explain the law of electrolysis and ionic theory
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Faraday's First Law of Electrolysis
From the brief explanation above, it is clear that the flow of current through the external battery circuit fully depends upon how many electrons get transferred from negative electrode or cathode to positive metallic ion or cations. If the cations have valency of two like Cu++ then for every cation, there would be two electrons transferred from cathode to cation. We know that every electron has negative electrical charge - 1.602 × 10 -19 Coulombs and say it is - e. So for disposition of every Cu atom on the cathode, there would be - 2.e charge transfers from cathode to cation.
Now say for t time there would be total n number of copper atoms deposited on the cathode, so total charge transferred, would be - 2.n.e Coulombs. Mass m of the deposited copper is obviously a function of the number of atoms deposited. So, it can be concluded that the mass of the deposited copper is directly proportional to the quantity of electrical charge that passes through the electrolyte. Hence mass of deposited copper m ∝ Q quantity of electrical charge passes through the electrolyte.
Faraday's First Law of Electrolysis states that only, According to this law, the chemical deposition due to flow of current through an electrolyte is directly proportional to the quantity of electricity (coulombs) passed through it. i.e. mass of chemical deposition, Where, Z is a constant of proportionality and is known as electro-chemical equivalent of the substance. If we put Q = 1 coulombs in the above equation, we will get Z = m which implies that electrochemical equivalent of any substance is the amount of the substance deposited on the passing of 1 coulomb through its solution. This constant of the passing of electrochemical equivalent is generally expressed in terms of milligrams per coulomb or kilogram per coulomb.
Faraday's Second Law of Electrolysis
So far we have learned that the mass of the chemical, deposited due to electrolysis is proportional to the quantity of electricity that passes through the electrolyte. The mass of the chemical, deposited due to electrolysis is not only proportional to the quantity of electricity passes through the electrolyte, but it also depends upon some other factor. Every substance will have its own atomic weight. So for the same number of atoms, different substances will have different masses. Again, how many atoms deposited on the electrodes also depends upon their number of valency. If valency is more, then for the same amount of electricity, the number of deposited atoms will be less whereas if valency is less, then for the same quantity of electricity, more number of atoms to be deposited. So, for the same quantity of electricity or charge passes through different electrolytes, the mass of deposited chemical is directly proportional to its atomic weight and inversely proportional to its valency. Faraday's second law of electrolysis states that, when the same quantity of electricity is passed through several electrolytes, the mass of the substances deposited are proportional to their respective chemical equivalent or equivalent weight.
Chemical Equivalent or Equivalent Weight
The chemical equivalent or equivalent weight of a substance can be determined by Faraday’s laws of electrolysis, and it is defined as the weight of that subtenancy which will combine with or displace the unit weight of hydrogen. The chemical equivalent of hydrogen is, thus, unity. Since valency of a substance is equal to the number of hydrogen atoms, which it can replace or with which it can combine, the chemical equivalent of a substance, therefore may be defined as the ratio of its atomic weight to its valency.
Arrhenius theory, theory, introduced in 1887 by the Swedish scientist Svante Arrhenius, that acids are substances that dissociate in water to yield electrically charged atoms or molecules, called ions, one of which is a hydrogen ion (H+), and that bases ionize in water to yield hydroxide ions (OH−). It is now known that the hydrogen ion cannot exist alone in water solution; rather, it exists in a combined state with a water molecule, as the hydronium ion (H3O+). In practice the hydronium ion is still customarily referred to as the hydrogen ion.
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