Characterization of Brazilian commercial milks by instrumental neutron activation analysis

Aiming at the determination of toxic and essential elements in Brazilian commercial bovine milk, 25 ultra high temperature (UHT) milk samples were acquired in the local market of Piracicaba, SP. The samples were freeze-dried and analyzed by instrumental neutron activation analysis (INAA) allowing the determination of Br, Ca, Co, Cs, Fe, K, Na, Rb and Zn. When the results were expressed as concentration (mg·l⁻¹) no significant differences were found. However, considering the dry matter, results showed a clear difference between the mass fractions (mg·kg⁻¹ d.w.) of skim milk and whole milk for the elements Br, Ca, K, Na, Rb and Zn, indicating that the removal of fat caused a concentration effect in the dry matter of skim milks. Discrepancies were found between the concentrations of Ca and Na measured by INAA and the values informed in the labels. Ca showed variations within 30% for most samples, while concentrations of Na were up to 190% higher than informed values. The sample preparation and the INAA procedure were appropriate for the determination of Br, Ca, Co, Cs, Fe, K, Na, Rb and Zn in milk samples.     

Electrophoretic analysis of snake venoms.

Electrophoretic analyses were conducted on snake venoms from 21 species representing Elapidae, Crotalidae and Viperidae. Denatured and native venoms were analyzed by polyacrylamide gel electrophoretic (PAGE) methods with sodium dodecyl sulfate (SDS) and without SDS. Both SDS-PAGE and PAGE profiles of venoms from different snake species indicate that some proteins and polypeptide components of these venoms have common electrophoretic characteristics suggesting a genetic relationship. Conversely, the electropherograms also showed the characteristic protein and polypeptide profiles that could differentiate one snake species from another. Therefore, both SDS-PAGE and PAGE profiles suggest that proteins and polypeptides with similar characteristics abound among subspecies or related species, although each venom has a unique profile that differentiates one species from the other.     

Determination of trace elements in Brazilian cigarette tobacco by neutron activation analysis

The determination of 14 trace elements /Ba, Ce, Co, Eu, Fe, Hf, La, Nd, Rb, Sb, Sc, Sm, Tb and Th/ has been carried out in three different brands of Brazilian cigarettes. The samples and standards were irradiated for 8 h at a thermal neutron flux of approx. 5×10¹² n cm^–2s^–1. After the irradiation, the -rays activity was measured on a Ge/Li/ detector coupled with a 4096-channel pulse height analyzer. The results were compared with those obtained for the tobacco from American, Iranian, Turkish, Pakistan and Yugoslavian cigarettes. The amount of each element transferred to the ashes was determined.     

Non-destructive analysis of inorganic impurities in Brazilian coals by epithermal neutron activation

Twenty-two elements were identified and determined in different Brazilian coal samples by an epithermal neutron activation technique developed by the authors. The detection limits and the uncertainties of the results show that the technique can be used for routine analysis. The analysis of the complex gamma-ray spectra and the evaluation of the interfering activities are discussed in detail.     

Multielemental analysis of Brazilian milk powder and bread samples by neutron activation

The concentrations of Na, Cl, Mn, Br, Fe, Zn, Rb, Sb, Sc, Cr, Al and Mg were determined in some types of bread and in some brands of milk powder consumed in the city of São Paulo (SP—Brasil), by instrumental neutron activation analysis. Radiochemical separations were carried out by means of retention of²⁴Na on hydrated antimony pentoxide (HAP) from a 8N HCl solution, after digestion of the organic matter. It was possible in this way to determine the radioisotopes⁶⁴Cu,^69mZn and¹⁴⁰La in the effluent solution. The detection limits of the trace elements analyzed in bread and milk powder samples were determined using the Currie and Girardi criterions.From a dissertation submitted by V. A. MAIHARA to the University of São Paulo in partial fullfillment of the requirements for a Master of Science Degree in Nuclear Technology.     

Uranium and thorium determination in Brazilian coals by epithermal neutron activation analysis

An experimental technique has been developed to determine impurities in coal. Uranium was determined by counting the²³⁹Np 106.1 keV -ray with a LEPS detector and thorium by counting the²³³Pa 311.8 keV -ray with a Ge(Li) detector. Seventeen coal samples were analyzed with an average precision of 3% and a quantitative determination limit of 0.153 g/g for uranium and 0.078 g/g for thorium. The technique allows determinations of up to twenty elements besides U and Th and can be applied in routine analysis.     

