Hydrodynamics of plate columns. IV. Interfacial area and the mass transfer coefficient in the gas-liquid mixture on sieve plates of separation columns; Theoretical study

1970 ◽  
Vol 35 (12) ◽  
pp. 3678-3685 ◽  
Author(s):  
V. Kolář
Author(s):  
Keshav C Ruthiya ◽  
John van der Schaaf ◽  
Ben F.M. Kuster ◽  
Jaap C Schouten

In this paper, the influence of carbon and silica particle slurry concentration up to 20 g/l (4 vol%) on regime transition, gas hold-up, and volumetric mass transfer coefficient is studied in a 2-dimensional slurry bubble column. From high speed video image analysis, the average large bubble diameter, the frequency of occurrence of large bubbles, the gas-liquid interfacial area, and the large bubble hold-up are obtained. The liquid side mass transfer coefficient is calculated from the volumetric mass transfer coefficient and the gas-liquid interfacial area. The lyophilic silica particles are rendered lyophobic by a methylation process to study the influence of particle wettability. The influence of organic electrolyte (sodium gluconate) and the combination of electrolyte and particles is also studied. It is found that lyophilic silica, lyophobic silica, and lyophobic carbon particles at concentrations larger than 2 g/l (0.4 vol%) decrease the gas hold-up and shift the regime transition point (where the first large bubbles appear) to a lower gas velocity. The volumetric mass transfer coefficient increases with gas velocity, increases with electrolyte concentration, decreases with slurry concentration, and is higher for lyophobic particles. The liquid side mass transfer coefficient increases with gas velocity, bubble diameter, and is higher for lyophobic particles. A correlation for the mass transfer coefficient based on dimensionless numbers is proposed for the heterogeneous regime.


2015 ◽  
Vol 31 (4) ◽  
Author(s):  
Reza Afshar Ghotli ◽  
Abdul Raman Abdul Aziz ◽  
Shaliza Ibrahim

AbstractA general review on correlations to evaluate mass transfer coefficients in liquid-liquid was conducted in this work. The mass transfer models can be classified into continuous and dispersed phase coefficients. The effects of drop size and interfacial area on mass transfer coefficient were investigated briefly. Published experimental results for both continuous and dispersed phase mass transfer coefficients through different hydrodynamic conditions were considered and the results were compared. The suitability and drawbacks of these correlations depend on the operating conditions and hydrodynamics. Although the results of these models are reasonably acceptable, they could not properly predict the experimental results over a wide range of designs and operating conditions. Therefore, proper understanding of various factors affecting mass transfer coefficient needs to be further extended.


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