ultra fast cooling of hot steel plate by air atomized spray with salt solution
TRANSCRIPT
ORIGINAL
Ultra fast cooling of hot steel plate by air atomized spraywith salt solution
Soumya S. Mohapatra • Satya V. Ravikumar • Jay M. Jha •
Akhilendra K. Singh • Chandrima Bhattacharya •
Surjya K. Pal • Sudipto Chakraborty
Received: 31 October 2012 / Accepted: 7 November 2013
� Springer-Verlag Berlin Heidelberg 2013
Abstract In the present study, the applicability of air
atomized spray with the salt added water has been studied
for ultra fast cooling (UFC) of a 6 mm thick AISI-304 hot
steel plate. The investigation includes the effect of salt
(NaCl and MgSO4) concentration and spray mass flux on
the cooling rate. The initial temperature of the steel plate
before the commencement of cooling is kept at 900 �C or
above, which is usually observed as the ‘‘finish rolling
temperature’’ in the hot strip mill of a steel plant. The heat
transfer analysis shows that air atomized spray with the
MgSO4 salt produces 1.5 times higher cooling rate than
atomized spray with the pure water, whereas air atomized
spray with NaCl produces only 1.2 times higher cooling
rate. In transition boiling regime, the salt deposition occurs
which causes enhancement in heat transfer rate by con-
duction. Moreover, surface tension is the governing
parameter behind the vapour film instability and this length
scale increases with increase in surface tension of coolant.
Overall, the achieved cooling rates produced by both types
of salt added air atomized spray are found to be in the UFC
regime.
List of symbols
Fa Air flow rate (N m3/h)
Fw Water flow rate (m3/s)
S1 Section 1 (mm)
S2 Section 2 (mm)
S3 Section 3 (mm)
Sc Salt concentration (mol/l)
T Temperature (�C)
T1 Temperature measured by thermocouple 1 (�C)
T2 Temperature measured by thermocouple 2 (�C)
T3 Temperature measured by thermocouple 3 (�C)
t Time (s)
X Direction along the length of the plate (mm)
Y Direction along the thickness of the plate (mm)
1 Introduction
The modern day requirements of high tensile strength
steel have placed a great emphasis on the rapid cooling
methods for the hot plate immediately after rolling. The
desired mechanical properties of steel are achieved during
cooling on the Run-Out table (ROT) of a hot strip mill.
During the cooling process, the thermo-metallurgical
phase transformation of steel takes place and that governs
the final mechanical properties. However, the slow
quenching rate generated by conventional laminar cooling
system, which is generally fitted in the ROT, cannot
generate the desired high tensile strength steel. According
to Lucas et al. [1], the rapid cooling rate has been the
main focus for the development of ultra fast cooling
(UFC) technologies.
UFC technique, depending upon the final microstructure
of dual phase steel, was investigated by Bin et al. [2]. Any
cooling process, for which the product of cooling rate (�C/
s) and plate thickness (mm) yields a number greater than
800, is called UFC technique.
S. S. Mohapatra � S. V. Ravikumar � J. M. Jha �A. K. Singh � C. Bhattacharya � S. Chakraborty (&)
Department of Chemical Engineering, Indian Institute
of Technology, Kharagpur 721032, India
e-mail: [email protected]
S. K. Pal
Department of Mechanical Engineering, Indian Institute
of Technology, Kharagpur 721302, India
123
Heat Mass Transfer
DOI 10.1007/s00231-013-1260-6
For rapid cooling operations, amongst all the liquid
coolants, water is the most economical and easily available
component. When water is used to cool a hot substrate at
high initial surface temperature, the Leidenfrost effect
plays an important role. Oliveria and Sousa [3] reported
that due to the aforesaid effect, a vapour layer covers the
hot surface and simultaneously reduces the heat transfer
rate.
Air atomized spray is found to be a promising cooling
system among different cooling methods reported by Mo-
hapatra et al. [4]. Moreover, the study made by Puschmann
and Specht [5] point out that the main advantage of air
atomized spray cooling is that a high volumetric flow of air
sweeps away the partially evaporated drops from the hot
surface. This phenomenon prevents the formation of a
stable vapour film at high surface temperature, but is
observed only at low mass flux. However, the investigation
made by Al-Ahmadi and Yao [6] depicts that cooling
occurs in transition boiling regime in the case of high-mass
flux atomized spray cooling also. As a result, in the
aforesaid case, high cooling rate is observed when it starts
from a high surface temperature.
In case of air atomized spray with high mass flux, the
droplet evaporation time plays an important role as repor-
ted by Bhattacharya et al. [7]. The study made by Qio and
Chandra [8, 9] revealed that droplet life time can be
decreased by making the droplet thin when it impinges the
hot plate, and creating high contact surface for heat transfer
by using surfactant added water. They noticed that cooling
enhancement was limited within the nucleate boiling
regime. Cui et al. [10] examined the effect of dissolving
gas and salt in boiling of water droplet. They concluded
that gas had little effect on boiling, and the dissolved salt in
water prevented the coalescence of vapour bubble inside
the droplet. In the follow up research by King et al. [11], it
was observed that dissolved salt decreased the droplet
vaporization rate due to the boiling point elevation.
Cui et al. [12, 13] experimentally studied salt added
water-spray cooling in the temperature range of
100–240 �C, and found that the dissolved salt in water
droplet deposits on the hot plate during evaporation. The
deposited salt penetrates the vapour film and touches the
water droplet. Therefore, the heat transfer occurs in con-
duction mode from the hot plate to the droplet and as a
consequence, the cooling in transition boiling regime of a
conventional spray cooling improved. The research with
dissolved salt in water has so far been limited to spray
cooling, and was conducted at a very low substrate tem-
perature (*240 �C) and low mass flux (\5 kg/m2 s) of
water.
