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12C05

Surface Chemistry

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Learning Objectives

Adsorption

Catalysis

Colloids

12C05 - Surface Chemistry

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Introduction to Surface Chemistry

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Surface Chemistry

It deals with phenomena that occur at the surfaces or interfaces

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Surface Chemistry

It deals with phenomena that occur at the surfaces or interfaces

Separating the bulk phases

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Surface Chemistry

It deals with phenomena that occur at the surfaces or interfaces

  • Liquid - Liquid
  • Liquid - Gas
  • Liquid - Solid
  • Solid - Gas
  • Solid - Solid

Types of Interfaces

Separating the bulk phases

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ConcepTest

Ready for challenge

7

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Q. : Why does a gaseous mixture not possess an interface ?

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Pause the Video

(Time Duration : 01 Minutes)

Q. : Why does a gaseous mixture not possess an interface ?

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Q. : Why does a gaseous mixture not possess an interface ?

Sol. :

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Q. : Why does a gaseous mixture not possess an interface ?

Sol. : Gases are completely mixed with each other.

Due to complete miscibility, there is no

interface in mixtures of gases

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Phenomena at Interface

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Crystallisation

Phenomena at Interface

Crystallisation of water

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Crystallisation

Phenomena at Interface

Crystallisation of water

Ice

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Crystallisation

Phenomena at Interface

Crystallisation of water

Ice

Medicines

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Crystallisation

Phenomena at Interface

Crystallisation of water

Sugar

Ice

Medicines

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Crystallisation

Phenomena at Interface

Crystallisation of water

Table salt

Sugar

Ice

Medicines

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Dissolution

Phenomena at Interface

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Dissolution

Phenomena at Interface

Dissolution of Table Salt

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Dissolution

Phenomena at Interface

Dissolution of Table Salt

Dissolution of Medicine

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Corrosion

Phenomena at Interface

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Corrosion

Phenomena at Interface

Surface of Iron

O2

H2O

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Corrosion

Phenomena at Interface

Surface of Iron

O2

H2O

Rusted Iron Object

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Phenomena at Interface

Heterogeneous catalysis

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Phenomena at Interface

Heterogeneous catalysis

Surface of Catalyst, Ni

Reactant, vanaspati oil

Product, vanaspati ghee

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Phenomena at Interface

Heterogeneous catalysis

Surface of Catalyst, Ni

Reactant, vanaspati oil

Product, vanaspati ghee

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Surface chemistry

Colloids

Catalysis

Adsorption

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12C05.1

Adsorption and its types

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12C05.1 Adsorption and its types

Learning Objectives

Absorption and Adsorption

Mechanism of Adsorption

Types of Adsorption

Characteristics of Physisorption

Characteristics of Chemisorption

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12C05.1

CV 1

Absorption and Adsorption

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Absorption

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Absorption

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One Substance is uniformly distributed throughout the bulk of the other substance

Absorption

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Adsorption

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Adsorption

Accumulation of molecular species at the surface of a solid or liquid

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Adsorbent

Accumulation of molecular species at the surface of a solid or liquid

Adsorption

Adsorbate

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Adsorbent

Accumulation of molecular species at the surface of a solid or liquid

Adsorption

Adsorbate

Accumulates at the surface

Solid, liquid or gas

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Adsorbent

Provides Surface for adsorption

Accumulation of molecular species at the surface of a solid or liquid

Solid or liquid

Adsorption

Adsorbate

Accumulates at the surface

Solid, liquid or gas

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Absorption vs Adsorption

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Absorption vs Adsorption

Absorbed

Particle

(In the bulk)

Liquid

Gas Particles

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Absorption vs Adsorption

Absorbed

Particle

(In the bulk)

Liquid

Absorption (bulk phenomenon)

Gas Particles

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Absorption vs Adsorption

Absorbed

Particle

(In the bulk)

Adsorbed

Particle

(At surface)

Adsorbent Surface

Gas Particles

Gas Particles

Liquid

Absorption (bulk phenomenon)

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Absorption vs Adsorption

Absorbed

Particle

(In the bulk)

Adsorbed

Particle

(At surface)

Adsorbent Surface

Adsorption (surface phenomenon)

Gas Particles

Gas Particles

Liquid

Absorption (Bulk phenomenon)

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Absorption vs Adsorption

Absorption

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Absorption vs Adsorption

Absorption

Adsorption

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Water vapours are adsorbed by silica gel

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Water vapours are absorbed by anhydrous CaCl2

Water vapours are adsorbed by silica gel

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Examples of some common adsorbents :

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Examples of some common adsorbents :

Charcoal

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Examples of some common adsorbents :

Charcoal

Silica gel

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Examples of some common adsorbents :

Charcoal

Silica gel

Alumina gel

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Adsorption in action

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Adsorption in action

Brown coloured NO2 gas

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Adsorption in action

Brown coloured NO2 gas

Activated charcoal

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Adsorption in action

Brown coloured NO2 gas

NO2 gas adsorbed by charcoal

Activated charcoal

Brown colour is disappeared

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Adsorption in action

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Adsorption in action

Gas Molecules

Molecules collide with wall and create pressure

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Adsorption in action

Gas Molecules

Pressure of gas = P

Molecules collide with wall and create pressure

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Adsorption in action

Gas Molecules

Adsorbent

Molecules collide with wall and create pressure

Pressure of gas = P

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Adsorption in action

Gas Molecules

Adsorbent

Molecules collide with wall and create pressure

Pressure of gas = P

Gas adsorbed by Adsorbate

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Adsorption in action

Gas Molecules

Pressure of gas = P

Pressure of gas < P

Molecules collide with wall and create pressure

Adsorbent

Gas adsorbed by Adsorbent

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Some basic terms related to adsorption

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Some basic terms related to adsorption

Desorption

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Some basic terms related to adsorption

Desorption

Process of removing adsorbate from surface of adsorbent

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Some basic terms related to adsorption

Desorption

Process of removing adsorbate from surface of adsorbent

Sorption

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Some basic terms related to adsorption

Desorption

Process of removing adsorbate from surface of adsorbent

Sorption

Adsorption and absorption take place simultaneously

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12C05.1

CV 2

Mechanism of Adsorption

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Mechanism of Adsorption

Two Aspects

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Mechanism of Adsorption

Net force on particle

Two Aspects

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Mechanism of Adsorption

Net force on particle

Thermodynamics of Adsorption

Two Aspects

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Net Force on Particle

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Net Force on Particle

Adsorbent

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Bulk particle

Net Force on Particle

Adsorbent

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Adsorbent

Bulk particle

Surface particle

Net Force on Particle

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Adsorbent

Bulk particle

Balanced force

Net force = 0

Surface particle

Net Force on Particle

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Adsorbent

Bulk particle

Balanced force

Net force = 0

Surface particle

Imbalanced force

Net Force on Particle

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Adsorbent

Bulk particle

Balanced force

Net force = 0

Surface particle

Imbalanced force

Net Force on Particle

Net force

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Adsorbent

Bulk particle

Balanced force

Net force = 0

Surface particle

Imbalanced force

Other particle

Net Force on Particle

Net force

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Adsorbent

Bulk particle

Balanced force

Net force = 0

Surface particle

Imbalanced force

Other particle

Net Force on Particle

Net force

Attraction

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Adsorbent

Bulk particle

Balanced force

Net force = 0

Surface particle

Imbalanced force

Other particle

Net Force on Particle

Adsorption due to imbalanced force

Net force

Attraction

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Thermodynamics of Adsorption

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Thermodynamics of Adsorption

Change in heat of adsorption

ΔH

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Thermodynamics of Adsorption

Change in heat of adsorption

Change in entropy

ΔH

ΔS

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Thermodynamics of Adsorption

Change in heat of adsorption

Change in entropy

Change in Gibbs free energy

ΔH

ΔS

ΔG

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Change in heat of adsorption, ΔH

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Change in heat of adsorption, ΔH

A

B

AB

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Change in heat of adsorption, ΔH

Attraction

ΔH = - ve

A

B

AB

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Change in heat of adsorption, ΔH

Attraction

ΔH = - ve

A

B

AB

AB

A

B

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Change in heat of adsorption, ΔH

Separation

ΔH = + ve

Attraction

ΔH = - ve

A

B

AB

AB

A

B

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Change in heat of adsorption, ΔH

Separation

ΔH = + ve

Attraction

ΔH = - ve

A

B

AB

AB

A

B

Occurs in adsorption

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Change in entropy, ΔS

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Change in entropy, ΔS

Adsorbate

Adsorbent

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Change in entropy, ΔS

Adsorbate

Adsorbent

Adsorbent

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Change in entropy, ΔS

Randomness decrease

Adsorbate

Adsorbent

Adsorbent

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Change in entropy, ΔS

Randomness decrease

ΔS = - ve

Adsorbate

Adsorbent

Adsorbent

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12C05.1 Adsorption and its types

