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Abu Zaid1996
Abu Zaid1996
TECHNOLOGY
ELSEVIER Powder Technology 89 ( 1996 ) 45 56
A rate dependent model for turbulent flows of dilute and dense two phase
solid-liquid mixtures
Sameer Abu-Zaid, Goodarz Ahmadi
Department of Mechanical and Aeronautic~d Engineering. Clarkson University, Potsdam, NY 13699-5725. USA
Abstract
The thermodynamically consistent rate dependent model for turbulent flow of dense two phase solid-liquid mixtures derived previously is
extended to cover the entire range of solids volume fraction. The modifications needed for the phasic viscosity, as well as the particulate
energy dissipation rate, are included. It is shown that the model contains the existing kinetic models for rapid granular flows and dilute
turbulent two phase flows as special limiting cases, The model is then used to study the problem of simple shear flow of a two phase solid-
liquid mixture. The phasic shear and normal stresses, normal stress differences, fluctuation kinetic energy, production, dissipation and
interaction energy supply are evaluated and discussed. The predicted stresses are compared with experimental data and good agreement is
observed.
Keywords." Turbulent flow: Two phase mixture: Solid liquid phase: Energy dissipation rate; Granular flow
Conservation of mass where d~ is the deviatoric part of the deformation rate tensor,
O / D t stands for the Jaumann derivative, /,f a n d / z ~' are the
at + ~ x ( u"z,<')
; =0 (l) coefficients of mean viscosity, pff and/.t '*Tare the coefficients
of turbulence (eddy) v i s c o s i t y , f T a n d p ~x are the fluctuation
Ou t O pressures. T f and T" are fluctuation time scales and a,/3 and
,,';:', > : 0 (2> ~"are some material parameters.
The constitutive equations for the interaction momentum
Balance o f linear momentum supply terms are given by
collisional contribution. The kinetic contribution which was the particle diameter. The non-collisional dissipation rate
derived for granular particles in a vacuum is expected to be becomes quite small as the solid volume fraction approaches
negligible due to the presence of the liquid phase. Coefficient the maximum packing limit. Furthermore, for very small par-
C"* is also introduced here to account for the reduction of ticles, the collisional contributions to the particulate energy
collisional effects as particle relaxation time becomes small. dissipation rate becomes negligible and e '~ is dominated by
A similar dependence of effective viscosity on particle relax- the non-collisional energy dissipation.
ation time was suggested earlier by Chen and Wood [ 7 ]. Stress constitutive equations given by Eqs. (9) and ( 11 )
The crowding effect of particles exhibits itself through the involve the fluctuation time scales of particulate and fluid
radial distribution function X. For spherical particles, Ma and phases. These are given by
Ahmadi [ 17] suggested
k+' 1 kf
T....... Tr=-= l (23)
1 + 2.5 u'~ + 4.59( u"): +4.52( ~'(')" e<, a,,(k~)l/2 ' @ at(U) '':
X= [ 1 - ( /,"+~/ e r a ) 3 1 0 6 7 N (16)
where the expressions for the dissipation rates as given by
which is in agreement with the exact virial expansion up to Eq. (20) are used. For spherical particles+ the values of par-
the ( ~,,~)3 term. ameters ad', ]3 ~ and ~'<+as suggested by Abu-Zaid and Ahmadi
The drag coefficient for spherical particles is given by [ 13 ] are given as
18/x~iv" [1 +0.1 (Res) u?S] 1
D~- d~ (1 --U"/Um) 25 ..... 17) ~t~=-( I - r2) ::5
2
where the particle Reynolds number is defined as 3 I[d'~l~
/ 3 " = ~ ( 1 -r2} 2~', ~'"=48('*" (24)
t,l;a I ,rl - <'I
Rea = Ul; 18 >
where
and/-*I; is the cocflicient of viscosity of the fluid phase, The d "+'= c<C"'+/'X( 1 - d ) ,
effects of solids volume fraction and particle Reynolds num-
ber on the drag coefficient are included in Eq. (17). C " " = 0 . 0 8 5 3 [ (Xu +') ~ + 3 . 2 + 12.18u~'X] (25)
The coefficient c in Eq. (13). the Lagrangian time scale Similarly, the coefficients o?, fit and (t are given by [ 18,19]
TL and the particle relaxation time r '~ are given by
I/3'1:
1 k' O ....L cr'=0.93, /T=0.54, (1= (26)
C= l +,r,,/T L, Tj.=0.16577, r"- DI; (19) 48
e~=a"(k")~/:, e~ = at(,('~) ~': 20) These coefficients of mean viscosity resemble those sug-
with gested by Ishii and Mishima [20] and are consistent with
Einstein's equation for the effective viscosity of dilute
1 - r 2 C fD suspensions.
