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  1. Potentiometry
    to determine the concentration of analyte, we measure potential differences, with little or no current passed
  2. Electrolysis
    to determine the concentration of analyte, we measure current differences, by applying a potential, to drive a redox reaction.
  3. What can you do with electrolysis-based techniques?
    • -- Determine concentration of analytes
    • -- Identify analytes
    • -- Characterize redox behavior of analytes (how much voltage does it take to drive the reaction)
    • -- Sweep generators, potentiostats, cells, and data acquistion/computers make up most systems
  4. Over potential
    the voltage needed to overcome the activation energy for a redox reaction to occur at the electrode. If you want the reaction to go fast (i.e. high current), then you apply high voltages.
  5. Ohmic potential
    the voltage needed to overcome the resistance of the solution (high resistance solutions do provide easy migration of the ions). Ohm’s Law: E = IR.
  6. Concentration polarization
    the concentration of ions at the surface of the electrode are less than they are in bulk solution.
  7. Overpotential
    the difference between the equilibrium potential and the actual potential
  8. Sources of polarization in cells
    • – Charge-transfer (kinetic) polarization:magnitude of current is limited by the rate of the electrode reaction(s) (the rate of electron transfer between the reactants and the electrodes)
    • – Concentration polarization: rate of material transport to electrode isinsufficient to maintain current
    • – Other effects (e.g. adsorption/desorption)
  9. Some electrochemical cells have significant currents
    • – Electricity within a cell is carried by moving ions – When small currents are involved, E = IR holds
    • – R depends on the nature of the solution
  10. When current in a cell is large, the actualpotential usually differs from that calculatedat equilibrium using the Nernst equation
  11. Coulometry
    measuring the flow of charge
  12. Electroanalytical techniques are categorized by:
    • • the excitation waveform:
    • – Variation in Applied Potential (E)• Step, repeat step, etc.
    • • Ramp (one way or cycled), etc
    • .– Variation in Applied Current (I)
    • • the response waveform
    • – (usually in this chapt, I vers. E) Voltammetry
  13. Potential Step Methods: apply voltage, then measure current or charge, before & after voltage is applied
    • Chronoamperometry (CA)
    • – Response:i (current) vs. t =time
    • Chronocoulometry (CC)
    • – Response:Q (accumulated charge) vs. t =time
    • All in unstirred solution.

  14. Chronoamperometry (CA)
    Before excitation, there is no current. After the excitation, the current starts high, And becomes smaller as material near the electrode gets used up.
  15. Chronocoulometry (CC)
    To determine the charge, we integrate the current
  16. Why would you use chronoamperometry or chronocoulometry????
    • Determination of:
    • – n (# of electrons)
    • – A (surface area of electrode)
    • – Do (diffusion coefficient of analyte)
    • Kinetics/reaction mechanism
    • Double potential step
    • – Generate species, their probe fate
  17. Amperometry
    A current proportional to the analyte concentration is monitored, usually at a fixed potential.
  18. Voltammetry
    A current proportional to the analyte concentration is monitored, at a variable, controlled potential.
  19. DC Polarography
    measures current flowing through the dropping mercury electrode (DME) as a function ofapplied potential
  20. Linear Sweep Voltammetry
    performed by applying a linear potential ramp in the same manner as DCP

    potential scan rate is usually much faster than with DCP (direct current polarography)

    LSV asymmetric peak-shaped I-E curve
  21. Applications of Linear Sweep Voltammetry
    • Determination of:
    • – n,A, Do, co
    • Energy of reactioins
    • Study of kinetics
    • Study of adsorption
    • Characterization of new materials
  22. Cyclic Voltammetry
    potential scans run from the starting potential to the end potential, then reverse from the end potential back to the starting potential
  23. Hydrodynamic Voltammetry
    Hydrodynamic voltammetry is performed with rapid stirring in a cell
  24. Light Interacts with Matter
  25. Isosbestic Point
    a set of absorption spectra for a set of solutions, plotted on the same chart, in which the sum of the concentrations of two principal absoring components, A and B, is constant
  26. The Scatchard Plot

Card Set Information

2011-04-27 20:52:02

Quant Analysis
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