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PHYSICAL CHEMISTRY
Thermo-chemistry
11-12 Heat of formation, heat of
reaction and heat of solution,
Hess’s law, calorimetry
1
THERMOCHEMISTRY
 Thermochemistry is the
branch of chemistry which
deals with the thermal
changes accompanying
chemical and physical
transformations. The aim of
thermochemistry is not only
the determination of energy
emitted or absorbed but
also to develop methods for
calculating these thermal
readjustments without
recourse to experiment.
2
THERMOCHEMISTRY
 For practical purpose it
is essential to know
whether the heat is
absorbed or evolved
and how much of it,
because if the heat is
evolved it must be
removed to effect
appropriate reaction
and if it is absorbed,
required amount of
heat must be supplied. 3
CHEMICAL REACTIONS
 A reaction always begins
with the breaking a few
bonds and ends with the
formation of a few new
bonds.
4
Since the reaction begins with breaking
of bonds, hence it invariably needs
energy to start. This energy is called
energy of activation.
THERMAL CHANGES IN CHEMICAL
REACTIONS
 Energy of activation is required to
start a reaction irrespective of the
fact whether the reaction is
exothermic or endothermic.
 The energy of activation is
actually the barrier between the
reactants and the products and
must be crossed by providing
energy to start the reaction
5
EXOTHERMIC REACTIONS
 In exothermic reactions the
total energy of the products is
less than the total energy of
the reactants. Hence, the
difference of energy is
released usually as heat.
 Since more energy is
released than activation
energy, the energy released
is more than enough to
activate more reactant
molecules. Hence once
activated the reaction goes
on by itself and no more
heating is required.
6
EXOTHERMIC REACTIONS
7
If the difference of
activation energy and the
total energy released is
less, the reaction is less
exothermic
If the difference of
activation energy and the
total energy released is
more, the reaction is more
exothermic
ENDOTHERMIC REACTIONS
 In endothermic reactions the total
energy of the products is greater
than the total energy of the
reactants. Hence, the difference
of energy is absorbed by the
system.
 Since the energy of products is
greater than the reactants, the
energy released after activation is
less than the activation energy
and is not sufficient to activate
more reactant molecules. That is
why endothermic reactions
require continuous supply of
energy (heat) for propagation of
reaction and the reaction stops as
and when the supply of heat is
interrupted. 8
ENDOTHERMIC REACTIONS
9
If the difference of activation
energy and the total energy
release is less, the reaction is
less endothermic
If the difference of
activation energy and the
total energy release is
more, the reaction is more
endothermic
HEAT OF FORMATION
 The heat of formation is the amount of heat absorbed or
evolved when a mole of a substance is formed from it’s
elements. For example if 2 grams of hydrogen are burned in
oxygen to form liquid water, 68.320 Kilo Calories of heat are
evolved.
H2 + ½ O2 = H2O ΔH = -68.320 Kcal
 The heat associated with chemical reaction not only depends
on whether the reaction is carried out at constant pressure but
also the amounts of substances. Hence if the amount of
hydrogen in the above reaction is doubled (i.e. 4 grams) the
amount of heat evolved will also be doubled, i.e. 68.320 x 2 =
136.640
10
HEAT OF FORMATION
H2 + ½ O2 = H2O
 In the above reaction:
 Whether the work will be done or not?
 If work is done, will it be negative (-) or positive (+)?
11
HEAT OF REACTION
 All chemical reactions are accompanied by
absorption or evolution of heat. This thermal
change is called heat of reaction.
 Tables of standard enthalpies of a large number of
substances are available and simply substituting
the values of enthalpies in a reaction, the heat of
reaction can be calculated.
 For example sodium carbonate reacts with HCl,
producing NaCl, CO2 and H2O; the heat of this
reaction can be calculated by the use of standard
enthalpies as follows:
12
HEAT OF REACTION
 By subtracting the total energy of reactants from
the total energy of products the heat of reaction
is obtained.
