Major and Trace Element Accumulation in Coastal Sediments along Southeastern Baja California Studied by Instrumental Neutron Activation Analysis and 210Pb Age-Dating

The vertical distribution of K, Rb, Cs, Ca, Sr, Ba, Fe, Cr, Co, Ni, Zn, Sc, Zr, Sb, Se and As was studied by means of instrumental neutron activation analysis in four sediment cores collected from the eastern shelf of tectonically active Baja California peninsula accompanied by ²¹⁰Pb age-dating. ²¹⁰Pb analysis was performed by extraction chromatography with measuring the ingrowing daughter 210Bi radioactivity by liquid-scintillation spectrometry. It was found that concentration variations of Se, As, Sb, Zr and Zn are probably controlled by the intensity and composition of the material supplied from the drainage basin constituted by volcanic and sedimentary rocks.     

Measurement of neutron-induced activation cross sections of lanthanum at 14.8 MeV

Cross-sections for (n,p), (n,α), (n,n′α), (n,t) and (n,2p) reactions have been measured on ¹³⁹La isotope at the neutron energy 14.8 MeV using the activation technique in combination with high-resolution gamma-ray spectroscopy. Neutrons were produced via the ³H(d,n)⁴He reaction using a solid tritium–titanium target. The neutron fluences were determined using the monitor reaction ²⁷Al(n,α)²⁴Na. The neutron energy in this measurement was determined by cross section ratios for the ⁹⁰Zr(n,2n)^89m+gZr and ⁹³Nb(n,2n)^92mNb reactions. Data are reported for the following reactions: ¹³⁹La(n,p)¹³⁹Ba, ¹³⁹La(n,α)¹³⁶Cs, ¹³⁹La(n,n′α)^135mCs, ¹³⁹La (n,t)^137mBa, and ¹³⁹La(n,2p)¹³⁸Cs. The cross sections were discussed and compared with experimental data found in the literature, and with the comprehensive evaluation data in ENDF/B-VII.0, JENDL-3.3, JEFF-3.1/A, and TENDL-2008 libraries.     

Cross-sections of 14 MeV neutron reactions producing short-lived nuclides

The cross-sections for the production of the short-lived nuclides:^26mAl,^197mAu,^136mBa,^79mBr,^139mCe,³⁴Cl,^167mEr,^114m3In,^114m2In,^38mK,^38mCl,²⁶Na,²⁰F,¹⁹²Re,^207mPb,^203mPb,^46mSc,^183mW,^90mZr obtained from (n, 2n), (n, n′), (n, alpha), (n,p) reactions using 14 MeV neutrons, were evaluated by the activation method. The experimental results of this work were compared with those obtained by other authors.     

Simultaneous quantification of 17 trace elements in blood by dynamic reaction cell inductively coupled plasma mass spectrometry (DRC-ICP-MS) equipped with a high-efficiency sample introduction system

A quadrupole inductively coupled plasma mass spectrometer (Q-ICP-MS) equipped with a dynamic reaction cell (DRC) and coupled with a desolvating nebulization system (APEX-IR) was employed to determine 17 elements (Al, As, Ba, Cd, Co, Cr, Li, Mn, Mo, Ni, Pb, Sb, Se, Sn, Sr, V, and Zr) in blood samples. Ammonia (for Al, Cr, Mn, and V) and O₂ (for As and Se) were used as reacting gases. Selection of the best flow rate of the gases and optimization of the quadrupole dynamic bandpass tuning parameter (RPq) were carried out, using digested blood diluted 1 + 9 with deionized water and spiked with 1 μg L⁻¹ of Al, Cr, Mn, V and 5 μg L⁻¹ of As and Se. Detection limits were determined in digested blood using the 3σ criterion. The desolvating system allowed a sufficient sensitivity to be achieved to determine elements at levels of ng L⁻¹ without detriment of signal stability. The accuracy of the method was tested with the whole blood certified reference material (CRM), certified for Al, As, Cd, Co, Cr, Mn, Mo, Ni, Pb, Sb, Se, and V, and with indicative values for Ba, Li, Sn, Sr, and Zr. The addition calibration approach was chosen for analysis. In order to confirm the DRC data, samples were also analyzed by means of sector field inductively coupled plasma mass spectrometry (SF-ICP-MS), operating in medium (m/Δm = 4000) and high (m/Δm = 10,000) resolution mode and achieving a good agreement between the two techniques.     

