Comparison and determination of elemental composition in Korean space foods using instrumental neutron activation analysis

A quantitative analysis of mineral contents in several kinds of foods is needed to obtain information on a comprehensive elemental composition as well as an investigation on the effects of human health and nutrition based on the dietary intake of mineral elements. In 2012, six kinds of new Korean space foods (KSF) such as sweet pumpkin porridge, dakgalbi (spicy grilled chicken), Manila clam porridge, ox leg bone-cabbage soup, ginseng-chicken porridge, and chicken curry rice were developed by KAERI, and the contents of more than 15 elements in the samples were determined using an instrumental neutron activation analysis. A certified reference material associated with a biological food sample was used for analytical quality control. The analytical results were evaluated according to the elemental concentrations with KSF samples and compared with the reported values. These results will be applied toward the identification of gamma-irradiated foods.     

Evaluation of soil to tea plant elemental correlation using instrumental neutron activation analysis

Instrumental neutron activation analysis using relative and k ₀-based internal monostandard methods were employed for determination of concentrations of 12 elements in soil and tea plants collected from three different tea producing regions in India namely Assam, Darjeeling and Kangra. A total of 17 tea leaf samples along with corresponding soil samples were analyzed for elemental content. The obtained concentration data was used for the soil–plant elemental correlation studies. Positive correlation was observed between elemental concentrations of tea plants and the associated soil with Pearson correlation coefficient values in the range 0.6–0.9 for ten elements. Variations in transfer factor values were also observed according to the geo-chemical variation.     

Rare-earth elemental analysis of banded iron-formations by instrumental neutron activation analysis

Representative banded iron-formations (BIFs) from various locations of the eastern Indian geological belt were investigated by instrumental neutron activation analysis (INAA). After pre-concentration, irradiation was carried out using a neutron flux of 5.1·10¹⁶ m⁻²·s⁻¹, 1.0·10¹⁵ m⁻²·s⁻¹ and 3.7·10¹⁵ m⁻²s⁻¹, with thermal, epi-thermal and fast neutrons, respectively. The activities in these samples were measured by a HPGe detector. Ten rare-earth elements, such as La, Ce, Nd, Sm, Eu, Tb, Ho, Tm, Yb and Lu, have been qualitatively identified and quantitatively estimated in these samples. The present investigation is an example of employing a pre-concentration method for high iron-containing ores prior to neutron activation analysis.     

Elemental analysis of Korean women’s blood serums using instrumental neutron activation analysis

Instrumental neutron activation analysis was used to assess the concentration of the inorganic trace elements in Korean women’s blood serums. It was found that a high concentration of Na and Cl incurs an analytical interference, but the 12 elements such as Br, Ca, Cl, Co, Cr, Cs, Fe, K, Na, Rb, Se and Zn could be determined under the condition of an interference minimization. Serum samples collected from 63 women were analyzed and the concentration level and range of the elements were evaluated. NIST SRMs were analyzed simultaneously for quality control. The average values of the Na and Cl determined in the serum samples were 3,365 and 3,533 mg/l, Ca was 96.4 mg/l and K was 191 mg/l. Besides, Br, Se and Zn have a concentration level of 6.46, 0.13 and 0.98 mg/l, respectively. It was found that there is no significant difference between the present values and the reported values.     

Determination of elemental levels in radiopharmaceuticals by instrumental neutron activation analysis

Instrumental neutron activation analysis (INAA) was applied to thedetermination of the concentration levels of Na, Mg, Al, Cl, K, Sc, Ti, V,Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Br, Rb, Sr, Zr, Mo, Ag, Cd, Sb, I, Cs,Ba, La, Ce, Nd, Sm, Eu, Tb, Dy, Yb, Lu, Hf, Ta, Hg, Th and U in three radiopharmaceuticals.The irradiation of the samples was carried out in a 0.5 kW Bariloche RA-6Research Nuclear Reactor and the induced gamma-activity was measured by gamma-spectrometry.INAA proves to be an accurate and precise technique to obtain a quick informationon the concentration levels of several minor and trace components in radiopharmaceuticals.The quantification of heavy toxic elements is required for the registrationof radiopharmaceuticals.     

Determination of the elemental contents in stream sediments collected from Cheongju city by instrumental neutron activation analysis

Sediment samples were collected from seven locations of the MeeHo stream in Cheongju city, strained out by a sieve, dried by an oven and pulverized by an agate mortar. Instrumental neutron activation analysis (INAA) was applied for the determination of the elemental contents in the sediment samples by using the NAA #1 and #2 irradiation holes of the HANARO research reactor and HPGe gamma-ray spectrometers. Twenty-five elements were determined by a relative method with NIST SRM 2711-Montan Soil and the ranges of the elemental contents for the seven locations were identified. The contamination levels for elements such as As, Ba, Cr, Mn, Fe and Zn were compared with the guidelines of USEPA. The detection limits and combined uncertainties for the hazardous elements such as As, Ba, Cr, Mn, Sb, V and Zn were estimated under the given analytical conditions.     