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Change in Gibbs Free Energy , ΔG

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12C05.1 Adsorption and its types

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Change in Gibbs Free Energy , ΔG

Ice

Water

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12C05.1 Adsorption and its types

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Change in Gibbs Free Energy , ΔG

Ice

Water

ΔG = - ve

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12C05.1 Adsorption and its types

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Change in Gibbs Free Energy , ΔG

Ice

Water

Spontaneous process

ΔG = - ve

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12C05.1 Adsorption and its type

12C05.1 Adsorption and its types

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Change in Gibbs Free Energy , ΔG

Ice

Water

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12C05.1 Adsorption and its types

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Change in Gibbs Free Energy , ΔG

Ice

Water

ΔG = + ve

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12C05.1 Adsorption and its types

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Change in Gibbs Free Energy , ΔG

Ice

Water

Non - spontaneous process

ΔG = + ve

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12C05.1 Adsorption and its types

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Change in Gibbs Free Energy , ΔG

Ice

Water

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Change in Gibbs Free Energy , ΔG

Ice

Water

ΔG = 0

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12C05.1 Adsorption and its types

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Change in Gibbs Free Energy , ΔG

Ice

Water

Equilibrium

ΔG = 0

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Thermodynamics of adsorption

Change in heat of adsorption, ΔH

Change in entropy, ΔS

Change in Gibbs free energy, ΔG

Bond breaking

ΔH = +ve

Bond making

ΔH = -ve

Randomness increase, ΔS = +ve

Spontaneous

ΔG = -ve

Equilibrium

ΔG = 0

Randomness decrease, ΔS = -ve

Non - spontaneous

ΔG = +ve

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110

Relation between ∆H, ∆S and ∆G

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Relation between ∆H, ∆S and ∆G

∆G = ∆H - T ∆S

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112

Relation between ∆H, ∆S and ∆G

∆G = ∆H - T ∆S

- ve

- ve

For adsorption

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Relation between ∆H, ∆S and ∆G

∆G = ∆H - T ∆S

- ve

- ve

∆G = - ∆H + T ∆S

For adsorption

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∆G = ∆H - T∆S

∆G = −∆H +T∆S

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∆G = ∆H - T∆S

∆G = −∆H +T∆S

At low Temperature

∆H < T∆S

∆G = - ve

Spontaneous Process

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∆G = ∆H - T∆S

∆G = −∆H +T∆S

At low Temperature

∆H < T∆S

∆G = - ve

Spontaneous Process

If Temperature increases

∆H = T∆S

∆G = 0

Equilibrium Condition

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12C05.1

CV 3

Types of Adsorption

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Types of Adsorption

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Types of Adsorption

Physical adsorption

Physisorption

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Types of Adsorption

Physical adsorption

Physisorption

Chemisorption

Chemicall adsorption

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Types of Adsorption

Adsorbate

Adsorbent

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Types of Adsorption

Adsorbate

Adsorbent

Weak van der Waals’ forces

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Types of Adsorption

Adsorbate

Adsorbent

Physisorption

Weak van der Waals’ forces

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Types of Adsorption

Adsorbate

Adsorbent

Physisorption

Weak van der Waals’ forces

Strong chemical bonds (Covalent or Ionic)

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Types of Adsorption

Adsorbate

Adsorbent

Physisorption

Chemisorption

Weak van der Waals’ forces

Strong chemical bonds (Covalent or Ionic)

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12C05.1

CV 4

Characteristics of Physisorption

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Characteristics of Physisorption

1 - Lack of specificity

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Characteristics of Physisorption

1 - Lack of specificity

Adsorbent

Different gases

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Characteristics of Physisorption

1 - Lack of specificity

Adsorbent

Different gases

Universal weak van der Waals’ force

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Characteristics of Physisorption

1 - Lack of specificity

Adsorbent

Different gases

Adsorbent

Universal weak van der Waals’ force

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Characteristics of Physisorption

1 - Lack of specificity

Adsorbent

Different gases

All types of gases can adsorbed

Adsorbent

Universal weak van der Waals’ force

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Characteristics of Physisorption

2 - Nature of adsorbate

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Characteristics of Physisorption

Adsorbent

Adsorbent

2 - Nature of adsorbate

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Characteristics of Physisorption

Adsorbent

Adsorbent

Adsorbent

2 - Nature of adsorbate

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Characteristics of Physisorption

Adsorbent

Adsorbent

Adsorbent

Adsorbent

2 - Nature of adsorbate

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Characteristics of Physisorption

Adsorbent

Adsorbent

Adsorbent

Adsorbent

2 - Nature of adsorbate

High critical temperature

More adsorption

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12C05.1 Adsorption and its types

ConcepTest

Ready for challenge

137

138 of 519

12C05.1 Adsorption and its types

Q. : What is the role of critical temperature, TC in adsorption of gases on solid surface?

139 of 519

12C05.1 Adsorption and its types

Pause the Video

(Time Duration : 02 Minutes)

Q. : What is the role of critical temperature, TC in adsorption of gases on solid surface?

140 of 519

12C05.1 Adsorption and its types

Q. : What is the role of critical temperature, TC in adsorption of gases on solid surface?

Sol. :

141 of 519

12C05.1 Adsorption and its types

Q. : What is the role of critical temperature, TC in adsorption of gases on solid surface?

Sol. : Critical temperature is one above which gases can't be liquefied, no matter

what the pressure is.

142 of 519

12C05.1 Adsorption and its types

Q. : What is the role of critical temperature, TC in adsorption of gases on solid surface?

Sol. : Critical temperature is one above which gases can't be liquefied, no matter

what the pressure is.

Critical temperature

Adsorption

143 of 519

12C05.1 Adsorption and its types

Q. : What is the role of critical temperature, TC in adsorption of gases on solid surface?

Sol. : Critical temperature is one above which gases can't be liquefied, no matter

what the pressure is.

Critical temperature

Adsorption

Gas

SO2

NH3

CO2

H2

TC (K)

430

406

304

33

Adsorption (ml)

380

180

48

4.5

Adsorption of some gases per g of adsorbate at their critical temperature

144 of 519

12C05.1 Adsorption and its types

ConcepTest

Ready for challenge

144

145 of 519

12C05.1 Adsorption and its types

Q. : On the basis of TC given in the following table, arrange the given gases in the

increasing order of adsorption under identical conditions.

Gas

H2

CO2

CH4

NH3

TC (K)

33

304

190

406

146 of 519

12C05.1 Adsorption and its types

Pause the Video

(Time Duration : 02 Minutes)

Q. : On the basis of TC given in the following table, arrange the given gases in the

increasing order of adsorption under identical conditions.

Gas

H2

CO2

CH4

NH3

TC (K)

33

304

190

406

147 of 519

12C05.1 Adsorption and its types

Q. : On the basis of TC given in the following table, arrange the given gases in the

increasing order of adsorption under identical conditions.

Sol. :

Gas

H2

CO2

CH4

NH3

TC (K)

33

304

190

406

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12C05.1 Adsorption and its types

Q. : On the basis of TC given in the following table, arrange the given gases in the

increasing order of adsorption under identical conditions.

Sol. :

Gas

H2

CO2

CH4

NH3

TC (K)

33

304

190

406

Intermolecular forces

Critical temp.

Adsorption

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12C05.1 Adsorption and its types

Q. : On the basis of TC given in the following table, arrange the given gases in the

increasing order of adsorption under identical conditions.

Sol. :

Order of TC = H2 < CH4 < CO2 < NH3

Gas

H2

CO2

CH4

NH3

TC (K)

33

304

190

406

Intermolecular forces

Critical temp.

Adsorption

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12C05.1 Adsorption and its types

Q. : On the basis of TC given in the following table, arrange the given gases in the

increasing order of adsorption under identical conditions.

Sol. :

Order of TC = H2 < CH4 < CO2 < NH3

Increasing order of Adsorption = H2 < CH4 < CO2 < NH3

Gas

H2

CO2

CH4

NH3

TC (K)

33

304

190

406

Intermolecular forces

Critical temp.

