Gas–liquid interfacial area and mass transfer coefficient in a co‐current down flow contacting column

The gas–liquid interfacial area and mass transfer coefficient for absorption of oxygen from air into water, aqueous glycerol solutions up to 1.5% (w/w) and fermentation medium containing glucose up to a 3% concentration were determined in a co‐current down flow contacting column (CDCC; 0.05 m i.d. and 0.8 m length). Experimental studies were conducted using various nozzle diameters at different gas and re‐circulation liquid rates. Specific interfacial area (a) is determined from the fractional gas hold‐up (ε_G) and the average bubble diameter (d_b). Once the interfacial area is determined, the volumetric mass transfer coefficient (k_La) is then used to evaluate the film mass transfer coefficient in the CDCC. The effects of operating conditions and liquid properties on the specific interfacial area were investigated. The values of interfacial area in air–aqueous glycerol solutions and fermentation media were found to be lower than those in the air–water system. As far as experimental conditions were concerned, the values of interfacial area obtained from this study were found to be considerably higher than those of the literature values of conventional bubble columns. The penetration theory is used to interpret the film mass transfer coefficient and results match the experimental k_L data reasonably well. Copyright © 2006 Society of Chemical Industry     

Oxygen Mass Transfer Rate in a Pressurized Lab‐Scale Stirred Bioreactor

Oxygen mass transfer from air to the liquid phase in bioreactors with aerobic cultures has long been a serious impairment to the productivity of various bioprocesses. An increase of the oxygen mass transfer rate (OTR) can be the key to overcome oxygen limitation. The influence of higher air pressure on OTR was measured and a significantly enhanced OTR could be obtained. The oxygen volumetric mass transfer coefficient (k_La) was described by a function of the air pressure in a stirred lab‐scale pressurized bioreactor. The correlation obtained proved that k_La slightly decreased with higher air pressure, following a power function.     

Interfacial Area and Liquid‐Side Volumetric Mass Transfer Coefficient in a Downflow Bubble Column

An experimental investigation was made to measure interfacial area, a, and liquid‐side volumetric mass transfer coefficient, k_La, in a downflow bubble column by chemical methods viz., absorbing CO₂ in aqueous sodium hydroxide and sodium carbonate/bicarbonate buffer solution respectively. The effect of gas and liquid flowrate and nozzle sizes on a and k_La were investigated. The experimental data obtained in the present system were analyzed and correlations were developed to predict a and k_La in terms of superficial gas velocity. The variation of a and k_La with specific power input were shown in graphical plot and compared with other gas‐liquid systems.     

Oxygen mass transfer coefficient in bubble column slurry reactor with ultrafine suspended particles and neural network prediction

The gas–liquid volumetric mass transfer coefficient was determined by the dynamic oxygen absorption technique using a polarographic dissolved oxygen probe and the gas–liquid interfacial area was measured using dual‐tip conductivity probes in a bubble column slurry reactor at ambient temperature and normal pressure. The solid particles used were ultrafine hollow glass microspheres with a mean diameter of 8.624 µm. The effects of various axial locations (height–diameter ratio = 1–12), superficial gas velocity (u_G = 0.011–0.085 m/s) and solid concentration (ε_S = 0–30 wt.%) on the gas–liquid volumetric mass transfer coefficient k_La_L and liquid‐side mass transfer coefficient k_L were discussed in detail in the range of operating variables investigated. Empirical correlations by dimensional analysis were obtained and feed‐forward back propagation neural network models were employed to predict the gas–liquid volumetric mass transfer coefficient and liquid‐side mass transfer coefficient for an air–water–hollow glass microspheres system in a commercial‐scale bubble column slurry reactor. © 2012 Canadian Society for Chemical Engineering     

Hydrodynamics,Mass Transfer and Gas Scrubbing in a Co‐current Droplet Column Operating at High Gas Velocities

The main objective of this work was to propose a new process for household fume incineration treatment: the droplet column. A feature of this upward gas‐liquid reactor which makes it original, is to use high superficial gas velocities (13 m s^–1) which allow acid gas scrubbing at low energy costs. Tests were conducted to characterize the hydrodynamics, mass transfer performances, and acid gas scrubbing under various conditions of superficial gas velocity (from 10.0 to 12.0 m s^–1) and superficial liquid velocity (from 9.4·10^–3 to 18.9·10^–3 m s^–1). The following parameters characterized the hydrodynamics: pressure drops, liquid hold‐ups, and liquid residence time distribution were identified and investigated with respect to flow conditions. To characterize mass transfer in the droplet column, three parameters were determined: the gas‐liquid interfacial area (a), the liquid‐phase volumetric mass transfer coefficient (k_La) and the gas‐phase volumetric mass transfer coefficient (k_Ga). Gas absorption with chemical reaction methods were applied to evaluate a and k_Ga, while a physical absorption method was used to estimate k_La. The influence of the gas and liquid velocities on a, k_La, and k_Ga were investigated. Furthermore, tests were conducted to examine the utility of the droplet column for the acid gas scrubbing, of gases like hydrogen chloride (HCl) and sulfur dioxide (SO₂). This is a process of high efficiency and the amount of pollutants in the cleaned air is always much lower than the regulatory European standards imposed on household waste incinerators.     

