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Understanding Infrared Spectroscopy

Brief introduction about it spectrophotometry

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0% found this document useful (0 votes)
51 views39 pages

Understanding Infrared Spectroscopy

Brief introduction about it spectrophotometry

Uploaded by

f2pmaster000
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPT, PDF, TXT or read online on Scribd

INFRARED SPECTROSCOPY

What is IR light?
Is a kind of electromagnetic radiation
which has wave region longer than
visible light, but shorter than radio
wave.
Low energy
What is IR region?

The wavelength region is 2.5-25 µm


The unit commonly used is
wavenumbers (cm-1 ) i.e. 4000-400
cm-1
Remember that Wavenumber is
proportional with energy (E) and
frequency (v), but reciprocal with
wavelength.
Light & Electromagnetic Spectrum
IR Application
Broadly applied in several area sort
of :
- Army
- Fire man
- Veterinary
- Pharmacy
- Electronic devices
- Remote sensing
IR spectrum
Divided into 3 regions
1. Near Infrared
2. Middle Infrared
3. Far Infrared
SPECTRUM IR
Ranges Far Middle Near
Infrared Infrared Infrared

Wavelength 50-1000µm 2.5-50µm 0.8-2.5µm


range

Wavelength 200-10cm-1 4000- 12500-4000


number 200cm-1 cm-1

Energy 0.025- 0.5-0.025eV 1.55-0.5eV


range 0.0012eV
Principles
When the certain molecules are exposed
to IR light, it will absorb the energy to
make the atoms of molecules vibrating
The vibration frequency depend on the
amount of atoms and the length and the
strength of atomic bonding
Molecule vibration is stimulated by
absorption radiation in the same
frequency with the frequency of its origin
vibrations
Energy Trends
Energy follows vibration frequency of atoms
-light atoms vibrate more rapidly: -CH, NH,
OH vibrations . 2800 cm-1
Multiple bonds vibrate more rapidly:
triple bonds : C≡C (2100-2200), C≡N
(2240- 2280)
Double bonds : C=O (1680-1750), C=C
(1620-1680)
Single bond : C-O (1025-1200)
Intensity Trends
Follows change in dipole caused by
vibrating atoms
– Polar bonds (strong bond dipoles) absorb
strongly
O-H
C=O, C=N
C-O
– Nonpolar bonds absorb weakly
C=C, C≡C
Follows overlapping bands
– CH bands tend to overlap
– Molecules contain many CH
– CH absorptions tend to be strong
PRINCIPLES
For each molecules, there is a
various kind of vibration occurs
What kind of sample be able to
absorb IR radiation?
Only vibration which alters molecule dipole
moment and having the IR absorption frequency
in the IR region

Gas molecules such as O2, H2 and Cl2 don’t have a


dipole moment, means no IR absorption occurs

SO2 and CO2 have a dipole moment so it will give


IR absorption
Every functional group has their own IR
absorption
The more complex in molecule structure,
the more complex in IR absorption
It is used to identify any functional group
presents in a molecule structure
IR Spectrum Distribution
1. 4000-2500 cm-1, absorption of atom
which is bond to H atom, ex: C-H, O-H
and N-H
2. 2500-2000 cm-1, triple bond, ex: C≡C ,
C≡N
3. 2000-1500 cm-1, double bond, ex: C=O,
C=C, C=N
4. 1500-400 cm-1, an absorption that
involves the deformation of other
bondings
Fingerprint region (<1500 cm-1)
Many bands & many overlaps
– Heavy atom stretches
– All bends, etc.
– Should have simple molecule (or other
evidence or structure) before intepreting
bands in this region
Overall pattern reflects molecular
structure
– Pattern from 1400-600 = molecular
fingerprints
Prosedure

IR light is passed through the sample, and the amount of energy which is
absorbed by the sample per cm wavelength will be recorded .
The IR light desired will be selected by monochromator before exposed to
the sample’ Interferometer is used for measuring all wavelength in one
running time.
The data will be translated into the graph which is plotted as wavelength
vs transmision
The graph might be compared to known standard reference
Instrumentation
Conventional method(dispersive
instrument)
– The monochromator being used to
select frequency of one radiation in one
time through the sample.
Peralatan
Spektrometer FTIR (Fourir Transform IR)
– Semua frekuensi yang diperlukan melalui instrument sekaligus
– Menggunakan interferometer contohnya Michelson Interferometer
– Teknik cepat dan pantas
– Digunakan dikebanyakan makmal kimia
Animation of FTIR
IR Components
A. IR Resources
– Quartz halogen
Nernst Glower lamp (run at 2000oC)
– Globar (made from Carbide silicon, run
at 1100oC)
IR Components
B. sample
1. solids
– A. Nujol mull
The sample is ground using a mortar and pestle to
give a very fine powder
A small amount is then mixed with nujol (liquid
paraffin) togive a paste
Several drops of this paste are then applied between
two sodium chloride plates (these do not absorb
infrared in the region of interest)
The plates are then place in the instrument sample
holder ready for scanning
IR Components
B. Potassium Bromide disk
– A verry small amount of the solid
(approximately 1-2 mg) is added to pure
potassium bromide powder (approximately 200
mg) and ground up as fine as possible
– This is then placed in a small die and put under
pressure mechanically. The pressure is
maintained for several minutes before
removing the die and the KBr disk formed
– The disk is then placed in a sample holder
ready scanning
Sample preparation
Sample preparation
2. thin films
– The infrared spectrum of thin film can be easily obtained
by placing a sample in a suitable holder, such as a card
with a slot cut for the sample window
– This method is often used for checking the calibration of
an instrument with a polystrirene sample as the band
produced by this material are accurately known
3. liquids
– This is possibly the simplest and the common method
for sample preparation
– A drop of the sample is placed between two potassium
bromide or sodium chloride circular plates to produce a
thin capillary film
– The plates are then placed in a holder ready for analysis
Sample preparation
4. gases
– To obtaine an infrared spectrum of a gas
requires the use of a cylindrical gas cell
with windows at each end composed of
an infrared inactive material such as
KBr, NaCl or CaF2
– The cell usually has an inlet and outlet
port with atap to enable the cell to be
easilly filled with the gas to be analyzed
instrumentation
C. monochromator/interferometer
– Break down the radiation of light to the
different wave region in one time
running process.
D. detector
– CCD (charge couple device)
– InGaAs (Indium Gallium Arsen)
– Pbs (Lead sulfide)
Instrumentation
Display
– Exhibit the collected data
– Translate the data to the graph
– The graph is plotted as transmision vs
frequnecy (wavenumbers)
Advantages
Provide the fingerprint for the sample
being analyzed
The installation of instrument to the
computer allows the comparison of
sample spectrum and standard
reference can be run simultaneously
Disadvantages
Rarely used for quantitative purpose
since the spectrum produced is too
complicated to determine one by one
The sample preaparation is quite
difficult, needs the skill to handle it.
aniline
phenol
Salycilic acid
ethanol
Contoh spektrum
allopurinol
phenytoin
References
David G. watson (2005).
Pharmaceuthical Analysis. Second
edition. Pp:115-128
[Link] [Link]./wiki/Infrared
spectroscopy
[Link]
~orglabs/procedures/Infrared
Spectroscopy/ir/IR%[Link]

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