Proton Concentration Cell: Finding Original pH with Initial EMF

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Discussion Overview

The discussion revolves around the operation of a proton concentration cell, specifically how to determine the original pH from the initial electromotive force (EMF) reading. Participants explore the implications of redox reactions, the role of the voltmeter, and the effects of current flow on concentration changes in the solutions involved.

Discussion Character

  • Technical explanation
  • Debate/contested
  • Mathematical reasoning

Main Points Raised

  • Some participants assert that the wire does not allow redox reactions to occur unless a closed circuit is established, which is necessary for electron transfer and concentration changes.
  • Others question how the EMF can remain stable if the concentration of H+ ions is altered during the redox process, suggesting that reaching equilibrium would render concentration measurements ineffective.
  • There is a discussion about the time it takes for equilibrium to be reached and how this affects the EMF reading, with some noting that the EMF does not drop to zero instantly.
  • One participant challenges the statement that "Fast electrode kinetics is desirable," arguing that the method for measuring concentrations may be destructive as it alters the concentrations being measured.
  • Another participant emphasizes that the reaction speed does not guarantee that it will occur quickly enough to maintain accurate EMF readings, suggesting that the current drawn by the voltmeter affects the charge buildup and thus the measured EMF.
  • It is noted that the EMF measured is not the true cell potential but rather a steady state potential under load, influenced by the resistance of the voltmeter and the kinetics of the reaction.

Areas of Agreement / Disagreement

Participants express differing views on the desirability of fast electrode kinetics and the implications of current flow on concentration measurements. The discussion remains unresolved with multiple competing perspectives on these points.

Contextual Notes

Participants highlight the dependence of the discussion on the specific context of the measurements and the assumptions regarding the voltmeter's operation and the kinetics of the reactions involved.

OmniReader
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Proton concentration cell is made by connecting with Pt wire two acid-base solutions and measuring emf. but wire allows redox reaction, changing conc of H+ in each solution. how is original pH found- with initial emf reading?
 
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Wire doesn't "allow redox reaction". For the reaction to take place you need a closed circuit. Then, speed of the reaction (and concentration changes) depend on the charge that flowed through the circuit. Controlling the charge you can control changes in the concentration.
 
ok, closed circuit allows transfer of electrons between the solutions so redox reaction occurs. this changes conc of species, so how does emf not change down to 0. as, won't it disturb emf reading, if you control or interfere the natural redox flow of electrons? but if you don't redox equilibrium will reached then conc measurement was pointless...
 
If you allow the current to flow long enough, you will reach equilibrium, and the EMF will go down to zero. But it is not something that happens instantly.

To measure EMF you use voltmeter - do you know how it works?
 
Borek said:
If you allow the current to flow long enough, you will reach equilibrium, and the EMF will go down to zero. But it is not something that happens instantly.

To measure EMF you use voltmeter - do you know how it works?

so statement "Fast electrode kinetics is desirable" is incorrect, we desire to see the initial emf. also isn't this destructive, we our method for reading concentrations is changing them...

I think I have grasped voltmeter concept from my book.
 
OmniReader said:
so statement "Fast electrode kinetics is desirable" is incorrect

Depends on the context. But generally speaking it is perfectly correct.

You are still missing the point. Just because the reaction CAN run fast, doesn't mean it WILL.

If you know how the voltmeter works, think what kind of currents flow through the voltmeter. Try to estimate concentration changes related to the current flowing through the voltmeter. How long will it take for the concentration change - and EMF drop - to be noticeable?
 
Borek said:
Depends on the context. But generally speaking it is perfectly correct.

You are still missing the point. Just because the reaction CAN run fast, doesn't mean it WILL.

If you know how the voltmeter works, think what kind of currents flow through the voltmeter. Try to estimate concentration changes related to the current flowing through the voltmeter. How long will it take for the concentration change - and EMF drop - to be noticeable?

Currents very tiny, so would take long for equilibrium to be reached. but still why fast electrode kinetics are desirable then?
 
Reaction creates charge on the electrodes. This charge is a source of potential difference. If the reaction is not fast enough to create enough charge in time (and while voltmeter draws a very tiny current, it still draws one, so the charge slowly disappears) the measured EMF will be lower than the real one (which should be measured using ideal voltmeter of infinite resistance - but such a device doesn't exist).

Technically what we measure is not the cell potential, but kind of a steady state potential of the cell under load. The higher the resistance the lower the load, the faster the reaction, the faster the charge buildup - the better the result.
 

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