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Research article
Department of Chemical Engineering, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, P. R. China
Department of Chemical and Biochemical Engineering, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, P. R. China
ABSTRACT: Electrostatics is an inevitable phenomenon in uidization processes and granular ow, where collisions
between particulates and walls with different materials occur. In this work, a two-dimensional computational uid dynamics
model based on the EulerianEulerian approach was applied and coupled with a rst-principles electrostatic model to
describe the gassolid two-phase ow behavior in a uid catalytic cracking (FCC) riser reactor under the electrostatic
conditions. The coupled model was used to predict the main gassolid ow distribution parameters in the FCC riser, such
as electric potential, particle volume fraction, gas-phase temperature, and gas-phase component fractions. The simulation
results showed that the electrostatic had a signicant inuence on the particle distribution in the bottom dense region of
the FCC riser, whereas it had a weak inuence in the upper dilute region at the cold-ow conditions. The simulation results
also showed that the electrostatic had a weak inuence on the particle concentration, gas-phase temperature, and lump
concentration distributions when the cracking reaction was considered. 2014 Curtin University of Technology and John
Wiley & Sons, Ltd.
KEYWORDS: FCC riser; EulerEuler approach; electrostatic modeling; CFD simulation
INTRODUCTION
It is well-known that riser reactor is very important for
uid catalytic cracking (FCC) process.[14] An
FCC system in the FCC riser reactor can be treated as a
gassolid two-phase system.[5,6] The gas phase consists
of vacuum gas oil, by-products, and products, and the
solid phase consists of catalyst particles. Because the
fresh FCC catalyst particles enter the riser as a single
component and the FCC reactions occur within those
particles when they are exposed to the gas phase,[7]
continuous and frequent contacts and collisions of
particleparticle, particlewall and particlegas must
exist, which leads to the formation of electrostatics.[8,9]
The motion of charged particles in the riser would result
in nonuniform electric eld.[10,11] Meanwhile, the
commercial FCC catalyst particles (<100 m) are
generally fabricated with 12 m Y-zeolite crystals
dispersed in an amorphous silica-alumina matrix, and
only those hydrocarbon species can penetrate through
the zeolite pores,[11] which further leads to the increase
of the electrostatics phenomenon in the riser.
*Correspondence to: Luo Zheng-Hong, Department of Chemical
Engineering, School of Chemistry and Chemical Engineering,
Shanghai Jiao Tong University, Shanghai 200240, P. R. China.
E-mail: luozh@sjtu.edu.cn
2014 Curtin University of Technology and John Wiley & Sons, Ltd.
Curtin University is a trademark of Curtin University of Technology
646
0
g
g
g
g
g
t
v
v
g g g g g g g g g P
t g g g
M
f gm
1
1;m
f m F qsm
Cp
T
Cp
v
T
grad
T
g
g
g
g
g
g
g
g
g
g
t
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Dgrad
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t
Asia-Pac. J. Chem. Eng. 2014; 9: 645655
DOI: 10.1002/apj
Electrostatic model
Rokkam et al.[42] have developed a rst-principles
electrostatic model to compute the electrostatic force
in olen polymerization FBRs. Herein, the suggested
electrostatic model is extended into the FCC riser.
The force acted on a charged particle in the
electromagnetic eld can be described as Lorentz force
equation, which is described as
F qE B
Lump symbol
Lump
Heavy parafnics
Medium parafnics
Light parafnics
Heavy naphthenics
Medium naphthenics
Light naphthenics
Heavy aromatics in resin
and asphaltene
Heavy aromatics expert
FAh
Medium aromatics
Light aromatics
Gasoline
Liquid petroleum gas
Dry gas
Coke
Ph
Pm
Pl
Nh
Nm
Nl
FAh
Ah
Am
Al
GO
LPG
DG
CK
(1)
Boiling
range ( C)
500
350-500
221350
500
350-500
221350
500+
F qE
(2)
500+
350500
221350
C5221
C3 + C4
C1 + C2 + H2
D qv
(3)
N
Path no.
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
Path
k01 (m3/kgcat/s)
E2 (kJ/kmol)
Path no.