13
HEAT OF REACTION AT CONSTANT PRESSURE
 If a reaction is carried out at constant pressure
the heat of reaction will be:
qp = ΔE + PΔV
= (Ep-Er) + P(Vp-Vr)
= (Ep+PVp) – (Er+PVr)
=Hp - Hr
= ΔH
ΔH = HH2O (l) – [HH2 (g) +H1/2 O2 (g)]
14
HEAT OF REACTION AT CONSTANT VOLUME
 At constant volume ΔV = 0, hence, heat of reaction
will be:
qv = ΔE = Ep - Er
15
HEAT OF SOLUTION
 Solution of one substance in another is
accompanied by absorption or evolution of heat and
this thermal effect is called heat of solution of the
substance.
 Per mole of dissolved substance, the heat of
solution at any given temperature and pressure
depends upon the amount of solvent in which
solution takes place. The grater the dilution the
greater the enthalpy of solution. Hence for heat of
solution it is essential to specify the number of
moles of solvent per mole of solute.
16
HEAT OF SOLUTION
 Sulphuric acid dissolves
in water with evolution of
heat. If one mole of
H2SO4 is dissolved in
water the heat evolved
depends on the number of
moles of water. It is
evident from results that,
the greater the dilution,
the greater is the ΔH.
Moles of water ΔH (cal)
0.5 -3810
1 -6820
2 -9960
3 -11890
4 -13120
6 -14740
10 -16240
3200 -20050
infinite -22990
17
HEAT OF SOLUTION
 The dilution of H2SO4 with water given by
equation:
H2SO4 (l) + aq = H2SO4 (aq)
The heat of solution, ΔH, for this process is
given by:
ΔH = H – (n1H1 + n2H2)
Where H1 and H2 are the enthalpies of two
pure solution constituents and H is the
enthalpy of solution.
18
HESS’S LAW OF HEAT SUMMATION
 As we have seen that E and H are functions of the
state of system and consequently ΔE and ΔH must
be true quantities, independent of path.
 It follows from this that the heat absorbed or
evolved in a chemical reaction is independent of the
particular manner in which the reaction is carried
out. This generalization of the statement is called
Hess’s law of heat summation.
 This principle makes it possible to calculate the
heats of many reactions which cannot be directly
measured.
19
HESS’S LAW OF HEAT SUMMATION
 If we intend to determine the enthalpy ΔH of the
following reaction:
2C (s)+ 2H2 (g) + O2 (g) = CH3COOH ΔH25 ºC = ?
 It is not possible to determine the enthalpy of this
reaction as the reaction does not occur in this
manner. However we can determine the enthalpy
of this reaction by a different way using Hess’s law.
20
HESS’S LAW OF HEAT SUMMATION
 Using the available calorimetric data for the following
reactions and Hess’s law we can calculate ΔH of acetic
acid.
21
HESS’S LAW OF HEAT SUMMATION
22
MEASUREMENT OF THERMAL CHANGES -
CALORIMETRY
 Heat changes involved in a reaction, are
determined using the instrument named
calorimeter. There are different types of
calorimeters, however, all essentially consists of an
insulated chamber filled with definite amount of
water. The actual reaction is carried out in a
separate chamber which is immersed in water. The
thermal changes occurring in the reaction chamber
directly bring about thermal changes in the water,
which are then measured and calculated.
23
CALORIMETRY
 The calorimeter is essentially an
insulated chamber filled with definite
amount of water in which reaction
chamber is immersed. The water in the
insulated chamber
 In an exothermic reaction, the heat
evolved is transferred to water and the
rise in temperature of water is
measured. The data then collected is
used to calculate the amount of heat
evolved in the reaction.
 In case of an endothermic reaction, the
heat is absorbed and the temperature
of water is lowered, which is measured
and corresponding heat change is
calculated. 24
CALORIMETRY
 Various types of calorimeters are used
to meet different requirements. The
one shown in the figure is called bomb
calorimeter. It consists of an outer
insulated housing and an inner
container containing pure water. The
reaction chamber, called bomb, is a
sealed vessel immersed in water. The
water is circulated using the stirrer to
keep the temperature homogenous
though out its body. The sample resting
on a boat in the reaction chamber is
ignited electrically and the heat changes
thus occurring are read from the
changes occurring in water.
