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Distillation
(part 2)
(Dr.) Mirza Salman Baig
Assistant Professor (Pharmaceutics)
AIKTC, School of Pharmacy,New Panvel
Affiliated to University of Mumbai (INDIA)
Distillation Types
• Azeotropic Distillation
• Extractive distillation
• Vacuum distillation
• Steam distillation
• Molecular Distillation
Azeotropic Distillation
Azeotropic Distillation
• Principle:- Addition of new
substance to the liquid mixture in
order to increase relative volitility
of one of two components and make
seperation easier.
• Ex- Benzene is added to mixture of
water and EtOH
Azeotropic Distillation
Ø This occurs because, when an azeotrope is
boiled, the resulting vapor has the same
ratio of constituents as the original mixture.
Ø Because their composition is unchanged by
distillation, azeotropes are also called
constant boiling mixtures.
Ø Positive azeotrope is 95.63% ethanol and
4.37% water (by weight).
Ø Ethanol boils at 78.4°C, water boils at 100°C,
but the azeotrope boils at 78.2°C.
Ø Negative azeotrope is hydrochloric acid at a
concentration of 20.2% and 79.8% water (by
weight). Hydrogen chloride boils at −84°C
and water at 100°C, but the azeotrope boils
at 110°C.
Azeotropic distillation
Ø Azeotropic distillation usually refers to the
specific technique of adding another
component to generate a new, lower-boiling
azeotrope that is heterogeneous (e.g.
producing two, immiscible liquid phases),
such as the example below with the addition
of benzene to water and ethanol.
Ø This practice of adding an entrainer which
forms a separate phase is a specific sub-set
of (industrial) azeotropic distillation methods,
or combination thereof.
Contd...
• Example - distillation of ethanol/water, using
normal distillation techniques, ethanol can
only be purified to approximately 96% .
• Some uses require a higher percentage of
alcohol, eg. when used as a gasoline
additive.
• Material separation agent- The addition of a
Material Separation Agent, such as benzene.
• Molecular sieves- For the distillation of
ethanol for gasoline addition, the most
common means of breaking the azeotrope is
the use of molecular sieves.
Extractive distillation
Extractive distillation
• 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.
• When third substance added to
azeotropic mixture is non volatile.
• Ex- Glycerien addion reduce
vapour pressure of water.
Extractive Distillation
(Contd...)
Ø The method of extractive distillation uses a
separation solvent, which is generally
nonvolatile, has a high boiling point and is
miscible with the mixture, but doesn't form an
azeotropic mixture.
Ø The solvent interacts differently with the
components of the mixture thereby causing
their relative volatilities to change.
Extractive Distillation
(Contd...)
• The solvent must alter the relative
volatility by a wide enough margin for a
successful result. The quantity, cost and
availability of the solvent should be
considered.
• The solvent should be easily separable
from the bottom product, and should not
react chemically with the components or
the mixture, or cause corrosion in the
equipment.
• A classic example is of aniline as suitable
solvent.
Distillation under reduced pressure
(Vacuum distillation)
Distillation under reduced pressure
(vacuum distillation)
• Liquid distillation at lower pressure than
normal boiling point by applying vacuum.
• Mass of vapour formed =
Vapour pressure of evaporating liquid /
External pressure
• Application-
– Preventing degradation of active components
– Changing physical form (to produce light porous
mass of Cascara sagrada extract.
Vacuum Distillation
Ø 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 pressure) causing
evaporation of the most volatile liquid(s)
(those with the lowest boiling points).
Ø This distillation method works on the
principle that boiling occurs when the
vapor pressure of a liquid exceeds the
ambient (sorrounding) pressure.
Vacuum distillation (Contd...)
• Vacuum distillation is used with or without
heating the solution.
• Temperature sensitive materials (such as
beta carotene) require vacuum distillation
to remove solvents from the mixture
without damaging the product.
• Vacuum distillation is sometimes referred
to as low temperature distillation.
• This type of distillation is in use in the oil
industry.
Advantages of Vacuum Distillation
Ø Industrial-scale vacuum distillation has
several advantages.
• One tool to reduce the number of stages
needed is to utilize vacuum distillation.
Vacuum distillation columns typically used in
oil refineries have diameters ranging up to
about 14 meters (46 feet), heights ranging up
to about 50 meters (164 feet), and feed rates
ranging up to about 25,400 cubic meters per
day (160,000 barrels per day).
• Vacuum distillation increases the relative
volatility of the key components in many
applications. Lower pressures increase
relative volatilities in most systems.
