chromatographypresentation

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    Chemical Ideas 7.6

    Chromatography

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    The general principle.Use to separate and identify

    components of mixtures.

    Several different types - paper, thin

    layer, gas-liquid. All use the principle of partition -

    affinity between two phases, toseparate mixtures of substances.

    Stationary phase & mobile phase.

    Compounds with greatest affinity for mobile phase travel further.

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    All chromatography needs :

    ChromatographyType

    Stationary phase Mobile phase

    Paper Paper Organic oraqueous solvent.

    Thin layer Silica gel

    supported onplastic film

    Organic or

    aqueous solvent.

    G.L.C. High boilingpoint liquid oninert solidsupport.

    Inert gas e.g.nitrogen.

    support material stationary phase

    solvent (or carrier gas ) mobilephase.

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    Thin Layer Chromatography - t.l.c.

    Series of spots formsCompare samples inmixture with knownsubstances.Measure R f values.

    Coloured compounds& colourlesscompounds.

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    Separation and identification.

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    Gas - Liquid Chromatography

    G.l.c.

    Sample introduced by syringe.

    Column separates components.(Heated in oven )

    Detector monitors compoundsemerging from outlet.

    Recorder plots signals asa chromatogram.

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    What happens in practice.

    Compounds that have high affinityfor mobile phase emerge first,(most volatile).

    Chromatogram charts recorderresponse against time.

    Each component - separate peak.

    Retention time characteristic ofthe compound under givenconditions.

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    F actors affecting retention

    time:

    length of column

    packing materialtype of carrier gas

    flow rate of carrier gas

    temperature of column.

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    Interpreting the trace

    Calibration known compounds are addedto the column and conditions keptconstant.

    Amount of substance area under peak /peak height.

    Relative proportions can be determined.

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    Uses of

    G.l.c.

    Very sensitive - small quantities of substances detected, explosives, drugs etc.Separation of pure substances for collection.Can be connected to mass spectrometer for direct identification of substances.