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Printed: 30.03.2017 16:01:18 | P3060660
Keywords:
Kohlrausch’s law, equivalent conductivity, temperature dependence o6 conductivity, Ostwald’s dilution law
Overview
Short description
Principle
It is possible to di66erentiate between strong and weak electrolytes by measuring their electrical conduc-tance. Strong
electrolytes 6ollow Kohlrausch’s law, whereas weak electrolytes are described by Ost-wald’s dilution law. The examination o6 the
concentration dependence o6 the conductivity allows the mo-lar conductivities o6 in6initely diluted electrolytes to be determined,
and 6acilitates the calculation o6 the degree o6 dissociation and the dissociation constants o6 weak electrolytes.
Safety instructions
When handling chemicals, you should wear suitable protective gloves, sa6ety goggles, and suitable clothing. Please re6er to the
appendix 6or detailed sa6ety instructions.
Safety instructions
When handling chemicals, you should wear suitable protective gloves, sa6ety goggles, and suitable clothing.
Acetic acid
H226: Flammable liquid and vapour.
H314: Causes severe skin burns and eye damage
P280: Wear protective gloves/protective clothing/eye protection/6ace protection
P305+351+338: IF IN EYES: Rinse cautiously with water 6or several minutes. Remove contact lenses i6 present and easy to do –
continue rinsing.
P310: Immediately call a POISON CENTER/doctor/…
Equipment
Tasks
1. Determine the concentration dependence o6 the electrical conductivity o6 potassium chloride and acetic acid.
2. Calculate the molar conductivity using data 6rom the measurements taken and determine the molar conductivity at in6inite
dilution by extrapolation.
3. Determine the dissociation constant o6 acetic acid.
Setup
Procedure
Procedure: When measuring the conductivity, always begin with the solution having the lowest concentration in each series o6
measurements. Be6ore each new measurement, thoroughly rinse the probe, the glass beaker and the magnetic stirrer bar, 6irst
with distilled water and then with the solution to be subsequently measured.
Determine the conductivity o6 the distilled water that is used 6or the dilution o6 the solutions and note the result. This is to
enable the conductivity o6 the water used to be taken into consideration in the evaluation.
Place a glass beaker containing a magnetic stirrer bar on the magnetic stirrer. Pour the 6irst potassium chloride solution to
be measured into the glass beaker, and immerse the previously well-rinsed conductivity cell to a depth o6 approximately 5
cm in the solution.
Adjust the magnetic stirrer bar to a medium stirring speed (Note: The stirring bar must not touch the measurement cell).
Start the measurement with
whereby in each case the solution with the next higher concentration is measured.
While recording the measuring series, pay strict attention to cleanliness as even the slightest trace o6 contaminants (e.g.
by carrying over some o6 one solution into another) would result in the registration o6 erroneous data.
Stop the measurement by pressing
In “measure” click on
Fig. 4: Settings 6or the conductivity o6 KCl solutions as 6unctions o6 the concentration.
Exchange the x values manually with the given concentration values in the right order.
Save the measurement (File > Save meausrement as…).
Fig. 5 shows the graph as it is now presented by the programme.
Call up the “Measure” programme and boot the experiment “Conductivity o6 strong and weak electrolytes: acetic acid”
(experiment > open experiment). The measurement parameters 6or this experiment are loaded now.
Carry out the measurements and the alterations using the same procedure as above.
Fig. 6 shows the graph as it is presented by the programme.
The substance constant is known as the speci6ic resistance; its reciprocal as the speci6ic conductivity, and the reciprocal o6
the resistance as the conductance . It is usual to use 6or metallic conductors and 6or electrolytes. The conductivity 6or an
electrolytic solution results in the 6ollowing:
I6 the conductivity o6 a solution is to be measured, then the measurements o6 the cell (length an area) must be known.
There6ore, the cell is usually calibrated with a solution with a known conductivity. The ratio o6 the measured to the tabulated
conductivity o6 a calibration solution directly provides the ratio o6 the length to the cross section. This ratio is also known as the
cell constant. Usually it can be 6ound in the accompanying test certi6icate.
As a result o6 the strong concentration dependency, the conductivity is not appropriate 6or comparing electrolytes. For these
purposes it is better to determine the molar conductivity . This is calculated 6rom the speci6ic conductivity and the
concentration (in mol . l-1) o6 the substance in the electrolyte solution:
When the concentration dependence o6 the conductivity in electrolytes is examined, one 6inds that the conductivity basically
increases with the concentration because the number o6 the charge carriers (ions) increases. The plot o6 molar conductivity
versus concentration can be calculated with
by setting the parameters as given in Fig. 7. In this operation you can also substract the conductivity o6 the distilled water. The
two diagrams 6or potassium chloride and acetic acid are shown in Fig. 8.
Fig. 8: Molar conductivities o6 aqueous potassium chloride and acetic acid solutions as 6unctions o6 the concentration.
The molar conductivity approaches a limit with increasing dilution. This is the conductivity at in6inite dilution. Kohlrausch
6ound the 6ollowing con6ormity to natural law 6or the concentration dependency o6 the molar conductivity 6or strong electrolytes:
According to Kohlrausch ‘s law, plotting the molar conductivity o6 KCl against the square root o6 the concentration should result
in a straight line. This line’s intersection with the ordinate is the molar conductiv-ity at in6inite dilution.
Weak electrolytes do not dissociate completely and have a lower conductivity than strong electrolytes. As the concentration
increases, the dissociation equilibrium shi6ts in the direction o6 non-dissociated molecules. The degree o6 dissociation α o6 weak
electrolytes is the quotient o6 the molar conductivity divided by the molar conductivity at in6inite dilution.
Ostwald’s dilution law is valid 6or weak electrolytes. It enables dissociation constants to be calculated:
The limiting value o6 the molar conductivity o6 weak electrolytes at in6inite dilution is 6irst reached at extremely low
concentrations; there6ore, exact measurements in this are no longer possible. Consequently cannot be obtained by
extrapolating -curves 6or weak electrolytes. The 6ollowing equation is derived by trans6orming Ostwald’s law o6
dilution:
From this equation it can be seen that a linear relationship exists between the reciprocal o6 the conductivity and the product o6
the molar conductivity and the concentration o6 weak electrolytes. Furthermore, Ostwald’s law o6 dilution shows that the molar
conductivity at in6inite dilution can be obtained 6rom the line’s point o6 intersection o6 the line with the ordinate over
.
Appendix
Disposal
The diluted solutions o6 potassium chloride and acetic acid can be disposed by rinsing into the drain.
Appendix
Acetic acid
H314: Causes severe P305 + 351 + 338: IF IN EYES: Rinse cautiously with water 6or
skin burns and eye several minutes. Remove contact lenses i6 present and easy to do.
damage. continue rinsing.
Danger