PAPER CHROMATOGRAPHY 纸张层析法

PAPER CHROMATOGRAPHY

INTRODUCTION

Chromatography is a technique that is used to separate and to identify components of a

mixture. This analytical technique has a wide range of applications in the real world since

many substances are mixtures of chemical compounds. In this lab, you will explore two

applications of chromatography - identification of an unknown ink sample and the separation of food colorings.

In paper chromatography, the sample mixture is applied to a piece of filter paper, the edge of the paper is immersed in a solvent, and the solvent moves up the paper by capillary action. Components of the mixture are carried along with the solvent up the paper to varying degrees, depending on the compound's preference to be adsorbed onto the paper versus being carried along with the solvent. The paper is composed of cellulose to which polar water molecules are adsorbed, while the solvent is less polar, usually consisting of a mixture of water and an

organic liquid. The paper is called the stationary phase while the solvent is referred to as the mobile phase. Performing a chromatographic experiment is basically a three-step process: 1) application of the sample, 2) "developing" the chromatogram by allowing the mobile phase to move up the paper, and 3) calculating Rf values and making conclusions.

In order to obtain a measure of the extent of movement of a component in a paper

chromatography experiment, we can calculate an "Rf value" for each separated

component in the developed chromatogram. An Rf value is a number that is defined as:

distance traveled by component from application point

R f = ----------------------------------------------------

distance traveled by solvent from application point

The distance traveled by the spot is measured to the MIDDLE of the spot.

R f = A/B

Forensic chemistry, the profession popularized by TV's "Quincy" is the application of

chemical techniques to law. Many samples that are received in a crime laboratory are

complex mixtures of chemical compounds and chromatography is often ideal for

separating and identifying these components. One example of this is the identification

of an unknown ink sample. Suppose the authenticity of a signature or the source of a

ransom note is in question. Using paper chromatography, it is often possible to identify

the source of the inks that were used and thereby provide strong evidence that can be

used in the courtroom

In the second part of the experiment, you will separate a mixture of three food colorings

using "reverse-phase" chromatography. In this type of chromatography, the stationary

phase is a non-polar material and the mobile phase is relatively polar. You will use a

commercial C18 cartridge, which contains very non-polar 18-carbon long chains as the

stationary phase. The mobile phase will be water and/or isopropyl alcohol (IPA).

AVOID EXCESSIVE HANDLING OF PAPER

1. The chromatography paper is cut in about 2.5 x 10 cm strips. Along one of the

shorter sides, draw a horizontal line in pencil (lead will not move) about 1.5 cm

from the edge of the strip. This will be your “base line”, the starting line where

the samples will be spotted.

2. Apply a dot of ink from each black felt tip pen on the baseline. Make sure dots

are evenly spaced on the baseline and not too close to the edge. It may be

helpful to use a pencil to mark the spots before placing the ink on the paper. See

the diagram below.

3. Label each spot in pencil so that you know what each spot is.

4. Stand the paper in the eluting solution. Taping the top of the strips to the side of

the beaker may be helpful.

B a s e L in

e

1. Remove the cartridge from the bottom of the syringe then remove the piston of

the syringe.

2. Insert the LONGER END of the C18 cartridge snugly onto the syringe tip. Be

careful to use the proper end and not put the cartridge on backwards.

3. Add solution as directed and insert the piston.

4. Flush solutions slowly through the cartridge. Faster is not better.

5. REMOVE CARTRIDGE BEFORE PULLING PLUNGER to add new solution to

avoid pulling air backwards through the column.

6. The cartridge should be cleaned with a 1:1 mixture of water:IPA until all coloring

is removed. Food coloring not removed may stain the column and make it less

effective.

SAFETY AND DISPOSAL

• The food coloring mixture will stain your skin and clothing. Handle with care.

• All of the solutions in this lab may be washed down the drain with water.

EXPERIMENTAL PROCEDURE

I .

A. This lab will be done as a collaboration between both lab pairs at a bench.

1. One lab pair will use 2 parts isopropanol to 1 part water as a solvent

(labeled 2:1 IPA).

