Development of gamma spectrometric method for the determination of thorium in phosphoric acid solution

2010 ◽  
Vol 98 (5) ◽  
Author(s):  
N. N. Mirashi ◽  
Satyajeet Chaudhury ◽  
S. K. Aggarwal

AbstractGamma spectrometric determination of thorium in sintered thoria dissolved in strong phosphoric acid was studied using a high purity germanium (HPGe) detector.

1977 ◽  
Vol 60 (5) ◽  
pp. 1018-1021 ◽  
Author(s):  
William M Smith

Abstract Reserpine-rescinnamine group alkaloids are extracted from Rauwolfia serpentina preparations into dimethylsulfoxide (DMSO)-methanol and diluted with 0.5N H2SO4. The chloroform extract of this solution is passed through a 0.1N NaOH-Celite column and then through a silica gel column. The weakly basic alkaloids trapped on the latter column are eluted with chloroform-methanol; a portion of the eluate is treated with a vanadium pentoxide-phosphoric acid solution, and the reserpine-rescinnamine content is determined by measuring the intensity of the resulting fluorescence. The following means and standard deviations (11 collaborators) were obtained for the determination of reserpine-rescinnamine group alkaloids in 4 samples of Rauwolfia serpentina (NF reference powder, 100 and 50 mg commercial tablets, and 45 mg synthetic tablet formulation) : 0.173%, 0.0050; 0.128%, 0.0030; 0.150%, 0.0069; and 0.142%, 0.0032; respectively. The method has been adopted as official first action.


2020 ◽  
Vol 58 (5) ◽  
pp. 464-470
Author(s):  
Yang Xu ◽  
Huailei Yang ◽  
Jihong Chi ◽  
Fang Wang ◽  
Huiwei Bao

Abstract A HPLC-DAD method was established for the simultaneous determination of eight components in Leonuri Herba from different habitats, as well as providing methodological reference for quality control of Leonuri Herba. In this study, absolute ethanol extracts of the medicinal material were considered as the sample solutions to be analyzed. Agilent ZORBAX SB-C18 column (250 mm × 4.6 mm, 5 μm) was used for determination maintained at the temperature of 30°C. Gradient elution was performed with a mobile phase of methanol (B)-0.1% phosphoric acid solution (A) at the flow rate of 1.0 mL·min−1. The analysis was carried out at the wavelength of 225, 280 and 320 nm. The measured eight components showed good linear relationships within their own concentration range. Average recoveries ranged from 98.83 to 100.36% with RSDs of 1.14~1.97%. The proposed method was found to be simple, accurate and reproducible, which provided an effective quantitative analytical method for quality control of Leonuri Herba from different habitats.


2009 ◽  
Vol 19 (01n02) ◽  
pp. 67-76
Author(s):  
SANJIV KUMAR ◽  
G. L. N. REDDY ◽  
V. S. RAJU

This paper deals with studies on Ge K α and K β escape peaks in particle induced X-ray emission (PIXE) spectra recorded by a high purity germanium (HPGe) detector. A knowledge of the energies and intensities of these escape peaks is desirable for accurate qualitative as well as quantitative analysis of elements by PIXE. The spectral interferences caused by Ge K escape peaks in the determination of Fe in U by PIXE are highlighted for illustration. A simple theoretical approach based on the production of Ge K X-rays inside the Ge crystal of the detector during the process of detection of the incident characteristic X-rays and the subsequent escape of a fraction of the produced radiations from the crystal, is described to calculate the intensity ratio of the Ge escape peak to its parent characteristic X-rays. The calculated values are in agreement with the experimental values and those estimated using the formulation provided in GUPIX software for PIXE. The Ge K escape peaks are very prominent; the intensities of Ge K α escape peaks, from bromine to silver, range from 15% to 6% of those of their respective K α X-rays. These intensities are, in general, considerably higher compared to those of Si escape peaks in spectra recorded by Si ( Li ) detector. Ge K escape peaks therefore may give rise to severe interferences. The present approach provides a precise (~8%) determination of the intensity of an escape peak and thereby facilitates a reliable PIXE analysis.


1978 ◽  
Vol 7 (4) ◽  
pp. 313-318 ◽  
Author(s):  
I.A.S. Mansour ◽  
G.H. Sedahmed ◽  
M.Z. El-Abd ◽  
A.M. Ahmed

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