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Atomic Absorption and Atomic Fluorescence Spectrometry

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Presentation on theme: "Atomic Absorption and Atomic Fluorescence Spectrometry"— Presentation transcript:

1 Atomic Absorption and Atomic Fluorescence Spectrometry
Chapter 9 Atomic Absorption and Atomic Fluorescence Spectrometry

2 Atomic Spectroscopy Atomization is by far the most critical step in atomic spectroscopy. In AAS and AFS there are two factors involved. The intensity of light source. The probability of transition.

3 Flame Atomization

4 Flame Structure

5 Flame Atomizer

6 Flame Atomizer

7 Electrothermal Atomizers
Graphite furnace atomic absorption spectrometry (GFAAS) is also known by various other acronyms, including electrothermal atomic absorption spectrometry (ETAAS). An ideal graphite furnace should fulfill the following requirements: A constant temperature in time and space during the interval in which free atoms are produced Quantitative atom formation regardless of the sample composition Separate control of the volatilization and atomization processes High sensitivity and good detection limits A minimum of spectral interferences

8 Specialized Atomization Techniques
Glow Discharge Atomization Hydride Atomization Cold-Vapor Atomization

9 Flame Atomic Absorption Spectroscopy

10 Radiation Sources Doppler Broadening Pressure Broadening
Electrodeless Discharge Lamps Source Modulation Hollow Cathode Lamps:

11 Spectrophotometers In general, the instrument must contain:
Narrow bandwidth to isolate the line chosen for measurement Sufficient glass filter Interchangeable interference filters Good-quality ultraviolet/visible monochromators Photomultiplier tubes

12 Spectrophotometers Single-Beam Double-Beam

13 Spectral Interferences
The Two-Line Correction Method The Continuum-Source Correction Method Background Correction Based on the Zeeman Effect Background Correction Based on the Source Self-Reversal

14 Chemical Interference
The equilibria of principle interest include: Formation of Compounds of Low Volatility Dissociation Reactions Ionization

15 Calibration Curves Should follow Beer’s Law

16 Standard Addition Method

17 Instrumentation Sources:
Hollow Cathode Lamp- only observed the fluorescent signal during pulses Electrodeless Discharge Lamp- produced intensities that exceed those of hollow cathode lamps Lasers- ideal source with high intensities and narrow bandwidths

18 Instrumentation Dispersive Instruments- They are made up of a modulated source, an atomizer, a monochromator or an interference filter system, a detector, and a signal processor and readout.  Nondispersive Instruments- They ideally are made up of a source, an atomizer, and a detector. Advantages: Simplicity and low-cost instrumentation Ready adaptability to multi-element analysis High-energy throughput and thus high sensitivity Simultaneous collection of energy from multiple lines, enhancing sensitivity

19 References www.anachemumu.se.htm www.aurora-instr.com/right.htm

20 References www.dq.fct.unl.pt/QOF/Chroma.html www-ssg.chem.utas.edu.au/


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