a"=C~'* ~ , , p " ~ ' - - j - + ~ , a'=C'D/ A ' 21)
The expression for the mean particulate pressure as derived
by Ahmadi I21 ] is given as
where r is the coeflicient of restitution, % = 3 . 9 1 and
C ~° = 0.165 are constants. The length macroscales of partic- p-~ = p-~ + p , l~
( ( ~, , _ ~ ,-'+
,)2 (28)
ulate and fluid turbulence, A ++and A ~, are given by
where the parameter ~ is given by
A " = C:~d / i t = C!,L(I P")
- - - (22) 3 L'"
C <~*' l-' m)
4( 1 - p,,)2 (29)
Here L is the characteristic length scale of the flow and C,~
and C'a are numerical constants. Values of C+[ =0.25 and Note that Eq. (28) is also consistent with the proposal of
C ~ = 0 . 1 0 are used in the subsequent studies. In Eqs. (20) McTigue et al. [ 22 ].
and (21), it is assumed that the particulate phase dissipation The fluctuation pressures in fluid and particulate phases
rate consists of two parts, collisional and non-collisional. At are given as [ 11 ]
low concentrations, where the collisional energy dissipation
is negligible, the particle dissipates energy in a manner similar P'~ = 201,
't
~/k' (30)
to that of the fluid phase with a length scale proportional to
48 S Abu-Z2#d, G. Ahmadi / Powder Technology 89 (1996) 45 56
and
r?t = - - p " T - - c ~ * ( & ) 2 ~ 2 + 52 (38)
p~T = p o p k (l +4t," X) +~ (1 - - r 2 ) (31)
_v++c°.p,>
(a~) °2 \ - ~ - T 2e"]52
] (39)
The particulate fluctuation pressure as given by Eq. (31)
includes both the kinetic and collisional effects.
¢~'.3 = --P+'T+c'~*(a,,,)2 6 Y- (40)
+ D[~((i + - a " ) =0 ( 32 )
tit = a " = u ( y) (34) Eqs. ( 38 ) -(40) and (43) -( 45 ) clearly show the anisotropy
of the particulate and the fluid normal stresses.
with For the case of a simple rapid shear flow, the total stresses
are the sum of the phasic stresses, that is:
du
= 5'= constant 35 I % = ~,,
A~jff-t,j,v (48)
where 5' is a constant shear rate. Here, for rapid shearing flow conditions, the collisional and
Using Eqs. (34) and (35), the evolution equations for the turbulence stresses dominate and, hence #,,<<pfc and
fluctuation energies as given by Eqs. (5) and (6) become /x,.<<pfr. Therefore, the effects of /x'~ and /xr may be
neglected.
C
"*-"
C Po
"v~'Ck~)1/2d52[1+ 4(a,)ek,,CU,j
--~+52 * ]
The corresponding total first and second normal stress dif-
ferences ¢h~and 4& may then be evaluated. These are
= p{{u¢+d'( k " ) 3 / 2 - 2D{{( ck I - k " ) 36) gh = re++- rtt = [C~*fi~k~(7~)z~'++tx'VTf~r]52 (49)
/112 ~ T3 t -- T22
0.545C*Plw'(k')~/2A~/2[l+ 4(a--~ktj~'~Y
]
Introducing the non-dimensional particulate fluctuation In this section, different limiting cases of the model are
energy k ~*, the fluctuation energy ratio ~L the density ratio discussed. While particular attention is given to the special
So and the particle Reynolds number Rea defined as case of simple shear flows, most results are applicable to
general flows.
