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This paper aims at the interfacial phenomena of liquid-liquid mass transfer and its characteristic. By using the real-time holographic technique, the concentration distributions on the aqueous side were obtained according to holographic diagrams of mass transfer of ethanol through the interface of oil and water at different initial concentrations. Furthermore, the concentrations near the interface and the mass transfer coefficients were attained. A correlation of concentration near the interface to the concentration of the solute in the oil side was proposed. An approach of interfacial energy with solute concentration was established, and the calculated results are at good agreement with the experimental data. It is indicated that the liquid-liquid mass transfer process is approximately in accordance with two-film theory, the interfacial performance may be changed by the addition of the solute, and the interface of liquid-liquid is nonequilibrium thermodynamically during the mass transfer process. __________ Translated from Chemical Engineering (China), 2007, 35(6): 1–3 [译自: 化学工程] 相似文献
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The effect of interfacial velocity and interfacial tension gradient on momentum, heat and mass transfer was studied theoretically. After reviewing current knowledge regarding interfacial velocity effects, the interfacial tension gradient effect is discussed as a numerical solution of the laminar boundary layer equations. The enhancement and suppression of interfacial mobility, and the rates of interphase momentum, heat and mass transfer were related to the Marangoni number. A diagram showing the effect of interfacial tension gradient on momentum, heat and mass transfer is presented. 相似文献
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A. Grahn 《Chemical engineering science》2006,61(11):3586-3592
Two-dimensional (2D) simulations of isothermal liquid-liquid mass transfer subject to surface tension- and buoyancy-driven hydrodynamic instabilities have been carried out. Simulation is based on the numerical solution of 2D equations of momentum and mass transport, using a combination of finite difference and finite volume methods. Two different cases have been considered: (1) buoyancy stable mass transfer, only surface tension-driven convection occurs; (2) surface tension-driven instability superseeded by buoyant convection. The faster attenuation of mass transfer coefficients in buoyancy stable situations is attributed to the merging of convection cells leading to a reduction in the number of renewal zones along the interface. Concentration profiles next to the interface reveal the diffusional nature of the mass transfer in the immediate interfacial neighbourhood. 相似文献
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An experimental study of transient drop rise velocities and mass transfer rates was carried out in the system toluene/acetone/water which is known to show interfacial instabilities. The rise velocity of toluene drops was studied without added solute (acetone) in the diameter range 1-3 mm and with added solute for 2 mm drops. The initial concentration of the transferred solute was varied from 0 to 30 g/L. The transient drop rise velocities were used to quantify the Marangoni effect since the drag coefficient depends on the strength of the Marangoni convection patterns caused by interfacial tension gradients. In addition, mass transfer measurements were carried out in order to determine the modification of the mass transfer rate due to Marangoni convection. Velocity and mass transfer measurements were then correlated via the contact time. Results reveal the existence of a range in which a critical value for the solute concentration can be defined for Marangoni convection. 相似文献
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Ying Shi 《Chemical engineering science》2008,63(13):3560-3563
A novel Hele-Shaw cell design for accurate experiments in liquid-liquid systems with and without chemical reactions is hereby presented. It allows the formation of a stably pinned, plane liquid-liquid interface in less than one second with a minimum shear flow. The underlying working principle and the performance for different solvent systems and gap widths are discussed. 相似文献
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Liquid-liquid binary mass transfer involving simultaneous transfer of an organic phase component to the aqueous phase and an aqueous phase component to the organic phase in water-n butanol and water-methyl ethyl ketone systems has been studied in a vertical ejector system. Correlations have been developed to predict both dispersed and continuous phase film capacity coefficients as function of various physical and dynamic variables of the system. 相似文献
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A simulation technique is developed to predict the performance of a two phase liquid-liquid continuous flow stirred tank reactor as an extractor. The dynamics of the dispersed phase droplet interactions and the microscopic interphase mass transfer in the turbulent flow field are digitally simulated using the interval of quiescence method. The use of realistic breakage and coalescence functions together with the natural evolution of the interactive drop population has made it possible to predict the dispersed phase drop size distribution and mass transfer efficiency in a rational manner from the known physicochemical properties of the dispersion and the operating conditions of the extractor. 相似文献
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Effect of interfacial mass transfer on the dispersion in segmented flow in straight capillaries
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Jaydeep B. Deshpande Amol A. Kulkarni 《American Institute of Chemical Engineers》2015,61(12):4294-4308
