CY6151 Engineering Chemistry 1 - PHASE RULE AND ALLOYS (Unit 4) – Lecture Notes

Anna University

CY6151 Engineering Chemistry - I

UNIT IV

PHASE RULE AND ALLOYS

Chemical reactions are of two types

1. Irreversible reaction homogeneous

2. Reversible reaction – it’s of two types

  • homogeneous
  • heterogeneous

B.heterogeneous reversible reaction --- its behaviour can be studied by PHASE RULE given by Willard Gibbs (1874).

Phase rule

The number of degree of freedom (F) of the system is related to number of components (C) and number of phases (P) by the following phase rule equation.

F = C-P+2

Explanation or meaning of terms

1. Phase (P)

Any homogeneous physically distinct and mechanically separable portion of a system which is separated from other parts of the system by definite boundaries.

a. Gaseous phase

All gases are completely miscible and there is no boundary between one gas and the other. For example: air – single phase

b.Liquid phase

It depends on the number of liquids present and their miscibilities.

i. If two liquids are immiscible, they will form three separate phases two liquid phase and one vapour phase. For example: benzene-water.

ii. If tow liquids are miscible, they will form one liquid phase and one vapour phase.

For example: alcohol – water. C .Solid phase

Every solid constitutes a separate phase

For example:

(i) Water system ------- three phases

(ii) Rhombic sulphur (s) à monoclinic sulphur (s) ----- two phase iii) Sugar solution in water ----- one phase

iv) CuSO4.5H2O(s) clip_image003 CuSO4.3H2O(s) + 2H2O(g) ---- three phases.

2. Component (C)

“The smallest number of independently variable constituents, by means of which the composition of each phase can be expressed in the form of a chemical equation”.

For example:

i) Water system ---- one component ( H2O )

ii) An aqueous system of NaCl --- two component ( NaCl , H2O )

iii) PCl5(s) clip_image003[1] PCl3 (l) + Cl2 (g) --- two component ,three phases

iv) CuSO4.5H2O(s) clip_image003[2] CuSO4.3H2O(s) + 2H2O(g) ---- three phases,two component

3. Degree of freedom(F)

“The minimum number of independent variable factors such as temperature, pressure and concentration, which much be fixed in order to define the system completely”.

i) Water system

image

F = Non variant (or) zero variant

image

F = univariant (one)

iii) For a gaseous mixture of N2 and H2, we must state both the pressure and temperature.

Hence,the system is bivariant.

PHASE DIAGRAM:

Phase diagram is a graph obtained by plotting one degree of freedom against another.

Types of phase diagrams

(i)P-T Diagram : used for one component system

(ii) T-C Diagram : used for two component system

APPLICATIONS OF PHASE RULE TO ONE COMPONENT SYSTEM The water system:

Water exists in three possible phases namely solid, liquid and vapour. Hence there can be three forms of equilibria.

image

Each of the above equilibrium involves two phases. The phase diagram for the water system is shown in the figure.

This phase diagram contains curves, areas, and triple.

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(i)Curve OA

The curve OA is called vaporisation curve, it represents the equilibrium between water and vapour. At any point on the curve the following equilibrium will exist.

image

The degree of freedom of the system is one, i.e, univariant. This is predicted by the phase rule.

F=C-P+2; F=1-2+2; F=1

This equilibrium (i.e. Line OA) will extend up to the critical temperature (347o C). Beyond the critical temperature the equilibrium will disappear only water vapour will exist.

(ii) Curve OB

The curve OB is called sublimation curve of ice, it represents the equilibrium between ice and vapour. At any point on the curve the following equilibrium will exist.

image

The degree of freedom of the system is one, i.e. univariant. This is predicted by the phase rule.

F = C – P + 2; F = 1-2=2 ; F=1

This equilibrium (line OB) will extend up to the absolute zero (-273o C), where no vapour can be present and only ice will exist.

iii) Curve OC

The curve OC is called melting point curve of ice, it represents the equilibrium between the ice and water. At any point on the curve the following equilibrium will exist.

image

The curve OC is slightly inclined towards pressure axis. This shows that melting point of ice decreases with increase of pressure.

The degree of freedom of the system is one i.e., univariant. iv) point O (triple point)

The three curves OA ,OB ,OC meet at a point “O” ,where three phases namely solid ,liquid and vapour are simultaneously at equilibrium .

This point is called triple point, at this point the following equilibrium will exist.

image

The degree of freedom of the system is zero i.e., nonvariant.This is predicted by the phase rule. F=C-P+2; F=1-3+2=0

Temperature and pressure at the point “O” are 0.0075 oC and 4.58 mm respectively. (v) Curve OB’: Metastable equilibrium

The curve OB’ is called vapour pressure curve of the super-cool water or metastable equilibrium where the following equilibrium will exist.

Super-cool water clip_image019 vapour

Sometimes water can be cooled below OoC without the formation of ice, this water is called super –cooled water. Super cooled water is unstable and it can be converted in to solid by seeding or by slight disturbance.

vi) Areas

Area AOC, BOC, AOB represents water, ice and vapour respectively .The degree of the freedom of the system is two.i.e. Bivariant.