Adsorption

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3 - Reversible nature

Characteristics of Physisorption

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3 - Reversible nature

Characteristics of Physisorption

Adsorbent

Gas

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3 - Reversible nature

Characteristics of Physisorption

Adsorbent

Adsorbent

Gas

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3 - Reversible nature

Characteristics of Physisorption

Adsorbent

Adsorbent

Gas

weak van der Waals’ force

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3 - Reversible nature

Characteristics of Physisorption

Adsorbent

Adsorbent

Adsorbent

Gas

weak van der Waals’ force

Easy desorption

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4 - Change with Pressure

Characteristics of Physisorption

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Pressure

Characteristics of Physisorption

Adsorption

4 - Change with Pressure

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Pressure

Characteristics of Physisorption

Piston

Gas molecules

Adsorbent

Adsorption

4 - Change with Pressure

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Pressure

Characteristics of Physisorption

Piston

Gas molecules

Adsorbent

Less adsorption

Low pressure

Adsorption

4 - Change with Pressure

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Pressure

Characteristics of Physisorption

Piston

Gas molecules

Adsorbent

Less adsorption

More adsorption

Low pressure

High pressure

Adsorption

4 - Change with Pressure

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ConcepTest

Ready for challenge

161

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12C05.1 Adsorption and its types

Q. : Why does physical adsorption increase with pressure?

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Q. : Why does physical adsorption increase with pressure?

Sol. :

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Q. : Why does physical adsorption increase with pressure?

Sol. : According to the Le–Chatelier’s principle, If we increase pressure of the system

at equilibrium state, the equilibrium will shift towards lesser number of gaseous

molecules to reduce the pressure of the system

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Q. : Why does physical adsorption increase with pressure?

Sol. : According to the Le–Chatelier’s principle, If we increase pressure of the system

at equilibrium state, the equilibrium will shift towards lesser number of gaseous

molecules to reduce the pressure of the system

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Q. : Why does physical adsorption increase with pressure?

Sol. : According to the Le–Chatelier’s principle, If we increase pressure of the system

at equilibrium state, the equilibrium will shift towards lesser number of gaseous

molecules to reduce the pressure of the system

Equilibrium state

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Q. : Why does physical adsorption increase with pressure?

Sol. : According to the Le–Chatelier’s principle, If we increase pressure of the system

at equilibrium state, the equilibrium will shift towards lesser number of gaseous

molecules to reduce the pressure of the system

Equilibrium state

At low P

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Q. : Why does physical adsorption increase with pressure?

Sol. : According to the Le–Chatelier’s principle, If we increase pressure of the system

at equilibrium state, the equilibrium will shift towards lesser number of gaseous

molecules to reduce the pressure of the system

Equilibrium state

At low P

At high P

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5 - Change with Temperature

Characteristics of Physisorption

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Adsorption is an exothermic process

Characteristics of Physisorption

5 - Change with Temperature

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Adsorption

Adsorption is an exothermic process

Temp.

Characteristics of Physisorption

5 - Change with Temperature

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Adsorption

Adsorption is an exothermic process

Temp.

Adsorbent

More adsorption

Characteristics of Physisorption

5 - Change with Temperature

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Adsorption

Adsorption is an exothermic process

Temp.

Adsorbent

Adsorbent

More adsorption

Less adsorption

Characteristics of Physisorption

5 - Change with Temperature

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Characteristics of Physisorption

5 - Change with Temperature

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Characteristics of Physisorption

Amount of gas adsorbed

Temperature

5 - Change with Temperature

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Characteristics of Physisorption

Amount of gas adsorbed

Temperature

5 - Change with Temperature

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Characteristics of Physisorption

Amount of gas adsorbed

Temperature

High adsorption

Low temp.

5 - Change with Temperature

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Characteristics of Physisorption

Amount of gas adsorbed

Temperature

High adsorption

Low adsorption

High temp.

Low temp.

5 - Change with Temperature

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Q. : Why does physisorption decrease with the increase of temperature?

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Q. : Why does physisorption decrease with the increase of temperature?

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Q. : Why does physisorption decrease with the increase of temperature?

Sol. :

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Q. : Why does physisorption decrease with the increase of temperature?

Sol. :

Adsorption is an exothermic process

ΔH = -ve

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Q. : Why does physisorption decrease with the increase of temperature?

Sol. :

Adsorption is an exothermic process

ΔH = -ve

From Le–Chatelier’s principle -

For an exothermic process, an increase in temperature shifts the process in backward direction - adsorption will decrease

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Q. : Why does physisorption decrease with the increase of temperature?

Sol. :

Adsorption is an exothermic process

ΔH = -ve

From Le–Chatelier’s principle -

For an exothermic process, an increase in temperature shifts the process in backward direction - adsorption will decrease

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6 - Enthalpy of Adsorption

Characteristics of Physisorption

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6 - Enthalpy of Adsorption

Characteristics of Physisorption

Adsorbent

Adsorbate

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6 - Enthalpy of Adsorption

Characteristics of Physisorption

Adsorbent

Weak van der Waals’ force

Adsorbate

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6 - Enthalpy of Adsorption

Characteristics of Physisorption

Adsorbent

Weak van der Waals’ force

Release less energy during adsorption

Only 20 to 40 kj mol-1

Adsorbate

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7 - Surface area of adsorbent

Characteristics of Physisorption

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7 - Surface area of adsorbent

Characteristics of Physisorption

Surface area of adsorbent Adsorption

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7 - Surface area of adsorbent

Characteristics of Physisorption

Surface area of adsorbent Adsorption

Dividing adsorbent

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Characteristics of Physisorption

Surface area of adsorbent Adsorption

Less surface area

Less adsorption

More surface area

More adsorption

Dividing adsorbent

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7 - Surface area of adsorbent

Characteristics of Physisorption

Surface area of adsorbent Adsorption

Less surface area

Less adsorption

More surface area

More adsorption

New surface for more adsorption

Dividing adsorbent

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8 - Activation energy

Characteristics of Physisorption

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8 - Activation energy

Characteristics of Physisorption

Weak van der Waal force is present b/w adsorbate and adsorbent

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8 - Activation energy

Characteristics of Physisorption

Weak van der Waal force is present b/w adsorbate and adsorbent

No appreciable activation energy is needed

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9 - Multilayer Adsorption

Characteristics of Physisorption

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9 - Multilayer Adsorption

Characteristics of Physisorption

Adsorbent

Adsorbate

Adsorbent

Multilayer Adsorption

1st Layer

2nd Layer

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9 - Multilayer Adsorption

Characteristics of Physisorption

Adsorbent

Adsorbate

Multilayer Adsorption

Due to Lack of specificity

Molecule can adsorbed on molecule

Adsorbent

1st Layer

2nd Layer

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Characteristics of Chemisorption

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1 - High Specificity

Characteristics of Chemisorption

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1 - High Specificity

Characteristics of Chemisorption

Adsorbent

Different gases

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1 - High Specificity

Characteristics of Chemisorption

Adsorbent

Different gases

Strongly Attracted towards adsorbent

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1 - High Specificity

Characteristics of Chemisorption

Adsorbent

Adsorbent

Different gases

Some specific gases can only be adsorbed

Strongly Attracted towards adsorbent

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2 - Irreversibility

Characteristics of Chemisorption

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2 - Irreversibility

Characteristics of Chemisorption

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2 - Irreversibility

Characteristics of Chemisorption

Strong chemical bond between adsorbate and adsorbent

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2 - Irreversibility

Difficult to separate adsorbent and adsorbate

Characteristics of Chemisorption

Strong chemical bond between adsorbate and adsorbent

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2 - Irreversibility

Difficult to separate adsorbent and adsorbate

Characteristics of Chemisorption

Strong chemical bond between adsorbate and adsorbent

Chemisorption is Irreversible

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3 - Change with Pressure

Characteristics of Chemisorption

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Pressure Adsorption

3 - Change with Pressure

Characteristics of Chemisorption

Like physisorption

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4 - Change with Temperature

Characteristics of Chemisorption

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Adsorbent

4 - Change with Temperature

Characteristics of Chemisorption

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Adsorbent

Adsorbent

4 - Change with Temperature

Characteristics of Chemisorption

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Adsorbent

Adsorbent

Adsorbent

4 - Change with Temperature

Characteristics of Chemisorption

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Amount of gas adsorbed

Temperature

4 - Change with Temperature

Characteristics of Chemisorption

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Amount of gas adsorbed

Temperature

4 - Change with Temperature

Characteristics of Chemisorption

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Amount of gas adsorbed

Temperature

Low tem.

Low adsorption

4 - Change with Temperature

Characteristics of Chemisorption

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Amount of gas adsorbed

Temperature

Low tem.

Low adsorption

Temp. increases

Adsorption increases

4 - Change with Temperature

Characteristics of Chemisorption

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Amount of gas adsorbed

Temperature

Low tem.

Low adsorption

High temp.

low adsorption

Temp. increases

Adsorption increases

4 - Change with Temperature

Characteristics of Chemisorption

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Q. : How does temperature change the chemical adsorption?

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(Time Duration : 01 Minutes)

Q. : How does temperature change the chemical adsorption?

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Q. : How does temperature change the chemical adsorption?

Sol. :

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Q. : How does temperature change the chemical adsorption?