Path
k01 (m3/kgcat/s)
E2 (kJ/kmol)
Ph Pm
Nh Nm
Ah Am
FAh Am
Ph Pl
Nh Nl
Ah Al
FAh Al
Ph GO
Nh GO
Ah GO
FAh GO
Ph LPG
Nh LPG
Ph DG
Nh DG
Ph CK
Nh CK
Ah CK
FAh CK
Pm Pl
Nm Nl
Am Al
Pm GO
18.77
19.25
1.817
0.5514
16.38
17.05
1.617
0.4342
0.2266
0.1374
0.0136
0.0054
5.77
6.20
63.18
64.99
3.366
4.754
41.82
40.50
833.90
944.00
773.80
1.263
7.21e+4
7.21e+4
7.21e+4
7.21e+4
7.21e+4
7.21e+4
7.21e+4
7.21e+4
3.04e+4
3.04e+4
3.76e+4
3.76e+4
4.32e+4
4.32e+4
6.32e+4
6.32e+4
5.00e+4
5.00e+4
5.44e+4
5.44e+4
7.21e+4
7.21e+4
7.21e+4
3.04e+4
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
Nm GO
Pm LPG
Nm LPG
Am LPG
Pm DG
Nm DG
Am DG
Pm CK
Nm CK
Am CK
Pl GO
Nl GO
Pl LPG
Nl LPG
Al LPG
Pl DG
Nl DG
Al DG
Pl CK
Nl CK
Al CK
GO LPG
GO DG
GO CK
0.4092
1.506
0.5742
0.0438
5.491
2.013
0.0324
1.704
1.061
5.611
1.257
1.986
2.258
1.506
0.033
15.20
10.14
0.0498
0.1363
0.1491
0.8254
1374.00
343.40
0.066
3.04e+4
4.32e+4
4.32e+4
2.76e+4
6.32e+4
6.32e+4
3.76e+4
5.00e+4
5.00e+4
5.44e+4
3.04e+4
3.04e+4
4.32e+4
4.32e+4
2.76e+4
6.32e+4
6.32e+4
3.76e+4
5.00e+4
5.00e+4
5.44e+4
1.18e+5
1.18e+5
5.61e+4
Frequency factor.
Activation energy.
2014 Curtin University of Technology and John Wiley & Sons, Ltd.
647
648
D 0 E P
(4)
(5)
0 m E qsm sm
(6)
m1
(8)
sm qsm
2:17
m1
g
1:20
0
g
(9)
(10)
Figure 1. Conguration and schematic of the 2D uid catalytic cracking riser used in
this study [(a) the whole riser and (b) the simulated 2D riser]. This gure is available in
colour online at www.apjChemEng.com
of the gas and solid volume fractions from the CFD model
to the electrostatic model as well as the electrostatic force
from the electrostatic model to the CFD model without
any assumptions for these transportations; the coupled
model is effective for describing the effect of the
electrostatic on the hydrodynamics in the FCC riser.
Description
Value
3
1560
6.0 105
0.14
1.2 104
0.1
0.2
0.1
0.38
4.5
1.255
1.732 105
2014 Curtin University of Technology and John Wiley & Sons, Ltd.
Description
Value
840.5
0.2625
0.2
0.1
1560
6.0 105
0.14
1.2 104
0.1
1.3932
733
420.0
0.5588
0.2663
0.1749
649
650
Figure 5. Particle volume fraction proles in the riser at hot-model condition [(a) 60 m
and (b) 120 m]. This gure is available in colour online at www.apjChemEng.com
2014 Curtin University of Technology and John Wiley & Sons, Ltd.
651
652
Figure 6. Mean radial uid catalytic cracking particle volume fraction distributions at various axial
Figure 9. Main mean gas-phase product yield distributions of the uid catalytic cracking riser. This
gure is available in colour online at www.apjChemEng.com
CONCLUSIONS
A 2D EulerianEulerian CFD model coupled with a
rst-principles electrostatic model was extended to
describe the gassolid two-phase ow behavior in an
FCC riser reactor under the electrostatic conditions.
The coupled model was used to predict the main gas
solid ow distribution parameters in the FCC riser,
such as electric potential, particle volume fraction,
gas-phase temperature, and gas-phase component
fractions. The following conclusions can be drawn on
the basis of the simulation results:
(1) Like other gassolid handling devices, obvious
electrostatic effects are found in FCC riser. The
electric potential distribution is inhomogeneous
because of the hydrodynamic segregation in the
riser when considering the electrostatics force.
(2) The simulation results also showed that the
electrostatic had a signicant inuence on the particle
distribution in the bottom dense region of the FCC
riser reactor, whereas it has a weak inuence in the
upper dilute region at the cold-ow conditions.
(3) The simulation results also showed that the
electrostatic has a weak inuence on the particle
concentration, gas-phase temperature, and main
product yields at the heat-model conditions.
As a whole, the coupling of the CFD model and the
electrostatics model leads to the iterative inuences
between the ow hydrodynamics and the electrostatics.
Further studies on the coupling modeling of the gassolid
Asia-Pac. J. Chem. Eng. 2014; 9: 645655
DOI: 10.1002/apj
653
654
NOMENCLATURE
B
CD
Cp
ds
E
fgm
fm
Fqsm
g
M
P
PS
q
qsm
Qr
Q
T
t
v
Wj
Yj
m
0
g
s
Subscripts
g Gas phase
s Solid phase
j Lump
2014 Curtin University of Technology and John Wiley & Sons, Ltd.
REFERENCES
[1] C.M. Xu, J.S. Gao, S.X. Lin, G.H. Yang. Analysis of
Catalytic Cracking Reaction Process, China Petroleum
Industry Press, Beijing, P. R. China, 2002.
[2] C. Zhu, Y. Jin, R. Patel, D.W. Wang, T.C. Ho. AIChE J.,
2011; 57, 31223131.
[3] C.K. Pashikanti, Y.A. Liu Fuel, 2011; 25, 52985319.
[4] J.W. Wang. Particuology, 2010; 8, 176185.
[5] C.N. Wu, Y. Cheng, Y.L. Ding, Y. Jin. Chem. Eng. Sci.,
2010; 65, 542549.