This is predicted by the phase rule

F=C-P=2; F=1-1+2; F=2

Two component alloy system or multi component equilibria

Reduced phase rule or condensed system

The system in which only the solid and liquid are considered and the gas phase is ignored is called a condensed system.since pressure kept constant, the phase rule becomes

F’ = C – P + 1

This equation is called reduced phase rule.

Classification of two component system

Based on the solubility and reactive ablity, the two component systems are classified in to three types.

1. Simple eutectic formation - A binary system consisting of two substances, which are completely miscible in the liquid state, but completely immiscible in the solid state, is known as eutectic (easy melt) system. They do not react chemically. Of the different mixtures of the two substances, the mixture having the lowest melting point is known as the eutectic mixture.

2. a) formation of compound with congruent melting point

b) Formation of compound with incongruent melting point

3. Formation of solid solution

Thermal analysis or cooling curve

Thermal analysis is a method involving a study of the cooling curves of various compositions of a system during solidification. The form of the cooling curve indicates the composition of the solid.

Ex: 1. Cooling curve of a pure solid.

Ex: 2. Cooling curve of a mixture A + B.

A cooling curve is a line graph that represents the change of phase of matter, typically from a gas to a solid or a liquid to a solid.

The independent variable (X-axis) is time and the dependent variable (Y-axis) is temperature. Below is an example of a cooling curve.

image

The initial point of the graph is the starting temperature of the matter, here noted as the "pouring temperature". When the phase change occurs there is a "thermal arrest", that is the temperature stays constant. This is because the matter has more internal energy as a liquid or gas than in the state that it is cooling to. The amount of energy required for a phase change is known as latent heat. The "cooling rate" is the slope of the cooling curve at any point.

A Pure substance in the fused or liquid state is allowed to cool slowly. The temperature is noted at different times.when represented graphically the rate of cooling will be a continuous from ‘a’ to ‘b’.

When the freezing point is reached and solid making its appearance there will be a break in the continuity of the cooling curve.The temperature will thereafter remain constant until the liquid is completely solidified.Thereafter the fall in temperature wil again become continuous.

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        a. Cooling curve of a pure substances        b. Cooling curve of a mixture

If a mixture of two solids in the fused state is cooled slowly we get a cooling curve . Here also first a continuous coling curve will be obtained as long as the mixture is in the liquid state .

When a solid phase begins to form there will be a break in the cooling curve .But the temperature will not remain constant unlike in the case of cooling of a purified substance.The temperature will decrease continuously but at a different rate.The fall of temperature will continue till the mixture forms a eutectic and the eutectic point is reached.

The temperature will thereafter remain constant until solidification is complete . Thereafter the fall of temperature will become uniform ,but the rate of fall will be different from that for a pure substance.

Uses of cooling curves

i) Percentage purity of the compounds can be noted from the cooling curve.

ii) The behaviour of the compounds can be clearly understood from the cooling curve. iii) The procedure of thermal analysis can be used to derive the phase diagram of any two component system.

BINARY ALLOY SYSTEM OR THE SIMPLE EUTECTIC SYSTEM The Lead – Sliver system

Since the system is studied at constant pressure,the vapour phase is ignorned and the condensed phase rule is rule is used.

F I= C-P+1

The phase diagram of lead –sliver system is shown in the figure

It contains lines,areas and the eutectic point.

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i) curve AO

The curve AO is known as freezing point curve of sliver.

Along the curve AO, solid Ag and the melt are in equilibrium.

Solid <------------> Ag melt

According to reduced phase rule

F’=C-P+1

C=2

P=2

F’=1

The system is univariant ii) curve BO

The curve BO is known as freezing point curve of lead .

Along the curve BO, solid Pb and the melt are in equilibrium.

Solid Pb <----------->melt

According to reduced phase rule

F’=C-P+1

C=2

P=2

F’=1

The system is univariant. iii) Point “ O ” (eutectic point)

The curves AO and BO meet at point ‘ O ‘ at a temperature of 303 o C ,where the three phases are in equilibrium.

Solid Pb + soild Ag <---------> melt

According to reduced phase rule

F’=C-P+1

C=2

P=3

F’=1

The system is non-variant.

The point “ O “ is called eutectic point or eutectic temperature and is corresponding composition,97.4 % Pb and 2.6 % Ag ,is called eutectic composition.below this point the eutectic compound and the metal solidfy.

iv) Areas

The area above the line AOB has a single phase( molten Pb + Ag ). According to reduced phase rule

F’=C-P+1

C=2

P=1

F’=2

The system is bi-variant.

The area below the line AO ,OB and point “O” have two phases and hence the system is univariant.

According to reduced phase rule

F’=C-P+1

C=2

P=2

F’=1

The system is uni-variant.

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The process of raising the relative proportion of Ag in the alloy is known as pattinson’s process.

The Pattinson process was patented in 1833. It depended on well-known material properties; essentially that lead and silver melt at different temperatures. The equipment consisted of a row of about 8-9 iron pots, which could be heated from below. Agentiferous lead was charged to the central pot and melted. This was then allowed to cool, as the lead solidified, it was skimmed off and moved to the next pot in one direction, and the remaining metal was then transferred to the next pot in the opposite direction. The process was repeated in the pots successively, and resulted in lead accumulating in the pot at one end and silver in that at the other. The process was economic for lead containing at least 250 grams of silver per ton.

