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.     

Trace elemental composition of Nigerian coal measured by neutron activation analysis

The instrumental neutron activation analysis (INAA) technique has been used to determine 17 major, minor, and trace elements in samples of the three major sources of Nigerian coal. The NBS Standard Reference Material, Coal SRM 1632, was also analyzed, for the purpose of verifying the accuracy of the method. The results obtained with it were in good agreement with the NBS certified values. The concentrations of the major elements determined for the Nigerian coal were found to be much lower than the mean values of those reported for coal samples from other parts of the world.     

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.     

Instrumental neutron activation analysis for the elemental analysis of cement

Cement is widely used as a construction material in Libya. Production plants introduce certain contaminants to the environment. The dust from such plants is carried away to neighbouring areas. This dust contains a substantial amount of contaminants depending on the origin of clays used in the production. In this study, a survey of elemental concentration of clay and cement was carried out to assess the environmental impact of such plants, especially those that are situated near residential and agricultural areas. Cement and clay samples, imported and locally produced, were analyzed. Instrumental neutron activation analysis was utilized to determine the elemental concentration of As, Ca, Ce, Co, Cr, Eu, Fe, Hf, La, Na, Rb, Sb, Sc, Sm, Ta, Th, U, Yb and Zn. Elevated concentrations of U and Th were found in a number of cement samples. The two nuclides are part of an elaborate decay scheme producing a range of radioactive elements, which emit alpha-, beta- and gamma-radiation. With ⁴⁰K, they could give elevated levels of background radiation in buildings resulting in higher exposure doses. This could pose a health hazard and a detrimental effect on the well being of residents, especially in poor ventillated buildings. Also, cement is the main component for constructing underground reservoirs for collecting rainwater for drinking in private residences, so some harmful elements could leach into water. This is the first comprehensive survey of commercial cement brands and clays used in Libya. These results are intended to build a database for trace element concentrations using INAA.     

Elemental analysis of traditional medicinal seeds by instrumental neutron activation analysis

Traditional medicinal seeds prescribed for specific treatment purposes, were purchased from local markets and analyzed by INAA. The samples were irradiated at Es-Salam research reactor, at a power of 5 MW for 6 h. The accuracy of the method was established by analyzing reference materials. Twenty elements were measured, with good accuracy and reproducibility. The concentration of elements determined, was found to vary depending on the seeds. The daily intake of essential and toxic elements was determined, and compared with the recommended values. The probable cumulative intake of toxic elements is well below the tolerance limits.     

Characterization of trace elements in medicinal herbs by instrumental neutron activation analysis

Medicinal herbs are often used as alternative medicines for healing and controlling some diseases in the world. This study focuses on the content of heavy and trace elements of some widely consumed herbs in Libya. Nine most popular herbs were analyzed by k ₀-instrumental neutron activation analysis. All the samples, SRM and flux monitors were irradiated for 7 and 10 hours under thermal neutron flux of 1.3·10¹³ cm⁻²·s⁻¹ at Tajoura nuclear reactor. In total, 33 elements were analyzed in different herbs. The variations in the concentration of the elements are attributed to soil composition and the climate in which the plant grows. The study showed that the toxic elements found in the samples were below the levels prescribed by health regulations. The precision and the accuracy of the results were evaluated by analyzing the reference materials Pine Needles SRM 1575 and Citrus Leaves SRM1572.     

Possibilities of the elemental analysis of dry biological material by fast neutron activation analysis

The applicability of a 400 kV neutron generator in the elemental analysis of dry biological material is considered. Data for the specific count-rates of 66 elements are given. A procedure for the determination of N, Mg, Si, P, K and Ca is described. The results for three Standard Reference Materials and some samples are given.     

Substoichiometry in neutron activation analysis technique

Neutron activation analysis has become one of the most sensitive and selective analytical technique for the determination of trace elements in a wide variety of matrices. Neutron activation involves the irradiation of the test sample and a standard of the element to be determined with thermal neutrons in a reactor, followed by dissolution of the test sample in the presence of carrier of the element to be determined. The carrier and radioisotopes are separated from the bulk of other induced activities (employing precipitation, solvent extraction, ion exchange etc.) and then the activity induced in the sample is measured on a suitable detector. The standard is treated identically. From the ratios of the activity of the sample and standard and the weight of the standard irradiated, the concentration of element in the test sample is calculated. A rapid, selective and sensitive method of radiochemical separation is subtoichiometric extraction in which the same amount of carrier is added to the irradiated test sample and standard. Exactly the same amount of reagent is added to both the sample and standard but in substoichiometric amounts, followed by the separation of the species formed by extracting it with an organic solvent. The activities of the extracts are measured. The amount of element present in the sample is calculated with help of the ratio of the activities and the weight of the standard taken. The advantages of the method are discussed. Application of substoichiometry in neutron activation has been elucidated with reference to the determination of Au in various samples by substoichiometric neutron activation analysis.     