Comparison of elemental composition of hair between osteoporotic and normal women by instrumental neutron activation analysis

Instrumental neutron activation analysis (INAA) was carried out on hair samples from a group of twenty patients undergoing a study of osteoporosis. Half of these were judged normal. Fourteen elements were measured but only calcium was found to have a correlation with the disease state. Calcium levels in hair were significantly lower (99% confidence level) in patients with osteoporosis. Conversely, calcium levels in the blood of osteoporotic patients were significantly higher (95% confidence level) than those in normals. Though the group studied was small it is felt that the levels of calcium in hair may be of value in diagnosing osteoporosis.     

Trace-element analysis of argyle diamonds using instrumental neutron activation analysis

Thirty four elements were determined by instrumental neutron activation analysis in colourless, brown, and pink diamonds, with and without inclusions. These were compared with data obtained for similar elements in the host lamproite rock. The natural radioactivity of these samples was measured by instrumental techniques, and found to be negligible.     

Determination of elemental concentrations in environmental plant samples by instrumental neutron activation analysis

The intake of leafy vegetables in daily diet is very important to meet our nutritional needs. Vegetables provide the essential elements which are necessary and recommended for human growth. However, due to rapid industrialization and urbanization our environment becomes polluted and this affects the normal growth of agricultural products and composition of environmental species. The elemental concentrations present in the environmental samples are good indicators to assess the toxicological levels due to pollution affects. In the present work we have analysed several vegetable plant samples by instrumental neutron activation analysis to determine the elemental concentrations at major, minor and trace levels. The leafy vegetables like spinach, red leafy veagetable, pui, gourd leaf, lettuce and katoua were chosen as these are extensively consumed by local peple in eastern part of India. We have determined 15 elements in the above mentioned vegetable samples and some of these are essential elements and some are toxic elements. It was found that Na and K were present as major elements, Fe and Zn as minor elements and As, Ce, Cr, Co, La, Mo, Rb, Sc, Sm, Sr as trace elements. The concentration level of Cr was found to be higher than that of recommended value certified by WHO and National environment quality control for human consumption. The validation of our analytical results have been performed by the Z-score tests through the determination of concentrations of the elements of interest in certified reference materials.     

Elemental analysis of local soda samples using instrumental neutron activation analysis

Nigerian soda samples have been analyzed for major, minor and trace elements using instrumental neutron activation analysis. The following elements were determined; Na, Sm, U, La, Cr, Eu, Zn, Hf, Fe, Sc, Ba, Rb, Cs, Co, Au, Yb, Lu, Th, Ce, Zr, Se, As and Ta. The samples appear safe to use in human diet, although they may still require industrial purification to bring down the level of nonessential elements and those that could be toxic when present at high concentration.     

Determination of elemental levels in medicinally important Indian leaves by instrumental neutron activation analysis

Levels of As, Ba, Br, Ca, Ce, Cl, Cr, Cs, Eu, Fe, Hg, I, K, La, Mg, Mn, Na, Ni, Rb, Sb, Sc, Sm, Sr, Th, Zn, and U have been determined in ten leaves widely used in ayurvedic medicine by instrumental neutron activation analysis (INAA). The neutron irradiations were performed with a 100 kW Triga nuclear reactor and the induced activity was counted with a gamma-ray spectrometer. Based on elemental levels obtained the utility of these leaves in medicine are discussed.     

Determination of uranium in ores using instrumental neutron activation analysis

An instrumental neutron activation analysis method based on the measurement of²³⁹Np has been developed for the determination of uranium in ores. The samples after 5 sec irradiation were cooled for 3 days and the gamma-ray spectra were measured with a 30 cm³ Ge(Li) detector. The precision and accuracy of the proposed method were determined by analysing IAEA Standard Uranium Ore samples.     

Study of size-fractionated coal-combustion aerosols using instrumental neutron activation analysis

The chemical composition of aerosols emitted during coal combustion was studied as a function of particle size down to 0.01 m. The aerosol collections were carried out in a 81 MW capacity boiler that burned Venezuelan coal in a circulating fluidized bed combustion chamber. The samples were analyzed with upstream of the electrostatic precipitator using a Berner low-pressure impactor, which was quipped with a cyclone pre-cutter to avoid overloading of the first impaction stages. The samples were analyzed by INAA for up to about 40 elements. The elemental concentrations in the particulate matter for each impaction stage were plotted as a function of stage number (particle size). For the elements Na, Al, K, Ca, Sc, Ti, V, Ga, La and Sm, the concentration variation was limited to a factor of 2 to 4, and the concentrations of these elements were lower for the initial and final impactor stages than for the intermediate particle sizes. The variations were also limited to a factor of 2–4 for Mn, Fe, As, Sb and Th, butall these elements showed increasing concentrations with decreasing particle size. Still other elements, such as Ni, Cr, Co, Za, W, Mo and the halogens, were highly enriched (up to 20–100 fold) in the fine particles when compared with the coarse particles.     

