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Abstract
E;ect of the liquid-phase viscosity (0.725 mPa s) and surface tension (3365 mN m1 ) on hydraulic and mass-transfer characteristics
in a bubble column with an up- ow ejector-type gas distributor was studied. The coalescent character of the aqueous batches was changed
by addition of a polymeric thickener, sucrose and an alcoholic foam breaker. Mass transfer was studied using steady-state physical
absorption of air.
Better performance of the ejector with swirl body for all tested liquid batches was achieved. Gas hold-up in the bubble column increased
with increasing viscosity and surface tension in all batches. Mass-transfer coeCcient in the ejector decreased with increasing viscosity
by 60% maximally in the maximum viscous coalescent batch. It was correlated within 10% using the gas monodispersion model.
Mass-transfer coeCcient in the column decreased with increasing viscosity by 30% maximally in the same coalescent viscous batch. It
was correlated with large relative error, 27%.
? 2002 Elsevier Science Ltd. All rights reserved.
Keywords: Ejector gas distributor; Hydrodynamics; Mass transfer; Multiphase reactors; Surfactant; Viscous liquids
0009-2509/02/$ - see front matter ? 2002 Elsevier Science Ltd. All rights reserved.
PII: S 0 0 0 9 - 2 5 0 9 ( 0 2 ) 0 0 1 6 5 - 3
2988 A. Elgozali et al. / Chemical Engineering Science 57 (2002) 29872994
literature where the in uence of the liquid-phase properties by adding the foam breaker OCENOL (a mixture of satu-
on the mass-transfer characteristics of ejector was studied. rated and unsaturated alcohol from the fraction C16 C18 ) in
So far, prediction of the e;ect of physical properties of the standard amount 3 ppm by volume. Symbols for the batches
liquid phase on the behavior of gasliquid dispersions and on containing OCENOL are distinguished by a cross or dot
the rate of interfacial mass transfer in both ejector and bub- inside. In addition, some experiments were made also us-
ble column seems to be a question without speciOc answer. ing an aqueous sucrose solution and water with and without
The aim of present work is to study the e;ect of OCENOL. All the experiments were carried out at temper-
liquid-phase viscosity and surface tension on the hydraulic ature 30 C and atmospheric pressure.
characteristics, i.e. gas suction rate, gas hold-up, and on Immersion densimeter, rotational viscometer RheoStress
volumetric liquid-side mass-transfer coeCcient, kL a, of the 100, and hanging-ring LAUDA Tensiometer TE 1 C=2 were
two reactor zones using two ejector conOgurations and used for the laboratory measurements of density L , viscos-
some selected Newtonian liquid batches. ity L , and surface tension , respectively.
The coalescence ratio of bubble pairs, , has been used
in the studies devoted to the bubble coalescence in relation
2. Experimental to physical properties of the liquid-phase, see Zahradn16k,
Kuncov1a, and Fialov1a (1999), and Zahradn16k, Fialov1a, and
2.1. Ejector Linek (1999). Brie y, gives a probability of coalescence
for a pair of identical air bubbles, synchronously discharged
Mechanical design of the applied ejectors is given in from two closely neighboring metallic capillaries to a small
Fig. 1. Ejector A includes swirl body inside the nozzle, while column Olled with stagnant tested uid. The parameter is
Ejector B instead of the swirl body includes mixing cham- of empirical character where = 1 for the well coalescent
ber, which has length to diameter ratio equals to 10. liquids like distilled water, while = 0 for non-coalescing
batches.
2.2. Experimental setup The oxygen di;usivity in aqueous SOKRAT solutions
was measured by the polarographic voltage-step transient
The schematic diagram of the experimental setup is shown measurement. The details of the experimental procedure can
in Fig. 2. The liquid batch was circulated between the ab- be found in Sobol16k, Tihon, Wein, and Wichterle (1998).
sorption EJ, BC, T2 and desorption PC, T1 branches of the The results given in Table 1, conOrm a week variation of
setup. In the co-current absorption branch, ambient air was the di;usivity with the polymer concentration, which is a
sucked by the ejector EJ, dispersed in liquid stream and in- well-known rule for a broad class of water soluble polymers.
