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Treatment of Data |
Table 4: Pv of the pure substances
Temperature (°C) |
Ethanol Pv (mmHg) |
Ethanol Pv
(kPa) |
n-Propanol Pv (mmHg) |
n-Propanol Pv
(kPa) |
56 |
286 |
38.1238 |
|
|
58 |
314 |
41.8562 |
|
|
60 |
344 |
45.8552 |
|
|
62 |
377 |
50.2541 |
|
|
64 |
412 |
54.9196 |
|
|
66 |
450 |
59.985 |
|
|
68 |
490 |
65.317 |
|
|
70 |
534 |
71.1822 |
|
|
72 |
581 |
77.4473 |
|
|
74 |
631 |
84.1123 |
286 |
38.1238 |
76 |
658 |
87.7114 |
300 |
39.99 |
78 |
|
|
343 |
45.7219 |
80 |
|
|
374 |
49.8542 |
82 |
|
|
408 |
54.3864 |
84 |
|
|
444 |
59.1852 |
86 |
|
|
483 |
64.3839 |
88 |
|
|
525 |
69.9825 |
90 |
|
|
570 |
75.981 |
Table 5:Logarithm of Vapor Pressure at different temperatures
1/T
(Kelvins)-1 |
Logarithm of vapour pressure of Ethanol
ln(Pv) |
Logarithm of vapour pressure of n-Propanol
ln(Pv) |
0.003038 |
3.640839 |
|
0.00302 |
3.73424 |
|
0.003002 |
3.825489 |
|
0.002984 |
3.917092 |
|
0.002966 |
4.00587 |
|
0.002949 |
4.094095 |
|
0.002931 |
4.179252 |
|
0.002914 |
4.265243 |
|
0.002897 |
4.349598 |
|
0.002881 |
4.432153 |
3.640839 |
0.002864 |
4.474052 |
3.688629 |
0.002848 |
|
3.822577 |
0.002832 |
|
3.909103 |
0.002816 |
|
3.996114 |
0.0028 |
|
4.080672 |
0.002784 |
|
4.164864 |
0.002769 |
|
4.248245 |
0.002754 |
|
4.330483 |
Treatment of Data
1.1 To find the vapour pressure
Formula: 
Symbol:
Pv = vapor pressure (kPa)
Pb = corrected barometric pressure (kPa)
DP = The pressure difference between the two legs of the manometers (kPa)
Sample calculation for pure ethanol at 56°C
DP=379mmHg
Pb =665.0mmHg



Note: This answer has to be converted into kPa, to convert the values, one must multiply the answer with the conversion factor of 0.1333.
Converting it into kPa
Pv(kPa) = Pv(mmHg) x 0.1333
Pv(kPa) = 286.0mmHg x 0.1333
Pv(kPa) = 38.12kPa
Sample calculation for pure n-propanol at 74°C
DP=379mmHg
Pb =665.0mmHg



Note: This answer has to be converted into kPa, to convert the values, one must multiply the answer with the conversion factor of 0.1333.
Converting it into kPa
Pv(kPa) = Pv(mmHg) x 0.1333
Pv(kPa) = 286.0mmHg x 0.1333
Pv(kPa) = 38.12kPa
1.2 To find the natural log of the vapor pressure in kPa
Formula: ln(Pv)
Symbol:
ln(): Natural log function
Pv: Vapor pressure (kPa)
This formula is for taking the natural log of the vapor pressure.
Sample calculation for Ethanol at 56°C
Pv= 38.12kPa
ln(Pv)
ln(38.12kPa)=3.64
Sample calculation for n-Propanol at 74°C
Pv= 38.12kPa
ln(Pv)
ln(38.12kPa)=3.64
1.3 To find the inverse of temperature
Formula: T-1=1/T
Symbols:
T-1= inverse of temperature (K-1)
T = Temperature (K)
Note: Temperature in Table 1 is in degrees Celsius. To convert degrees Celsius into Kelvins, one must add the temperature in Celsius by 273.15K to obtain the temperature in Kelvins.
Sample calculations for 56°C
T-1=1/T
T-1= 1/(56+273.15K)
T-1= 0.003038K-1
1.4 To find coeffiecient A
Formula: 
Symbol:
A = Constant (K)
Dy = Change of y coordinate ln(Pv)
Dx = Change of x coordinate (K-1)
This formula is derived from the original slope formula:
. Using the line of best fit, one can find an approximation value for coefficient A.
Sample calculation for ethanol
Two points from line of best fit (0.00286, 4.476) and (0.0030, 3.83)

or
-A= linear regression by input the x (Inverse temperature) and y (ln(Pv) values on Table 4 in calculator and use the function LinReg(Ax+B)
A= 4907.94K
Sample calculation for n-propanol
Two points from line of best fit (0.00285, 3.82) and (0.00277, 4.25)

or
-A= linear regression by input the x (Inverse temperature) and y (ln(Pv) values on Table 4 in calculator and use the function LinReg(Ax+B)
A= 5554.37K
1.5 To find coefficient C
Formula: 
Symbol:
ln(Pv): The natural log of pressure
T: The temperature at certain pressure (K)
A: Coefficient (K)
C: Coefficient
This equation is from the relationship between vapor pressure and temperature.
Sample Calculation for ethanol at 56°C
ln(Pv)=3.64
A=4907.94K
T=56°C+273.15K=329.15K



Sample Calculation for n-propanol at 74°C
ln(Pv)=3.64
A=5554.37K
T=74°C+273.15K=347.15K



