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Bala subramanian
Dr.M.SUBAS.C.BOSE
MASS TRANSFER Transfer of material from one homogeneous phase to another. With or without phase change.
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
DIFFUSION The term mass transfer Diffusion is used to denote the transference of a component in a mixture from a region where its concentration is high to a region where the concentration is lower. Mass transfer process can take place in a gas or vapour or in a liquid, and it can result from the random velocities of the molecules (molecular diffusion) or from the circulating or eddy currents present in a turbulent fluid (eddy diffusion).
Dr.M.SUBAS.C.BOSE
A simple example of a mass transfer process is that occurring in a box consisting of two compartments, each containing a different gas, initially separated by an impermeable partition. When the partition is removed the gases start to mix and the mixing process continues at a constantly decreasing rate until eventually (theoretically after the elapse of an infinite time) the whole system acquires a uniform composition. The process is one of molecular diffusion in which the mixing is attributable solely to the random motion of the molecules. The rate of diffusion is governed by Pick's Law, first proposed by FlCK(I) in 1855 which expresses the mass transfer rate as a linear function of the molar concentration gradient. In a mixture of two gases A and B, assumed ideal, Pick's Law for steady state diffusion may be written as:
Dr.M.SUBAS.C.BOSE
DIFFUSION IN BINARY GAS MIXTURES 10.2.1, Properties of binary mixtures If A and B are ideal gases in a mixture, the ideal gas law, equation 2.15, may be applied to each gas separately and to the mixture: PAV = nART PBV = nRRT PV = nRT where nA and HB are the number of moles of A and B and n is the total number of moles in a volume V, and PA , PB and P are the respective partial pressures and the total pressure.
Dr.M.SUBAS.C.BOSE
Equimolecular counterdiffusion When the mass transfer rates of the two components are equal and opposite the process is said to be one of equimolecular counterdiffusion. Such a process occurs in the case of the box with a movable partition, referred to in Section 10.1. It occurs also in a distillation column when the molar latent heats of the two components are the same. At any point in the column a falling stream of liquid is brought into contact with a rising stream of vapour with which it is not in equilibrium. The less volatile component is transferred from the vapour to the liquid and the more volatile component is transferred in the opposite direction. If the molar latent heats of the components are equal, the condensation of a given amount of less volatile component releases exactly the amount of latent heat required to volatilise the same molar quantity of the more volatile component. Thus at the interface, and consequently throughout the liquid and vapour phases, equimolecular counterdiffusion is taking place.
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
The removal of one or more selected components from a mixture of gases by absorption into a suitable liquid is the second major operation of chemical engineering that is based on interphase mass transfer controlled largely by rates of diffusion. Thus, acetone can be recovered from an acetoneair mixture by passing the gas stream into water in which the acetone dissolves while the air passes out. Similarly, ammonia may be removed from an ammoniaair mixture by absorption in water. In each of these examples the process of absorption of the gas in the liquid may be treated as a physical process, the chemical reaction having no appreciable effect
Dr.M.SUBAS.C.BOSE
The transfer unit The group (dy/ye y), which is used in Chapter 11, has been defined by CHILTON and COLBURN(52) as the number of overall gas transfer units NOG. The concept of the transfer unit is also introduced in Volume 1, Chapter 10. The application of this group to the countercurrent conditions in the absorption tower is now considered. Over a small height dZ, the partial pressure of the diffusing component A will change by an amount dPAG.
Dr.M.SUBAS.C.BOSE
Reflux drum
1
Rectifying section stages
Reflux
Distillate
2 f
Feed Stage
Feed
Boilup
N
Partial reboiler Bottoms
Dr.M.SUBAS.C.BOSE
Distillation and V-L Equilibria Types of Distillation Action on an Ideal Plate Mass Balance in a Distillation Column Determination of Ideal Number of Plates McCabe Thiele Analysis Differential or batch distillation Flash or equilibrium distillation Continuous Rectification Binary systems
Dr.M.SUBAS.C.BOSE
MASS TRANSFER 0PERATIONS Differential distillation: The simplest examples of batch distillation at a single stage.
