Volumetric mass transfer coefficients in an internal loop airlift reactor with low‐density particles

The influence of organic additives (propanol, benzoic acid, isoamyl alcohol and carboxymethylcellulose) on the volumetric mass transfer coefficient, k_La, in an internal loop airlift reactor with low‐density particles (nylon‐6 and polystyrene) was investigated. The k_La values increased with increase in superficial gas velocity, U_sg, and decreased with increase in solid loading. A draft tube to reactor diameter ratio, D_R/D, of 0.4 gave maximum k_La values. The addition of benzoic acid and propanol increased the k_La values owing to their coalescence inhibiting characteristics. The addition of isoamyl alcohol decreased k_La, owing to the formation of rigid bubbles and recirculation of small bubbles having a low oxygen content. The k_La values decreased with increase in the concentration of the non‐Newtonian fluid carboxymethylcellulose (CMC). The proposed correlations predicted the experimental data well. Copyright © 2006 Society of Chemical Industry     

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.     

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     

Gas‐Liquid Mass Transfer Rates and Impeller Power Consumptions for Industrial Vessel Design

Volumetric mass transfer coefficients (k_La) and power input (P) are often the key parameters in the design of gas‐liquid contactors. However, due to the limitations of most measurement methods, there is a lack of reliable data for predicting k_La for non‐coalescent batches under high energy dissipation rates. Accurate k_La and P correlations are proposed. The reliability of the correlations is ensured by using experimental data from a wide range of process conditions conducted in multiple‐impeller vessels of both laboratory scale and pilot scale, and including both non‐coalescent and coalescent batches. Applying the proposed correlations, the scale‐up and optimization of industrial vessels can be performed more accurately.     

Studies on the hydrodynamic behavior and mass transfer in a down‐flow jet loop reactor with a coaxial draft tube

The effects of certain pertinent parameters such as gas and liquid flow rates and nozzle position on the behavior of a down‐flow jet loop reactor (DJR) have been studied. The mean residence times of gas and liquid phases and the gas holdup within the reactor have been measured. In addition, the overall volumetric mass transfer coefficient, and the influence of the gas flow rate and the position of the nozzle inside the draft tube on the latter has been determined. Correlations have been presented for the gas holdup and k_La which take into account the length of the draft tube and the nozzle immersion height. The k_La values obtained at different power per unit volume (P/V) values in the DJR used in the present study compare favorably with data presented for stirred tanks and bubble columns in the literature. The liquid residence time distribution (RTD) within the reactor has been studied by tracer analysis for various operating conditions and nozzle immersion height and the results are indicative of the high mixing intensities that can be obtained in such reactions. © 2001 Society of Chemical Industry     

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.     

Influence of top‐section design and draft‐tube height on the performance of airlift bioreactors containing water‐in‐oil microemulsion

The mixing and mass transfer characteristics of draft‐tube airlift bioreactors (DTAB) for a water‐in‐kerosene microemulsion, as a cold model of petroleum biodesulfurization, were studied. Incomplete gas disengagement at the top‐section of the DTAB and hence high gas recirculation were obtained with the microemulsion system for all the top‐section configurations employed in the present study especially at the high airflow rates. The ratio (S) of the volumes of the riser and the downcomer to the top‐section together with the gas disengagement abilities of the gas separator were both found to affect the mixing performance of the DTAB employed for the microemulsion system. Increase in the draft‐tube height resulted in significant increase in the mixing time (t_m) and a slight increase in the overall volumetric oxygen transfer coefficient (k_La). Increase in the diameter of the top‐section and the height of the liquid above the draft‐tube led to a decrease in k_La, the latter effect being less prominent. New correlations were developed that predicted the mixing time and oxygen transfer coefficients obtained in the present work with reasonable accuracy. Copyright © 2004 Society of Chemical Industry     

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.     