Sol. :

Amount of gas adsorbed

Temperature

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Q. : How does temperature change the chemical adsorption?

Sol. :

Amount of gas adsorbed

Temperature

Initially adsorption increases

Temperature gives heat for reaction

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Q. : How does temperature change the chemical adsorption?

Sol. :

Amount of gas adsorbed

Temperature

temperature gives heat for reaction

Initially adsorption increases

Due to exothermic nature excess heat breaks the bonds b/w adsorbate and adsorbent

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5 - Enthalpy of Adsorption

Characteristics of Chemisorption

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5 - Enthalpy of Adsorption

Adsorbent

Adsorbate

Characteristics of Chemisorption

Strong chemical bonds

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5 - Enthalpy of Adsorption

Adsorbent

Adsorbate

Characteristics of Chemisorption

Strong chemical bonds

Release high energy during adsorption

80 – 240 kJ mol-1

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6 - Surface area of adsorbent

Characteristics of Chemisorption

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6 - Surface area of adsorbent

Surface area of adsorbent Adsorption

Characteristics of Chemisorption

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7 - Activation energy

Characteristics of physisorption

Characteristics of Chemisorption

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7 - Activation energy

Characteristics of physisorption

Strong chemical bonds are present b/w adsorbate and adsorbent

Characteristics of Chemisorption

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7 - Activation energy

Characteristics of physisorption

Strong chemical bonds are present b/w adsorbate and adsorbent

Sometimes high activation energy is needed

Characteristics of Chemisorption

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Characteristics of Chemisorption

8 - Unimolecular layer Adsorption

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Characteristics of Chemisorption

8 - Unimolecular layer Adsorption

Chemical bond will be formed between adsorbent and adsorbate only

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8 - Unimolecular layer Adsorption

Characteristics of Chemisorption

Chemical bond will be formed between adsorbent and adsorbate only

Adsorbate

Adsorbent

Unimolecular layer

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Q. : What are the major differences between physisorption and chemisorption?

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Q. : What are the major differences between physisorption and chemisorption?

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Q. : What are the major differences between physisorption and chemisorption?

Sol. :

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Q. : What are the major differences between physisorption and chemisorption?

Sol. :

Physisorption

Chemisorption

Van der Waals’ forces

Chemical bonds

Not specific nature

Highly specific

Reversible nature

irreversible nature

Low enthalpy of adsorption

High enthalpy of adsorption

Low activation energy

High activation energy

Multimolecular layers

Unimolecular layer

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ConcepTest

Ready for Challenge

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Q. : What are the major factors which influence the adsorption of a gas on a solid?

(NCERT Exercise Question 5.4, pg no. 148)

247

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Q. : What are the major factors which influence the adsorption of a gas on a solid?

(NCERT Exercise Question 5.4, pg no. 148)

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(Time Duration : 02 Minutes)

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Question : What are the factors which influence the adsorption of a gas on a solid?

(NCERT Exercise Question 5.4, pg no. 148)

Sol. :

249

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Question : What are the factors which influence the adsorption of a gas on a solid?

(NCERT Exercise Question 5.4, pg no. 148)

Sol. :

250

Extent of adsorption depends on nature of adsorbent and adsorbate

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Question : What are the factors which influence the adsorption of a gas on a solid?

(NCERT Exercise Question 5.4, pg no. 148)

Sol. :

251

Surface area of the adsorbent Adsorption

Extent of adsorption depends on nature of adsorbent and adsorbate

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Question : What are the factors which influence the adsorption of a gas on a solid?

(NCERT Exercise Question 5.4, pg no. 148)

Sol. :

252

Surface area of the adsorbent Adsorption

Pressure of gas Adsorption

Extent of adsorption depends on nature of adsorbent and adsorbate

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Question : What are the factors which influence the adsorption of a gas on a solid?

(NCERT Exercise Question 5.4, pg no. 148)

Sol. :

253

Extent of adsorption depends on nature of adsorbent and adsorbate

Surface area of the adsorbent Adsorption

Pressure of gas Adsorption

Temperature

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Question : What are the factors which influence the adsorption of a gas on a solid?

(NCERT Exercise Question 5.4, pg no. 148)

Sol. :

254

Extent of adsorption depends on nature of adsorbent and adsorbate

Surface area of the adsorbent Adsorption

Pressure of gas Adsorption

Temperature

Physisorption

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Question : What are the factors which influence the adsorption of a gas on a solid?

(NCERT Exercise Question 5.4, pg no. 148)

Sol. :

255

Extent of adsorption depends on nature of adsorbent and adsorbate

Surface area of the adsorbent Adsorption

Pressure of gas Adsorption

Temperature

Physisorption

Chemisorption, initially

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Question : What are the factors which influence the adsorption of a gas on a solid?

(NCERT Exercise Question 5.4, pg no. 148)

Sol. :

256

Extent of adsorption depends on nature of adsorbent and adsorbate

Surface area of the adsorbent Adsorption

Pressure of gas Adsorption

Temperature

Physisorption

Chemisorption, initially

At high Temp.

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: Reference Questions :

Intext Questions : 5.1 and 5.3 (NCERT page no. 129)

Exercise Questions : 5.1, 5.2, 5.3, 5.6, 5.8, 5.10 ( NCERT page no. 148)

Workbook Questions : 2, 3, 9,

257

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Adsorption Isotherm

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Learning Objectives

Adsorption Isotherm

Freundlich adsorption Isotherm

Adsorption from Solution Phase

Applications of Adsorption

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CV 1

Adsorption Isotherm

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Adsorption Isotherm

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Adsorption Isotherm

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Amount of gas adsorbed

Adsorption Isotherm

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Amount of gas adsorbed

Pressure

Adsorption Isotherm

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Amount of gas adsorbed

Pressure

At constant temperature

Adsorption Isotherm

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Adsorption Isotherm

Amount of gas adsorbed

Pressure

At constant temperature

Explain by Freundlich

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Freundlich adsorption isotherm

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Freundlich adsorption isotherm

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Freundlich adsorption isotherm

An equation to relate amount of gas adsorbed with pressure at constant temperature

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Freundlich adsorption isotherm

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x/m = Extent of adsorption

Freundlich adsorption isotherm

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x/m = Extent of adsorption

x = Mass of gas adsorbed

Freundlich adsorption isotherm

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x/m = Extent of adsorption

x = Mass of gas adsorbed

m = Mass of absorbent

Freundlich adsorption isotherm

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x/m = Extent of adsorption

x = Mass of gas adsorbed

m = Mass of adsorbent

p = Pressure

Freundlich adsorption isotherm

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x/m = Extent of adsorption

x = Mass of gas adsorbed

m = Mass of adsorbent

p = Pressure

k = Constant

Freundlich adsorption isotherm

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x/m = Extent of adsorption

x = Mass of gas adsorbed

m = Mass of adsorbent

p = Pressure

k = Constant

n = Constant

Freundlich adsorption isotherm

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x/m = Extent of adsorption

x = Mass of gas adsorbed

m = Mass of adsorbent

p = Pressure

k = Constant

n = Constant

Depend on nature of gas, adsorbent and temperature

Freundlich adsorption isotherm

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Graphical representation of Freundlich adsorption isotherm

At Constant Temperature

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Graphical representation of Freundlich adsorption isotherm

At Constant Temperature

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Graphical representation of Freundlich adsorption isotherm

There are three possible cases

At Constant Temperature

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Cases of Freundlich adsorption isotherm

At low pressure

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Cases of Freundlich adsorption isotherm

At low pressure

At high pressure

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Cases of Freundlich adsorption isotherm

At moderate pressure

At low pressure

At high pressure

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Case - 1

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Case - 1

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Case - 1

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Case - 1

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Case - 1

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Case - 1

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Case - 2

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Case - 2

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Case - 2

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Case - 2

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Case - 2

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Case - 2

PS

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Case - 3

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Case - 3

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Case - 3

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Case - 3

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Case - 3

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Validity of Freundlich adsorption isotherm

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Validity of Freundlich adsorption isotherm

Freundlich adsorption isotherm equation

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Validity of Freundlich adsorption isotherm

Freundlich adsorption isotherm equation

Taking logarithm

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Validity of Freundlich adsorption isotherm

Freundlich adsorption isotherm equation

Taking logarithm

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Validity of Freundlich adsorption isotherm

Freundlich adsorption isotherm equation

Taking logarithm

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Validity of Freundlich adsorption isotherm

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Validity of Freundlich adsorption isotherm

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Validity of Freundlich adsorption isotherm

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Validity of Freundlich adsorption isotherm

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Validity of Freundlich adsorption isotherm

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Slope = m =

Validity of Freundlich adsorption isotherm

Intercept = c = log k

Comparing with

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Comparing log form of Freundlich equation with the equation of straight line

vs

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Limitations of Freundlich adsorption isotherm

  • Freundlich equation has no theoretical basis
  • Equation does not explain the independent nature of adsorption at high pressure
  • Constants K and n are not real constants as they depend on temperature and nature of the gas

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Q. : A curve between log x/m and log p is found to be straight line with a slope of 45° and intercept 0.3010. Calculate the amount of gas adsorbed at 0.2 atm pressure.