 Since the process takes place at
constant volume, the reaction vessel is
specially constructed to withstand high
pressure.
25
CALORIMETRY
 The simple calorimeter used
in student laboratories is the
styrofoam coffee cup. The
coffee cup is covered by the
lid and a thermometer
inserted through the lid
reads the temperature
changes.
 Styrofoam is a good thermal
insulator over a short time
and provides good results
for students experimantal
work.
26
CALORIMETRY – CALCULATING THERMAL
DATA
Heat flow is calculated by using the
equation:
q = C x m x ΔT
Where “q” is the heat flowing through
system boundary, “C” is the specific
heat, “m” is the mass of system and
“ΔT” is rise or fall of temperature.
27
PROBLEM 1
 consider a chemical reaction which occurs in 200
grams of water with an initial temperature of
25.0°C. The reaction is allowed to proceed in the
coffee cup calorimeter. As a result of the reaction,
the temperature of the water changes to 31.0°C.
Calculate the enthalpy change (ΔH) of this reaction
in Joules.
N.B. The specific heat of water is = 4.18 J/g,˚C
28
PROBLEM 1 - SOLUTION
 The change in temperature of water is used to calculate the heat
evolved or absorbed in the reaction. Use is made of the following
equation:
q = C x m x ΔT
while q = ΔH
 where C is the specific heat capacity, m is the mass and ΔT is the
change in temperature of water.
C = 4.18 J/g ˚C
M = 200 g
ΔT = (31.0 – 25.0) = 6.0 ˚C
qwater = 4.18 J/g,°C x 200 g x (31.0°C - 25.0°C)
= 5.016 kJ
 Since we know that the reaction is exothermic hence the sign for ΔH
will be negative, therefore ΔH for the reaction will be:
ΔH = - 5.016 kJ
29
PROBLEM 2
When 7.1 g of NH4NO3 was added to
100 g of water at 18.2 ºC, the
temperature of solution dropped to
12.8 ºC. Calculate the enthalpy
change, ΔH of solution for 1 mole of
NH4NO3.
(specific heat capacity of water =
4.184 J g-1K-1)
30

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Basic Civil Engineering first year Notes- Chapter 4 Building.pptx
 

Lecture of thermo-chemistry and calorimetery

  • 1. PHYSICAL CHEMISTRY Thermo-chemistry 11-12 Heat of formation, heat of reaction and heat of solution, Hess’s law, calorimetry 1
  • 2. THERMOCHEMISTRY  Thermochemistry is the branch of chemistry which deals with the thermal changes accompanying chemical and physical transformations. The aim of thermochemistry is not only the determination of energy emitted or absorbed but also to develop methods for calculating these thermal readjustments without recourse to experiment. 2
  • 3. THERMOCHEMISTRY  For practical purpose it is essential to know whether the heat is absorbed or evolved and how much of it, because if the heat is evolved it must be removed to effect appropriate reaction and if it is absorbed, required amount of heat must be supplied. 3
  • 4. CHEMICAL REACTIONS  A reaction always begins with the breaking a few bonds and ends with the formation of a few new bonds. 4 Since the reaction begins with breaking of bonds, hence it invariably needs energy to start. This energy is called energy of activation.
