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ftnd conservation of energy becomes where in the temperature range 500 to 1000 deg K the reaction
rate is [10]
i[rh(h + ?)] = ±ThE(hE + Yf) + Qc, (5) */ = (9.5 - 0.005T) X 1011 (10)
The plus sign is for injection (evaporator) and the minus sign where T has the units deg K and kf has the units cm /sec-moles 2 . 6
for suction (condenser). The total heat transfer rate per unit The process of liquid formation in the supersaturated vapor
stream can be separated into two distinct steps: (1) the forma-
length QE to the outside wall of the heat pipe is
tion of the liquid nuclei and (2) the subsequent growth of these
QE = QCOIIY ± irishf, (6) nuclei into relatively large liquid drops. The classical theory for
the droplet nucleation rate yields [11—13]
and is positive in the evaporator, negative in the condenser, and
zero in the adiabatic region. /P\2 M haft V 4irar* ;
Assuming the monatomic and diatomic species are perfect J = (11)
~3kT~
gases, the density of the mixture of diatomic vapor, monatomic
vapor, and liquid can be written where r*, the critical radius, is given by
2<TM
(7) (12)
H (1 - p)R2T(l + a) pLRTlnP/Ps
PL P
and where a is the flat-film value of surface tension. The rate
and the x-derivative of the enthalpy of the mixture becomes of growth of a droplet of radius r can be expressed as [11]
dh dT da fir 1 Pn
dx
= (1 /*)'• {«cpi + (1 - a)cp[
dx 1}
dx dt VZir [
PL LVRT VRTD.
(13)
N a + N a <=* Na 2
kb
(l4)
can be written [9] K^/TI^]^**+!"•*'
— Nomenclature-
A = cross-sectional area of vapor jection or suction per X axial distance measured
passage unit length from upstream end of
constant-pressure specific m,D = liquid flow rate evaporator
heat Thy = vapor flow rate, rhv = rhyi a = degree of dissociation of
specific heat of monatomic + mV2 vapor, a = rhvi/{rhvi +
vapor rhyi = monatomic vapor flow rate rhvi)
specific heat of diatomic va- rhvi = diatomic vapor flow rate aE = degree of dissociation of in-
por Mi = molecular weight of mon- jected or rejected vapor,
CpL = liquid specific heat atomic sodium otB^=Tfim/(mm + mm)
D = diameter of vapor passage iV = Avogadro's number = liquid-mixture mass ratio,
/ = friction factor P = static pressure p, E = ThhlirriD + rhv)
h = enthalpy P», Pant = saturation pressure = viscosity
h/g = enthalpy of evaporation Pr = Prandtl number = density
h = enthalpy of monatomic QE = heat transfer to outside wall = surface tension
vapor of heat pipe per unit = wall shear stress
h = enthalpy of diatomic vapor length (d\m\
Qconv = heat transfer from liquid- = rate of change in molal
ti = convection heat transfer co- \ dt /„,
vapor interface to vapor concentration of mon-
efficient
by convection atomic sodium vapor due
J = critical droplet nucleation to chemical reaction
rate R = gas constant
Rz = gas constant of diatomic (drhi\
k, = reaction rate rate of change in flow rate
sodium ^ (XX / eond
Kv = equilibrium constant of liquid sodium due to
Res = Reynolds number, Rez> =
KT = thermal conductivity homogeneous vapor con-
VD/v
densation
enthalpy of dimerization, T = temperature of vapor
ID = ID — hi — hi TE = temperature of liquid-vapor Subscripts
rate of mass injection or interface 1 = denotes monatomic sodium
riiE = suction per unit length ^sat = saturation temperature 2 = denotes diatomic sodium
rate of monatomic mass in- V = axial velocity of vapor L = denotes liquid
rtiEi = jection or suction per unit VE = transverse velocity of va- V = denotes vapor
length por at liquid-vapor inter- E = denotes state of injected or rejected
rate of diatomic mass in- face vapor
FRICTIONLESS 1 REACTING-
PERFECT GAS X
X
h-
100
I
-EQUILIBRIUM
s
II
x WESTINGHOUSE HEAT PIPE
0
0
400 500 600
2001
FROZEN
10'
100
3X10'^
500 600
TE (X = 0), °C
Fig. 1 Sonic-limit heat transfer rate
400
Within the evaporator region, the injected fluid is assumed
to be superheated vapor with an equilibrium composition OLE cor- Fig. 2 Variation of axial drop in vapor temperature and vapor super-
responding to the local static pressure P and the local interface saturation at choking point
temperature TE (equations to determine the equilibrium com-
position are found in [9]). The magnitude of the interfacial
KT
superheat was taken to be [14] h = 0.023 — (Refl) 0 - 8 (Pr) 0 - 3 (20)
TE — Tsl
[ rhE "
27TO. Pht.
