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FT-IR Instrument
Components
• Source
• Michelson Interferometer
• Sample
• Detector
Sources
• Black body radiators
• Inert solids resistively heated to 1500-2200 K
• Max radiation between 5000-5900 cm-1
(2-1.7
µm), falls off to about 1 % max at 670 cm-1
(15
µm)
• Nernst Glower – cylinder made of rear earth
elements
• Globar- SiC rod
• CO2 laser
• Hg arc (Far IR), Tungsten filament (Near IR)
Michaelson Interferometer
• 1014
Hz is too fast for the rapid changes in
power to be directly measured as a
function of time.
• Can not measure the FID signal directly
• Interferometer creates a replicate
interference pattern at a frequency that is
a factor of 1010
times slower
• 104
-105
Hz can be measured electronically
• f = (2vm/c)ν = 10-10
ν, vm = 1.5 cm/s
Michaelson Interferometer
• Beam splitter
• Stationary mirror
• Moving mirror at constant velocity
• Motor driven Micrometer screw
• He/Ne laser; sampling interval, control
mirror velocity
Source
Stationary mirror
Moving mirror
Sample
Detector
Beam Splitter
PMT
HeNe laser
Sample
• Sample holder must be transparent to IR- salts
• Liquids
– Salt Plates
– Neat, 1 drop
– Samples dissolved in volatile solvents- 0.1-10%
• Solids
– KBr pellets
– Mulling (dispersions)
• Quantitative analysis-sealed cell with
NaCl/NaBr/KBr windows
Detector
• Transducers
– The heating effect of radiation
• Thermal transducer- black body, small, very low
heat capacity- ∆T=10-3
K, housed in vacuum,
signal is chopped
• Thermocouples
– Two junctions of dissimilar metals, An and Bi
– One is IR detector, one is reference detector
– Potential difference that develops in proportional to
∆T; detection of ∆Ts of 10-6
K is possible
FT-IR detectors
• Pyroelectric tranducers (PTs)
• Pyroelectric substances act as temperature-
dependent capacitors
• Triglycine sulfate is sandwiched between two
electrodes. One electrode is IR transparent
• The current across the electrodes is
Temperature dependent
• PTs exhibit fast response times, which is why
most FT instruments use them
Photoconducting transducers
• Thin film of a semi-conducting material
• IR radiation promotes non-conducting electrons
to a higher energy conducting state.
• The voltage drop across the thin film is a
measure the Power of the IR beam.
• PbS for near IR can be operated at RT
• Hg/Cd/Te can be used in the mid-IR and far IR,
but must be cooled to 77 K
• Superior response characteristics
• Great for GC-IRs
Setting up an experiment
• Factors you can control
– Spectral Resolution
– Number of scans averaged
– These combine to determine the overall time required
to collect a spectrum
Signal/Noise ratio α N1/2
If S/N ratio is 3 for 1 scan, you can expect the S/N to
increase to 30 if you collect and average 100 scans
Selectivity
• Offers much more selectivity that UV-vis
spectroscopy
• Absorption peaks are narrow in comparison and
the energies of the absorption bands are unique
for sets of functional groups
• Thus qualitative information is readily obtained
from IR spectra
• Correlation charts and compilations of IR
spectra for unknown matching
• But IR spectra do not have the specificity that
NMR spectra or electron impact mass spectra
tend to exhibit
Sensitivity
• This is perhaps the major shortcoming of
this technique when compared to
fluorescence, or especially mass
spectrometry
• However, Beer’s law type analysis are
possible and fairly routine using FT-IR
• Detection limits are in the ppm range (µM)
ATR
• Attenuated total reflectance
• More dense media to less dense media
• Complete reflectance
• Evanescent wave
• Penetrates several micrometers
IR beam
sample
Diamond tip

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Ft ir instrument

  • 2. Components • Source • Michelson Interferometer • Sample • Detector
  • 3. Sources • Black body radiators • Inert solids resistively heated to 1500-2200 K • Max radiation between 5000-5900 cm-1 (2-1.7 µm), falls off to about 1 % max at 670 cm-1 (15 µm) • Nernst Glower – cylinder made of rear earth elements • Globar- SiC rod • CO2 laser • Hg arc (Far IR), Tungsten filament (Near IR)
  • 4. Michaelson Interferometer • 1014 Hz is too fast for the rapid changes in power to be directly measured as a function of time. • Can not measure the FID signal directly • Interferometer creates a replicate interference pattern at a frequency that is a factor of 1010 times slower • 104 -105 Hz can be measured electronically • f = (2vm/c)ν = 10-10 ν, vm = 1.5 cm/s
  • 5. Michaelson Interferometer • Beam splitter • Stationary mirror • Moving mirror at constant velocity • Motor driven Micrometer screw • He/Ne laser; sampling interval, control mirror velocity
  • 7. Sample • Sample holder must be transparent to IR- salts • Liquids – Salt Plates – Neat, 1 drop – Samples dissolved in volatile solvents- 0.1-10% • Solids – KBr pellets – Mulling (dispersions) • Quantitative analysis-sealed cell with NaCl/NaBr/KBr windows
  • 8. Detector • Transducers – The heating effect of radiation • Thermal transducer- black body, small, very low heat capacity- ∆T=10-3 K, housed in vacuum, signal is chopped • Thermocouples – Two junctions of dissimilar metals, An and Bi – One is IR detector, one is reference detector – Potential difference that develops in proportional to ∆T; detection of ∆Ts of 10-6 K is possible
  • 9. FT-IR detectors • Pyroelectric tranducers (PTs) • Pyroelectric substances act as temperature- dependent capacitors • Triglycine sulfate is sandwiched between two electrodes. One electrode is IR transparent • The current across the electrodes is Temperature dependent • PTs exhibit fast response times, which is why most FT instruments use them
  • 10. Photoconducting transducers • Thin film of a semi-conducting material • IR radiation promotes non-conducting electrons to a higher energy conducting state. • The voltage drop across the thin film is a measure the Power of the IR beam. • PbS for near IR can be operated at RT • Hg/Cd/Te can be used in the mid-IR and far IR, but must be cooled to 77 K • Superior response characteristics • Great for GC-IRs
  • 11. Setting up an experiment • Factors you can control – Spectral Resolution – Number of scans averaged – These combine to determine the overall time required to collect a spectrum Signal/Noise ratio α N1/2 If S/N ratio is 3 for 1 scan, you can expect the S/N to increase to 30 if you collect and average 100 scans
  • 12. Selectivity • Offers much more selectivity that UV-vis spectroscopy • Absorption peaks are narrow in comparison and the energies of the absorption bands are unique for sets of functional groups • Thus qualitative information is readily obtained from IR spectra • Correlation charts and compilations of IR spectra for unknown matching • But IR spectra do not have the specificity that NMR spectra or electron impact mass spectra tend to exhibit
  • 13. Sensitivity • This is perhaps the major shortcoming of this technique when compared to fluorescence, or especially mass spectrometry • However, Beer’s law type analysis are possible and fairly routine using FT-IR • Detection limits are in the ppm range (µM)
  • 14. ATR • Attenuated total reflectance • More dense media to less dense media • Complete reflectance • Evanescent wave • Penetrates several micrometers IR beam sample Diamond tip