Modeling of heat and mass transfer processes in phase transformation cycle of sprayed water into gas: 3. Energy and thermal states analysis of slipping droplet in a humid air flow.
Miliauskas, G. ; Maziukiene, M. ; Ramanauskas, V. 等
Nomenclature [B.sub.T]--Spalding transfer number; D--mass
diffusivity, [m.sup.2]/s;
[F.sub.o]--Fourier number; g--evaporation velocity, kg/s;
[k.sup.-.sub.c]--effective thermal conductivity parameter;
L--latent heat of evaporation, J/kg; m--vapour mass flux,
kg/([m.sup.2]s);
Nu--Nusselt number; p--pressure, Pa; P--symbol of free parameter in
heat-mass transfer; [bar.P]--dimensionless parameter in heat-mass
transfer; [??]--average parameter in heat-mass transfer; Pe--Peclet
number; Pr--Prandtl number; q--heat flux, W/[m.sup.2]; r--radial
coordinate, m; Re Reynolds number; S--area, [m.sup.2]; T--temperature,
K; [eta]--non-dimensional radial coordinate; [lambda]--thermal
conductivity, W/(m K); [mu]- molecular mass, kg/kmol; [rho]- density,
kg/[m.sup.3]; [tau]- time, s;
subscripts
c--convection; "c"--convective heating; "c +
r"--convective-radiative heating; C--droplet centre;
co--condensation; e--equilibrium evaporation; f--phase change; g--gas;
i--time index in a digital scheme; it--number of iteration; IT--index of
closing iteration; I--index of control time; j--index of radial
coordinate; J--index of droplet surface; k--conduction; "
k"--conductive heating; l--liquid; m--mass average; r--radiation;
rt--dew point; R--droplet surface; v--vapor; vg--vapor-gas mixture;
0--initial state; [SIGMA]--total; [infinity]--far from a droplet;
superscripts
+--external side of a droplet surface; ---internal side of a
droplet surface.
[B.sub.T]--Spalding transfer number; D--mass diffusivity,
[m.sup.2]/s;
[F.sub.o]--Fourier number; g--evaporation velocity, kg/s;
[k.sup.-.sub.c]--effective thermal conductivity parameter;
L--latent heat of evaporation, J/kg; m--vapour mass flux,
kg/([m.sup.2]s);
Nu--Nusselt number; p--pressure, Pa; P--symbol of free parameter in
heat-mass transfer; [bar.P]--dimensionless parameter in heat-mass
transfer; [??]--average parameter in heat-mass transfer; Pe--Peclet
number; Pr--Prandtl number; q--heat flux, W/[m.sup.2]; r--radial
coordinate, m; Re Reynolds number; S--area, [m.sup.2]; T--temperature,
K; [eta]--non-dimensional radial coordinate; [lambda]--thermal
conductivity, W/(m K); [mu]- molecular mass, kg/kmol; [rho]- density,
kg/[m.sup.3]; [tau]- time, s;
subscripts
c--convection; " c"--convective heating; "c +
r"--convective-radiative heating; C--droplet centre;
co--condensation; e--equilibrium evaporation; f--phase change; g--gas;
i--time index in a digital scheme; it--number of iteration; IT--index of
closing iteration; I--index of control time; j--index of radial
coordinate; J--index of droplet surface; k--conduction; "
k"--conductive heating; l--liquid; m--mass average; r--radiation;
rt--dew point; R--droplet surface; v--vapor; vg--vapor-gas mixture;
0--initial state; [SIGMA]--total; [infinity]--far from a droplet;
superscripts
+--external side of a droplet surface;- --internal side of a
droplet surface.
1. Introduction
Many thermal technologies are based on by droplets heat transfer
and phase transformations. Therefore, researchers' attention for
water heat transfer processes and for heat exchange and phase
transformations of hydrocarbon and other liquids dispersed into droplets
do not decrease [1-6]. A liquid droplets phase transformation cycle
combines condensing, unsteady and equilibrium evaporation modes [tau]
[equivalent to] 0 / [[tau].sub.co] / [[tau].sub.nf] / [[tau].sub.f] An
intensive interaction of heat and mass transfer processes sets when a
heat supplying conditions for droplets are rapidly changing. Droplet
environment provides thermal energy by processes of heat exchange and
liquid vapour condensation on the surface of the droplet. In
condensation mode a supplying heat warmth the liquid in a droplet. At
unsteady evaporation mode heat is being provided by heat transfer, where
a part of heat vaporizes a liquid. At equilibrium evaporation mode all
heat that is provided for the droplet participates in liquid
evaporation. Peculiarities of interaction between phases determine the
droplet thermal state, which has a reversible impact for a droplet
energy state variation in phase transformation cycle.