Uses of eutectic system

1.suitable alloy composition can be predicted with the help of eutectic systems.

2.eutectic systems are used in preparing solders ,used for joining two metal pieces together.

Melting point

It is the temperature at which the solid and liquid phases, having the same composition ,are in equilibrium.

Solid A <------> solid B

Eutectic point

It is the temperature at which two solids and a liquid phase are in equilibrium .

Solid A + solid B <-----> Liquid

Triple point

It is the temperature at which three phases are in equilibrium.

Solid <---->liquid<-------> vapour

By definition ,

All the eutectic points are melting points, but all the melting points need not be eutectic points. ll ly , all the eutectic points are triple points ,but all the triple points need not be eutectic points. Uses (or) merits of phase rule

1. It is a convenient method of classifying the equilibrium states in terms of phases ,components and degree of freedom.

2. It helps in deciding whether the given number of substances remain in equilibrium or not.

Limitations of phase rule

1.phase rule can be applied for the systems in equilibrium.

2.only three variables like P,T & C are considered ,but not electrical, magnetic and gravitational forces.

Definition

ALLOYS

An alloy is defined as “homogeneous solid solution of two or more different element one of which at least is essentially a metal”. Alloy containing Hg as a constituent element are called amalgams.

Properties of alloys

1) Alloy are harder less malleable and possess lower melting point than their component metals

2) Alloys possess low electrical conductivity

3) Alloys resist corrosion and the action of acids

Importance or need of making alloys

1. To increase the hardness of the metal

Example

Gold and silver are soft metal they are alloyed with copper to make them hard

2. To lower the melting points of the metal

Example

Wood metal (an alloy of lead, bismuth, tin and cadmium) melts at 60.5⁰c which is far below the melting points of any of these constituent metals

3. To resist the corrosion of the metal

Example

Pure iron rested but when it is alloyed with carbon chromium (stainless steel) which resists corrosion

4. To modify chemical activity of the metal

Example

Sodium amalgam is less active than sodium but aluminium amalgam is more active than aluminium

5. To modify the colour of the metal

Example

Brass an alloy of copper (red) and size (silver-white) is white colour.

6. To get good casting of metal

Example

An alloy of lead with 5% tin and 2% antimony is used fro casting printing type due toits good casting property

Functions (or) effects of alloying elements

Addition of small amount of certain metals such as Ni, Cr, Mo, Mn, Si, v and Al impart special properties like hardness, tensile strength, resistance to corrosion and coefficient of expansion on steel. Such products are known as special steel or alloy steels

Some important alloying element and their functions are given in table

CLASSIFICATION (OR) TYPES OF ALLOYS

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PROPERTIES

1. High yield point & strength

2. Sufficient formability,ductility & weldability

3. Corrosion & abrasion resistant

4. Less distortion & cracking

5. High temperature strength

IMPORTANT FERROUS ALLOYS (i)NICHROME

Nichrome is an alloy of nickel & chromium

COMPOSITION

Nickel – 60%

Chromium – 12%

Iron – 26%

Manganese – 2%

PROPERTIES

1. Good resistance to oxidation & heat

2. High melting point & electrical resistance

3. Withstand heat up to 1000-1100⁰C

USES

1. Used for making resistance coils,heating elements in stoves & electric irons

2. Used in making parts of boilers,steam lines stills,gas turbines,aero engine valves,retorts,annealing boxes.

(ii)ALNICO

Alnico is an alloy of aluminium-nickel-cobalt .

COMPOSITION

Aluminium – 8-12%

Nickel – 14-28%

Cobalt – 5-35%

PROPERTIES

1. Excellent magnetic properties & high melting point

2. Magnetized to produce strong magnetic fields as high as 1500 gauss

TYPES OF ALNICO ALLOYS

Alnico alloys are of two types

1. ISOTROPIC ALNICO

It is effectively magnetized in any direction

2.ANISOTROPIC ALNICO

It possess preffered direction of magnetization.

Anisotropic alnico possesses greater magnetic capacity in their preffered orientation than isotropic alnico.

USES

1. Used as permanent magnets in motors,generators,radio speakers microphones,telephone receivers & galvanometers.

(iii)STAINLESS STEELS (or)CORROSIOPN RESISTANT STEELS

· These are alloy steels containing chromium together with other elements such as nickel,molybdenum,etc.

