Potentiometry, Electrochemical cell, construction and working of indicator an...Vandana Devesh Sharma
Potentiometry - Electrochemical cell -Construction and working of reference (Standard hydrogen, silver chloride electrode and calomel electrode)
Indicator electrodes (metal electrodes and glass electrode)
Methods to determine end point of potentiometric titration
and applications
Potentiometry is the method to find the concentration of solute in
A given solution by measuring the potential between two Electrodes
(reference and Indicator electrode) . Potentiometric titration involves
the measurement of the potential of the indicator electrode and
reference electrode.
In potentiometric titration reference and indicator electrodes are
immersed in the solution of particular analyte (titrand) and
potential of indicator electrode is measured with relation to
reference electrode.
Titrant is added in analyte (Titrand) and change in potential is noted
down.
At the end point there is sharp change in potential on indicator
electrode.
Graph is plotted between the indicator electrode potential and
volume of titrant added.
This method is used for determination of sharp end point.
Types of Potentiometric Titration
1. Acid-base titration 2. Redox Titration 3.Complexometric titration 4. Precipitation Titration
Potentiometry, Electrochemical cell, construction and working of indicator an...Vandana Devesh Sharma
Potentiometry - Electrochemical cell -Construction and working of reference (Standard hydrogen, silver chloride electrode and calomel electrode)
Indicator electrodes (metal electrodes and glass electrode)
Methods to determine end point of potentiometric titration
and applications
Potentiometry is the method to find the concentration of solute in
A given solution by measuring the potential between two Electrodes
(reference and Indicator electrode) . Potentiometric titration involves
the measurement of the potential of the indicator electrode and
reference electrode.
In potentiometric titration reference and indicator electrodes are
immersed in the solution of particular analyte (titrand) and
potential of indicator electrode is measured with relation to
reference electrode.
Titrant is added in analyte (Titrand) and change in potential is noted
down.
At the end point there is sharp change in potential on indicator
electrode.
Graph is plotted between the indicator electrode potential and
volume of titrant added.
This method is used for determination of sharp end point.
Types of Potentiometric Titration
1. Acid-base titration 2. Redox Titration 3.Complexometric titration 4. Precipitation Titration
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2. ACKNOWLEGEMENT
I wish to express my deep gratitude and sincere thanks to
the principal Mrs. Asha kapoor for her encouragement
and for all the facilities that she provided for this project
work.
I extend my hearty thanks to Mrs. Priti Kulshresth, who
guided me to the successful completion of this project. I
take this opportunity to express my deep sense of
gratitude for this invaluable guidance constant
encouragement, immense motivation, which has sustained
my efforts at all stages of this Project work.
I can’t forget to offer my sincere thanks to my parents and
also to my classmates who helped me to carry out this
project successful and for their valuable advice and
support, which I received from then time to time.
SATYAM GIRI
XII-A Signature of Teacher
3. CERTIFICATE
This is to certify that the project entitled, “Electrochemical
Cell” submitted by “Satyam Giri” in partial fulfilment of the
requirements for CBSE in “PCM” at “Shivalik School” is an
authentic work carried out by him under my supervision
and guidance.
To the best of my knowledge, the matter embodied in the
project has not been submitted to any other institute.
Mrs.Priti Kulshresth
P.G.T Chemistry
4. INDEX
S.no Topic
1 INTRODUCTION
2 EXPERIMENTAL SETUP
3 SALT BRIDGE AND ITS FUNCTION
4 STANDARD EMF OF AN
ELECTROCHEMICAL CELL
5 SOME IMPORTANT FEATURES
6 PROCEDURE
7 OBSERVATIONS
8 CONCLUSION
9 BIBLIOGRAPHY
5. INTRODUCTION
Electro Chemical Cell
Whenever a redox reaction is allowed to take place directly
in a single beaker, it is found that the solution becomes
hot. For example, when zinc is placed in a copper solution,
the solution is found to be warmer as the reaction
proceeds according to the equation.
Zn(s) +Cu (aq) ZnSo4 (aq) +Cu(s)
Similar results are observed when a rod of copper is
placed in silver solution. The reaction taking place as
follows:
Cu(s) +2AgNo3+2Ag
Thus, we conclude that whenever a redox takes place
directly in a single in a single beaker, chemical energy in
the form of heat is produced. By suitable means it is
possible to bring out the redox reaction indirectly so as to
convert the chemical energy into the electrical energy.
Representation of an Electrochemical Cell
An electrochemical cell is represented in a manner an
illustrated below.
Zn/Zn2+
||Cu2+
/Cu
I.e. by convention, the electrode on which oxidation takes
place is written on the left-hand side and the other
electrode on which reduction takes place is written on the
6. right-hand side. The electrode of the left-hand side is
written by writing the symbol of the metal first followed by
the symbol of the ion with its concentration in brackets.