Starting with a still pot, initially full, heated at a constant rate. In this process the vapour formed on boiling the liquid is removed at once from the system.
Since this vapour is richer in the more volatile component, with this result the composition of the product progressively alters. Thus, whilst the vapour formed over a short period is in equilibrium with the liquid
At the end of the process the liquid, which has been vaporized, is removed as the bottom product.
Dr.M.SUBAS.C.BOSE
Let S be the number of mols of material in the still and x be the mol fraction of component A. Suppose an amount dS, containing a mol fraction y of A, be vaporised. Then a material balance on component A gives:
ydS = d (Sx)
= S dx + x Ds The integral on then right-hand side can be solved graphically if the equilibrium relationship between y and x is available. Thus, if over the range concerned the equilibrium relationship is a straight line of the form y= m x + c
Dr.M.SUBAS.C.BOSE
This process consists of only a single stage, a complete separation is impossible unless the relatively volatility is finite. Application is restricted to conditions where a preliminary separation is to be followed by a more rigorous distillation, where high purifies is not required, or where the mixture is very easily separated
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
It is not effective separating components of comparable volatility, which requires the use of distillation with reflux
By definition a vapour leaving a plate are brought into equilibrium. Assume that the plates are numbered serially from top down and that the plate under consideration is the nth plate from the bottom. Then the immediately above plate n is plate n-1, and the immediately below is n+1.
Dr.M.SUBAS.C.BOSE
Vn,yn
Plate n
Ln-1,Xn-1
Vn+1,yn+1 Ln ,xn
Plate n+1
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Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
To develop a method for the design of distillation units to give the desired fractionation, it is necessary to determine the numbers of trays. Before that the heat and material flows over the trays, the condenser and the reboiler must be established Thermodynamic data is required to establish how much mass transfer is needed to establish equilibrium between the stream leaving each tray. The diameter of the column will be dictated by the necessity to accommodate the desired flow rates, to operate within the available drop in pressure, while at the same time affecting the desired degree of mixing of the stream on each tray.
Dr.M.SUBAS.C.BOSE
Let the process be analysed simply for a binary mixture of A and B as follows:
Let F be the number of mols per unit of feed of mol fraction xf of A. D be the number of mols per unit time of vapour formed with y the mol fraction of A and B be the number of mols per unit time of liquid with x the mol fraction of A. Then an overall mass balance gives: F=D+B Component A balance FxF = D xD + B xB
Dr.M.SUBAS.C.BOSE
D xF xB F xD xB B xD xF F xD xB
Net flow rates. Quantity D is the difference between the flow rates of the streams entering and leaving the top of the column. A material balance around the condenser and accumulator in the gives:
D Va La
Dr.M.SUBAS.C.BOSE
Dx D VaYa La xa Vn 1 yn 1 Ln xn
Quantity D xD is the net flows rate of the component A upward in the upper section of the column. It too is constant throughout this part of the equipment. In the lower section of the column the net flow rates are also constant but, are in a downward direction.
Dr.M.SUBAS.C.BOSE
The net flow of total material equals B; that of the component A is BxB. The following equations apply:
Operating lines:
There are two sections in the column; there are also two operating lines, one for the rectifying section and other for the stripping section.
yn 1
Ln Va ya La xa xn Vn 1 Vn 1
For the first section (rectifying section) the operation line is represented by:
y n 1
Ln Dx D xn Ln D Ln D
Dr.M.SUBAS.C.BOSE
Vm1 ym1 Lm xm Bx B
For the section below the feed plate, a material balance over control surface II gives
y n 1 Ln Dx D xn Ln D Ln D
Rearranging this equation and taking into account that the slope is the ratio of liquid flow to the vapour flow, and also eliminating Vm+1
y m 1
Lm Bx B xm Lm B Lm B
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
Feed Line:
Cold feed : It is assumed that the entire feed stream adds to the liquid flowing down the column. Feed at bubble point: no condensation is required to heat the feed. Feed partial vapour: the liquid portion of the feed becomes part of the L and the vapour portion becomes part of V Feed saturated vapour the entire feed becomes part of the V Feed superheated: part of the liquid from the rectifying column is vaporized to cool the feed to a state of saturated vapour.