· Chromium-16% or more

· Carbon-0.3-1.5%

PROPERTIES

1. Resist corrosion by atmospheric gases & also by other chemicals.

2. Protection against corrosion is due to the formation of dense, non- porous,tough film of chromium oxide at the metal surface. If the film cracks, it gets automatically healed up by atmospheric oxygen

TYPES OF STAINLESS STEEL

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1. HEAT TREATABLE STAINLESS STEEL

COMPOSITION Carbon-1.2%

Chromium-less than 12-16% PROPERTIES

Magnetic,tough & can be worked in cold condition

USES

1. Can be used up to 800⁰C

2. Good resistant towards weather & water

3. In making surgical instruments,scissors,blades,etc.

2.HEAT TREATABLE STAINLESS STEEL PROPERTIES

· Possess less strength at high temperature

· Resistant to corrosion

TYPES OF NON HEAT TREATABLE STAINLESS STEEL (a)MAGNETIC TYPE

COMPOSITION

Chromium-12-22% Carbon-0.35%

PROPERTIES

1. Can be forged,rolled & machined

2. Resist corrosion

USES

Used in making chemical equipments& automobile parts.

(b)NON MAGNETIC TYPE COMPOSITION

Chromium-18-26%

Nickel-8-21%

Carbon-0.15%

Total % of Cr & Ni is more than 23%. EXAMPLE:18/8 STAINLESS STEEL COMPOSITION: Chromium-18%

Nickel-8%

PROPERTIES

1. Resistance to corrosion.

2. Corrosion resistance is increased by adding molybdenum

USES

In making household utensils,sinks,dental & surgical instruments.

NON FERROUS ALLOYS

· Do not contain iron as one of the main constituent.

· Main constituents are copper,aluminium,lead,tin,etc.

PROPERTIES

1. Softness & good formability

2. Attractive (or) very good colours

3. Good electrical & magnetic properties

4. Low density & coefficient of friction

5. Corrosion resistance

IMPORTANT NON FERROUS ALLOYS

1. COPPER ALLOYS (BRASS)

Brass contains mainly copper & zinc

PROPERTIES

· Greater strength, durability & machinability

· Lower melting points than Cu & Zn

· Good corrosion resistance & water resistance property

2.BRONZE(COPPER ALLOY)

Bronze contains copper & tin

PROPERTIES

· Lower melting point

· Better heat & electrical conducting property

· Non-oxidizing,corrosion resistance & water resistance property.

3.SOLDERS

Solders are low- melting alloys of tin & lead

PROPERTIES

Solder is melted to join metallic surfaces ,especially in the fields of electronic &

plumbing

USES

1. Used in electrical industry

2. Alloy with 50% tin is general-purpose solder

3. For sealing automotive radiator cores.

4. As fuses for fire-extinguishing equipments,boiler plugs,etc.

Heat treatment of alloys (steel)

Heat treatment is defined as” the process of heating and cooling of solid steel article under carefully controlled condition”. During heat treatment certain physical properties are altered without altering its chemical composition

Objectives (or) purpose of heat treatment

Heat treatment causes

i. Improvement in magnetic and electrical properties ii. Refinement of grain structure

iii. Removal of the imprisoned trapped gases iv. Removal of internal stress

v. Improves fatique and corrosion resistance

Types of heat treatment of alloys (steel)

1. Annealing

Annealing means softening. This is done by heating the metal to high temperature followed by slow cooling in a furnace.

Purpose of annealing

i. It increases the machinability

ii. It also removes the imprisoned gases

Types of annealing

Annealing can be done in two types

i. Low temperature annealing (or) process annealing ii. High temperature annealing 9or) full annealing

Low temperature annealing (or)process annealing

It involves in heating steel to a temperature below the lower critical point followed by slow cooling

Purpose

1. It improves mashinability by reliving the internal stress or internal strain

2. It increases ductility and shock resistance

3. It reduce hardness

(i) High temperature annealing (or) fault annealing

It involves in heating to a temperature about 30 to 50C above the higher critical temperature and holding it at that temperature for sufficient time to allow the internal changes to take place and then cooled room temperature

The approximate annealing temperature of various grades of carbon steel are

1. Mild steel=840-870⁰c

2. Medium carbon steel=780-840⁰c

3. High carbon steel=760-780⁰c

Purpose

1. It increases the ductility and machinability

2. It makes the steel softer, together with an appreciable increases in its toughness

2.Hardening (or) quenching

· It is the process of heating steel beyond the critical temperature and then suddenly cooling it either in oil or brine water or some other fluid.

· The faster the rate of cooling harder will be the steel produced.

· Medium and high carbon steel can be hardened but low carbon steel cannot hardened

Purpose

1. It increases its resistance to wear ability ,to cut other metal and strength .

2. It increases abrasion resistance.

3. Used for making cutting tools.

3. TEMPERING

· It is the process of heating the already hardened steel to a temperature lower than its own hardening temperature & then cooling it slowly.

· The reheating controls the development of the final properties

· Thus,

(a)For retaining strength & hardness, reheating temperature should not exceed 400⁰C.

(b) For developing better ductility & toughness, reheating

temperature should be within 400-600⁰C.

Purpose

1. It removes stress &strains that might have developed during quenching.

2. Increased toughness & ductility.

3. Used for cutting tools like blade,cutters etc.

4. NORMALISING

It is the purpose of heating steel to a definite temperature (above its higher critical temperature) & allowing it to cool gradually in air. Purpose

1. Recovers homogeneity

2. Refines grains.

3. Removes internal stresses

4. Increases toughness

5. Used in engineering works

NOTE: The difference between normalised & annealed steel are

1. A normaled steel will not be as soft as annealed steel.

2. Also normalizing takes much lesser time than annealing.

5.CARBURIZING

· The mild steel article is taken in a cast iron box within containing small pieces of charcoal(carbon material).