Cross-sections for formation of <Superscript>178m2</Superscript>Hf and <Superscript>179m2</Superscript>Hf through reactions on natural hafnium at neutron energy 14.8 ± 0.2 MeV

The cross sections for formation of metastable state of ¹⁷⁸Hf (^178m2Hf, 574.215 keV, 31 y) and ¹⁷⁹Hf (^179m2Hf, 362.55 keV, 25.05 d) through reactions induced by 14.8 ± 0.2 MeV neutrons on natural hafnium were measured for the first time. The monoenergetic neutron beam was produced via the ³H(d, n)⁴He reaction on ZF-300-II Intense Neutron Generator at Lanzhou University. Induced gamma activities were measured by a gamma-ray spectrometer with high-purity germanium (HPGe) detector. Measurements were corrected for gamma-ray attenuations, random coincidence (pile-up), dead time and fluctuation of neutron flux. The neutron fluence were determined by the cross section of ⁹³Nb(n, 2n)^92mNb reaction. The neutron energy in the measurement were by the cross section ratios of ⁹⁰Zr(n, 2n)^89m+gZr and ⁹³Nb(n, 2n)^92mNb reactions.     

Investigation of the impurity concentrations and product activities of some targets used in radioisotope production: a neutron activation analysis study

Neutron activation analysis using the k ₀ standardization method (k ₀-NAA) and fast neutron activation analysis using reactor fission neutrons, were used to determine the impurity concentrations in WO₃, MoO₃, SnO₂ and TeO₂ targets. The radioimpurities ¹²⁴Sb, ¹³⁴Cs, ⁶⁰Co, ⁸⁷Rb, ¹⁸²Ta, ²³³Pa, ⁶⁵Zn, ⁵⁹Fe, ^110mAg, ⁵¹Cr, ⁹⁵Zr, ⁷⁵Se and ^114mIn were found in the irradiated targets and their origin either neutron capture reactions, or threshold reactions or both were identified. The specific activities of ¹⁸⁷W, ¹⁸⁸Re, ^99mTc, ^113mIn, ^117mSn and ¹³¹I radioisotopes were determined. It is shown that the epithermal neutron flux significantly contributes to the isotopes characterized with high Q₀ values. It is shown that the ^117mSn isotope can be produced with a high specific activity using the fast neutron component of the reactor neutron spectrum.     

Precise simultaneous determination of zirconium and hafnium in silicate rocks,meteorites and lunar samples

A precise, sensitive and rapid analytical technique has been developed for the simultaneous determination of Zr and Hf in natural silicate matrices. The technique is based on radiochemical neutron activation analysis and employs a rapid fusion dissolution of the sample and simultaneous precipitation of the Zr−Hf pair with p-hydroxybenzene arsonic acid in an acidic medium. The indicator radionuclides,⁹⁵Zr and¹⁸¹Hf, are counted with a pair of high resolution Ge(Li) detectors and the⁹⁵Zr activity is corrected for the contribution from U fission. The chemical yields of the radiochemical separation are based on Hf carrier, which quantitatively carries both Zr and Hf. The yield is determined by reactivation of the processed samples and standards with a²⁵²Cf isotopic neutron source and by counting the 18.6 sec half-life^179mHf. The sensitivity, precision and accuracy of the procedure are demonstrated by replicate analyses of several standard rocks, meteorites and lunar samples which exhibit a wide range of Zr and Hf abundances.     