Droplets phase transformation cycle is determined by sprayed liquid
and carrier gas flow parameters. Liquid spray dispersity, a two-phase
flow velocity and a temperature can be considered the essential
parameters of sprayed liquid. Parameter of liquid vapour condensation in
gas mixture is very important for heat and mass transfer intensity. A
phase transformation cycle starts with condensing phase transformation
mode, when sprayed pure liquid temperature is lower than a dew point
temperature [[bar.T].sub.0] = [T.sub.rt]/[T.sub.0] > 1. In condensing
phase mode a droplet is heated up and therefore grows rapidly. In
condensing mode droplet heats up to dew point temperature and in
unsteady evaporation mode droplets dispersity is defined. A droplet
slipping in gas flow has a bright effect for condensing phase
transformation mode that causes a longer term of liquid vapour
condensation on a droplet surface by enhanced convective heating
conditions [5]. A longer duration of condensing phase transformation
means extended droplet surface heating to dew point temperature. A bit
more liquid vapour condenses on the droplet surface therefore a droplet
is larger at the end of condensing mode. Peculiarity of slipping droplet
in condensing phase transformation mode can be based by intensive inner
layers warming, compared with the case of a stable liquid, which is
caused by fluid circulation. This requires assessment of droplet energy
state in phase transformation cycle. It necessitate analysis of heat and
mass flows on the droplet surface by conditions of a complex transfer
processes. A problem of temperature gradient in a droplet rises when
defining the intensity of the processes. This gradient is highly
dependent from a droplet definition methodology. When a liquid is stable
in a droplet, then temperature gradient in a droplet can be defined by
integral type model that is convenient for numerical research [7].
Integral type model combines heat spread in droplet by conduction and
radiation.
However, liquid can circulate in a droplet. These presumptions are
made by non-isothermal in a droplet and by friction forces that arises
on the droplet surface [1, 8, 9]. Archimedes forces rises in
non-isothermal droplet. Their effect for liquid stability depends from
droplet dispersity. In common occurring technologies such as liquid fuel
burning, fireplaces or air conditioning systems droplets are quite
small. Rising Archimedes forces in droplets are week and do not cause a
fluid circulation [7]. A forced fluid circulation is arising in a
slipping droplet. This circulation is described by Navier-Stokes
equation system. It is impossible to solve this system analytically. Its
numerical solution was analyzed in work [10]. This solution is receptive
for machine counting and is difficult to apply for iterative scheme.
This article presents an energy state balance assessment
methodology of sliding droplet in gas. In humid air slipping water
droplet case is analyzed as well as energy and thermal states need for
complex analysis is justified.
2. Research method
Energy state change is defined by connection of droplet internal
and external heat transfer and by phase transformation processes that is
ongoing on its surface. In case of condition [T.sub.g] > [T.sub.i] a
droplet external heat transfer ensures continuous heat supply for a
droplet in all phase transformation cycle. Heating intensity is
described by density function of total heat flow on a droplet surface
external side:
[q.sup.+.sub.[SIGMA],"c+r"]([tau]) =
[q.sup.+.sub.r]([tau]) + [q.sup.+.sub.c]([tau]) (1)
In non-radiant environment for warming droplet case [q.sub.r] = 0,
so [q.sup.+.sub.[SIGMA]] [equivalent to] [q.sup.+.sub.c]. In droplet
phase transformation cycle a convective heating heat flow is described
by expression:
[MATHEMATICAL EXPRESSION NOT REPRODUCIBLE IN ASCII] (2)
where phase transformation impact for convective heating is taken
into account by the Spalding transfer parameter [B.sub.T] [5]. A droplet
slip velocity [DELTA][w.sub.l] = [w.sub.l] - [w.sub.g] defines a
convection heating intensity, that determines Reynolds number Re = 2R
[absolute value of [DELTA]w] [[rho].sub.g] /[[mu].sub.vg], where a gas
density is chosen according to temperature [T.sub.d], and liquid vapor
and gas mixture dynamic viscosity coefficient is selected by temperature
according to "1/3" rule: [T.sub.vg] [equivalent to] [T.sub.R]
+ ([T.sub.g] - [T.sub.R])/ 3.