· It is heated to about 900 to 950C & allow it for sufficient time,so that the

carbon is absorbed to required depth .

· The article is then allowed to cool slowly within the box itself.

· The outer skin of the article is converted into high carbon steel containing about 0.8 to 1.2% carbon.

Purpose

To produce hard surface on steel article

6.NITRIDING

Purpose

· Nitriding is the process of heating the metal alloy in presence of ammonia to about 550C.

· The nitrogen (obtained by the dissociation of ammonia)

combines with the surface of the alloy to form hard nitride.

To get super-hard surface.

CY6151 Engineering Chemistry 1 - PHOTOCHEMISTRY AND SPECTROSCOPY (Unit 3) Lecture Notes

Anna University

CY6151 Engineering Chemistry - I

UNIT III

Spectroscopy

ANALYTICAL CHEMISTRY

· Analytical chemistry is concerned with the identification of a substance, the elucidation of its structure and quantitative analysis of its composition.

· It is an interdisciplinary branch of science which deals with various disciplines of chemistry such as inorganic, organic, physical, industrial and biochemistry

INSTRUMENTAL METHODS

The methods dependent upon measurement of an electrical property and those based upon determination of the extent to which radiation is absorbed or upon assessment of the intensity of emitted radiation, all require the use of a suitable instrument, eg. Polarograph, spectrophotometer etc., and in consequence such methods are referred to as instrumental methods.

The growth of instrumental methods (or) analysis is related to the developments in the field of electronics, so instrumental methods of chemical analysis have become the backbone of experimental chemistry.

ANALYTICAL TECHNIQUES –SPECTROSCOPY

Spectroscopy is the branch of science dealing with the study of interaction of electromagnetic radiation with matter.

It is a powerful tool available for the study of atomic and molecular structure and it is also used in the analysis of most of the samples.

Types of Spectroscopy:-

The study of spectroscopy is divided into two types. They are,

1. Atomic spectroscopy

2. Molecular spectroscopy.

Atomic Spectroscopy

It deals with the interactions of electromagnetic radiation with atoms.

Molecular Spectroscopy

It deals with the interaction of electromagnetic radiation with molecules.

Differences between atomic spectra and molecular spectra

Atomic Spectra

Molecular Spectra

1 It occurs from the interaction of atoms and electromagnetic radiation.

It occurs from the interaction of molecules and electromagnetic radiation

2. It is a line spectra

It is a complicated spectra.

3.It is a due to electronic transition in an element

It is due to vibrational, rotational and electronic transition in a molecule

Electromangnetic radiation (or) Electromagnetic energy (or) Radiant energy

Electromagnetic radiation is produced due to the interaction between the electric field and the magnetic field.

Electromagnetic radiation is divided into number of regions according to their wave length.

It can be represented as, λ (lambda)

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Wave length (λ)

It is the distance between two successive crests of a wave.

It is denoted by ‘λ’. Wave length is expressed in meters and to express very short wave

clip_image003lengths nanometer (nm,10-9m), picometer (pm,10-12m) or ‘non SI’ Units Angstrom (Ao,10-10m)

clip_image004λ

clip_image0051 second

Frequency (ע)

It is the number of waves crossing a point in unit time. It is denoted by, ע

clip_image006Frequency is expressed in s-1(or) Hertz, (Hz).

Velocity of light ( c )

The product of the wavelength and the frequency is a constant called the velocity of light

(or) speed of light. That is,

c = λ

Where,

c - speed of light;

ע - frequency;

λ - wave length

c = 2.998 X 108 ms-1

c = 3 X 108 ms-1

Wave number image

It is the reciprocal of the wave length. It is denoted by ע

Wave number is expressed in units of per centimeter,

Electromagnetic spectrum (EMS)

The arrangement of all types of electromagnetic radiations in the increasing order of their wavelength or decreasing order of their frequency is known as ‘Electromagnetic Spectrum’.

S. No.

Type of radiation

Wave

length

Frequency

1

Gamma rays

10-11

1019

2

X ray

10-9

10-17

3

UV

10-7

1015

4

Visible

10-6

1014

5

IR

10-5

1013

6

Micro waves

10-3

1011

7

Radio waves (low energy)

102

106

PRINCIPLE OF ATOMIC SPECTROSCOPY Spectrum

When a beam of polychromatic light is passed through a prism or grating it splits up into seven different colour. The set of colours thus obtained is called a spectrum.

The complete spectrum may extend from gamma rays of wave length 10-13 m to radiowaves of wavelength 105m.

Classification of spectra

There are two main classes of spectra namely,

1. Absorption Spectrum.

2. Emission Spectrum.

Absorption spectrum

When white light (ie.having all the wave length) is passed through an absorbing substance and then observed through a spectroscope, it is found that certain colours (or) wave lengths are missing and dark lines appear at their places. The specrtrum so obtained is called absorption spectrum.

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Emission spectrum

When the light emitted by a substance is passed through a prism and examined directly with a spectroscope, the spectra obtained is referred to as emission spectrum.

