Biomedical subjects

S B Manohar

Publications and source records attributed to S B Manohar.

8 recordsLinked to original sources

PubMed2003

Development of an internal monostandard instrumental neutron activation analysis method based on in situ detection efficiency for analysis of large and nonstandard geometry samples.

A k0-based internal monostandard instrumental neutron activation analysis method for determination of relative elemental concentration in samples of large size and irregular geometry has been developed. In this method, one of the elements present in the sample is used as comparator. A priori knowledge of the concentration of one of the constituents is required to convert the relative concentration into absolute values. The problems of gamma-ray self-attenuation and geometrical effects that arise in the assay of large and nonstandard geometry samples were overcome by an in situ relative detection efficiency calibration procedure, which requires one or more activation products emitting gamma-rays over a wide range of the spectrum. To minimize the problem of neutron flux perturbations that may arise in large samples, irradiations were carried out using a thermal column with thermal neutron component of more than 99.9%. The method has been standardized with samples of silica (approximately 0.5 kg) and water (0.5 L) spiked with known amounts of different elements and has been advantageously applied to some alloy and metal samples of irregular geometry, where complete compositional characterization was carried out using mass balance. This approach is highly valuable for analysis of large, irregularly shaped samples if not too high demands are set to the degree of accuracy.

Journal Article↗

PubMed2002

Selective preconcentration and determination of chromium(VI) using a flat sheet polymer inclusion sorbent: potential application for Cr(VI) determination in real samples.

A method for sorption preconcentration of Cr(VI) from aqueous samples was developed using a polymer inclusion sorbent (PIS). The PIS used in this method was prepared by physical inclusion of Aliquat-336 in the matrix formed by cellulose triacetate and 2-nitrophenyl octyl ether. This sorbent was found to be stable, cost-effective, efficient for preconcentration of Cr(VI) present in the aqueous samples, and amenable to direct quantitative analysis of Cr(VI) held in it by neutron activation analysis and spectrophotometry. The quantifying of Cr(VI) in PIS by spectrophotometry was carried out by developing color directly on the PIS after reacting it with 1,5-diphenylcarbazide. The distinct color developed on the PIS even at very low concentrations of Cr(VI) suggests its possible use for field determination of Cr(VI). The composition of PIS was optimized to obtain maximum uptake of Cr(VI) without sacrificing uniformity in terms of thickness and distribution of ion-exchange sites, stability, and time required for quantitative sorption of Cr(VI) from aqueous samples. The Cr(VI) species held in the PIS, mainly HCrO4- and CrO4(2-), were found to vary as a function of pH of the aqueous samples from which Cr(VI) was preconcentrated. A close agreement was found in the abundances of Cr(VI) species held in the PIS with those reported in the literature for aqueous solutions at different pH. The variation of Cr(VI) species as a function of pH was found to have a significant impact on the tolerance to anions on the uptake of Cr(VI) in the PIS. The high selectivity of PIS toward Cr(VI) from aqueous solution at pH = 2 was explained on the basis of hydration of anions. The uptake of Cr(VI) was found to be fairly constant (88 +/- 3%) up to nearly complete exchange of counterions present in the PIS. The method developed in the present work was successfully used for the preconcentration of Cr(VI) from tap water and seawater samples containing low levels of Cr(VI).

Anion Exchange Resins↗

PubMed2002

Separation of 48V and 48,49Cr in 7Li irradiated Sc2O3 target by liquid-liquid extraction.

A radiochemical heavy ion activation procedure was carried out for the simultaneous production of carrier-free 48V and 48,49Cr in 7Li ion irradiated Sc2O3 target, followed by the separation of the individual radio-elements in pure form through liquid-liquid extraction using liquid cation exchanger, di-(2-ehtylhexyl) phosphoric acid. Liquid anion exchanger, trioctylamine, was used to obtain extractants from aqueous acid solutions under different experimental conditions.

Journal Article↗

PubMed2002

Validation of a neutron activation analysis method using k0-standardization.

A neutron activation analysis method using k0-standardization has been adopted for multielement analysis using our research reactors. Gold has been used as the comparator. The input parameters, used for calculation of elemental concentration, such as subcadmium to epithermal neutron flux ratio (f), the epithermal neutron flux shape factor (alpha), and the absolute efficiency of the detector (epsilon) have been determined. The values of k0-factors and Q0 (the ratio of resonance integral to thermal neutron cross section) have been taken from the literature. The validity of applying this method in our laboratory is evaluated by analyzing the elemental concentrations with respect to the certified values in eight reference materials of different origin obtained from USGS, IAEA and NIST. The percent deviation of the measured elemental concentrations are found to be within +/- 15% to that of the certified values whereas the percent relative standard deviation ranged from 2% to 10% for most of the elements analyzed.

Journal Article↗

PubMed2002

Heavy metal concentration and distribution in a dated sediment core of Nainital Lake in the Himalayan region.

The concentrations and distribution of the elements, including heavy metals such as As, Ba, Br, Co, Cr, Cs, Fe, Ga, K, Mn, Na, Rb, Sc, Sr, Th and Zn, were investigated in dated sediment cores of Nainital Lake located in the Himalayan region, in Uttar Pradesh state of India, which is considered as a remote background area. The concentrations of the elements were measured by instrumental neutron activation analysis using the k0 method. The International Atomic Energy Agency certified reference material SL-3 was used to evaluate the accuracy of the method. The normalized data for a series of elements were used to understand the source of loading. Elements like Br, Co, Cr, Fe, K, Mn and Zn show a negative correlation with increasing depth whereas elements like As, Ba, Cs, Na and Rb show a positive correlation with increasing depth. By considering the concentration for the bottom segments of the core as close to the baseline concentration, recent flux values for different elements were calculated. An increase in the flux value was observed for Br, Cr, Fe, K, Mn and Zn, which can be attributed to anthropogenic contribution in recent years.

Environmental Monitoring↗

PubMed2001

Separation of carrier-free 181Re produced in 16O-irradiated thulium target.

Heavy ion activation of natural Tm2O3 with 90 MeV 16O beam results in the formation of carrier-free short-lived 181Ir and 181Os which ultimately decay out to 181Re in the matrix. The liquid cation exchanger, HDEHP, has effectively been utilized as an extractant for quantitative separation of bulk thulium target matrix from carrier-free rhenium radionuclide.

Journal Article↗

PubMed2000

Multielement analysis in cereals and pulses by k0 instrumental neutron activation analysis.

The concentrations of some elements in a few varieties of cereals and pulses are determined by Instrumental Neutron Activation Analysis using a single comparator method (k0-standardised NAA method). A total of 15 elements are measured. The method was validated by analysing the Standard Reference Material (SRM-1571) of NIST; the results are within +/-10% of the reported values for the majority of the elements. The measured concentrations of major and minor elements are analysed in terms of the average intake of mineral content and the role of these elements in terms of the nutritional value.

Diet↗

PubMed1999

Separation of carrier free 151,152Tb produced in 16O irradiated lanthanum oxide matrix.

Charged particle activation of natural La2O3 with approximately 78.5 MeV 16O results in the formation of carrier free 151,152Tb isotopes in the matrix. The liquid cation exchanger, HDEHP, has effectively been utilised as an extractant in the quantitative separation of the activation products from the bulk target matrix of lanthanum oxide.

Cation Exchange Resins↗