Its Is The Process By Which A Iron Nail Is Been Coated With Copper Plate.Electroplating is a process that uses electrical current to reduce dissolved metal cations so that they form a coherent metal coating on an electrode. The term is also used for electrical oxidation of anions onto a solid substrate, as in the formation silver chloride on silver wire to make silver/silver-chloride electrodes. Electroplating is primarily used to change the surface properties of an object (e.g. abrasion and wear resistance, corrosion protection, lubricity, aesthetic qualities, etc.), but may also be used to build up thickness on undersized parts or to form objects by electroforming.
The process used in electroplating is called electrodeposition. It is analogous to a galvanic cell acting in reverse. The part to be plated is the cathode of the circuit. In one technique, the anode is made of the metal to be plated on the part. Both components are immersed in a solution called an electrolyte containing one or more dissolved metal salts as well as other ions that permit the flow of electricity. A power supply supplies a direct current to the anode, oxidizing the metal atoms that comprise it and allowing them to dissolve in the solution. At the cathode, the dissolved metal ions in the electrolyte solution are reduced at the interface between the solution and the cathode, such that they "plate out" onto the cathode. The rate at which the anode is dissolved is equal to the rate at which the cathode is plated, vis-a-vis the current flowing through the circuit. In this manner, the ions in the electrolyte bath are continuously replenished by the anode.[1]
Other electroplating processes may use a non-consumable anode such as lead or carbon. In these techniques, ions of the metal to be plated must be periodically replenished in the bath as they are drawn out of the solution.[2] The most common form of electroplating is used for creating coins such as pennies, which are small zinc plates covered in a layer of copper. [3]Process[edit]
Electroplating of a metal (Me) with copper in a copper sulfate bath
The cations associate with the anions in the solution. These cations are reduced at the cathode to deposit in the metallic, zero valence state. For example, in an acid solution, copper is oxidized at the anode to Cu2+ by losing two electrons. The Cu2+ associates with the anion SO42- in the solution to form copper sulfate. At the cathode, the Cu2+ is reduced to metallic copper by gaining two electrons. The result is the effective transfer of copper from the anode source to a plate covering the cathode.
The plating is most commonly a single metallic element, not an alloy. However, some alloys can be electrodeposited, notably brass and solder.
Its Is The Process By Which A Iron Nail Is Been Coated With Copper Plate.Electroplating is a process that uses electrical current to reduce dissolved metal cations so that they form a coherent metal coating on an electrode. The term is also used for electrical oxidation of anions onto a solid substrate, as in the formation silver chloride on silver wire to make silver/silver-chloride electrodes. Electroplating is primarily used to change the surface properties of an object (e.g. abrasion and wear resistance, corrosion protection, lubricity, aesthetic qualities, etc.), but may also be used to build up thickness on undersized parts or to form objects by electroforming.
The process used in electroplating is called electrodeposition. It is analogous to a galvanic cell acting in reverse. The part to be plated is the cathode of the circuit. In one technique, the anode is made of the metal to be plated on the part. Both components are immersed in a solution called an electrolyte containing one or more dissolved metal salts as well as other ions that permit the flow of electricity. A power supply supplies a direct current to the anode, oxidizing the metal atoms that comprise it and allowing them to dissolve in the solution. At the cathode, the dissolved metal ions in the electrolyte solution are reduced at the interface between the solution and the cathode, such that they "plate out" onto the cathode. The rate at which the anode is dissolved is equal to the rate at which the cathode is plated, vis-a-vis the current flowing through the circuit. In this manner, the ions in the electrolyte bath are continuously replenished by the anode.[1]
Other electroplating processes may use a non-consumable anode such as lead or carbon. In these techniques, ions of the metal to be plated must be periodically replenished in the bath as they are drawn out of the solution.[2] The most common form of electroplating is used for creating coins such as pennies, which are small zinc plates covered in a layer of copper. [3]Process[edit]
Electroplating of a metal (Me) with copper in a copper sulfate bath
The cations associate with the anions in the solution. These cations are reduced at the cathode to deposit in the metallic, zero valence state. For example, in an acid solution, copper is oxidized at the anode to Cu2+ by losing two electrons. The Cu2+ associates with the anion SO42- in the solution to form copper sulfate. At the cathode, the Cu2+ is reduced to metallic copper by gaining two electrons. The result is the effective transfer of copper from the anode source to a plate covering the cathode.