1.6 To find the latent heat vaporization
Formula: 
Symbol:
A= Constant (K)
DHv= Latent heat of vaporization (kJ/kg)
R= Universal gas constant (8.314kJ/molK)
This formula is derived from the relationship between the parameter A, the gas constant, and DHv. If parameter A is known, one can find the latent heat of vaporization using the above formula.
Sample Calculation for ethanol
A= 4907.94K
R=8.314kJ/molK



Sample Calculation for n-propanol
A= 5554.37K
R=8.314kJ/molK



Note: The latent heat should be in kJ/kg. To convert the units into kJ/kg, one must divide the above value by the molar mass.
Ethanol:

n-Propanol:

1.7 To find the normal boiling point
Formula: 
Symbol:
ln(Pv)= the natural log of pressure
Tb=Normal boiling point (K)
A =Coefficient (K)
C =Coefficient
This equation is from the relationship between vapor pressure and temperature. By knowing the values of A, C and the vapor pressure at normal boiling point (101.325kPa), one can find the value for the normal point using the equation above.
Sample Calculation for ethanol
Pv=101.325kPa
A= 4907.94K




Sample Calculation for n-propanol
Pv=101.325kPa
A= 5554.37K




1.8 To find Percentage of Error
Formula: 
This formula is to calculate the percentage of error by finding the difference between theoretical and experimental value, and then divide by the theoretical value multiply by 100% to obtain the percentage.
Sample calculation for DHv of Ethanol
Acquired Value: 885.71kJ/kg
Accepted Value: 838.00kJ/kg



Table 6: Percentage of Error
|
%Error (%) |
DHv of Ethanol |
5.69 |
DHv of n-Propanol |
|
Tb of Ethanol |
1.06 |
Tb of n-Propanol |
0.05 |
Table 7: Vapour pressure of different mixtures in different temperature
|
Liquid Mixture Composition (Volumes of Ethanol: Volumes of n-Propanol) |
Temperature (°C) |
1:0 (kPa) |
8:1 (kPa) |
4:1 (kPa) |
1:1 (kPa) |
1:4 (kPa) |
1:8 (kPa) |
0:1 (kPa) |
56 |
38.1238 |
|
|
|
|
|
|
58 |
41.8562 |
40.2566 |
38.9236 |
|
|
|
|
60 |
45.8552 |
44.1223 |
42.656 |
|
|
|
|
62 |
50.2541 |
48.3879 |
46.7883 |
39.8567 |
|
|
|
64 |
54.9196 |
52.9201 |
51.1872 |
43.7224 |
|
|
|
66 |
59.985 |
57.8522 |
55.986 |
47.8547 |
|
|
|
68 |
65.317 |
63.0509 |
61.0514 |
52.2536 |
39.5901 |
|
|
70 |
71.1822 |
68.7828 |
66.5167 |
57.0524 |
43.4558 |
38.5237 |
|
72 |
77.4473 |
74.9146 |
72.5152 |
62.2511 |
47.4548 |
42.1228 |
|
74 |
84.1123 |
81.313 |
78.7803 |
67.7164 |
51.8537 |
46.1218 |
38.1238 |
76 |
87.7114 |
84.7788 |
82.2461 |
70.649 |
54.2531 |
48.2546 |
39.99 |
78 |
|
|
|
80.1133 |
61.7179 |
54.9196 |
45.7219 |
80 |
|
|
|
86.7783 |
67.0499 |
59.8517 |
49.8542 |
82 |
|
|
|
|
72.9151 |
65.0504 |
54.3864 |
84 |
|
|
|
|
79.0469 |
70.649 |
59.1852 |
86 |
|
|
|
|
85.7119 |
76.7808 |
64.3839 |
88 |
|
|
|
|
|
83.1792 |
69.9825 |
90 |
|
|
|
|
|
|
75.981 |
1.8 To find number of moles
Formula: 
Symbol:
Volume = volume of substance in composition (m3) (note: the volume are based on unit of 1m3, but it does not mean that the volume of the substance is 1m3)
Density: Density of the substance (kg/m3)
Molar mass-1= Molar mass inverse (kmol/kg)
Sample Calculation for Ethanol 1:0 mixture
Volume of Ethanol: 1m3
Density of Ethanol: 785.05kg/m3
Molar mass of Ethanol: 1kmol/46.07kg



Table 8: Moles of substance in different Mixture Composition
Composition
(Volume of Ethanol: Volume of n-Propanol |
Mole of Ethanol (kmol) |
Mole of n-Propanol (kmol) |
1:0 |
17.04 |
0 |
8:1 |
136.32 |
13.31 |
4:1 |
68.16 |
13.31 |
1:1 |
17.04 |
13.31 |
1:4 |
17.04 |
53.24 |
1:8 |
17.04 |
106.48 |
0:1 |
0 |
13.31 |
1.8 To find mole fraction
Formula: 
Symbol:
Moles of substance = mole of a substance (kmol)
Moles of Composition = nethanol + nn-Propanol (kmol)
Table 9: Mole Fraction of different Mixture Composition
Composition
(Volume of Ethanol: Volume of n-Propanol |
Mole fraction of Ethanol |
Mole Fraction of n-Propanol |
1:0 |
1 |
0 |
8:1 |
0.911047 |
0.088953 |
4:1 |
0.836627 |
0.163373 |
1:1 |
0.56145 |
0.43855 |
1:4 |
0.242459 |
0.757541 |
1:8 |
0.137953 |
0.862047 |
0:1 |
0 |
1 |
|
|
|
|