Use Of Neutron Activation Analysis Research Articles

Raw material choices and technical practices as indices of cultural change: Characterizing obsidian consumption at 'Mycenaean' Quartier Nu, Malia (Crete).

This paper takes a practice-based approach to the study of cultural identity, focusing on how raw material and technical choices involved in the production of quotidian tools served to both reproduce, and reflect a social group's very way of being. We then consider the (dis)continuity of obsidian blade-making traditions from Middle-Late Bronze Age Malia (north-central Crete), i.e., before and after a period of island-wide destructions, and appearance of foreign elements believed to reflect the arrival of a population from the Greek mainland (Mycenaeans). Methodologically this involves an integrated, 'thick description' obsidian characterisation study to detail long-term cultural traditions, including the use of Neutron Activation Analysis (NAA) to source the raw materials of 36 artifacts. The results show a significant degree of continuity in the community's lithic traditions, suggesting that many of the innovative features at Malia can be interpreted in terms of local factions appropriating new and foreign means of social distinction, rather than wholescale changes in community composition.

A pilot study on the use of neutron activation analysis and multivariate statistics for the provenance of Jamaican Cannabis sativa L (Marijuana)

The aim of this study was to use instrumental neutron activation analysis and multivariate analysis to determine the provenance of Jamaican Cannabis sativa L. Sixty-three samples were collected from various areas in Jamaica, with no other data but their known or self-reported growing regions. The samples were analysed for Al, As, Br, Ca, Cd, Co, Cs, Fe, K, La, Mg, Mn, Na, Rb, Sb, Sc, Sm, Sr, V, and Zn. The resulting elemental data were statistically evaluated using agglomerative hierarchical cluster analysis and principal component analysis. Cluster analysis was able to group the samples into their known or reported growing regions with a high degree of accuracy. Principal component analysis was also able to elucidate some of the underlying geochemical factors that could explain the clustering. These included the underlying bauxitic geochemistry and the influence of fertilizer inputs. Of the analysed elements, Al, As, Cd, Co, Fe, K, La, Mg, Mn, Sc, Sm, V, and Zn appear to be most significant in identifying the growing regions of the cannabis samples. Results indicate the promise of this methodology with an increased dataset and potentially further refinement of the identifying elements.

Determination of the content of impurity elements in a sample of high purity India by the method of radiochemical neutron activation analysis

The present article is devoted to the development of a method for neutron activation analysis of a microimpurity composition of high-purity indium with the radiochemical separation of indium radionuclides from radionuclides of the determined elements by extraction chromatography in the system tributyl phosphate (TBP) - solutions of hydrobromic acid (HBr).Neutron activation analysis (NAA) has a special place among the physical methods for determining the trace composition of high-purity substances. Low detection limits, the possibility of simultaneous determination of a large number of impurity elements from one sample, no correction for the control experiment, the possibility of using inactive carriers in separating traces of radionuclides of impurity elements from matrix elements ensured the widespread use of NAA in the analysis of highly pure substances.The developed technique allows separating matrix radionuclides from radionuclides of impurity elements with high efficiency and determination of 28 impurity elements in high-purity indium with detection limits of 0.7 ppm to 0.05 ppb.

Anthropogenic radionuclides in Antarctic biota – dosimetrical considerations

The article presents results of the research on artificial radionuclides (137Cs, 90Sr, 241Am) in the Antarctic environment. Samples of 12 species from the marine environment: Pygoscelis adeliae, Pygoscelis papua, Macronectes giganteus, Pagodroma nivea, Catharacta antarctica, Leptonychotes weddellii, Mirounga leonina, Harpagifer antarcticus, Chaenocephalus aceratus, Nacella concinna, Himantothallus grandifolius, Iridaea cordata (bones, feathers, soft tissues, eggs' shells of birds, bones, skin, fur of mammals, fish, mollusks’ soft tissues and shells, algae) and samples of 4 species from the terrestrial environment: Sanionia uncinata, Usnea antarctica, Usnea aurantiaco-atra, Deschampsia antarctica (mosses, lichens, grass) were investigated. Differences in the accumulation of 137Cs between marine and terrestrial ecosystem were shown, which are mostly due to conservatism of mosses and lichens and active removal of cesium by animal body. Furthermore discrepancy between mosses and lichens in the radioceasium accumulation was statistically proven with the additional use of Neutron Activation Analysis. Moreover, the internal weighted dose rates assessment was prepared using the ERICA Tool. The dose rates were relatively low, not exceeding several dozen nGy/h. Nonetheless, one species – Pagodroma nivea, was significantly outstanding due to the highest weighted dose rate it is burdened with.

