Inductively coupled plasma atomic absorption spectrometry

Que-Hee and Boyle [70] analysed soils for total silicon using Parr bomb digestion with hydrofluoric-nitric-perchloric acid followed by inductively coupled plasma atomic absorption spectrometry. 

Until now, little attention has been given to the analysis of ancient copper alloys with LA-ICP-MS. This type of material is usually analyzed with fast or instrumental neutron activation analysis (FNAA or INAA), particle induced X-ray emission (PIXE), X-ray fluorescence (XRF), inductively coupled plasma-atomic emission spectrometry or inductively coupled plasma-atomic absorption spectrometry (ICP-AES or ICP-AAS). Some of these techniques are destructive and involve extensive sample preparation, some measure only surface compositions, and some require access to a cyclotron or a reactor. LA-ICP-MS is riot affected by any of these inconveniences. We propose here an analytical protocol for copper alloys using LA-ICP-MS and present its application to the study of Matisse bronze sculptures. 

Inductively coupled plasma atomic absorption spectrometry (Sect. 2.55) and neutron activation analysis (Sect. 2.55) have both been applied to the determination of platinum in multi-metal mixtures. 

AMS = accelerated mass spectroscopy FAAS = flame atomic absorption spectrometry GC/ED = gas chromatography/electron capture detector GFAAS graphite furnace atomic absorption spectrometry ICP-AES = inductively couples plasma-atomic absorption spectrometry NA = not applicable NAA = neutron activation analysis... 

A more recent addition to the AES family uses high temperature plasma to promote emission. Inductively coupled plasma atomic absorption spectrometry (ICP-AES) has the advantage that a wide range of elements may be measured simultaneously. However, great problems with spectral interferences restrict the value of this technique for complex mixture such as sediments. 

Inductively coupled plasma - atomic absorption spectrometry 10.0 pg/1 to 1000 mg/1... 

Inductively coupled plasma atomic emission spectrometry Electrothermal atomic absorption spectrometry High pressure liquid chromatography... 

Magnesium deficiency has been long recognized, but hypermagnesia also occurs (Anderson and Talcott 1994). Magnesium can be determined in fluids by FAAS, inductively coupled plasma atomic emission spectrometry (ICP-AES) and ICP-MS. In tissue Mg can be determined directly by solid sampling atomic absorption spectrometry (SS-AAS) (Herber 1994a). Both Ca and Mg in plasma/serum are routinely determined by photometry in automated analyzers. 

ASTM. 1998a. ASTME1613. Standard test method for analysis of digested samples for lead by inductively coupled plasma atomic emission spectrometry (ICP-AES). Flame Atomic Absorption (FAAS), or Graphite Furnace Atomic Absorption (GFAA) Techniques. American Society for Testing and Materials. 

Measurement techniques that can be employed for the determination of trace metals include atomic absorption spectrometry, anodic stripping voltammetry, differential pulse cathodic stripping voltammetry, inductively coupled plasma atomic emission spectrometry, liquid chromatography of the metal chelates with ultraviolet-visible absorption and, more recently, inductively coupled plasma mass spectrometry. 

It is seen by examination of Table 1.11(b) that a wide variety of techniques have been employed including spectrophotometry (four determinants), combustion and wet digestion methods and inductively coupled plasma atomic emission spectrometry (three determinants each), atomic absorption spectrometry, potentiometric methods, molecular absorption spectrometry and gas chromatography (two determinants each), and flow-injection analysis and neutron activation analysis (one determinant each). Between them these techniques are capable of determining boron, halogens, total and particulate carbon, nitrogen, phosphorus, sulphur, silicon, selenium, arsenic antimony and bismuth in soils. 

The analytical techniques used for additives analysis are reviewed below. They are mainly chromatographic but enzymatic, flow injection analysis, inductively coupled plasma-atomic emission spectrometry and atomic absorption methods are also used. 

Table 5.2 Summary of selected analytical methods for molecular environmental geochemistry. AAS Atomic absorption spectroscopy AFM Atomic force microscopy (also known as SFM) CT Computerized tomography EDS Energy dispersive spectrometry. EELS Electron energy loss spectroscopy EM Electron microscopy EPR Electron paramagnetic resonance (also known as ESR) ESR Electron spin resonance (also known as EPR) EXAFS Extended X-ray absorption fine structure FUR Fourier transform infrared FIR-TEM Fligh-resolution transmission electron microscopy ICP-AES Inductively-coupled plasma atomic emission spectrometry ICP-MS Inductively-coupled plasma mass spectrometry. Reproduced by permission of American Geophysical Union. O Day PA (1999) Molecular environmental geochemistry. Rev Geophysics 37 249-274. Copyright 1999 American Geophysical Union...