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 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 “dead-end” autoclave reactors

Gas-liquid volumetric mass transfer coefficients, (k_La), have been obtained for “dead-end” autoclave reactors operated in two different modes: (a) gas introduced into the gas phase, and (b) gas introduced through a dip-tube in the liquid. Three different methods of k_La determination have been compared. Effects of agitation speed, impeller diameter, gas to liquid volume ratio (V_g/V_L), position of the impeller and reactor size on k_La have been investigated. The k_La data were found to be correlated as: k_La = 1.48 × 10^?3 (N)^2.18 (V_g/V_L)^1.88 (d_I/d_T)^2.16 (h₁/h₂)^1.16 The critical speed of surface breakage, at which transition from the surface convection to the surface entrainment regime occurs, was also determined for different impeller positions, impeller diameters and gas to liquid volume ratios.     

Effect of catalyst loading on gasliquid mass transfer in a slurry reactor: A statistical experimental approach

A statistical experimental design was employed to study the effects of pressure, temperature, catalyst loading, and mixing speed on the solubilities (C*) and volumetric gas/liquid mass transfer coefficients (k_L^a) for H₂, N₂, CO, CH₄ and C₂H₄ in a liquid mixture of hexanes containing iron oxide catalyst in a 4-litre agitated autoclave. Statistical correlations for k_L^a values for the gases used were developed. Mixing speed and solid concentration showed the strongest effects on k_L^a. At low catalyst concentrations, a maximum in k_L^a was observed and at concentrations > 37 mass%, k_L^a decreased by more than one order of magnitude.     

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.     

Statistical assessment of gas/liquid mass transfer in slurry-phase propylene polymerization process

A statistical approach was developed to investigate the effects of pressure, temperature, mixing speed and solid concentration on k_La for gaseous hydrogen, ethylene, and propylene in liquid n-hexane containing solid polypropylene powder in a 4-litre agitated reactor. The solubilities of the gases appeared to follow Henry's Law. Statistical correlations to predict k_La were proposed and response surfaces were constructed. k_La values appeared to reach a maximum around 15 mass% and sharply decrease above 30 mass%. The effects of pressure and temperature on k_La were found to depend on the gas-liquid system and operating conditions used.     

Efficiency of a Gas‐Liquid Contactor for the Oxygenation of Activated Sludge: Assessment of Mass Transfer Coefficient

The aim of this work is to investigate a co‐current air‐liquid downward flow bubble column with air entrainment by liquid injection nozzle in order to use it as an aerator in activated sludge treatment plants. The study concerns the determination of mass transfer efficiency by measuring the mass transfer coefficient, k_La, both in clean water and in activated sludge. In clean water, this parameter is determined by three methods, i.e., gassing out method, absorption with chemical reaction and off‐gas method. In activated sludge medium, k_La values are measured by two methods, i.e., sludge reoxygenation and the hydrogen‐peroxide method. The values of k_La obtained in clean water are compared to those obtained in sludge, enabling the assessment of the α factor, i.e., ratio of oxygen transfer coefficient sludge/clean water. The results are in good agreement with those reported previously in the literature.     

A three‐phase fluidized bed reactor in the combined anaerobic/aerobic treatment of wastewater