The role of NAA in securing the accuracy of analytical results in the inorganic trace analysis

The unique value of the neutron activation analysis (NAA) for analytical quality assurance is demonstrated through its contribution to the certification of the reference materials over the time span of 40 years. Ratio primary reference measurement procedures i.e. definitive methods, based on radiochemical NAA, play an important role in confirming the validity of the certified values established in the international intercomparisons. Real analytical situations where the use of NAA was critical to get accurate results are presented. The dangers associated with the possible non-availability of the NAA in the near future are indicated.

Marginalized Potters and Ceramic Compositional Groups: Neutron Activation Analysis of Contemporary Pottery from Tigray, Northern Highland Ethiopia

The study presents the results of neutron activation analysis (NAA) of contemporary pottery from Tigray Regional State, northern highland Ethiopia. This is the first regional-scale study of ceramic composition of Tigray’s pottery and is part of an ethnoarchaeological study of the material and social contexts of pottery production and consumption in Tigray’s Eastern (Misraqawi), Central (Mehakelegnaw), and North-western (Semien Mi’irabawi) zones. The analysis identifies clear compositional groups with strong regional patterns, an encouraging result for the use of NAA to study Tigray’s ancient pottery trade. Significantly, the study further contributes to discussions of how mutually constituted social identities of potters and consumers affect compositional patterning in the distribution of pottery in market networks.

Use of neutron activation analysis and LC–ICP-MS in the development of candidate reference materials for As species determination

Arsenic (As) is widely found in marine organ- isms, mainly as organic arsenical compounds. With the introduction of regulations for As species in foodstuffs and for environmental control, it has become more important to quantify the amount of arsenic species present. To address this concern new reference materials (RMs) for validation and quality assurance of As speciation measurements are being developed, including a tuna fish tissue and a robalo liver tissue. Instrumental neutron activation analysis (INAA) is used in this work as a proven analytical tool for As determinations and for validating the As mass fraction determined by liquid chromatography coupled to induc- tively coupled mass spectrometry (LC-ICP-MS) in extracts of the candidate RMs and other fish samples including certified RMs. Various methods for the extraction of water- soluble As species were evaluated. The best results were acquired after methanol/acetone/water extraction yielding in 93 % extractable As in the tuna RM. This procedure was used for the LC-ICP-MS studies. The results demonstrate that INAA can account for 100 % of the distribution of As species in analytical processes. It complements LC-ICP- MS for the validation of the characterization of As species in the development of RMs for such species. Excellent agreement of measured results in certified RMs with the reported values confirms the validity of the applied procedures.

Use of Neutron Activation Analysis and Inductively Coupled Plasma Mass Spectrometry for the Determination of Trace Elements in Pediatric and Young Adult Prostate