The literature asserts that the dissolved salt in water
enhances the cooling in transition boiling regime due to the
deposition of salt on the hot surface. Therefore, the authors
expect an improvement of cooling rate in the transition
boiling regime (900–600 �C) of an air atomized spray with
salt-water. The reasons are—prevention of vapour bubble
coalescence inside the droplet, the effect of deposition of
salt on the cooling surface and the effect of superposed air
flow and foaming.
The degree of film boiling depends on the extent of
vapour bubble generation and its coalescence. Since the
dissolved salt in water droplet prevents the vapour bubble
coalescence, the film boiling effect is expected to be a
minimum in this case. Additionally due to salt deposition,
the vapour film in the transition boiling regime collapses,
and as a result an enhancement in cooling is expected.
Therefore, in the current research, salt added air-atomized
spray cooling has been studied at a high initial surface
temperature (*900 �C), which is generally found to be in
the transition boiling regime, and high mass flux of water
to examine its applicability in achieving UFC rate for a hot
steel plate.
2 Experimental configuration
Experimental setup has been initially fabricated to conduct
the required number of experiments according to the
Design of Experiment (DOE) methodology followed in
the current work. After the experimentations, the surface
heat flux and the surface temperatures have been calcu-
lated for the interpretation of the heat transfer data. In
addition to the above, to understand the heat transfer
mechanism during cooling, the spray behaviours have also
been investigated.
2.1 Experimental procedure
Systematic experiments have been conducted on a 100
mm 9 100 mm AISI 304 steel plate of 6 mm thickness.
For the measurement of temperature during experimenta-
tion, three K-type thermocouples having diameter 3 mm
each (T1, T2 and T3) were inserted in the plate. The exact
locations of the thermocouples within the steel plate have
been shown in Fig. 1. By following the methodology
proposed by Li and Wells [14], in the current work ther-
mocouples were placed parallel to the quenching surface to
avoid the error induced due to the thermocouple hole
diameter. The temperature data were recorded at a sam-
pling rate of 10 data per second during experimentation
with the help of a data acquisition system (NI-USB-6210,
from National Instrument, USA).
The steel plate was initially heated to a temperature of
1,050 �C. After attaining the desired temperature
(1,050 �C) and proper thermal soaking in the muffle fur-
nace, the compressor and pump were switched on for air
Heat Mass Transfer
123
and water spray respectively. The water temperature for
each experiment was maintained at 25 �C. The hot steel
plate was then taken out from the muffle furnace and put
on the cooling pad. The spray was showered from a full
cone air-assisted atomizer (Lechler 170.801) at a fixed
nozzle to plate distance (60 mm), and the atomizer was
kept vertically downward to get the maximum gravity
effect. The time–temperature data was recorded continu-
ously and saved in a file. The experiments were conducted
with various water flow rates (6.67 9 10-5–
16.67 9 10-5 m3/s) and at different salt concentrations
(0–0.4 mol/l) of sodium chloride (NaCl) and magnesium
sulphate (MgSO4). The solution was prepared with the
proper ratio of water at 25 �C and salt. During the
experimentation, the air flow rate was maintained at
40 N m3/h. A complete schematic diagram of the experi-
mental setup is shown in Fig. 2.
2.2 Estimation of surface heat flux
In the current work, the prediction of surface heat flux and
calculation of surface temperature have been done from the
measured temperature inside the plate, by using an inverse
heat conduction software (INTEMP) developed by Trujillo
and Busby [15]. The ‘‘INTEMP’’ is widely used by the
scientific community for the inverse heat conduction
problem; therefore, in the current research also, INTEMP
software has been used. INTEMP solves both linear and
nonlinear inverse heat conduction problems with unknown
surface heat flux, as claimed by Busby and Trujillo [16].
The plate used in the current experiment was 6 mm
thick and square in shape. Therefore, the heat transfer
within the plate can be modelled as a two dimensional
transient heat conduction problem with unknown surface
heat flux. Hence, in INTEMP, a 2-D planar thermal model
Fig. 1 Sketch of thermocouple
installation locations
Heat Mass Transfer
123
of 100 mm length and 6 mm thickness corresponding to
the actual steel plate has been considered. In INTEMP, for
the prediction of surface heat flux and surface tempera-
tures, the plate geometry has been discretised into 3,340
quadratic element with four nodes per element. The dis-
cretisation has been performed by using GAMBIT soft-
ware. In meshing, 0.06 mm increment in the direction of
X-axis and 0.03 mm in Y-axis have been contemplated,
and as a result a total of 3,528 nodes have been found.
For boundary conditions, all plate surfaces were
assumed to be adiabatic, except the top impinging surface.
The top non-adiabatic surface has been divided into three
flux sections. The first section extends from x = 0 to
35 mm (S1), the second section from x = 35 to 65 mm
(S2), whereas the third section is from x = 65 to 100 mm
(S3).
In the current calculation, the measured thermocouple
data were given as the input at the nodes, which belong to
the location of the thermocouples inserted inside the metal
plate. The nodes corresponding to the locations where the
temperature measurements occur are numbered as—1,715
at position (20, 3); 1,765 at (50, 3) and 1,797 at (70, 3)
respectively. Based on the above information, INTEMP
predicts the transient surface heat flux in all the sections
Fig. 2 Schematic diagram of the experimental setup
Fig. 3 Computational domain
of the steel plate for INTEMP
Fig. 4 Measured temperature and predicted temperature by INTEMP
with time
Heat Mass Transfer
123
and also calculates the transient surface temperatures at
each node. Figure 3 shows the entire computational
domain.
