Theoretical plate: Difference between revisions
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A '''theoretical plate''' in many [[chemical engineering]] separation processes is a hypothetical zone or stage in which two phases, such as the [[liquid]] and [[vapor]] phases of a substance, establish an [[Vapor-liquid equilibrium|equilibrium]] with each other. Those zones or stages may also be referred to as a '''theoretical tray''' or an '''equilibrium stage'''. The performance of many separation processes depends on having a series of equilibrium stages and is enhanced by providing more such stages. In other words, having more theoretical plates increases the efficacy of the separation process be it either a [[Continuous distillation|distillation]], [[absorption (chemistry)|absorption]], [[chromatography|chromatographic]], [[adsorption]] or similar process. | A '''theoretical plate''' in many [[chemical engineering]] separation processes is a hypothetical zone or stage in which two phases, such as the [[liquid]] and [[vapor]] phases of a substance, establish an [[Vapor-liquid equilibrium|equilibrium]] with each other. Those zones or stages may also be referred to as a '''theoretical tray''' or an '''equilibrium stage'''. The performance of many separation processes depends on having a series of equilibrium stages and is enhanced by providing more such stages. In other words, having more theoretical plates increases the efficacy of the separation process be it either a [[Continuous distillation|distillation]], [[absorption (chemistry)|absorption]], [[chromatography|chromatographic]], [[adsorption]] or similar process. | ||
==Applications== | ==Applications== |
Revision as of 20:13, 1 August 2008
A theoretical plate in many chemical engineering separation processes is a hypothetical zone or stage in which two phases, such as the liquid and vapor phases of a substance, establish an equilibrium with each other. Those zones or stages may also be referred to as a theoretical tray or an equilibrium stage. The performance of many separation processes depends on having a series of equilibrium stages and is enhanced by providing more such stages. In other words, having more theoretical plates increases the efficacy of the separation process be it either a distillation, absorption, chromatographic, adsorption or similar process.
Applications
The concept of theoretical plates and trays or equilibrium stages is used in the design of many different types of separation.
Distillation columns
The concept of theoretical plates in designing distillation processes has been discussed in many reference texts.[1][2][3][4][5] Any physical device that provides good contact between the vapor and liquid phases present in industrial-scale distillation columns or laboratory-scale glassware distillation columns constitutes a "plate" or "tray". Since an actual, physical plate is rarely a 100% efficient equilibrium stage, the number of actual plates is more than the required theoretical plates.
where: | |
= the number of actual, physical plates or trays | |
= the number of theoretical plates or trays | |
= the plate or tray efficiency |
So-called bubble-cap or valve-cap trays are examples of the vapor and liquid contact devices used in industrial distillation columns. The trays or plates used in industrial distillation columns are fabricated of circular steel plates and usually installed inside the column at intervals of about 60 to 75 cm (24 to 30 inches) up the height of the column. That spacing is chosen primarily for ease of installation and ease of access for future repair or maintenance.
For example, a very simple tray would be a perforated tray. The desired vapor and liquid contacting would occur as the vapor flowing upwards through the perforations would contact the liquid flowing downwards through the perforations. In current modern practice, as shown in the adjacent diagram, better contacting is achieved by installing bubble-caps or valve caps located at each perforation to promote the formation of vapor bubbles flowing through a thin layer of liquid maintained by a weir on each tray.
To design a distillation unit or a similar chemical process, the number of theoretical trays or plates (that is, hypothetical equilibrium stages), , required in the process should be determined, taking into account a likely range of feedstock composition and the desired degree of separation of the components in the output fractions. In industrial continuous fractionating columns, is determined by starting at either the top or bottom of the column and calculating material balances, heat balances and equilibrium flash vaporizations for each of the succession of equilibrium stages until the desired end product composition is achieved. The calculation process requires the availability of a great deal of vapor-liquid equilibrium data for the components present in the distillation feed, and the calculation procedure can be very complex.[1][2][4]
In an industrial distillation column, the N t required to achieve a given separation also depends upon the amount of reflux used. Using more reflux decreases the number of plates required and using less reflux increases the number of plates required. Hence, the calculation of is usually repeated at various reflux rates. is then divided by the tray efficiency, , to determine the actual number of trays or physical plates, , needed in the ditillation column. The final design choice of the number of trays to be installed in a distillation column is then selected based upon an economic balance between the cost of additional trays and the cost of using a higher reflux rate.
There is a very important distinction between the theoretical plate terminology used in discussing conventional distillation trays and the theoretical plate terminology used in the discussions below of packed bed distillation or absorption or in chromatography or other applications. The theoretical plate in conventional distillation trays has no height. It is simply a hypothetical equilibrium stage. However, the theoretical plate in packed beds, chromatography and other applications is defined as having a height.
Distillation and absorption packed beds
Distillation and absorption separation processes using packed beds for vapor and liquid contacting have an equivalent concept referred to as the plate height or the height equivalent to a theoretical plate (HETP). [1][4] HETP arises from the same concept of equilibrium stages as does the theoretical plate and is numerically equal to the absorption bed length divided by the number of theoretical plates in the absorption bed (and in practice is measured in this way).
where: | |
= the number of theoretical plates (also called the "plate count") | |
= the total bed height | |
= the height equivalent to a theoretical plate |
The material in packed beds can either be random dumped packing (1-3" wide) such as Raschig rings or structured sheet metal. Liquids tend to wet the surface of the packing and the vapors contact the wetted surface, where mass transfer takes place.
Chromatographic processes
The theoretical plate concept was also adapted for chromatographic processes by the British chemists and Nobel Prize winners, Martin and Synge. The IUPAC's Gold Book provides a definition of the number of theoretical plates in a chromatography column.[6]
The same equation applies in chromatography processes as for the processes, namely:
where: | |
= the number of theoretical plates (also called the "plate count") | |
= the total column length | |
= the height equivalent to a theoretical plate |
Other applications
The concept of theoretical plates or trays applies to other processes as well, such as capillary electrophoresis and some types of adsorption.
References
- ↑ 1.0 1.1 1.2 Kister, Henry Z. (1992). Distillation Design, First Edition. McGraw-Hill. ISBN 0-07-034909-6.
- ↑ 2.0 2.1 King, C.J. (1980). Separation Processes. McGraw Hill. 0-07-034612-7.
- ↑ McCabe, W., Smith, J. and Harriott, P. (2004). Unit Operations of Chemical Engineering, Seventh Edition. McGraw Hill. ISBN 0-07-284823-5.
- ↑ 4.0 4.1 4.2 Perry, Robert H. and Green, Don W. (1984). Perry's Chemical Engineers' Handbook, Sixth Edition. McGraw-Hill. ISBN 0-07-049479-7.
- ↑ B.S. Furnis et al (1989). Vogel's Textbook of Practical Organic Chemistry, 5th Edition. Longman Scientific. ISBN 0-582-46236-3.
- ↑ Definition of the number of plates (in chromatography) IUPAC Gold Book