Mass transfer distillation

The situation is very much poorer for stmctured rather than random packings, in that hardly any data on Hq and have been pubHshed. Based on a mechanistic model for mass transfer, a way to estimate HETP values for stmctured packings in distillation columns has been proposed (91), yet there is a clear need for more experimental data in this area. 

Simultaneous heat and mass transfer also occurs in drying processes, chemical reaction steps, evaporation, crystallisation, and distillation. In all of these operations transfer rates are usually fixed empirically. The process can be evaluated using either the heat- or mass-transfer equations. However, if the process mechanism is to be fully understood, both the heat and mass transfer must be described. Where that has been done, improvements in the engineering of the process usually result (see Process energy conservation). 

Examination of this equation will show that the required heat transfer area for the heat recovery section per unit mass of distillate produced, increases significantly when PR is increased, and decreases slightly as the number of heat recovery stage, is increased. 

Ordinary diffusion involves molecular mixing caused by the random motion of molecules. It is much more pronounced in gases and Hquids than in soHds. The effects of diffusion in fluids are also greatly affected by convection or turbulence. These phenomena are involved in mass-transfer processes, and therefore in separation processes (see Mass transfer Separation systems synthesis). In chemical engineering, the term diffusional unit operations normally refers to the separation processes in which mass is transferred from one phase to another, often across a fluid interface, and in which diffusion is considered to be the rate-controlling mechanism. Thus, the standard unit operations such as distillation (qv), drying (qv), and the sorption processes, as well as the less conventional separation processes, are usually classified under this heading (see Absorption Adsorption Adsorption, gas separation Adsorption, liquid separation). 

To determine the mass-transfer rate, one needs the interfacial area in addition to the mass-transfer coefficient. For the simpler geometries, determining the interfacial area is straightforward. For packed beds of particles a, the interfacial area per volume can be estimated as shown in Table 5-27-A. For packed beds in distillation, absorption, and so on in Table 5-28, the interfacial area per volume is included with the mass-transfer coefficient in the correlations for HTU. For agitated liquid-liquid systems, the interfacial area can be estimated... 

TABLE 5-28 Mass Transfer Correlations for Packed Two-Phase Contactors—Absorption, Distillation, Cooling Towers, and Extractors (Packing Is Inert)... 

Experimental values of Hqg -nd Hql for a number of distillation systems of commercial interest are also readily available. Extrapolation of the data or the correlations to conditions that differ significantly from those used for the original experiments is risky. For example, pressure has a major effect on vapor density and thus can affect the hydrodynamics significantly. Changes in flow patterns affeci both mass-transfer coefficients and interfacial area. 

This section also includes a treatment of distillation-type separations from a rate-based point of view that utilizes principles of mass transfer and heat transfer. Section 14 also presents details of that subject as applied to absorption and stripping. 

Example 8 Calculation of Rate-Based Distillation The separation of 655 lb mol/h of a bubble-point mixture of 16 mol % toluene, 9.5 mol % methanol, 53.3 mol % styrene, and 21.2 mol % ethylbenzene is to be earned out in a 9.84-ft diameter sieve-tray column having 40 sieve trays with 2-inch high weirs and on 24-inch tray spacing. The column is equipped with a total condenser and a partial reboiler. The feed wiU enter the column on the 21st tray from the top, where the column pressure will be 93 kPa, The bottom-tray pressure is 101 kPa and the top-tray pressure is 86 kPa. The distillate rate wiU be set at 167 lb mol/h in an attempt to obtain a sharp separation between toluene-methanol, which will tend to accumulate in the distillate, and styrene and ethylbenzene. A reflux ratio of 4.8 wiU be used. Plug flow of vapor and complete mixing of liquid wiU be assumed on each tray. K values will be computed from the UNIFAC activity-coefficient method and the Chan-Fair correlation will be used to estimate mass-transfer coefficients. Predict, with a rate-based model, the separation that will be achieved and back-calciilate from the computed tray compositions, the component vapor-phase Miirphree-tray efficiencies. 

The HETP of a packed-tower section, valid for either distillation or dilute-gas absorption and stripping svstems in which constant molal overflow can be assumed and in which no chemical reactions occur, is related to the height of one overall gas-phase mass-transfer unit Hqc by the equation... 

Bakowsld [B/ Chem. Eng., 8, 384, 472 (1963) 14, 945 (1969)]. It is based on tbe assumption that tbe mass-transfer rate for a component moving to tbe vapor phase is proportional to tbe concentration of tbe component in tbe liquid and to its vapor pressure. Also, tbe interfacial area is assumed proportional to liquid depth, and surface renewal rate is assumed proportional to gas velocity. The resulting general equation for binaiy distillation is... 

Note that the product of the mass-transfer coefficient and the interfacial area is a volumetric coefficient and obviates the need for a value of the interfacial area. While areas for mass transfer on plates have been measured, the experimental contacting equipment cuffered significantly from that used for commercial distillation or gas absorption, and the reported areas are considered unreliable for design purposes. 

For total-reflux distillations carried out in packed columns, regions of loading and flooding are identified by their effects on mass-transfer efficiency, as shown in Fig. 14-47. Gas and liquid rate increase... 

Mass Transfer Relationships for calculating rates of mass transfer between gas and liquid in packed absorbers, strippers, and distillation columns may be found in Sec. 5 and are summarized in Table, 5-28. The two-resistance approach is used, with rates expressed as transfer units ... 

While the carbon dioxide/caiistic test method has become accepted, one should use the results with caution. The chemical reaction masks the effect of physical absorption, and the relative values in the table may not hold for other cases, especially distillation applications where much of the resistance to mass transfer is in the gas phase. Background on this combination of physical and chemical absorption may Be found earher in the present section, under Absorption with Chemical Reaction. ... 

There are several important eomponents in a distillation column, each of which is used either to transfer heat energy or enhance mass transfer. The major components in a typical distillation are ... 

Figures 4.34 and 4.35 represent two extreme cases. Drying processes represent the case shown in Fig. 4.34 and distillation processes represent Fig. 4.35. Neither case represents a convective mass transfer case while the gas flow is in the boundary layer, other flows are Stefan flow and turbulence. Thus Eqs. (4.243) and (4.244) can seldom be used in practice, but their forms are used in determining the mass transfer factor for different cases.

Distillation is probably Ihe most widely used separation (mass transfer) process in the chemical and allied industries. Its applications range from the rectification of alcohol, which has been practiced since antiquity, lo the fractionation of crude oil. The separation of liquid mixtures by distillation is based on differences in volatility between the components. The greater the... 

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