[6] A. Hany, R. Sohrab. Chem. Eng. Technol., 1997; 20,
118130.
[7] R. Sadeghbeigi. Fluid Catalytic Cracking: Design, Operation,
and Troubleshooting of FCC Facilities, Gulf Publishing
Company, Houston, USA, 2000.
[8] J. Ciborowski, A. Wlodarski. Chem. Eng. Sci., 1962; 17, 2332.
[9] Y.F. Zhang, Y. Yang, H. Arastoopour. AIChE J., 1996; 42,
15901599.
[10] E.W.C. Lim, Y. Zhang, C.H. Wang. Chem. Eng. Sci., 2006;
61, 78897908.
[11] G. Hendrickson. Chem. Eng. Sci., 2006; 61, 10411064.
[12] A.H. Park, H.T. Bi, J.R. Grace. Chem. Eng. Sci., 2002; 57,
153162.
[13] M. Kashyap, D. Gidaspow, M. Driscoll. Powder Technol.,
2008; 183, 441453.
[14] F. Wang, J.D. Wang, Y.R. Yang. Ind. Eng. Chem. Res., 2008;
47, 95179526.
[15] C.L. Briens, M.A. Bergougnou, I.I. Inculet, T. Baron, J.D.
Hazlett. Powder Technol., 1992; 70, 5762.
[16] R.K. Gupta, V. Kumar, V.K. Srivastava. Int. J. Chem. React.
Eng., 2010; 8, 140.
[17] J.S. Gao, C.M. Xu, S.X. Lin, G.H. Yang. AIChE J., 1999; 45,
10951113.
[18] J.S. Gao, J. Chang, C.X. Lu, C.M. Xu. Particuology, 2008;
6, 5971.
[19] J.S. Gao, X.Y. Lan, Y.P. Fan, J. Chang, G. Wang, C.X. Lu,
C.M. Xu. Chem. Eng. Sci., 2009; 64, 43024316.
[20] J.W. Wang, Q. Zhou, K. Hong, W. Wang, J.H. Li. Chem.
Eng. Sci., 2012; 75, 349358.
[21] J.W. Wang, Y.B. Liu. Powder Technol., 2010; 197, 241246.
[22] M.T. Shah, R.P. Utikar, M.D. Tade, V.K. Pareek. Chem. Eng.
J., 2011; 168, 812821.
[23] S.P. Egendla, G.J. Heynderickx, G.B. Marin. AIChE J., 2012;
58, 268284.
[24] S.K. Nayak, S.L. Joshi, V.V. Ranade. Chem. Eng. Sci., 2005;
60, 60496066.
[25] A. Dutta, D. Constales, G.J. Heynderickx. Chem. Eng. Sci.,
2012; 83, 93109.
[26] J. Li, Z.H. Luo, X.Y. Lan, C.M. Xu, J.S. Gao. Powder
Technol., 2013; 237, 569580.
[27] I.S. Han, C.B. Chung. Chem. Eng. Sci., 2001; 56, 19731990.
[28] J.S. Gao, X.Y. Lan, Y.P. Fan, J. Chang, G. Wang, C.X. Lu,
C.M. Xu. AIChE J., 2009; 55, 16801694.
[29] J. Chang, F.D. Meng, L.Y. Wang, K. Zhang, H.G. Chen, Y.P.
Yang. Chem. Eng. Sci., 2012; 78, 128143.
[30] J. Chang, K. Zhang, F.D. Meng, L.Y. Wang, X.L. Wei.
Particuology, 2012; 10, 184195.
[31] A.K. Das, E. Baudrez, G.B. Marin, G.J. Heynderickx. Ind.
Eng. Chem. Res., 2003; 42, 26022617.
[32] J.H. Li, M. Kwauk. Chem. Eng. Sci., 2003; 58, 521535.
[33] H.R. Nazif, H.B. Tabrizi. Appl. Math. Model., 2013; 37,
24452459.
[34] S. Wang, G.D. Liu, H.L. Lu, Y.C. Yang, P.F. Xu, L.Y. Sun.
Powder Technol., 2012; 228, 5668.
[35] G.C. Lopes, L.M. Rosa, M. Mori, J.R. Nunhez, W.P.
Martignoni. Comput. Chem. Eng., 2011; 35, 21592168.
[36] J.Q. Gan, H. Zhao, A.S. Berrouk, C.H. Yang, H.H. Shan. Ind.
Eng. Chem. Res., 2011; 50, 1151111520.
[37] M.T. Shah, R.P. Utikar, M.O. Tade, V.K. Pareek, G.M.
Evans. Chem. Eng. Sci., 2011; 66, 32913300.
[38] Y. Behjat, S. Shahhosseini, M.A. Marvast. Chem. Eng. Res.
Des., 2011; 89, 978989.
[39] N. Ellis, M. Xu, C.J. Lim, S. Cloete, S. Amini. Ind. Eng.
Chem. Res., 2011; 50, 46974706.
Asia-Pac. J. Chem. Eng. 2014; 9: 645655
DOI: 10.1002/apj
2014 Curtin University of Technology and John Wiley & Sons, Ltd.
655