To check the accuracy of the nodal temperature pre-
diction by INTEMP, the predicted temperature for node
number 1,765 has been compared with the measured
temperature (T2). These temperatures have been compared,
because both the temperatures correspond to the same
location of the steel plate. From the comparison (Fig. 4), it
is seen that there is a close match (below 0.05 % error)
between the values estimated by the INTEMP software and
that measured by thermocouples.
2.3 Characterization of salt solution
The dissolved salt in water changes the surface tension
depending upon the nature and concentration of the salts.
Hence, the aqueous solution was characterized for the
aforesaid physical property of water.
Surface tension is an important parameter which influ-
ences the droplet contact angle with the solid surface. The
effect of salt concentration on the surface tension is shown
in Fig. 5. All the measurements shown in the said figure are
the average values of three repeated measurements taken
by using a surface tension meter (Model No: 232, Testing
Instruments, Kolkata, India).
In Fig. 5, it can be seen that the surface tension of water
marginally increases with an increasing NaCl concentra-
tion, and this is quite consistent with the information
reported in the literature. Sodium chloride dissolves per-
fectly in water, and as a result its surface tension at 25 �C
increases by adding NaCl, which in turn induces attractive
forces on the surface of the water molecule. However, the
surface tension of water decreases up to an MgSO4 salt
concentration of 0.05 mol/l. The same trend line was also
observed by the Cui et al. [12].
2.4 Spray characterization
The parameters which influence the air atomized spray are
droplet diameter, spray area and impingement density. The
details about each parameter has been described below. By
using the data sheet provided by Lechler Company
(GmbH), the variation of volumetric mean diameter of the
droplet with the water flow rate is as shown in Fig. 6. At a
constant air flow rate of 40 Nm3/h, it can be seen that the
droplet diameter increases with an increase in water flow
rate. The maximum droplet diameter of 170 lm was found
at a water flow rate of 16.67 9 10-5 m3/s, whereas the
minimum diameter of 88 lm was obtained at
6.67 9 10-5 m3/s.
Fig. 5 Variation of surface tension with salt concentrationFig. 6 The variation of droplet diameter with water flow rate
Fig. 7 Photograph taken at the moment spray impinges on the hot
plate
Heat Mass Transfer
123
To observe the spray impinging area, photographs were
taken by a digital camera during experiments. Figure 7
shows one such photograph taken during the experiment
with salt added (NaCl concentration 0.1 mol/l) air-atom-
ized spray. The nozzle height (60 mm) and the spray angle
(60�) data have been used to calculate the spray area. From
Fig. 7, it was noticed that a dark circle having radius equal
to the radius of the spray area appeared. The forced con-
vection cooling in the direct spray impinging area lowers
the surface temperature, compared to the surrounding red
hot zone leading to this dark circle. From the dark circle, it
was apparent that thermocouples T3 and T2 were in the
direct spray impinging area, whereas thermocouple T1 lies
outside.
The local variation of the spray impingement density
with the different water flow rates is shown in Fig. 8. All
impingement density measurements were taken by using an
indigenously designed and fabricated Patternator. Here, it
is found that the impingement density varies within the
radial distance of ±22 mm from the spray axis. The same
observation was also found from the photograph taken
during cooling. It was also noticed that the local
impingement density decreases with an increase in distance
from the spray axis, and the maximum value has been
achieved at the spray centre. The same trend line was also
observed by Alam et al. [17]. Moreover, it was also
observed that the local impingement density increases with
an increase in water flow rate. The maximum impingement
density was observed at a water flow rate of
16.67 9 10-5 m3/s and the minimum was found at
6.67 9 10-5 m3/s. The average impingement density of
air-atomized spray increases with an increase in water flow
rate and this is shown in Fig. 9. In the current research, the
average impingement density varies in the range of
82–255 kg/m2 s in the said water flow rate range. In the
present work, since the water impingement density depends
on the flow rate, the cooling rates and the surface heat flux
have been represented as a function of flow rate instead of
water impingement density.
2.5 Experimental uncertainty
In the present case, the measured variables are temperature
(Ti, inside temperature) and impingement density. The
main sources of uncertainty in temperature measurements
are temperature fluctuations and uncertainty in the loca-
tions of the thermocouples. All measurements were taken
thrice and their average was considered for the final cal-
culation. From the average data, the maximum uncertainty
is found to be 4 %.
3 Results and discussion
In the current investigation, the effect of water flow rate
and salt concentration on the heat transfer characteristics of
an air atomized spray has been studied for both types of
salts (NaCl and MgSO4), and from the experimental data,
relevant mathematical correlations have been developed.
Four sets of experiments have been designed which is
presented in Table 1.
3.1 Experiment with NaCl
3.1.1 Cooling curve
As per the DOE, a total of 20 experiments were performed,
and the time–temperature data were recorded for each of
these experiments. From these time–temperature histories,
by using INTEMP software, the surface heat flux and
surface temperature have been estimated. Here, only one
Fig. 8 Variation of water impingement density with water flow rate Fig. 9 Variation of average impingement density with water flow
rate
Heat Mass Transfer
123
such result is given as a sample case to understand the
cooling behavior of the steel plate during the experiment.
