Double Beam spectrometer - PowerPoint PPT Presentation

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Double Beam spectrometer

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... A 2 Plot versus concentration Use to asses purity of ... sample of DNA you have ... Slide 11 Slide 12 Slide 13 Absorbance ratios and differences Applications ... – PowerPoint PPT presentation

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Title: Double Beam spectrometer


1
Double Beam spectrometer
  • Provides a signal that is largely free of drift
    in the source and detector without requiring
    really expensive components
  • Beam alternates very fast between sample and
    reference cells.
  • Dont need to keep zeroing

2
Sample Cells
  • Usually 1 cm pathlength
  • Glass visible
  • Quartz UV
  • Plastic disposable beware solvents
  • 5 cm or 10 cm for dilute samples
  • Smaller cells for small samples
  • Flow through cells
  • Temperature control
  • Gas cells longer
  • Fibre optic probes

3
Fibre Optics
  • Fibres of glass, usually about 120 µm in
    diameter.

4
Fibre Optic Probe
5
Derivative Spectroscopy
  • Can determine flat maxima more precisely
  • Isolate shoulders
  • Distinguish weak signals from background

6
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7
Photometric Titration
Solution 2 x 10-3 M in Bi3 and Cu2 Titrant
EDTA At 745 nm, neither cation, nor reagent,
absorbs Bi complex forms first more stable
but doesnt absorb The cu complex does absorb at
745 nm
8
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9
Reaction rates
  • Following enzyme kinetics
  • Determine enzymes
  • Determine substrates

10
Stop Flow Methods
  • For fast reactions
  • Two syringes driven at same rate
  • Solutions flow into mixing chamber
  • When plunger hits stop, measurement starts
  • Generally measure initial rates of reactions

11
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12
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13
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14
Absorbance ratios and differences
  • Measure A at two ?
  • Use A1/A2 or A1 A 2
  • Plot versus concentration
  • Use to asses purity of samples to check just
    one component is present
  • Eg ratio of A 260 nm A 280 nm indicates how pure
    A sample of DNA you have.

15
Applications
  • Metal ion analysis
  • eg iron II or III
  • React with ligands to get intense colours
  • Reduce Fe III with hydroxylamine or hydroquinone
    etc
  • Can extract the complexes into isoamyl alcohol
    for a cleanup/preconcentration step
  • 0.1 - 0.005 µg/mL are typical LODs

16
Organic/Biologicals
  • Most common application
  • Many absorb strongly
  • May need to derivatize
  • eg alcohol with phenyl isocyanate to give alkyl
    carbamates 280 nm
  • Free amino acids react with ninhydrin
    blue/purple 575 nm aa analyzers

17
Automated clinical methods
  • Many samples/hour
  • Expensive to buy
  • Can run many samples unattended

18
Centrifugal Analysis
  • Combines robotic pipettors
  • Centrifuge
  • Spectrophotometer
  • Computer
  • Increases sample throughput
  • Reduces volume of sample and reagents

19
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20
  • Eliminates chemistry changeover time
  • No set-up equilibrium time
  • Used for water quality measurements
  • Based on standard procedures
  • Liquids are dispensed into separate compartments
    attached to the cuvettes
  • Cuvettes are round a rotor. When rotor is spun,
    reagents are propelled into cuvettes.
  • All reactions start together good for kinetics

21
  • Samples and standards are mixed and run in
    parallel.
  • Identical conditions are ensured for all cuvettes
  • Can analyze 110 samples/hour
  • Rotor spins at 2000 revolutions /min
  • Get an average of 7 readings/sample

22
Water Pollution Analysis
  • Molybdenum blue method
  • (NH4)3 P (Mo3O10)4 yellow
  • Reduce with hydroquinone, Sn II or Fe II
  • Get a polymer of Mo of different oxidation states
  • Not stoichiometrically well-defined but is blue
  • As, Si interfere so they can also be determined
    this way

23
Air Pollution Analysis- SO2
  • Collect by bubbling through 0.1 M sodium
    tetrachloromercurate
  • HgCl42- 2SO2 2H2O ? Hg(SO3)22-
    4Cl- 4H
  • Treat with formaldehyde and p-rosaniline to give
    red-violet colour 569 nm
  • 0.005 ppm by volume
  • NO2 interferes above 2 ppm

24
Advantages Visible
  • Less interferences
  • Often higher molar absorptivities
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