The questions about the androgen control and the involvement of trace elements in prostatic reproductive function still remain unanswered. One valuable way to elucidate the situation is to compare the values for the prostatic mass fractions of trace elements in pre-and post-pubertal boys. The effect of age on the mass fraction of 54 trace elements in intact prostate of 50 apparently healthy 0-30 years old males was investigated by neutron activation analysis and inductively coupled plasma mass spectrometry. Mean values (M ± SΕΜ) for mass fraction (milligram per kilogram, on dry-weight basis) of trace elements were: Ag 0.062 ± 0.008, Al 80 ± 18, Au 0.0092 ± 0.0024, B 5.9 ± 3.5, Be 0.0034 ± 0.0009, Bi 0.018 ± 0.010, Br 26 ± 3, Cd 0.26 ± 0.05, Ce 0.049 ± 0.012, Co 0.035 ± 0.004, Cr 0.49 ± 0.07, Cs 0.036 ± 0.005, Dy 0.0072 ± 0.0018, Er 0.0040 ± 0.0011, Fe 100 ± 10, Gd 0.0065 ± 0.0018, Hg 0.031 ± 0.004, Ho 0.0013 ± 0.0004, La 0.034 ± 0.007, Li 0.064 ± 0.009, Mn 1.69 ± 0.15, Mo 0.54 ± 0.13, Nb 0.013 ± 0.004, Nd 0.025 ± 0.006, Ni 4.1 ± 0.6, Pb 1.3 ± 0.2, Pr 0.0058 ± 0.0015, Rb 14.5 ± 0.8, Sb 0.051 ± 0.006, Sc 0.013 ± 0.002, Se 0.54 ± 0.03, Sm 0.0055 ± 0.0015, Sn 0.22 ± 0.05, Tb 0.0012 ± 0.0004, Th 0.0076 ± 0.0020, Ti 2.8 ± 0.5, Tl 0.0032 ± 0.0009, Tm 0.00064 ± 0.00017, U 0.0025 ± 0.0004, Y 0.036 ± 0.010, Yb 0.0037 ± 0.0012, Zn 281 ± 32, and Zr 0.16 ± 0.04. The upper limit of mean mass fraction of As, Eu, Ga, Hf, Ir, Lu, Pd, Pt, Re, and Ta were: As ≤ 0.069, Eu ≤ 0.0012, Ga ≤ 0.071, Hf ≤ 0.049, Ir ≤ 0.00054, Lu ≤ 0.00063, Pd ≤ 0.014, Pt ≤ 0.0029, Re ≤ 0.0048, and Ta ≤ 0.010. This work revealed that there is a significant tendency for the mass fractions of Cd, Se and Zn in the prostate tissue of healthy individuals to increase with age from the time of birth up to 30 years. It was also shown that high levels of Al, Au, B, Br, Cr, Ga, Li, and Ni mass fraction in prostate tissue do not indicate a direct involvement of these elements in the reproductive function of prostate.

Dispersal and fate of dredged materials disposed of in the Changjiang Estuary determined by use of an in situ rare earth element tracer

To investigate the dispersal pattern and the fate of dredged materials disposed at a pre-selected disposal site, a field tracer experiment was conducted in the North Passage of the Changjiang Estuary during the 2005 flood season. Three tons of dredged materials were mixed with 2.792 kg of sodium hexachloroiridate (IV) hexahydrate (SHH), which contained the rare earth element tracer iridum (Ir). Sampling was conducted at pre-selected sections of the estuary on the second, third and fourth day after the release of dredged materials. All samples were evaluated by use of neutron activation analysis. The majority of the dredged material was dispersed nearly parallel to the navigation channel and deposited between the channel and the south dike. Only a small quantity of dredged materials entered or crossed the navigation channel, and the back silting ratio in the navigation channel was about 5%. The dredged materials also dispersed southeasterly beyond two dike heads.

Use of neutron activation analysis for determination of gold in some human scalp hair samples

In the Egyptian society, it is usual until now that females wear extensively gold jewelry since their birth. The present work is carried out to determine gold content in scalp hair samples from some selected female donors of various ages. Instrumental Neutron Activation Analysis, with gamma ray spectrometry was applied for this study. The obtained data are compared with the available published data for analysis of hair samples from other countries. The correlation between age and gold concentration in hair samples is discussed. Interpretation of the influence of other factors which possibly may affect the contents of gold in the analyzed hair samples is also presented.

A trial proficiency test of eight NAA laboratories in Asia using stream sediments

Eight neutron activation analysis research groups from seven countries have participated in a trial proficiency test under the auspices of the Forum for Nuclear Cooperation in Asia. Three stream sediment reference materials were used in the test. A high degree of proficiency was found in the quantification of Co and Sc and more than 20 elements were well quantified by the majority of laboratories. The results support the use of neutron activation analysis, as practised by the participants, for geochemical mapping. The data produced in this study may provide an opportunity to improve the characterisation of the three reference materials.

Use of neutron activation analysis for the characterization of single-wall carbon nanotube materials

Instrumental neutron activation analysis (INAA) and prompt gamma neutron activation analysis (PGAA) were used to characterize a variety of single-wall carbon nanotube (SWCNT) materials from different principal production processes, as well as a material containing SWCNTs together with other carbon species, catalyst residues, and trace element contaminants to be issued by the National Institute of Standards and Technology for characterization and distribution as Standard Reference Material SRM 2483 Carbon Nanotube Soot. INAA proved to be well suited for the direct determination of catalyst and contaminant trace elements requiring only minimal sample preparation. PGAA complemented the INAA data in particular with determinations of the light elements. Carbon and hydrogen results provided information on the materials purity and storage properties. Strategies for the quality assurance of the measurements in these new materials were developed. INAA and PGAA data were provided for the value assignment of mass fractions of catalyst and trace elements in the candidate SRM and a systematic overview was obtained of the catalyst and trace element contaminants associated with each of the major production routes.

