Hydride generation-flame atomic absorption spectrometry

Kabengera, C., Bodart, P., Hubert, P., Thunus, L., Noirfalise, A. Optimization and validation of arsenic determination in foods by hydride generation flame atomic absorption spectrometry. J. AOAC Int. 85, 122-127 (2002)... 

Total dissolved Fe and Mn were analyzed directly by flame atomic absorption spectrometry (AAS). As was measured by AAS with hydride generation (HG-FIAS). Total dissolved Se concentrations were determined by hydride-generation atomic fluorescence spectrometry (Chen etal., 2005). 

Hydride generation for analytical use was introduced at the end of the 1960s using arsine formation (Marshal Reaction) in flame atomic absorption spectrometry (FAAS). A simple experimental setup for a hydride generator is shown in Figure 5.18. Today, hydride generation,91,92 which is the most widely utilized gas phase sample introduction system in ICP-MS, has been developed into... 

H. Matusiewicz and M. Krawczyk, Determination of total antimony and inorganic antimony species by hydride generation in situ trapping flame atomic absorption spectrometry a new way to (ultra)trace speciation analysis, J. Anal. At. Spectrom., 23, 2008, 43-53. 

In an interlab oratory study involving 160 accredited hazardous materials laboratories reported by Kimbrough and Wakakuwa [28], each laboratory performed a mineral acid digestion on five soils spiked with arsenic, cadmium, molybdenum, selenium and thallium. Analysis of extracts was carried out by atomic emission spectrometry, inductively-coupled plasma mass spectrometry, flame atomic absorption spectrometry and hydride generation atomic absorption spectrometry. 

Spectrometric techniques based on atomic absorption or the emission of radiation flame atomic absorption spectrometry (FAAS), electrothermal atomic absorption spectrometry (ETAAS), inductively coupled plasma-optical emission spectrometry (ICP-OES), inductively coupled plasma-mass spectrometry (ICP-MS), and cold vapor (CV)/hydride generation (HG), mainly for trace and ultratrace metal determinations. 

ETA-AAS, Electrothermal Atomization Atomic Absorption Spectrometry FAAS, Flame Atomic Absorption Spectrometry HG-AAS, Hydride Generation Atomic Absorption Spectrometry ICP-AES, Inductively Coupled Plasma Atomic Emission Spectrometry ID-MS, Isotopic Dilution Mass Spectrometry NAA, Neutron Activation Analysis Q-ICP-MS, Quadrupole Inductively Coupled Plasma Mass Spectrometry SS-Z-ETA-AAS, Solid Sampling Zeeman Atomic Absorption Spectrometry Z-ETA-AAS, Zeeman Electrothermal Atomization Atomic Absorption Spectrometry... 

Hahn MH, Kuennen RW, Caruso JA, et al. 1981. Determination of trace amounts of selenium in corn, lettuce, potatoes, soybeans, and wheat by hydride generation/condensation and flame atomic absorption spectrometry. J Agric Food Chem 29 792-796. 

Detection limits are presented for 61 elements by ten analytical determinative methods FAAS flame atomic absorption spectrometry ETAAS electrothermal atomization atomic absorption spectrometry HGAAS hydride generation atomic absorption spectrometry including CVAAS cold vapor atomic absorption spectrometry for Hg ICPAES(PN) inductively coupled plasma atomic emission spectrometry utilizing a pneumatic nebulizer ICPAES(USN) inductively coupled plasma atomic emission spectrometry utilizing an ultrasonic nebulizer ICPMS inductively coupled plasma mass spectrometry Voltammetry TXRF total reflection X-ray fluorescence spectrometry INAA instrumental activation neutron analysis RNAA radiochemical separation neutron activation analysis also defined in list of acronyms. 

Atomic absorption spectrometry, belonging to a class of techniques also defined as optical atomic spectrometry, has been for some four decades - and continues to be - one of the most important, dominant determinative techniques. It includes flame atomic absorption spectrometry (FAAS), electrothermal atomization atomic absorption spectrometry (ETAAS) (including graphite furnace AAS (GFAAS), carbon rod AAS, tantalum strip AAS), and gaseous generation (cold vapor AAS for Hg, hydride gener-... 

Metalloid compounds are usually determined by flowing-stream techniques hyphenated with hydride generation (HG)-atomic absorption or atomic fluorescence spectrometry. The continuous operation mode inherent to flow injection is specially suited for the latter detection technique as the tetrahyd-roborate reagent is a potential source of hydrogen for supporting the flame. Analyte preconcentration is frequently needed to detect the typical levels of metalloid species found in water matrices. In this context, cold trap collection of generated hydrides, sorbent extraction microcolumn methods, sorption... 

FP, flame photometry FAAS, flame atomic absorption spectrometry ETAAS, electrothermal atomic absorption spectrometry ICP-AES, inductively coupled plasma-atomic emission spectrometry ICP-MS, inductively coupled plasma-mass spectrometry HG, hydride generation CV, cold vapor AFS, atomic fluorescence spectrometry ASV, anodic stripping voltammetry PSA, potentiometric stripping... 

Numerous methods have been pubUshed for the determination of trace amounts of tellurium (33—42). Instmmental analytical methods (qv) used to determine trace amounts of tellurium include atomic absorption spectrometry, flame, graphite furnace, and hydride generation inductively coupled argon plasma optical emission spectrometry inductively coupled plasma mass spectrometry neutron activation analysis and spectrophotometry (see Mass spectrometry Spectroscopy, optical). Other instmmental methods include polarography, potentiometry, emission spectroscopy, x-ray diffraction, and x-ray fluorescence. 