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Pause the Video

(Time Duration : 02 Minutes)

Q. : A curve between log x/m and log p is found to be straight line with a slope of 45° and intercept 0.3010. Calculate the amount of gas adsorbed at 0.2 atm pressure.

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Q. : A curve between log x/m and log p is found to be straight line with a slope of 45° and intercept 0.3010. Calculate the amount of gas adsorbed at 0.2 atm pressure.

Sol. : Given - curve between log x/m and log p is straight line

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Q. : A curve between log x/m and log p is found to be straight line with a slope of 45° and intercept 0.3010. Calculate the amount of gas adsorbed at 0.2 atm pressure.

Sol. : Given - curve between log x/m and log p is straight line

Slope =

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Q. : A curve between log x/m and log p is found to be straight line with a slope of 45° and intercept 0.3010. Calculate the amount of gas adsorbed at 0.2 atm pressure.

Sol. : Given - curve between log x/m and log p is straight line

Slope =

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12C05.2 Adsorption Isotherm

Q. : A curve between log x/m and log p is found to be straight line with a slope of 45° and intercept 0.3010. Calculate the amount of gas adsorbed at 0.2 atm pressure.

Sol. : Given - curve between log x/m and log p is straight line

Slope =

Intercept =

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12C05.2 Adsorption Isotherm

Q. : A curve between log x/m and log p is found to be straight line with a slope of 45° and intercept 0.3010. Calculate the amount of gas adsorbed at 0.2 atm pressure.

Sol. : Given - curve between log x/m and log p is straight line

Slope =

Intercept =

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12C05.2 Adsorption Isotherm

Q. : A curve between log x/m and log p is found to be straight line with a slope of 45° and intercept 0.3010. Calculate the amount of gas adsorbed at 0.2 atm pressure.

Sol. : Given - curve between log x/m and log p is straight line

Slope =

Intercept =

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Q. : A curve between log x/m and log p is found to be straight line with a slope of 45° and intercept 0.3010. Calculate the amount of gas adsorbed at 0.2 atm pressure.

Sol. : Given - curve between log x/m and log p is straight line

Slope =

Intercept =

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12C05.2

CV 2

Adsorption from Solution Phase

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Adsorption from Solution Phase

Solids can adsorb solutes from solutions

Iodine solution

Iodine solution with charcoal

Colourless iodine solution

Adding charcoal

Colour adsorbed by charcoal

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12C05.1 Adsorption and its type

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Adsorption from Solution Phase

Litmus solution

Colourless solution

Animal charcoal

Colouring agent of litmus solution is adsorbed by animal charcoal

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12C05.2 Adsorption Isotherm

ConcepTest

Ready for Challenge

327

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12C05.2 Adsorption Isotherm

Q. : Why does White precipitate of Mg(OH)2 turn blue in magneson reagent?

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12C05.2 Adsorption Isotherm

Pause the Video

(Time Duration : 02 Minutes)

Q. : Why does White precipitate of Mg(OH)2 turn blue in magneson reagent?

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12C05.2 Adsorption Isotherm

Q. : Why does White precipitate of Mg(OH)2 turn blue in magneson reagent?

Sol. : Blue coloured Magneson gets adsorbed on the surface of white ppt of Mg(OH)2

White precipitate of Mg(OH)2

Magneson reagent

Blue precipitate of Mg(OH)2

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12C05.1 Adsorption and its types

ConcepTest

Ready for challenge

331

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12C05.1 Adsorption and its types

Question : Why does a blue colour of methylene blue solution fade on adding small

amount of activated charcoal ?

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12C05.1 Adsorption and its types

Pause the Video

(Time Duration : 02 Minutes)

Question : Why does a blue colour of methylene blue solution fade on adding small

amount of activated charcoal ?

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12C05.1 Adsorption and its types

Question : Why does a blue colour of methylene blue solution fade on adding small

amount of activated charcoal ?

Solution : The colouring agent of methylene blue is adsorbed by activated charcoal.

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12C05.1 Adsorption and its types

Question : Why does a blue colour of methylene blue solution fade on adding small

amount of activated charcoal ?

Solution : The colouring agent of methylene blue is adsorbed by activated charcoal.

Methylene blue

Blue colour faded by charcoal

Activated charcoal

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Adsorption from Solution Phase

Some important observations for adsorption from solution phase

  • Extent of adsorption depends on the nature of the adsorbent and the adsorbate

  • Extent of adsorption 1 / Temperature

  • Extent of adsorption Surface area of the adsorbent

  • Extent of adsorption Concentration of the solute in solution

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337

Adsorption from Solution Phase

Mechanism

Precise mechanism

Freundlich equation approximately describes the behaviour of

adsorption from solution

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338

Adsorption from Solution Phase

Describes with the help of Freundlich equation

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339

Adsorption from Solution Phase

To calculate the value of constants k and n

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12C05.2

CV 3

Applications of Adsorption

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Applications of adsorption

1 - Production of high vacuum

Remaining traces of air can be adsorbed by charcoal from a vessel evacuated by a vacuum pump to provide a very high vacuum

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342

Applications of adsorption

1 - Production of high vacuum

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343

Applications of adsorption

1 - Production of high vacuum

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344

Applications of adsorption

2 - Gas masks

Gas mask loaded with activated charcoal or any other safe adsorbents is usually used for breathing in coal mines to adsorb poisonous gases

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345

Applications of adsorption

3 - Control of humidity

Silica and aluminium gels can adsorb moisture very effectively

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346

Applications of adsorption

4 - Removal of colouring matter

Animal charcoal

removes colours of solutions by adsorbing coloured impurities

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347

Applications of adsorption

5 - Heterogeneous catalysis

Adsorption of reactants on the solid

surface of the catalysts increases the rate of reaction

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348

Applications of adsorption

6 - Separation of inert gases

A mixture of noble gases can be separated by adsorption on coconut charcoal at different temperatures

Difference in degree of adsorption of gases

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349

Applications of adsorption

7 - In curing diseases

Adsorption of drug on the germs can kill them or stop their growth

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350

Applications of adsorption

8 - Adsorption indicators

Surfaces of certain precipitates such as silver halides have the property of adsorbing some indicator dyes like eosin, fluorescein, etc.

Characteristic colour indicated the end point

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12C05.1 Adsorption and its type

: Reference Questions :

Exercise Questions : 5.5 ( NCERT page no. 148)

Workbook Questions : 6, 10

351

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PSV

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12C05.1 Adsorption and its type

  • ICE

353

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CT

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12C05.3

Catalysis

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CV 1

Catalysis and its types

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Catalysis

2KClO3

653-873 K

2KCl + 3O2

2KClO3

473-633 K

2KCl + 3O2

MnO2

Slow

Comparatively Fast

Mass and composition remains unchanged

Can alter rate of reaction

Catalyst

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Substances, which accelerate the rate of a chemical reaction and themselves remain chemically and quantitatively unchanged after the reaction, are known as catalysts, and the phenomenon is known as catalysis

Catalysis

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Promoters and poisons

N2(g) + 3H2(g)

2NH3(g)

Fe

Mo

N2(g) + 3H2(g)

2NH3(g)

Fe

H2S

Enhance the activity of catalyst

Decrease the activity of catalyst

Promoters

Poisons

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Types of Catalysis

Homogeneous

Heterogeneous

Reactants products and the catalyst are in the same phase

Reactants products and the catalyst are in different phase

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Homogeneous Catalysis

2SO2(g) + O2(g)

2SO2(g)

NO(g)

CH3COOCH3(l) + H2O(l)

CH3COOH(aq) + CH3OH(aq)

HCI(l)

C6H12O6 (aq) + C6H12O6(aq)

C12H22O11 (aq) + H2O(l)

H2SO4(l)

Lead chamber process

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Heterogeneous Catalysis

2SO2(g) + O2(g)

2SO2(g)

Pt(S)

4NO(g) + 6H O(g)

4NH (g) + 5O (g)

Ni(S)

Haber’s process

N2(g) + 3H2(g)

2NH3(g)

Fe(S)

Ostwald’s process

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CV 2

Adsorption Theory of Heterogeneous Catalysis

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Adsorption Theory of Heterogeneous Catalysis

Explains the mechanism of heterogeneous catalysis

Modern adsorption theory of catalysis

Old adsorption theory

of catalysis

Intermediate compound formation theory

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Old Adsorption Theory of Catalysis