Mercury exposure and risk of cardiovascular disease in two U.S. cohorts.

Exposure to methylmercury from fish consumption has been linked to a potentially increased risk of cardiovascular disease, but evidence from prior studies is equivocal. Beneficial effects of the ingestion of fish and selenium may also modify such effects. Among subjects from two U.S. cohorts (a total of 51,529 men and 121,700 women) whose toenail clippings had been stored, we prospectively identified incident cases of cardiovascular disease (coronary heart disease and stroke) in 3427 participants and matched them to risk-set-sampled controls according to age, sex, race, and smoking status. Toenail mercury and selenium concentrations were assessed with the use of neutron-activation analysis. Other demographic characteristics, cardiovascular risk factors, fish consumption, and lifestyle habits were assessed by means of validated questionnaires. Associations between mercury exposure and incident cardiovascular disease were evaluated with the use of conditional logistic regression. Median toenail mercury concentrations were 0.23 μg per gram (interdecile range, 0.06 to 0.94) in the case participants and 0.25 μg per gram (interdecile range, 0.07 to 0.97) in the controls. In multivariate analyses, participants with higher mercury exposures did not have a higher risk of cardiovascular disease. For comparisons of the fifth quintile of mercury exposure with the first quintile, the relative risks were as follows: coronary heart disease, 0.85 (95% confidence interval [CI], 0.69 to 1.04; P=0.10 for trend); stroke, 0.84 (95% CI, 0.62 to 1.14; P=0.27 for trend); and total cardiovascular disease, 0.85 (95% CI, 0.72 to 1.01; P=0.06 for trend). Findings were similar in analyses of participants with low selenium concentrations or low overall fish consumption and in several additional sensitivity analyses. We found no evidence of any clinically relevant adverse effects of mercury exposure on coronary heart disease, stroke, or total cardiovascular disease in U.S. adults at the exposure levels seen in this study. (Funded by the National Institutes of Health.).

Notes on the Chlorite-Schist Industry of Madagascar’s Southeast Coast

This paper reports on different aspects of the Matitanana archaeological project relating to the chlorite-schist stone vessels found in southeastern Madagascar. Quarry sites discovered near the modern city of Mananjary are described, as are other non-quarry sites with evidence for the working of chlorite-schist material near Manakara and the Matitanana River valley to the south. A preliminary attempt to link the production and consumption sites, through the use of neutron activation analysis, suggests that some of the Matitanana artifacts did come from the Mananjary quarries, that other artifacts came from other as yet unknown quarries, and that both of these groups differ in their trace elements from the stone commonly found near Vohémar. It is hoped that future research will be able to further clarify many of these issues.

A new perspective on Late Holocene social interaction in Northwest Alaska: results of a preliminary ceramic sourcing study

This research examines the evidence for prehistoric ceramic exchange networks over the last 2000 years in northwest Alaska through the use of neutron activation analysis of ceramic artifacts. Results from ceramic analysis on eight coastal and inland archaeological sites identified three source macrogroups and three associated subgroups. Clay source diversity and shared source macrogroups between geographically distant sites suggest the use of multiple sources and/or the movement of pots between production locales, mirroring related patterns in pottery stylistic data. Although additional analytical work is needed to fully understand the changing character of clay procurement and ceramic distribution across this time period, this study provides exploratory data on past ceramic production and distribution that hints at changes in exchange and territoriality in northwest Alaska during the late Holocene.

Use of neutron activation analysis for evaluating the efficiency of water treatment to remove heavy metal ions by zone freezing

The efficiency of zone freezing for potable water treatment to remove inorganic impurities was examined. The content of impurities in model solutions before and after zone freezing was evaluated by neutron activation analysis with the formation of 56Mn, 116m In, and 198Au radionuclides. The zone freezing procedure is the most efficient at low ice front velocities (no greater than 0.15 cm h−1).

