Non-destructive neutron activation analysis of the Naragh meteorite

The concentration of 18 elements in the Naragh meteorite that fell in Iran on August 18, 1974, has been measured by neutron activation analysis employing a high resolution Ge(Li) detector.     

Determination of chlorine distribution in silicon dioxide by neutron activation

A neutron activation method for the determination of chlorine distribution in silicon dioxide on the surface of Si wafers has been developed. After irradiation of the sample with a standard, successive layers are removed from the oxide surface by chemical etching and the chlorine content in the solutions obtained is determined gamma-spectrometrically. Using a Ge(Li) detector, a lower limit of determination of 1.0·10⁻⁷ g was obtained. This limit can be improved by using a NaI(Tl) detector. The error of chlorine determination is discussed.     

Determination of rare earths in silicate rocks by epithermal neutron activation and a simple group separation

The determination of nine rare earth elements in rock samples by epithermal neutron activation, followed by a simple group-separation procedure and Ge(Li) γ-ray spectrometry, is described. This method is found to be advantageous for the determination of Nd, Gd, Ho, Er and Lu by means of the short-lived nuclides¹⁴⁹Nd,¹⁵⁹Gd,¹⁶⁶Ho,¹⁷¹Er and^176m Lu. Precision for La, Sm and Eu is similar to that of thermal neutron activation, that for Dy is worse. Samples of the standard rocks, basalt BCR-1 and granite G-2, were analyzed by this procedure and the results obtained are compared with previously reported data.     

Determination of titanium in bauxite: A comparison of neutron activation analysis with the X-ray fluorescence method

The determination of the titanium content of bauxite samples of various origin was studied by thermal neutron activation and X-ray analysis. A²⁵²Cf-fission neutron source and a Ge(Li) detector as well as a³H exciting source and a Si(Li) detector were used in the investigations. Within equal measuring times and with a sample weight of 8 g the sensitivity of the activation method is 0.35 w% Ti with an absolute statistical error less than 10%, while that of the X-ray method is 0.06 w% Ti and the absolute statistical error does not exceed 5%.     

Instrumental neutron activation analysis of Obsidian rock

An instrumental neutron activation analysis technique has been developed for the simultaneous determination of up to 30 elements including major, minor and trace elements in Obsidian Rock (a proposed NBS-SRM-278). INAA method involves both short and long irradiations followed by gamma-ray activity measurement with a Ge(Li) detector. The accuracy of the procedure has been checked by analyzing IAEA Reference Materials.     

Activation analysis of bromine in rock samples

A simple method for the radiochemical neutron activation analysis of bromine in rock samples is described. The irradiated samples are ignited in an induction furnace in a flow of air for four minutes. The bromine expelled is collected onto activated charcoal which is measured using a Ge(Li) detector. The yield of the chemical separation is 85–100% and the detection limit is 7 ppb. The method is discussed and results for the analysis of 14 USGS standard rock samples are presented.     

Multielement analysis of Chinese Environmental Reference Materials by instrumental neutron activation analysis

Instrumental neutron activation analysis (INAA) has been applied for the simultaneous determination of up to 33 elements including major, minor and trace elements in the environmental reference materials soil and coal fly ash from China. The procedure involves both short and long irradiations followed by the measurement of the gamma spectra with a Ge(Li) detector. The analytical results are presented and discussed.     

A new system of gamma-ray spectrometry for activation analysis

A new system of γ-ray spectrometry has been designed and constructed. This system performs a precise, quick and automatic activation analysis using our nuclear reactor (TRIGA-II Research Reactor) as a neutron source. The main components are detector system consisted of a high resolution Ge(Li) detector settled in a shielding cabinet and a well-type NaI(Tl) scintillation counter for anti-Compton measurement, and data acquisition and spectra analysis system performed independently by two mini computer. The system has operated for atmospheric aerosols as an example of activation analysis.     

Neutron activation analysis of high purity silver using high resolution gamma-spectrometry

A method of neutron activation determination of microimpurities in high purity silver has been developed. For matrix activity separation the extraction of silver by dibuthylsulfide (DBS) was employed. The purification coefficient was 10⁸ after triple extraction. Using Ge(Li) detector it was possible to determine 30 elements simultaneously in silver samples.     

Preconcentration of silver from rocks by extraction with bismuth dibenzyldithiocarbamate prior to neutron activation analysis

The method developed for determining trace levels of silver in geological materials involves the extraction of silver with a toluene solution of bismuth dibenzyldithiocarbamate followed by neutron activation of the extract. At pH 2 and in the presence of 0.1M EDTA, silver is quantitatively extracted. Under these conditions only small amounts of copper are coextracted. The detection limits of silver for three different modes of neutron activation analysis: /three cycles with Ge/Li/ detector, one cycle with Ge/Li/ detector and one cycle with NaI/Tl/ detector/ were 12, 20 and 11 ng g^–1, respectively.     