Mass transfer behaviour of gas-liquid jet loop reactors

A special type of jet loop reactor (JLR), designed for continuous operation and short residence times was investigated with regard to its mass transfer behaviour, described by the volumetric mass transfer coefficient k_La. The jet stream and superficial gas velocities are varied in two JLRs of different sizes, equipped with different nozzles. Fully desalinated water, 0.08 molar NaCI solution and solutions of different concentration of carboxymethyl cellulose (CMC) are used as the liquid phase. A steady-state physical method is employed to determine k_La: air oxygen is purged from the liquid phase by gaseous nitrogen. The measurements show that the reactor is characterized by high power density and high mass transfer performance. No limit of mass transfer capacity was observed in the chosen ranges of volumetric gas and liquid flow rates, i.e. at a given jet stream velocity, the relationship between k_La and the superficial gas velocity is nearly linear. The investigations show that the mass transfer contributed by the jet stream largely depends on liquid phase composition.     

Gas–liquid mass transfer studies for biomass support materials in a bioreactor

BACKGROUND: Oxygen mass transfer can be described and analyzed by means of the mass transfer coefficient k_La, which is the most important parameter involved in the design and operation of mixing–sparging equipment for bioreactors. In the present study, the effect of biomass support materials on the gas–liquid mass transfer coefficient was studied in a bioreactor under variable process conditions. The biomass support materials used were activated carbon, pumice and loofa sponge. RESULTS: Compared with the case with distilled water only, the presence of the biomass support materials negatively influenced mass transfer. On the other hand, the mass transfer coefficient increased with increased impeller speed, air flow rate and temperature; and decreased with the increase of liquid viscosity and biomass support material concentration for all cases. CONCLUSIONS: Evaluation of the experimental data showed that k_La values were affected by process variables. Besides the major exponential correlations used in the literature, satisfactory linear correlations for the relationship between the k_La and process variables were obtained. Copyright © 2010 Society of Chemical Industry     

Mass Transfer Characteristics of Syngas Components in Slurry System at Industrial Conditions

The gas‐liquid mass transfer behavior of syngas components, H₂ and CO, has been studied in a three‐phase bubble column reactor at industrial conditions. The influences of the main operating conditions, such as temperature, pressure, superficial gas velocity and solid concentration, have been studied systematically. The volumetric liquid‐side mass transfer coefficient k_La is obtained by measuring the dissolution rate of H₂ and CO. The gas holdup and the bubble size distribution in the reactor are measured by an optical fiber technique, the specific gas‐liquid interfacial area aand the liquid‐side mass transfer coefficient k_L are calculated based on the experimental measurements. Empirical correlations are proposed to predict k_L and a values for H₂ and CO in liquid paraffin/solid particles slurry bubble column reactors.     

Gas‐liquid mass transfer in low‐ and medium‐consistency pulp suspensions

The volumetric gas—liquid mass transfer coefficient (k_La) was measured for low‐ and medium‐consistency pulp suspensions using the cobalt‐catalyzed sulfite oxidation technique. Mass transfer rates were measured in a high‐shear mixer for a range of operating parameters, including the rotor speed (N = 10 to 50 rev/s), gas void fraction (X_g = 0.10 to 0.40) and fibre mass concentration (C_m = 0.0 to 0.10). k_La measurements were compared with the macroscale flow regime in the vessel (characterized using photographic techniques) and correlated with energy dissipation, gas void fraction and suspension mass concentration in the mixer. We found that gas‐liquid mass transfer was significantly reduced in pulp suspensions, even for low suspension concentrations. Part of this reduction was associated with dissolved components leached from the fibres into the liquid phase. This could account for reductions in k_La of up to 30% when compared with distilled water. The fibres further reduced k_La, with the magnitude of the decrease depending on the fibre mass concentration. Correlations were developed for k_La and compared with results available in the literature.     

Influence of current density on oxygen transfer in an electroflotation cell

The objective of this work is to study the transfer of oxygen from gas to liquid phase in an electroflotation cell. The measurements were performed in a laboratory scale cell using insoluble electrodes, titanium coated with ruthenium oxide as anode and stainless steel as cathode. The volumetric mass transfer coefficient K _L a, was characterized for clean tap water as liquid phase for different values of current density (J). The global coefficient of mass transfer based on the liquid film, K _L , and the specific interfacial area, a, were characterized. A model which relates K _L a to current density was established. Different evaluation criteria of oxygen transfer in electroflotation process were determined and compared with other aeration process.     

