Information about Batch Distillation
Batch distillation[1] refers to the use of distillation in batches, meaning that a mixture is distilled to separate it into its component fractions before the distillation still is again charged with more mixture and the process is repeated. This is in contrast with continuous distillation where the feedstock is added and the distillate drawn off without interruption.
Batch distillation has always been an important part of the production of seasonal, or low capacity and high-purity chemicals. It is a very frequent separation process in the pharmaceutical industry and in wastewater treatment units.
The pot is filled with liquid mixture and heated. Vapour flows upwards in the rectifying column and condenses at the top. Usually, the entire condensate is initially returned to the column as reflux. This contacting of vapour and liquid considerably improves the separation. Generally, this step is named start-up. After some time, a part of the overhead condensate is withdrawn continuously as distillate and it is accumulated in the receivers, and the other part is recycled into the column as reflux.
Owing to the differing vapour pressures of the distillate, there will be a change in the overhead distillation with time, as early on in the batch distillation the components with a lower vapour pressure wil be evaporated first. As the supply of the material is limited and lighter components are removed, the relative fraction of heavier components will increase as the distillation progresses.
During operation (after charging the pot and starting up the system) the high boiling constituents are primarily separated from the charge mixture. The liquid in the pot is depleted in the high boiling constituents, and enriched in low boiling ones. The high boiling product is routed into the bottom product receivers. The residual low boiling product is withdrawn from the charge pot. This mode of batch distillation is very seldom applied in industrial processes.
Lelkes et al.[11] published a feasibility method for the separation of minimum boiling point azeotropes by continuously entrainer feeding batch distillation. This method has been applied for the use of a light entrainer in the batch rectifier and stripper by Lang et al. (1999)[12] and it applied for maximum azeotropes by Lang et al.[13] Modla et al.[9] extended this method for batch heteroazeotropic distillation under continuous entrainer feeding.
Batch distillation has always been an important part of the production of seasonal, or low capacity and high-purity chemicals. It is a very frequent separation process in the pharmaceutical industry and in wastewater treatment units.
Batch rectifier
The simplest and most frequently used batch distillation configuration is the batch rectifier, including the alembic and pot still. The batch rectifier consists of a pot (or reboiler), rectifying column, a condenser, some means of splitting off a portion of the condensed vapour (distillate) as reflux, and one or more receivers.The pot is filled with liquid mixture and heated. Vapour flows upwards in the rectifying column and condenses at the top. Usually, the entire condensate is initially returned to the column as reflux. This contacting of vapour and liquid considerably improves the separation. Generally, this step is named start-up. After some time, a part of the overhead condensate is withdrawn continuously as distillate and it is accumulated in the receivers, and the other part is recycled into the column as reflux.
Owing to the differing vapour pressures of the distillate, there will be a change in the overhead distillation with time, as early on in the batch distillation the components with a lower vapour pressure wil be evaporated first. As the supply of the material is limited and lighter components are removed, the relative fraction of heavier components will increase as the distillation progresses.
Batch stripper
The other simple batch distillation configuration is the batch stripper. The batch stripper consists of the same parts as the batch rectifier. However, in this case, the charge pot is located above the stripping column.During operation (after charging the pot and starting up the system) the high boiling constituents are primarily separated from the charge mixture. The liquid in the pot is depleted in the high boiling constituents, and enriched in low boiling ones. The high boiling product is routed into the bottom product receivers. The residual low boiling product is withdrawn from the charge pot. This mode of batch distillation is very seldom applied in industrial processes.
Middle vessel column
A third feasible batch column configuration is the middle vessel column. The middle vessel column consists of both a rectifying and a stripping section and the charge pot is located at the middle of the column.Feasibility studies
Generally, the feasibility studies of batch distillation are based on analyses of the following maps:- Residue Curve map
- still path map
- distillate path map
- different column profile maps
- an infinite number of equilibrium stages
- an infinite reflux ratio
- a negligible tray hold-up in the two column sections
- a quasi-steady state in the column
- a constant molar overflow
Lelkes et al.[11] published a feasibility method for the separation of minimum boiling point azeotropes by continuously entrainer feeding batch distillation. This method has been applied for the use of a light entrainer in the batch rectifier and stripper by Lang et al. (1999)[12] and it applied for maximum azeotropes by Lang et al.[13] Modla et al.[9] extended this method for batch heteroazeotropic distillation under continuous entrainer feeding.