The remaining results have, however, been used to analyze
the effect of salt concentration and water flow rate on the
cooling rate, as illustrated later.
Figure 10 shows the temperature acquired by the ther-
mocouples at different locations of the plate during cool-
ing. The experimental conditions at which the experiments
were conducted are—water flow rate of 13.33 9 10-5 m3/s
and sodium chloride (NaCl) concentration of 0.1 mol/l.
Before the atomized spray was turned on, the three ther-
mocouples show the same temperature, which confirms
proper thermal soaking inside the muffle furnace. Fur-
thermore, Fig. 10 also shows that up to initial 37 s, the heat
loss is due to natural convection and radiation, because
some time is required to bring out the hot plate from the
muffle furnace and place it properly on the cooling pad.
After this initial time period, the heat loss significantly
increases with an increase in time due to forced convection
and boiling heat transfer caused by the atomized spray, and
consequently the temperature falls sharply. It was also
observed that there are 1.5 and 4 s delay in cooling for
thermocouples T3 and T1 respectively. The reason being
that, the thermocouple T1 is not under the direct spray
impingement section, whereas T3 is the second nearest
thermocouple from the spray centre.
The experimental data corresponding to Fig. 10 has
been used for the estimation of surface heat flux. The
transient variation of the estimated surface heat flux is
shown in Fig. 11. The point at which atomized spray
cooling starts in Fig. 10 has been considered as the initial
time (time = 0) for Fig. 11. Here it was observed that the
surface heat flux increases with an increase in time up to
2.65 s, and thereafter decreases. This could be due to the
change in heat transfer mechanism. For better under-
standing of the heat transfer mechanism, the boiling curve
Table 1 Design of experiment
Sl. No. Name of salt Name of variables Max. level Min. level Levels
1 NaCl Water flow rate (m3/s) 16.67 9 10-5 6.67 9 10-5 6.67 9 10-5, 10 9 10-5, 13.33 9 10-5, 16.67 9 10-5
2 NaCl Salt concentration (mol/l) 0.4 0 0, 0.1, 0.2, 0.3, and 0.4
3 MgSO4 Water flow rate (m3/s) 16.67 9 10-5 6.67 9 10-5 6.67 9 10-5, 10 9 10-5, 13.33 9 10-5, 16.67 9 10-5
4 MgSO4 Salt concentration (mol/l) 0.4 0 0, 0.1, 0.2, 0.3, and 0.4
Fig. 10 Temperature-time history for NaCl added air atomized spray
cooling
Fig. 11 Estimated surface heat flux and calculated surface temper-
ature with time for NaCl
Fig. 12 Boiling curve for air atomized spray with salt (NaCl)
Heat Mass Transfer
123
of the salt added air-atomized spray cooling has been
shown in Fig. 12.
For the boiling curve of air-atomized spray with salt, the
surface heat flux has been plotted as a function of surface
temperature (Fig. 12). Here, it was seen that transition
boiling regime cooling occurs in the temperature range of
900–525 �C, and the surface heat flux reaches the maxi-
mum value (CHF) of 1.9 MW/m2 at T = 525 �C. There-
after, the surface heat flux decreases with a decrease in
surface temperature, because the boiling regime changes
from transition to nucleate. Hence, in Fig. 11, the surface
heat flux is directly proportional to the time from
t = 0–2.65 s, due to the early onset of transition boiling
regime and thereafter, the surface heat flux decreases with
time due to the cooling in nucleate boiling regime. The film
boiling mechanism which weakens the heat transfer rate
has not been found in the experimental study of air-atom-
ized spray cooling. This is due to the fact that in air-
atomized spray cooling the finer droplets of water with
higher momentum touch the hot surface, gets deformed
increasing the contact area, the conduction heat transfer
takes place through the contact area, the water temperature
inside the droplet rises and it starts evaporating. Before the
droplet evaporates completely, they are swept away from
the plate surface by high velocity superposed air flow.
Hence, the formation of vapour film is prevented as there is
no occurrence of water pool on the hot surface unlike the
pure water jet impingement cooling. The same has also
been observed in the authors’ earlier studies with air-
atomized spray cooling system [18–20].
3.1.2 Transient variation of surface heat flux
The variation of surface heat flux with time at different salt
concentrations is shown in Fig. 13. Here, it was observed
that all the curves show a similar trend that initially
increases with an increase in time, and then decreases. The
increasing nature corresponds to the cooling in transition
boiling regime, whereas the decreasing characteristic of the
surface heat flux is due to the cooling in nucleate boiling
regime.
Figure 13 shows that the surface heat flux at any time
increases with an increase in salt concentration up to
0.1 mol/l, and thereafter shows a decreasing trend with an
increase in cooling in both the boiling regimes. In the
nucleate boiling regime, up to a salt concentration of
0.1 mol/l, the cooling enhancement could be due to the
prevention of the vapour bubble coalescence, which always
promotes the nucleate boiling.
In the transition boiling regime, up to a salt concentra-
tion of 0.1 mol/l, the surface heat flux mainly increases due
to the effect of salt deposition on the hot plate during the
droplet evaporation. As suggested in the literature, this
deposited salt breaks through the vapour layer insulating
the hot plate, and touches the water droplet during cooling.
Therefore, the heat transfer takes place by conduction
mode from the hot plate to the water droplet through the
deposited salt, and enhances the surface heat flux in the
transition boiling regime. However, the improvement in
surface heat flux with an increase in salt concentration in
the transition boiling regime is lesser compared to the
nucleate boiling regime. This could be due to insufficient
amount of salt deposition, which might not be adequate to
significantly enhance the surface heat flux.
