HYDRODYNAMICS IN A COCURRENT GAS-LIQUID TRICKLE BED AT ELEVATED PRESSURES

被引:82
作者
WAMMES, WJA
MIDDELKAMP, J
HUISMAN, WJ
DEBAAS, CM
WESTERTERP, KR
机构
[1] Dept. of Chemical Engineering, Chemical Reaction Engineering Laboratories, University of Twente, Enschede
关键词
D O I
10.1002/aic.690371210
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Data on design and operation of trickle beds at elevated pressures are scarce. In this study the influence of the gas density on the liquid holdup, the pressure drop, and the transition between trickle and pulse flow has been investigated in a trickle-bed reactor operating up to 7.5 MPa and with nitrogen or helium as the gas phase. Gas-liquid interfacial areas have been determined up to 5.0 MPa by means of CO2 absorption from CO2/N2 gas mixtures into amine solutions. A comparison of the results from nitrogen as the gas phase to those of helium shows that at equal gas densities the hydrodynamic states are the same. The gas-liquid interfacial area increases when operating at higher gas densities. When the determined dimensionless interfacial areas a(gl)/a(s) are all within the range 0.25-0.8, the trickle-bed reactor is suggested to operate in the trickle-flow regime. The gas density has a strong influence on the liquid holdup. Due to the higher pressure gradients at elevated gas densities, the liquid holdup decreases noticeably. Besides, the boundary between the trickle-flow and pulse-flow regime shifts toward higher liquid throughputs: the region for trickle-flow operation becomes larger. For the liquid holdup and the pressure gradient in the trickle-flow regime, correlations derived based on dimensionless numbers can be applied to high-pressure trickle beds.
引用
收藏
页码:1849 / 1862
页数:14
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