k '~ k' S p[ { Red_Pl¢124/
k'~* = d25'2' [] = k--~' ° - pl;' /xl; (51) For the limit of small size particles, the production and
dissipation terms in the particulate phase energy equation as
Eqs. (36) and (37) may be restated in a non-dimensional given by Eq. (36) become negligible. It then follows that
form as
k" = ckt (60)
oe
where c is given by Eq. (19). Using Eq. (60) in Eq. (14),
the expression for particulate viscosity becomes
36v ~'
+(c[~-l)(k"*) I/2 -0 (52) i~uT = CO.~,~p~u,,,d( ckt)1/2 (61)
( 1 - u'~/um)es""'Red
where
C'*[ ~l 1
0.545-~g-[l+4~af.)gk~,,i)-a'*,~k~*]v' (53) T°
C "* - (62)
TL( 1 -- p'~/pm) 3
f t - 1 , . /2 36u'~
~-~77~(k )' i l 7----,2s, =0 (53) Using Eq. (20) in Eq. (14), the turbulent viscosity of the
- v°'/urn) " '~Re.
fluid phase may be restated as
where i.zrr = c f * C*a p ro( 1 - ~,o,) ( kr) i /Z / a j (63)
a '~*=a'd, a j*=atd, d*=d/A 1 (54)
The ratio of the turbulent viscosities is now given by
are dimensionless. When the particle Reynolds number, the
density ratio and the solid volume fraction are specified, Eqs. = d* (64)
(68) and (69) form a set of two non-linear algebraic equa- i~ T 1-v"(I+r~/TL)I/2C f* C ~f
tions for determining the dimensionless particulate fluctua- where Eqs. ( 61 ) and (63) are used. Thus, for small particles,
tion energy and the fluctuation energy ratio. the fluctuation kinetic energy equation for the particulate
The non-dimensionalized components of the stress tensor phase reduces to Eq. (60) and the fluctuation viscosities of
are defined as the particulate and fluid phases are given by Eqs. (61) and
(63), respectively.
-7,: (55)
As the solids volume fraction becomes small, the phasic
¢ ~J fi S~ d 2
fluctuation energy Eqs. (36) and (37) reduce to
where
fi= p,'~u'~ + pl;(1 - ~,~') (56) kt.= 0.545 1 + 4(ar)akJ j,
is the density of the mixture. The non-dimensional first and
In this case
second normal stress differences are given as
c"* = :/TL, &=0.27, c"* = 1, A t.= CfAL (66)
I//? = r~2 - - ~'~11 (57)
and and Eq. (64) reduces to
,r e*
I't~'v 3S°u'~ - - d * C fD (67)
tx'w - ( 1 + r=/TL) 1/2 TL
Using Eq. (19), the ratio of the particle relaxation time to
the fluid turbulent Lagrangian time scale may be evaluated. Eq. (67) for the viscosity ratio shows a trend of variation
Restated in terms of non-dimensional parameters, the result with ,r~/TL which is similar to the equation suggested by
is given by Chen and Wood [7]. However, Eq. (67) is more general in
that it includes the effects of the solid volume fraction and
r'~/Tt = 0 . 3 3 7 ( 1 - u°'/ Um)25~''ReaS<clt*(k"*fl) 1'2 (59)
the physical properties of particles. Accordingly, an increase
where the dimensionless groups are defined in Eqs. (51 ) and in solid volume fraction, particle diameter and density ratio
(54). leads to an increase in turbulent viscosity of the particulate
Numerical solutions of Eqs. (52) and (53) and the vari- phase.
