Neutron activation analysis INAA

Instiximental neutron activation analysis (INAA) is considered the most informative and highly sensitive. Being applied, it allows detecting and determination of 30-40 elements with the sensitivity of 10 -10 g/g in one sample. The evident advantage of INAA is the ability to analyze samples of different nature (filters, soils, plants, biological tests, etc.) without any complex schemes of preliminai y prepai ation. 

Atomic absorption spectroscopy of VPD solutions (VPD-AAS) and instrumental neutron activation analysis (INAA) offer similar detection limits for metallic impurities with silicon substrates. The main advantage of TXRF, compared to VPD-AAS, is its multielement capability AAS is a sequential technique that requires a specific lamp to detect each element. Furthermore, the problem of blank values is of little importance with TXRF because no handling of the analytical solution is involved. On the other hand, adequately sensitive detection of sodium is possible only by using VPD-AAS. INAA is basically a bulk analysis technique, while TXRF is sensitive only to the surface. In addition, TXRF is fast, with an typical analysis time of 1000 s turn-around times for INAA are on the order of weeks. Gallium arsenide surfaces can be analyzed neither by AAS nor by INAA. 

Homogeneity Determinations with Instrumental Neutron Activation Analysis (INAA)... 

WVGES has not had analytical laboratory facilities since the 1970 s so contract geochemical analyses are a necessity. After considering a variety of sources for analytical work including both university and government laboratories, we decided to use a commercial lab, located in Ontario, which specializes in analyses for the mineral exploration industry (they have since expanded into the environmental field as well). For the sake of consistency, each sample is analyzed using the same set of techniques, a combination of Instrumental Neutron Activation Analysis (INAA) and Selective Extraction-Ignition Coupled Plasma spectroscopy that yield results for 49 elements - Au, Ag, As, Ba, Br, Ca, Co, Cr, Cs, Fe, Hf, Hg, Ir, Mo, Na, Ni, Rb, Sb, Sc, Se, Sn, Sr, Ta, Th, U, W, Zn, La, Ce, Nd, Sm, Eu, Tb, Yb, Lu, Cu, Pb, Mn, Cd,... 

Cluster analysis Is used to determine the particle types that occur in an aerosol. These types are used to classify the particles in samples collected from various locations and sampling periods. The results of the sample classifications, together with meteorological data and bulk analytical data from methods such as instrunental neutron activation analysis (INAA). are used to study emission patterns and to screen samples for further study. The classification results are used in factor analysis to characterize spatial and temporal structure and to aid in source attribution. The classification results are also used in mass balance comparisons between ASEM and bulk chemical analyses. Such comparisons allow the combined use of the detailed characterizations of the individual-particle analyses and the trace-element capability of bulk analytical methods. 

With analytical methods such as x-ray fluorescence (XRF), proton-induced x-ray emission (PIXE), and instrumental neutron activation analysis (INAA), many metals can be simultaneously analyzed without destroying the sample matrix. Of these, XRF and PEXE have good sensitivity and are frequently used to analyze nickel in environmental samples containing low levels of nickel such as rain, snow, and air (Hansson et al. 1988 Landsberger et al. 1983 Schroeder et al. 1987 Wiersema et al. 1984). The Texas Air Control Board, which uses XRF in its network of air monitors, reported a mean minimum detectable value of 6 ng nickel/m (Wiersema et al. 1984). A detection limit of 30 ng/L was obtained using PIXE with a nonselective preconcentration step (Hansson et al. 1988). In these techniques, the sample (e.g., air particulates collected on a filter) is irradiated with a source of x-ray photons or protons. The excited atoms emit their own characteristic energy spectrum, which is detected with an x-ray detector and multichannel analyzer. INAA and neutron activation analysis (NAA) with prior nickel separation and concentration have poor sensitivity and are rarely used (Schroeder et al. 1987 Stoeppler 1984). 

First, we analyzed samples for a large number of elements to Identify any elements, regardless of toxicity or typical concentration, that would provide signals for the presence of material from certain types of sources. Both ambient samples and particles from sources were analyzed by Instrumental neutron activation analysis (INAA), by which one can often measure about 35 elements In Individual samples (17), As the Important elements Pb, N1 and Cd are not consistently, If ever, observed by INAA, they were often measured by other methods. As INAA Is sensitive to very small amounts of obscure elements, we have obtained reliable data for elements such as Ga, Hf, Sc, In, W and many rare earths which pose no known health hazard at present levels and contribute Insignificant amounts of mass to TSP. However, as discussed below, many trace elements have already been shown to be Important In receptor... 

In this work, we use a University of Washington low pressure impactor (LPI) and instrumental neutron activation analysis (INAA) to determine the elemental composition of aerosols from a two 430 MWe coal-utility boilers, ranging in diameter from less than 0.07 to about 10 )Jm, and to investigate the modification of the aerosol by a modern flue-gas desulfurization system. A preliminary account of the work is presented here. 

All impactor and filter samples were analyzed for up to 45 elements by instrumental neutron activation analysis (INAA) as described by Heft ( ). Samples were irradiated simultaneously with standard flux monitors in the 3-MW Livermore pool reactor. The x-ray spectra of the radioactive species were taken with large-volume, high-resolution Ge(Li) spectrometer systems. The spectral data were transferred to a GDC 7600 computer and analyzed with the GAMANAL code (1 ), which incorporates a background-smoothing routine and fits the peaks with Gaussian and exponential functions. 

