An unknown mixture is pushed passed what is called the stationary phase in a continuous stream, it can be a solid in the case of TLC, or a liquid as is the case in many forms of GC. The exact nature of the stationary phase is not so important, what is important is that the individual components of the unknown mixture interact with the stationary phase in some way. Ones that interact more strongly and prefer to stay associated with the stationary phase versus in solution (or in the gas phase) will move slowly and be held back in the stream. Species that interact weakly move more swiftly through the stream. In this manner the different components of the mixture can be separated out by the amount of time it takes for them to elute : move through a column of stationary phase.
A measure of how strongly or weakly a compound is retained is the Retention Factor (RF) or Retention Time. In TLC the RF of a compound can be used to identify it from tabulated values. The retention factor is the ratio of the distance traveled by the compound up the plate versus the distance traveled by the solvent front. The RF for a given compound is (relatively) unique as it depends upon the structure and chemistry of that compound.
In this instructable I will describe how one can prepare their own silica gel TLC (Thin-Layer Chromatograph) plates. In this form of chromatography the stationary phase is a thin layer of silica, a type of finely divided silicon dioxide, deposited on a glass slide. The analyte is "spotted" on the plate using an eye-dropper or micropipette and the whole plate is placed in a beaker with a small amount of solvent in the bottom such that the solvent level is just above the bottom of the plate. The solvent moves up the plate by capillary action, pulling the pigment along with it. The different chemical species in the pigment interact with the silica in differing ways and this affects the degree to which they are pulled up the plate, which is how the separation is effected.
A more basic version of this substitutes a strip of sturdy paper in place of the TLC plate, in which case the cellulose of the paper fills the role of the stationary phase instead of silica. Paper chromatography has its limitations, however, usually making themselves visible as smearing or poor separation. This is why thin layer chromatography is usually employed. It operates in much the same way as paper chromatography in so far as development, however peak separation is generally better (amongst other things).
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Signing UpStep 1Gather the materials
- an oven, generally comes with houses
- a weigh scale, nothing too fancy should be accurate to one tenth of a gram, e.g This digital scale from Amazon
- an old plastic bottle you don't care about, not too large (I used a 150mL one)
- a pan, for resting the plates on and for putting in the oven.
- a mortar and pestle, larger ones are easier to work with than smaller ones
- a syringe, 10cc minimum, plastic works fine, I got mine from Home Depot
- glass slides, you can also use sheets of tin or plastic, basically anything stiff that won't interact with water
- Anhydrous Calcium Sulfate, a.k.a. Plaster of Paris, I liberated mine from an artsy friend
- Water, from the tap, or distilled if impurities are an issue
- Silica Gel - This is the desiccant in those little packets you find in medicine bottles and assorted what-nots.
The final materials are needed for constructing a developing chamber and developing slides of plant pigments:
- a mason jar with lid. it should be just taller than the glass slides such that you could prop a slide up in it easily
- filter paper, you can also use sturdy sketch paper, I use 10mm filter paper
- eye dropper or pasteur pipette
- acetone 50mL
- hexane 50mL
- a pencil
- a graduate cylinder
- some leaves, from which to extract the chlorophylls and xanthophylls
- clean sand for grinding with, mine is from the beach.
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