Multielemental hair composition of Brazilian Indian populational groups by instrumental neutron activation analysis

In the present paper, for the first time the multielemental compositionof hair samples of Indian populations living in the Xingu Park Reservation,in the Brazilian Amazonic region has been determined, by INAA. Irradiationswere carried out at the Interfaculty Reactor Institute (Delft, The Netherlands)and, using a combination of different irradiation and decay times, about 40elements could be determined in the hair. Previous analysis made at the RadiochemistryDivision of IPEN/CNEN-SP (Brazilian Nuclear Energy Commission) of hair samplesof a Brazilian control population allowed the determination of 20 elements,also by INAA. Comparison of the data obtained for the Indian populations andthe controls showed very significant differences in elemental compositionsfor some elements, like Hg, Mn and Al while for others, like Cu and Zn, theconcentrations were similar. A discussion of the differences found for otherelements also is made in the present paper.     

Determination of mercury in head hair of Brazilian populational groups by neutron activation analysis

In the present work, determination of mercury in the head hair of populational groups living near a heavily industrialized region in São Paulo and of Indians living in the Xingu park in the Amazonic region, was carried out by instrumental neutron activation analysis. A control group of people with no suspicion of contamination by mercury was also studied. The range of mercury concentrations found up to now were: for the control group from 0.26 to 02.5 ppm; for the Indians from 6.9 to 34 ppm, and for the industrialized region inhabitants: from 0.30 to 3.0 ppm.     

Analysis of small biopsy samples by neutron activation analysis

An accurate knowledge of the ratio Ca/P in bone biopsies is very useful in the diagnosis of osteoporosis. Similarly, measurements on muscle biopsies are important in understanding the disturbance of intracellular fluid and electrolyte (Na, Cl, K and P) balance in patients with metabolic myopathies (muscle diseases) and acid-base disturbances including renal failure. The ratio Ca/P in normal subjects was found to be 2.30. Similarly, the ratio K/P was found to be very nearly constant in normal subjects.     

Ocean-sediment analysis by neutron activation

Neutron activation analysis (NAA) techniques have been developed and applied to the analysis of marine sediments. More than 150 core sites have been sampled in the northwestern Gulf of Mexico. More than 500 surface and subsurface sediment samples have been analyzed for Ba, Cr, Fe, and various other elements of interest. Typical concentrations at various locations are given. An extensive half-life study was performed to verify that gamma lines, used for quantitation exhibited the decay parameters expected to the parent radionuclide. Suggested gamma lines are presented for a few elements of particular interest to ocean-sediment analysis.     

Quantitative evaluation of blood elements by neutron activation analysis in mice immunized with <Emphasis Type="Italic">Bothrops</Emphasis> snake venoms

Mice genetically selected for high antibody responsiveness (H_III) were immunized against different Bothrops species snake venoms from distinct region of Brazil. The Neutron Activation Analysis technique was used to evaluate the whole blood concentrations of elements of clinical relevance [Ca, Cl, K, Mg and Na] in order to establish a potential correlation between antibody response and blood constituents after Bothrops venom administration for clinical screening of envenomed patients.     

Analysis of foods for iodine by epithermal neutron activation analysis

Epithermal-neutron activation analysis (ENAA) was applied to the analysis of foods for iodine. The procedure involves irradiation of wet foods in a boron nitride, vessel, followed by direct counting of the 442.9 keV gamma ray of¹²⁸I without any processing of the sample. Three research reactors were evaluated for use in determining iodine by ENAA. The University of Virginia reactor at Charlottesville was chosen for this study because the reactor facilities minimized thermal heating of the boron nitride vessel, enabling irradiation of larger, more representative analytical portions. Iodine concentrations ranging from <0.003 to 0.74 g/g are reported for 17 different food matrices.     

Analysis of sewage sludge and cover soil by neutron activation analysis

The Korean government reported that in 2005, 4395 tons/day of sewage sludge were generated from sewage disposal facilities in Korea and only 11.03% of it was reused. In addition, as a direct landfill of sewage sludge was forbidden from June 2003, research for a relevant disposal technique has been increasing. In this study, the aims were to analyze the collected sewage sludge samples and to evaluate the possibility for their reuse by a comparison of the elemental contents from a sewage sludge and a cover soil. Sludge samples were collected from a sewage disposal plant in Daejeon city and the cover soil was produced by a dilution of a sewage sludge with quicklime. Instrumental neutron activation analysis was employed to determine the elemental contents in the samples. Twenty seven elements were analyzed and their concentrations were compared.     