During the late 1960s and early 1970s, neutron activation analysis provided a new way to measure bulk chemical composition. Neutron activation analysis utilizes (n,y) reactions to identify elements. A sample is placed in a nuclear reactor where thermal neutrons are captured by atoms in the sample and become radioactive. When they decay, the radioactive isotopes emit characteristic y-rays that are measured to determine abundances. Approximately 35 elements are routinely measured by neutron activation analysis. A number of others produce radioactive isotopes that emit y-rays, but their half-lives are too short to be useful. Unfortunately, silicon is one of these elements. Other elements do not produce y-ray-emitting isotopes when irradiated with neutrons. There are two methods of using neutron activation to determine bulk compositions, instrumental neutron activation analysis (INAA) and radiochemical neutron activation analysis (RNAA). 

Quantitative trace element analysis of diamond by LA-ICP-MS using different synthetic multielement carbon based standards (e.g., cellulose pellets) is discussed by Rege et al 2, whereby 13C was used for internal standardization. Concentrations of 41 elements were determined in two fibrous diamonds from Jwaneng Botswana (JWA 110 and 115) by relative sensitivity coefficients measured using the synthetic cellulose standard. The analytical data were verified by means of instrumental neutron activation analysis (INAA) and proton induced X-ray emission (PIXE).72... 

Methods and technology were developed and used at the NASA Plum Brook Reactor (PBR) to analyze trace elements in pollution-related samples by instrumental neutron activation analysis (INAA). This work is significant because it demonstrates that INAA is a useful analytic tool for monitoring trace elements in a variety of sample matrices related to environmental protection. In addition to coal, other samples analyzed for trace elements included fly ash, bottom ash, crude oil, fuel oil, residual oil, gasoline, jet fuel, kerosene, filtered air particulates, various ores, stack... 

Battelle has developed instrumental neutron activation analysis (INAA) techniques which permit very sensitive and accurate multielement analysis of approximately 40 elements in coal and fly ash. These techniques, which will be described in this work, form the basis for extensive environmental studies of the effluent from coal-powered generating facilities and other pollution sources. 

In most obsidian provenance studies, the ability to employ compositional differences to discriminate between sources depends, to a certain extent, on the number of elements measured. Because instrumental neutron activation analysis (INAA) is capable of measuring 25-30 elements in obsidian with excellent precision, numerous combinations of trace and major elements are available for comparing differences between sources. The main requirements for success are that all sources have been located and analyzed, and that the internal variation measured within the sources be smaller than the compositional differences measured between the sources (23). 

Trace elemental analysis of ancient ceramics has been proven a very useful tool for tracing the circulation of this material. Instrumental neutron activation analysis (INAA) was for years the analytical technique of choice to measure the composition of ceramics because of the large number of elements it could determine and its good sensitivity. Lately, a few publications have shown that laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) could provide similar results as INAA more quickly and at lower cost. A protocol has been developed to determine 51 elements using LA-ICP-MS and tested it on Wari period ceramics previously analyzed using INAA. We show how INAA and LA-ICP-MS analysis lead to the same conclusion in terms of sample groupings. 

Trace element studies of ceramics have been undertaken for the purpose of locating source regions for archaeological materials since the 1960s. While a number of techniques have been used for this purpose, by far the most common and most effective has been instrumental neutron activation analysis (INAA), largely due to its excellent sensitivity, precision, accuracy and the large number of elements it can measure simultaneously. 

Forty-four of the 55 samples were chemically characterized by X-ray fluorescence (XRF). Thirty-seven of these samples were also characterized mineralogically by X-ray diffraction (XRD). Finally, 11 out of the 44 samples analyzed by XRD (4 specimens from La Cueva Pintada site and 7 from the San Francisco s convent) were analyzed by instrumental neutron activation analysis (INAA). Additionally, 11 samples from San Francisco convent, which had an insufficient weight to be characterized by XRF, were analyzed by INAA as well. XRD analyses are now being conducted for the 18 samples not yet characterized. 

The following section focuses on the variability of the clay bodies or pastes of the glazed ceramics previously characterized by LA-ICP-MS and LA-TOF-ICP-MS. The purpose of this study is to compare the variation in the ceramic pastes with the different glaze decorative technologies through time. The variability in the ceramic pastes will be characterized through instrumental neutron activation analysis (INAA) and petrographic analysis. 

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). 

As, Sb, and Au determined by instrumental neutron activation analysis (INAA). Hg determined by cold vapor atomic absorption (CVAA). nd = not determined. 

V. E. Negretti de Bratter, S. Recknagel, D. Gawlik, Speciation of Se, Fe and Zn in human milk whey the use of instrumental neutron activation analysis (INAA) to corroborate element profiles measured with inductively coupled plasma atomic emission spectrometry (ICP-AES), Fresenius J. Anal. Chem., 353 (1995), 137-142. 

Trace element compositions of airborne particles are important for determining sources and behavior of regional aerosol, as emissions from major sources are characterized by their elemental composition patterns. We have investigated airborne trace elements in a complex regional environment through application of receptor models. A subset (200) of fine fraction samples collected by Shaw and Paur (1,2) in the Ohio River Valley (ORV) and analyzed by x-ray fluorescence (XRF) were re-analyzed by instrumental neutron activation analysis (INAA). The combined data set, XRF plus INAA, was subjected to receptor-model interpretations, including chemical mass balances (CMBs) and factor analysis (FA). Back trajectories of air masses were calculated for each sampling period and used with XRF data to select samples to be analyzed by INAA. 

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