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Experiment 5:

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Objectives To learn the separation technique of column chromatography. ... Mix slurry Add slurry Drain solvent COLUMN CHROMATOGRAPHY: Loading the column ... – PowerPoint PPT presentation

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Title: Experiment 5:


1
Experiment 5
  • COLUMN CHROMATOGRAPHIC PURIFICATION OF
    NITROANILINES

2
Objectives
  • To learn the separation technique of column
    chromatography.
  • To separate constitutional isomers of
    o-nitroaniline from p-nitroaniline using this
    technique.
  • To analyze the purity of the isolated compounds
    using TLC and HPLC.

3
Before coming to lab
  • Prepare the Pre-lab notebook entry for this
    experiment!
  • It is highly recommended that you watch a short
    video prior to coming to lab! Simply copy and
    paste the following link into your address bar
  • http//www.youtube.com/watch?vEytuRMS1154feature
    related
  • Please note that this is an example of how column
    chromatography experiments are performed,
    however our procedure may be slightly different.

4
TLC VS.COLUMN CHROMATOGRAPHY
Polar components (b) adsorb more strongly to the
polar silica gel and elute after the less polar
components, which move more quickly with the
non-polar (relative to silica gel) solvent.
5
COLUMN CHROMATOGRAPHYGeneral Procedure
  • Prepare column
  • Load column
  • Develop column
  • Collect fractions
  • Analyze fractions

6
OVERVIEW
  • Run column to separate the nitroaniline compounds
    from one another.
  • Collect the compounds in separate test tubes as
    they elute from the column.
  • Perform a TLC experiment to determine which test
    tubes contain pure o-nitroaniline and which
    contain pure p-nitroaniline.
  • Combine pure p-nitroaniline fractions in one
    container, combine pure o-nitroaniline fractions
    in another.
  • Evaporate solvent to concentrate samples.
  • Prepare an HPLC vial of each sample and submit
    for analysis.

7
COLUMN CHROMATOGRAPHYPreparing the column
  • MATERIALS
  • 50 mL SOLVENT 1
  • 30 mL SOLVENT 2
  • 20 mL SOLVENT 3
  • 20 cc SiO2 gel

8
COLUMN CHROMATOGRAPHYPreparing the column
Mix slurry
Add slurry
Drain solvent
9
COLUMN CHROMATOGRAPHYLoading the column
Add concentrated sample solution with spiraling
motion
Rinse sides of column with solvent to remove
excess sample
Allow column rinse to load into silica gel
10
COLUMN CHROMATOGRAPHYDeveloping the column
SLOWLY add solvent to column to elute compounds
11
COLUMN CHROMATOGRAPHYCollecting fractions
  • Once individual fractions are collected, you
    will perform a TLC experiment to determine which
    test tubes contain which nitroaniline compound.
  • You should prepare ONE TLC plate, with up to 7
    lanes per plate.
  • Remember to apply the original sample mixture
    solution as your standard.

12
COLUMN CHROMATOGRAPHYAnalyzing fractions by TLC
  • In order to evaluate the success of the
    separation after the column, TLC analysis is
    performed.
  • By applying the original nitroaniline mixture
    solution (STD) along with the sample solutions
    from the individual fractions collected, the
    fractions containing pure compounds can be
    identified.
  • Once the pure fractions are identified, they
    will be combined in an effort to produce a pure
    sample of each nitroaniline compound for further
    analysis.
  • Since the UV detector on the HPLC is more
    sensitive than the human eye, HPLC analysis will
    be performed on the samples prepared after TLC
    analysis to ensure the correct fractions were
    combined during the experiment.

13
TABLE 5.1
Compound Standard Rf Value Rf value Fraction 1 Rf value Fraction 2 Rf value Fraction 3 Rf value Fraction 4 Rf value Fraction 5 Rf value Fraction 6
o-nitroaniline
p-nitroaniline
  • Rf values are unit less and 2 decimal places
    ONLY!
  • Individual fractions may contain a single
    compound or both compounds as the column
    proceeds.
  • Fractions containing a single compound are
    considered PURE fractions, while those containing
    both compounds are considered MIXED (IMPURE)
    fractions.

14
HPLC SAMPLE PREPARATION
  • Place a small amount of crystals of each purified
    sample into a small auto analyzer vial. Add 1 mL
    of HPLC solvent.
  • Place sample vial into vial slot in sample tray
    and sign out on vial slot sheet.
  • Any samples with visible solid in them will be
    DISCARDED!

15
HPLC SAMPLE PREPARATION
HPLC sample prep area located in balance room
To operate dispenser on solvent bottle, pull up
on plunger and push down SLOWLY!
16
TABLE 5.2
Compound Standards Component 1 Component 1 Component 2 Component 2
Compound Rt (min) Rt (min) HPLC Area Rt (min) HPLC Area
o-nitroaniline
p-nitroaniline
  • Samples containing a single compound are
    considered PURE samples, while those containing
    both compounds are considered MIXED (IMPURE)
    samples.
  • Be sure to attach both sample chromatograms to
    final lab report!

17
SAFETY CONCERNS
  • Ethyl acetate and hexane are flammable. Never
    use these solvents around an open flame or hot
    hot plate.
  • o-nitroaniline and p-nitroaniline are toxic if
    ingested or inhaled. Wear safety goggles all
    times during the experiment!
  • GLOVES are available upon request.

18
WASTE MANAGEMENT
  • Place all liquid waste into the container marked
    LIQUID ORGANIC WASTE.
  • Place used TLC capillaries in the broken glass
    container.
  • Place TLC plates in yellow solid waste trashcan
    under the supply hood.
  • Leave the columns containing SiO2 gel suspended
    in hood.

19
For Next Lab
  • Lab Quiz 1 will be given at the beginning of
    lab.
  • We will do Experiment 3 after the lab quiz.
  • There is NO pre-lab notebook entry for Experiment
    3!
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