ations of non-dimensional stress are described in the subse- For dilute mixtures, the collisional part of the solid phase
quent sections. pressure becomes negligible and Eq. (31 ) reduces to
50 S Abu-Zaid. G, Ahmadi I Powder Technology 89 (1996) 45 56
- - - Fluid Stress
t
solids volume fraction increases towards the maximum pack-
ing limit, Eqs. (15) and ( 2 2 ) l e a d t o
0 *
C"*=1, C I*=1, A"=CI~d (74)
lC z= 10
O Bognold (1954) I 0 H o n e s e n d Inman
- - rotel S t r e s s - - Totel S t r e s s
...... Particulate Stress ...... Pdrtlculate Stress
-- Fluid S t r e s s
10 --- Fluid S t r e s s 0 /
lO
¢ .-'"
//
." [
/" i
10 ~ I ,
O.OO O,10 O.½0 0.30 0.-40 O.5O O.60 0.70 1°~.oo o.Io o.~o 0.;0 o~o o.go o.go 0.70
SOLID V O L U M E FRACTION SOLID VOLUME FRACTION
Fig. 2. Variations of non-dimensional normal stress with solid volume frac- Fig. 4. Variations of non-dhnensional normal stress with solid volume frac-
tion. Comparison with the experimental data of Bagnold [ I } for 1.32 m m tion. Comparison with the expemnental data of Hanes and lmnan [ 3 ] ('or
wax beads in water 1.1 m m glass beads in water.
lO=. 6.0
0 Hones ond Inrnon - - SO = 1.00
- - Total Stress \ ...... So = 2.48
...... Porticulote Stress
--- Fluid S t r e s s
~'4.0
lO
L,J e
?, z
2.0
ft.
.'-.\
0.0 "- i i- " r I I I
10 -~ "'"" ~
o.oo o30 o.~o o.~o o.~o o.so o.~o 0.7o 0,00 0.10 0.20 0.30
SOLID VOLUME FRACTION
0,4-0 0.50 0.60 0.70
SOLID VOLUME FRACTION
Fig. 3. Variations of non-dimensional shear stress with solid volume fraction. Fig 5. Variations of non-dimensional first normal stress difference with
Comparison with the experimental data of Hanes and lnman [ 3 ] for 1.1 m m solid volume fraction for different density ratios.
glass beads in water
3.0
- - So = 1.00
. . . . . . So = 2.48
are shown in Fig. 3 and Fig. 4. The experimental data of --- So = 2 0 0 0
Hanes and l n m a n [ 3 ] for total stress components are repro-
duced in these figures for comparison. The width of the exper-
imental shear cell was 1.6 cm and the shear rate was in the ~ 2.0
0.5 5.0
...... So = 2,48 Total Energy Production
OC" - - So = 1 . 0 0 ...... Solid Phase Energy Production
LO --- Fluid Phase Energy Production
5 4.0
0.4
z
§s
530
0..3
2.0
5
D 0.2
c)
F-- 1.0
(3.
1 O.O 0.8
- - Production
0.7 ...... Dissipation
- - So = 1.00 --- Source
8.0 ....... So = 2.48
0.6
~ 0.5
m
. 0.4
o 0.3
~ 4.0
'"', /
c~ 0.2
/
ff 2.0 0.1
O.O
O.O -01
o.oo 0.40 o.~o 030 0.40 o.go o.go 0.70 o.oo o30 o.:~o O..~o o.J.o o.~o o.~o o.70
SOLID VOLUME FRACTION SOLID VOLUME FRACTION
Fig. 8. Variations of non-dimensional fluid fluctuation kinetic energy with Fig. 10. Variations of non-dimensional fluctuation energy production,dis-
solid volume fraction for glass beads and two different density ratios, sipation and source terms of the fluid phase with solid volume fraction for
1.32 m m particles and So = 1.0.
transferred away from the fluid phase. The process is reversed figure clearly shows that, for u"< 0.5, fluctuation energy is
at higher solid volume fractions and the fluid phase receives being transferred from the fluid phase to the particulate phase.
