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Dagondon
CHROMATOGRAPHY
Experiment 4
I.
Objectives
To learn the techniques of paper chromatography and thin layer chromatography
To apply chromatographic methods in the separation of the compounds of a mixture
To identify an unknown by comparing Rf value and other characteristics with those
of a standard.
II. Data and Discussion
A. Separation of Plant Pigments by Paper Chromatography
Sample: San Fransisco (Codiaeum variegatum)
Solven
9:1 (v/v) pet-ether-acetone
t
System
Spot
X
Y
Rf
Color
no.
1. 1
3.40
0.32
1
Yellowcm
cm
Green
1.8
3.40
0.53
2
Redcm
cm
orange
Rf
0.85
cm
-
2.8
Cm
0.30
Color
YellowGreen
-
The first set-up separated two pigments with the colours of yellow-green and redorange. With the use of a polar solvent, the red-orange pigment obtained a higher rf value
(the red-orange pigment rose higher than the yellow-green pigment). This signifies that the
red-orange pigment is more polar than the yellow-green pigment. This is because the solvent
used is polar and therefore by the rule of thumb, like dissolves like, polar substances will
be soluble in polar solvents and thus, would be eluted last (placed at the top of the strip).
The red-orange pigment has lower affinity to stationary phase and high affinity to mobile
phase. The second set-up, only the yellow-green pigment was identified. This indicates that
the yellow-green pigment is less polar. This is because, the solvent used in this set-up was
non-polar and therefore the red-orange pigment didnt dissolve in it. To generalize, when
using a polar solvent, a polar substance will migrate higher in the paper and the same goes
for non-polar solvents.
In conclusion, the solvent system 9:1 (v/v) pet-ether-acetone is more beneficial and
more appropriate to be used as solvent in separating the pigments of the San Francisco
leaves (Codiaeum variegatum) than 9:1:1 (v/v/v) pet-ether-diethyl ether- acetone.
B. Analysis of the Component Dyes of Black Ink by TLC
Solvent System: 6:2:2 (v/v/v) n-butanol-ethanol-NH3
Sample: Pilot (black)
Spot
X
Y
No.
2
2.2 cm
3.4 cm
3
2.7 cm
3.4 cm
Rf
Color
0.65
0.79
Violet
Yellow
Trial2
Trial1
Trial2
Trial1
Trial2
Trial1
Trial2
Trial1
Trial2
X
(cm)
6.0
6.1
5.7
5.7
3.1
3.2
6.2
6.0
3.2
3.2
Y
(cm)
7.2
7.2
7.2
7.2
7.2
7.2
7.2
7.2
7.2
7.2
Rf
0.83
0.85
0.79
0.79
0.43
0.44
0.86
0.83
0.44
0.44
Color
Dark
violet
Dark
Viole
t
Light
Violet
Light
Violet
Light
Viole
t
Light
Violet
Dark
violet
Dark
Violet
Light
Viole
t
Light
Viole
t
Ave
Rf
0.84
0.79
0.44
0.85
0.44
Three amino acids (Phenylalanine, Tyrosine and Aspartic acid) and one unknown
were tested under paper chromatography. The solvent used was 2 % ammonium hydroxideisopropyl alcohol. The development of the spots is due to the polarity affinity of the amino
acids to its solvent. The above table summarizes the results including the amino acids
respective rf values. The unknown was found out to be a mixture of two amino acids
namely, phenylalanine and aspartic acid yielding almost the rf values of the said amino
acids.
Phenylalanine and also the unknown (since it contained phenylalanine) travelled
the highest. This signifies that they have a higher affinity to the mobile phase (solvent)
since they easily travelled easily and farther from it. Aspartic acid (which was also in the
unknown), on the other hand, has travelled the lowest distance signifying a lower affinity
towards the mobile phase.
III.
QUESTIONS
1. What would be the effect of the following errors in the chromatographic work?
a. The solvent level in the developing chamber is higher than the spotted sample.
The spot will be smudged and will be dissolved by the solvent and thus would yield no
result.
b. Too much sample is applied to the paper
Too much sample applied on the paper would mean a spot with a large diameter on the
chromatogram. In this case, the sample may combine with adjacent samples and hence,
would make color identification difficult.
c. The paper is allowed to remain in the chamber after the solvent front has reached the top
of the plate.
The solvent front will reach the maximum point and therefore would alter the value of R f
since the value of Y (distance travelled by solvent from the origin) will continue to
increase while X (distance travelled by compound from the origin) will remain.
2. Why is it necessary to cover the developing chamber tightly during the development of
the chromatogram?
The chamber was covered tightly to avoid the evaporation of the volatile solvents in the
developing chamber. Another reason is to prevent the chromatogram to dry up since if
this would happen, it will be difficult to locate the solvent front.
3. Identify your unknown. Explain clearly how you made this identification.
The amino acids that were identified in the unknown are phenylalanine and aspartic
acid. These acids were identified through the comparison made from the height of
distance travelled of the amino acids and the unknown with respect to the origin. It was
found out that the distance travelled of the said amino acids coincides with the distance
travelled of the unknown. The Rf values also verified this assumption.
4. Can TLC or paper chromatography be used to separate and identify very volatile
substances? Explain your answer.
No, Thin-Layer Chromatography or paper chromatography cannot be used to separate
and identify very volatile substances. Volatile substances will be dry easily because of it
will evaporate quickly and thus will make identification harder and not feasible.
5. Why were you required to handle the chromatographic paper only at its corners in part C?
The chromatogram was handled only on the sides to prevent it to absorb any unnecessary
moistures and contaminations that may be present in our fingers.
IV. Conclusion
5.