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ATOMIC
ABSORPTION
SPECTROSCOPY
ADVANCES IN CLINICAL
BIOCHEMISTRRY
Presented to:
Dr. Sibtain Ahmad
Presented by:
Kulsoom MPH-BC-22-02
Hafsa Hashmi MPH-BC-22-32
CONTENTS:
• Introduction
• Principle of AAS.
• Instrumentation.
• Applications.
INTRODUCTION:
• Atomic Absorption Spectroscopy is a very common
technique for detecting metals and metalloids in
samples.
• It is very reliable and simple technique.
• It can analyze over 62elements.
• It also measures the concentration of metals in the
sample.
HISTORY:
• The first atomic absorption spectrometer was built
by CSIRO scientist AlanWalshin1954.Showninthe
picture Alan Walsh(left) ,with a spectrometer.
PRINCIPLE:
• The technique uses basically the principle that free atoms (gas)
generated in an atomizer can absorb radiation at specific
frequency.
• Atomic-absorption spectroscopy quantifies the absorption of
ground state atoms in the gaseous state.
• The atoms absorb ultraviolet or visible light and make
transitions to higher electronic energy levels. The analyte
concentration is determined from the amount of absorption.
• Concentration measurements are usually determined from a
working curve after calibrating the instrument with standards
Of known concentration. Atomic absorption is a very common
technique for detecting metals and metalloids in environmental
samples.
THEORY:
Schematic diagram of AAS:
LIGHT SOURCE:
• Hollow Cathode Lamp are the most common radiation
source in AAS.
• It contains a tungsten anode and a hollow cylindrical
cathode made of the element to be determined.
• These are sealed in a glass tube filled with an inert gas
(neon or argon ) .
• Each element has its own unique lamp which must be
used for that analysis .
Hollow Cathode Lamp:
NEBULIZER:
• Suck up liquid samples at controlled rate and create a
fine aerosol spray for introduction into flame.
• Mix the aerosol and fuel and oxidant thoroughly for
introduction into flame.
Atomizer
• Elements to be analyzed needs to be in atomic sate.
• Atomization is separation of particles into individual
molecules and breaking molecules into atoms.
• This is done by exposing the analyte to high
temperatures in a flame or graphite furnace .
ATOMIZERS:
FLAME ATOMIZER:
• To create flame, we need to mix an oxidant gas and a
fuel
• Gas in most of the cases air-acetylene flame or
nitrous oxide-acetylene flame is used.
• liquid or dissolved samples are typically used with
flame atomizer.
FLAME ATOMIZER:
GRAPHITE TUBE ATOMIZER:
• Uses a graphite coated furnace to vaporize the sample.
• In GFAAS sample, samples are deposited in a small
graphite coated tube which can then be heated to vaporize
and atomize the analyte.
• The graphite tubes are heated using a high current power
supply.
MONOCHROMATOR:
• This is a very important part in an AA spectrometer. It is
used to separate out all of the thousands of lines.
• A monochromator is used to select the specific
wavelength of light which is absorbed by the sample, and
to exclude other wavelengths.
• The selection of the specific light allows the
determination of the selected element in the presence of
others
DETECTOR:
• The light selected by the monochromator is directed
onto a detector that is typically a photomultiplier tube ,
whose function is to convert the light signal into an
electrical signal proportional to the light intensity.
• The processing of electrical signal is fulfilled by a signal
amplifier.
• The signal could be displayed for readout.
CalibrationCurve
• A calibration curve is used to determine the unknown
concentration of an element in a solution.
• The instrument is calibrated using several solutions of known
concentrations.
• The absorbance of each known solution is measured and then a
calibration curve of concentration vs absorbance is plotted.
• The sample solution is fed into the instrument, and the absorbance
of the element in this solution is measured
• The unknown concentration of the element is then calculated
from the calibration curve.
APPLICATIONS:
• Determination of even small amounts of metals
(lead, mercury, calcium, magnesium, etc) as follows:
• Environmental studies: drinking water, ocean
water,soil.