Advantages of Vacuum Distillation
• A second advantage of vacuum distillation is
the reduced temperature requirement at lower
pressures. For many systems, the products
degrade at high temperatures.
• Vacuum distillation can improve a separation
by:
• Prevention of product degradation or polymer
formation because of reduced pressure
leading to lower tower bottoms temperatures.
• Increasing capacity, yield, and purity.
• Another advantage of vacuum distillation is
the reduced capital cost, at the expense of
slightly more operating cost. Utilizing vacuum
distillation can reduce the height and diameter,
and thus the capital cost of a distillation
column.
Distillation under reduced
pressure (Vacuum distillation)
Distillation under reduced
pressure (industrial scale)
Steam distillation
Steam distillation
• Principle - Mixture of immiscible
liquids bigin to boil when the sum of
there vapour pressure is equal to
atmospheric pressure.
• Application Separation of high boiling
point liquid from non volatile impurity.
• Ex- to separate toulene / water.
Steam Distillation still (industrial scale)
Molecular Distillation
Molecular Distillation
Ø A special application of the simple
distillation is molecular distillation,
known also as evaporative distillation or
short path distillation.
Ø Theory of molecular distillation:-
The mean free path of a molecule is
defined as the average distance through
which a molecule can move without
coming into collision with another.
Ø For material that are regarded as non
volatile under ordinary conditions of
temperature and pressure are generally
removed by increasing the mean free path.
Mean free path
• Average distance through a molecule can move
without collision with other molecules.
Molecular Distillation
• It is the distillation processes where
each molecule in vapour phase
travels mean free path and get
condense on condenser surface
without intercollision.
• Distance between evaporating
surface and condensor surface is
approx. equal to mean free path.
• Short path distillation
Molecular Distillation (cont.)
Characteristics of the molecular
distillation process:-
• Very high vacuum
• Evaporating surface must be close to
the condensing surface
• The liquid area is large to avoid
boiling and evolution of the vapors is
from surface only.
Molecular Distillation (cont.)
Applications of molecular distillation:-
Ø Purification of oils
Ø Separation of vitamins
Wiped film molecular still
• Evaporative
distill insted
of boiling
• High vacuum
• short path
Centrifugal molecular still
• Feed introduced
in center
• Rotation of bucket
form the film
which is heated
by radiation.
• Vapouts condense
at condensor
surface.
Distillation types

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Distillation types

  • 1. Distillation (part 2) (Dr.) Mirza Salman Baig Assistant Professor (Pharmaceutics) AIKTC, School of Pharmacy,New Panvel Affiliated to University of Mumbai (INDIA)
  • 2. Distillation Types • Azeotropic Distillation • Extractive distillation • Vacuum distillation • Steam distillation • Molecular Distillation
  • 4. Azeotropic Distillation • Principle:- Addition of new substance to the liquid mixture in order to increase relative volitility of one of two components and make seperation easier. • Ex- Benzene is added to mixture of water and EtOH
  • 5. Azeotropic Distillation Ø This occurs because, when an azeotrope is boiled, the resulting vapor has the same ratio of constituents as the original mixture. Ø Because their composition is unchanged by distillation, azeotropes are also called constant boiling mixtures. Ø Positive azeotrope is 95.63% ethanol and 4.37% water (by weight). Ø Ethanol boils at 78.4°C, water boils at 100°C, but the azeotrope boils at 78.2°C. Ø Negative azeotrope is hydrochloric acid at a concentration of 20.2% and 79.8% water (by weight). Hydrogen chloride boils at −84°C and water at 100°C, but the azeotrope boils at 110°C.
  • 6. Azeotropic distillation Ø Azeotropic distillation usually refers to the specific technique of adding another component to generate a new, lower-boiling azeotrope that is heterogeneous (e.g. producing two, immiscible liquid phases), such as the example below with the addition of benzene to water and ethanol. Ø This practice of adding an entrainer which forms a separate phase is a specific sub-set of (industrial) azeotropic distillation methods, or combination thereof.
  • 7. Contd... • Example - distillation of ethanol/water, using normal distillation techniques, ethanol can only be purified to approximately 96% . • Some uses require a higher percentage of alcohol, eg. when used as a gasoline additive. • Material separation agent- The addition of a Material Separation Agent, such as benzene. • Molecular sieves- For the distillation of ethanol for gasoline addition, the most common means of breaking the azeotrope is the use of molecular sieves.
