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1.
Correlations that allow determination of gas film mass transfer coefficients (kGat, kGaw) and liquid film mass transfer coefficients (kLaw) for packing materials used in biofilters and biotrickling filters for air pollution control are presented. Lava rock, polyurethane foam cubes (PUF), Pall rings, porous ceramic beads, porous ceramic Raschig rings, and various compost-woodchips mixtures were used as packing materials. The functionality of gas and liquid velocity on mass transfer coefficients (kGat,kGaw,kLaw) obtained experimentally (see Part 1 of this paper) was correlated using modified Onda-type equations. The correlation equations helped to better understand the sensitivity of gas and liquid velocities on mass transfer, and the effects of packing wetting. Each packing had a different functionality with gas and liquid velocity and different wetting property, hence different correlation equations were needed for the different packing materials. Most of the fitted data fell within ±20% of the experimental values.  相似文献   

2.
Overall mass transfer coefficients (KGa and KLa) were determined experimentally for four different‐nature packing materials used in gas‐phase biotrickling filters. A simple methodology based on overall mass balances and following a standard procedure allowed to calculate the mass transfer coefficients under different operating conditions corresponding to usual biotrickling filtration situations. Results showed an increase of mass transfer resistance when increasing the empty bed residence time (EBRT) of the reactor for all packing materials. Experimental results were fitted to existing and well‐accepted correlations used in conventional biofilter or biotrickling filter modeling. The comparison of experimental and theoretical data showed huge discrepancies. Simple correlations for the experimental data obtained in this study were also suggested.  相似文献   

3.
The interfacial area in the Taylor (slug) gas–liquid flow in a microchannel was measured by the Danckwerts' (chemical) method, using CO2 absorption from the CO2/N2 mixture into KHCO3/K2CO3 buffer solutions, containing NaOCl as a catalyst. The rate of absorption was determined and the Danckwerts' plots were constructed. Reasonable agreement with the geometrical area measured photographically was obtained. This fact allowed to determine for the first time the mass transfer coefficients separately for liquid film and liquid caps. A correlation for the calculation of mass transfer coefficients has been proposed.  相似文献   

4.
Volumetric mass transfer coefficients in liquid and vapour phases in distillation column were measured by the method consisting of a fitting of the concentration profile of liquid phase along the column obtained by the integration of a differential model to the experimental one. The mathematical model of distillation process includes mass and energy balances and the heat and mass transfer equations. The film model flux expressions with the convective transport contributions have been considered in the transfer equations. Vapour and liquid phases are supposed to be at their saturated temperatures along the column. Effect of changes of phase flows and physical properties of phases on the mass transfer coefficients along the column and non-ideal thermodynamic behaviour of the liquid phase have been taken into account. The concentration profiles of liquid phase are measured in the binary distillation of the ethanol-water and methanol-ethanol systems at total reflux on metal Pall Rings and Intalox saddles 25 mm in the column with diameter of 150 mm. The distillation mass transfer coefficients obtained by the fitting procedure are compared with those calculated from absorption data using Onda's, Billet's and Linek's correlations. The distillation heat transfer coefficients calculated from the model assuming saturated temperatures in both phases are compared with those calculated from the Chilton-Colburn and penetration model analogy between mass and heat transfer. The results have confirmed an agreement neither between distillation and from absorption correlations calculated mass transfer coefficients nor between analogy and from enthalpy balance calculated heat transfer coefficients. Also the concentration profiles obtained by the integration of the differential model of the distillation column using the coefficients from absorption correlation have differed from the experimental profiles considerably.  相似文献   

5.
The absorption of oxygen and styrene in water-silicone oil emulsions was independently studied in laboratory-scale bubble reactors at a constant gas flow rate for the whole range of emulsion compositions (0-10% v/v). The volumetric mass transfer coefficients to the emulsions were experimentally measured using a dynamic absorption method. It was assumed that the gas phase contacts preferentially the water phase. In the case of oxygen absorption, it was found that the addition of silicone oil hinders oxygen mass transfer compared to an air-water system. Decreases in kLaoxygen of up to 25% were noted. Such decreases in the oxygen mass transfer coefficient, which imply longer aeration times to transfer oxygen, could represent a limiting step in biotechnological processes strongly dependent on oxygen concentration. Nevertheless, as the large affinity of silicone oil for oxygen enables greater amounts of oxygen to be transferred from the gas phase, it appears that the addition of more than 5% silicone oil should be beneficial to increase the oxygen transfer rate. In the case of styrene absorption, it was established that the volumetric mass transfer coefficient based on the emulsion volume is roughly constant with the increase in the emulsion composition. In spite of the relatively high cost of silicone oil, water-silicone oil emulsions remain relevant to treat low-solubility volatile organic compounds, such as styrene, in low-concentration gas streams.  相似文献   

