Lab 2
Lab 2
Kevin Brew
04/20/08
Experiment 2: Partial Molal Volume
Abstract
aqueous sodium chloride were recorded with a density meter so that the partial molal
volumes, and ultimately, the partial molal volumes at infinite dilution, could be
calculated. For potassium chloride and sodium chloride, the partial molal volumes at
infinite dilution of the salts were calculated to be 25.18 mL/mol and 15.19 mL/mol,
respectively. These differ from literature values by 6.23% and 26.85%, respectively.
Error sources include inadequate mixing of the solutions, evaporation and the small range
of the solutions.
Introduction:
Amagat’s law states that volumes are approximately additive. However, this does
not apply to solutions whose concentrations are to be known to a high degree of accuracy.
water to a measured amount of salt and obtaining the weight of water by difference. In
1770 Millero reported that volume decreases when salts are added to a specific volume of
water. This effect was explained as electrostriction: the volume contracts due to
interaction of the polar solvent around the ions. However, this phenomenon occurs in
explains this deviation from ideal behavior through partial molal quantities. The most
(2)
(3)
The partial molal volume considers the change in molal volume with the increase in
moles of material:
Since partial molal volumes are functions of concentration but not the total number of
where V is total volume. Taking component 1 to be water and component 2 to be the salt,
the volume of solution can be determined with static amounts of solvent (water) and
varying amounts of salt. Since molality is the concentration of solute per kg of solvent, it
is intuitive to take the amount of water fixed at 1000 g. With the molality of the solution
and the molecular weight of the salt used and the measured density of the solution, the
power series, yielding a fit equation whose derivative with respect to molality yields the
expressed as:
Since both partial molal volumes are functions of concentration, they can be expressed at
infinite dilution for a single value. At infinite dilution for the partial molal volume of
water, the effects of solvated ions on the solvent are null. The partial molal volume of salt
at infinite dilution reflects the effects of electrostriction on water due to the solvated ions.
The values of partial molal volumes at infinite dilution depend on the equation used to fit
the data and how well is extrapolates to m = 0. Thus, it is imperative that density be
Procedure:
Five solutions of KCl with varying molalities between 0.05 m and 2.00 m were
prepared by weighing salt by difference in a jar with lid. 20 mL of distilled water was
added to the jar and the mass was recorded. This was used to calculate the molality of the
solution. The DMA 4500 was turned on and its temperature was adjusted to 25.00°.
Distilled Water was injected and then the air line was reconnected and the pump was
turned on. The density was then taken. Once the density read that of air (between 0.0011-
0.0014 g/mL), a syringe of distilled water was put into the injection port and distilled
water was injected. The density for water was recorded at least 3 times for different
portions until consistency (within 0.0001g/mL). Then the syringe was rinsed twice with
small portions of the KCl solution and was then filled with the solution. The solution was
injected partially and density was recorded. This was repeated until 3 consistent values of
density were reported for the solution, again using different portions. The syringe was
rinsed with another solution of KCl and the density was measured as before. This was
repeated for the remaining KCl solutions. Then the entire procedure was repeated using
Weights, molalities, and densities for water, sodium chloride and potassium
chloride were recorded in Table 1. It must be noted that instead of using 0.5 to 2.0 molal
solutions as the procedure indicated, 0.01 to 0.5 molal solutions for sodium chloride and
0.06 to 0.5 molal solutions for potassium chloride were used. With the data obtained,
Figure 1, which shows the relationship between density and molality for each salt, was
produced. The graphs indicate a quadratic relationship between density and molality; as
molality increases, density increases as well. R-squared values of 0.99872 for sodium
chloride and 0.99346 for potassium chloride indicate that the data obtained is precise.
molal volume of water, V1, the partial molal volume of the salts, V2, and the apparent
partial molal volume, φ. The volume as a function of molality was calculated using
equation 6, the partial molal volume of water using equation 8, the partial molal volume
of the salts using equation 7 and the apparent molal volume using equation 11. It is to be
noted that the partial molal volume of water is somewhat constant across different
molalities but the partial molal volume of the salts decreases greatly with increasing
molality.
Figure 2 represents the relationship between the partial molal volume of the salt
and molality; both graphs show a quadratic relationship. As molality increases, partial
molal volume of the salt increases as well. R-squared values for figure 2 are not as high
Table 3 is a summary of the values for an infinite dilution using three different
methods of calculation. By taking the derivative of the fit equation for volume versus
molality in the form V = A + B*m+C*m2. An expression for the partial molal volume is
molality approaching 0. This results in the infinite dilution of V2 being equal to the fit
again, but use the fit equation obtained in figure 3. A third method is to do the same but
use figure 4. This data shows that method 2 is the most reliable with only a 8.6%
deviation from the literature value for NaCl and a 6.2% deviation for KCl.