In the case of salt concentration higher than 0.1 mol/l,
the effect produced due to the rise in surface tension of
resulting droplet dominates over the salt deposition, and
vapor bubble coalescence to enhance the heat transfer.
Moreover, surface tension is the governing parameter
behind the vapour film wave length of instability and this
wave length scale increases with increase in surface tension
of coolant. This instability length scale is a function of
surface tension, density of liquid and gas, and expressed as
the following equation [21]:
k ¼ rgðql � qgÞ
!1=2
ð1Þ
where r is surface tension, ql is density of liquid, qg is
density of gas, and g is acceleration due to gravity.
Therefore, the maximum surface heat flux has been
observed at a salt concentration of 0.1 mol/l.
3.1.3 Effect of water and salt concentration on average
surface heat flux and cooling rate
The steel strip/plate in the temperature range of
900–600 �C is cooled on the ROT, where the cooling rate
Fig. 13 Varition of surface heat flux with time at different concen-
trations of salt (NaCl)
Heat Mass Transfer
123
is an important parameter to control its mechanical/met-
allurgical properties. So, in the present work the average
surface heat flux and the cooling rate have been estimated
for the surface temperature drop of 900–600 �C. Figure 14
depicts that for all levels of water flow rates, the average
heat flux increases with an increase in salt concentration,
and reaches the maximum value at a salt concentration of
0.1 mol/l. The maximum average heat flux is obtained at a
salt concentration of 0.1 mol/l and water flow rate of
16.67 9 10-5 m3/s. Moreover, it is also noticed that the
average surface heat flux increases with an increase in
water flow rate at a constant salt concentration. This is due
to the fact that at higher water flow rate the impingement
density is also high, and this enhances the critical heat flux
(CHF) and nucleate boiling heat flux.
By using Design Expert Software version 6.0, a math-
ematical correlation (Eq. 2) has been developed involving
the surface heat flux, water flow rate and the surfactant
concentration. The determination coefficient for this cor-
relation is 0.99 which shows a proper fitting of this cor-
relation to the current experimental data.
qS ¼ 1:68þ 0:31� FW þ 0:075� SC � 0:034� F2w
� 0:49� S2C ð2Þ
The variation of average surface cooling rate with the water
flow rate and the salt concentration is shown in Fig. 15.
The figure shows that at constant water flow rate, cooling
rate gradually increases with an increase in salt concen-
tration, and reaches the maximum value at a salt concen-
tration of 0.1 mol/l. Thereafter, the cooling rate decreases
with an increase in salt concentration. The same trend is
observed for all levels of water flow rates.
The maximum cooling rate (178 �C/s) was observed at a
water flow rate of 16.67 9 10-5 m3/s, and the achieved
cooling rate was found to be in the ultra fast domain of an
AISI-304 steel plate. In addition to the above, by using
Design Expert Software version 6.0, a correlation which
relates cooling rate with water flow rate (Fw) and salt
concentration (Sc) is given Eq. 3. The determination
coefficient (R2) of the developed correlation is 0.99.
Z ¼ 158:28þ 21:33� FW þ 0:33� SC � 10:97� F2W
� 23:97� S2C � 4:5� FW � Sc
ð3Þ
3.1.4 Effect of salt (NaCl) concentration on critical heat
flux (CHF) and critical surface temperature (TCHF)
Figure 16 shows the estimated CHF and critical surface
temperature (TCHF) as a function of salt concentration. The
CHF increases from 1.4 to 2.58 MW/m2, while the salt
concentration increases from 0 to 0.1 mol/l. The deposited
salt on the cooling surface increases the surface roughness
of the hot substrate during cooling, and this process is the
main reason for the variation in CHF. After a concentration
Fig. 14 Variations of average surface heat flux with salt (NaCl)
concentration
Fig. 15 Cooling rate variation with salt (NaCl) concentration
Fig. 16 The variation of CHF and TCHF with salt (NaCl)
concentration
Heat Mass Transfer
123
of 0.1 mol/l, the CHF shows a decreasing nature with an
increase in salt concentration. In addition to the above, it is
also observed that the critical surface temperature vary
from 575 to 605 �C when the salt concentration changes
from 0 to 0.1 mol/l.
3.2 Experiment with MgSO4 salt
3.2.1 Cooling curves
Figure 17 shows the temperature measured by the ther-
mocouples at different positions of the steel plate during
atomized spray cooling with MgSO4 added water. The
experiments were performed at water flow rate of
13.3 9 10-5 m3/s, magnesium sulphate (MgSO4) concen-
tration of 0.1 mol/l and an air flow rate of 40 N m3/h.
Before the atomized spray is turned on, the three thermo-
couples exhibit the same temperature, which indicates the
uniformity of temperature at different locations before air
atomized spray cooling.
Figure 18 shows the variation of estimated surface
heat flux and surface temperature with time. The surface
heat flux increases with an increase in time up to 2 s
and thereafter shows a decreasing trend. This is because
of the two different boiling regimes (Fig. 19) at two
varying range of surface temperatures. Here, it is
observed that the transition boiling regime cooling
occurs in the temperature range of 900–570 �C, which
corresponds to the time period of 0–2 s in Fig. 18.
Furthermore, it is also found that below 570 �C, the
nucleate boiling initiates.