Reactants in gaseous state or in solutions, are adsorbed on the surface of the solid catalyst

Increase in concentration of reactants on the surface increases rate of reaction

Adsorption being an exothermic process, the heat of adsorption is utilised in

enhancing the rate of the reaction

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Intermediate compound formation theory

Explains the catalytic action of the catalyst

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367

It is the combination

Modern adsorption theory of catalysis

Modern adsorption theory of catalysis

Old adsorption theory

of catalysis

The catalytic activity is localised on the surface of the catalyst

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Modern adsorption theory of catalysis

Diffusion of reactants to the surface of the catalyst

Adsorption of reactant molecules on the surface of the catalyst

Desorption of reaction products from the catalyst surface

Formation of an intermediate on the catalyst’s surface due to chemical reaction

Diffusion of reaction products away from the catalyst’s surface

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A

B

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A

B

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378

A

B

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379

A

B

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A

B

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381

A

B

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Modern adsorption theory of catalysis

Limitations

Advantages

Explains -

  • Why catalyst remains unchanged in mass and chemical composition at the end of the reaction

  • Why catalyst is effective even in small quantities

does not explain -

  • Action of catalytic promoters

  • Action of catalytic poisons

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Important features of solid catalysts

Selectivity

Activity

  • Activity of a catalyst depends upon the strength of chemisorption
  • Reactants must get adsorbed reasonably strongly on to catalyst to become active
  • However, highly strong adsorption make reactant molecules immobile
  • Other reactants are left with no space on catalyst surface for adsorption
  • For hydrogenation, catalytic activity increases from Group 5 - 11 metals with maximum activity being shown by groups 7- 9 elements of the periodic table

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Important features of solid catalysts

Selectivity

Activity

  • Ability of a catalyst to direct a reaction to yield a particular product selectively
  • Selectivity of different catalysts for same reactants can be different

CO(g) + 3H2(g)

CH4(g) + H2O(g)

Ni

CO(g) + 2H2(g)

CH3OH(aq)

Cu/ZnO-Cr2O3

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CV 2

Shape Selective Catalysis

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Shape Selective Catalysis

A catalytic reaction that depends upon -

Pore structure of the catalyst

Size of the reactant and product molecules

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Shape Selective Catalysis

A catalytic reaction that depends upon -

Pore structure of the catalyst

Size of the reactant and product molecules

Zeolites are good shape-selective catalysts

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12C05.3 Catalysis

388

Zeolites

What are the Zeolites ?

How they act as Shape Selective Catalysts ?

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12C05.3 Catalysis

389

What are the Zeolites ?

They are microporous aluminosilicates

3-D network of silicates in which some silicon atoms are replaced by aluminium atoms giving Al–O–Si framework

Reactions taking place in zeolites depend upon the size and shape of reactant and product molecules as well as upon pores and cavities of the zeolites

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390

How they act as Shape Selective Catalysts ?

Zeolites are good shape selective catalysts

because of their honeycomb-like structures

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391

Uses of Zeolites

It converts alcohols directly into gasoline (petrol) by dehydrating them

Zeolites are widely used as catalysts in petrochemical industries for cracking of hydrocarbons

An important zeolite catalyst used in the petroleum industry is ZSM-5

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CV 2

Enzyme Catalysis

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Enzyme Catalysis

Where they act as catalyst

When reactions are catalysed by enzymes

What are enzymes

How they act as catalyst

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What are Enzyme

Enzymes are complex nitrogenous organic compounds which are produced by living plants and animals

They are actually protein molecules of high molecular mass

They are very effective catalysts as they catalyse numerous reactions, especially those connected with natural processes

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Where they act as catalyst ❓

Enzymes are, thus, termed as biochemical catalysts and the phenomenon is known as biochemical catalysis

Many reactions occur in bodies of animals and plants to maintain life process are catalysed by enzymes

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Homogeneous Catalysis

1 - Inversion of cane sugar

2 - Conversion of glucose into ethyl alcohol

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397

Homogeneous Catalysis

3 - Conversion of starch into maltose

4 - Conversion of maltose into glucose

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398

Homogeneous Catalysis

5 - Decomposition of urea

Curd

Milk

Lacto Bacilli

6 - Conversion of milk into curd

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Homogeneous Catalysis

Peptides

Proteins

Pepsin

Amino acids

Proteins

Trypsin

7 - In stomach

8 - in intestine

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Characteristics of enzyme catalysis

High efficiency

pH dependent

Highly specific

Affected by activators and co-enzymes

Temp. dependent

Affected by inhibitors and poisons

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Characteristics of enzyme catalysis

1- High efficiency - One molecule of an enzyme may transform one million molecules of the reactant per minute

2 - Highly specific nature - Each enzyme is specific for a given reaction

For example - the enzyme urease catalyses the hydrolysis of urea only. It does not catalyse hydrolysis of any other amide

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402

Characteristics of enzyme catalysis

3 - Optimum temperature - Rate of an enzyme reaction becomes maximum at definite temperature, called the optimum temperature.

Optimum temperature range for enzymatic activity is 298-310K. Human body temperature being 310 K is suited for enzyme-catalysed reactions

Temp. other than optimum temperature, will decreases the enzyme activity

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403

Characteristics of enzyme catalysis

4 - Optimum pH - Rate of an enzyme-catalysed

reaction is maximum at a particular pH called optimum pH

Optimum pH is between pH values 5-7

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12C05.3 Catalysis

404

Characteristics of enzyme catalysis

5 - Effect of activators and co-enzymes - The enzymatic activity is increased in the presence of certain substances, known as co-enzymes

It has been observed that when a small non-protein (vitamin) is present along with an enzyme, the catalytic activity is enhanced considerably

Activators are generally metal ions such as Na+, Mn2+, Co2+, Cu2+,

etc. These metal ions, when weakly bonded to enzyme molecules,

increase their catalytic activity. Amylase in presence of sodium

chloride i.e., Na+ ions are catalytically very active

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405

Characteristics of enzyme catalysis

6 - Effect of inhibitors and poisons - Like ordinary catalysts, enzymes

are also inhibited or poisoned by the presence of certain substances.

The inhibitors or poisons interact with the active functional groups

on the enzyme surface and often reduce or completely destroy the

catalytic activity of the enzymes. The use of many drugs is related

to their action as enzyme inhibitors in the body

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Characteristics of enzyme catalysis

Mechanism of enzyme catalysis - There are a number of cavities present on the surface of colloidal particles of enzymes. These cavities are of characteristic shape and possess active groups such as -NH2, -COOH, -SH, -OH, etc. These are actually the active centres on the surface of enzyme particles. The molecules of the reactant (substrate), which have complementary shape, fit into these cavities just like a key fits into a lock. On account of the presence of active groups, an activated complex is formed which then decomposes to yield the products. Thus, the enzyme-catalysed reactions may be considered to proceed in two steps.

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407

Characteristics of enzyme catalysis

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408

Characteristics of enzyme catalysis

Step 1: Binding of enzyme to substrate to form an activated complex.

E + S → ES≠

Step 2: Decomposition of the activated complex to form product.

ES≠ →E +

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12C05.4

Colloids

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12C05.2 Adsorption Isotherm and Freundlich adsorption Isotherm

  • Colloids
  • Classification of Colloids
  • Mechanism of micelle formation
  • Cleansing action of soaps
  • Preparation of Colloids

410

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CV 1

Colloids

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12C05.4 Colloids

412

FC

On the basis of study of diffusion of solutions through an animal membrane, Thomas Graham divided the various solute-solvent systems in two categorie

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12C05.4 Colloids

413

FC

On the basis of study of diffusion of solutions through an animal membrane, Thomas Graham divided the various solute-solvent systems in two categorie

Crystalloids

Colloids

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12C05.4 Colloids

414

FC

On the basis of study of diffusion of solutions through an animal membrane, Thomas Graham divided the various solute-solvent systems in two categorie

Crystalloids

Colloids

Def. Some crystalline substances whose solutions were able to pass through an animal membrane

E.g. Aq. solution of sugar, urea, sodium chloride

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12C05.4 Colloids

415

FC

On the basis of study of diffusion of solutions through an animal membrane, Thomas Graham divided the various solute-solvent systems in two categorie

Crystalloids

Colloids

Def. Some crystalline substances whose solutions were able to pass through an animal membrane

E.g. Aq. solution of sugar, urea, sodium chloride

Def. Some amorphous substances whose solutions were unable to pass through the membrane

E.g. Solutions of glue, gelatin, gum Arabic etc

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12C05.4 Colloids

416

FC

On the basis of study of diffusion of solutions through an animal membrane, Thomas Graham divided the various solute-solvent systems in two categorie

Crystalloids

Colloids

Def. Some crystalline substances whose solutions were able to pass through an animal membrane

E.g. Aq. solution of sugar, urea, sodium chloride

Def. Some amorphous substances whose solutions were unable to pass through the membrane

E.g. Solutions of glue, gelatin, gum Arabic etc

Division was not successful as certain substances can act as crystalloids and colloids

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12C05.4 Colloids

417

FC

Division of solute-solvent systems

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418

FC

Division of solute-solvent systems

On the basis of the size of solute particles

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419

FC

Division of solute-solvent systems

True solution

On the basis of the size of solute particles

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420

FC

Division of solute-solvent systems

True solution

Suspension

On the basis of the size of solute particles

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421

Division of solute-solvent systems

True solution

Suspension

Colloids

On the basis of the size of solute particles

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True Solution

  • Particles of solute in a true solution are either tiny single molecules or ions
  • True solutions are homogeneous system
  • The size of dispersed particles less than 1 nm, i.e. 10-9
  • These particles cannot be seen even with a microscope
  • True solutions pass through ordinary filter paper and animal membranes
  • E.g. Sodium chloride, sugar, urea etc. form true solutions in water.