• Foodindustry.
• Pharmaceutical industry
Any Question???
Thank you

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ATOMIC absorption spectrometery.pptx

  • 2. ADVANCES IN CLINICAL BIOCHEMISTRRY Presented to: Dr. Sibtain Ahmad Presented by: Kulsoom MPH-BC-22-02 Hafsa Hashmi MPH-BC-22-32
  • 3. CONTENTS: • Introduction • Principle of AAS. • Instrumentation. • Applications.
  • 4. INTRODUCTION: • Atomic Absorption Spectroscopy is a very common technique for detecting metals and metalloids in samples. • It is very reliable and simple technique. • It can analyze over 62elements. • It also measures the concentration of metals in the sample.
  • 5. HISTORY: • The first atomic absorption spectrometer was built by CSIRO scientist AlanWalshin1954.Showninthe picture Alan Walsh(left) ,with a spectrometer.
  • 6. PRINCIPLE: • The technique uses basically the principle that free atoms (gas) generated in an atomizer can absorb radiation at specific frequency. • Atomic-absorption spectroscopy quantifies the absorption of ground state atoms in the gaseous state. • The atoms absorb ultraviolet or visible light and make transitions to higher electronic energy levels. The analyte concentration is determined from the amount of absorption. • Concentration measurements are usually determined from a working curve after calibrating the instrument with standards Of known concentration. Atomic absorption is a very common technique for detecting metals and metalloids in environmental samples.
  • 9. LIGHT SOURCE: • Hollow Cathode Lamp are the most common radiation source in AAS. • It contains a tungsten anode and a hollow cylindrical cathode made of the element to be determined. • These are sealed in a glass tube filled with an inert gas (neon or argon ) . • Each element has its own unique lamp which must be used for that analysis .
  • 11. NEBULIZER: • Suck up liquid samples at controlled rate and create a fine aerosol spray for introduction into flame. • Mix the aerosol and fuel and oxidant thoroughly for introduction into flame.
  • 12. Atomizer • Elements to be analyzed needs to be in atomic sate. • Atomization is separation of particles into individual molecules and breaking molecules into atoms. • This is done by exposing the analyte to high temperatures in a flame or graphite furnace .
  • 14. FLAME ATOMIZER: • To create flame, we need to mix an oxidant gas and a fuel • Gas in most of the cases air-acetylene flame or nitrous oxide-acetylene flame is used. • liquid or dissolved samples are typically used with flame atomizer.
  • 16. GRAPHITE TUBE ATOMIZER: • Uses a graphite coated furnace to vaporize the sample. • In GFAAS sample, samples are deposited in a small graphite coated tube which can then be heated to vaporize and atomize the analyte. • The graphite tubes are heated using a high current power supply.
  • 17. MONOCHROMATOR: • This is a very important part in an AA spectrometer. It is used to separate out all of the thousands of lines. • A monochromator is used to select the specific wavelength of light which is absorbed by the sample, and to exclude other wavelengths. • The selection of the specific light allows the determination of the selected element in the presence of others
  • 18. DETECTOR: • The light selected by the monochromator is directed onto a detector that is typically a photomultiplier tube , whose function is to convert the light signal into an electrical signal proportional to the light intensity. • The processing of electrical signal is fulfilled by a signal amplifier. • The signal could be displayed for readout.
  • 19. CalibrationCurve • A calibration curve is used to determine the unknown concentration of an element in a solution. • The instrument is calibrated using several solutions of known concentrations. • The absorbance of each known solution is measured and then a calibration curve of concentration vs absorbance is plotted. • The sample solution is fed into the instrument, and the absorbance of the element in this solution is measured • The unknown concentration of the element is then calculated from the calibration curve.
  • 20. APPLICATIONS: • Determination of even small amounts of metals (lead, mercury, calcium, magnesium, etc) as follows: • Environmental studies: drinking water, ocean water,soil. • Foodindustry. • Pharmaceutical industry