The brain selenoproteome: priorities in the hierarchy and different levels of selenium homeostasis in the brain of selenium‐deficient rats

The application of radionuclides for the localization of essential trace elements in vivo and the characterization of their binding proteins is a story of intermittently made improvements of the techniques used for their detection. In this study we present the use of neutron activation analysis and different autoradiographic imaging methods including real-time digital autoradiography to reveal new insights in the hierarchy of selenium homeostasis. Selenoproteins containing the essential trace element selenium play important roles in the CNS. Although the CNS does not show the highest selenium concentration in the case of selenium-sufficient supply in comparison with other organs, it shows a high priority for selenium uptake and retention in the case of dietary selenium deficiency. To characterize the hierarchy of selenium supply in the brain, in vivo radiotracer labeling with (75)Se in rats with different selenium status was combined with autoradiographic detection of (75)Se in brain tissue sections and (75)Se-labeled selenoproteins after protein separation by two-dimensional gel electrophoresis. This study demonstrates significant differences in the uptake of (75)Se into the brain of rats with different selenium status. A brain region-specific uptake pattern of the radiotracer (75)Se in selenium-deficient rats could be revealed and the CSF was identified as a key part of the brain selenium homeostasis.

Determination of cadmium in Arctic air filters by epithermal neutron activation analysis and Compton suppression

Arctic pollution is a problem of great concern, because its characteristics (transportation, assimilation into the environment, etc.) are complex and not fully understood. Detection of elemental constituents has been undertaken through the use of neutron activation analysis and Compton suppression (to lower the detection limits for radionuclides characteristic of mainly single gamma-ray emission) to discover possible pollutant sources. The goal of this project was to perform a feasibility study to determine the suitability of neutron activation analysis (NAA) to evaluate cadmium concentrations on air filters collected in the Arctic.

Development of suitable plastic standards for X-ray fluorescence analysis

For the adoption of the EU directive “Restriction on use of certain Hazardous Substances” and “Waste Electrical and Electronic Equipment” using X-ray fluorescence analysis suitable standard materials are required. Plastic standards based on acrylonitrile–butadiene–styrene terpolymer, containing the regulated elements Br, Cd, Cr, Hg and Pb were developed and produced as granulates and solid bodies. The calibration materials were not generated as a dilution from one master batch but rather the element concentrations were distributed over nine independent calibration samples. This was necessary to enable inter-elemental corrections and empirical constant mass absorption coefficients. The produced standard materials are characterized by a homogenous element distribution, which is more than sufficient for X-ray fluorescence analysis. Concentrations for all elements except for Br could be determined by Inductively Coupled Plasma Atomic Emission Spectroscopy after microwave assisted digestion. The concentration of Br was determined by use of Neutron Activation Analysis at Hahn-Meitner-Institute in Berlin, Germany. The correlation of the X-ray fluorescence analysis measurements with the values determined using Inductively Coupled Plasma Atomic Emission Spectroscopy and Neutron Activation Analysis showed a very good linearity.

Diffusion of sulfuric acid solutions in Nylon 6,6 monitored by neutron activation analysis

AbstractNylon 6,6 is an excellent material for the study of the diffusion mechanism and associated mechanical performance of polymers saturated with aqueous solutions of varying pH at different temperatures. The diffusion profile was studied for samples saturated at temperatures ranging from 20 to 90°C in solutions decreasing in pH from distilled water to 1.0M sulfuric acid. The presence of sulfuric acid molecules within the diffusing solutions acts to promote hydrolysis of the polyamide molecules. The degree of hydrolysis is dependent on saturation temperature and solution pH. The extent of degradation was evaluated via changes to mechanical performance and inherent viscosity and often results in a reduction of the stress at yield, flexural modulus, and inherent viscosity on increasing temperature and decreasing pH. The use of neutron activation analysis allowed for an evaluation of the sulfur content within the samples as a function of diffusing time. This demonstrated that although the mechanical performance decreases rapidly on initial exposure to the aqueous medium, this is likely due to plasticization. As diffusion time progresses, the sulfur content within the sample continues to rise to a level where the acid/water molar ratio is much higher in the sample than that of the bulk. This results in an enhancement of the degradation process as time progresses. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 2476–2487, 2005