6.
The influences of operating parameters such as channel size, flow rate, and void fraction on the mass transfer rate in the gas–liquid slug flow are investigated to establish a design method to determine the parameters for rapid mass transfer. From the experimental results, the turnover index, including the slug linear velocity, its length, and the channel size that represents the turnover frequency of the internal circulation flow, is proposed. For PTFE tube in which no liquid film exists in slug flow, a master curve is derived from the relationship between the mass transfer coefficient and the turnover index. For each channel material, the Sherwood number is also roughly correlated with the Peclet number. These correlations make it possible to arbitrarily determine a set of operating parameters to achieve the desired mass transfer rate. However, the turnover index and the Peclet number include the slug length, which cannot be controlled directly. The relationship between the slug length and the operating parameters is also investigated. The slug volume mainly depends on the inner diameter (i.d.) of a union tee. At a fixed union tee i.d., the slug length is controlled through the exit i.d. of the channel connected to the union tee and the void fraction. Thus, the final slug length depends on the union tee and exit channel inner diameters. At low flow rates, the gas and liquid collision angle is significant in determining the slug length.  相似文献   

7.
An experimental study of steady-state selective catalytic reduction (SCR) of NOx with NH3 on both Fe-ZSM-5 and Cu-ZSM-5 monolithic catalysts was carried out to investigate the extent of mass transfer limitations in various SCR reactions. Catalysts with different washcoat loadings, washcoat thicknesses and lengths were synthesized for this purpose. SCR system reactions examined included NO oxidation, NH3 oxidation, standard SCR, fast SCR and NO2 SCR. Comparisons of conversions obtained on catalysts with the same washcoat volumes but different washcoat thicknesses indicated the presence of washcoat diffusion limitations. NH3 oxidation, an important side reaction in SCR system, showed the presence of washcoat diffusion limitations starting at 350 °C on Fe-zeolite and 300 °C on Cu-zeolite catalysts. Washcoat diffusion limitations were observed for the standard SCR reaction (NH3+NO+O2) on both Fe-zeolite (≥350 °C) and Cu-zeolite (≥250 °C). For the fast (NH3+NO+NO2) and NO2 SCR (NH3+NO2) reactions, diffusion limitations were observed throughout the temperature range explored (200–550 °C). The experimental findings are corroborated by theoretical analyses. Even though the experimentally observed differences in conversions clearly indicate the presence of washcoat diffusion limitations, the contribution of external mass transfer was also found to be important under certain conditions. The transition temperatures for shifts in controlling regimes from kinetic to washcoat diffusion to external mass transfer are determined using simplified kinetics. The findings indicate the necessity of inclusion of mass transfer limitations in SCR modeling, catalyst design and optimization.  相似文献   

8.
Volatile organic compounds (VOCs) cause nuisance to humans and the environment. Recent legislation encourages industrialists to set up equipment for treating their VOC-loaded gaseous effluents. This piece of research studies the absorption process, using a viscous organic absorbent (di(2-ethylhexyl) adipate=DEHA) to treat a toluene-loaded vent gas, in terms of hydrodynamics and mass transfer. It is shown that DEHA does not lead to an excessive pressure drop. Correlations predicting hydrodynamic parameters from previous literature are summarised and tested against experimental results. It is shown that acceptable prediction accuracy can be achieved for counter-current pressure drop and liquid hold-up. Treatment efficiency for the toluene-loaded vent gas is shown to be very good. Calculation of mass transfer constants (kLa) enables to test literature correlations against the experimental results. The mass transfer is supposed to be limited by the liquid-side resistance. Our experimental results showed that the kLa of the system depends on the liquid velocity but also on the gas velocity. This behaviour has also been observed by the few authors who have used viscous fluids in their experiments, but is contrary to all the authors who have work on low-viscosity fluids. It is therefore clear that the influence of viscosity on the phenomenon is considerable. Not one current correlation is currently accurate in the case of a viscous absorbent.  相似文献   

9.
Conventional design of circulating fluidized beds requires the knowledge of dispersion and mass transfer coefficients, expressed in dimensionless forms as Sherwood numbers. However, these are known to vary by five or more orders of magnitude. Furthermore, the Sherwood numbers for fine particles reported in the literature are several orders of magnitude lower than the Sherwood number of two for diffusion to a single particle. We have shown that by replacing the particle diameter in the conventional Sherwood number with cluster or bubble diameter, the modified Sherwood number is again of the order of two.We have also shown that the kinetic theory based computational fluid dynamics codes correctly compute the dispersion and mass transfer coefficients. Hence, the kinetic theory based computational fluid dynamics codes can be used for fluidized bed reactor design without any such inputs.  相似文献   