The electrode on the right-hand side is written by first
writing the ion along with its concentration in brackets
followed by the symbol of the metal.
Experimental Setup
A zinc rod is placed in the zinc sulphate solution taken in a
beaker. A copper rod is placed in the copper sulphate
solution taken in another beaker. The two rods are
connected by a wire and two solutions are connected by a
salt bridge.
Salt bridge and Its Function
A salt-bridge is a U-shaped tube containing concentrated
solution of an inert electrolyte like KCL, KNO3 , K2SO4 etc.
An inert electrolyte is one whose ions do not take part in
the redox reaction and also do not react with electrolyte
used. The function of the salt bridge is to allow the
movement of the ions from one solution to the other
without mixing of the two solutions. Thus, whereas the
electrons flow in the outer circuit in the wire, the inner
circuit is completed by the flow of ions from one solution to
the other through the salt bridge moreover, it helps to
maintain the electrical neutrality of the solution of the two
half cells.
7. Thus, the main functions of the salt bridge are:
To complete the electrical circuit by allowing the ions
to flow from one solution to the other without mixing of
the two solutions.
To maintain the electrical neutrality of the solutions in
the two half cells.
Let us see what would happen if the salt bridge were not
used in the cells show in the following diagram. Electrons
are given out by the zinc electrode where
they will neutralize some of the Cu2+
ions of the solution.
Thus So4
2-
ions will not leave and the solution will acquire a
negative charge. At the same time, Zn2+
ions produced
from zinc plate will enter ZnSo4 solution. After some time,
the flow of electrons will stop and hence the current stops
flowing.
Standard EMF of an Electrochemical Cell
An electrochemical cell is based on reaction which can be
split into the two half reactions:
Oxidation half reaction
Reduction half reaction
Standard EMF of the cell:
Where,
Ecell = Electrode Potential of the cell
8. Ecathode = Electrode Potential of the oxidation half
reaction
Eanode= Electrode Potential of the oxidation half reaction
According to Nernst Equation, the relation between
concentration of electrode and the standard electrode
potential can be given as:
Ecell = Ecathode - Eanode
E = Eo
– 0.059/n Log [M]/ [Mn+
]
Where,
E= Electrode Potential at non-standard conditions
Eo
=Electrode potential at standard conditions
n= Number of electrons transferred in the equation
[M]=concentration of the metal
[Mn+
]=concentration of metal ion
9. Some Important Features
The electrode at which oxidation takes place is called
the anode. The electrode at which the reduction takes
place is called the cathode.
Since electrons are produced at the zinc electrodes,
this electrode is rich in electrons, which pushes the
electrons into the external circuit and hence it is
designated as the negative pole. The other electrode,
i.e. the copper electrode is in the need of electrons for
the reduction of Cu2+
ions into the Cu.
The electrons flow from the negative pole to the
positive pole in the external circuit. However,
conventionally, this current is set to flow in the
opposite direction.
The oxidation of Zn into ions produces excess of Zn2+
ions in the left beaker. This creates an
unbalanced positive charge in the solution. To
maintain electrical neutrality of the solution in the two
beakers, the cations and anions move through the salt
bridge.
As copper from copper sulphate solution is deposited
on the copper electrode and sulphate ions migrate to
the other side, the concentration of the copper
sulphate solution decreases. As the cell operates
consequently, the current falls.
Evidently, the weight of the copper rod will increase
while that of zinc rod will decrease as the cell works.
10. Procedure
Take two clean beakers.
In one beaker take 0.5M copper sulphate solution and
in the other take 0.5M zinc sulphate solution.
Take a copper strip and clean it using a sandpaper.
Dip the copper strip into the beaker containing the 1M
copper sulphate solution.
Similarly, take a zinc strip and clean it using a
sandpaper.
Then dip into the beaker containing 1M zinc sulphate
solution.
Take a salt bridge and connect the two solutions using
the salt bridge.
Take a voltmeter and connect the copper strip to the
positive terminal and the zinc strip to the negative
terminal using connecting wires.
Note the positive of the pointer in the voltmeter and
record the reading.
Repeat the experiment by taking different
concentration of zinc sulphate and the copper
sulphate solutions.
11. Observations
S.no. MCuSo4 MZnSo4 EMF
1 0.5 0.5 0.98V
2 0.5 0.25 0.81V
3 0.25 0.25 0.90V
Conclusion
With these observations, we conclude that EMF of the cell
increases with decreases in the concentration of the
electrolyte around the anode and the increase in the
concentration of the electrolyte around the cathode.
12. Bibliography
1.Chemistry Part-1, Textbook for class XII
2.http://www.chemistryexplained.com/Di-
Fa/Electrochemistry.html
3.http://en.wikipedia.org/wiki/Daniell_cell
4.http://chemcollective.org/chem/electrochem/step2_cell