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COLLIGATIVE PROPERTIES
OF SOLUTIONS
• The word “colligative” has been adapted or
taken from the Latin word “colligatus” which
means “bound together”.
• “A colligative property is a property of a
solution that is dependent on the ratio
between the total number of solute particles
(in the solution) to the total number of
solvent particles.”
• Colligative properties are not dependent on
the chemical nature of the solution’s
components.
• Thus, colligative properties can be linked to
several quantities that express the
concentration of a solution, such as molarity,
normality, and molality.
• The four colligative properties that can be
exhibited by a solution are:
1. Boiling point elevation
2. Freezing point depression
3. Relative lowering of vapor pressure
4. Osmotic pressure
1. Lowering of Vapor Pressure
• In a pure solvent, the entire surface is occupied
by the molecules of the solvent.
• If a non- volatile solute is added to the solvent,
the surface now has both solute and solvent
molecules; thereby fraction of surface covered by
solvent molecules gets reduced.
• Since the vapour pressure of the solution is solely
due to solvent alone, at the same temperature
the vapour pressure of the solution is found to be
lower than that of the pure solvent.
• If P0 is the vapour pressure of pure solvent
and Ps is the vapour pressure of the solution.
The difference P0 – Ps is termed as lowering in
vapour pressure. The ratio P0 – Ps / P0 is
known as the relative lowering of vapour
pressure.
• Raoult, in 1886, established a relation
between relative lowering in vapour pressure
and mole fraction. The relationship is known
as Raoult’s law.
• It states that
• “the relative lowering in vapour pressure of a
dilute solution is equal to the mole fraction of
the solute present in the solution”
• If n moles of solute is dissolved in N moles of
the solvent, then according to Raoult’s law
• P0 – Ps / P0 = n / n + N
2. Elevation in Boiling Point
• The boiling point of a liquid is the temperature at
which the vapour pressure is equal to atmospheric
pressure.
• We know that on the addition of a non-volatile liquid
to a pure solvent, the vapour pressure of a solution
decrease.
• Therefore to make vapour pressure equal to
atmospheric pressure we have to increase the
temperature of the solution.
• The difference in the boiling point of the solution and
the boiling point of the pure solvent is termed as
elevation in boiling point.
• If T0b is the boiling point of the pure solvent and Tb is the boiling
point of the solution then elevation in boiling point is given as
∆Tb =T0b-Tb
• Experimental results show that there is a relation between
elevation in boiling point and molality ‘m’ of the solute present in
solution
– ∆Tb ∝ m
– ∆Tb = kb m
– Where,
– kb = molal elevation constant
– Substituting the value of ‘m’ in the above relation we get
– ∆Tb = 1000 x kb x m2 / M2 x m1
• Where,
–m2 = mass of solvent in g
–M1 = mass of solvent in kg
–M2 = molar mass of solute
3. Depression in Freezing Point
• The freezing point of a substance is defined as the
temperature at which the vapour pressure of its liquid is
equal to the vapour of the corresponding solid.
• According to Raoult’s law when a non-volatile solid is added
to the solvent its vapour pressure decreases and now it
would become equal to that of solid solvent at a lower
temperature.
• The difference between the freezing point of the pure
solvent and its solution is called depression in freezing
point.
• If T0
f is the freezing point of the pure solvent and Tf is the
freezing point of the solution then depression in freezing
point is given as
• ∆Tf =T0
f-Tf
• Just like elevation in boiling point, depression
in freezing point is also directly related to
molality ‘m’.
• ∆Tf = 1000 x kf x m2 / M2 x m1
• Where,
• kf = molal depression constant
• m2 = mass of solvent in g
• M1 = mass of solvent in kg
• M2 = molar mass of solute
4. Osmotic Pressure
• When a semipermeable membrane is placed between a solution and
solvent, it is observed that solvent molecules enter the solution
through the semipermeable membrane and the volume of the solution
increases.
• The semi-permeable membrane allows only solvent molecules to pass
through it but prevents the passage of bigger molecules like solute.
• This phenomenon of the spontaneous flow of solvent molecules
through a semipermeable membrane from a pure solvent to a solution
or from a dilute to a concentrated solution is called osmosis.
• The flow of solvent molecules through the semipermeable membrane
can be stopped if some extra pressure is applied from the solution
side.