10.
In this work, the effects of surface-active contaminants on mass transfer coefficients kLa and kL were studied in two different bubble contactors. The oxygen transfer coefficient, kL, was obtained from the volumetric oxygen transfer coefficient, kLa, since the specific interfacial area, a, could be determined from the fractional gas holdup, ε, and the average bubble diameter, d32. Water at different heights and antifoam solutions of 0.5- were used as working media, under varying gas sparging conditions, in small-scale bubble column and rectangular airlift contactors of 6.7 and capacity, respectively. Both the antifoam concentration and the bubble residence time were shown to control kLa and kL values over a span of almost 400%. A theoretical interpretation is proposed based on modelling the kinetics of single bubble contamination, followed by sudden surface transition from mobile to rigid condition, in accordance with the stagnant cap model. Model results match experimental kL data within ±30%.  相似文献   

11.
Desorption of oxygen and hydrogen from various liquids (water, 0.8 molar sodium sulphate solution) containing suspended particles of activated carbon at various solid loading was investigated. The desorption was used to avoid supersaturation effect which was observed during oxygen and hydrogen absorption into liquid saturated with nitrogen. Experiments were carried out in a stirred cell with flat gas-liquid interface at and atmospheric pressure. An increase of kL upon addition of the particles was observed. Enhancement factor increases with increasing contact time of the particles with liquid reaching maximum steady-state value of approx. 3 after sufficiently long time (a few hours) regardless of solid loading , agitator frequency and solute gas (O2,H2). The results fit the correlation (e is specific power dissipated by agitator in liquid and D is molecular diffusivity of gas absorbed) with the exponent for liquids without and for the liquids with the particles. It indicates that the interface is rigid in absence of particles and hinders the motion of liquid along the interface forming boundary layer while in the presence of particles the interface is completely mobile and surface renewal proceeds according to the penetration model. These results confirm a finding of Kaya and Schumpe (2005) that the enhancement of mass transfer in the cell at the presence of hydrophobic solids is due to clean-up of the interface from surfactants by their adsorption on hydrophobic solids rather than by a “shuttle mechanism” exerted by particles with a high adsorption capacity for the transfer component.  相似文献   

12.
In this study, the absorption of carbon dioxide by the absorbent which was composed of 2-amino-2-methyl-l-propanol (AMP) + piperazine (PZ) or methyldiethanolamine (MDEA) + piperazine (PZ) in polyvinylidinefluoride (PVDF) and polypropylene (PP) membrane contactors werewas examined. Three resistances were considered in each hollow fiber, i.e., liquid-film diffusion, membrane diffusion, and gas-film diffusion. The mass transfer resistance of membrane km was influenced by the wetting ratio using an absorbent with higher reaction rate. The wetting ratio was affected by contact angle between the membrane and absorbent and the viscosity of absorbent. The calculated absorption rates considering wetting ratio of membrane and using the modified correlation equation of gas-phase mass transfer coefficient were reasonably agreeable to those of measured ones (standard deviation, 4%). The fractional resistance of each transport step during the experiments was then determined. The rate-controlling step was dominated by the resistance of gas-film diffusion with mixed absorbents. The absorption rates of CO2 increase with the increasing of gas flow rates in the most experimental cases. The resistance of liquid-film diffusion was only important using an absorbent with lower reaction rate. The rate-controlling step was the membrane diffusion only at higher gas flow rate with the absorbent composed of AMP and PZ in PVDF hollow fiber membrane contactor.  相似文献   

13.
The two-equation porous medium model has been widely employed for modeling the flow-through monolithic catalytic converter. In this model, the interfacial heat and mass transfer coefficients have been usually obtained using the asymptotic Nusselt and Sherwood numbers with some suitable assumptions. However, previously it seemed that there existed some misunderstanding in adopting these Nusselt and Sherwood numbers. Up to now, the Nusselt number based on the fluid bulk mean temperature has been used for determining the interfacial heat and mass transfer coefficients. However, the mass and energy balance formulations in the two-equation model indicate that the Nusselt number should be evaluated based on the fluid mean temperature instead of the fluid bulk mean temperature. Therefore, in this study, to correctly model the heat and mass transfer coefficients, the Nusselt number based on the fluid mean temperature was newly obtained for the square and circular cross-sections under two different thermal boundary conditions (i.e., constant heat flux and constant temperature at the wall). In order to do that, the present study employed the numerical as well as analytical method.  相似文献   

