8
TITRATION THEORY
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measured potential can then be used to determine the analytical quantity of interest, generally a
component concentration of the analyte solution. The potential that develops in the electrochemical
cell is the result of the free energy change that would occur if the chemical phenomena were to
proceed until the equilibrium condition has been satisfied.
There are many types of titrations where potentiometry can be used,e.g., pH electrodes for acid-base
titrations, platinum ORP electrodes in redox titrations, ion selective electrodes, such as chloride or
fluoride for a specific ion titration, and silver electrodes for argentometric (silver-based) titrations.
An example of potetiometric titrations are shown below. Figure 2 “A” is the pH of a solution vs.
the volume of titrant and “B” is the potential from a chloride electrode vs. the volume of AgNO
3
.
2.1.3 Spectrophotometric Titrations
The name comes from the method used to detect the endpoint of the titration, not its
chemistry. Highly colored indicators that change color during the course of the titration are
available for many titrations. More accurate data on the titration curve can be obtained if the
light absorption is monitored instrumentally using a light source, a simple monochromator
and a photodetector, rather than visually determining the color or light absorption change.
Light absorption by either an indicator or by one of the reactants or products can be used to
monitor the titration.
In the first titration curve, Figure 3 “A”, the absorption of a metal-indicator complex is being
monitored. The absorption is constant while the metal is complexed by the EDTA titrant. The
metal indicator complex was stripped, causing a sharp break in the titration curve. The point
where all the metal is complexed and stripped from the indicator is the equivalence point. This point
is marked by “e.p.” on the graph.
In the second titration curve, Figure 3 “B”, the metal complex is being measured while being
titrated with EDTA. The new complex being formed is not colored and does not absorb light.
The extrapolated intersection of the two lines determines the equivalence point.
Figure 2
A
B
Summary of Contents for HI 902 Color
Page 6: ...6 QUICK START GUIDE TITRATOR CONNECTIONS Front View Rear View sale ponpe com www ponpe com ...
Page 18: ...18 QUICK START GUIDE QS 902C 10 10 sale ponpe com www ponpe com ...
Page 22: ...1 2 INTRODUCTION sale ponpe com www ponpe com ...
Page 24: ...1 2 INTRODUCTION sale ponpe com www ponpe com ...
Page 26: ...2 2 SETUP sale ponpe com www ponpe com ...
Page 36: ...3 2 USER INTERFACE sale ponpe com www ponpe com ...
Page 44: ...4 2 GENERAL OPTIONS sale ponpe com www ponpe com ...
Page 100: ...5 44 METHODS sale ponpe com www ponpe com ...
Page 102: ...6 2 TITRATION MODE sale ponpe com www ponpe com ...
Page 106: ...6 6 TITRATION MODE sale ponpe com www ponpe com ...
Page 138: ...8 2 AUXILIARY FUNCTIONS sale ponpe com www ponpe com ...
Page 148: ...9 2 MAINTENANCE PERIPHERALS sale ponpe com www ponpe com ...
Page 160: ...A1 2 APPENDIX 1 sale ponpe com www ponpe com ...
Page 164: ...A2 2 APPENDIX 2 sale ponpe com www ponpe com ...
Page 170: ...A3 2 APPENDIX 3 sale ponpe com www ponpe com ...
Page 174: ...A3 6 APPENDIX 3 sale ponpe com www ponpe com ...
Page 176: ...A4 2 APPENDIX 4 sale ponpe com www ponpe com ...
Page 184: ...A5 2 APPENDIX 5 sale ponpe com www ponpe com ...
Page 193: ...A5 11 APPENDIX 5 ...
Page 194: ...A5 12 APPENDIX 5 MAN902C 10 10 ...
Page 196: ...1 2 INTRODUCTION ...
Page 224: ...2 TITRATION THEORY sale ponpe com www ponpe com ...
Page 248: ...26 TITRATION THEORY Titr THEORY 901 902 04 10 ...