2. One lab pair will use 1 part isopropanol to 2 parts water as a solvent

(labeled 1:2 IPA).

B. Obtain a strip of chromatography paper about 2.5 cm wide by 10 cm tall.

Along one of the shorter sides, draw a horizontal line in pencil about

1.5 cm from the edge of the strip. This will be your “base line”, the

starting line where the samples will be spotted. Graphite will not be

carried up the chromatography paper. This baseline will be used later in the calculations of Rf values.

C. Using the black felt tip pens, apply generous dots of ink on the baseline

according to the diagram in the "TECHNIQUES" section.

D. With a pencil, label each dot with the identity of the pen from which the ink came.

E. Obtain a paper strip from your instructor that is marked with one of the three

pens. This is the unknown ink sample that you must identify.

F. Once your two strips are prepared, set up a developing chamber using a 400 ml

beaker.

G.

H.

I.

J.

II .

1. Pour some of the developing solvent in the beaker, using only enough solvent to cover the bottom of the beaker (about 5-10 mL). 2. Remember, one lab pair will use 1:2 IPA and the other lab pair will use 2:1 IPA. Place the paper strips into the developing chamber so that the edge near the ink spots is submerged in the solvent. THE INK SPOT MUST BE ABOVE THE SOLVENT LEVEL. You should avoid allowing the paper strips to touch each other or the sides of the beaker. (Taping the top of the strips to the outside of the beaker may be helpful.) Once you have inserted the paper, cover the chamber with a watchglass and make sure the solvent is progressing up the paper. When the solvent has risen almost to the top of the paper strip, remove the strip from the chamber and immediately mark the level to which the solvent has risen and circle each spot present on the strip with a pencil. (The solvent front and the spots will continue to move for several minutes after removing the strip from the beaker.) Measure the distance each spot traveled and calculate Rf values for each spot. Use the circles you drew around each spot with your pencil and not the actual spot! Turn your chromatogram in as part of your report. A. B. Remove the piston and insert the LONG END of the C18 cartridge snugly into the syringe tip. Add 5 mL of IPA, insert the piston, and slowly flush at a flow rate not

exceeding 5-10 mL per minute. It is important to not flush liquid through the cartridge more rapidly than 10 mL per minute. Repeat this step with another 5 mL portion of IPA.

Flush with two 5 mL portions of distilled water.

Add about 1 mL of the food coloring mixture to the syringe, insert the

piston, and push the mixture onto the cartridge. As you push the sample through the cartridge, immediately begin collecting the drops in a test

tube. The first color comes off quickly.

1. Once the 1 mL of food coloring mixture is pushed onto the

cartridge, add water to the syringe and push it through the cartridge

until all the yellow is gone. Collect the yellow liquid. The process

of pushing solvent(s) through a cartridge is called elution. In this

case, water elutes the yellow color.

2. The remaining colors in the mixture must be removed by eluting

with a water/IPA mixture. Prepare a 1% IPA solution by placing 5

mL of water into the syringe and adding 1 drop of IPA. Mix well by

shaking the syringe. Push this solution through the cartridge and

collect all the colors that come off. If coloring still remains on the

cartridge, prepare a 2% IPA solution by adding 2 drops of IPA to 5

mL of water, mix, and elute this solution through the cartridge.

Continue to increase the percentage of IPA (3% - 3 drops IPA + 5

mL water, 4% - 4 drops IPA + 5 mL water, etc.) until all or most of

the coloring has been removed from the cartridge. A 5% IPA C. D.

3.

E.

F. Make sure the cartridge is clean before returning it.

4. See what would happen if several of the separated colored solutions were mixed. - Try to make a green solution from the colors you separated. solution may be the most concentrated solution needed to remove all of the colors from the cartridge. Any coloring residue remaining on the cartridge should be removed using a 1:1 IPA:water mixture. This residue may need to be collected. Save the separated colored solutions for the next part.