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Suspension

  • Suspensions have larger particles
  • Suspensions are heterogeneous systems
  • Size of particles in a suspension is more than 1000 nm (i.e., >10-6 m)
  • Particles are either visible to naked eye or can be seen under a microscope
  • Suspensions easily pass through ordinary filter paper and animal membranes
  • E.g. Stirred muddy water

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424

FC

Colloids

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12C05.4 Colloids

425

FC

Colloids

Def. Colloid is a heterogeneous system in which one substance is dispersed (dispersed phase) as very fine particles in another substance called dispersion medium

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426

FC

Colloids

On the basis of the size of the solute particles, colloids are exist between suspensions and solutions

Def. Colloid is a heterogeneous system in which one substance is dispersed (dispersed phase) as very fine particles in another substance called dispersion medium

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Properties of Colloids

  • Colloid is a heterogeneous system
  • Size of dispersed particles is between 1 nm-1000 nm (i.e. 10-9-10-6 m)
  • Particles are not large enough to be seen with naked eye
  • Particles can be seen with the help of an ultra microscope
  • Colloidal solutions can pass through ordinary filter paper but not through an animal membrane
  • Colloidal particles have an enormous surface area per unit mass as a result of their small size
  • E.g. Solution of Gum Arabic, gelatin, glue etc. in water

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PSV

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CT

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CV 2

Classification of Colloids

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12C05.4 Colloids

431

FC

Classification of Colloids

Colloids are classified on the basis of the following criteria -

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432

FC

Classification of Colloids

1 - Physical state of dispersed phase and dispersion medium

Colloids are classified on the basis of the following criteria -

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FC

Classification of Colloids

1 - Physical state of dispersed phase and dispersion medium

Colloids are classified on the basis of the following criteria -

2 - Nature of interaction between dispersed phase and dispersion

medium

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434

FC

Classification of Colloids

1 - Physical state of dispersed phase and dispersion medium

3 - Type of particles of the dispersed phase

Colloids are classified on the basis of the following criteria -

2 - Nature of interaction between dispersed phase and dispersion

medium

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435

FC

Depending upon the physical states of dispersed phase and dispersion

Medium, there are eight types of colloidal systems

Classification based on physical state of dispersed phase and dispersion medium

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Table : Types of colloids

Classification based on physical state of dispersed phase and dispersion medium

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437

Classification based on physical state of dispersed phase and dispersion medium

Some important points

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438

  • Gaseous mixtures are homogeneous and hence are not colloidal systems
  • Most biological fluids are aqueous sols (solids dispersed in water)
  • if the dispersion medium is water, the sol is called aquasol or hydrosol
  • if the dispersion medium is alcohol, it is called alcosol

Classification based on physical state of dispersed phase and dispersion medium

Some important points

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FC

Classification Based on Nature of Interaction between Dispersed Phase and Dispersion Medium

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440

FC

Classification Based on Nature of Interaction between Dispersed Phase and Dispersion Medium

Lyophilic (solvent attracting)

Lyophobic (solvent repelling)

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441

FC

Classification Based on Nature of Interaction between Dispersed Phase and Dispersion Medium

Lyophilic (solvent attracting)

Lyophobic (solvent repelling)

If water is the dispersion medium - Hydrophilic

If water is the dispersion medium - Hydrophobic

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Lyophilic Colloids (solvent attracting)

  • Can be easily formed by mixing dispersed phase and dispersion medium
  • Also called reversible sols because - If the dispersion medium is separated from the dispersed phase (say by evaporation), the sol can be reconstituted by simply remixing with the dispersion medium

  • These are quite stable and cannot be easily coagulated.
  • E.g. sol of gum, gelatine, starch, rubber, etc., with a suitable dispersion medium

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Lyophobic Colloids (solvent repelling)

  • Can not be easily formed by mixing dispersed phase and dispersion medium
  • Also called irreversible sols because - If the dispersion medium is separated from the dispersed phase the sol can not be reconstituted by simply remixing with the dispersion medium
  • These are not quite stable and thus, easily coagulated small amounts of electrolytes
  • They need stabilising agents for their preservation
  • E.g. metals and their sulphides

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444

FC

Classification Based on Type of Particles of the Dispersed Phase

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445

FC

Classification Based on Type of Particles of the Dispersed Phase

Multimolecular

colloids

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446

FC

Classification Based on Type of Particles of the Dispersed Phase

Multimolecular

colloids

Macromolecular

colloids

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447

FC

Classification Based on Type of Particles of the Dispersed Phase

Multimolecular

colloids

Macromolecular

colloids

Associated

colloids (Micelles)

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Multimolecular Colloids

Def. When a large number of atoms or smaller molecules aggregate together to form colloidal species, the new species is termed as Multimolecular colloid.

E.g. gold sol and Sulphur (S8) sol

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FC

Macromolecular Colloids

Def. When in a solution the size of the macromolecules is in the colloidal range, the system is termed as Multimolecular colloid

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FC

Macromolecular Colloids

Def. When in a solution the size of the macromolecules is in the colloidal range, the system is termed as Multimolecular colloid

These colloids are quite stable and resemble true solutions in many respects

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FC

Macromolecular Colloids

Def. When in a solution the size of the macromolecules is in the colloidal range, the system is termed as Multimolecular colloid

E.g. Natural - Starch, cellulose, proteins and enzymes, etc.

Man made - Polythene, nylon, polystyrene, synthetic rubber, etc.

These colloids are quite stable and resemble true solutions in many respects

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FC

Associated colloids (Micelles)

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FC

Associated colloids (Micelles)

Some substances like soaps at low concentrations behave as normal strong electrolytes

At higher concentrations the aggregate and show colloidal behaviour

454 of 519

12C05.4 Colloids

454

FC

Associated colloids (Micelles)

Some substances like soaps at low concentrations behave as normal strong electrolytes

At higher concentrations the aggregate and show colloidal behaviour

455 of 519

12C05.4 Colloids

455

FC

Associated colloids (Micelles)

Some substances like soaps at low concentrations behave as normal strong electrolytes

At higher concentrations the aggregate and show colloidal behaviour

Micelle

456 of 519

12C05.4 Colloids

456

FC

Conditions for Micelle formation

457 of 519

12C05.4 Colloids

457

FC

Conditions for Micelle formation

Kraft temperature (Tk)

Critical micelle concentration (CMC)

458 of 519

12C05.4 Colloids

458

FC

Conditions for Micelle formation

Kraft temperature (Tk)

Critical micelle concentration (CMC)

The temperature above which micelles formation takes place

459 of 519

12C05.4 Colloids

459

Conditions for Micelle formation

Kraft temperature (Tk)

Critical micelle concentration (CMC)

The temperature above which micelles formation takes place

The Concentration above which micelles formation takes place

For soap CMC is 10–4 to 10–3 mol L–1

FC

460 of 519

PSV

461 of 519

CT

462 of 519

CV 3

Mechanism of Micelle formation

463 of 519

12C05.4 Colloids

463

Mechanism of micelle formation

This mechanism can be explained with the example of soap solutions

464 of 519

12C05.4 Colloids

464

Mechanism of micelle formation

This mechanism can be explained with the example of soap solutions

Soap

Def. Soap is sodium or potassium salt of a higher fatty acids.