Determination of uranium in human head hair of a Brazilian populational group by epithermal neutron activation analysis

Hair analysis is extensively used in forensic sciences, assessment of occupational or environmental exposure and in some cases also for clinical and nutritional studies. Hair has a series of advantages in relation to other biomonitors, like blood and urine, since it is very easy to collect, very stable at room temperature and it represents not only instantaneous concentrations, but it can reveal the exposure along a given period of time. The assessment of environmental or occupational exposure to uranium is generally done by means of urine analysis, although a few papers have described attempts to use hair as a biomonitor. In the present work, epithermal neutron activation analysis has been used to establish base-line concentrations for a Brazilian populational group, living in Sao Paulo and not exposed to uranium, either environmentally or occupationally. For quality control, the reference materials Pine Needles NIST 1575 and Basalt USGS BCR-1 were used. The concentrations obtained for the control population studied up to now varied from about 2 to 50 ng·g⁻¹.     

Low level mercury analysis by neutron activation analysis

During the years 1974–77 about 200 low level mercury analyses on samples with less than 1000 ng Hg/kg were made at the Danish Isotope Centre. This paper describes our method of neutron activation analysis for low level mercury analysis. The accuracy of the mercury analyses is shown by the results of the determinations on NBS standard, SRM 1642, and on intercalibration analyses. The accuracy found is better than 10% for samples with about 100–300 ng Hg/kg and better than 10 ng Hg/kg for samples with less than 100 ng Hg/kg. The limit of detection for the analyses is about 1–5 ng Hg/kg, depending on the sample and the exact method of analysis. The lowest standard deviations on duplicate analyses are about 1 ng Hg/kg. The general level found in sea water is about 10 ng Hg/kg, in ground water about 50 ng Hg/kg, and in rain water about 100 ng Hg/kg.     

Determination of trace elements in Brazilian rice grains and in biological reference materials by neutron activation analysis

Instrumental neutron activation analysis was applied to the determination of the elements Na, K, Br, As, Rb, Zn, Co, Fe and Sc in Brazilian rice samples and in biological standards. Hg and Se concentrations were determined by using a simple radiochemical separation. The chemical procedure was carried out by means of distillation of Hg and Se in HBr medium and subsequent precipitation of selenium by sodium metabisulfite and mercury by thioacetamide. The accuracy of the instrumental and radiochemical methods was evaluated by means of analysis of the Reference Materials NBS-Bovine Liver, Bowen's Kale and NBS-Rice Flour.     

Use of multivariate and neutron activation analysis on studying element interrelationships in Brazilian phosphorite

Methods to determine U, Th, and other constituent elements in mineral matrices through Instrumental Neutron Activation Analysis (INAA), have been widely utilized due to their capability to extract a large quantity of information from small samples. In the present work, an experimental methodology based on INAA associated to the cluster statistics technique was used to determine the uranium concentration and its correlation with other elements present in the mineral phosphorites from the northeast region of Brazil. Data for 22 elements including rare-earth elements are presented. A good correlation between uranium and rare-earth elements is observed. For the transition metals, correlation with uranium was not noted.     

Multielement analysis of lichen by instrumental neutron activation analysis

Lichen (species Trypethelium Eluteriae) is analysed for different elements. Nondestructive instrumental neutron activation analysis is employed for the multielemental analysis. Gamma-ray spectrometry is used for the identification and quantitative estimation of elements. Concentrations of 24 elements are reported. Gamma-ray spectrum of the lichen irradiated for 16 hours, delayed for 10 days, and counted for 10 hours on a 50 cm³ coaxial Ge(Li) detector is given.     

Elemental analysis of limestone by instrumental neutron activation analysis

Limestone samples from Assuit Governrate in Upper Egypt were subjected to elemental analysis by instrumental neutron activation analysis and X-ray fluorescence techniques. The samples were properly prepared together with their standards and simultaneously irradiated in a neutron flux of the order 7 × 1011 n/cm² s using TRIGA research reactor at Mainz. After activation the samples were subjected to γ-ray spectrometry using a high purity germanium detection system and computerized multichannel analyzer. Nineteen elements: Na, Ca, Mn, Fe, Sc, Cr, Co, Zn, Sn, La, Ce, Nd, Eu, Sm, Yb, Lu, Hf, Th and U were analyzed. X-ray fluorescence spectrometry have been also used. The presence of any elements in higher or lower levels in certain limestone samples is contingent on the occurrence of its bearing minerals, nature of parent sediments and depositional environments of these sediments. The major elements in the samples were also observed to be among the elements that had high enrichment factors in the study of suspended dust particulate within and around cement industries. This confirms cement as the major contributor to the airborne particulate matter in the environs.