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IN HEAT AND MASS TRANSF~I~ 0094-4548/82/030221-06502.00/0 Vol. 9, pp. 221-226, 1982 © Pergamon Press Ltd. Printed in the United states
FURTHER EXPERIMENTS ON TRANSIENT SWELLING
DURING POOL BOILING
J,P. Gupta , A. ShaDma & D. Garg Chemical Engineering Department India~ Institute of Technolo~
Kanpur-208016, India
(Communicated by J.H. Whitelaw)
Pool boiling equipment are extensively use4 to produce
distilled water for boiler feed, to concentrate dilute solutloms, to
provide vapor reflux at the bottom of distillati~ column and,
lately, also as am emergency condenser for high pressure steam in
nuclear power plants. A large amount of space is arbitrarily left
above the liquid level for the dise~gagemeat uE the entrained liquid
droplets from the vapor. For the power plant reboilers, Kern [13
states that the liquid level is malntained at 50~ of the shell diame-
ter, while for the kettle reboilers, it is kept at approximately 60~,
the remainder of the space bei~ 'adequate' for the disengagement of
the entrained liquid dropletS.
The above rules-of-thumb were satisfactory for small units
used in the ¥1ftees when Kern wrote his famous book. However, with
larger sizes and high pressures currently in use, it is very important
that the units be slzed properly since the thickness of the shell
and hence its cost are related to the pressure and radius.
221
222 J.P. Gupta, A. Sha_rn~ and D. C~rg Vol. 9, No. 3
An importent factor which had ben ignored until veEy recently
is the signiflcant increase or swelli~ in the 2-phase level due to
the vapor generation. This cuts down the net available dlsengagement
spaae. In a poorly sized unit, the disengagement space may redt~e to
nil. Therefore the knowledge of swelling 18 important to properly
si -e up the hoiling ulp-ent [2J. singh [3] dmlo
the first set of relatiun8 add an iterati~e analytical prooedure to
calculate the swelled level° This has been verified experimer~allY
by T ~ o n ~, Gupte [ 4 ] us~.g water .
Since the publicatlon of [4], other researaheEs and equl~ent
designers have ~ked if the model would hold for other liquids
solutiun8 with viscosities and surface ter~|iun8 different than th~
of water. In this paper we report the results obtained by using
liquids of different densities, viscosities ~d surface tensiO~o It
turns out that indeed the model holds for them a~8o and hence Qaa~ be
used in design using any liquid or solution° This also cancludes our
curr~t experimental program in thl8 area,
The equil~er~ used has been described I~ detail by Tando~
& Gupta [4~. Briefly, it was a glass column calibrat Id in units
of OeOOS-m with a 2-kW immersion heater 8=rewed into the bottom
flange. Rest of the dimensions are shown in Fig.(I) of RIg.J4] °
The liquids used were salt and sugar solutions listed in
T a b l e l ,
Vol. 9, No. 3 TRANSII~XTf SHT~Z.TL',IG DURING POOL BO]XJ_h~ 223
Table I
PROPERTIES OF SOLUTIONS USED
CAll solutions made in distilled water. Percent composition in weight percent)
Solution
,~oncentrat ions
Boiling Point, B.P., C)
Density
~B.P. , , J ,
Vlscosity,-7 25C
( Zo3kg/m. e. ) "~ B.P.
Surf ace / 25(:: renslon
( 10 3N/m) S.P,
Sugar Solutions
10~
(100.5)
1135
1041 i
1.233
0.33
29.8
22.5
20~ 30~
(iO1.O) (102.O)
1172 1210
1075 1110
1.7 3.0
0.336 0.341
30.7 31.62
23.2 23.9
Salt (NaCI) Solutions
10~
(lO4.o)
1184
1083 i
m
0.337
31.5
23.5
21.8%
(107.O) ii
1256
1146
0.347
33,6
25.1
These solutions were chosen because cf their practical nature
since these are used in the manufacture cf iodized and free flowing
salt and in sugar production by evaporation In units where pool
boiling Is encountered. Besides, these cover a range of parameters
which represent a large number of other pure liquids and solutions
as well. All the solutions used were made in distilled water.
One solution1 at a time was filled into the glass colmun upto
a height of approximately o~e meter and heated by means of the
immersion heater. When the heating was started, the level increased
224 J.P. Oupta, A. Sharma and D. Garg Vol. 9, No. 3
due to decrease in density• The liquid level Just before boiling
was noted. The increase in the level due to the release of vapor
during boiling was thal noted. This level, due to the vary nature
of boiling, is not a steady value but has a range of a few centi-
meters. At times, a momentary spurt would temporarily raise the
2-phase level further by 0.015 to O.02-m. Experiments were repeated
by varying the initial height of the liquid. The proQedure for this
is glven in .
R e s u l t s
The mathematical modal given by Singh told Gt~pta ~3~ was used
to calculate the swelled height by the iterative tectmique described
therein •
For the liquids tested (Table 1), the results ace given in
Fig.( 1). The ope~ symbols denote the values calculated from the
model while the short vertical lines denote the experimental values
which, as discusse6 above, varied within a few centimeters. It
includes the O.015 to O•02-m sudden bursts scmet~es enco~altered in
the system.
The work reported here ind in Ref.[4] conclusively demonstrate
the usefulness of our mathematical model ~3~ in calculatlng the
swelled height c~ the 2-phase mixture in a pool boiling equil~ent.
This should give a new confidence to the designers who otherwise
find it difficult to calculate the exact dlseng~ement sp~e
available in a pool boiling equipment and end up doing a significant
overde s Ign.
Vol. 9, No. 3 TRANSI]~f SWELLII~DURING POOL BOILIk~ 225
Acknewleduemem:
H e l p provided by Dr.P.CoNigam• Chemistry Department, IoI.T.
Kanpur in measurements of eurfaos tensi~ Is gratefully acknowledged.
0
2.
3.
4,
D•Q.Kerne 'Prc~ess Heat Transfer' • McGraw-Hill• New York (1950).
K.J.Bella 'Heat Exchangers w~th phase change.• Invited Lecture• Int, S e m i n a r cm Advancements in Heat Exchangers, Dubrovnlk• Yugoslavia• September, 1981.
K°P.S~gh & J.P.Guptat 'Transient swelling cf llqu~ level during pool boiling in ml emergen~ condenser', Letters i~ Heat Mass Trarls~er, 8( I)• 25-33 ( 1981)o
Nears Tando~ & JoP,Gupta• 'Experiments oll transient swelZing during pool boiling'• Letters in Heat Mass T~ansf~r • 8( 3), 247-252 (1981).
226 J.P. Gupta, A. Sharma and D. Garg Vol. 9, No. 3
1-10
1.00
o 10°1o sugar solut ion
V 20°•0 sugar solution
A 30010 sugar solution
O 10°1o NoCI so lu t ion
o 21.8Olo NQCI solut ion
0.90
E 0.80 c
c
0.70
~n 0-60
0.50
0.40
0.30 " 0.30 0-40 0-50 0.60 0.70 0.80 0-90 1-00 1.10
In i t i a l height, m
FIG, 1
S w e l l e d H e i g h t v s . I n i t i a l H e i g h t f o r V a r i o u s 8 o l u t i o a e