Determination of trace elements in quartz glass by use of LINA-Spark–ICP–MS as a new method for bulk analysis of solid samples

The determination of trace elements in pure quartz glass samples has been performed by coupling an ICP quadrupole mass spectrometer with the LINA-Spark-Atomizer, an IR laser ablation system dedicated to direct bulk and surface analysis of solid samples. Linear calibration curves were obtained for nine elements (Na, Al, Ca, Ti, Cr, Mn, Zr, Ba, and Pb) in the ng g^–1 range with detection limits of less than 10 ng g^–1 for Ca, Cr, Mn, Zr, Ba, and Pb and in the range of 120–220 ng g^–1 for Na, Al, and Ti. The distance between the laser focal point and the sample surface has a significant influence on signal intensity and precision, both of which can be improved by a factor of approximately two by focusing the laser 15 mm behind the sample surface. Aerosol moistening reduced the standard deviation of the signal intensity by a factor of 2–4. Signal instability, which resulted from different ablation rates or variations in the transmission of the mass spectrometer, were compensated by use of the simultaneously measured SiAr⁺ ion as an internal standard. Under these conditions precision was usually better than 5% RSD. The results were compared with those obtained by use of a commercial LA–ICP–MS system. With this instrumentation linear calibration curves were achieved for three elements only (Al, Ti, and Pb), showing that LA–ICP–MS is less appropriate for bulk analysis in the ng g^–1 range.     

Chemical characterization and 210Pb dating in wetland sediments from the Nhecolândia Pantanal Pond, Brazil

Summary Pantanal, located in the central region of South America, is recognized as one of the world's largest freshwater wetlands. In order to verify possible changes in this environment, a study was undertaken in Nhecolandia Pantanal, Mato Grosso do Sul State, Brazil. Two sediment cores from the Salina do Meio pond (SM1 and SM2) and one core from a small flood land named Baía (B5) were collected in 2001. The elements As, Ba, Br, Ce, Co, Cr, Cs, Eu, Fe, Hf, La, Lu, Na, Nd, Rb, Sb, Sc, Sm, Ta, Tb, Th, U, Yb, Zn and Zr were determined by instrumental neutron activation analysis (INAA). Cluster and factorial analysis were applied to the chemical data. The sedimentation rate in the SM2 core was determined by ²¹⁰Pb method and the mean value found was 0.61 cm ^. y^-1. The results obtained in the present study showed that recent geochemical processes such as desorption, precipitation and dissolution can contribute for the high water alkalinity and salinity in the saline ponds.     

Determination of metal impurities in ultrapure CaCl2 and MgCl2 by ICP OES

An effective, rapid and simple analytical method for the determination of Na, K, Ca, Mg, Cd, Pb, Ba, Fe, Mn, Sr, Zr, Cu, Zn and Al at mg kg⁻¹ levels in the ultrapure salts MgCl₂ and CaCl₂ using optical emission spectrometry was developed. Optimisation of the operation conditions was performed with real samples of ultrapure MgCl₂ and CaCl₂. The results of the determination with multi-elemental water standards were compared to the internal standardisation, the standard addition method, and the maximum allowable content of the above mentioned elements in pure chemicals. The method was shown to be very sensitive with the following limits of detection: Na 1.01, K 3.12, Ca 0.263, Mg 0.275, Cd 0.0832, Pb 0.482, Ba 0.0153, Fe 0.0528, Mn 0.0473, Sr 0.0203, Zr 0.638, Cu 0.0732, Zn 0.0686 and Al 0.459 (all in mg kg⁻¹). The method exhibited satisfactory precision, high analytical recoveries, linear responses of an accuracy of at least 4 orders of magnitude and low contamination susceptibility.     

Cross section measurements for 141Pr(n,γ)142Pr reaction at neutron energies from 13.5 to 14.8?MeV

Activation cross-sections were measured for the ¹⁴¹Pr(n,??)¹⁴²Pr reaction at three different neutron energies from 13.5 to 14.8?MeV. The fast neutrons were produced via the ³H(d,n)⁴He reaction on Pd-300 neutron generator. The natural high-purity Pr₂O₃ powder was used as target material. Induced gamma activities were measured by a high-resolution gamma-ray spectrometer with high-purity germanium detector. Measurements were corrected for gamma-ray attenuations, random coincidence (pile-up), dead time and fluctuation of neutron flux. The neutron fluences were determined by the cross section of ²⁷Al(n,??)²⁴Na reaction. The neutron energy in the measurement were by the cross section ratios of ⁹⁰Zr(n,2n)^89m+gZr and ⁹³Nb(n,2n)^92mNb reactions. The data for ¹⁴¹Pr(n,??)¹⁴²Pr reaction cross sections are reported to be 3.3?±?0.2, 2.7?±?0.2 and 2.2?±?0.2 mb at 13.5?±?0.2, 14.1?±?0.2, and 14.8?±?0.2?MeV incident neutron energies, respectively. Results were discussed and compared with some corresponding values found in the literature.     