Dr.M.SUBAS.C.BOSE
Reflux Ratio:
The analysis of fractionating columns is facilitated by the use of a quantity called reflux ratio. Two ratios are used, one is the ratio of the reflux to the overhead product and the other is the ratio of the reflux to the vapour. Both ratios refer to quantities in the rectifying section. The equations for those ratios are
RD
If the operation lines equations are divided D, the result is, for constant molar overflow,
L V D D D
and
RV
L L V LD
Dr.M.SUBAS.C.BOSE
Reflux Ratio:
The y intercept of this line is xD/(RD+1). The concentration xD is set by the conditions of the design. RD, the reflux ratio, is an operating variable that can be controlled at will by adjusting the split between reflux and overhead product or by changing the amount of vapour formed in the reboiler for a given flow rate of the overhead product. A point at the upper end of the operating line can be obtained by setting xn equal to xD in the equation above. A point at the upper end of the operating line can be obtained by setting xn equal to xD in the previous equation.
yn 1 RD xD x R 1 xD D D RD 1 RD 1 RD 1 or yn 1 xD
The operating line for the rectifying section then intersects the diagonal at point (xD, xD).
Dr.M.SUBAS.C.BOSE
xF
Dr.M.SUBAS.C.BOSE
There is a minimum reflux ratio below which it is impossible to obtain the desired enrichment, however many plates are used.
xF
Dr.M.SUBAS.C.BOSE
Rm x xF D or Rm 1 xD xF
Rm
e
y F xF
xF
Dr.M.SUBAS.C.BOSE
McCabe -Thiele principles Construction the operation lines: Locate the feed line Calculate the y-axis intercept xD/(RD + 1) of the rectifying line and plot that line through the intercept and the point (xD, xD) Draw the stripping line through point (xB,xB) and the intersection of the rectifying line with the feed line.
Dr.M.SUBAS.C.BOSE
Effect the feed condition on feed line: If the feed is a cold liquid, the feed line slopes will be upward and to the right; if the feed is a saturated liquid, the line is vertical; if the feed is a mixture of liquid and vapour, the lines slopes upward and to the left and the slope is the negative of the ratio of the liquid to the vapour; if the feed is saturated vapour the line is horizontal and if the feed is superheated vapour. The lines slope downward and to the left.
Dr.M.SUBAS.C.BOSE
Feed Plate location After the location of the feed plate the construction of the number of ideal trays is found by the usual step-by step construction. The process can begin at the top and also a total condenser is used.
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
Dr.M.SUBAS.C.BOSE
LiquidLiquid Extraction
13.1. INTRODUCTION The separation of the components of a liquid mixture by treatment with a solvent in which one or more of the desired components is preferentially soluble is known as liquidliquid extractionan operation which is used, for example, in the processing of coal tar liquids and in the production of fuels in the nuclear industry, and which has been applied extensively to the separation of hydrocarbons in the petroleum industry. In this operation, it is essential that the liquid-mixture feed and solvent are at least partially if not completely immiscible and, in essence, three stages are involved: (a) Bringing the feed mixture and the solvent into intimate contact, (b) Separation of the resulting two phases, and (c) Removal and recovery of the solvent from each phase.
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Dr.M.SUBAS.C.BOSE
Continuous Extraction
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Dr.M.SUBAS.C.BOSE
General principles of Leaching Leaching is concerned with the extraction of a soluble constituent from a solid by means of a solvent. The process may be used either for the production of a concentrated solution of a valuable solid material, or in order to remove an insoluble solid, such as a pigment, from a soluble material with which it is contaminated. The method used for the extraction is determined by the proportion of soluble constituent present, its distribution throughout the solid, the nature of the solid and the particle size.