The effect of interfacial mass transfer on the extent of dispersion in liquid‐liquid segmented flow in straight capillaries is studied. In the absence of interfacial mass transfer, dispersion coefficient was seen to go through a minimum with increasing flow rates. In the presence of mass transfer, physicochemical properties of both the phases and slug lengths were seen to vary along the capillary length. The extent of dispersion was always higher in the presence of interfacial mass transfer. The predictions using axial dispersion model deviated noticeably for larger capillaries as the model does not account for varying buoyancy, dynamic contacting, and Marangoni convection. Simulations of a first‐order interfacial reaction considering varying slug lengths showed a significant change in optimum operating parameters than the conventional approach. A special case of “drop‐on‐demand” type of controlled two‐phase flow in capillaries was also studied. © 2015 American Institute of Chemical Engineers AIChE J, 61: 4294–4308, 2015 相似文献
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Dr. Henryk Sawistowski 《化学,工程师,技术》1973,45(18):1093-1098
Surface-tension-induced interfacial convection (Marangoni phenomena) can appear as a result of mass and heat transfer, compression and dilatation of surface films or their non-Newtonian behaviour and owing to presence in the interface of electrostatic charges. In process engineering problems the mass transfer effect is usually predominant and, depending on the geometry of the system, leads to surface renewal or changes in interfacial area. The surface renewal phenomena can appear as instabilities or disturbances and their effect on mass transfer is presented for transfer to and from drops as well as across flat interfaces in stirred and laminar flow contactors. Mass transfer coefficients and drag coefficients of drops are compared under conditions of undisturbed (diffusional) transfer, cellular convection and interfacial turbulence for stable and unstable direction of transfer. The importance of gravitational instability is indicated. 相似文献
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Mean droplet diameter of the dispersed phase in pulsed plate extraction columns was measured for binary and ternary systems. A change in the droplet size in the presence of solute, dependent on such factors as the direction of mass transfer, droplet size in the binary system, radio of diffusion coefficients, viscosity of the continuous phase, interfacial tension and driving force for extraction was observed. Two new empirical correlations of mean droplet sizes in mass transfer conditions are proposed. These correlations have been successfully applied to other extraction columns. 相似文献
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A non-interfering technique has been used to measure the concentration of ozone in pairs of bubbles injected into a bed of inactive 390 μm glass beads fluidized by ozone-free air. The transfer of the ozone tracer from the bubble phase to the dense phase is enhanced when compared to the transfer from isolated bubbles in the same particles and the same column. Bubble growth is also greater for the case where pairs of bubbles are introduced than when bubbles are present in isolation. Enhancement of interphase mass transfer for interacting bubbles in the present work and in previous studies incr with particle size and can be explained in terms of enhancement of the throughflow (or convective) component of transfer while the diffusive component unaltered. This mechanism leads to new equations for estimating interphase mass transfer in freely bubbling fluidized beds. 相似文献
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《Chemical engineering science》1970,25(6):1081-1090
A photographic technique was used to determine mass transfer rates from single drops immediately following formation. Measurements were made on a system expected to exhibit interfacial tension driven convection and comparisons are drawn to predictions for stable systems and to measurements in the presence of surfactant. Unusually high mass transfer coefficients are reported. 相似文献
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《化学工程》2016,(3):1-8
气液反应界面传质的强化是当今高效和节能反应器研究的重要课题,弄清反应器内的气液传质机理是对气液反应器进行数学描述的关键。反应过程的能效和物效与体系中的传质系数k_G,k_L,k_S以及相界面面积a等参数直接相关,这些参数受气泡尺寸、分布、表观气速和气含率等因素的制约。就确定的体系和反应条件而言,这些因素会因反应器的结构尤其是搅拌和混合方式的变化而异。文章从理论上分析了影响气液界面传质的各因素,建立了较为详细的理论模型。理论计算结果表明:气泡大小是影响气液界面传质和最终反应速率的重要流体力学参数,微米级气泡对反应过程的强化作用明显。能量耗散率是决定体系气泡大小的深层原因,强化气液反应器设计时应重点考虑。 相似文献
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《Chemical engineering science》1959,9(4):225-241
The effect of the surface active agents sodium hexadecanyl sulphate and sodium undecanyl sulphate on the rate of mass transfer, droplet oscillation and terminal velocity has been studied during extraction of o-nitrophenol and iodine from aqueous solutions by single drops of carbon tetrachloride. The effect is caused by the pure surface active agents and does not depend on the presence of impurities. The hydrodynamic character of the effect has been confirmed. A comparison with solid spheres shows that the surface active agents can make the rates of mass transfer and the terminal velocities equal to those for solid bodies, internal circulation, oscillation and the zig-zag path being completely eliminated. Evidence is presented indicating that the high rates of mass transfer obtained in the absence of surface active agents, about three times that for solid spheres, are not caused by the droplet oscillation, and that, at the most, they can be accounted for only partly by internal circulation. It is suggested that the explanation must be sought in the micro structure of the flow pattern. 相似文献
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A rate-based model formass transfer in liquid-liquid extraction (LLX) has been developed usingthree distinct stages of drop formation, drop fall or rise and drop coalescence. Binary diffusivities in infinite dilution as well as for concentrated
multicomponent mixtures were used to estimate the Maxwell-Stefan binary mass transfer coefficients for both the phases. The
mass transfer resistances associated with these coefficients have been categorized in four configurations. Because of the
very large number of computations associated with repeated calculations of mass transfer coefficients, alocal model has been incorporated. Acomparative study between rate-based and non-equilibrium simulator and our bench scale experiments (LLX of toluene-acetone-water system) has
been done. The stage-wise composition profiles of acetone in water and toluene phase of the experimental and simulation runs
have been compared by using the relative error square analysis. Based on this analysis, best mass transfer combination and
mass transfer resistance model has been selected. 相似文献