14.
Absorption of hydrophobic volatile organic compounds (VOCs): dimethylsulfide (DMS), dimethyldisulfide (DMDS) and toluene, in organic solvents: di-(2-ethyl)hexyladipate (DEHA), n-hexadecane, oleyl alcohol and PEG 400, was studied. In order to characterise the absorption capacity of various VOC/solvent systems, the Henry's constant (H) was determined. DMS was found to be the least absorbable in all the selected solvents. Amongst these solvents, DEHA was found to be the most efficient to absorb the considered VOCs. The effect of water addition to the considered solvents (emulsions) on the Henry's constants was examined and confirmed a decreasing VOC absorption for an increasing amount of water in solvent. Finally, to quantify the process rapidity, the absorption rate (N) and the overall liquid mass transfer coefficient (KLa) were measured for some selected couples VOC/solvent and revealed a superior efficiency of DEHA compared to other solvents in trapping DMS, DMDS and toluene.  相似文献   

15.
Posidonia oceanica residues were extracted with supercritical CO2 in order to isolate phenolic compounds. The process was optimized by developing a mathematical model based on mass transfer mechanism consisting of adsorption of supercritical fluid on the solid particles, desorption of solute and convective transfer of solute phase along the column. Henry relation between solute concentrations on the surface of the solid (Cs) and in the solid (q) was approximated in order to describe the adsorption/desorption equilibrium. The model parameters such as solid-liquid film mass transfer coefficient (kf), molecular diffusivity coefficient (DAB) and axial dispersion (Dax) were estimated using empirical methods. The linear driving force model was applied to improve the yield of total phenolic acid recovery. The optimum parameters were elicited as 25 MPa, 323.15 K and a co-solvent mass ratio of 20% yielding 34.97 μg per gram of dry feed and the model satisfactorily described the extraction yield which can be used for scale-up purposes.  相似文献   

16.
The mass transfer process in a perforated rotating disk contactor (PRDC) using a toluene-acetone-water system was investigated.The volumetric overall mass transfer coefficients are calculated in a PRDC column.Both mass transfer directions are considered in experiments.The influences of operating variables containing agitation rate,dispersed and continuous phase flow rates and mass transfer in the extraction column are studied.According to obtained results,mass transfer is significantly dependent on agitation rate,while the dispersed and continuous phase flow rates have a minor effect on mass transfer in the extraction column.Furthermore,a novel empirical correlation is developed for prediction of overall continuous phase Sherwood number based on dispersed phase holdup,Reynolds number and mass transfer direction.There has been great agreement between experimental data and predicted values using a proposed correlation for all operating conditions.  相似文献   

17.
《分离科学与技术》2012,47(16):2706-2717
ABSTRACT

Experimental and numerical studies were conducted on the mass transfer efficiency of new wire gauze structured packing. For serving this purpose, various operational conditions were studied to assess the optimal parameters such as HETP of PACK-2100 in the distillation column. The results indicate that the HETP values are enhanced in comparison to conventional ones. In addition, the HETP slowly increases from 4 to 6 cm as mass flow rates of air and liquid flow are increased. The numerical simulations were also performed to describe the performance of the PACK-2100. The Eulerian-Eulerian multiphase approach is applied to calculate the value of HETP and pressure drop. The computational results confirmed that our experimental results. The average relative error between CFD predictions and the experimental data for the prediction of mass transfer efficiency is 20.45%.  相似文献   

18.
A mathematical model describing the heat and mass transfer in the dryer section of a paper machine has been applied to the production data from four paper machines. Model predictions for the machine speed are compared to actual machine speeds for a total of 163 data sets. The mathematical model assumes that the temperature and moisture content remain homogeneous in the thickness direction of the sheet. For three paper machines producing paper with basis weights ranging from 0.056 to 0.159 kg d.s./m2 the model predictions are adequate. For the paper machine producing the heaviest grades with basis weights ranging from 0.189 to 0.390 kg d.s./m2 the model predictions are flawed by a systematic error. For low machine velocities/high basis weights the machine velocity is over-predicted and for high machine velocities/low basis weights the machine velocity is under-predicted. This systematic error is caused by the assumption of homogeneous moisture content and temperature within the sheet being severely in error for thick sheets.  相似文献   

19.
We present results from experiments and numerical simulations of contact between a non-reactive gas (N2O and CO2) and a physical solvent (H2O) occurring in a polypropylene (PP) hollow fiber membrane contactor. The closed-loop liquid flow within the experimental setup provides transient curves representing the progressive saturation of the solvent by the gas. We develop an in-house numerical model to fully characterize the gas/liquid mass transfer both in the non-wetted and in the wetted modes, i.e., when the liquid starts partially wetting the pores of the membrane. Using experiments and numerical simulations, we show that the Henry constant (H) and the molecular diffusion coefficient of a non-reactive gas absorbing into a liquid solvent can be extracted by parameter estimation. Both parameters are obtained within a single experiment at a constant temperature and the comparison with temperature-dependant correlations yields excellent agreement over the whole range of temperature studied in this work. Simulations show a partial wetting of the membrane pore by the liquid meniscus during a contact between CO2 and H2O, possibly due to the plasticizer effect of CO2 inside the membrane contactor fibers.  相似文献   

20.
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