3.2.2 Transient variation of heat flux
To observe the transient variation of surface heat flux at
different salt concentrations, experiments were conducted
at a water flow rate of 13.33 9 10-5 m3/s and air flow rate
of 40 N m3/h. The variation of estimated surface heat flux
Fig. 17 Temperature-time history for MgSO4 added air atomized
spray cooling
Fig. 18 Estimated surface heat flux and surface temperature with
time for MgSO4
Fig. 19 Boiling curve for air atomized spray with salt (MgSO4)
Fig. 20 Varition of surface heat flux with time for different
concentrations of salt (MgSO4)
Heat Mass Transfer
123
with time is shown in Fig. 20. Here, it was noticed that
initially surface heat flux increases with an increase in time
due to the early initiation of transition boiling, and there-
after decreases with time because of cooling in the nucleate
boiling regime.
In the nucleate boiling regimes, the surface heat flux is
enhanced due to the decrease in surface tension of the
resulting salt added water, production of foaming during
cooling, and the prevention of vapor bubble coalescence
inside the evaporating droplets. In Sect. 2.3, it was dis-
cussed that the surface tension of water decreases with an
increase in salt concentration up to 0.05 mol/l. As a result,
droplet contact angle with the solid surface decreases with
an increase in salt concentration. Due to the said phe-
nomenon, high contact area is produced during droplet
evaporation, and thereby droplets evaporate at a faster rate
from the hot plate.
The dissolved salt in water prevents vapor bubble
coalescence inside the evaporating droplets, and this
process minimizes the film boiling affect. Foaming is also
observed during air-atomized spray cooling with salt, and
this could be another reason for the surface heat flux
enhancement. Due to the foaming, the heat transfer rate
enhances. The above mentioned effect on heat transfer
becomes stronger with an increase in salt concentration up
to 0.05 mol/l. However, above a salt concentration of
0.05 mol/l, all the said positive effects enhance the sur-
face heat flux, except the effect produced due to a
decrease in surface tension. This is because above
0.05 mol/l of salt concentration, the surface tension of the
resulting solution starts increasing with an increase in salt
concentration.
In the transition boiling regimes, the surface heat flux
enhances because of the dominating effects of salt depo-
sition on the hot plate, and the prevention of vapor bubble
coalescence inside the evaporating droplet. In the previous
section, it was discussed that deposition of salt on the hot
plate increases the surface heat flux by minimizing the
negative effect produced due to the unstable vapour film
during cooling.
Beyond salt concentration of 0.05 mol/l, the surface
tension increases with an increase in salt concentration, and
as a result droplet contact angle increases. But, the effect is
not significant, and therefore an increasing trend of surface
heat flux with the salt concentration has been noticed in the
transition boiling regime.
In case of MgSO4 added air atomized spray cooling, the
effect due to salt deposition was the controlling factor.
Moreover, the chances of salt deposition increase with an
increase in salt concentration. As a result, the surface heat
flux shows an increasing trend with an increase in salt
concentration.
3.2.3 Effect of water flow rate and salt concentration
on both average surface heat flux and cooling rate
The average surface heat flux and surface temperature for
900–600 �C drop are shown in Figs. 21 and 22 respectively.
Figure 21 depicts that the average surface heat flux increases
with an increase in salt concentration at a constant water flow
rate. The maximum variation in surface heat flux is observed
when the concentration changes from 0 to 0.1 mol/l. The
average surface heat flux increases with an increase in water
flow rate due to the increase in water impingement density.
By using Design Expert Software version 6.0, a correlation
describing surface heat flux as a function of salt concentration
and water flow rates has been shown in Eq. 4. The determi-
nation coefficient (R2) for the aforesaid correlation is 0.98.
qS ¼ 2:03þ 0:21� Fw þ 0:54� SC þ 0:04� F2a � 0:36
� S2c � 0:075� Fa � Sc ð4Þ
Fig. 21 Variations of average surface heat flux with salt (MgSO4)
concentration
Fig. 22 Variation of cooling rate with salt (MgSO4) concentration
Heat Mass Transfer
123
Similarly, the average surface cooling rates at different
water flow rates and salt concentrations are given in
Fig. 22. The maximum cooling rate of 242 �C/s has been
achieved at a water flow rate of 16.67 9 10-5 m3/s and salt
concentration of 0.4 mol/l, and moreover this achieved
cooling rate was found to be in the UFC regime of a 6 mm
thick AISI-304 steel plate. The developed correlation by
using Design Expert Software version 6.0 (R2 = 0.99) is
shown in Eq. 5.
Z ¼ 198þ 20:83� Fa þ 40:83� S c þ 10:64� F2a
� 21:38� S2c � 4:75� Fa � Sc ð5Þ
3.2.4 Effect of salt (MgSO4) concentration on critical
surface heat flux (CHF) and critical surface
temperature (TCHF)
High value of critical surface heat flux and corresponding
temperature have been of great practical interest in many
applications related to metal quenching especially in
cooling operations such as UFC of a hot steel plate.
Therefore, the effect of salt concentration on critical sur-
face heat flux and critical surface temperature was studied
in great detail and is as shown in Fig. 23. The CHF
increases with an increase in salt concentration. The same
trend was observed by Cui et al. [13] for salt added con-
ventional spray cooling. The maximum CHF has been
observed at a salt concentration of 0.4 mol/l, and the
obtained value is almost twice that obtained for air-atom-
ized spray cooling with pure water. This could be due to
the salt deposition, which increase the surface roughness
value and thereby CHF. In addition to the above, it is also
found that the critical surface temperature changes from
550 to 610 �C with an increase in salt concentration from 0
to 0.4 mol/l. This is due to the fact that at higher salt
concentrations, the Leidenfrost temperature transits to a
higher value according to Huang and Carey [22], and as a
result the critical surface temperature also increases to a
higher value with an increase in salt concentration.
