Distillation Column
Distillation Column
Distillation Column
Distillation
Distillation is a kind of seperation technique of two or more volatile liquid compunds by using the difference in boiling points and relative volatility. The process takes place in a column, and two heat exchangers. In the column two phases, liquid and gas, are distributed to enrich the vapor in more volatile compounds and enrich the liquid phase on less volatile compounds. Mass transfer is the key to a successful distillation.
Disadvantages
It has simple flowsheet, low capital investment, and low risk. If components to be separated have a high relative volatility difference and are thermally stable, distillation is hard to beat.
Distillation has a low energy efficiency and requires thermal stability of compounds at their boiling points. It may not be attractive when azeotropes are involved or when it is necessary to separate high boiling components, present in small concentrations, from large volumes of a carrier, such as water.
Types of Distillation
Continous Distillation
The mixture which is to be seperated is fed to column at one or more points. Liquid mixture runs down the column while vapor goes up. Vapor is produced by partial vaporisation of the mixture which is heated in reboiler. Then vapor is partially condensed to earn back the less volatile compounds to the column to seperate as bottom product. (reflux)
Batch Distillation
The oldest operation used for seperation of liquid mixtures. Feed is fed from bottom,where includes reboiler, to be processed. Numbers of accumulator tanks are connected to collect the main and the intermediate distillate fractions.
Semi-batch Distillation
Semi-batch distillation is very similar to batch distillation. Feed is introduced to column in a continous or semi-continous mode. It is suitable for extractive and reactive distillations.
For batch distillation, it is enough to use only one column to seperate multicomponent liquid mixture. One sequence of operation is enough to seperate all the components in a mixture.
For continous distillation, to seperate multicomponent liquid mixtures, more than one columns are necessary to be used. One column is dedicated to seperate a specific mixture and specific operation.
Equipment Designs
It is the most widely used kind of distillation column. Trays are shaped to maximize the liquid-vapor contact and increase the mass transfer area. Tray types include sieve, valve and bubble cap.
behavior
Moderate Can Low
Suitable Feed
/ Nozzle sizes
Height = # actual stages x tray spacing + space allowance for feed/draws + sump + top volume Tray spacing for most applications is 18-24 inches Rule of thumb could be to add 1- 2 nozzle diameters to the total height for feeds and draws Sumps sized on liquid residence time. Two to five minutes is typical.
Bubble Caps
Bubble Cap
Bubble Caps
Sieve trays Sieve trays are simply metal plates with holes in them. Vapour passes straight upward through the liquid on the plate. The arrangement, number and size of the holes are design parameters.
Sieve Tray
Sieve Tray
Column Diameter
Column
diameter is chosen to provide a comfortable range of operating between flooding and weeping. A typical operating range is about 70% of the flooding velocity. The flooding velocity is determined by correlations An approach to flooding is used to get the actual superficial velocity (based on column diameter). Downcomers take up about 5-20% of column area Diameters should be rounded to standard dimensions
Disadvantages
Least expensive colum for diameters greater than 0.6m The liquid-vapor contact in the cross-flow of plate columns is more effective than countercurrent-flow in packed columns. Cooling coils can be easily added to the plate column Can handle high liquid flow rates.
Higher pressure drops than packed columns Foaming can occur because the liquid is agitated by the vapor flowing up through it.
Packed Beds
Packings can be provided either as dumped or stacked. Dumped packing consistutes of bulk inert materials. Stacked packing is includes meshwork which has the same diameter with the column. Important criterias for packings are efficent contact (liquid-vapor), resistence to flow, flow capacity, resistance of packing against corrosion.
pressure drop / smaller diameter Random packing scale-up for HETP is difficult; structured packing scale-up is predictable HETP prediction less well developed than for trays Low to moderate cost for random packing; high cost for structured packing Not suitable for fouling service
Random packing Structured packing Trade-off pressure drop vs. HETP vs. cost
of packing
Column
diameter
Height
Feeds
of packing
and offtakes
HETP
HETP
is difficult to generalize and is a function of the type of packing, the system being separated and the hydraulics of the column. Experimental or vendor-supplied values are used.
When the diameter is less than 0.6m it is less expensive than the plate column. Packing is able to handle corrosive materials. Lower pressure drop than in plate columns. Good for thermally sensitive liquids.
Can break during installation or due to thermal expansion. Not cost efficient for high liquid flow rates. Contact efficiencies are decreased when the liquid flow rate is too low.
Because of the high operation and installation costs, low energy efficiency, vacuum distillation appears to be uneconomical in the commercial applications.
Azeotropic Distillation
This type of distillation is used for processes that produce almost 100 percent alcohol with help of an organic solvent and two additional distillations. A solvent (pentane, gasoline etc.) is added to distillation product comming out of the usual distillation column. Mixture is fed to another distillation column which seperates it into a top product and a bottom product. Distillate of this column is fed to a third column which distills out the solvent leaving the mixture of alcoholwater. Solvent is recycled and never gets out. System is hard to design and it is more complicated comparing to ordinary distillation system.