Inductively coupled plasma mass spectrometry sample preparation

Brown,]. A., Kunz, F.W., and Belitz, R. K. (1991). Characterization of automotive catalysts using inductively coupled plasma mass spectrometry Sample preparation.J. /4 [Pg.199]

Gold is a useflil caUbration standard for this method (see Radioactive tracers). Whereas similar sensitivities can be achieved by inductively coupled plasma mass spectrometry (qv), the latter requires more extensive sample preparation to overcome interference by other metals such as copper (64). 

The very low Hg concentration levels in ice core of remote glaciers require an ultra-sensitive analytical technique as well as a contamination-free sample preparation methodology. The potential of two analytical techniques for Hg determination - cold vapour inductively coupled plasma mass spectrometry (CV ICP-SFMS) and atomic fluorescence spectrometry (AFS) with gold amalgamation was studied. 

The complex of the following destmctive and nondestmctive analytical methods was used for studying the composition of sponges inductively coupled plasma mass-spectrometry (ICP-MS), X-ray fluorescence (XRF), electron probe microanalysis (EPMA), and atomic absorption spectrometry (AAS). Techniques of sample preparation were developed for each method and their metrological characteristics were defined. Relative standard deviations for all the elements did not exceed 0.25 within detection limit. The accuracy of techniques elaborated was checked with the method of additions and control methods of analysis. 

Detailed examination of another madder preparation proved that the sample can be premordanted with alum. [ 19] After hydrolysis performed with hydrochloric acid and extraction with M-amyl alcohol, only four colourants are found alizarin, purpurin, and probably lucidin and ruberythric acid. Additionally, signals at m/z 525 and 539 are observed in the mass spectrum. Analysis of the preparation by inductively coupled plasma mass spectrometry (ICP MS) shows that aluminium and calcium are the main inorganic components of the sample. This is why it was suggested that the signal at m/z 539 can be attributed to the complex of aluminium with alizarin, and the second one, observed at m/z 525, to an aluminium-calcium cluster. 

Techniques for analysis of different mercury species in biological samples and abiotic materials include atomic absorption, cold vapor atomic fluorescence spectrometry, gas-liquid chromatography with electron capture detection, and inductively coupled plasma mass spectrometry (Lansens etal. 1991 Schintu etal. 1992 Porcella etal. 1995). Methylmercury concentrations in marine biological tissues are detected at concentrations as low as 10 pg Hg/kg tissue using graphite furnace sample preparation techniques and atomic absorption spectrometry (Schintu et al. 1992). 

Soil samples were wet sieved into (a) 2-4 mm, (b) 1-2 mm, (c) 0.5-1 mm, (d) 250-500 i m, (e) 125-250 am, (f) 63-125 j,m and (g) <63 j.m fractions. A ferruginous/magnetic fraction (m) was also prepared from the 2-4 mm fraction. Soil fractions were crushed, digested with HNO3/HCI/HF/HCIO4 and then analysed by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) for Al, Ca, Cu, Fe, K, Mn, Na, P, S and Zn. Inductively Coupled Plasma Mass Spectrometry (ICP-MS) was used to determine Ag, As, Cd, Pb and Sb because of the lower detection limits by this method. The mineralogy of selected samples was determined by qualitative X-ray diffractometry. 

Inductively coupled plasma-mass spectrometry (ICP-MS) has been utilized as a bulk technique for the analysis of obsidian, chert and ceramic compositional analyses 12-14). However, due to the high level of spatial variation of ceramic materials, increased sample preparation is necessary with volatile acids coupled with microwave digestion (MD-ICP-MS) to properly represent the variability of ceramic assemblages IS, 16). Due to the increased sample preparation and exposure to volatile chemicals, researchers have continued to utilize neutron activation analysis (INAA) as the preferred method of chemical characterization of archaeological ceramics (77). 

A. P. Vonderheide, M. Montes-Bayon, J. A. Caruso, Solid-phase microextraction as a sample preparation strategy for the analysis of seleno amino acids by gas chromatography D inductively coupled plasma mass spectrometry,Analyst, 127 (2002), 49D53. 

Several isotopes (see Isotopes Isotope Labeling) of Cd are known, and 8 are stable (Table 3). For " Cd and " Cd, the nnclear spin is 1/2 and they are used for NMR studies of Cd compounds and in biological fields (see Cadmium Organometallic Chemistry). " Cd is used in the nuclear industry because of its high neutron cross section. Unstable isotopes are prepared from nuclear reactions. Cd stable isotope composition in geological and meteorite samples has been investigated using multiple collector inductively coupled plasma mass spectrometry. ... 

Kingston, H.M., Walter, P.J. The art and science of microwave sample preparations for trace and ultratrace elemental analysis. In Montaser, A. (ed.) Inductively Coupled Plasma Mass Spectrometry, pp. 33-81. Wiley-VCH, New York (1998)... 

E.W. Hoppe, et al., "Use of Electrodeposition for Sample Preparation and Rejection Rate Prediction for Assay of Electroformed Ultra High Purity Copper for Th and U Prior to Inductively Coupled Plasma Mass Spectrometry," submitted for publication to J. Radioanal. Nucl. Chem., 2006. 

ICP-OES continues to dominate the market because of its ease of use and relatively low maintenance cost. Inductively coupled plasma mass spectrometry (ICP-MS) is a very powerful state-of-the-art technique used for metal analysis of all kinds of samples but requires highly skilled operators. A vast amount of information is received that is not necessarily required as part of problem-solving or routine support. The cost difference and relative freedom from maintenance problems would favour ICP-OES. This book is aimed at practitioners requiring multi-elemental analysis in industrial, environmental, pharmaceutical and research laboratories, where information on identification and quantification is required on a regular basis. The main focus of this book will be on sample preparation, a topic overlooked in most books on atomic spectroscopy. It is aimed at most ICP-OES and ICP-MS users to show that the instrument is useless unless the sample is prepared in a suitable state that can be used to accurately and precisely quantify the metals present. 

The uranium content of a sample can be determined by fluorometry, alpha-spectrometry, neutron activation analysis (NAA), (IAEA 2000), or inductively coupled plasma mass spectrometry (ICP-MS) (Baglan etal. 1999). For uranium, isotope analysis may be carried out using ICP-MS (Uchida etal., 2000). In most cases, measurements of environmental levels or biological materials require preliminary sample preparations such as ashing and dissolution in acid, followed by either solvent extraction or ion exchange (PUvio and... 

Fig. 3.19. Ion-pair chromatography with phosphorus-specific inductively coupled plasma mass spectrometry detection of organic matter isolated from the Experimental Nutrient Removal (ENR) wetland outflow (dotted line) and Water Conservation Area 2A (solid line). Chromatography conditions and sample preparation as described in Eigs 3.11 and 3.12.

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