3.3 Comparative study (NaCl and MgSO4)
3.3.1 Transient surface heat flux
To compare the effect of two different types of salts during
air atomized spray cooling illustrated earlier, experiments
were conducted at water flow rate of 16.67 9 10-5 m3/s,
air flow rate of 40 N m3/h and with pure water and salt
added water (Sc = 0.1 mol/l for both NaCl and MgSO4).
The variation of surface heat flux with time for different
type of salt is shown in Fig. 24.
The initial surface heat flux (at t = 0) achieved for air-
atomized spray with pure water and both types of saline
water are 0.6, 0.7 and 2.3 MW/m2 respectively. This dif-
ference between salt added air-atomized spray and pure
water is mainly due to the occurrence of cooling in dif-
ferent boiling regimes at high initial surface temperatures.
But, the difference between two types of salt added air-
atomized spray is mainly due to the occurrence of foaming
in case of MgSO4 added air atomized spray.
Another reason could be the insufficient amount of salt
deposition at the beginning of cooling. However, it is
expected that the deposition becomes significant with an
increase in time, and subsequently prove to be an important
factor in the cooling enhancement. The literature reveals
that the chances of film rupture increase with an increase in
the possibility of salt deposition and moreover, the depo-
sition intensity depends on the rate of diffusion of a dis-
solved salt in water. When the droplet evaporates from the
hot surface, the salt concentration increases in the
remaining liquid. This causes a local increment of ionic
strength at the droplet and hot surface interface, promoting
Fig. 23 The variation of CHF and TCHF with salt (MgSO4)
concentration
Fig. 24 Comparative study among the transient effect of different
types of salts
Heat Mass Transfer
123
deposition of salt on the hot surface. The lower the rate of
diffusion of salt from the region of high concentration to
the bulk liquid, the higher is the formation and stability of
the salt deposition.
According to the Cui et al. [12], the mass diffusion
coefficient of MgSO4 is much lower in water than that of
NaCl and therefore, a higher amount of salt is likely to
deposit in case of MgSO4 added atomized spray cooling.
As a result, the surface heat flux obtained for MgSO4 added
water atomized spray in transition boiling regime is higher
than that with NaCl. In addition to the above, significant
difference in critical surface heat flux has also been
observed. Among the three cooling process, the maximum
CHF has been found in case of air-atomized spray with the
salt (MgSO4), whereas air-atomized spray with pure water
produces minimum critical surface heat flux. Furthermore,
the critical surface heat flux in case of air-atomized spray
with salt (MgSO4) was observed much earlier than the
Fig. 25 Comparison of the average surface heat flux of two different
types of saltFig. 26 Comparison of the average cooling rate of two different
types of salt
Fig. 27 Photographs during air
atomized spray cooling at
different conditions
Heat Mass Transfer
123
other two types of air- atomized spray (with pure water and
with NaCl added water). Therefore, salt (MgSO4) added air
atomized spray cooling was found to be one of the efficient
cooling methods for fast quenching operation.
3.3.2 Average surface heat flux
Figure 25 shows the achieved average heat flux at a water
flow rate of 16. 67 9 10-5 m3/s for both NaCl and MgSO4
added air-atomized spray. In case of MgSO4 added air-
atomized spray, the average surface heat flux increases
with an increase in salt concentration, and shows the
maximum value of 2.4 MW/m2 at a salt concentration of
0.4 mol/l. But, in case of NaCl added air-atomized spray,
the maximum average surface heat flux (2 MW/m2) has
been observed at a salt concentration of 0.1 mol/l, and
thereafter it shows a decreasing trend with an increase in
salt concentration. The maximum observed average surface
heat flux in case of MgSO4 added air-atomized spray is
20 % higher than that with NaCl added water. Similarly,
the maximum average cooling rate in case of MgSO4 added
air atomized spray cooling is 35 % higher than that
obtained in case of NaCl (Fig. 26).
3.3.3 Visual comparison
Figure 27 shows the photographs taken after the different
types of air atomized spray (air atomized spray with the salt
and without salt) impinge the hot surface. The first pho-
tograph was taken after 0.5 s from the time of impinge-
ment, and the subsequent photographs were taken at a time
interval of 1 s. It was observed that in case of air atomized
spray with the MgSO4 and NaCl, at t = 0.5 s, a black dark
circle appears around the spray centre, and this indicates a
significantly colder region which is also an evidence of fast
cooling. However, in case of pure water, the dark circle
appears after 1.5 s from the starting of the spray. The
successive photographs also show that in case of MgSO4,
the dark circle moves at a faster rate than the other two
cases.
4 Conclusion
The experimental studies of UFC of a 6 mm thick hot static
AISI-304 steel plate by salt added air atomized spray has
been successfully conducted. The results depict that salt
added air atomized spray enhances the surface heat flux in
nucleate boiling regime, because of the suppression of the
vapor bubble coalescence inside an evaporating droplet and
also due to the occurrence of foaming. Moreover, the
surface heat flux in transition boiling regime is also
enhanced, and this could be due to the deposition of salt on
the hot surface during cooling. Therefore, the obtained
cooling rate (242 �C/s) in case of MgSO4 added air
atomized spray cooling and (178 �C/s) for the case of NaCl
were found to be in the UFC regime of a 6 mm thick AISI-
304 steel plate.