See also
- Azeotrope
- Azeotropic distillation
- Extractive distillation
- Fractional distillation
- Heteroazeotrope
- Pot still
- Steam distillation
- Vacuum distillation
- Theoretical plate
References
1. ^ Kister, Henry Z. (1992). Distillation Design, 1st Edition, McGraw-Hill. ISBN 0-07-034909-6.
2. ^ Bernot C., M. Doherty, M. and M. F. Malone, Patterns of composition change in multicomponent batch distillation, Chem. Eng. Sci., 45, 1207, (1990)
3. ^ Ewell, R. H. and L. M. Welch, Rectification in Ternary Systems Containing Binary Azeotropes, Industrial Engineering Chemistry, 37, 1224,(1945)
4. ^ Pham, H. N. and M. F. Doherty, Design and synthesis of heterogeneous azeotropic distillations II. Residue curve maps, Chem. Eng. Sci., 45, 1987-1843, (1990)
5. ^ Rodriguez-Donis I, V. Gerbaud and X. Joulia, Feasibility of Heterogeneous Batch Distillation Processes, AIChE Journal, 48 (6), 1168, (2002)
6. ^ Rodriguez-Donis Y., J. A. Equijarosa, V. Gerbaud and X. Joulia, Heterogeneous Batch-extractive Distillation of Minimum Boiling Azeotropic Mixtures, AIChE Journal, 49 (12), 3074, (2003)
7. ^ Skouras S., V. Kiva and S. Skogestad, Feasible separations and entrainer selection rules for heteroazeotropic batch distillation, Chemical Engineering Science, 60, 2895, (2005)
8. ^ Skouras S., S. Skogestad and V. Kiva, Analysis and Control of Heteroazeotropic Batch Distillation, AIChE Journal, 51 (4), 1144-1157, (2005)
9. ^ Modla G., P. Lang, B. Kotai and K. Molnar, Batch Heteroazeotropic Rectification of a Low Relative Volatility Mixture under Continuous Entrainer Feeding, AIChE Journal, 49 (10), 2533, (2003)
10. ^ * Lang P. and Modla G., Generalised method for the determination of heterogeneous batch distillation regions, Chem. Eng. Sci., 61, 4262-4270, (2006)
11. ^ Lelkes Z., P. Lang, P. Moszkowicz, B. Benadda and M. Otterbein, Batch extractive distillation: the process and the operational policies, Chem. Eng. Sci., 53,1331 (1998)
12. ^ Lang, P., Lelkes Z., Otterbein M., Benadda B., Modla G. ”Feasibility studies for batch extractive distillation with a light entrainer”, Comp. Chem. Eng., 23, S93-S96, (1999).
13. ^ Lang P., G. Modla, B. Benadda and Z. Lelkes, Homoazeotropic Distillation of Maximum Azeotropes in a Batch Rectifier with Continuous Entrainer Feeding: I. Feasibility Studie, Comp. Chem. Eng., 24, 1465, (2000)
2. ^ Bernot C., M. Doherty, M. and M. F. Malone, Patterns of composition change in multicomponent batch distillation, Chem. Eng. Sci., 45, 1207, (1990)
3. ^ Ewell, R. H. and L. M. Welch, Rectification in Ternary Systems Containing Binary Azeotropes, Industrial Engineering Chemistry, 37, 1224,(1945)
4. ^ Pham, H. N. and M. F. Doherty, Design and synthesis of heterogeneous azeotropic distillations II. Residue curve maps, Chem. Eng. Sci., 45, 1987-1843, (1990)
5. ^ Rodriguez-Donis I, V. Gerbaud and X. Joulia, Feasibility of Heterogeneous Batch Distillation Processes, AIChE Journal, 48 (6), 1168, (2002)
6. ^ Rodriguez-Donis Y., J. A. Equijarosa, V. Gerbaud and X. Joulia, Heterogeneous Batch-extractive Distillation of Minimum Boiling Azeotropic Mixtures, AIChE Journal, 49 (12), 3074, (2003)
7. ^ Skouras S., V. Kiva and S. Skogestad, Feasible separations and entrainer selection rules for heteroazeotropic batch distillation, Chemical Engineering Science, 60, 2895, (2005)
8. ^ Skouras S., S. Skogestad and V. Kiva, Analysis and Control of Heteroazeotropic Batch Distillation, AIChE Journal, 51 (4), 1144-1157, (2005)
9. ^ Modla G., P. Lang, B. Kotai and K. Molnar, Batch Heteroazeotropic Rectification of a Low Relative Volatility Mixture under Continuous Entrainer Feeding, AIChE Journal, 49 (10), 2533, (2003)
10. ^ * Lang P. and Modla G., Generalised method for the determination of heterogeneous batch distillation regions, Chem. Eng. Sci., 61, 4262-4270, (2006)
11. ^ Lelkes Z., P. Lang, P. Moszkowicz, B. Benadda and M. Otterbein, Batch extractive distillation: the process and the operational policies, Chem. Eng. Sci., 53,1331 (1998)
12. ^ Lang, P., Lelkes Z., Otterbein M., Benadda B., Modla G. ”Feasibility studies for batch extractive distillation with a light entrainer”, Comp. Chem. Eng., 23, S93-S96, (1999).
