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The analytical (total) concentration of a reactant R at the i th titration point is given by = + [] + where R 0 is the initial amount of R in the titration vessel, v 0 is the initial volume, [R] is the concentration of R in the burette and v i is the volume added. The burette concentration of a reactant not present in the burette is taken to be ...
Standard solutions are generally prepared by dissolving a solute of known mass into a solvent to a precise volume, or by diluting a solution of known concentration with more solvent. [1] A standard solution ideally has a high degree of purity and is stable enough that the concentration can be accurately measured after a long shelf time. [2]
Active mass was defined in the 1879 paper as "the amount of substance in the sphere of action". [14] For species in solution active mass is equal to concentration. For solids, active mass is taken as a constant. , a and b were regarded as empirical constants, to be determined by experiment.
Back titration is a titration done in reverse; instead of titrating the original sample, a known excess of standard reagent is added to the solution, and the excess is titrated. A back titration is useful if the endpoint of the reverse titration is easier to identify than the endpoint of the normal titration, as with precipitation reactions
Thermometric iodometric titrations employing thiosulfate as a titrant are also practical, for example in the determination of Cu(II). In this instance, it has been found advantageous to incorporate the potassium iodide reagent with the thiosulfate titrant in such proportions that iodine is released into solution just prior to its reduction by ...
In analytical chemistry, potentiometric titration is a technique similar to direct titration of a redox reaction. It is a useful means of characterizing an acid . No indicator is used; instead the electric potential is measured across the analyte , typically an electrolyte solution.
This method, in practical terms, is non-destructive since only a very small amount of the analyte is consumed at the two-dimensional surface of the working and auxiliary electrodes. In practice, the analyte solution is usually disposed of since it is difficult to separate the analyte from the bulk electrolyte , and the experiment requires a ...
The popularity of the Karl Fischer titration (henceforth referred to as KF) is due in large part to several practical advantages that it holds over other methods of moisture determination, such as accuracy, speed and selectivity. KF is selective for water, because the titration reaction itself consumes water.