Gas Holdup and Volumetric Mass Transfer Coefficient in a Slurry Bubble Column

The gas holdup, ?, and volumetric mass transfer coefficient, k_La, were measured in a 0.051 m diameter glass column with ethanol as the liquid phase and cobalt catalyst as the solid phase in concentrations of 1.0 and 3.8 vol.‐%. The superficial gas velocity U was varied in the range from 0 to 0.11 m/s, spanning both the homogeneous and heterogeneous flow regimes. Experimental results show that increasing catalyst concentration decreases the gas holdup to a significant extent. The volumetric mass transfer coefficient, k_La, closely follows the trend in gas holdup. Above a superficial gas velocity of 0.04 m/s the value of k_La/? was found to be practically independent of slurry concentration and the gas velocity U; the value of this parameter is found to be about 0.45 s^–1. Our studies provide a simple method for the estimation of k_La in industrial‐size bubble column slurry reactors.     

A contribution to the measurement of oxygen mass transfer in a laboratory pressure reactor

A method was used to measure the liquid‐side volumetric coefficient of oxygen mass transfer (k_La) in closed, semi‐batch pressure reactors used in hydrometallurgical laboratories. In this method, the oxygen pressure was monitored as oxygen was continuously sparged into a pressure vessel containing a sodium sulfite solution. A material balance equation was derived for oxygen in the vessel and the experimental data were fitted to this equation. From the constant parameters of the equation, k_La was calculated. The solution in the vessel also contained an appropriate amount of cobalt catalyst so that oxygen was consumed rapidly by oxidation of sulfite to sulfate. Under these conditions, the oxygen concentration in the bulk liquid phase could be assumed to be equal to zero. Values of k_La determined by the method under various conditions were reproduced within 12% deviation from the average values. k_La was found to increase moderately with temperature in the range of 25 to 75 °C, with an activation energy of 33.09 ± 1.33 kJ mol⁻¹. The presence of hydrophobic or hydrophilic solids was found to have a deleterious effect on k_La. © 2000 Society of Chemical Industry     

Measurement of mass transfer coefficient in an airlift reactor with internal loop using coalescent and non‐coalescent liquid media

In this work the sulfite oxidation (SOM), dynamic pressure‐step (DPM) and gassing‐out (GOM) methods were compared for volumetric mass transfer coefficient measurement in an airlift reactor with internal loop. As a liquid phase both, non‐coalescent and coalescent media were used. Among the methods discussed here, the mass transfer coefficient (k_La) values obtained by the DPM appear as the most reliable as they were found to be independent of oxygen concentration in the inlet gas, which confirmed the physical correctness of this method. The difference between data measured using air and oxygen was not higher than 10%, which was comparable to the scatter of experimental data. It has been found that the sulfite oxidation method yielded k_La values only a little higher than those obtained by the DPM and the difference did not exceed 10%. Up to an inlet gas velocity (U_GC) of ?0.03 m s^?1 the GOM using oxygen as a gas medium gave k_La values in fact identical with those obtained by the DPM. At higher flows of the inlet gas, the GOM yielded k_La values as much as 15% lower. The enhancement in oxygen mass transfer rate determined in non‐coalescent media was estimated to be up to +15%, when compared with a coalescent batch. The experimental dependence of k_La vs the overall gas hold‐up was described by an empirical correlation. 1 Copyright © 2004 Society of Chemical Industry     

Improving Gas‐Liquid Mass Transfer in Bubble Columns by Applying Low‐Frequency Vibrations

We show that application of low‐frequency vibrations, in the 50–200 Hz range, to the liquid phase of an air‐water bubble column causes significantly smaller bubbles to be generated at the distributor plate. For bubble column operation in the homogeneous flow regime, measurements of the volumetric mass transfer coefficient using the oxygen absorption technique show that the increase in the k_La values ranges from 50–100 % depending on the flow rate. It is concluded that application of low‐frequency vibration has the potential of improving the performance of bubble columns.     

Comparison of Hydrodynamics and Mass Transfer in Airlift and Bubble Column Reactors Using CFD

Computational Fluid Dynamics (CFD) is used to compare the hydrodynamics and mass transfer of an internal airlift reactor with that of a bubble column reactor, operating with an air/water system in the homogeneous bubble flow regime. The liquid circulation velocities are significantly higher in the airlift configuration than in bubble columns, leading to significantly lower gas holdups. Within the riser of the airlift, the gas and liquid phases are virtually in plug flow, whereas in bubble columns the gas and liquid phases follow parabolic velocity distributions. When compared at the same superficial gas velocity, the volumetric mass transfer coefficient, k_La, for an airlift is significantly lower than that for a bubble column. However, when the results are compared at the same values of gas holdup, the values of k_La are practically identical.     