13. ^ Lang P., G. Modla, B. Benadda and Z. Lelkes, Homoazeotropic Distillation of Maximum Azeotropes in a Batch Rectifier with Continuous Entrainer Feeding: I. Feasibility Studie, Comp. Chem. Eng., 24, 1465, (2000)
Further reading
- Perry, Robert H. and Green, Don W. (1984). Perry's Chemical Engineers' Handbook, 7th Edition, McGraw-Hill. ISBN 0-07-049841-5.
- Johann G. Stichlmair, James R. Fair (1998). Distillation: principles and practice. Wiley-VCH. ISBN 0-471-25241-7.
- I.M. Mujtaba (2004). Batch Distillation:Design and Operation. Imperial College Press. ISBN 1-86094-437-X.
- Hilmen Eva-Katrine, Separation of Azeotropic Mixtures:Tools for Analysis and Studies on Batch Distillation Operation, Thesis, Norwegian University of Science and Technology Department of Chemical Engineering, (2000).
- Beychok, Milton (May 1951). "Algebraic Solution of McCabe-Thiele Diagram". Chemical Engineering Progress.
Concepts in distillation | |
|---|---|
| Principles | Raoult's law, Dalton's law, Reflux, Fenske equation, McCabe-Thiele method, Theoretical plate |
| Industrial processes | Batch distillation, Continuous distillation, Fractionating column |
| Laboratory methods | Rotary evaporator, Kugelrohr, Spinning band distillation |
| Techniques | Fractional distillation, Vacuum distillation, Extractive distillation, Reactive distillation, Dry distillation, Destructive distillation, Azeotropic distillation, Steam distillation |
Distillation is a method of separating chemical substances based on differences in their volatilities in a boiling liquid mixture. Distillation usually forms part of a larger chemical process, and is thus referred to as a unit operation.
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Continuous distillation, a form of distillation, is an ongoing separation in which a mixture is continuously (without interruption) fed into the process and separated fractions are removed continuously as output streams as time passes during the operation.
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A pharmaceutical company, or drug company, is a commercial business whose focus is to research, develop, market and/or distribute drugs, most commonly in the context of healthcare. They can deal in generic and/or brand medications.
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Wastewater is any water that has been adversely affected in quality by anthropogenic influence. It comprises liquid waste discharged by domestic residences, commercial properties, industry, and/or agriculture and can encompass a wide range of potential contaminants and
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alembic (From Arabic,Al-ambiq الأنبيق ) is an alchemical still consisting of two retorts connected by a tube. Technically, the alembic is only the upper part (the capital or still-head
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A pot still is a type of still used in distilling spirits such as whisky or brandy. Heat is applied directly to the pot in which the mash (in the case of whisky) or wine (in the case of Cognac) is contained.
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Reboilers are heat exchangers typically used to provide heat to the bottom of industrial distillation columns. They boil the liquid from the bottom of a distillation column to generate vapors which are returned to the column to drive the distillation separation.
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Reflux is a technique used in industrial and laboratory distillations. It is also used in chemistry to apply energy to reactions over a long time.
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Reflux in industrial distillation
The term reflux [1][2]..... Click the link for more information.