Basic techniques for speciation analysis are typically composed of a succession of analytical steps, e.g. extraction either with organic solvents (e.g. toluene, dichloromethane) or different acids (e.g. acetic or hydrochloric acid), derivatisa-tion procedures (e.g. hydride generation, Grignard reactions), separation (gas chromatography (GC) or high-performance liquid chromatography (HPLC)), and detection by a wide variety of methods, e.g. atomic absorption spectrometry (AAS), mass spectrometry (MS), flame photometric detection (FPD), electron capture detection (ECD), etc. Each of these steps includes specific sources of error which have to be evaluated. 

Valkirs et al. [755,756] compared two methods for the determination of pg L 1 levels of dialkyltin and tributyltin species in marine and estuarine waters. The two methods studied were hydride generation followed by atomic absorption spectrometry and gas chromatography with flame photometric detection. Good agreement was obtained between the results of the two methods. Down to 0.0 lmg kg 1 of butyltin compounds, including tri- -butyl tin and tri-n-butyl tin oxide, could be detected. 

Maintaining the quality of food is a far more complex problem than the quality assurance of non-food products. Analytical methods are an indispensable monitoring tool for controlling levels of substances essential for health and also of toxic substances, including heavy metals. The usual techniques for detecting elements in food are flame atomic absorption spectroscopy (FAAS), graphite furnace atomic absorption spectrometry (GF AAS), hydride generation atomic absorption spectrometry (HG AAS), cold vapour atomic absorption spectrometry (CV AAS), inductively coupled plasma atomic emission spectrometry (ICP AES), inductively coupled plasma mass spectrometry (ICP MS) and neutron activation analysis (NAA). 

Whatever the analytical method and the determinand may be, the greatest care should be devoted to the proper selection and use of internal standards, careful preparation of blanks and adequate calibration to avoid serious mistakes. Today the Antarctic investigator has access to a multitude of analytical techniques, the scope, detection power and robustness of which were simply unthinkable only two decades ago. For chemical elements they encompass Atomic Absorption Spectrometry (AAS) [with Flame (F) and Electrothermal Atomization (ETA) and Hydride or Cold Vapor (HG or CV) generation]. Atomic Emission Spectrometry (AES) [with Inductively Coupled Plasma (ICP), Spark (S), Flame (F) and Glow Discharge/Hollow Cathode (HC/GD) emission sources], Atomic Fluorescence Spectrometry (AFS) [with HC/GD, Electrodeless Discharge (ED) and Laser Excitation (LE) sources and with the possibility of resorting to the important Isotope... 

The introduction of atomic absorption spectrometry in 1955 by Walsh has brought about a preferred analytical technique among clinical chemists in the field of element determinations. Flame atomic absorption atomization techniques with solution aspiration is not sufficiently sensitive (detection limits varies from 0,05-3 mg Se/L for most clinical applications where sub-mg/L concentrations are encountered. The sensivity can, however, be improved by generation of volatile selenium hydride and subsequent atomization in argon-hydrogen flames or electrically heated quartz tubes. Electrothermal atomization of solutions in graphite tubes has developed rapidly since the analytical use was first proposed and studied by L vov (1961). For most clinical chemists this technique may be the most appropriate technique to analyze samples for low concentrations of selenium. 

Atomic absorption spectrometry (AAS) is nowadays one of the most important instrumental techniques for quantitative analysis of metals (and some few metalloids) in various types of samples and matrices. The history of atomic absorption spectrometry dates back to the discovery of dark lines in the continuous emission spectrum of the sun by WoUaston in 1802. The lines are caused by the absorption of the elements in the atmosphere of the sun. His work was taken up and further pursued by Fraunhofer in 1814. In 1860, Kirchhoff and Bunsen demonstrated that the yellow hne emitted by sodium salts when introduced into a flame is identical with the so-caUed D-Hne in the emission spectrum of the sun. However, it took nearly one century before this important discovery was transferred into a viable analytical technique. In 1955, Alan Walsh published the first paper on atomic absorption spectroscopy [4]. At the same time, and independently of Walsh, AUce-made and Wilatz pubhshed the results of their fundamental AAS experiments [5, 6]. But it was the vision of Walsh and his indefatigable efforts that eventually led to the general acceptance and commercialisation of AAS instrumentation in the mid-1960s. Further instrumental achievements, such as the introduction of the graphite furnace and the hydride generation technique, in the second half of the 1960s further promoted the popularity and applicability of the technique. 

Atomic absorption spectrometry is commonly used to measure a wide range of elements as shown in Table 2. Such techniques as flame, graphite furnace, hydride generation, and cold vapor are employed. Measurements are made separately for each element of interest in turn to achieve a complete analysis these techniques are relatively slow to use. More sensitive, but also more expensive, multielement analytical techniques such as inductively coupled plasma-atomic emission spectrometry and inductively coupled plasma-mass spectrometry can be used if lower (pgl and below) detection limits are required. These detectors can also be coupled with separation systems if speciation data, e.g., Cr(III) and Cr(VI), are needed. 

Acid digestion or extraction, atomic absorption spectrometry (flame, cold vapor, hydride generation, and electrothermal), emission spectroscopy (plasma and flame), spectrophotometry, anodic stripping voltametry... 

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