# Fractionating column

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A fractional column is an essential item used in distillation of liquid mixtures so as to separate the mixture into its component parts, or fractions, based on the differences in volatilities. Fractionating columns are used in small scale laboratory distillations as well as for large-scale industrial distillations.

## Laboratory fractionating columns

Figure 1: Fractional distillation apparatus using a Liebig condenser.

A laboratory fractionating column is a piece of glassware used to separate vaporized mixtures of liquid compounds with close volatility. It can also be called a fractional column. Most commonly used is either a Vigreux column or a straight column packed with glass beads or metal pieces such as Raschig rings.

Fractionating columns help to separate the mixture by helping the mixed vapors to cool, condense, and vaporize again in accordance with Raoult's law. With each condensation-vaporization cycle, the vapors are enriched in a certain component. A larger surface area allows more cycles, improving separation. This is the rationale for a Vigreux column or a packed fractionating column. Spinning band distillation achieves the same outcome by using a rotating band within the column to force the rising vapors and descending condensate into close contact, achieving equilibrium more quickly.

In a typical fractional distillation, a liquid mixture is heated in the distilling flask, and the resulting vapor rises up the fractionating column (see Figure 1). The vapor condenses on glass spurs (known as trays or plates) inside the column, and returns to the distilling flask, refluxing the rising distillate vapor. The hottest tray is at the bottom of the column and the coolest tray is at the top. At steady-state conditions, the vapor and liquid on each tray reach an equilibrium. Only the most volatile of the vapors stays in gas form all the way to the top, where it may then proceed through a condenser, which cools the vapor until it condenses into a liquid distillate. The separation may be enhanced by the addition of more trays (to a practical limitation of heat, flow, etc.).

Figure 2: Typical industrial fractionating columns

## Industrial fractionating columns

Fractional distillation is one of the unit operations of chemical engineering.[1][2] Fractionating columns are widely used in the chemical process industries where large quantities of liquids have to be distilled.[3][4][5] Such industries are the petroleum processing, petrochemical production, natural gas processing, coal tar processing, brewing, liquified air separation, and hydrocarbon solvents production and similar industries but it finds its widest application in petroleum refineries. In such refineries, the crude oil feedstock is a complex, multicomponent mixture that must be separated, and yields of pure chemical compounds are not expected, only groups of compounds within a relatively small range of boiling points, also called fractions. That is the origin of the name fractional distillation or fractionation. It is often not worthwhile separating the components in these fractions any further based on product requirements and economics.

Distillation is one of the most common and energy-intensive separation processes. Effectiveness of separation is dependent upon the height and diameter of the column, the ratio of the column's height to diameter, and the material that comprises the distillation column itself.[6] In a typical chemical plant, it accounts for about 40% of the total energy consumption.[7] Industrial distillation is typically performed in large, vertical cylindrical columns (as shown in Figure 2) known as "distillation towers" or "distillation columns" with diameters ranging from about 65 centimeters to 6 meters and heights ranging from about 6 meters to 60 meters or more.

Figure 3: Chemical engineering schematic of a continuous fractionating column
Figure 4: Chemical engineering schematic of typical bubble-cap trays in a fractionating column

Industrial distillation towers are usually operated at a continuous steady state. Unless disturbed by changes in feed, heat, ambient temperature, or condensing, the amount of feed being added normally equals the amount of product being removed.

The amount of heat entering the column from the reboiler and with the feed must equal the amount heat removed by the overhead condenser and with the products. The heat entering a distillation column is a crucial operating parameter, addition of excess or insufficient heat to the column can lead to foaming, weeping, entrainment, or flooding.

Figure 3 depicts an industrial fractionating column separating a feed stream into one distillate fraction and one bottoms fraction. However, many industrial fractionating columns have outlets at intervals up the column so that multiple products having different boiling ranges may be withdrawn from a column distilling a multi-component feed stream. The "lightest" products with the lowest boiling points exit from the top of the columns and the "heaviest" products with the highest boiling points exit from the bottom.

Industrial fractionating columns use external reflux to achieve better separation of products.[3][5] Reflux refers to the portion of the condensed overhead liquid product that returns to the upper part of the fractionating column as shown in Figure 3.

Inside the column, the downflowing reflux liquid provides cooling and condensation of upflowing vapors thereby increasing the efficacy of the distillation tower. The more reflux and/or more trays provided, the better is the tower's separation of lower boiling materials from higher boiling materials.

The design and operation of a fractionating column depends on the composition of the feed and as well as the composition of the desired products. Given a simple, binary component feed, analytical methods such as the McCabe–Thiele method[5][8][9] or the Fenske equation[5] can be used. For a multi-component feed, simulation models are used both for design, operation, and construction.

Bubble-cap "trays" or "plates" are one of the types of physical devices, which are used to provide good contact between the upflowing vapor and the downflowing liquid inside an industrial fractionating column. Such trays are shown in Figures 4 and 5.

The efficiency of a tray or plate is typically lower than that of a theoretical 100% efficient equilibrium stage. Hence, a fractionating column almost always needs more actual, physical plates than the required number of theoretical vapor–liquid equilibrium stages.

Figure 5: Section of fractionating tower of Figure 4 showing detail of a pair of trays with bubble caps
Figure 6: Entire view of a Distillation Column

In industrial uses, sometimes a packing material is used in the column instead of trays, especially when low pressure drops across the column are required, as when operating under vacuum. This packing material can either be random dumped packing (1–3 in or 2.5–7.6 cm wide) such as Raschig rings or structured sheet metal. Liquids tend to wet the surface of the packing, and the vapors pass across this wetted surface, where mass transfer takes place. Differently shaped packings have different surface areas and void space between packings. Both of these factors affect packing performance.

## References

1. ^ Editors: Jacqueline I. Kroschwitz and Arza Seidel (2004). Kirk-Othmer Encyclopedia of Chemical Technology (5th ed.). Hoboken, New Jersey: Wiley-Interscience. ISBN 0-471-48810-0.
2. ^ McCabe, W., Smith, J. and Harriott, P. (2004). Unit Operations of Chemical Engineering (7th ed.). McGraw Hill. ISBN 0-07-284823-5.
3. ^ a b Kister, Henry Z. (1992). Distillation Design (1st ed.). McGraw-Hill. ISBN 0-07-034909-6.
4. ^ King, C.J. (1980). Separation Processes (2nd ed.). McGraw Hill. ISBN 0-07-034612-7.
5. ^ a b c d Perry, Robert H.; Green, Don W. (1984). Perry's Chemical Engineers' Handbook (6th ed.). McGraw-Hill. ISBN 0-07-049479-7.
6. ^ "Distillation Columns". Brewhaus. Retrieved 4 August 2015.
7. ^ Felder, R.; Roussea, W. (2005). Elementary Principles of Chemical Processes (3rd ed.). Wiley. ISBN 978-0-471-68757-3.
8. ^ Beychok, Milton (May 1951). "Algebraic Solution of McCabe-Thiele Diagram". Chemical Engineering Progress.
9. ^ Seader, J. D.; Henley, Ernest J. (1998). Separation Process Principles. New York: Wiley. ISBN 0-471-58626-9.