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Absorption Laws

These are,

There are two laws which govern the absorption of light by the molecules.

1. Lambert’s law

2. Beer’s law.

Lambert’s Law

When a beam of monochromatic light is passed through a solution of an

absorbing substance, the rate of decrease of intensity of radiation (‘dI’) with thickness of the absorbing solution (‘dx’) is directly proportional to the intensity of incident radiation (I). Mathematically, the law is expressed as,

image

Where,

k = absorption co-efficient.

On integrating the above expression between the limits,

I = Io at x = 0 and I = I at x = l

We get

image

-ln I/ Io = Kl

ln Io/ I = Kl

Kl = ln Io/ I

By taking natural logarithm,

Kl = 2.303 log Io / I

Beer’s Law

When a beam of monochromatic light is passed through a solution of an absorbing substance, the rate of decrease of intensity of radiation (‘dI’ ) with thickness of absorbing solution (‘dx’) is directly proportional to the intensity of incident radiation (I), as well as concentration of the solution( c).

Mathematically, it is expressed as

image

Where,

K = Absorption co-efficient.

On integrating the above expression between the limits,

I = Io at x = 0

I = I at x = l

We get,

image

-ln I/ Io = Kcl

ln Io/ I = Kcl

By taking natural logarithms,

2.303 log Io/ I = Kcl

log Io/ I = K / 2.303 . cl

where,

log Io/ I = εcl

ε = K / 2.303, is called the molar absorption coefficient and

log Io/ I = A, is called the absorbance

A = εcl

This equation is known as Beer – Lambert’s Law

Limitations of Beer – Lambert’s Law

This law is not obeyed if the radiation used in polychromatic.

1. It is applicable only for dilute solutions.

2. It is not applied to suspensions.

3. Deviation may occur, if the solution contains impurities.

UV – Visible Spectroscopy:

Absorption radiation in the UV (wave length range = 200 – 400 nm) and Visible (wave length range = 400 – 750 nm) regions of the electromagnetic spectrum results transitions between electronic levels. This is due to the larger energy change corresponds to 100 – 100,000 kJ/mol which cause simultaneous change in vibrational and rotation energies.

image

Generally energy change due to electronic transition is greater than that of vibrational and rotational transitions. Hence the UV and Visible spectra of simple molecules exihibit narrow absorption peaks.

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Permitted energy levels in UV and Visible regions.

The vibrational and rotational fine structure lines are not observed during the spectrum is run in solution. This is because of the physical interactions between sample organic molecule and the solvent molecule, cause collisional broadening of the lines.

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Electronic absorption spectrum of a solution of benzene in hexane.

The above spectra of benzene shows larger peaks at 250 nm due to the presence of П electrons and smaller peaks & troughs indicate vibrations of molecules.

Types of electrons in organic molecules involving in transitions:

1. σ electrons.

2. П electrons.

3. Non – bonding electrons.

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According to Molecular orbital theory, the interaction of atomic orbitals leads to the formation of “bonding” and “anti – bonding” molecular orbitals. The relative energies of bonding, anti – bonding and non – bonding molecular orbitals are given in the following diagram.

Bonding and antibonding orbitals.

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Molecules absorb radiation from UV – Visible region and undergo various transitions. During this transition, an electron from one of the filled σ, П or non – bonding orbitals get excited to vacant σ* or П* orbitals. Corresponding to possible excitations, there are various transitions are possible as follows.

These transitions are classified into two types as follows:

1. Allowed transition:

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2. Forbidden transition:

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The order of transition is

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Out of the above possible transitions, the last three ones account for the absorption in 200

– 800 nm region of electromagnetic radiation and first three transitions requires much higher energy, thus the molecules with n or П electrons give rise to characteristic spectra in the region 200 – 800 nm of electromagnetic region.

Chromophores:

The structural units of the compound having n or П electrons, absorbs

selective wavelength of UV – Visible radiation are called chromophores.

Example: - N=N- , C=C, C=O, etc.

Auxochromes:

The polar groups with lone pair of electrons support the intensity of chromophores are called auxochromes.

Example: .. ..

-O – H , - O – R , etc...

clip_image040

Bathochromic shift:

Absorption and intensity shifts.

It is also called red shift. The substitution of a selective group in a molecule makes the absorption to longer wavelength is called bathochromic shift.

Example: Alkyl substitution on olefins.

Hypsochromic shift:

It is also called blue shift. The substitution of a selective group in a molecule make the absorption to shorter wavelength is called hypsochromic shift. Example: Chlorine substitution on olefins.

Hyperchromic effect:

The substitution of a selective group in a molecule causes increase in the intensity of absorption maximum of the molecule, and then the effect is called hyperchromic effect. Example: Methyl substitution on benzene.

Hypochromic effect:

The substitution of a selective group in a molecule causes decrease in the intensity of absorption maximum of the molecule, and then the effect is called hypochromic effect. Example: Chlorine substitution on benzene.

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UV – Visible Spectrophotometer: Instrumentation:

Components:

Block diagram for a UV – Visble spectrophotometer.

