (recallExperiment9.1) However, before a liquid comes up to temperature, or if
temper-a very smtemper-all rtemper-ate of forced convection continuously repltemper-aces wtemper-arm liquidwith cool liquid, we can justly ask what the effect of a cool liquid bulkmight be
Figure 9.16 shows how a typical boiling curve might be changed if
Tbulk < Tsat: We know, for example, that in laminar natural convection,
q will increase as (T w − Tbulk) 5/4 or as [(T w − Tsat) + ∆Tsub] 5/4, where
∆Tsub ≡ Tsat− Tbulk During nucleate boiling, the influence of subcooling
on q is known to be small The peak and minimum heat fluxes are known
to increase linearly with ∆Tsub These increases are quite significant The film boiling heat flux increases rather strongly, especially at lower
heat fluxes The influence of ∆Tsub on transitional boiling is not welldocumented
Gravity
The influence of gravity (or any other such body force) is of concern cause boiling processes frequently take place in rotating or acceleratingsystems The reduction of gravity has a significant impact on boiling
be-processes aboard space vehicles Since g appears explicitly in the tions for qmax, qmin, and qfilm boiling, we know what its influence is Both
equa-qmax and qmin increase directly as g 1/4 in finite bodies, and there is an
additional gravitational influence through the parameter L However,
when gravity is small enough to reduce R below about 0.15, the
Trang 5hydrody-§9.6 Transition boiling and system influences 493
Figure 9.16 The influence of subcooling on the boiling curve.
namic transitions deteriorate and eventually vanish altogether Although
Rohsenow’s equation suggests that q is proportional to g 1/2in the
nucle-ate boiling regime, other evidence suggests that the influence of gravity
on the nucleate boiling curve is very slight, apart from an indirect effect
on the onset of boiling
Forced convection
The influence of superposed flow on the pool boiling curve for a given
heater (e.g., Fig.9.2) is generally to improve heat transfer everywhere But
flow is particularly effective in raising qmax Let us look at the influence
of flow on the different regimes of boiling
Trang 6Influences of forced convection on nucleate boiling Figure9.17showsnucleate boiling during the forced convection of water over a flat plate.Bergles and Rohsenow [9.36] offer an empirical strategy for predictingthe heat flux during nucleate flow boiling when the net vapor generation
is still relatively small (The photograph in Fig.9.17 shows how a stantial buildup of vapor can radically alter flow boiling behavior.) Theysuggest that
• qFCis the single-phase forced convection heat transfer for the heater,
as one might calculate using the methods of Chapters6and7
• q B is the pool boiling heat flux for that liquid and that heater from
eqn (9.4)
• q iis the heat flux from the pool boiling curve evaluated at the value
of (T w −Tsat) where boiling begins during flow boiling (see Fig.9.17)
An estimate of (T w − Tsat)onset can be made by intersecting the
forced convection equation q = hFC(T w − T b ) with the following
con-Peak heat flux in external flows The peak heat flux on a submerged
body is strongly augmented by an external flow around it Althoughknowledge of this area is still evolving, we do know from dimensionalanalysis that
qmax
ρ g h fg u ∞ = fnWeD , ρ f ρ g
(9.39)
Trang 7§9.6 Transition boiling and system influences 495
Figure 9.17 Forced convection boiling on an external surface.
where the Weber number, We, is
Kheyrandish and Lienhard [9.38] suggest fairly complex expressions
of this form for qmax on horizontal cylinders in cross flows For a
cylin-drical liquid jet impinging on a heated disk of diameter D, Sharan and
Trang 8Lienhard [9.39] obtained
qmax
ρ g h fg ujet =0.21 + 0.0017ρ f ρ g
djet D
range of the data
The influence of fluid flow on film boiling Bromley et al [9.40] showedthat the film boiling heat flux during forced flow normal to a cylindershould take the form
for u2∞ /(gD) ≥ 4 with h fg from eqn (9.29) Their data fixed the constant
at 2.70 Witte [9.41] obtained the same relationship for flow over a sphereand recommended a value of 2.98 for the constant
Additional work in the literature deals with forced film boiling onplane surfaces and combined forced and subcooled film boiling in a vari-ety of geometries [9.42] Although these studies are beyond our presentscope, it is worth noting that one may attain very high cooling rates usingfilm boiling with both forced convection and subcooling
9.7 Forced convection boiling in tubes
Flowing fluids undergo boiling or condensation in many of the cases inwhich we transfer heat to fluids moving through tubes For example,such phase change occurs in all vapor-compression power cycles and
refrigerators When we use the terms boiler, condenser, steam generator,
or evaporator we usually refer to equipment that involves heat transfer
within tubes The prediction of heat transfer coefficients in these systems
is often essential to determining U and sizing the equipment So let us
consider the problem of predicting boiling heat transfer to liquids flowingthrough tubes
Trang 9Figure 9.18 The development of a two-phase flow in a vertical
tube with a uniform wall heat flux (not to scale)
497
Trang 10Relationship between heat transfer and temperature difference
Forced convection boiling in a tube or duct is a process that becomes veryhard to delineate because it takes so many forms In addition to the usualsystem variables that must be considered in pool boiling, the formation
of many regimes of boiling requires that we understand several boilingmechanisms and the transitions between them, as well
Collier and Thome’s excellent book, Convective Boiling and tion [9.43], provides a comprehensive discussion of the issues involved
Condensa-in forced convection boilCondensa-ing Figure9.18 is their representation of the
fairly simple case of flow of liquid in a uniform wall heat flux tube in
which body forces can be neglected This situation is representative of a