Reflux is a technique used in industrial and laboratory distillations. It is also used in chemistry to apply energy to reactions over a long time.
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Reflux in industrial distillation
The term reflux [1][2]..... Click the link for more information.
Node: Residue curves begin and end at nodes.
Stable node: The component or azeotrope with the highest boiling point in the region. All the residue curves in the region point to (terminate) at this point.
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Stable node: The component or azeotrope with the highest boiling point in the region. All the residue curves in the region point to (terminate) at this point.
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In the physical sciences, a phase is a set of states of a macroscopic physical system that have relatively uniform chemical composition and physical properties (i.e. density, crystal structure, index of refraction, and so forth).
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An azeotrope is a mixture of two or more pure compounds (chemicals) in such a ratio that its composition cannot be changed by simple distillation.[1] This is because when an azeotrope is boiled, the resulting vapor has the same ratio of constituents as the
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In chemistry, azeotropic distillation[1] is any of a range of techniques used to break an azeotrope in distillation. In chemical engineering, azeotropic distillation
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Extractive distillation is defined as distillation in the presence of a miscible, high boiling, relatively non-volatile component, the solvent, that forms no azeotrope with the other components in the mixture.
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Fractional distillation is the separation of a mixture into its component parts, or fractions, such as in separating chemical compounds by their boiling point by heating them to a temperature at which several fractions of the compound will evaporate.
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A heteroazeotrope is an azeotrope where the vapour phase coexists with two liquid phases.
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Examples of heteroazeotropes
- Benzene - Water NBP 69.2 °C
- Dichloromethane - Water NBP 38.5 °C
See also
- Azeotrope
- Batch distillation
- Distillation
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A pot still is a type of still used in distilling spirits such as whisky or brandy. Heat is applied directly to the pot in which the mash (in the case of whisky) or wine (in the case of Cognac) is contained.
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Steam distillation is a special type of distillation (a separation process) for temperature sensitive materials like natural aromatic compounds.
Many organic compounds tend to decompose at high sustained temperatures.
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Many organic compounds tend to decompose at high sustained temperatures.
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Vacuum distillation is a method of distillation whereby the pressure above the liquid mixture to be distilled is reduced to less than its vapor pressure (usually less than atmospheric) causing evaporation of the least volatile liquid(s) (those with the highest boiling points).
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A theoretical plate in many 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.
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Distillation Design
Author Henry Z. Kister
Language English
Subject(s) Chemical engineering: Distillation design
Publisher McGraw-Hill
Publication date 1992 (1st Edition)
Media type Hardback
Pages 710
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Author Henry Z. Kister
Language English
Subject(s) Chemical engineering: Distillation design
Publisher McGraw-Hill
Publication date 1992 (1st Edition)
Media type Hardback
Pages 710
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Relative volatility is a measure comparing the vapor pressures of the components in a liquid mixture of chemicals. This quantity is widely used in designing large industrial distillation processes.
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Perry's Chemical Engineers' Handbook
Author Perry, R.H. and Green, D.W. (Editors)
Language English
Subject(s) Chemical Engineering
Publisher McGraw-Hill
Publication date June 1997 (7th Edition)
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Author Perry, R.H. and Green, D.W. (Editors)
Language English
Subject(s) Chemical Engineering
Publisher McGraw-Hill
Publication date June 1997 (7th Edition)
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Distillation is a method of separating chemical substances based on differences in their volatilities in a boiling liquid mixture. Distillation usually forms part of a larger chemical process, and is thus referred to as a unit operation.
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Raoult's law states that
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- The vapor pressure of an ideal solution is dependent on the vapor pressure of each chemical component and the mole fraction of the component present in the solution [1].
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Dalton's law (also called Dalton's law of partial pressures) states that the total pressure exerted by a gaseous mixture is equal to the sum of the partial pressures of each individual component in a gas mixture.
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Reflux is a technique used in industrial and laboratory distillations. It is also used in chemistry to apply energy to reactions over a long time.
..... Click the link for more information.
Reflux in industrial distillation
The term reflux [1][2]..... Click the link for more information.
The Fenske equation in continuous fractional distillation is an equation used for calculating the minimum number of theoretical plates required for the separation of a binary feed stream by a fractionation column that is being operated at total reflux (i.e.
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