Chem111.1 Exer7 SampleCalc.v1

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Exercise 7

Surface Tension of Pure Liquids and Solutions


Sample Calculations
1. Calculation of MMmoist air
%𝑅𝐻 𝑃𝐻2 𝑂@ 𝑅𝑇
Χ 𝐻2 𝑂 = ( )
100 𝑃𝑐,𝑎𝑡𝑚
1 𝑎𝑡𝑚
80% 0.0037831 𝑥106 𝑃𝑎 ( )
Χ 𝐻2 𝑂 =( ) 101325 𝑃𝑎
100 29.36 𝑖𝑛𝐻𝑔 (25.4 𝑚𝑚) ( 1 𝑎𝑡𝑚 )
𝑖𝑛 760 𝑚𝑚𝐻𝑔
Χ 𝐻2 𝑂 = 0.03044002609
Χ 𝑁2 = 0.79(1 − Χ 𝐻2 𝑂 ) = 0.79(1 − 0.03044002609 ) = 0.7659523794

Χ 𝑂2 = 0.21(1 − Χ 𝐻2 𝑂 ) = 0.21(1 − 0.03044002609 ) = 0.2036075945

𝑀𝑀𝑚𝑜𝑖𝑠𝑡 𝑎𝑖𝑟 = Χ 𝐻2 𝑂 MM𝐻2 𝑂 + Χ 𝑁2 MM𝑁2 + Χ 𝑂2 MM𝑂2


g g g
𝑀𝑀𝑚𝑜𝑖𝑠𝑡 𝑎𝑖𝑟 = (0.03044002609 ) (18.016 ) + (0.7659523794) (28.02 ) + (0.2036075945) (32 )
mol mol mol
g
𝑀𝑀𝑚𝑜𝑖𝑠𝑡 𝑎𝑖𝑟 = 28.52601937
mol

2. Calculation of ρo
𝑃𝑉 = 𝑛𝑅𝑇
𝑚
𝑃𝑉 = ( ) 𝑅𝑇
𝑀𝑀
𝑚 𝑃(MM𝑚𝑜𝑖𝑠𝑡 𝑎𝑖𝑟 )
𝜌𝑜 = =
𝑉 𝑅𝑇
25.4 𝑚𝑚 1 𝑎𝑡𝑚 g
𝑚 29.36 𝑖𝑛𝐻𝑔 ( 𝑖𝑛 ) (760 𝑚𝑚𝐻𝑔) (28.52601937 mol)
𝜌𝑜 = =
𝑉 𝐿 𝑎𝑡𝑚
(0.082056 ) (28 + 273.15)𝐾
𝑚𝑜𝑙 𝐾
𝑔
𝜌𝑜 = 1.132724094𝑥10−3
𝑐𝑚3

3. Calculation of A and B
𝛾
= 𝐴∆ℎ − 𝐵
𝜌 − 𝜌𝑜
Plotted values (Day 1):
𝛾
𝑥 = ∆ℎ 𝑦=
𝜌 − 𝜌𝑜
𝑑𝑦𝑛𝑒
71.1833 𝑐𝑚
water 4.1 𝑔
(0.995647 − 1.132724094𝑥10−3 )
𝑐𝑚3
𝑑𝑦𝑛𝑒
22.4275 𝑐𝑚
acetone 4 𝑔
(0.888 − 1.132724094𝑥10−3 )
𝑐𝑚3
𝑑𝑦𝑛𝑒
22.69494
ethyl acetate 3.2 𝑐𝑚
𝑔
(0.77825 − 1.132724094𝑥10−3 ) 3
𝑐𝑚

Using Linear Regression analysis:


𝑐𝑚2
Slope: 𝐴 = 27.14455232 𝑠2

𝑐𝑚3
y-int: −𝐵 = −60.22167829 𝑠2

𝑐𝑚3
𝐵 = 60.22167829
𝑠2

R2 = 0.2721225414

4. Calculation of ρsoln
𝑚𝑝𝑦𝑐+𝑠𝑜𝑙𝑛 − 𝑚𝑝𝑦𝑐
𝜌𝑠𝑜𝑙𝑛 = 𝜌
𝑚𝑝𝑦𝑐+𝐻2 𝑂 − 𝑚𝑝𝑦𝑐 𝐻2 𝑂@𝑤𝑎𝑡𝑒𝑟 𝑏𝑎𝑡ℎ 𝑡𝑒𝑚𝑝=30℃
24.1108 𝑔 − 14.1897 𝑔 𝑔
𝜌𝑠𝑜𝑙𝑛 = (0.995646 )
24.1714 𝑔 − 14.1897 𝑔 𝑐𝑚3
𝑔
𝜌𝑠𝑜𝑙𝑛 = 0.9896013235
𝑐𝑚3

5. Calculation of 𝛾
𝛾 = (𝐴∆ℎ − 𝐵)( 𝜌𝑠𝑜𝑙𝑛 − 𝜌𝑜 )
𝑐𝑚2 𝑐𝑚3 𝑔
𝛾 = [27.14455232 2
(4.6 𝑐𝑚) − (60.22167829 2 )] [0.9896013235 − 1.132724094𝑥10−3 ] ( 3 )]
𝑠 𝑠 𝑐𝑚
𝑔
𝛾 = 63.89783503
𝑠2

