Saturated calomel electrode

Last updated September 18, 2023

The saturated calomel electrode (SCE) is a reference electrode based on the reaction between elemental mercury and mercury(I) chloride. It has been widely replaced by the silver chloride electrode, however the calomel electrode has a reputation of being more robust. The aqueous phase in contact with the mercury and the mercury(I) chloride (Hg₂Cl₂, "calomel") is a saturated solution of potassium chloride in water. The electrode is normally linked via a porous frit to the solution in which the other electrode is immersed. This porous frit is a salt bridge.

Theory of electrolysis

Solubility product

The electrode is based on the redox reactions

{\ce {Hg2^2+ + 2e^- <=> 2Hg(l)}},\qquad {\ce {with}}\quad E_{{\ce {Hg2^2+/Hg}}}^{0}=+0.80\ {\ce {V}}

{\ce {Hg2Cl2 + 2e^- <=> 2Hg(l) + 2Cl^-}},\qquad {\ce {with}}\quad E_{{\ce {Hg2Cl2/Hg, Cl-}}}^{0}=+0.27\ {\ce {V}}

The half reactions can be balanced to the following reaction

{\ce {Hg2^2+ + 2Cl^- + 2Hg(l) <=> Hg2Cl2(s) + 2Hg(l)}},\qquad {\ce {with}}\quad E_{{\ce {Hg2Cl2/Hg2^2+, Cl-}}}^{0}=+0.53\ {\ce {V}}

.

Which can be simplified to the precipitation reaction, with the equilibrium constant of the solubility product.

{\ce {Hg2^2+ + 2Cl^- <=> Hg2Cl2(s)}},\qquad K_{sp}=a_{{\ce {Hg2^2+}}}a_{{\ce {Cl-}}}^{2}=[{\ce {Hg2^2+}}]\cdot [{\ce {Cl-}}]^{2}

The Nernst equations for these half reactions are:

{\begin{cases}E_{{\frac {1}{2}}{\ce {cathode}}}&=E_{{\ce {Hg_2^2+/Hg}}}^{0}-{\frac {RT}{2F}}\ln {\frac {1}{a_{{\ce {Hg2^2+}}}}}\qquad &{\text{in which}}\quad E_{{\ce {Hg2^2+/Hg}}}^{0}=+0.80\ {\ce {V}}.\\E_{{\frac {1}{2}}{\ce {anode}}}&=E_{{\ce {Hg2Cl2/Hg,Cl-}}}^{0}-{\frac {RT}{2F}}\ln a_{{\ce {Cl-}}}^{2}\qquad &{\text{in which}}\quad E_{{\ce {Hg2Cl2/Hg, Cl-}}}^{0}=+0.27\ {\ce {V}}.\\\end{cases}}

The Nernst equation for the balanced reaction is:

{\begin{aligned}E_{{\ce {cell}}}&=E_{{\frac {1}{2}}{\ce {cathode}}}-E_{{\frac {1}{2}}{\ce {anode}}}\\&=E_{{\ce {Hg2Cl2/Hg2^2+, Cl-}}}^{0}-{\frac {RT}{2F}}\ln {\frac {1}{{\ce {[Hg2^2+]}}\cdot {\ce {[Cl^-]}}^{2}}}\\&=E_{{\ce {Hg2Cl2/Hg2^2+, Cl-}}}^{0}-{\frac {RT}{2F}}\ln {\frac {1}{K_{sp}}}\qquad {\text{in which}}\quad E_{{\ce {Hg2Cl2/Hg2^2+, Cl-}}}^{0}=+0.53\ {\ce {V}}\end{aligned}}

where E⁰ is the standard electrode potential for the reaction and a_Hg is the activity for the mercury cation.

At equilibrium,

\Delta G=-nFE=0\mathrm {J/mol}

, or equivalently

E_{\text{cell}}=0\ \mathrm {V}

.

This equality allows us to find the solubility product.

E_{\text{cell}}=E_{{\ce {Hg2Cl2/Hg2^2+, Cl-}}}^{0}-{\frac {RT}{2F}}\ln {\frac {1}{{\ce {[Hg2^2+]}}\cdot {\ce {[Cl^-]}}^{2}}}=+0.53+{\frac {RT}{2F}}\ln {K_{sp}}=0\ {\ce {V}}

{\begin{aligned}\ln {K_{sp}}&=-0.53\cdot {\frac {2F}{RT}}\\K_{sp}&=e^{-0.53\cdot {\frac {2F}{RT}}}\\&=[{\ce {Hg2^2+}}]\cdot [{\ce {Cl-}}]^{2}=1.184\times 10^{-18}\end{aligned}}

Due to the high concentration of chloride ions, the concentration of mercury ions ( ${\ce {[Hg2^2+]}}$ ) is low. This reduces risk of mercury poisoning for users and other mercury problems.

SCE potential

{\ce {Hg2Cl2 + 2e- <=> 2Hg(l) + 2Cl^-}},\qquad {\ce {with}}\quad E_{{\ce {Hg2Cl2/Hg, Cl-}}}^{0}=+0.27\ {\ce {V}}

{\begin{aligned}E_{{\frac {1}{2}}{\ce {SCE}}}&=E_{{\ce {Hg2Cl2/Hg,Cl-}}}^{0}-{\frac {RT}{2F}}\ln a_{{\ce {Cl-}}}^{2}\\&=+0.27-{\frac {RT}{F}}\ln[{\ce {Cl-}}].\end{aligned}}

The only variable in this equation is the activity (or concentration) of the chloride anion. But since the inner solution is saturated with potassium chloride, this activity is fixed by the solubility of potassium chloride, which is: $.mw-parser-output .sfrac{white-space:nowrap}.mw-parser-output .sfrac.tion,.mw-parser-output .sfrac .tion{display:inline-block;vertical-align:-0.5em;font-size:85%;text-align:center}.mw-parser-output .sfrac .num,.mw-parser-output .sfrac .den{display:block;line-height:1em;margin:0 0.1em}.mw-parser-output .sfrac .den{border-top:1px solid}.mw-parser-output .sr-only{border:0;clip:rect(0,0,0,0);height:1px;margin:-1px;overflow:hidden;padding:0;position:absolute;width:1px}342 g/L/74.5513 g/mol = 4.587 M @ 20 °C$ . This gives the SCE a potential of +0.248 V vs. SHE at 20 °C and +0.244 V vs. SHE at 25 °C,^[1] but slightly higher when the chloride solution is less than saturated. For example, a 3.5M KCl electrolyte solution has an increased reference potential of +0.250 V vs. SHE at 25°C while a 1 M solution has a +0.283 V potential at the same temperature.

Application

The SCE is used in pH measurement, cyclic voltammetry and general aqueous electrochemistry.

This electrode and the silver/silver chloride reference electrode work in the same way. In both electrodes, the activity of the metal ion is fixed by the solubility of the metal salt.

The calomel electrode contains mercury, which poses much greater health hazards than the silver metal used in the Ag/AgCl electrode.

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References

↑ Sawyer, Donald T.; Sobkowiak, Andrzej; Roberts, Julian L. (1995). Electrochemistry for Chemists (2nd ed.). Wiley. p. 192. ISBN 978-0-471-59468-0.

Banus MG (June 1941). "A Design for a Saturated Calomel Electrode". Science. 93 (2425): 601–602. doi:10.1126/science.93.2425.601-a. PMID 17795970. S2CID 39905013.

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[1] Sawyer, Donald T.; Sobkowiak, Andrzej; Roberts, Julian L. (1995). Electrochemistry for Chemists (2nd ed.). Wiley. p. 192. ISBN 978-0-471-59468-0.

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