Graphite furnace atomic absorption spectrometry (GFAAS) is also known by various other acronyms, including electrothermal atomic absorption spectrometry (ETAAS). Briefly, the technique is based on the fact that free atoms will absorb light at frequencies or wavelengths characteristic of the element of interest (hence the name atomic absorption spectrometry). Within certain limits, the amount of light absorbed can be linearly correlated to the concentration of analyte present. Free atoms of most elements can be produced from samples by the application of high temperatures. In GFAAS, samples are deposited in a small graphite tube, which can then be heated to vaporise and atomize the analyte. The atoms absorb ultraviolet or visible light and make transitions to higher electronic energy levels. Applying the Beer-Lambert law directly in AA spectroscopy is difficult due to variations in the atomization efficiency from the sample matrix, and nonuniformity of concentration and path length of analyte atoms (in graphite furnace AA). Concentration measurements are usually determined from a working curve after calibrating the instrument with standards of known concentration.
GFAA spectrometry instruments have the following basic features: 1. a source of light (lamp) that emits resonance line radiation; 2. an atomization chamber (graphite tube) in which the sample is vaporized; 3. a monochromator for selecting only one of the characteristic wavelengths (visible or ultraviolet) of the element of interest; 4. a detector, generally a photomultiplier tube (light detectors that are useful in low-intensity applications), that measures the amount of absorption; 5. a signal processor-computer system (strip chart recorder, digital display, meter, or printer).
Mode Of Operation
Most currently available GFAAs are fully controlled from a personal computer that has Windows-compatible software. Aqueous samples should be acidified (typically with nitric acid) to a pH of 2.0 or less. Discoloration in a sample may indicate that metals are present in the sample. For example, a greenish colour may indicate a high nickel content, or a bluish colour may indicate a high copper content. A good rule to follow is to analyze clear samples first, and then analyze coloured samples. It may be necessary to dilute highly coluored samples before they are analyzed.
After the instrument has warmed up and been calibrated, a small aliquot (usually less than 100 microliters (μL) and typically 20 μL) is placed, either manually or through an automated sampler, into the opening in the graphite tube. Click to see a cross-sectional view of a graphite tube The sample is vaporized in the heated graphite tube; the amount of light energy absorbed in the vapor is proportional to atomic concentrations. Analysis of each sample takes from 1 to 5 minutes, and the results for a sample is the average of triplicate analysis.