  • 9. Extractive distillation • 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. • When third substance added to azeotropic mixture is non volatile. • Ex- Glycerien addion reduce vapour pressure of water.
  • 10. Extractive Distillation (Contd...) Ø The method of extractive distillation uses a separation solvent, which is generally nonvolatile, has a high boiling point and is miscible with the mixture, but doesn't form an azeotropic mixture. Ø The solvent interacts differently with the components of the mixture thereby causing their relative volatilities to change.
  • 11. Extractive Distillation (Contd...) • The solvent must alter the relative volatility by a wide enough margin for a successful result. The quantity, cost and availability of the solvent should be considered. • The solvent should be easily separable from the bottom product, and should not react chemically with the components or the mixture, or cause corrosion in the equipment. • A classic example is of aniline as suitable solvent.
  • 12. Distillation under reduced pressure (Vacuum distillation)
  • 13. Distillation under reduced pressure (vacuum distillation) • Liquid distillation at lower pressure than normal boiling point by applying vacuum. • Mass of vapour formed = Vapour pressure of evaporating liquid / External pressure • Application- – Preventing degradation of active components – Changing physical form (to produce light porous mass of Cascara sagrada extract.
  • 14. Vacuum Distillation Ø 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 pressure) causing evaporation of the most volatile liquid(s) (those with the lowest boiling points). Ø This distillation method works on the principle that boiling occurs when the vapor pressure of a liquid exceeds the ambient (sorrounding) pressure.
  • 15. Vacuum distillation (Contd...) • Vacuum distillation is used with or without heating the solution. • Temperature sensitive materials (such as beta carotene) require vacuum distillation to remove solvents from the mixture without damaging the product. • Vacuum distillation is sometimes referred to as low temperature distillation. • This type of distillation is in use in the oil industry.
  • 16. Advantages of Vacuum Distillation Ø Industrial-scale vacuum distillation has several advantages. • One tool to reduce the number of stages needed is to utilize vacuum distillation. Vacuum distillation columns typically used in oil refineries have diameters ranging up to about 14 meters (46 feet), heights ranging up to about 50 meters (164 feet), and feed rates ranging up to about 25,400 cubic meters per day (160,000 barrels per day). • Vacuum distillation increases the relative volatility of the key components in many applications. Lower pressures increase relative volatilities in most systems.
  • 17. Advantages of Vacuum Distillation • A second advantage of vacuum distillation is the reduced temperature requirement at lower pressures. For many systems, the products degrade at high temperatures. • Vacuum distillation can improve a separation by: • Prevention of product degradation or polymer formation because of reduced pressure leading to lower tower bottoms temperatures. • Increasing capacity, yield, and purity. • Another advantage of vacuum distillation is the reduced capital cost, at the expense of slightly more operating cost. Utilizing vacuum distillation can reduce the height and diameter, and thus the capital cost of a distillation column.
  • 18. Distillation under reduced pressure (Vacuum distillation)
  • 21. Steam distillation • Principle - Mixture of immiscible liquids bigin to boil when the sum of there vapour pressure is equal to atmospheric pressure. • Application Separation of high boiling point liquid from non volatile impurity. • Ex- to separate toulene / water.
  • 22. Steam Distillation still (industrial scale)
  • 24. Molecular Distillation Ø A special application of the simple distillation is molecular distillation, known also as evaporative distillation or short path distillation. Ø Theory of molecular distillation:- The mean free path of a molecule is defined as the average distance through which a molecule can move without coming into collision with another. Ø For material that are regarded as non volatile under ordinary conditions of temperature and pressure are generally removed by increasing the mean free path.
  • 25. Mean free path • Average distance through a molecule can move without collision with other molecules.
  • 26. Molecular Distillation • It is the distillation processes where each molecule in vapour phase travels mean free path and get condense on condenser surface without intercollision. • Distance between evaporating surface and condensor surface is approx. equal to mean free path. • Short path distillation
  • 27. Molecular Distillation (cont.) Characteristics of the molecular distillation process:- • Very high vacuum • Evaporating surface must be close to the condensing surface • The liquid area is large to avoid boiling and evolution of the vapors is from surface only.
  • 28. Molecular Distillation (cont.) Applications of molecular distillation:- Ø Purification of oils Ø Separation of vitamins
  • 29. Wiped film molecular still • Evaporative distill insted of boiling • High vacuum • short path
  • 30. Centrifugal molecular still • Feed introduced in center • Rotation of bucket form the film which is heated by radiation. • Vapouts condense at condensor surface.