A group separation scheme for radiochemical neutron activation analysis for 24 trace elements in rocks and minerals

A group separation scheme has been developed for radiochemical neutron activation analysis for Ca, Cu, Zn, Ga, Rb, Sr, Zr, Sb, Cs, Ba, La, Nd, Sm, Eu, Gd, Tb, Ho, Tm, Yb, Lu, Hf, Ta, W and Th in a wide variety of silicate rocks and minerals, especially ultrabasic rocks and mafic minerals. The samples are decomposed in a hydrofluoric acid-nitric acid mixture in a PTFE-lined bomb. The soluble fluorides (Cu, Zn, Ga, Rb, Zr, Sb, Cs, Ht, Ta, W and Pa) are separated into three groups of elements by sequential elution from a cationexchange resin. The insoluble fluorides (Ca, Rb, Sr, Cs, Ba and REE) are dissolved and purified from interfering iron and scandium activities by extraction with tri-n-butyl phosphate. If necessary, the four main groups can be purified further from interfering activities such as ⁵⁹Fe, ⁵¹Cr and ⁶⁰Co. The accuracy and reproducibility of the procedure were tested by repeated analysis of U.S. Geological Survey standard granite G-2, andesite AGV-1 and dunite DTS-1.     

Activation cross-section measurements for producing short-lived nuclei with 14 MeV neutrons—Ge, Pd, Yb

Activation cross sections for ⁷⁰Ge(n,p)⁷⁰Ga, ⁷⁴Ge(n,p)⁷⁴Ga, ¹⁰⁸Pd(n,p)¹⁰⁸Rh, ¹¹⁰Pd(n,α)¹⁰⁷Ru, and ¹⁷⁴Yb(n,p)¹⁷⁴Tm reactions producing short-lived nuclei with half-lives of several minutes were measured in the energy between 13.5 and 14.8 MeV using activation technique in this work. All cross-section values were relatively obtained on the basis of the standard cross section of ⁹³Nb(n,2n)^92mNb or ²⁷Al(n,α)²⁴Na, and the neutron energies were measured by the method of cross-sectional ratios for ⁹⁰Zr(n,2n)^89m+gZr to ⁹³Nb(n,2n)^92mNb reactions. Careful attention on corrections was paid to neutron irradiation and induced activities measurement. The measured results were discussed and compared with the previous works.     

Measurement of dispersion numbers for 36 and 100% tri-isoamyl phosphate solvents equilibrated with aqueous nitric acid solutions

The cross sections for the ¹¹⁸Sn (n, α)¹¹⁵Cd, ¹²⁰Sn (n, α)^117gCd and ¹²⁰Sn (n, α)^117mCd reactions have been measured in the neutron energy range of 13.5–14.6 MeV using the activation technique and a coaxial HPGe γ-ray detector. The fast neutrons were produced by the T (d, n) ⁴He reaction. The neutron energies in the measurements were determined by cross section ratios for ⁹³Nb(n,2n)^92mNb and ⁹⁰Zr(n, 2n)^89m+gZr reactions. The results of present work were discussed and compared with theoretical calculation data, measurement results found in the literature and with the comprehensive evaluation data in ENDF/B-VII.0, CENDL-3.1, JENDL-4.0 libraries.     

Determination of lead,cadmium and thallium by neutron activation analysis in environmental samples

A radiochemical procedure for simultaneous determination of lead (²⁰³Pb), thallium (²⁰²TI) and cadmium (¹¹⁵Cd^115mIn) after fast neutron activation, based on ion-exchange separation from bromide medium and additional purification steps for Pb and Tl is described. Radioactive tracers²¹⁰Pb and¹⁰⁹Cd were used for determination of the chemical yields of Pb and Cd; for Tl it was determined gravimetrically. Two standard reference materials, BCR CRM No. 146 Sewage Sludge and NIST SRM 1633a Coal Fly Ash were analyzed and satisfactory agreement with certified values was obtained.     

