Abstract
Iodine is a chemical element with critical physiological roles and its determination using instrumental analysis is not trivial. Inductively coupled plasma spectrometry associated with either optical emission (ICP-OES) or mass spectrometry (ICP-MS) may be employed, but each alternative presents limitations considering iodine behavior in argon plasma and the occurrence of interferences. Sample preparation is also a critical issue when using sample introduction by pneumatic nebulization due to memory effects. This critical review discusses the literature dealing with sample preparation followed by ICP-OES or ICP-MS for iodine determination in a plethora of samples. It is shown that the best figures of merit may be reached using sample preparation in alkaline medium followed by ICP-MS measurements.
Notes
aLOD: limit of detection.
bCRMs: certified reference materials.
cMultiwave: pressure and temperature controlled equipment for microwave-assisted sample digestion in closed vessels.
dPMD: pressure controlled equipment for microwave-assisted sample digestion in closed vessels.
eHPA: high-pressure asher.
fTMAH: tetramethylammonium hydroxide.
gIS: internal standard.
hNAA: neutron activation analysis.
iTXRF: total reflection X-ray fluorescence.
jCFA-C: water-soluble tertiary amines.
kPC-NAA: pre-irradiation combustion-neutron activation analysis.
mSAM: standard additions method.
aLOD: limit of detection.
bCRMs: certified reference materials.
cSAM: standard additions method.
dIS: internal standard.