Why do we have to vapourise the metal ions in AAS before they will absorb light energy? It seems that in UV Vis spec, the compounds will absord light energy without being vapourised.
Please explain the vapourisation process in AAS
Thank you.
As psyxwar has hinted, AAS works only if what you're analysing absorbs at the same wavelength as that which is emitted from a metal lamp. These metal lamps themselves only work on pure metals. What your flame does is reduce the metal ions to elemental form. In UV Vis, you're analysing for the metal ions; in AAS, you're analysing for the metal atom. UV Vis would be using different wavelengths to AAS. Problem with UV Vis is that you'd have to run a test of which wavelengths in solution would be absorbed well as these can change even if the ion is the same.
As anyone doing uni chem would know, copper (II) nitrate dissolved in water has a distinctly different colour to [Cu(NH
3)
6](NO
3)
2 (aq). So, using UV Vis, you would have to scan and find the right wavelength. Using AAS, you just inject the sample without any extra modifications.
I've done AAS; it is REALLY simple xD