Radiation source:

Hydrogen or deuterium lamps are used. It provides stable, continuous and sufficient intensity.

Filter:

It is also called monochromator. It permits the radiation of required wavelength only.

Cell:

It is a transparent and uniformly constructed container which contains

either sample solution or reference solvent.

Detectors:

It converts the absorbed radiation into current. There are three types of detectors, viz., Barrier layer cell, photo multiplier tube and photo cell.

Recorder: It converts the signal reaches to itself into spectrum of a molecule.

Working:

The radiation from the source is passed through the monochromator where it splitted into two equal beams, one half is passed into the sample cell and another half is passed into the reference cell containing solvent. The detector will measure the comparison of intensities of beam of light. If the sample absorbs light then the intensity of sample beam is less than the intensity of reference beam. It will be recorded as a signal in recorder. The instruments gives output graph (absorption spectrum) of a plot of the wavelength verses absorbance (A) of

the light at each wavelength, where A = log (I0/I).

clip_image046clip_image054

  UV – Visble spectra : (a) benzene in ethanol              (b) naphthalene in methanol.

Applications of UV spectroscopy:

1. It is used to determine the structure of vitamins, detecting steric hindrance, study rates of reactions and determine the dissociation constants of acids and bases from the change of absorption spectra with pH.

2. It is used to determine the dissociation energy of a molecule accurately from the wavelength.

3. It provides the information regarding moment of inertia, vibrational frequency and interatomic distances of diatomic molecules.

4. It is used to identify the cis and trans isomers of a compound from absorption spectra.

5. It is used to know the purity of a compound.

6. It is used to determine the structure of organic compounds. For example,

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isatin can be assigned following two possible structures:

However, the corresponding structures of two possible methyl ethers are known to us.

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On comparison of the spectra of isatin with that of two methyl isomers (III) and (IV), the spectrum of isatin is similar to that of N-methyl ether (III). Hence isatin is assigned the structure (I).

7. It is used in quantitative analysis to determine the concentration of unknown sample by using Beer – Lambert’s equation, A = E c l.

IR spectroscopy:

The spectra of a molecule arised in IR region (12500 cm – 1 – 50 cm – 1 )

due to the absorption of energy and transition occurs between different vibrational levels. Hence it is called vibration spectroscopy.

image

All types of molecules cannot interact with IR radiation. Only those molecules which exhibit change in dipole moment during a vibration can exhibit IR spectra.

Evidently, the homo-nuclear diatomic molecules like H2, O2, N2, Cl2, etc do not show change in dipole moment during vibration. Consequently, these do not exhibit IR

spectra. The hetero- nuclear diatomic / polyatomic molecules like HCl, BeCl2, NH3, CH4, CO2, C6H6, etc shows change in dipole moment and thus they exhibit IR spectra.

The IR spectral region at 1400 cm – 1 – 700 cm – 1 gives rich, intense and clear absorption bands for all functional groups in the organic compounds. This region is called finger – print region. It is used to identify the functional group present in the organic compound, Identify the molecule and find out the characteristics of the molecule.

The IR spectral region at 4000 cm – 1 – 600 cm – 1 gives intense absorption bands associated with bending and stretching vibrations of particular functional group in organic compounds. This region is called group frequency region. It is used to identify the types of functional groups present in organic molecules.

The molecules have certain number of vibrational modes. It can be calculated using the following formulae.

(a)For a linear molecule, No of fundamental vibrational mode = 3n – 5

(b)For a non – linear molecule, No of fundamental vibrational mode = 3n – 6

where n = number of atoms in a molecule.

Molecule

HCl

BeCl2

NH3

CH4

CO2

C6H6

FVM

1

4

6

9

4

30

Stretching and bending vibrations in water molecule:

Water molecule has non – linear structure. It has three fundamental vibrational modes which are corresponding to the frequencies 3652 cm – 1 (Symmetric stretching vibration), 3756 cm – 1 (Asymmetric stretching vibration) and 1596 cm – 1 (Bending vibration) respectively.

image

Generally stretching frequency is greater than bending frequency, because more energy is required to stretch the bond than to bend. All the above three vibrations are IR active and giving IR spectra at various frequencies. Hence IR active molecule undergoes change in dipole moments.

Stretching and bending vibrations in water molecule:

Carbon dioxide molecule has linear structure. It has four fundamental vibrational modes which are corresponding to the frequencies 1340 cm – 1 (Symmetric stretching vibration), 2350 cm – 1 (Asymmetric stretching vibration) and twice 666 cm – 1 (In plane bending vibration and Out of plane bending vibration) respectively.

image

In symmetrical stretching, both bonds are shortened or elongated to the same extent. Hence there is no change in dipole moment. So it is IR inactive.

In asymmetrical stretching, one of the bonds is shortened and the other is elongated. Hence there is change in bond length and dipole moment. So it is IR active.

In bending, both in-plane and out of plane bending involves variation of bond angle.

Hence there is change in bond angle and dipole moment. So it is IR active.