fairly low heat flux at the wall The vapor fraction, or quality, of the flow
increases steadily until the wall “dries out.” Then the wall temperaturerises rapidly With a very high wall heat flux, the pipe could burn outbefore dryout occurs
Figure9.19, also provided by Collier, shows how the regimes shown inFig.9.18are distributed in heat flux and in position along the tube Noticethat, at high enough heat fluxes, burnout can be made to occur at any sta-
tion in the pipe In the subcooled nucleate boiling regime (B in Fig.9.18)
and the low quality saturated regime (C), the heat transfer can be
pre-dicted using eqn (9.37) in Section 9.6 But in the subsequent regimes
of slug flow and annular flow (D, E, and F ) the heat transfer mechanism
changes substantially Nucleation is increasingly suppressed, and ization takes place mainly at the free surface of the liquid film on thetube wall
vapor-Most efforts to model flow boiling differentiate between
nucleate-boiling-controlled heat transfer and convective boiling heat transfer In
those regimes where fully developed nucleate boiling occurs (the later
parts of C), the heat transfer coefficient is essentially unaffected by the
mass flow rate and the flow quality Locally, conditions are similar to poolboiling In convective boiling, on the other hand, vaporization occursaway from the wall, with a liquid-phase convection process dominating
at the wall For example, in the annular regions E and F , heat is convected
from the wall by the liquid film, and vaporization occurs at the interface
of the film with the vapor in the core of the tube Convective boilingcan also dominate at low heat fluxes or high mass flow rates, where wallnucleate is again suppressed Vaporization then occurs mainly on en-trained bubbles in the core of the tube In convective boiling, the heattransfer coefficient is essentially independent of the heat flux, but it is
Trang 11§9.7 Forced convection boiling in tubes 499
Figure 9.19 The influence of heat flux on two-phase flow behavior.
strongly affected by the mass flow rate and quality
Building a model to capture these complicated and competing trends
has presented a challenge to researchers for several decades One early
effort by Chen [9.44] used a weighted sum of a nucleate boiling heat
trans-fer coefficient and a convective boiling coefficient, where the weighting
depended on local flow conditions This model represents water data to
an accuracy of about ±30% [9.45], but it does not work well with most
other fluids Chen’s mechanistic approach was substantially improved
in a more complex version due to Steiner and Taborek [9.46] Many other
investigators have instead pursued correlations built from dimensional
analysis and physical reasoning
To proceed with a dimensional analysis, we first note that the liquid
and vapor phases may have different velocities Thus, we avoid
Trang 12intro-ducing a flow speed and instead rely on the the superficial mass flux, G,
through the pipe:
Physical arguments then suggest that the dimensional functional
equa-tion for the flow boiling heat transfer coefficient, hfb, should take the following form for saturated flow in vertical tubes:
hfb= fnhlo, G, x, h fg , q w , ρ f , ρ g , D
(9.45)
It should be noted that other liquid properties, such as viscosity and
con-ductivity, are represented indirectly through hlo This functional tion has eight dimensional variables (and one dimensionless variable, x)
equa-in five dimensions (m, kg, s, J, K) We thus obtaequa-in three more
dimension-less groups to go with x, specifically
Bo≡ q w
Trang 13§9.7 Forced convection boiling in tubes 501
Table 9.4 Fluid-dependent parameter F in the Kandlikar
cor-relation for copper tubing Additional values are given in [9.47]
When the convection number is large (Co 1), as for low quality,
nucleate boiling dominates In this range, hfb /hlorises with increasing Bo
and is approximately independent of Co When the convection number
is smaller, as at higher quality, the effect of the boiling number declines
and hfb /hloincreases with decreasing Co
Correlations having the general form of eqn (9.49) were developed
by Schrock and Grossman [9.48], Shah [9.49], and Gungor and
Winter-ton [9.50] Kandlikar [9.45, 9.47, 9.51] refined this approach further,
obtaining good accuracy and better capturing the parametric trends His
method is to calculate hfb/hlofrom each of the following two correlations
and to choose the larger value:
where “nbd” means “nucleate boiling dominant” and “cbd” means
“con-vective boiling dominant”
In these equations, the orientation factor, f o, is set to unity for
ver-tical tubes4 and F is a fluid-dependent parameter whose value is given
4 The value for horizontal tubes is given in eqn (9.52).
Trang 14in Table9.4 The parameter F arises here for the same reason that
fluid-dependent parameters appear in nucleate boiling correlations: surfacetension, contact angles, and other fluid-dependent variables influencenucleation and bubble growth The values in Table9.4are for commer-cial grades of copper tubing For stainless steel tubing, Kandlikar recom-
mends F = 1 for all fluids Equations (9.50) are applicable for the
satu-rated boiling regimes (C through F ) with quality in the range 0 < x ≤ 0.8.
For subcooled conditions, see Problem9.21
Example 9.9
0.6 kg/s of saturated H2O at T b = 207 ◦C flows in a 5 cm diameter
ver-tical tube heated at a rate of 184,000 W/m2 Find the wall temperature
at a point where the quality x is 20%.
Solution. Data for water are taken from Tables A.3–A.5 We first
compute hlo
G = A m˙
pipe = 0.001964 0.6 = 305.6 kg/m2sand
Relo= GD
µ f = (305.6)(0.05) 1.297 × 10 −4 = 1.178 × 105From eqns (7.42) and (7.43):
... class="text_page_counter">Trang 14in Table9.4 The parameter F arises here for the same reason that
fluid-dependent parameters appear in...
497
Trang 10Relationship between heat transfer and temperature difference
Forced... flow and annular flow (D, E, and F ) the heat transfer mechanism
changes substantially Nucleation is increasingly suppressed, and ization takes place mainly at the free surface of the