Faraday's laws of electrolysis

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Michael Faraday

Faraday's laws of electrolysis are quantitative relationships based on the electrochemical research published by Michael Faraday in 1833.[1][2][3]

First law

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Michael Faraday reported that the mass (m) of a substance deposited or liberated at an electrode is directly proportional to the charge (Q, for which the SI unit is the ampere-second or coulomb).[3] mQmQ=Z

Here, the constant of proportionality, Z, is called the electro-chemical equivalent (ECE) of the substance. Thus, the ECE can be defined as the mass of the substance deposited or liberated per unit charge.

Second law

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Faraday discovered that when the same amount of electric current is passed through different electrolytes connected in series, the masses of the substances deposited or liberated at the electrodes are directly proportional to their respective chemical equivalent/equivalent weight (E).[3] This turns out to be the molar mass (M) divided by the valence (v)

mE;E=molar massvalence=Mvm1:m2:m3:=E1:E2:E3:Z1Q:Z2Q:Z3Q:=E1:E2:E3:Z1:Z2:Z3:=E1:E2:E3:

The modern form of the second law is F=Ne where F is the Faraday constant, N is Avogadro's number and e is the elementary charge. This form requires an understanding of chemical valence unavailable in Faraday's time.[4]: 72 

Derivation

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A monovalent ion requires one electron for discharge, a divalent ion requires two electrons for discharge and so on. Thus, if x electrons flow, xv atoms are discharged.

Thus, the mass m discharged is m=xMvNA=QMeNAv=QMvF where

Mathematical form

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Faraday's laws can be summarized by

Z=mQ=1F(Mv)=EF

where M is the molar mass of the substance (usually given in SI units of grams per mole) and v is the valency of the ions .

For Faraday's first law, M, F, v are constants; thus, the larger the value of Q, the larger m will be.

For Faraday's second law, Q, F, v are constants; thus, the larger the value of Mv (equivalent weight), the larger m will be.

In the simple case of constant-current electrolysis, Q = It, leading to

m=ItMFv

and then to

n=ItFv

where:

  • n is the amount of substance ("number of moles") liberated: n=mM
  • t is the total time the constant current was applied.

For the case of an alloy whose constituents have different valencies, we have m=ItF×iwiviMi where wi represents the mass fraction of the ith element.

In the more complicated case of a variable electric current, the total charge Q is the electric current I(τ) integrated over time τ:

Q=0tI(τ)dτ

Here t is the total electrolysis time.[5]

Applications

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See also

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References

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  1. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  2. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  3. ^ a b c Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  4. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  5. ^ For a similar treatment, see Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).

Further reading

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