Surfactant Effects on Aeration Performance of Stirred Tank Reactors

The effect of surfactants on aeration performance in stirred tank reactors (STR) at high rates of foaming is studied. The volumetric oxygen transfer coefficient (k_La) and foaming activity estimated as foaming height (H_f) were determined. Biotechnology of lipopeptide biosurfactants from aerobic organisms, e.g., Bacillus subtilis were addressed. Using model solutions of known foam‐generating properties, high‐molecular weight surfactin and low‐molecular weight sodium dodecyl sulphate (SDS), as well as impellers of different types, with flat and fluid‐foil blades, clues on the concentration dependence of STR oxygen transfer and foaming as well as options for foam reduction in the presence of biosurfactant were sought. In response to a two‐fold decrease of surface tension by surfactin, k_La values decreased up to 30 % but remained within the range expected for the mixing system in water; the experiments with SDS showing stronger dependence on surfactant concentration and surface tension. Mixing of surfactant media by a standard six‐blade disc turbine (RT) imposed rate limitations on gassing. A low‐shear impeller Narcissus (NS) could be used to avoid bulk foam outflow, while preserving k_La values that remained unchanged. The ‘power per unit volume' correlation of k_La in stirred tanks is tested in the presence of surfactin.     

Instantaneous Mass Transfer under Gas‐Liquid Taylor Flow in Circular Capillaries

The mass transfer process under CO₂‐water Taylor flow was experimentally investigated in circular capillaries with different lengths. The measured volumetric mass transfer coefficient k_La was found to reduce with the increase of mass transfer time under the same operational conditions. With computational fluid dynamics simulations, the instantaneous k_La values decreased sharply at the initial stage of the mass transfer process. The effects of numerous experimental parameters on separated contribution of k_La were investigated for different dimensionless mass transfer times. The instantaneous k_La values for arbitary transfer times could be calculated and agreed well with experimental data.     

On the Effect of Surfactant on Mass Transfer to Water–Glycerol Solutions in a Pulsed Baffled Reactor

This paper describes the effect of surfactant (0·025%w/w octanol) on mass transfer of oxygen into water–glycerol solutions of viscosity up to 21 mPa s in a pulsed baffled reactor. We also report the effect of air entrainment on the volumetric mass transfer coefficient in the open reactor system. The results show that the presence of octanol in solutions increases the mass transfer rate for all the experimental conditions tested, in particular, a higher percentage increase in k_La was obtained for more viscous solutions. This behaviour can be attributed to the non-coalescing characteristics of the octanol that is added to the water–glycerol solutions. The results of air entrainment on k_La suggest that the effect of the surface air entrained into the system on k_La measurement is insignificant. © 1997 SCI.     

Gas‐Liquid Mass Transfer in Fibrous Bed Reactor with Counter‐Current Liquid Recycle

In this work, the gas‐liquid mass transfer in a lab‐scale fibrous bed reactor with liquid recycle was studied. The volumetric gas‐liquid mass transfer coefficient, k_La, is determined over a range of the superficial liquid velocity (0.0042–0.0126 m.s^–1), gas velocity (0.006–0.021 m.s^–1), surface tension (35–72 mN/m), and viscosity (1–6 mPa.s). Increasing fluid velocities and viscosity, and decreasing interfacial tension, the volumetric oxygen transfer coefficient increased. In contrast to the case of co‐current flow, the effect of gas superficial velocity was found to be more significant than the liquid superficial velocity. This behavior is explained by variation of the coalescing gas fraction and the reduction in bubble size. A correlation for k_La is proposed. The predicted values deviate within ± 15 % from the experimental values, thus, implying that the equation can be used to predict gas‐liquid mass transfer rates in fibrous bed recycle bioreactors.     

Gas‐Liquid Mass Transfer in Pulp Retention Towers

The volumetric gas‐liquid mass transfer rate, k_La, was measured under batch conditions in a 0.28 m diameter laboratory‐scale retention column. Tests on water, and on unbleached kraft (UBK) pulp suspensions (mass fractions, C_m from 0.013 to 0.09) were made with air or nitrogen sparged through the column at superficial gas velocities between 0.0015 to 0.05 m/s. k_La varied with suspension mass concentration and superficial gas velocity, initially decreasing with increasing mass concentration, reaching a minimum between C_m = 0.03 and 0.06, and then increasing. The minimum in k_La coincided with a change in hydrodynamics within the column, from bubble column behaviour below C_m = 0.03 to porous solid behaviour above C_m = 0.06.