Even we have three active vibrations at 2350 cm – 1 666 cm – 1 and 666 cm – 1 respectively, we get two absorption band only, One at 2350 cm – 1 and another one at 666 cm – 1

image

Components:

Radiation source:

The Nernst glower (Oxides of Zr, Y and Er) is heated to 1500 radiation, which is used as radiation source.

C to give IR

Optical prism: It is also called mirror, which is used to reflect the radiation on filter.

Filter:

It is also called monochromator, which sent the individual frequencies to the detector.

Amplifier: It amplifies the current received from the detector.

Motor: It drives the wedge.

Recorder: It draws the IR spectrum, based on the movement of wedge.

Working:

The IR radiation from radiation source is splitted into two equal half beams; one half is passed into the sample cell and another half is passed into the reference cell containing solvent respectively. Then these beams are fall on the mirror and reflected to the monochromator, where the selective radiation is sent to the detector. The radiation received by the detector is converted into current. It is amplified and coupled to the motor which drives a wedge. Based on the movement of the wedge the recorder draws the absorption bands on the chart. Finally, we get a spectrum as a graph of Transmittance verses wave number from the IR spectrophotometer.

Applications:

1. It is used to identify the presence of functional groups in organic compounds.

For example, IR spectra of both benzaldehyde and acetophenone shows absorption peak at 1700 cm – 1

This indicates that the presence of keto group

(C=O) in both the compounds.

2. It is used to detect the presence of impurities in organic compounds, by comparing the IR spectra of the pure (shows actual absorption bands) and impure (shows extra absorption bands) compounds.

3. It is used to distinguish inter and intra molecular hydrogen bonding in organic compounds.

4. It is used to study the molecular symmetry, dipole moment, structure, bond angle and bond length, etc. of various organic and inorganic compounds.

5. It is used to distinguish positional isomers of organic compounds.

6. It is used in rapid quantitative analysis of mixture of compounds.

7. It is used to study the kinetics of a reaction

CY6151 Engineering Chemistry - I - CHEMICAL THERMODYNAMICS (Unit 2) Lecture Notes


Anna University

CY6151 Engineering Chemistry - I

Unit 2 Lecture Notes

 CHEMICAL THERMODYNAMICS 


CY6151 Engineering Chemistry - I - POLYMER CHEMISTRY Lecture Notes

Anna University

CY6151 Engineering Chemistry - I

Common to all Department

Unit 1 Lecture Notes

POLYMER CHEMISTRY


V+ Now Provides Nov / Dec 2013 Important Questions for Anna University Chennai


Vidyarthiplus (V+) is now providing Nov / Dec 2013 Important Questions for Anna University , Chennai Examination. The Important Questions were provided from various college students through the "Study Material Upload" tool.

Students are requested to submit your Important Questions with us so that we can share and help your friends. At Present we are receiving more than 10 Study Materials per day, Each Study Material is validated by V+ Staff's and are updated to V+ with the Creator's Credit.


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Chennai CBSE - 2014 Board Exam


Central Board of Secondary Education , Chennai

Chennai CBSE Board Exam for 10th and 12th will start from March 1st 2014.

This time 1.8 Lakh Students are writing the 10th Exam and 80 thousand Students are writing 12th Exam.

Timetable will be soon published.. Stay Connected with V+.



State-level chess competition for school students - Tamil Nadu

 State level chess competition for school students was held on Today (Friday) at Nehru Stadium in Chennai. The 360 students won in the regional level took part in the final competition.

The competition winners and their prize details will be announced in one or two days. Chief Minister Jayalalithaa announced that in order to promote the ability of Students , the school chess competition was introduced.

Across the state on August 23 school level competition was held with 11 lakh 25 thousand students from 55 thousand schools.

Anna University - Project Training 2013


SMART AND SECURE ENVIRONMENT RESEARCH LABORATORY

DEPARTMENT OF COMPUTER SCIENCE AND ENGINEERING

Anna University, Chennai-25.

Projects Topics:
  • Artificial Intelligence.
  • Attack simulation tool for lPv6 Environment — DDaS.
  • Bluetooth based Secure Routing Protocol.
  • Buffer Management in video Conference.
  • Cloud/Web Services Security.
  • Configuration, routing updates, service location.
  • C Content Distribution, Software Distribution.
  • Data Mining.
  • Distributed Interactive Online Gaming.
  • Graph Theory, Game Theory.
  • Hidden Semi Markov Model for Network Prediction.
  • Mobile Agent Communications.
  • C Network Coding.
  • Next Generation Internet.
  • Quality of Service in 3G and 46 Networks.
  • Software Defined Networks.
  • Source Address Verification using Soft Router.
  • Telemedicine.
  • Wireless Sensor Network Security.

Eligibility:
CEG, Anna University candidates pursuing 2nd or 3rd year of B.E (CSE)IB.Tech (IT) students are eligible to apply.

Period of the Project: The contact period far the project will be one month during 27th November - 21th December 2013.

How ta apply: 
Resume should be send ta sse@annauniv.edu on or before 06.11.2013.

Note:
Shortlisted Candidates will be intimated through E.Mail on or before 08.1 1.2013.

Coordinator:
C. Chellappan,
Professor and Dean, DCSE,
Anna University, Chennai.
Contact : Ph: 044.22358025.