A combination of empirical model [11] for effective thermal
conductivity and integral model of heat spread in droplet by
conductivity-radiation [7] are adapted to define the heat exchange in a
droplet. A heat flow that is leaded to the droplet is described by
modified Fourier law of heat spread:
[q.sup.-.sub.c] ([tau]) = -[k.sup.-.sub.c] ([tau])
[[lambda].sub.1]([tau]) [partial derivative][T.sub.1](3)
A forced liquid circulation influence for heat spread in a droplet
is evaluated by effective thermal conductivity parameter, which is
defined by methodology [11] as function [k.sup.-.sub.c] = f ([Pe.sub.l])
of Peclet number. The temperature gradient in equation (3) is defined by
methodology [7].
Heat flow which participates in phase transformations is calculated
by water vapor flow density on the surface of a droplet:
[q.sup.-.sub.f]([tau]) = [m.sup._.sub.v]([tau])L([tau]) (4)
On a droplet surface, expressions (2)-(4) is applied to concretize
an energy balance condition [MATHEMATICAL EXPRESSION NOT REPRODUCIBLE IN
ASCII] for all modeled droplet heating cases. A balance condition
requires matching of heat flows that flows in and flows from the surface
of the droplet. In outspread form a balance condition becomes a
transcendental system of algebraic and integral equations, because its
solutions are unambiguous only then, when the droplet surface
temperature function of time [T.sub.R]([tau]) is defined. This function
is defined by iterative technique according to method [5]. However, the
temperature distribution inside the droplet T(r < R, [tau]), can only
be defined by case assumptions of non-circulating fluid. At numerical
experiment attention is taken into account to phase transformation in
technologies of heat recovery from humid combustion products. Water
injection takes an important place for gas mixture cleaning and for
additional irrigation [7]. Peculiarities of convective heating was
highlight by modeling a water droplets of 278 K temperature at unsteady
phase transformation mode in 500 K temperature humid gas flow
([[bar.p].sub.v,[infinity]] = 0.3, when p = 0.1 MPa). Droplets primary
slipping is defined by Reynolds number values 0, 5, 10, 20, 40, and 80
for 2[R.sub.0] = 150 x [10.sup.-6] m droplet diameter, when a gas flow
velocity is [w.sub.g] [equivalent to] 10 m/s. These [Re.sub.0] number
values were ensured by primaries velocities [w.sub.l,0] m/s: 10, 11.12,
12.25, 14.49, 18.98 and 27.97, respectively. Fourier number application
in time scale was carried out in numerical experiment. The main
attention is laid on for unsteady phase transformation mode 0 /
[Fo.sub.nf]. In numeric control scheme for condensing mode 21 control
time moments are provided for time grid formation. Condensing mode
duration [FO.sub.co] is defined [F.sub.O] [equivalent to] 0 /
[FO.sub.co] (Fig. 1).
[FIGURE 1 OMITTED]
Unchanging individual time step [DELTA][Fo.sub.i] = [Fo.sub.co]
/([I.sub.co] - 1), when [I.sub.co] = 21 was kept in each modeled cycle.
A droplet surface temperature function [T.sub.R]([F.sub.o]) is defined
according to (10) - (18) schemes in work [5]. Other parameters functions
P(Fo) of heat and mass transfer are defined in parallel. At numerical
experiment process a condition matching of heat flows that flows in and
flows from a droplet surface is satisfied (Fig. 2.) by a strict
requirement:
[absolute value of 1 - [q.sup.-.sub.c](Fo) + [q.sup.+.sub.f](Fo)/
[q.sup.+.sub.c] (Fo)] x 100% < [[delta].sub.R] [equivalent to] 0.01%
(5)
[FIGURE 2 OMITTED]
In phase transformation cycle a gas surrounding gives the heat for
a droplet by heat transfer (together with condensing heat or without a
heat that is necessary for evaporation process):
[Q.sup.+.sub.J,co] + [Q.sup.+.sub.J,ng] + [Q.sup.+.sub.J,eg] =
[Q.sup.+.sub.J] (6)
According to expression (6) described heat quantity can be defined
according to heat flow density average values [[??].sup.-.sub.c,i] in a
droplet that is distinguish at time intervals
[MATHEMATICAL EXPRESSION NOT REPRODUCIBLE IN ASCII] (7)
Because of physical nature change in phase transformation modes at
heat flow in a droplet [7], peculiarities of phase transformation cycle
modes should be taken into account when defining [[??].sup.-.sub.c,i].