Accurate measurement of bromine contents in plastic samples by instrumental neutron activation analysis

Accurate measurements of bromine contents in plastic samples were made by the direct comparator instrumental neutron activation analysis (INAA). Individual factors affecting the measurements were comprehensively evaluated and compensated, including the volatility loss of bromine from standard comparators, the background bromine level in the filter papers used for preparation of the standard comparators, nuclear interference, γ-ray spectral interference and the variance among replicates of the samples. Uncertainty contributions from those factors were thoroughly evaluated and included in the uncertainty budgeting of the INAA measurement. ⁸¹Br was chosen as the target isotope, and the INAA measurements for bromine were experimentally confirmed to exhibit good linearity within a bromine content range of 10–170 μg. The established method has been applied to the analysis of eight plastic samples: four commercially available certified reference materials (CRMs) of polyethylene and polystyrene and four acrylonitrile butadiene styrene (ABS) samples prepared as the candidate reference materials (KRISS CRM 113-01-012, -013, -014 and -015). The bromine contents of the samples were calculated at three different γ-ray energies and compared, showing good agreement. The results of the four CRMs also showed good consistency with their certified values within the stated uncertainties. Finally, the bromine contents of the ABS samples were determined with expanded uncertainties (at a 95% level of confidence) between 2.5% and 5% in a bromine content range of 25–900 mg kg⁻¹.     

Erros in instrumental neutron activation analysis

Equations are derived for the statistical and systematic error in INAA. It is possible to use them for the definition of limits of decision, detection and determination.     

Errors in instrumental neutron activation analysis

Equations are derived for the statistical and systematic error in INAA based on single photopeaks. They may serve to predict the applicability of the method or to judge data obtained under well-known conditions.     

Determination of aluminium contents in selected food samples by instrumental neutron activation analysis

Food and food products are the main sources of Aluminium entering the human body. In order to know aluminium contents in food and food products, selected 26 samples from local market were analyzed by instrumental neutron activation analysis (INAA) using reactor neutrons and high resolution gamma-ray spectrometry. INAA using 1,779 keV γ-ray of ²⁸Al (2.24 min) was used for aluminium concentrations in the range of 33–529 mg kg^?1. Two NIST standard reference materials (SRMs) and two IAEA reference materials (RMs) were analyzed by INAA for quantification of aluminium as a part of method validation.     

Determination of the elemental distribution in cigarette components and smoke by instrumental neutron activation analysis

Cigarette smoking is a major source of particles released in indoor environments. A comprehensive study of the elemental distribution in cigarettes and cigarette smoke has been completed. Specifically, concentrations of thirty elements have been determined for the components of 15 types of cigarettes. Components include tobacco, ash, butts, filters, and cigarette paper. In addition, particulate matter from mainstream smoke (MS) and sidestream smoke (SS) were analyzed. The technique of elemental determination used in the study is instrumental neutron activation analysis. The results show that certain heavy metals, such as As, Cd, K, Sb and Zn, are released into the MS and SS. These metals may then be part of the health risk of exposure to smoke. Other elements are retained, for the most part, in cigarette ash and butts. The elemental distribution among the cigarette components and smoke changes for different smoking conditions.     

Multielement comparison of instrumental neutron activation analysis techniques using reference materials

Several instrumental neutron activation analysis techniques (parametric, comparative, and k_o-standardization) are evaluated using three reference materials. Each technique is applied to National Institute of Standards and Technology standard reference materials, SRM 1577a (Bovine Liver) and SRM 2704 (Buffalo River Sediment), and the United States Geological Survey standard BHVO-1 (Hawaiian Basalt Rock). Identical (but not optimum) irradiation, decay, and counting schemes are employed with each technique to provide a basis for comparison and to determine sensitivities in a routine irradiation scheme. Fifty-one elements are used in this comparison; however, several elements are not detected in the reference materials due to rigid analytical conditions (e.g., insufficient length of irradiation or activity for radioisotope of interest decaying below the lower limit of detection before counting interval). Most elements are normally distributed around certified or consensus values with a standard deviation of 10%. For some elements, discrepancies are observed and discussed. The accuracy, precision, and sensitivity of each technique are discussed by comparing the analytical results to consensus values for the Hawaiian Basalt Rock to demonstrate the diversity of multielement applications.