In figure 3, φ is plotted against m1/2 for both salts. It was found that there is a
linear relationship between φ and m1/2 for NaCl but a quadratic relationship for KCl. This
could be due to the small range of molalities used. The values for R-squared are not as
desirable as those in previous graphs, values of 0.5847 for NaCl and 0.96381 for KCl
were acquired. The quadratic relationship for KCl, although more accurate, does not fit
If the salt solutions followed the Debye-Huckel theory, the equation for φ{m} would
provide a single slope of 1.868 for all 1,1-electrolites at 25ºC. This slope changes
depending on charge and temperature. The relationship between φ-1.86m1/2 and m1/2 is
shown in figure 4. φº is the intercept at m=0. The value φº for NaCl was found to be
14.24 and 25.18 for KCl. This means a deviation from the literature value of 14.3% and
6.2% respectively. The graph for NaCl is linear whereas KCl is quadratic. Once again,
Table 4 presents information on the differences between the partial molal values of KCl
and NaCl, and between KBr and NaBr at an infinite solution. It is noted that the
difference between the partial molal volumes and the apparent molal volumes of KCl and
NaCl decreases with decreasing molality. We determined that since both KCl and KBr,
and NaCl and KBr are 1,1 electrolytes the difference between them would be equal. The
literature indicates a difference of 6.9 between the partial molal volumes of ions of Cl and
Br. The reason for the disparity between the literature value and the experimental values
1.010
Data: Data1_B
Model: Parabola
Equation: y = A + B*x + C*x^2
Weighting:
1.005 y No weighting
Chi^2/DoF = 7.3015E-8
R^2 = 0.99872
0.995
0.0 0.1 0.2 0.3 0.4 0.5 0.6
Molality (mol NaCl/kg H2O)
1.020
1.015
KCl Data
Polynomial Fit
Density (g/mL)
1.010
Data: Data1_D
Model: Parabola
Equation: y = A + B*x + C*x^2
1.005 Weighting:
y No weighting
Chi^2/DoF = 5.9627E-7
R^2 = 0.99346
1.000
A 0.99619 ±0.00028
B 0.05073 ±0.00314
C -0.00683 ±0.00612
0.995
1014
1012
NaCl Data
1010
Polynomial Fit
1008
Volume (mL)
996
KCl Data
1015 Polynomial Fit
1010
Volume (mL)
Data: Data1_D
Model: Parabola
1005 Equation: y = A + B*x + C*x^2
Weighting:
y No weighting
Chi^2/DoF = 5.07679
1000 R^2 = 0.91877
A 998.41765 ±0.82639
B 64.29841 ±9.15573
C -55.60144 ±17.87097
995
1/2
φ versus Molality for NaCl
Data: Data1_B
Model: Line
20 Equation: y = A + B*x
Weighting:
y No weighting
Chi^2/DoF = 0.25021
R^2 = 0.58474
φ (ml/mol)
A 15.19251 ±0.59586
B 4.71179 ±1.14624
18
Data
Linear Fit
16
0.3 0.4 0.5 0.6 0.7 0.8
1/2 1/2
Molality (mol/kg)
1/2
φ versus Molality for KCl
28.6
28.4 Data
Quadratic Fit
28.2
28.0
Model: Parabola
Equation: y = A + B*x + C*x^2
27.6 Weighting:
y No weighting
26.8
0.35 0.40 0.45 0.50 0.55 0.60 0.65 0.70 0.75
1/2 1/2
Molality (mol/kg)
Figure 4: φ-1.86m1/2 vs m1/2 for NaCl and KCl Solutions
Data
Linear Fit
18
1/2
φ – 1.86m
Data: Data1_B
Model: Line
17 Equation: y = A + B*x
Weighting:
y No weighting
Chi^2/DoF = 0.3561
R^2 = 0.58821
16 A 14.23929 ±0.60596
B 5.00133 ±1.08048
1/2
φ – 1.86m1/2 vs. m for KCl
27.2
27.0 Data
Quadratic Fit
26.8
1/2
Data: Data1_D
φ – 1.86m
Model: Parabola
Equation: y = A + B*x + C*x^2
Weighting:
26.6
y No weighting
Chi^2/DoF = 0.01126
R^2 = 0.87445
26.4
A 25.17698 ±0.60723
B 4.02248 ±2.31626
C -1.91707 ±2.11387
26.2
The sodium chloride partial molar volume at infinite dilution, 15.19 mL/mol, is
significantly different than a literature value of 16.63 mL/mol by 8.64%. Running more
determinations at greater range of molalities might have lead to the better results than
those obtained. The potassium chloride partial molar volume at infinite dilution, 25.18
error between the literature and experimental values for the partial molar volume of
sodium chloride at infinite dilution is 6.23%. This error is smaller than the error in the
potassium chloride measurements. Reasons for these errors include evaporation of water
from the salt chloride solutions during density measurements, not mixing the solutions
thoroughly could have lead to errors, and also the small range of molalities may not
References:
A. Poisson and J. Chanu, Limnology and Oceanography, Vol. 21, No. 6. (Nov., 1976), pp.
853-861.
Coulture, A.M., Laidler, K.J.. "Partial Molal Volume of Ions in Aqueous Solutions."