  • 5. THERMAL CHANGES IN CHEMICAL REACTIONS  Energy of activation is required to start a reaction irrespective of the fact whether the reaction is exothermic or endothermic.  The energy of activation is actually the barrier between the reactants and the products and must be crossed by providing energy to start the reaction 5
  • 6. EXOTHERMIC REACTIONS  In exothermic reactions the total energy of the products is less than the total energy of the reactants. Hence, the difference of energy is released usually as heat.  Since more energy is released than activation energy, the energy released is more than enough to activate more reactant molecules. Hence once activated the reaction goes on by itself and no more heating is required. 6
  • 7. EXOTHERMIC REACTIONS 7 If the difference of activation energy and the total energy released is less, the reaction is less exothermic If the difference of activation energy and the total energy released is more, the reaction is more exothermic
  • 8. ENDOTHERMIC REACTIONS  In endothermic reactions the total energy of the products is greater than the total energy of the reactants. Hence, the difference of energy is absorbed by the system.  Since the energy of products is greater than the reactants, the energy released after activation is less than the activation energy and is not sufficient to activate more reactant molecules. That is why endothermic reactions require continuous supply of energy (heat) for propagation of reaction and the reaction stops as and when the supply of heat is interrupted. 8
  • 9. ENDOTHERMIC REACTIONS 9 If the difference of activation energy and the total energy release is less, the reaction is less endothermic If the difference of activation energy and the total energy release is more, the reaction is more endothermic
  • 10. HEAT OF FORMATION  The heat of formation is the amount of heat absorbed or evolved when a mole of a substance is formed from it’s elements. For example if 2 grams of hydrogen are burned in oxygen to form liquid water, 68.320 Kilo Calories of heat are evolved. H2 + ½ O2 = H2O ΔH = -68.320 Kcal  The heat associated with chemical reaction not only depends on whether the reaction is carried out at constant pressure but also the amounts of substances. Hence if the amount of hydrogen in the above reaction is doubled (i.e. 4 grams) the amount of heat evolved will also be doubled, i.e. 68.320 x 2 = 136.640 10
  • 11. HEAT OF FORMATION H2 + ½ O2 = H2O  In the above reaction:  Whether the work will be done or not?  If work is done, will it be negative (-) or positive (+)? 11
  • 12. HEAT OF REACTION  All chemical reactions are accompanied by absorption or evolution of heat. This thermal change is called heat of reaction.  Tables of standard enthalpies of a large number of substances are available and simply substituting the values of enthalpies in a reaction, the heat of reaction can be calculated.  For example sodium carbonate reacts with HCl, producing NaCl, CO2 and H2O; the heat of this reaction can be calculated by the use of standard enthalpies as follows: 12
  • 13. HEAT OF REACTION  By subtracting the total energy of reactants from the total energy of products the heat of reaction is obtained. 13
  • 14. HEAT OF REACTION AT CONSTANT PRESSURE  If a reaction is carried out at constant pressure the heat of reaction will be: qp = ΔE + PΔV = (Ep-Er) + P(Vp-Vr) = (Ep+PVp) – (Er+PVr) =Hp - Hr = ΔH ΔH = HH2O (l) – [HH2 (g) +H1/2 O2 (g)] 14
  • 15. HEAT OF REACTION AT CONSTANT VOLUME  At constant volume ΔV = 0, hence, heat of reaction will be: qv = ΔE = Ep - Er 15
  • 16. HEAT OF SOLUTION  Solution of one substance in another is accompanied by absorption or evolution of heat and this thermal effect is called heat of solution of the substance.  Per mole of dissolved substance, the heat of solution at any given temperature and pressure depends upon the amount of solvent in which solution takes place. The grater the dilution the greater the enthalpy of solution. Hence for heat of solution it is essential to specify the number of moles of solvent per mole of solute. 16
  • 17. HEAT OF SOLUTION  Sulphuric acid dissolves in water with evolution of heat. If one mole of H2SO4 is dissolved in water the heat evolved depends on the number of moles of water. It is evident from results that, the greater the dilution, the greater is the ΔH. Moles of water ΔH (cal) 0.5 -3810 1 -6820 2 -9960 3 -11890 4 -13120 6 -14740 10 -16240 3200 -20050 infinite -22990 17
  • 18. HEAT OF SOLUTION  The dilution of H2SO4 with water given by equation: H2SO4 (l) + aq = H2SO4 (aq) The heat of solution, ΔH, for this process is given by: ΔH = H – (n1H1 + n2H2) Where H1 and H2 are the enthalpies of two pure solution constituents and H is the enthalpy of solution. 18