Determination of the elemental composition of copper and bronze objects by neutron activation analysis

A method for the elemental analysis of copper and bronze objects is described. Na, Co, Ni, Cu, Zn, As, Ag, Sn, Sb, W, Ir and Au are determined through instrumental neutron activation analysis. Mg, Al, V, Ti and Mn are determined after chemical separation using anionic exhange. The detection limits for a number of other elements are also given. Results for NBS standard reference materials are presented and the results compared with the recommended values. The agreement is good. The results of the analysis of five ancient bronze and two copper objects are presented.     

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.     

Circadian rhythm of elemental concentration in Japanese morning-glory revealed by neutron activation analysis

Elemental concentration in each tissue of Japanese morning-glory (Pharbitis nil) during the growth was analyzed by INAA. Plants were grown in water culture for 4 days under 12-hour light and 12-hour dark condition. During the growth, 10 plants in the same developmental stage were periodically harvested. Then the plants were separated into 9 tissues to determine elemental concentration and water content. There was an elemental specific profile within the plant tissue, for example, Na and K concentrations were high in root whereas Mg and Ca concentrations were high at the upper part of the plants. Among the elements studied, Ca and Mg showed rhythmical change in concentration, increased during the day and decreased during the night. This tendency was especially noted at shoot apex. However, water content in all of the tissue was increased about 6 hours prior to the light period and showed maximum in the middle of the light period. About 6 hour difference of water content movement to those of Ca and Mg concentration suggested that water movement drives more dynamic change of each elemental concentration within a plant.     

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 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.     

Analysis of platinum for certain elemental imparities by neutron activation

Silver, ruthenium, cobalt, iron, zinc, cadmium and mercury are determined in platinum by neutron-activation analysis. The scheme developed requires the removal of the platinum matrix by reduction and the sequential separation of the elements by ion-exchange chromatography. The method is suitable for the simultaneous determination (at the ppm level) of these elements in milligram quantities of platinum.     

A study of the elemental composition of diabases by instrumental neutron activation and X-ray fluorescence analysis

The distribution of the elemental composition was studied mainly for microelements in the diabases of the Pechenga suite subjected to various changes. Investigations were conducted by a combination of instrumental neutron activation INAA and X-ray fluoresence XRFA analyses. The INAA was conducted with sample weights of 20–100 mg exposed to irradiation in a nuclear reactor by a flux of neutrons ≈10¹³ n·cm⁻²·s⁻¹. Measurements were carried out by means of a semi-conductor gamma-spectrometer with a Ge(Li) detector. The determination of Al, Mn, Mg, Ti, V, Ca was conducted by short-lived isotopes, while the determination of Na, Sc, Fe, Co, Cr, Hf, Th, La, Ce, Sm, Eu, Yb, Lu by longlived ones. For XRFA samples weighing up to 2 g were irradiated by means of an¹⁰⁹Cd isotope source and were measured by a spectrometer with a Si(Li) detector and beryllium window. By this method we determined the Sr, Zr an Nb contents. Continuous distribution histograms were plotted for the concentration of 22 elements and some of their ratios. Considerable variations in microelemental composition observed in a number of cases make it possible to assess the character of past processes of diabasic change.     

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.     

Analysis of menthol in three traditional Chinese medicinal herbs and their compound formulation by GC-MS

A GC-MS method was developed for identification and determination of menthol in three traditional Chinese medicinal herbs and their compound formulation, a granule for treating colds. Volatile oil was simultaneously distilled and extracted into ethyl ether in a unique glass extractor. The separation was performed on an HP-5 MS column. The standard addition method was used for quantitative determination of menthol content in herbal materials and in the granule. A component in the samples was chosen as the internal standard. The contents were calculated with the ratio of peak area percentage. Menthol was identified as the main component in Mentha haplocalyx Briq., and also existed in spikes of Schizonepeta tenuifolia Briq., Folium perilla frutescens (L.) Britt. and granules. The quantitative calibration range was 0.21-10.5 mg/mL. Good precision was demonstrated by an RSD < 4.0%. The mean content of menthol in Mentha haplocalyx Briq., spikes of Schizonepeta tenuifolia Briq., Folium perilla frutescens (L.) Britt. and granules was 121, 0.234, 1.03 and 1.84 mg/kg respectively.     

Investigation of elemental models in senile dementia and depressives using neutron activation analysis

Instrumental neutron activation analysis has been used to determine the concentration of a range of elements in hair and blood samples, separated into erythrocytes and plasma, obtained from two groups of women, senile demented (9) and depressives (16), and their respective controls (17 and 9). The results suggest that the senile dementia group has significantly higher Al concentrations in erythrocytes and hair relative to the controls but no significant correlation between the aluminium content of hair and that of blood exists. Further, Zn concentrations determined in the erythrocytes and plasma of these subjects were lower compared to the control values. Vanadium levels above our detection limit for the element were found in seven cases out of a total of sixteen in the depressive group. Vanadium was also found to be at higher concentration in the hair of the depressive group compared to the controls. Again no significant correlation was found to exist between the concentration of vanadium in hair and in erythrocyte sample for these seven subjects.