energy from the particulate phase. Fig. 1 l also shows that the The transported energy is quite large at small solid volume
fluid phasic fluctuation energy supply for the wax bead par- fraction and decreases with ~,% At high solid volume fractions
ticles is slightly higher than that of the glass bead particles. the process is reversed and the particulate phase loses energy
For 0.11 mm diameter glass beads-water mixtures, the through the interaction effects. As noted in the Appendix,
phasic particulate and fluid energy budgets are shown in interaction energy supplies include the interaction energy
Fig. 12 and 13. For u"<0.45, Fig. 12 clearly shows that the dissipation. Thus, they are not equal in magnitude and oppo-
fluctuation energy production by the particulate phase is neg- site in sign and their net sum is always negative. These qual-
ligibly small and the energy dissipation rate is nearly balanced itative variations are clearly observed in Fig. 14.
by the energy supply. For ~,~> 0.5, however, the collision To study the effect of particle diameter on stresses,
mechanism takes over and the particulate fluctuation energy mixtures of water and glass bead particles are considered.
production increases rapidly with ~,% In this range, the par- Eqs. (52) and (53) are solved for several values o f d a n d u '~
ticulate fluctuation energy supply becomes negative which and the corresponding phasic and total shear stresses are
indicates loss of phasic fluctuation energy. Fig. 13 shows that evaluated. Eqs. (41), (46) and (48) and an average value
the fluid phase energy production is generally higher than its of 3~= 200 s--~ are used in these analyses. The resulting
dissipation. The fluid interaction energy supply is negative stresses are shown in Fig. 15-17. Fig. 16 shows that as the
and fluctuation energy is being transferred from the fluid particle diameter increases, the phasic particulate shear stress
phase to the particulate phase. Hence, for small size particles, increases rapidly. Fig. 17 indicates that shear stress of the
the fluid phase dominates the fluctuation energy production fluid phase does not vary with particle size. The total shear
for almost the entire range of solids volume fraction except stresses shown in Fig. 15 have a minimum at some interme-
for the highly dense mixtures. diate value of u". It is also observed that the total shear stress
Variations of the phasic energy supplies for 0.11 mm glass increases significantly with d for large values of u '~. However,
beads-water mixtures with u '~ are shown in Fig. 14. This it is not affected by changes in d at small solid volume
fractions.
40.0
- - Production
. . . . . . Dissipation 50.0
.... Source
30.0
k Solid Phase Energy Source
\
....... Fluid Phase Energy Source
30.0
20.0 \
\\
~ O.D
~_ ,
-I0.0
-10.0 "
-30.0 ,""
-20.0 /
o.oo o.1o o.~o o.~o o.4o' 0.5o' 0.40 0.7o ,,
SOLID VOLUME FRACTION -50.0 ~
Fig. 12. Variations of non-dimensional fluctuation energy production, dis- o.oo o.1o 0.20 0.30 o.;,o o.~o o.oo 0.70
SOLID VOLUME FRACTION
sipation and source terms of the particulatephase with solid volume fraction
Fig. 14. Variations of non-dimensional phasic fluctuation energy source with
for 0.11 mm particles and S~= 2.48.
solid volume fraction for O.l l m m glass particles and S o = 2 . 4 8 .
50.0
r 30.0
: 10.0
N lO
-30.0
/
t
-5o.o ~,
o.oo o.1o o.~o 0.30 o.;,o o.~o 0.40 0.70
SOLID VOLUME FRACTION 1
o.oo o.~o olo oJo o.~o o.go o.~o 0.70
Fig. 13. Variations of non-dimensional fluctuation energy production, dis- SOLID VOLUME FRACTION
sipation and source terms of the fluid phase with solid volume fraction for Fig. 15. Variations of dimensional total shear stress with solid volume frac-
O. 11 m m particles and So = 2.48. tion for different values of particle diameter.
54 S Abu-Zatd, (i. A h m a d i / P o w d e r 7 e c h m d o g y b~9 (I 996) 4 5 - 5 6
10 8. Conclusions
...... d=l,10 mm ,"" /
,"
Appendix A. Fluctuation energy sources where R, ~ is the autocorrelation function of the fluid velocity
defined as
The phasic fluctuation energy supplies defined by Ahmadi
a n d M a [ l l ] are RI)(~-) = t,l"(t + ~ ' ( t ) (At0)
where t,t, and c / " are the fluctuation velocities of the partic- ~=~(l-c) (AI2)
ulate and fluid phases, and a bar stands for the expected value. Using Eqs. ( A I 2 ) and (A5) if follows that
Here it is assumed that the solids volume fraction does not
vary appreciably and the differences between mass weighted td'~"s' = 2 D ~ ( k ~ - k ' ) (AI3)
and regular fluctuating velocities are ignored.