(15) was taken for the turbulent flow case [17].
The thermophysical properties of sodium were obtained from
[18-21]. A comprehensive review of those properties pertinent
Whereas in the evaporator TE > Tsat, in the adiabatic region
to this study is contained in [9].
the interfacial temperature is equal to the local values of satura-
tion temperature. The temperature of the interface within the
condenser region is obtained from equation (15) where the minus Analytical Results
sign is now applicable. I t is assumed t h a t in the condenser re- The equations given above can be rearranged to form a system
gion the rejected fluid TOE leaves the vapor passage at the local of five simultaneous first-order ordinary differential equations
saturation temperature and pressure and t h a t the vapor com- t h a t can be solved numerically for a, fj., P, T, and V as functions
position CXE is the same as t h a t of the bulk vapor a. The fluid of x, provided QE is specified. These were solved by digital
removed from the vapor passage by suction is assumed to be computer by means of a R u n g e - K u t t a integration scheme. At
pure vapor; no liquid enters or leaves the vapor passage a t the the upstream end of the evaporator (x —*• 0), the vapor Mach
liquid-vapor interface. In all cases, both the evaporator mass number is small and the incompressible equations of motion can
injection rate and condenser mass suction rate were taken to be be used to generate the initial conditions needed for the first
uniform over the lengths of the evaporator and condenser regions. step in the integration.
The relation The calculations were made for two different heat pipes. One,
with a 1.846-cm-dia vapor passage, a 17.8-cm-long evaporator,
2x2
/= (16) a 5.1-cm-long adiabatic region, and a 19.0-cm-long condenser
ReD section, corresponds to an experimental sodium heat pipe of
2 Dzakowic et al. [2]. The second heat pipe, tested by Kemme of
Los Alamos Scientific Laboratory [1], had a 1.04-cm-dia vapor
was used for all laminar shear-stress calculations in the evaporator passage, a 40-em-long evaporator, a 10-cm-long adiabatic re-
[15] and gion, and a 75-cm-long condenser.
The calculations were performed in several steps to determine
(17) the relative importance of the various phenomena. The first
Rer>
set of results for the Westinghouse heat pipe are summarized in
for the adiabatic and condenser regions. The equation Figs. 1 and 2. The droplet nucleation rate / was artificially
set to zero (flow frozen with respect to phase change) and the
0.079 chemical reaction was alternately taken to be frozen (kf = 0 ) , in
/ (18)
(Res) 1 /* equilibrium (see [7] and [9] for a description of the equilibrium
calculations) and reacting at a rate given by equation (10). In
was used for all turbulent flow conditions [16] with transition all these calculations, the evaporator heat transfer rate QE was
assumed to occur at R e s = 2000. The equation adjusted until sonic flow was attained at the inlet to the con-
denser.
h = 3.66 - (19) Table 1 shows the rates of heat transfer required to cause
D
sonic vapor flow at the condenser inlet of the Westinghouse heat
was used for the laminar-flow convective heat transfer coefficient pipe. Over the temperature range considered, the differences
and between the heat transfer rates for the three cases were less than
REACTING FLOW
WITH FRICTION
2 J I L_L ui
*'° I L V s'oo1 ' ' 600 700 r-o
To=650°C
Te (X = 0), °C Q = 7 2 3 0 WATTS
r-
< 0.923 CM. RADIUS
Fig. 3 Sonic-limit heat transfer rate CRITICAL NUCL.
10 15 20
,200 DISTANCE CM
0 10 20 30 40
DISTANCE X, CM