Ipchmclass12th Converted1 191208134113
Ipchmclass12th Converted1 191208134113
Ipchmclass12th Converted1 191208134113
Paper Chromatography
Prepared by: -
Sandesh Walke
Class XII
Acknowledgment
Sandesh Walke
Class 12th
Content
• Certificate
• Acknowledgement
• Introduction
• Principal of Chromatography
• Sources of error
• Bibliography
Introduction
Paper chromatography was discovered by Synge and Martin in the year 1943.
Principal of Paper Chromatography
• Cut the paper into desired shape and size depending upon work to be carried
out.
• The starting line is marked on the paper with an ordinary pencil 5cm from the
bottom edge.
• On the starting line marks are made 2cm apart from each other .
Working of Chromatographic paper
• A horizontal line is drawn near one end (about 1.5 cm from the bottom edge) of the
paper.
• The sample needs to be separated is placed as a small drop or line on to the paper
using capillary tube. Labelling the drop by a pencil with an alphabet or number help
to identify the compound later. The drops are then soaked on the paper and dried.
• The paper is then placed into a sealed container with a swallow layer of suitable
solvent (M.P). The solvent level must be lower than the pencil line or drop on it.
The container needs to be covered to stop the solvent to evaporate.
• The solvent rises up the paper chromatography taking each component of the
sample with it. The components travel with the solvent depends on three things:
✓ The polarity of the sample molecule. The non-polar components travel faster
than the polar component.
✓ The attraction between the sample molecule and the solvent or solvent mixture.
✓ The attraction between the sample and the silica.
• When the solvent rises near the end of the paper then the paper should be taken
out from sealed container and air dried. The paper with separated bands of
components are then observed under UV-light.
• This is what causes the different liquids within our original liquid mixture to spread
out on the solid.
Paper Chromatography
✓ Column Chromatography: -
✓ Thin layer Chromatography (TLC)
✓ Gas Chromatography
➢ Here the solvent travels up the chromatographic paper. Both descending and
ascending paper chromatography are used for the separation of organic and
inorganic substances. The sample and solvent move upward.
➢ Like conventional type, the solvent flows against gravity. The spots are kept at
the bottom portion of paper and kept in a chamber with mobile phase solvent
at the bottom.
The retention factor (Rƒ) may be defined as the ratio of the distance traveled by the
solute to the distance traveled by the solvent. It is used in chromatography to quantify
the amount of retardation of a sample in a stationary phase relative to a mobile phase.
Rƒ values are usually expressed as a fraction of two decimal places.
• If Rƒ value of a solution is zero, the solute remains in the stationary phase and
thus it is immobile.
• The ratio of the distance moved up or travelled by the components from the origin
or point of application to the distance moved up by the solvent from the same
point.
For example, if a compound travels 9.9 cm and the solvent front travels 12.7 cm, the
Rƒ value = (9.9/12.7) = 0.779 or 0.78. Rƒ value depends on temperature and the
solvent used in experiment, so several solvents offer several Rƒ values for the same
mixture of compound. A solvent in chromatography is the liquid the paper is placed in,
and the solute is the ink which is being separated.
Factors affecting Rf Value
• The temperature
• The purity of the solvents used
• The quality of the paper, adsorbents & impurities
• present n the adsorbents
• Chamber saturation techniques, method of drying and development
• The distance travelled by the solute & solvent
• Chemical reaction between the substances being partitioned.
• pH of the solution
• In many cases it has been observed that the solvent front is run off the end of
the paper. Rx value is thus used,
• It is the ratio of distance travelled by the sample and the distance travelled by
the standard. Rx value is always closer to 1.
• Mobile phase composition
• Stationary phase
• Concentration of analyte
• Particle size
• In liquid chromatography, in general, the mobile phase pH is an important
parameter
• In reversed-phase liquid chromatography (hydrophobic retention
chromatography) the solvent type and concentration are important factors
Sources of error
• Development: -
➢ Improper adjustment of the paper in the tank leads to this error so the
paper should be held vertically.
➢ Do chamber saturation.
• Detection: -
• A few drops of the mixture of colored pigments are placed on the filter paper
(stationary phase) and it is then slowly submerged into a jar of solvent (mobile
phase).
• As the solvent rises up the paper, it dissolves the molecules present in the
mixture, their solubility depending on their polarity.
• Spotting of the sample is done with the help of a capillary tube or automated
applicator.
• The sample is applied as a neat spot on a horizontal line drawn with a pencil
close to one edge.
• Allow the spot to dry and then immerse the paper in the developing chamber
as per the selected technique with the marked spot above the solvent level.
• The solvent begins to move and draws the sample components differentially
along with it.
• At the end of the development take out the paper and mark the solvent front with
another line.
Applications of Paper Chromatography: -
• To inspect cosmetics.