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Electrochemical Measurement Systems: Difference between revisions

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Indirect vs Direct Ion-Selective Electrodes (ISEs)
Indirect vs Direct Ion-Selective Electrodes (ISEs)


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{| class="wikitable"
|+
!
!Indirect ISE
!Direct ISE
|-
|Principle
|
* Sample is diluted (generally between 1:16 to 1:34) before the ion concentration is measured
|
* Sample is directly measured without a dilution step
|-
|Benefits
|
|
|-
|Limitations
|
|
|}

Revision as of 21:01, 20 September 2025

Types of Electrodes

  • Glass Electrodes
    • H+, Na+, K+, Li+, Ag+ NH4+
  • pH Combination Electrodes
  • Solid State Electrodes
    • Cl-
  • Liquid Ion-Exchange
    • K+ (valinomycin binds K+ in centre ring)
    • Ca2+ (organo-phosphate salt in PVC)
  • Compound Gas Electrodes
    • pCO2 (Severinghaus CO2 electrode)
      • CO2 diffuses past first membrane and alters pH of internal bicarbonate buffer → lowers pH
    • pO2 (Clark electrode)
      • o2 reduced at platinum cathode, releasing electrons
  • Enzyme Electrodes
    • Non-ionic compounds
    • Glucose, urea, etc.
    • Measure ions generated from enzymatic reactions

Indirect vs Direct Ion-Selective Electrodes (ISEs)

test2

Indirect ISE Direct ISE
Principle
  • Sample is diluted (generally between 1:16 to 1:34) before the ion concentration is measured
  • Sample is directly measured without a dilution step
Benefits
Limitations