Chemical Engineering Laboratory-1 (CHE F312) Lab Report Engineering Chemistry Lab E-1 Thin Layer Chromatography
Chemical Engineering Laboratory-1 (CHE F312) Lab Report Engineering Chemistry Lab E-1 Thin Layer Chromatography
Chemical Engineering Laboratory-1 (CHE F312) Lab Report Engineering Chemistry Lab E-1 Thin Layer Chromatography
(CHE F312)
Lab Report
Engineering Chemistry Lab
E-1
Thin Layer Chromatography
Group 14
Vedant Desai
Pratyush Srivastava
Hritik Vinayak Lal
Apoorv Kaushik
Index Page
THEORY:
TLC is one of the fastest and least expensive out of several chromatographic
techniques used. It is a separation process which is based on the principle of
differential adsorption, i.e. the difference in interaction of molecules i.e Basically the
relative polarities to an inert solid dipped in an organic solvent or solvent mixture.
The stationary phase used in this case is silica gel or alumina coated on a glass
plate.
The components are distributed among the stationary phase and the solvent
depending upon the relative polarities of the compound and the solvent. TLC takes
advantage of the fact that different compounds will have different solubility, different
extent of adsorption and different polarities as compared to each other. Hence, these
compounds travel at different speeds and hence cover different distances on the
plate.
Polar compounds are strongly attracted to the polar adsorbent while nonpolar
compounds are held weakly as compared to polar. When a nonpolar solvent is
passed through the adsorbent, nonpolar compounds are released easily whereas
because polar adsorbents have high affinity for polar compounds, they are retained.
Whereas when a moderately polar solvent is passed through the adsorbent, both
polar and nonpolar compounds are discharged but since there is still an attraction
between the polar compounds and polar adsorbent,the non polar counterpart moves
faster on the plate.
In this experiment we use TLC to identify the components of an over the counter
analgesic.
APPARATUS REQUIRED: TLC
chamber ,TLC plates ,Micro
Capillaries,Ruler ,Test Tubes ,Spatula, Small Beaker ,Pencil
OBSERVATION:
Avg - - - 0.622
Rf, Avg =
(0.642+ 0.611 + 0.611)/3 = 0.62233
DISCUSSION:
PRATYUSH :
5.In TLC, we use a stationary phase (in this case silica gel) which is deposited over
a glass or aluminium support.Here, 99/1 mixture of ethyl acetate/glacial acetic acid
was used as the mobile phase.The solution used to dissolve the analgesic here is
50/50 mixture of Ethanol/Ethyl acetate
6.When we dip the TLC plate in an organic solvent, different compounds will move
upwards at different rates due to capillary action ,according to their relative polarities
and concentrations, allowing the separation of different components.
7.TLC works on the differential adsorption of compounds on the absorbent and the
polarity of the solvent used. The relative polarity of the compounds plays an
essential role in the mobility of compounds in the solvent (especially if it is nonpolar).
The compounds travel different distances on the plate; these distances are marked
and the Rf values are calculated and compared with the standard literature values to
identify the compounds.Due to different polarities, the binding forces result in
accumulation of non polar materials upwards from the origin point on the sheet.
Aspirin = 0.45
Caffeine = 0.08
Acetaminophen = 0.24
Ibuprofen = 0.60
9.Applications of TLC:
3.It is being used in chemistry for the separation and identification of compounds that
resemble each other to a large extent.
4.It is also used for identification of cations and anions in inorganic chemistry.
5.TLC is also useful in separation of biochemical constituents from its body fluids,
blood plasma,urine etc
10.Limitations of TLC:
2.One of its limitations is that it cannot tell the difference between enantiomers and
isomers of some compounds.
3.Another disadvantage of TLC is that to identify the compounds, the Rf values for
them must be known beforehand.
Aspirin 0.45
Caffeine 0.08
Acetaminophen 0.24
6. There is possibility of many errors and problems as well during TLC such
as:
a. Non uniform thickness of silica layer on plate can cause significant
amount of errors. Ideal thickness should be around 0.2mm.
b. Streaking: If the sample spot is too concentrated, the substance will
travel up the stationary phase as a streak rather than a single
separated spot.
c. Spotting: the sample spot will be washed off into the solvent before it
travels up the TLC plate if the sample is not above the solvent level.
7. Applications Of TLC :
● Purity of sample can be carried out with TLC. Direct comparison is
done between the sample and the standard or authentic sample; if any
impurity is detected, then it shows extra spots and this can be detected
easily.
● Thin layer chromatography can be employed in purification, isolation
and identification of natural products like volatile oil or essential oil,
fixed oil, waxes, alkaloids, glycosides, steroids etc.
● In food and cosmetic industry: TLC method is used for separation and
identification of colors, preservatives, sweetening agents, and various
cosmetic products.
● TLC is used in separation of multicomponent pharmaceutical drugs and
detection of its impurities.
● Analyzing the dye composition of fibers in forensics.
8. Disadvantages
a. Only qualitative analysis is possible, not quantitative.
b. Stationary phase layer thickness cannot always be maintained
uniformly all over the plate while preparing it in lab
c. It cannot tell the difference between enantiomers and some isomers.
d. Since TLC operates as an open system, factors such as humidity and
temperature can affect results.
e. It is difficult to replicate the results precisely in the experiment as we
get slightly different values every time.
HRITIK:
9. Applications Of TLC :
Purity of any sample: Purity of sample can be carried out with TLC. Direct
comparison is done between the sample and the standard or authentic
sample; if any impurity is detected, then it shows extra spots and this can be
detected easily.
● One of its limitations is that TLC cannot tell the difference between
isomeric and enantiomeric forms of a compound. This is because the
chiral pairs of a molecule exhibit the same physical properties.
●Stationary phase layer thickness cannot be maintained uniformly all over the
plate.
APOORV:
The average Rf v alue of the compound on which the TLC experiment was conducted
was found to be 0.622. When we compare this to the standard literature values
of the four substances present which are:
1.Aspirin - 0.45
2.Caffeine - 0.08
3.Acetominphen - 0.24
4.Ibuprofen - 0.60
We can conclude that the substance on which the experiment was conducted
was Ibuprofen,because the obtained Rf v alue i.e 0.622 is closest to the Rf
value of Ibuprofen i.e 0.60.
REFERENCES :
● https://chrominfo.blogspot.com/2018/10/advantages-and-disadvantages-
of-thin.html#:~:text=1%20There%20is%20a%20no%20longer%20stationa
ry%20are,Usually%2C%20it%20is%20not%20automatic.%20More%20ite
ms...%20
● https://en.wikipedia.org/wiki/Thin-layer_chromatography#:~:text=Thin-la
yer%20chromatography%20%28TLC%29%20is%20a%20chromatograph
y%20technique%20used,usually%20silica%20gel%2C%20aluminium%20
oxide%20%28alumina%29%2C%20or%20cellulose.