Use of cyclotron-produced fast neutrons in activation analysis

The determination of 15 elements: Pb, Sr, Ba, ti, Ca, Sc, Cs, Zr, Rb, Cr, Se, Ni, Y, Co and Zn was investigated by fast neutron activation analysis using 80 MeV deuterons on various environmental samples. Detection limits of these elements from interference-free spectra were calculated.     

Use of very short-lived nuclides in nondestructive activation analysis with a fast shuttle rabbit

The use of 0.80 sec^207m Pb for the nondestructive determination of lead is described. The 0.570 MeV gamma-ray activity is measured, and corrections are made to allow for the rapid decrease of the dead-time during the measurements. A sensitivity of about 1400 cps/mg Pb and a precision of ±4 % were obtained with a neutron flux of 5·10¹² n·cm^?2·sec^?1. The influence of possible interferences was studied. The fast shuttle rabbit used in this type of analysis is described.     

A comparative study of trace elements in water from various sources in surrounding areas of Nagpur city (India) by instrumental neutron activation analysis

Instrumental neutron activation analysis (INAA) has been used for the determination of 27 elements (Ag, Au, Ba, Br, Ce, Co, Cr, Cs, Eu, Fe, Ga, Hg, Hf, K, La, Mn, Na, Sb, Sc, Se Sr, Th, P, Ta, Tb, Zn and Zr) in 15 water samples collected from different sources (reservoirs, well, borewell, sewage tank, river, rain) in and around Nagpur city (central India) including doubly distilled and a sea water sample from Bombay. Sample residues after evaporation were irradiated at a thermal neutron flux of 10¹²–10¹³ n·cm^–2·s^–1 for 10 min, 1d and 1wk and counted using a HPGe detector and an 4k MCA at different intervals. Several environmental standards from NIST (USA), NIES (Japan) and USGS rock were also analysed for quality assurance. Wide variations in elemental concentrations have been observed in water samples from different sources. Most elemental concentrations in drinking water from various sources, are within ISI/WHO limits. Sea water showed very high concentrations of Ba, Cr, Co, Fe, Hg, Sb, Se and Zn. For doubly distilled and rain waters, however, very low elemental concentrations of Ba, Ce, Fe, Sc, Hg, Se, Sr and Th were observed.     

Accelerated denitration by formic acid accompanied with residual acid-electrolytic trimming

The fruit bodies of wild-growing higher fungi (macromycetes), commonly called mushrooms, of various genera and species collected in localities with different geochemical features and man-made burden in the Czech Republic were analyzed by different modes of activation analysis. The elements Na, Mg, Al, S, Cl, K, Ti, V, Mn, Cu, Br, Ba and Dy were determined by short-term instrumental neutron activation analysis (INAA). Short-term epithermal INAA (ENAA) was used for determination of I and other elements, such as Rb, Ag, and U. The elements Na, K, Sc, Cr, Fe, Co, Cu, Zn, As, Se, Br, Rb, Ag, Cd, Sb, Cs, Ba, La, Ce, Sm, Eu, Hf, Au, Hg and Th were determined by long-term INAA, whereas long-term ENAA enabled determination of several other elements, such as Ni, Ta, W and U. The analytical possibilities of instrumental photon activation analysis (IPAA) using a microtron were also explored and found useful for determination of several additional elements, namely Sr, Y, Zr, Nb, and Pb. High concentrations of several essential and toxic trace elements found (up to hundreds of mg^.g^-1, dry mass) should be of concern in nutritional studies, because mushrooms form non-negligible part of diet in many countries, especially in Middle and East Europe.     

Radioactive and stable elements’ concentration in medicinal plants from Brazil

Since the early days of mankind, plants have been used as food and for medicinal purposes. Still, little information exists in literature about the activity concentration of ²³⁸U and ²³²Th decay products, as well as stable element concentrations in Brazilian plants. Activity concentrations of ²²⁶Ra, ²²⁸Ra and ²¹⁰Pb, and chemical concentrations of As, Ba, Br, Cs, Co, Cr, Cu, Eu, Fe, Hf, La, Lu, Rb, Sb, Sc, Sm, Ta, Tb, Yb, Zn and Zr were determined in ten samples commonly used in Brazilian medicinal plants.