Generally, given as RCOONa+

E.g., sodium stearate CH3(CH2)16COONa+, which is a major component of many bar soaps

465 of 519

12C05.4 Colloids

465

Properties of soap

  • When dissolved in water, it dissociates into RCOO and Na+ ions
  • RCOOions, however, consist of two parts-
  • A non-polar, hydrophobic, long hydrocarbon chain R, also called tail
  • A polar, hydrophilic group COO , also called head

466 of 519

12C05.4 Colloids

466

Representation of soap

467 of 519

12C05.4 Colloids

467

Representation of soap

Sodium stearate (C17H35COONa+) - before dissociation

468 of 519

12C05.4 Colloids

468

Representation of soap

Sodium stearate (C17H35COONa+) - before dissociation

Sodium stearate (C17H35COONa+) - after dissociation

469 of 519

12C05.4 Colloids

469

Representation of soap

470 of 519

12C05.4 Colloids

470

Representation of soap

  • Tail
  • Non-polar
  • Hydrophobic
  • Water repellent
  • Oil or dirt soluble

471 of 519

12C05.4 Colloids

471

Representation of soap

  • Tail
  • Non-polar
  • Hydrophobic
  • Water repellent
  • Oil or dirt soluble
  • Head
  • Polar nature
  • Hydrophilic
  • Water loving
  • Water soluble

472 of 519

12C05.4 Colloids

472

FC

Micelles Formation

473 of 519

12C05.4 Colloids

473

FC

Micelles Formation

Polar RCOO ions are present on the surface with their COO groups in water and the hydrocarbon chains R staying away from it and remain at the surface

Below CMC

474 of 519

12C05.4 Colloids

474

FC

Micelles Formation

Polar RCOO ions are present on the surface with their COO groups in water and the hydrocarbon chains R staying away from it and remain at the surface

Below CMC

Arrangement of RCOO below CMC

475 of 519

12C05.4 Colloids

475

FC

Micelles Formation

anions are aggregate to form a spherical shape with their hydrocarbon chains pointing towards the centre of the sphere with COO part remaining outward on the surface of the sphere

Abow CMC

476 of 519

12C05.4 Colloids

476

FC

Micelles Formation

anions are aggregate to form a spherical shape with their hydrocarbon chains pointing towards the centre of the sphere with COO part remaining outward on the surface of the sphere

Abow CMC

Arrangement of RCOO above CMC

477 of 519

CV 4

Cleansing action of Soap

478 of 519

12C05.4 Colloids

478

Cleansing Action of Soaps

479 of 519

12C05.4 Colloids

479

Cleansing Action of Soaps

Soap

Hydrophobic

Hydrophilic

480 of 519

12C05.4 Colloids

480

Cleansing Action of Soaps

Soap

Hydrophobic

Hydrophilic

Cleansing action of soap is due to micelle formation around grease or oil droplet in such a way that hydrophobic part of the stearate ions is in the oil hydrophilic part projects out of the oil

481 of 519

12C05.4 Colloids

481

Cleansing Action of Soaps

Dirt - grease or oil

Soap

Hydrophobic

Hydrophilic

Cleansing action of soap is due to micelle formation around grease or oil droplet in such a way that hydrophobic part of the stearate ions is in the oil hydrophilic part projects out of the oil

482 of 519

12C05.4 Colloids

482

Cleansing Action of Soaps

483 of 519

PSV

484 of 519

CT

485 of 519

CV 4

Preparation of Colloids

486 of 519

12C05.4 Colloids

486

FC

Preparation of Colloids

487 of 519

12C05.4 Colloids

487

FC

Preparation of Colloids

1 - Chemical methods

2 - Electrical disintegration or

Bredig’s Arc method

3 - Peptization

488 of 519

12C05.4 Colloids

488

FC

Chemical Methods

489 of 519

12C05.4 Colloids

489

FC

Chemical Methods

Double Decomposition

Oxidations

Reduction

Hydrolysis

490 of 519

12C05.4 Colloids

490

FC

Chemical Methods

Double Decomposition

Oxidations

Reduction

Hydrolysis

Chemical change in which two compounds in a solution react to form two new compounds by the mutual exchange of radicals

491 of 519

12C05.4 Colloids

491

FC

Chemical Methods

Double Decomposition

Oxidations

Reduction

Hydrolysis

Oxidation is gaining oxygen or loss of electrons

Equation

492 of 519

12C05.4 Colloids

492

FC

Chemical Methods

Double Decomposition

Oxidations

Reduction

Hydrolysis

Reduction is gaining hydrogen or gain of electrons

Equation

493 of 519

12C05.4 Colloids

493

FC

Chemical Methods

Double Decomposition

Oxidations

Reduction

Hydrolysis

Chemical breakdown of a compound due to reaction with water

Equation

494 of 519

12C05.4 Colloids

494

FC

Electrical disintegration or Bredig’s Arc method

495 of 519

12C05.4 Colloids

495

FC

Electrical disintegration or Bredig’s Arc method

Electric arc is struck between electrodes of the metal immersed in the dispersion medium

496 of 519

12C05.4 Colloids

496

FC

Electrical disintegration or Bredig’s Arc method

Electric arc is struck between electrodes of the metal immersed in the dispersion medium

Bredig’s Arc method

497 of 519

12C05.4 Colloids

497

FC

Electrical disintegration or Bredig’s Arc method

Electric arc is struck between electrodes of the metal immersed in the dispersion medium

The intense heat produced evaporates the metal

Bredig’s Arc method

498 of 519

12C05.4 Colloids

498

FC

Electrical disintegration or Bredig’s Arc method

Electric arc is struck between electrodes of the metal immersed in the dispersion medium

The intense heat produced evaporates the metal

Vapour of metal can be converted to colloidal size by condensation

Bredig’s Arc method

499 of 519

12C05.4 Colloids

499

Peptization

500 of 519

12C05.4 Colloids

500

Peptization

Def. Peptization is the process of converting a precipitate (ppt.) into colloidal sol by shaking it with dispersion medium in the presence of an electrolyte

501 of 519

12C05.4 Colloids

501

Peptization

Def. Peptization is the process of converting a precipitate (ppt.) into colloidal sol by shaking it with dispersion medium in the presence of an electrolyte

The electrolyte used for this purpose is called peptizing agent

This method is generally applied to convert freshly prepared ppt. into colloidal sol

502 of 519

12C05.4 Colloids

502

FC

Mechanism of Peptization

503 of 519

12C05.4 Colloids

503

FC

Mechanism of Peptization

Precipitate

Dispersion medium

Electrolyte

+

+

504 of 519

12C05.4 Colloids

504

FC

Mechanism of Peptization

Precipitate adsorbs one of the ions of the electrolyte on its surface

Precipitate

Dispersion medium

Electrolyte

+

+

505 of 519

12C05.4 Colloids

505

FC

Mechanism of Peptization

Precipitate adsorbs one of the ions of the electrolyte on its surface

This causes the development of positive or negative charge on precipitates

Precipitate

Dispersion medium

Electrolyte

+

+

506 of 519

12C05.4 Colloids

506

FC

Mechanism of Peptization

Precipitate adsorbs one of the ions of the electrolyte on its surface

This causes the development of positive or negative charge on precipitates

Precipitate breaks up into smaller particles of the size of a colloid

Precipitate

Dispersion medium

Electrolyte

+

+

507 of 519

PSV

508 of 519

CT

509 of 519

12C05.1 Adsorption and its type

: Reference Questions :

Exercise Questions : 5.9, 5.11, 5.12, 5.14, 5.18, 5.25 ( NCERT page no. 148)

Workbook Questions : 6, 10

509

510 of 519

12C05.

Purification, Properties and Applications of Colloids

511 of 519

12C05.5 Purification, Properties and Applications of Colloids

  • Purification of Colloidal Solutions
  • Properties of Colloids
  • Applications of Colloids
  • Emulsions

511

512 of 519

CV 1

Purification of Colloidal Solutions

513 of 519

12C05.5 Purification, Properties and Applications of Colloids

513

Purification of Colloidal Solutions

The process used for reducing the amount of impurities to a requisite minimum is known as purification of colloidal solution

Why is purification necessary

  • Colloidal solutions generally contain excessive amount of electrolytes and some other soluble impurities

  • Presence of traces of electrolyte is essential for stability of colloidal solution, larger quantities coagulate it

514 of 519

12C05.5 Purification, Properties and Applications of Colloids

514

Methods of Purifications

Dialysis

Electro dialysis

Ultrafiltration

By membrane

By electricity

By ultra filter paper

515 of 519

12C05.4 Colloidal state

515

types

True solution

Suspension

Cant separate particles

Easily separa particles

Colloids

516 of 519

12C05.4 Colloidal state

516

types

True solution

Suspension

Cant separate particles

Easily separa particles

Colloids

517 of 519

12C05.4 Colloidal state

517

types

True solution

Suspension

Cant separate particles

Easily separa particles

Colloids

518 of 519

12C05.4 Colloidal state

518

types

True solution

Suspension

Cant separate particles

Easily separa particles

Colloids

519 of 519

12C05.4 Colloidal state

519

types

True solution

Suspension

Cant separate particles

Easily separa particles

Colloids