troduced to the bubble column BC (height 1:46 m and di-
ameter 0:3 m). The over ow from BC was stored in tank T2 2.4. Calculation procedure
and pumped to the top of desorption column PC. In the col-
umn, the oxygen dissolved in the liquid batch was stripped 2.4.1. Gas hold-up
o; by nitrogen introduced to the tank T1 and then to bottom Gas hold-up in the ejector was calculated assuming the
of the column PC, packed with 1 m of polypropylene Pall zero slip velocity of the phases
rings 25 mm. In some mass-transfer experiments, a twisted
QG
metallic sheet as shown in Fig. 2, was mounted inside T1 G; ej = : (1)
QL + Q G
to suppress the bubbles content at the input to the absorp-
tion unit. Experiments with the installed metallic sheet are Acceptability of this approach was discussed e.g. by Achar-
referred as MT2, while without the guarding sheet referred jee, Bhat, Mitra, and Roy (1975), Dirix and van der Wiele
as MT1. Polarographic dissolved oxygen probe was used to (1990), and Raghuram and Das (1997). Gas hold-up in the
determine oxygen concentrations in the liquid stream at in- column was calculated from
let and outlet of the ejector and bubble column (see Fig. 2) Qh
after reaching a steady state. G; col = ; (2)
QH
where Qh and QH are deOned in Fig. 2.
2.3. Liquid batches and their physical properties
2.4.2. kL aej in the ejector
The list of all used liquid batches with their physical The oxygen mass balance in ejector was described assum-
properties and the symbols used in the Ogures are given in ing constant and co-current plug ow of both phases
Table 1. Viscosity of the aqueous batches was modiOed
by addition of the commercial thickener SOKRAT (a wa- QL dcL; ej = kL aej (cG; ej =mO2 cL; ej ) dV = QG dcG; ej : (3)
ter soluble liquid polymer based on acrylonitrile and acrylic Solving this equation gives the expression for kL aej
acid in ratio 2 : 1). The resulting solutions displayed Newto- in
QL 1 (cG; ej =mO2 cL; ej )
nian ow behavior. An extensive foaming, which seriously kL aej = ln out : (4)
complicated the mass transfer experiments, was suppressed Vej 1 + QL =mO2 QG (cG; ej =mO2 cL; ej )
A. Elgozali et al. / Chemical Engineering Science 57 (2002) 29872994 2989
Fig. 2. Experimental setup. BC: bubble column; EJ: ejector distributor; QH : height di;erence between the pressure taps of two manometer tubes giving
the di;erence Qh of liquid levels; PC: packed column; QG and QL : gas suction rates and liquid ow rates measured by using turbine ow meters; T1
and T2: storage tanks.
Table 1
Physical properties of the liquid batches at 30 C with corresponding symbols used in Ogures
Coalescent batches
Distilled water 995 0.7 65.4 2.57 100
Distilled water & OCENOL 996 0.7 33.5 2.57 100
3% SOKRAT & OCENOL 1004 10.2 37.5 2.52 100
6% SOKRAT & OCENOL 1007 16.2 42.8 2.48 100
10% SOKRAT & OCENOL 1011 24.4 45.4 2.42 100
58% Sucrose 1270 25.6 57.0 0.17 95
Non-coalescent batches
0.5% SOKRAT 998 1.5 64.5 2.56 1.8
3% SOKRAT 1004 10.2 54.6 2.52 3.2
6% SOKRAT 1007 16.2 52.5 2.48 3.5
10% SOKRAT 1011 24.4 48.7 2.42 10
2990 A. Elgozali et al. / Chemical Engineering Science 57 (2002) 29872994
Table 2
Empirical constants for Eq. (8)
K (ma2b3c sa+b+2c ) (4:5 5:9) 109 (1:92 0:74) 106 (5:30 11:70) 106
a 0:67 0:04 0:72 0:01 0:44 0:01
b 0:22 0:02 0:14 0:01 0:13 0:02
c 1:95 0:12 1:26 0:04 1:41 0:20
Relative error 27.4% 8.0% 7.5%
Fig. 6. Mass-transfer correlation for the ejectors. Calculated values are Notation
according to the penetration model, Eq. (9).
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