The plating is most commonly a single metallic element, not an alloy. However, some alloys can be electrodeposited, notably brass and solder.
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2. Electrolytic Conduction VS Electrolytic Conduction
Metallic Conduction Electrolytic Conduction
Conduction in Metals Conduction in Electrolyte
Due to Free Electrons Due to Free Ions
Chemical Properties remains intact Chemical properties alter with the decomposition ions
e.g Sodium, Iron, Nickle e.g Sodium Chloride
3. Cont.
• In Electrolytic conduction, Current IS CARRIED OUT BY POSITIVE OR
NEGATIVE IONS. (EITHER IN AQUEOUS OR MOLTEN State
• Ionization is a process when ionic compounds when fused or
dissolved in water splits into its ions.
4. Electrochemical Cells
The devices that are used to drive spontaneous or
non-Spontaneous reaction.
Types :
1. Electrolytic Cells
2. Galvanic Cells
5. 1. Electrolytic Cell:
• Electrolytic Cell: A cell where a battery forces a redox reaction to occur (non-
spontaneous reaction). Opposite of a voltaic cell.
• Uses:
• 1) To obtain group 1 and group 2 metals. Electrolysis of salts, "Salt splitting".
• 2) Electroplating: plating a metal on top of another (Ex. Gold plated jewelry)
6. Parts of electrolytic cells
• Electrolytic cells have only one cell.
• Electrolytic cells are powered by a battery or power source. Converts electrical
to chemical energy.
• Anode - still the site of oxidation. Assigned as the POSITIVE electrode.
• Cathode - still the site of reduction. Assigned as the NEGATIVE electrode.
8. Electrolysis of a Molten Salt:
• Molten salt breaks up into ions in solution
•NaCl(l) → ________________
• Na+ is attracted to negative cathode and is reduced
_______________________
• Cl1- is attracted to the positive anode and is oxidized
________________________
9. Electrolysis of Aqueous Salt:
• Aqueous solutions will always have water (H2O). When aqueous solutions are
electrolysed the products are not always the same as when molten salts are
electrolysed.
• When you electrolyse sodium chloride solution the products at the electrodes
are:
Anode: chlorine
Cathode: hydrogen
• The hydrogen at the cathode comes from water. Water is a weak electrolyte.
Water dissociates/ ionise slightly to give hydrogen ions and hydroxide ions.
H2O (l) ⇌ H+ (aq) + OH– (aq)
11. Electrolysis
• The electrochemical reactions that occurs are the electrodes during electrolytic
conduction constitute the phenomena of electrolysis.
13. Galvanic or Voltoic Cell:
• Galvanic cells (aka voltaic cells) are electrochemical cells in which
spontaneous redox reactions produce a flow of electrons, ie
electricity.
Anode : -ive
Cathode: +ive
14. Components of Galvanic Cell:
• Two half cell
• Voltmeter and Wire
• Salt Bridge
• Functions:
• It Neutralizes both compartment
• Provide Connection
15. Working: Voltaic Cells
• A typical cell looks
like this.
• The oxidation occurs
at the anode.
• The reduction
occurs at the
cathode.
16. Working: Voltaic Cells
Once even one
electron flows from
the anode to the
cathode, the
charges in each
beaker would not be
balanced and the
flow of electrons
would stop.
17. • Therefore, we use a
salt bridge, usually a
U-shaped tube that
contains a salt
solution, to keep the
charges balanced.
➢Cations move toward
the cathode.
➢Anions move toward
the anode.
Working: Voltaic Cells
18. • In the cell, then,
electrons leave the
anode and flow
through the wire to
the cathode.
• As the electrons
leave the anode, the
cations formed
dissolve into the
solution in the
anode compartment.
Working: Voltaic Cells
19. • As the electrons
reach the cathode,
cations in the
cathode are
attracted to the now
negative cathode.
• The electrons are
taken by the cation,
and the neutral
metal is deposited
on the cathode.
Working: Voltaic Cells
20. Electrode Potential:
• The potential setup when an electrode is in contact with one molar
solution of its own ions at 298K is known as standard potential or
standard reduction potential of the elements. It is represented as Eo
21. Electromotive Force (emf)
• The potential difference between the
anode and cathode in a cell is called
the electromotive force (emf).
• It is also called the cell potential, and is
designated Ecell.