6. Calculation of surface tension of 1-propanol


𝛾 = −𝜇𝑅𝑇 (ln 𝑐) + 𝑐𝑜𝑛𝑠𝑡.
Plotted values:
𝑔 𝑑𝑦𝑛𝑒
𝑥 = ln 𝑐 𝑦 = 𝛾, 𝑠2 = 𝑐𝑚

ln 0.60 63.89783503
ln 0.50 69.33683333
ln 0.40 74.84357785
ln 0.30 80.2518497
ln 0.20 91.16151563
ln 0.05 96.53010979

Using linear regression analysis:


Slope: −𝜇𝑅𝑇 = −12.80445756 𝑑𝑦𝑛𝑒/𝑐𝑚
𝑑𝑦𝑛𝑒
y-int: 62.41499533 𝑐𝑚

R2 = 0.8490381453

7. Calculation of µ (surface concentration of the excess no. of moles solute per unit area)
From the slope:
−𝜇𝑅𝑇 = −12.80445756 𝑑𝑦𝑛𝑒/𝑐𝑚

−12.80445756 𝑑𝑦𝑛𝑒/𝑐𝑚
𝜇=
−𝑅𝑇
𝑑𝑦𝑛𝑒 𝑁 100 𝑐𝑚 𝑚 2
−12.80445756 𝑐𝑚 ( 5 )( 𝑚 )( )
10 𝑑𝑦𝑛𝑒 1𝑥1010 Å
𝜇=
𝐽 𝑁𝑚 𝑚𝑜𝑙
− (8.314 )( 𝐽 )( ) (30 + 273.15)𝐾
𝑚𝑜𝑙 𝐾 6.0221367𝑥1023 𝑚𝑜𝑙𝑒𝑐𝑢𝑙𝑒𝑠
𝑚𝑜𝑙𝑒𝑐𝑢𝑙𝑒𝑠
𝜇 = 0.03059455931
Å2

8. Calculation of ECAPM (effective cross-sectional area per molecule)


1
𝐸𝐶𝐴𝑃𝑀 =
𝜇
1
𝐸𝐶𝐴𝑃𝑀 =
𝑚𝑜𝑙𝑒𝑐𝑢𝑙𝑒𝑠
0.03059455931
Å2
Å2
𝐸𝐶𝐴𝑃𝑀 = 32.68555007
𝑚𝑜𝑙𝑒𝑐𝑢𝑙𝑒

9. Calculation of Katayama constant, K, and critical temperature, Tc (Day 2)


2
𝑀 3
Katayama equation: 𝛾 (𝜌−𝜌 ) = −𝐾𝑇 + 𝐾𝑇𝑐 ; MM(1-propanol) = 60.094 g/mol
𝑜

Plotted values:
2
𝑀 3
x=T y= 𝛾( )
𝜌−𝜌𝑜
2
3
𝑑𝑦𝑛𝑒 60.094 𝑔 𝑚𝑜𝑙 −1
y= 33.39412603 ((0.7958−𝜌 ) 𝑔 )
303.15 K 𝑐𝑚 𝑜 3
𝑐𝑚

= 597.1754122 𝑑𝑦𝑛𝑒 ∗ 𝑐𝑚 𝑚𝑜𝑙 −2/3


308.15 K 563.6376725
313.15 K 432.6871528
318.15K 399.5023008
323.15 K 398.8377945
328.15 K 398.1710666
333.15 K 397.4849157

Using linear regression analysis:


2
Slope:−𝐾 = −6.884671854 𝑑𝑦𝑛𝑒 ∗ 𝑐𝑚 𝑚𝑜𝑙 −3 𝐾 −1
2
y-int: 𝐾𝑇𝑐 = 2645.714967 𝑑𝑦𝑛𝑒 ∗ 𝑐𝑚 𝑚𝑜𝑙 −3
R2 = 0.732678368

Solving for Katayama constant:


From slope:
2
−𝐾 = −6.884671854 𝑑𝑦𝑛𝑒 ∗ 𝑐𝑚 𝑚𝑜𝑙 −3 𝐾 −1
2
𝐾 = 6.884671854 𝑑𝑦𝑛𝑒 ∗ 𝑐𝑚 𝑚𝑜𝑙 −3 𝐾 −1

Solving for critical temperature, Tc:


From y-intercept:
2
𝐾𝑇𝑐 = 2645.714967 𝑑𝑦𝑛𝑒 ∗ 𝑐𝑚 𝑚𝑜𝑙 −3
2

2645.714967 𝑑𝑦𝑛𝑒∗𝑐𝑚 𝑚𝑜𝑙 3
𝑇𝑐 = 𝐾
2

2645.714967 𝑑𝑦𝑛𝑒∗𝑐𝑚 𝑚𝑜𝑙 3
𝑇𝑐 = 2

6.884671854 𝑑𝑦𝑛𝑒∗𝑐𝑚 𝑚𝑜𝑙 3 𝐾−1

𝑇𝑐 = 384.290642 𝐾

10. Percent error of Tc


𝑒𝑥𝑝𝑒𝑟𝑖𝑚𝑒𝑛𝑡𝑎𝑙 − 𝑡ℎ𝑒𝑜𝑟𝑒𝑡𝑖𝑐𝑎𝑙
% 𝑒𝑟𝑟𝑜𝑟 = 𝑥100
𝑡ℎ𝑒𝑜𝑟𝑒𝑡𝑖𝑐𝑎𝑙
384.290642 𝐾 − 536.78 𝐾
% 𝑒𝑟𝑟𝑜𝑟 = 𝑥100
536.78 𝐾
% 𝑒𝑟𝑟𝑜𝑟 = −28.40816684 %

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