NAA—See Neutron activation analysis

To date, a few methods have been proposed for direct determination of trace iodide in seawater. The first involved the use of neutron activation analysis (NAA) [86], where iodide in seawater was concentrated by strongly basic anion-exchange column, eluted by sodium nitrate, and precipitated as palladium iodide. The second involved the use of automated electrochemical procedures [90] iodide was electrochemically oxidised to iodine and was concentrated on a carbon wool electrode. After removal of interference ions, the iodine was eluted with ascorbic acid and was determined by a polished Ag3SI electrode. The third method involved the use of cathodic stripping square wave voltammetry [92] (See Sect. 2.16.3). Iodine reacts with mercury in a one-electron process, and the sensitivity is increased remarkably by the addition of Triton X. The three methods have detection limits of 0.7 (250 ml seawater), 0.1 (50 ml), and 0.02 pg/l (10 ml), respectively, and could be applied to almost all the samples. However, NAA is not generally employed. The second electrochemical method uses an automated system but is a special apparatus just for determination of iodide. The first and third methods are time-consuming. 

The most frequently applied analytical methods used for characterizing bulk and layered systems (wafers and layers for microelectronics see the example in the schematic on the right-hand side) are summarized in Figure 9.4. Besides mass spectrometric techniques there are a multitude of alternative powerful analytical techniques for characterizing such multi-layered systems. The analytical methods used for determining trace and ultratrace elements in, for example, high purity materials for microelectronic applications include AAS (atomic absorption spectrometry), XRF (X-ray fluorescence analysis), ICP-OES (optical emission spectroscopy with inductively coupled plasma), NAA (neutron activation analysis) and others. For the characterization of layered systems or for the determination of surface contamination, XPS (X-ray photon electron spectroscopy), SEM-EDX (secondary electron microscopy combined with energy disperse X-ray analysis) and... 

For many years there was no sufficiently specific method for the identification of characteristic GSRs. One could not see metallic particles because of their small size (5-50 pm) and their presence was ascertained indirectly by means of colouring chemical reactions or such instrumental methods as atomic absorption spectroscopy (AAS), neutron activation analysis (NAA) or XRF. These methods, however, are... 

Before starting the preparation of the candidate CRM, a preliminary test was carried out on a small sample of 50 g wet sediment, which was dried for 15 h at 60°C, ground in a porcelain mortar, homogenized for 10 min in a Turbula mixer and subsequently analyzed for various trace metals by Neutron Activation Analysis (NAA) (see Table 11.1) and for its particle size distribution (Figure 11.1), after which the powder was examined microscopically (Figure 11.2). This semi-quantitative check was carried out to verify the initial trace element levels in order to establish whether the preparation steps listed below could be carried out free of contamination and whether the resulting material was of the required quality ... 

Methods for quantitative analysis of Co indude flame and graphite-furnace atomic absorption spectrometry (AAS e.g., Welz and Sperling 1999), inductively coupled plasma emission spectrometry (ICP-AES e.g., Schramel 1994), neutron activation analysis (NAA e.g., Versieck etal. 1978), ion chromatography (e.g., Haerdi 1989), and electrochemical methods such as adsorption differential pulse voltammetry (ADPV e.g., Ostapczuk etal. 1983, Wang 1994). Older photometric methods are described in the literature (e.g.. Burger 1973). For a comparative study of the most commonly employed methods in the analysis of biological materials, see Miller-Ihli and Wolf (1986) and Angerer and Schaller... 

Neutron activation analysis (NAA) - See Techniques for Materials Characterization, page 12-1. 

Similar processes have an important part in neutron activation analysis (NAA, see 0 Chap. 30 in Vol. 3) as well as in natural processes such as the formation of radiocarbon (see Sect. 17.17 in Chap. 17 of Vol. 2) in the atmosphere via the reaction... 

Besides XRD, other important studies are elemental analysis, either by chemical or physical methods, such as neutron activation analysis (NAA), x-ray fluorescence (XRF), or x-ray energy dispersive spectroscopy (X-EDS), for example (see Sections 7.6.1, 7.3.3, and 7.5.2, respectively) the advantage of these methods is that they are non destructive, as oppossed to wet chemical analysis. Additionally, IR spectroscopy can bring useful complementary information. Sometimes, the chemical composition is required along XRD analysis to fully identify a mineral. Also, thermal analysis (Section 7.6.5) is a useful tool in the qualitative and, sometimes, quantitative determination of clay minerals. 

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