Determination of absorption correction by the ?two masses? method for XRF analysis of intermediate samples

2003 ◽  
Vol 32 (2) ◽  
pp. 113-118 ◽  
Author(s):  
Rafa? Sitko ◽  
Jerzy Jurczyk
2020 ◽  
Vol 35 (12) ◽  
pp. 2920-2927
Author(s):  
Jorge Machado ◽  
Patrícia Miguel Carvalho ◽  
Ana Félix ◽  
Delfin Doutel ◽  
José Paulo Santos ◽  
...  

In this work, we aim at achieving the most accurate quantitative determination of elements in human tissues by means of X-ray fluorescence spectrometry using the external calibration approach.


1992 ◽  
Vol 41 (11) ◽  
pp. 589-592
Author(s):  
Toshihisa MARUTA ◽  
Shigeru YOKOYAMA ◽  
Hideki KOBAYASHI ◽  
Takeshi YAMANE

2020 ◽  
Vol 8 ◽  
Author(s):  
Sergio Augusto Barcellos Lins ◽  
Stefano Ridolfi ◽  
Giovanni Ettore Gigante ◽  
Roberto Cesareo ◽  
Monica Albini ◽  
...  
Keyword(s):  
X Ray ◽  

2015 ◽  
Vol 1 (3) ◽  
pp. 151
Author(s):  
Sojitra Rajanit ◽  
Paras Virani ◽  
Hashumati Raj

A new simple, economical, precise and accurate method are described for the simultaneous determination of Nifedipine (NIF) and Metoprolol Succinate (MET) in combined tablet dosage form. The proposed method was applied for the determination of Nifedipine and Metoprolol Succinate in synthetic mixture, for determination of sampling wavelength, 10?g/ml of each of NIF and MET were scanned in 200-400 nm range and sampling wavelengths were 313nm for NIF and 275.40nm for MET are selected for development and validation of absorption correction method. For this method linearity observed in the range of 5-25?g/ml for NIF and 25-125?g/ml for MET, and in their pharmaceutical formulation with mean percentage recoveries 100.68 and 100.33, respectively. The method was validated according to ICH guidelines and can be applied for routine quality control testing.


1982 ◽  
Vol 26 ◽  
pp. 409-414
Author(s):  
T. K. Smith ◽  
T. K. Ball

Many analysts use a wet or dry oxidation treatment prior to determination of minor and trace elements in non-fossilised vegetation. This stage is often unnecessary for XRFS since the technique is sufficiently sensitive for many purposes to permit the analysis of unashed material. Indeed, inaccurate results may be obtained if volati1es are lost, if no correction is made for loss on ignition, or if such correction is of large magnitude.


1973 ◽  
Vol 17 ◽  
pp. 269-278
Author(s):  
P. S. Ong ◽  
E. L. Cheng ◽  
G. Sroka

AbstractThe computerized fluorescence radiation induced energy dispersive analyzer (FRIEDA) (1) described earlier uses an x-ray beam with a well defined energy for the excitation of fluorescence radiation, and an Si(Li) detector to measure the total x-ray spectra emitted. Such a system can also simultaneously provide supplemental data for the determination of the dry mass and the sample mass absorption which is necessary for accurate quantitation of the results. This instrumental capabillty has been utilized in the measurement of the trace elements iron, copper, and zinc in serum.Known amounts of two elements are thoroughly mixed with the sample. One element has a ‘high energy’ K line, the other a ‘low energy’ K line. The ratio of these intensities, in the absence of absorption, is a known constant and dependent only on the relative amounts of the respective elements, and on the energy of the exciting radiation. Whenever absorption is present, the ratio will change in a manner directly related to the mass absorption of the sample for these radiations.


1985 ◽  
Vol 39 (6) ◽  
pp. 1040-1042 ◽  
Author(s):  
C. T. Yap ◽  
S. M. Tang

Quantitative determination of barium in Chinese porcelains from the seventeenth century to modern times together with some modern non-Chinese porcelains was made with the use of calibration curves obtained by the addition method. All Chinese porcelains from K'ang Hsi (Kangxi, 1662–1722) up to World War II were found to have a barium content between 100 ppm and 130 ppm. For those made after World War II, the barium content varies from 60 ppm to 7000 ppm, and only a few pieces are in the range from 100 ppm to 130 ppm, making it possible to identify most of the modern fake reproductions.


2015 ◽  
Vol 8 (6) ◽  
Author(s):  
Asghar Maziar ◽  
Daryoush Shahbazi-Gahrouei ◽  
Mohammad Bagher Tavakoli ◽  
Vahid Changizi

RADIOISOTOPES ◽  
1979 ◽  
Vol 28 (1) ◽  
pp. 24-26 ◽  
Author(s):  
Kenji TAKEDA ◽  
Tetsutaro HONDA ◽  
Masayasu NOGUCHI

1994 ◽  
Vol 51 (2) ◽  
pp. 197-206 ◽  
Author(s):  
S.M. Simabuco ◽  
V.F. Nascimento Filho

Three certified samples of different matrices (Soil-5, SL-1/IAEA and SARM-4/SABS) were quantitatively analysed by energy dispersive X-ray fluorescence with radioisotopic excitation. The observed errors were about 10-20% for the majority of the elements and less than 10% for Fe and Zn in the Soil-5, Mn in SL-1, and Ti, Fe and Zn in SARM-4 samples. Annular radioactive sources of Fe-55 and Cd-109 were utilized for the excitation of elements while a Si(Li) semiconductor detector coupled to a multichannel emulation card inserted in a microcomputer was used for the detection of the characteristic X-rays. The fundamental parameters method was used for the determination of elemental sensitivities and the irradiator or transmission method for the correction of the absorption effect of characteristic X-rays of elements on the range of atomic number 22 to 42 (Ti to Mo) and excitation with Cd-109. For elements in the range of atomic number 13 to 23 (Al to V) the irradiator method cannot be applied since samples are not transparent for the incident and emergent X-rays. In order to perform the absorption correction for this range of atomic number excited with Fe-55 source, another method was developed based on the experimental value of the absorption coefficients, associated with absorption edges of the elements.


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