At condensing phase transformation mode a gas surrounding gives thermal
energy in heat transfer process together with vapour phase
transformation heat that condensates on the surface of a droplet. At
unsteady evaporation mode a convective heat warmth and evaporates a
droplet. In equilibrium evaporation mode a convectional heat can only
evaporates the droplet and enthalpy of cooling down droplet can
participate in evaporation:
[MATHEMATICAL EXPRESSION NOT REPRODUCIBLE IN ASCII] (9)
[FIGURE 3 OMITTED]
[FIGURE 4 OMITTED]
A droplet slipping in gas flow is decreasing because of the impact
of resistance forces. The fastest droplet velocity change is in
condensing phase transformation mode, while in evaporation mode a
droplet slipping becomes negligible in term [approximately equal to] 5 x
[[bar.F]o.sub.oco] (Fig. 3). Then a case of heating by conductivity
approach in practice. Therefore at a droplet energy state analysis the
main attention is given for condensing and unsteady evaporation modes.
3. Energy evaluation of unsteady phase transformation mode
A droplet energy state graphical interpretation, in freely chosen
time Azi intervals at condensing and unsteady evaporation modes is
reflected in Fig 4. In condensation phase transformation mode a droplet
diameter increases from 2[R.sub.0] to 2[R.sub.co], therefore [R.sub.i]
> [R.sub.i-1]. At evaporation mode a droplet diameter decreases from
2[R.sub.co] to zero, therefore [R.sub.i] < [R.sub.i-1].
[FIGURE 5 OMITTED]
[FIGURE 6 OMITTED]
[FIGURE 7 OMITTED]
[FIGURE 8 OMITTED]
At condensation phase transformation mode droplet convective
heating intensity exceeds analogous solid particle heating case, when
phase transformation does not expose on its surface. In unsteady
evaporation mode a droplet heating intensity is weaker than solid
particle, while in regime change moment, matches it black points (Fig.
5. Droplet slipping in gas flow has a bright impact for convective heat
flow that warmth a droplet (Fig. 6), and also has an impact for phase
transformation heat flow (Fig. 7). In unsteady phase transformation mode
at a droplet liquid is heated up intensively (8 Fig. a), its surface
temperature increases, and temperature difference [DELTA]T = [T.sub.g] -
[T.sub.R] that reflects external heat exchange driving force, decreases
(Fig. 9). Therefore convective heating intensity suffocates in unsteady
condensing and evaporation phase transformation modes (Fig. 6).
[FIGURE 9 OMITTED]
In condensation mode a growing heat exchange area has a bright
impact for convective heat flow density that is provided for a droplet
(Fig. 10.). A warming liquid expansion and liquid vapour condensation on
the surface causes a droplet surface area growth in condensation mode.
Surface water evaporation compensates liquid expansion in unsteady
evaporation mode. At balance moment of these factors extreme point forms
in droplet surface variation curve therefore a droplet surface area
start to decrease.
[FIGURE 10 OMITTED]
[FIGURE 11 OMITTED]
At equilibrium evaporation mode a droplet surface decreases
linearly and satisfies a well known law [D.sup.2] [12]. For a more
extensive evaluation of droplet phase transformation peculiarities needs
to make a broader numerical research. Gas humidity and temperature, as
well temperature of sprayed water and heat transfer of a droplet would
be angular aspects. This is one of the future research topics. In
unsteady phase transformation mode a heat that is provided for a droplet
by convection from a gas surrounding is reflected in Fig. 11, while heat
change that participates in phase transformation process is presented in
Fig. 12.