Dr.M.SUBAS.C.BOSE
Factors influencing the rate of extraction The selection of the equipment for an extraction process is influenced by the factors which are responsible for limiting the extraction rate. Thus, if the diffusion of the solute through the porous structure of the residual solids is the controlling factor, the material should be of small size so that the distance the solute has to travel is small. On the other hand, if diffusion of the solute from the surface of the particles to the bulk of the solution is the controlling factor, a high degree of agitation of the fluid is required.
Dr.M.SUBAS.C.BOSE
EQUIPMENT FOR LEACHING Processes involved Three distinct processes are usually involved in leaching operations: (a) Dissolving the soluble constituent. (b) Separating the solution, so formed, from the insoluble solid residue. (c) Washing the solid residue in order to free it of unwanted soluble matter or to obtain as much of the soluble material as possible as the product. Leaching has in the past been carried out mainly as a batch process although many continuous plants have also been developed. The type of equipment employed depends on the nature of the solidwhether it is granular or cellular and whether it is coarse or fine. The normal distinction between coarse and fine solids is that the former have sufficiently large settling velocities for them to be readily separable from the liquid, whereas the latter can be maintained in suspension with the aid of only a small amount of agitation.
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Dr.M.SUBAS.C.BOSE
INTRODUCTION - ADSORPTION Although adsorption has been used as a physical-chemical process for many years, it is only over the last four decades that the process has developed to a stage where it is now a major industrial separation technique. In adsorption, molecules distribute themselves between two phases, one of which is a solid whilst the other may be a liquid or a gas. The only exception is in adsorption on to foams, a topic which is not considered in this chapter. Unlike absorption, in which solute molecules diffuse from the bulk of a gas phase to the bulk of a liquid phase, in adsorption, molecules diffuse from the bulk of the fluid to the surface of the solid adsorbent forming a distinct adsorbed phase.
Dr.M.SUBAS.C.BOSE
The adsorption which results from the influence of van der Waals forces is essentially physical in nature. Because the forces are not strong, the adsorption may be easily reversed. In some systems, additional forces bind absorbed molecules to the solid surface. These are chemical in nature involving the exchange or sharing of electrons, or possibly molecules forming atoms or radicals. In such cases the term chemisorption is used to describe the phenomenon. This is less easily reversed than physical adsorption, and regeneration may be a problem. Chemisorption is restricted to just one layer of molecules on the surface, although it may be followed by additional layers of physically adsorbed molecules.
Dr.M.SUBAS.C.BOSE
MASS TRANSFER 0PERATIONS MOISTURE CONTENT RELATIONSHIPS: MOISTURE/SOLID EQUILIBRIUM RELATIONSHIPS DEFINED ON THE BASIS OF RELATIVE HUMIDITY AT A SPECIFIC TEMPERATURE EQUILIBRIUM AMOUNT OF MOISTURE TENDS TO DECREASE WITH INCREASING TEMPERATURE.
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MASS TRANSFER 0PERATIONS MOISTURE CONTENT VARIABLES BASED ON THE MASS OF MOISTURE RELATIVE TO THE MASS BONE DRY SOLID
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DRYING RATE CURVES: DEPEND ON WHETHER HEAT ORMASS TRANSFER CONTROLS FREE MOISTURE VS. TIME DRYING RATE VS. MOISTURE CONTENT
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DRYING REGIMES CONSTANT RATE - NO LIMIT TO MASS TRANSFER IN SOLID PHASE SURFACE MOISTURE TRANSFER NEAR SURFACE FALLING RATE MOISTURE FLUX THROUGH THE SOLID IS HINDERED CRITICAL POINTS OCCUR BETWEEN CONSTANT RATE AND FALLING RATE WITH A CHANGE IN THE FALLING RATE DRYING MECHANISM.
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