which is an explicit expression for the fluid interaction energy
For a dilute suspension, an expression R)r the fluctuation
supply.
energy supply of the particulate phase was derived by Ahmadi
Suppose that the particles are made to fluctuate by some
and Ma [11]"
external means in a motionless fluid, Eq. ( A I 3 ) implies that
pc~u'~s ~ = 2D~{( c U - k ~) ( A3 ) at the equilibrium condition, k ~ = k ~ will be reached. Eq.
(A3), on the other hand, indicates that when particles
where c is given by Eq. ( 19).From Eqs. ( A I ) and (A2) it
encounter a fluid turbulence, they could acquire a fluctuating
follows that
energy of k '~ = ckq Thus, the large and heavy particles fluc-
p o t ' S~ ' ±
. . .p.o. .v. . . .~ -- _ D'~(),f -t'~') 2 (A4) tuate less than the light and smaller ones.
It should be pointed out that Eqs. (A3) and (AI 3) are also
Using Eq. (A3), Eq. (A4) may be restated as
thermodynamically consistent. For an isothermal mixture, the
entropy inequality imposes the following restriction on the
pl)ulst=2D~{ U ~ - c k t - w; (A51
interaction energy supply terms [ 11 ]:
, ! • I)
where a, = ~ - t,, is the difference in fluctuating v eloci- (plluts t + p~u'~s~) >_0 (A14)
ties. In the earlier work of Ahmadi and Ma [ 111 g',,t2 was where it is assumed that thermal coldness is much less than
neglected and #~Wts~= - p ~ , " s " was used. It was also sug-
that of turbulence.
gested that this additional loss of energy be accounted for as Substituting for the interaction energy supply terms from
part of the dissipation rates. In this Appendix, derivation of
Eqs. (A3) and (A13) into Eq. ( A I 4 ) , it follows that
an explicit expression for ~w ~-is attempted.
The equation of motion of a single particle in a turbulent
flow field written in terms of relative velocity is given by
(1 - c ) k ' = ('r~/TL)k.'.>O
1 +'r"/TL-
(A15)
[16] G. Ahmadi and S. Abu-Zaid, J Non-Newtonian Fluid Mech., 35 [21] G. Ahmadi, Adv. Water Res., 10 (1987) 32.
(1990) 15. [22] D.F. McTigue, R.C. Gilver and J.W. Nunziato, J. Rheol., 30 (1986)
[ 17] DN. Ma and G Ahmadi, J. Chem. Phys., 84 (1986) 3449. 1053.
[23] A. Einstein, Ann. Phys., 19 (1906) 289.
[ 18] G Ahmadi and S.J. Chowdhury, Appl. Math. Modelings, 15 (1991)
[24] J. Cao, G. Ahmadi and M. Massoudi, J. Fluid Mech., 316 (1996) 197.
516.
[ 25 ] S. Abu-Zaid and G. Ahmadi, Powder Technol., 67 ( 1991 ) 1.
[ 19] S.J. Chowdhury and G. Ahmadi, Int. J. Non-Linear Mech., 27 ( 1992 ) [26] O.T. Walton and R.L. Braun, Acta Mech., 63 (1986) 73.
705. [27] C.S. Campbell and A. Gong, J. Fluid Mech., 164 (1986) 107.
[20] M. Ishii and K. Mishima, Nucl. Design, 87 (19841 107 [28] D. Thomas, J. Colloid Sci. , 20 (1965) 267.