• This pressure that just stops the flow of solvent is called osmotic
pressure of the solution.
• Osmotic pressure is a colligative property as it depends on
the number of solute present and not on the nature of the
solute.
• Experimentally it was proved that osmotic pressure (⫪) is
directly proportional to molarity(C) and temperature(T).
• Mathematically, ⫪ = CRT where R is the gas constant.
• ⇒ ⫪ = (n2/V) RT
• Here, V is the volume of solution in liters and n2 is moles of
solute
• If m2 is the weight of solute and M2 molar mass of solute,
then n2= m2/M2
• ⫪ = m2 RT / M2V
• Thus by knowing the values of ⫪,W2, T and V we can
calculate the molar mass of the solute.
Different Solutions
• Hypotonic solution: A
hypotonic solution has a
lower osmotic pressure
than that of the
surrounding i.e, the
concentration of solute
particles is less than that of
the surrounding. If the
hypotonic solution is
separated by
semipermeable membrane
then water moves out of
the hypotonic solution.
• Hypertonic solution: A
hypertonic solution has a
higher osmotic pressure
than that of the
surrounding i.e, the
concentration of solute
particles is more than
that of the surrounding. If
the hypertonic solution is
separated by
semipermeable
membrane then water
moves inside the
hypertonic solution.
• Isotonic solution: Two
solutions having the
same osmotic pressure
at a given temperature
are known as an
isotonic solution. When
such solutions are
separated by a semi-
permeable membrane
than there is no
osmosis.
APPLICATIONS OF COLLIGATIVE
PROPERTIES IN PHARMACY
• Colligative properties are properties that are related to
the ratio of particle (ions or molecules of a solute to
the number of particles in the solvent. This can also be
expressed as the concentration of the dissociated or
dissolved particle in a solution. This can be used to
identify substances in pharmaceutical analysis, but
there are easier ways to identify substances. It is
unlikely that a dispensing pharmacy would utilize such
properties with one exeption. If the pharmacy is in a
cold climate and there is snow and ice on the ground,
various salts are used to lower the freezing point of the
ice below the ambient temperature in order to melt the
ice. Pharmacies would use this to keep their sidewalks
clear of frozen water.

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COLLIGATIVE PROPERTIES OF SOLUTIONS.pptx

  • 2. • The word “colligative” has been adapted or taken from the Latin word “colligatus” which means “bound together”.
  • 3. • “A colligative property is a property of a solution that is dependent on the ratio between the total number of solute particles (in the solution) to the total number of solvent particles.” • Colligative properties are not dependent on the chemical nature of the solution’s components. • Thus, colligative properties can be linked to several quantities that express the concentration of a solution, such as molarity, normality, and molality.
  • 4. • The four colligative properties that can be exhibited by a solution are: 1. Boiling point elevation 2. Freezing point depression 3. Relative lowering of vapor pressure 4. Osmotic pressure
  • 5. 1. Lowering of Vapor Pressure • In a pure solvent, the entire surface is occupied by the molecules of the solvent. • If a non- volatile solute is added to the solvent, the surface now has both solute and solvent molecules; thereby fraction of surface covered by solvent molecules gets reduced. • Since the vapour pressure of the solution is solely due to solvent alone, at the same temperature the vapour pressure of the solution is found to be lower than that of the pure solvent.
  • 6.
  • 7. • If P0 is the vapour pressure of pure solvent and Ps is the vapour pressure of the solution. The difference P0 – Ps is termed as lowering in vapour pressure. The ratio P0 – Ps / P0 is known as the relative lowering of vapour pressure. • Raoult, in 1886, established a relation between relative lowering in vapour pressure and mole fraction. The relationship is known as Raoult’s law.
  • 8. • It states that • “the relative lowering in vapour pressure of a dilute solution is equal to the mole fraction of the solute present in the solution” • If n moles of solute is dissolved in N moles of the solvent, then according to Raoult’s law • P0 – Ps / P0 = n / n + N
  • 9. 2. Elevation in Boiling Point • The boiling point of a liquid is the temperature at which the vapour pressure is equal to atmospheric pressure. • We know that on the addition of a non-volatile liquid to a pure solvent, the vapour pressure of a solution decrease. • Therefore to make vapour pressure equal to atmospheric pressure we have to increase the temperature of the solution. • The difference in the boiling point of the solution and the boiling point of the pure solvent is termed as elevation in boiling point.