Other frequently used methods for determining fluoride include ion and gas chromatography [150,204,205] and aluminium monofluoride (AIF) molecular absorption spectrometry [206,207]. Less frequently employed methods include enzymatic [208], catalytic [209], polarographic [210] and voltammetric methods [211], helium microwave-induced [212] or inductively coupled plasma atomic emission spectrometry [213], electrothermal atomic absorption spectrometry [214], inductively coupled plasma-mass spectrometry [215], radioactivation [216], proton-induced gamma emission [217], near-infrared spectroscopy [218] and neutron activation analysis [219]. 

Flame AAS (often abbreviated FAAS) was until recently the most widely used method for trace metal analysis. However, it has now largely been superseded by inductively coupled plasma atomic emission spectrometry (see Chapter 4). It is particularly applicable where the sample is in solution or readily solubilized. It is very simple to use and, as we shall see, remarkably free from interferences. Its growth in popularity has been so rapid that on two occasions, the mid-1960s and the early 1970s, the growth in sales of atomic absorption instruments has exceeded that necessary to ensure that the whole face of the globe would be covered by atomic absorption instruments before the end of the century. 

A number of instrumental analytical techniques can be used to measure the total phosphorus content of organophosphorus compounds, regardless of the chemical bonding of phosphorus within the molecules, as opposed to the determination of phosphate in mineralized samples. If the substances are soluble, there is no need for their destruction and for the conversion of phosphorus into phosphate, a considerable advantage over chemical procedures. The most important methods are flame photometry and inductively coupled plasma atomic emission spectrometry the previously described atomic absorption spectrometry is sometimes useful. 

In the test method, the coal or coke to be analyzed is ashed under controlled conditions, digested by a mixture of aqua regia and hydrofluoric acid, and finally dissolved in 1% nitric acid. The concentration of individual trace elements is determined by either inductively coupled plasma-atomic emission spectrometry (ICPAES) or inductively coupled plasma-mass spectrometry (ICPMS). Selected elements that occur at concentrations below the detection limits of ICPAES can be analyzed quantitatively by graphite furnace atomic absorption spectrometry (GFAA). 

The application of inductively coupled plasma atomic emission spectrometry and graphite furnace atomic absorption spectrometry to the determination of cadmium (and molybdenum) in soils has been discussed by Baucells et al. [53]. Baucells et al. chose the 228.802 nm cadmium line because it is well resolved from the 228.763 nm iron line with the spectrometer used in this work. Background measurements could only be carried out at +0.05 nm. These workers obtained good agreement between cadmium values obtained by direct graphite furnace atomic absorption spectrometry and inductively coupled plasma atomic emission spectrometry. Chelation extraction procedures that require extensive sample handling are avoided. 

The determination of chromium is also discussed under Multi-Metal Analysis of Soils in Sect. 2.55 (atomic absorption spectrometry), Sect. 2.55 (inductively coupled plasma atomic emission spectrometry), Sect. 2.55 (emission spectrometry), Sect. 2.55 (photon activation analysis), Sect. 2.55 (neutron activation analysis), and Sect. 2.55 (differential pulse anodic stripping voltammetry). 

Kimbrough and Wakakuwa [276,330] reported on an interlaboratory comparison study involving 160 accredited hazardous materials laboratories. Each laboratory performed a mineral acid digestion on five soils spiked with arsenic, cadmium, molybdenum, selenium and thallium. The instrumental detection methods used were inductively coupled plasma atomic emission spectrometry, inductively coupled plasma mass spectrometry, flame atomic absorption spectrometry, electrothermal atomic absorption spectrometry and hydride generation atomic absorption spectrometry. At most concentrations, the results obtained with inductively coupled plasma atomic emission spectrometry... 

The most widely used spectrochemical methods are flame atomic absorption spectrometry (FAAS), electrothermal atomization atomic absorption spectrometry (ETA-AAS), and inductively coupled plasma atomic emission spectrometry (ICP-AES). Some work has been performed using inductively coupled plasma mass spectrometry (ICP-MS) and the unique properties of Hg have allowed the use of cold vapor (CV) A AS. It is beyond the scope of this chapter to describe these well-established and well-accepted spectrochemical techniques. The reader is referred to several excellent texts which describe in detail the basic principles, instrumentation, and method development of these analytical techniques [1-4]. The most toxic elements, such as As, Cd, Cr, Pb, and particularly Hg have been the most widely studied. Other metals, such as Ba, Cu, Fe, Mn, V, and Zn, have also been investigated. 

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