Editing Atomic absorption spectroscopy (section)

==== Flame atomizers ====
The oldest and most commonly used atomizers in AAS are flames, principally the air-acetylene flame with a temperature of about 2300&nbsp;°C and the nitrous oxide<ref name="Koirtyohann1991" /> system (N<sub>2</sub>O)-acetylene flame with a temperature of about 2700&nbsp;°C. The latter flame, in addition, offers a more reducing environment, being ideally suited for analytes with a high affinity to oxygen.

[[File:FP8800GM.jpg|thumb|A laboratory flame photometer that uses a propane operated flame atomizer]]

Liquid or dissolved samples are typically used with flame atomizers. The sample solution is aspirated by a pneumatic [[analytical nebulizer]], transformed into an [[aerosol]], which is introduced into a spray chamber, where it is mixed with the flame gases and conditioned in a way that only the finest aerosol droplets (< 10&nbsp;μm) enter the flame. This conditioning process reduces interference, but only about 5% of the aerosolized solution reaches the flame because of it.

On top of the spray chamber is a burner head that produces a flame that is laterally long (usually 5–10&nbsp;cm) and only a few mm deep. The radiation beam passes through this flame at its longest axis, and the flame gas flow-rates may be adjusted to produce the highest concentration of free atoms. The burner height may also be adjusted so that the radiation beam passes through the zone of highest atom cloud density in the flame, resulting in the highest sensitivity.

The processes in a flame include the stages of desolvation (drying) in which the solvent is evaporated and the dry sample nano-particles remain, [[vaporization]] (transfer to the gaseous phase) in which the solid particles are converted into gaseous molecule, atomization in which the molecules are dissociated into free atoms, and [[ionization]] where (depending on the ionization potential of the analyte atoms and the energy available in a particular flame) atoms may be in part converted to gaseous ions.

Each of these stages includes the risk of interference in case the degree of phase transfer is different for the analyte in the calibration standard and in the sample. Ionization is generally undesirable, as it reduces the number of atoms that are available for measurement, i.e., the sensitivity.

In flame AAS, a steady-state signal is generated during the time period when the sample is aspirated. This technique is typically used for determinations in the mg L<sup>−1</sup> range and may be extended down to a few μg L<sup>−1</sup> for some elements.