  • 10. • If T0b is the boiling point of the pure solvent and Tb is the boiling point of the solution then elevation in boiling point is given as ∆Tb =T0b-Tb • Experimental results show that there is a relation between elevation in boiling point and molality ‘m’ of the solute present in solution – ∆Tb ∝ m – ∆Tb = kb m – Where, – kb = molal elevation constant – Substituting the value of ‘m’ in the above relation we get – ∆Tb = 1000 x kb x m2 / M2 x m1
  • 11. • Where, –m2 = mass of solvent in g –M1 = mass of solvent in kg –M2 = molar mass of solute
  • 12. 3. Depression in Freezing Point • The freezing point of a substance is defined as the temperature at which the vapour pressure of its liquid is equal to the vapour of the corresponding solid. • According to Raoult’s law when a non-volatile solid is added to the solvent its vapour pressure decreases and now it would become equal to that of solid solvent at a lower temperature. • The difference between the freezing point of the pure solvent and its solution is called depression in freezing point. • If T0 f is the freezing point of the pure solvent and Tf is the freezing point of the solution then depression in freezing point is given as
  • 13. • ∆Tf =T0 f-Tf • Just like elevation in boiling point, depression in freezing point is also directly related to molality ‘m’. • ∆Tf = 1000 x kf x m2 / M2 x m1 • Where, • kf = molal depression constant • m2 = mass of solvent in g • M1 = mass of solvent in kg • M2 = molar mass of solute
  • 14. 4. Osmotic Pressure • When a semipermeable membrane is placed between a solution and solvent, it is observed that solvent molecules enter the solution through the semipermeable membrane and the volume of the solution increases. • The semi-permeable membrane allows only solvent molecules to pass through it but prevents the passage of bigger molecules like solute. • This phenomenon of the spontaneous flow of solvent molecules through a semipermeable membrane from a pure solvent to a solution or from a dilute to a concentrated solution is called osmosis. • The flow of solvent molecules through the semipermeable membrane can be stopped if some extra pressure is applied from the solution side. • This pressure that just stops the flow of solvent is called osmotic pressure of the solution.
  • 15.
  • 16. • Osmotic pressure is a colligative property as it depends on the number of solute present and not on the nature of the solute. • Experimentally it was proved that osmotic pressure (⫪) is directly proportional to molarity(C) and temperature(T). • Mathematically, ⫪ = CRT where R is the gas constant. • ⇒ ⫪ = (n2/V) RT • Here, V is the volume of solution in liters and n2 is moles of solute • If m2 is the weight of solute and M2 molar mass of solute, then n2= m2/M2 • ⫪ = m2 RT / M2V • Thus by knowing the values of ⫪,W2, T and V we can calculate the molar mass of the solute.
  • 17. Different Solutions • Hypotonic solution: A hypotonic solution has a lower osmotic pressure than that of the surrounding i.e, the concentration of solute particles is less than that of the surrounding. If the hypotonic solution is separated by semipermeable membrane then water moves out of the hypotonic solution.
  • 18. • Hypertonic solution: A hypertonic solution has a higher osmotic pressure than that of the surrounding i.e, the concentration of solute particles is more than that of the surrounding. If the hypertonic solution is separated by semipermeable membrane then water moves inside the hypertonic solution.
  • 19. • Isotonic solution: Two solutions having the same osmotic pressure at a given temperature are known as an isotonic solution. When such solutions are separated by a semi- permeable membrane than there is no osmosis.
  • 20. APPLICATIONS OF COLLIGATIVE PROPERTIES IN PHARMACY • Colligative properties are properties that are related to the ratio of particle (ions or molecules of a solute to the number of particles in the solvent. This can also be expressed as the concentration of the dissociated or dissolved particle in a solution. This can be used to identify substances in pharmaceutical analysis, but there are easier ways to identify substances. It is unlikely that a dispensing pharmacy would utilize such properties with one exeption. If the pharmacy is in a cold climate and there is snow and ice on the ground, various salts are used to lower the freezing point of the ice below the ambient temperature in order to melt the ice. Pharmacies would use this to keep their sidewalks clear of frozen water.