Determination of reactor neutron spectra with multicomponent activation detectors

A procedure is described for the functional fitting of reactor neutron spectra with C/Eⁿ and fission spectra. The method is applied to multicomponent activation detector measurements in a Triga research reactor. In multicomponent detectors a mixture of several detector materials is irradiated as a single unit and measured simultaneously for all reaction products with a Ge(Li) gamma ray spectrometer.     

In situ activation analysis of marine sediments with252Cf

A seabed nuclear probe has been developed which permits the measurement of up to 33 elements at the parts per thousand to parts per million levels in continental shelf areas. The probe consists of a neutron irradiation source,²⁵²Cf, which neutron activates the elements in the minerals of interest. These resulting radioactive elements emit characteristic gamma radiation which is analyzed in situ in 2- to 10 min counting intervals with a Ge(Li) detector system. Details of the irradiation source, the Ge(Li) detector, and spectra taken in situ in a marine environment are discussed with respect to the detection of the minerals at concentrations of economic interest.     

Determination of rare earth elements and heavy metals in river water by preconcentration on chelex 100 and neutron activation

The neutron activation determination of rare earth elements and heavy metals in river water has been studied with Chelex 100 resin as a preconcentration agent. The resin is applied directly as a support for irradiation and for radiochemical separation. The radioactive rare earth elements are recovered selectively and quantitatively from the irradiated resin by elution with hot 1 M sodium carbonate solution; radioactive heavy metals are recovered with 2 M nitric acid. Activities from each eluate are counted with a Ge(Li) detector connected to a multichannel analyzer; La, Sm, Eu, Dy, Mn, Cu and Zn can be determined. The recoveries were almost quantitative and the measurement of chemical yield was unnecessary.     

Determination of rare earths in low grade uranium ores and SRM-rock by instrumental neutron activation analysis

An instrumental neutron activation analysis technique has been developed for simultaneous determination of 10 REE in low grade U/Zr ores and other geological materials. The samples were irradiated with reactor neutrons for 2 min to 8 hrs followed by a cooling of 30 min to 3 weeks. The γ-ray activity was measured with a semi-planar Ge(Li) detector. A precision of 5% has been obtained by the repeated analysis of NBS-SRM. The technique is relatively simple and adaptable on the routine basis.     

Determination of rare-earth eleemnts in rock samples by neutron activation analysis

A Ge(Li) detector combined with cation exchange separation has been used for the determination of 12 rare-earth elements (La, Ce, Nd, Sm, Eu, Gd, Tb, Ho, Er, Tm, Yb, and Lu) in rock samples by neutron activation analysis. After purification by the conventional hydroxide-fluoride precipitation, the rare-earth elements are separated into two fractions, light (La-Tb) and heavy (Ho-Lu), by EDTA cation exchange, and the γ-activities of the two fractions are measured by a Ge(Li) detector. The heavy rare-earths, such as Ho, Er, and Tm, can be easily γ-counted without serious interference from the intense Compton background and photopeaks due to the light rare-earths such as¹⁴⁰La,¹⁵³Sm,¹⁵²Eu, and¹⁶⁰Tb. The chemical yields (60%) for the individual rare-earths are determined by a reactivation technique. The results obtained for the U.S. Geological Survey standard rocks G-1 and W-1 are compared with the previously reported data.     

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.     

Routine multielement instrumental neutron activation analysis of silicate rocks using short-lived radionuclides

By means of thermal neutron activation and countings on the small planar and large coaxial Ge(Li) detector, 13 elements are determined in various silicate rocks, using short-lived radionuclides with half-lives from 2 min to 15 h. A method of routine analysis with simple dead-time and pile-up correction is described and tested with the standard rocks AGV-1 and G-2.     

14.8 MeV neutron activation cross-sections for (n,p) and (n, α) reactions of some rare earth nuclides

The activation cross-sections for sixteen (n, p) and (n, α) reactions on rare earth nuclides were measured at 14.8 MeV neutron energy. A Ge(Li) detector was used for the radioactivity measurements. The measured cross-sections are compared with the semi-empirical predictions of LEVKOVSKII³ and BAYHURST and PRESTWOOD.¹⁶     

Simultaneous determination of rubidium,cesium, chromium and phosphorus in rocks by neutron activation and a simple group separation

A neutron activation method is devised for the simultaneous determination of Rb, Cs, Cr and P in silicate rocks. After alkaline fusion and removal of the insoluble hydroxides, the filtrate is assayed for Rb, Cs and Cr by Ge(Li) γ-spectrometry and for P by β-counting. An additional hydroxide scavenging step permits the γ-spectrometric measurements to be performed by means of a sodium iodide detector. Results obtained on some standard rocks are in good agreement with previous neutron activation data obtained by methods based on more complicated radiochemical procedures.