  • 19. HESS’S LAW OF HEAT SUMMATION  As we have seen that E and H are functions of the state of system and consequently ΔE and ΔH must be true quantities, independent of path.  It follows from this that the heat absorbed or evolved in a chemical reaction is independent of the particular manner in which the reaction is carried out. This generalization of the statement is called Hess’s law of heat summation.  This principle makes it possible to calculate the heats of many reactions which cannot be directly measured. 19
  • 20. HESS’S LAW OF HEAT SUMMATION  If we intend to determine the enthalpy ΔH of the following reaction: 2C (s)+ 2H2 (g) + O2 (g) = CH3COOH ΔH25 ºC = ?  It is not possible to determine the enthalpy of this reaction as the reaction does not occur in this manner. However we can determine the enthalpy of this reaction by a different way using Hess’s law. 20
  • 21. HESS’S LAW OF HEAT SUMMATION  Using the available calorimetric data for the following reactions and Hess’s law we can calculate ΔH of acetic acid. 21
  • 22. HESS’S LAW OF HEAT SUMMATION 22
  • 23. MEASUREMENT OF THERMAL CHANGES - CALORIMETRY  Heat changes involved in a reaction, are determined using the instrument named calorimeter. There are different types of calorimeters, however, all essentially consists of an insulated chamber filled with definite amount of water. The actual reaction is carried out in a separate chamber which is immersed in water. The thermal changes occurring in the reaction chamber directly bring about thermal changes in the water, which are then measured and calculated. 23
  • 24. CALORIMETRY  The calorimeter is essentially an insulated chamber filled with definite amount of water in which reaction chamber is immersed. The water in the insulated chamber  In an exothermic reaction, the heat evolved is transferred to water and the rise in temperature of water is measured. The data then collected is used to calculate the amount of heat evolved in the reaction.  In case of an endothermic reaction, the heat is absorbed and the temperature of water is lowered, which is measured and corresponding heat change is calculated. 24
  • 25. CALORIMETRY  Various types of calorimeters are used to meet different requirements. The one shown in the figure is called bomb calorimeter. It consists of an outer insulated housing and an inner container containing pure water. The reaction chamber, called bomb, is a sealed vessel immersed in water. The water is circulated using the stirrer to keep the temperature homogenous though out its body. The sample resting on a boat in the reaction chamber is ignited electrically and the heat changes thus occurring are read from the changes occurring in water.  Since the process takes place at constant volume, the reaction vessel is specially constructed to withstand high pressure. 25
  • 26. CALORIMETRY  The simple calorimeter used in student laboratories is the styrofoam coffee cup. The coffee cup is covered by the lid and a thermometer inserted through the lid reads the temperature changes.  Styrofoam is a good thermal insulator over a short time and provides good results for students experimantal work. 26
  • 27. CALORIMETRY – CALCULATING THERMAL DATA Heat flow is calculated by using the equation: q = C x m x ΔT Where “q” is the heat flowing through system boundary, “C” is the specific heat, “m” is the mass of system and “ΔT” is rise or fall of temperature. 27
  • 28. PROBLEM 1  consider a chemical reaction which occurs in 200 grams of water with an initial temperature of 25.0°C. The reaction is allowed to proceed in the coffee cup calorimeter. As a result of the reaction, the temperature of the water changes to 31.0°C. Calculate the enthalpy change (ΔH) of this reaction in Joules. N.B. The specific heat of water is = 4.18 J/g,˚C 28
  • 29. PROBLEM 1 - SOLUTION  The change in temperature of water is used to calculate the heat evolved or absorbed in the reaction. Use is made of the following equation: q = C x m x ΔT while q = ΔH  where C is the specific heat capacity, m is the mass and ΔT is the change in temperature of water. C = 4.18 J/g ˚C M = 200 g ΔT = (31.0 – 25.0) = 6.0 ˚C qwater = 4.18 J/g,°C x 200 g x (31.0°C - 25.0°C) = 5.016 kJ  Since we know that the reaction is exothermic hence the sign for ΔH will be negative, therefore ΔH for the reaction will be: ΔH = - 5.016 kJ 29
  • 30. PROBLEM 2 When 7.1 g of NH4NO3 was added to 100 g of water at 18.2 ºC, the temperature of solution dropped to 12.8 ºC. Calculate the enthalpy change, ΔH of solution for 1 mole of NH4NO3. (specific heat capacity of water = 4.184 J g-1K-1) 30