Aerobic degradation or polishing is an essential step in the combined anaerobic/aerobic treatment of wastewater. In this study, a type of porous glass beads was used for immobilization of microbial cells in a three‐phase aerobic fluidized bed reactor (AFBR) with an external liquid circulation. The effects of superficial gas and liquid velocities on bed expansion, solid and gas hold‐ups and specific oxygen mass transfer rate, k_La, were investigated. A tracer study showed that the mixing and flow pattern in the 8 dm³ reactor could be simulated by a non‐ideal model of two continuous stirred tank reactors (CSTRs) in series. By treating an effluent from an upflow anaerobic sludge blanket (UASB) digester, the distribution of suspended and immobilized biomass in the reactor as well as the kinetics of COD removal were determined. The specific oxygen mass transfer rate, k_La, at a superficial gas velocity of 0.7 cm s⁻¹ dropped by about 30% from 32 h⁻¹ in tap water to 22 h⁻¹ after a carrier load of 15% (v/v) was added. The measured k_La further dropped by about 20% to 18 h⁻¹ in the wastewater, a typical value of the bubbling fermenters with no stirring. Compared with the aerobic heterotrophs under optimum growth conditions, the microbes in this reactor which was fed with anaerobic effluent plus biomass behaved like oligotrophs and showed slow specific COD removal rates. This might be attributed to the presence of a significant amount of obligate anaerobes and facultative organisms in the aerobic reactor. This was confirmed by a relatively low intrinsic oxygen uptake rate of the microbial population in the reactor, 94 mg O₂ dm⁻³ h⁻¹ or 19 mg O₂g VS⁻¹ h⁻¹. © 1999 Society of Chemical Industry     

A computational method for determination of the mass-transfer coefficient in packed-bed immobilized enzyme reactors

A computational method was developed that determined the mass-transfer coefficient k_L or the volumetric mass-transfer coefficient k_La in packed-bed immobilized enzyme (IME) reactors. To study the performance of this method, two experimental systems were considered where an enzyme was immobilized on a non-porous support surface (surface-IME system) or within a porous support (pore-IME system). The values of k_L and k_La determined in these packed-bed IME reactor systems were successfully expressed in terms of the substrate concentration at the reactor inlet and the liquid flow rate. Furthermore, the correlations obtained for k_L and k_La were used to calculate the unconverted fractions of substrate at the reactor outlet. Comparison showed that the calculated results were in satisfactory agreement with the experimental values.     

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.     

CFD Prediction of the Critical Agitation Speed for Complete Dispersion in Liquid‐Liquid Stirred Reactors

A computational fluid dynamics (CFD) model is adopted to simulate the turbulent immiscible liquid‐liquid flow in a stirred vessel based on a two‐fluid model with a k‐ϵ‐A_P turbulence model. An improved inner‐outer iterative procedure is adopted to deal with the impeller rotation in a fully baffled stirred tank. Different drag formulations are examined, and the effect of the droplet size on both the dispersed phase holdup distribution and the velocity field is analyzed. Two different numerical criteria are tested for determining the critical impeller speed for complete dispersion. The simulated critical impeller speeds are generally in good agreement with the correlations in the literature when the fixed droplet size is properly selected. This demonstrates that the modeling approach and the numerical criteria proposed in this work are promising for predicting the dispersion characteristics in liquid‐liquid stirred tanks.     

Semi‐theoretical prediction of volumetric mass transfer coefficients in bubble columns with organic liquids at ambient and elevated temperatures

A semi‐theoretical approach for predicting k_La values (referred to liquid volume) in 18 organic liquids [acetone, aniline, 1‐butanol, benzene, cyclohexane, decalin, 1,2‐dichloroethane, 1,4‐dioxane, ethanol (96%), ethylacetate, ethylbenzene, ligroin, methanol, nitrobenzene, 2‐propanol, tetralin, toluene, and xylene] at various operating conditions (including elevated temperatures and pressures) was developed. It was found that the approach is applicable regardless of the hydrodynamic regime (at u_G ≤ 0.1 m/s). Temperatures up to 353 K and pressures up to 0.5 MPa were tested. Two different distributors (multiple‐hole and single‐hole type) were employed. The liquid‐phase mass transfer coefficient k_L was calculated theoretically from the penetration theory on the basis of original definition of gas–liquid contact time. The interfacial area a was defined with respect to the liquid volume. It was found that their product k_La must be multiplied by some correction factor in order to take account of the non‐spherical (ellipsoidal) shape of the bubbles. When the correction term is correlated to both the Eötvös number (Eo) and the dimensionless temperature ratio, 198 experimental k_La values can be fitted reasonably well (average relative error 9.3%).