[FIGURE 12 OMITTED]
Heat is being provided for a droplet by convection in whole phase
transformation cycle, therefore a provided heat amount is consistently
growing. In phase transformation balance assessment the evolved heat
considered to be positive in condensation process, while a heat that is
required for water evaporation considered to be negative. Therefore at
the end of condensation mode in curve [Q.sup.+.sub.J,f] (Fo) of phase
transformation heat dynamics an extreme point observes. Liquid
evaporation starts from this point. Evaporation process continues due to
a part of heat that is provided by convection. In condensation process,
a released heat of phase transformation gets a bright effect from
droplet slipping in gas: [Q.sup.+.sub.J,f] ([Re.sub.0], Fo [equivalent
to] [Fo.sub.co]) x [10.sup.4], J is 3.195, 3.433, 4.159, 5.033, 5.649,
5.893, when Re is 0, 5, 10, 20, 40 and 80, respectively. The same heat
amount is used at initial state of unsteady evaporation, that is defined
by time moment [Q.sup.+.sub.J,f]([Re.sub.0], Fo) [equivalent to] 0 (Fig.
12 points x).
Therefore in condensation phase transformation mode a heat amount
that is provided for a droplet is [Q.sup.+.sub.J,f] ([Re.sub.0] >
[Fo.sub.co])j [Q.sup.+.sub.J,f] ([Re.sub.0] > [Fo.sub.co]). It is
leaded to droplet by internal heat convection [Q.sup.-.sub.J,f]
([Re.sub.0], [Fo.sub.co]) x [10.sup.4], J: 4.985, 6.063, 7.546, 9.403,
10.933, and 11.962 when Re is 0, 5, 10, 20, 40 and 80, respectively. In
a droplet water is heated from [T.sub.l,0] = 278 to [T.sub.l,m] (Fo
[equivalent to] [Fo.sub.co]). Heat amount that is leaded to a droplet by
internal heat convection (Fig. 13) is defined by condition
[Q.sup.-.sub.J,f] (Fo) [equivalent to] [Q.sup.-.sub.J,f](fo [equivalent
to] [Fo.sub.nf]), which enables to define unsteady phase transformation
duration [Fo.sub.nf]([Re.sub.0]) from scientific assessment: 2.68,
1.739, 1.849, 1.999, 2.128, 2.186, when Re is 0, 5, 10, 20, 40 and 80,
respectively (Fig. 13, b). In equilibrium evaporation mode a liquid in a
droplet is not heated anymore. For droplet that is heated up by
conductively this is reflected by condition [[bar.Q].sup.-.sub.J,f] (Fo
>[Fo.sub.nf])= 1.
Internal heat convection in slipping droplet can still going on,
but convection leads out heat from cooling down droplet to its surface
and stimulates an evaporation process. This is reflected by the
condition [[bar.Q].sup.-.sub.J,f] (Fo > [Fo.sub.nf])< 1.
For integrated droplet energy and thermal state change analysis it
is required to define a droplet warming dynamics in all phase
transformation cycle. A thermal state analysis of circulating water in a
droplet is quite complicated and would extend this work. It would be one
of the future research topics.
[FIGURE 13 OMITTED]
4. Conclusions
Water droplets slipping have a maximum impact for droplets heat
transfer in humid gas at condensation phase transformation mode. A set
analysis of energy state balance for different speeds moving droplets
shows, that essential role falls far liquid circulation that is caused
by friction forces that arises on the surface of the slipping droplet.
For this reason, heat is leaded out to central layers of the droplet
more intensively. Therefore droplet heats up gradually; a temperature
gradient in surface layers is lower than at conductivity heating case
and droplet surface heats up till a dew point longer. On the surface of
a droplet slipping in humid gas liquid vapor condenses more intensively
therefore a droplet diameter grows in condensation mode.
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Received April 29, 2015
Accepted June 23, 2015
G. Miliauskas *, M. Maziukiene *, V. Ramanauskas **
* Kaunas university of technology, K.Donelaicio 20, Kaunas,
LT-44239, Lithuania, E-mail: gimil@ktu.lt
** UAB "Enerstena", Raktazoliq 21, Kaunas, LT-52181,
Lithuania, E-mail: vramanauskas@enerstena.lt
http://dx.doi.org/10.5755/j01.mech.21.5.12167