In case of NaCl added air atomized spray cooling, the
transient surface heat flux as well as the average surface
heat flux increases with an increase in salt concentration up
to 0.1 mol/l, and thereafter it shows a decreasing trend.
Therefore, the maximum average cooling rate of (178 �C/s)
has been observed at a salt concentration of 0.1 mol/l.
However, in case of MgSO4 added air atomized spray
cooling, the transient and average surface heat flux
increases with an increase in salt concentration and the
maximum cooling rate of 242 �C/s was observed at a salt
concentration of 0.4 mol/l.
In case of NaCl added air atomized spray, the critical
surface heat flux increases from 1.4 to 2.58 MW/m2 with
an increase in salt concentration from 0 to 0.1 mol/l, but in
case of MgSO4, the critical surface heat flux shows an
increasing trend with an increase in salt concentration up to
0.4 mol/l.
References
1. Lucas A, Simon P, Bourdon G, Herman JC, Riche P, Neutjens J,
Harlet P (2004) Metallurgical aspect of ultra fast cooling in front
of down-coiler. Steel Res Int 75:139–146
2. Bin H, Hua LX, Guo-dong W, Guang-fu S (2005) Development
of cooling process technique in hot strip mill. J Iron Steel Res Int
12:12–16
3. Oliveria MSA, Sousa ACM (2001) Neural network analysis of
experimental data for air/water spray cooling. J Mater Process
Technol 113:439–445
4. Mohapatra SS, Chakraborty S, Pal SK (2012) Experimental
studies on different cooling process to achieve ultra fast cooling
rate for hot steel plate. Exp Heat Transf 25:111–126. doi:10.1080/
08916152.2011.582567
5. Puschmann F, Specht E (2004) Transient measurement of heat
transfer in metal quenching with atomized sprays. Exp Thermal
Fluid Sci 28:607–615. doi:10.1016/j.expthermflusci.2003.09.004
6. Al-Ahmadi HM, Yao SC (2008) Spray cooling of high temper-
ature metals using high mass flux industrial nozzle. Exp Heat
Transf 21:38–54. doi:10.1080/08916150701647827
7. Bhattacharya P, Samanta AN, Chakraborty S (2009) Spray
evaporative cooling to achieve ultra fast cooling in run out table.
Int J Therm Sci 48:1741–1747. doi:10.1016/j.ijthermalsci.2009.
01.015
8. Qio YM, Chandra SM (1997) Experiments on adding a surfactant
to water drops boiling on a hot surface. Math Phys Eng Sci
453:673–689
9. Qio YM, Chandra SM (1998) Enhancement of spray cooling by
addition of surfactant water spray on a hot surface. J Heat Transf
304:63–71. doi:10.1115/1.2830070
10. Cui Q, Chandra S, McCahan S (2001) The effect of dissolving
gases or solids in water droplets boiling on a hot surface. J Heat
Transf 123:719–728. doi:10.1115/1.1376394
Heat Mass Transfer
123
11. King MD, Yang JC, Chien WS, Grosshandler WL (1997)
Evaporation of a small water droplet containing an additive. In:
Proceedings of the 32nd national heat transfer conference, vol 4,
pp 45–57
12. Cui Q, Chandra S, McCahan S (2003) The effect of dissolving
salts in water spray used for quenching a hot surface: part-1
boiling of single droplets. J Heat Transf 125:326–332. doi:10.
1115/1.1532010
13. Cui Q, Chandra S, McCahan S (2003) The effect of dissolving
salts in water spray used for quenching a hot surface: part-2 spray
cooling. J Heat Transf 125:333–338. doi:10.1115/1.1532011
14. Li D, Wells MA (2004) Effect of surface thermocouple instal-
lation on the discrepancy of the measured thermal history and
predicted surface heat flux during a quench operation. Metall
Mater Trans B 36:343–354
15. Trujillo DM, Busby HR (2003) INTEMP—inverse heat transfer
analysis—user’s manual. TRUCOMP CO. FOUNTAIN VAL-
LEY, Canada, pp 1–47
16. Busby HR, Trujillo DM (1985) Numerical solution to a two-
dimensional inverse heat conduction problem. Int J Numer Meth
Eng 21:349–359
17. Alam U, Krol J, Specht E, Schmidt J (2008) Enhancement and
local regulation of metal quenching using atomized sprays.
J ASTM Int 5:1–10. doi:10.1520/JAI101805
18. Ravikumar SV, Jha JM, Sarkar I, Mohapatra SS, Pal SK, Cha-
kraborty S (2013) Achievement of ultrafast cooling rate in a hot
steel plate by air-atomized spray with different surfactant addi-
tives. Exp Thermal Fluid Sci 50:79–89
19. Ravikumar SV, Jha JM, Mohapatra SS, Sinha A, Pal SK, Cha-
kraborty S (2013) Experimental study of the effect of spray
inclination on ultrafast cooling of a hot steel plate. Heat Mass
Transf 49:1509–1522
20. Ravikumar SV, Jha JM, Mohapatra SS, Pal SK, Chakraborty S
(2013) Influence of ultrafast cooling on microstructure and
mechanical properties of steel. Steel Res Int. doi:10.1002/srin.
201200346
21. Lamb H (1993) Hydrodynamics. Cambridge University Press,
United Kingdom
22. Huang C, Carey V (2007) The effect of dissolved salt on the
leidenfrost transition. Int J Heat Mass Transf 50:269–282. doi:10.
1016/j.ijheatmasstransfer.2006.06.031
Heat Mass Transfer
123