Interlaboratory and Interinstrumental Spectrochemical Precision: Comparison of dc Carbon Arc Optical Emission Spectrographic, Atomic Absorption, and X-ray Fluorescence Spectrometric Procedures

1976 ◽  
Vol 30 (3) ◽  
pp. 335-343 ◽  
Author(s):  
Isaac B. Brenner ◽  
L. Gleit ◽  
A. Harel

A cooperative investigation has been performed to test long-term interlaboratory and interinstrumental accuracy and precision of a dc carbon arc optical emission spectrographic method for determining the common trace and minor elements in silicate rocks and minerals. Comparisons are made with determinations by atomic absorption and X-ray fluorescence spectrometric procedures to indicate agreement or bias of the analytical results, and the presence of systematic errors.

2015 ◽  
Vol 114 ◽  
pp. 52-57 ◽  
Author(s):  
Aleksandra Wandzilak ◽  
Mateusz Czyzycki ◽  
Edyta Radwanska ◽  
Dariusz Adamek ◽  
Kalotina Geraki ◽  
...  

1980 ◽  
Vol 34 (1) ◽  
pp. 39-43 ◽  
Author(s):  
J. J. Labrecque ◽  
H. Schorin

A comparison of an atomic absorption method and x-ray fluorescence procedure for the analysis of the major constituents in Venezuelan laterites from Serranía de los Guaicas and bauxites is presented. These methods are also compared to other classical methods. The accuracy and precision of both these techniques are within the requirements needed. The HF-H3BO3 decomposition step is a disadvantage in the atomic absorption method because of the uncertainty in a complete sample dissolution of bauxites, but it has been shown to be suitable for Venezuelan laterites. The x-ray fluorescence technique presented herein is also limited because of its sample preparation, i.e., the use of expensive Pt-Au crucibles and the large quantity of sample needed.


Author(s):  
Roberta de Oliveira Resende Ribeiro ◽  
Eliane Teixeira Mársico ◽  
Carla da Silva Carneiro ◽  
Julia Siqueira Simoes ◽  
Micheli da Silva Ferreira ◽  
...  

1981 ◽  
Vol 25 ◽  
pp. 127-131
Author(s):  
Hasso Schorin

Laterites and bauxites are residual products derived from a wide variety of rocks by intensive chemical weathering under strongly oxidizing and leaching conditions. Generally the main constituents of these residues are Fe, Al and Ti present in form of hydroxides and/or oxides. The content of silica depends on the thoroughness of the leaching process. The behaviour of trace and minor elements as Ga, Zn, Cu, Ni, Mn and Cr during the laterite/bauxite formation is not yet well established. Precise and accurate analyses of these elements are a prerequisite for such investigations. In this paper the standard addition method is presented and the results are compared with those obtained by calibration standardization. The accuracy and the precision of the methods as well as the distinction limit and the limit of detection for each element are given.


1980 ◽  
Vol 24 ◽  
pp. 329-332
Author(s):  
J. L. de Vries ◽  
N. V. Philips

If we want to evaluate the present state of X.R.S., we should do this in perspective with other methods, e.g. Optical Emission and Atomic Absorption Spectrometry.One way to compare would be to estimate the number of papers published or given at conferences on these three methods. Table 1 gives a survey af some meetings. It is evident that X.R.S. is less talked about than the other methods. The rejuvenation of OES, thanks to the Plasma sources, can also clearly be seen.


1980 ◽  
Vol 45 (3) ◽  
pp. 715-719
Author(s):  
Anna Sopková ◽  
Katarína Radváková

The decomposition of two lanthanoid minerals, viz fluorocarbonate bastnasite and phosphate monazite, is described. Iron present in the solution obtained is removed on anion exchanger. Atomic absorption spectrophotometry was applied to the determination of the minor elements present in the mineral, viz. copper, lead, calcium and magnesium. The measurement conditions for the determination of these elements in microquantities were established by using model solutions, and the accuracy and precision of determination were evaluated.


Mineralogia ◽  
2008 ◽  
Vol 39 (1-2) ◽  
pp. 31-40 ◽  
Author(s):  
John Rakovan ◽  
Yun Luo ◽  
Olaf Borkiewicz

Synchrotron microanalytical methods in the study of trace and minor elements in apatiteSynchrotron X-ray facilities have the capability for numerous microanalytical methods with spatial resolutions in the micron to submicron range and sensitivities as low as ppm to ppb. These capabilities are the result of a high X-ray brilliance (many orders of magnitude greater than standard tube and rotating anode sources); a continuous, or white, spectrum through the hard X-ray region; high degrees of X-ray columniation and polarization; and new developments in X-ray focusing methods. The high photon flux and pulsed nature of the source also allow for rapid data collection and high temporal resolution in certain experiments. Of particular interest to geoscientists are X-ray fluorescence microprobes which allow for numerous analytical techniques including X-ray fluorescence (XRF) analysis of trace element concentrations and distributions; X-ray absorption spectroscopy (XAS) for chemical speciation, structural and oxidation state information; X-ray diffraction (XRD) for phase identification; and fluorescence microtomography (CMT) for mapping the internal structure of porous or composite materials as well as elemental distributions (Newville et al. 1999; Sutton et al. 2002; Sutton et al. 2004).We have employed several synchrotron based microanalytical methods including XRF, microEXAFS (Extended X-ray Absorption Fine Structure), microXANES (X-ray Absorption Near Edge Structure) and CMT for the study of minor and trace elements in apatite (and other minerals). We have also been conducting time resolved X-ray diffraction to study nucleation of and phase transformations among precursor phases in the formation of apatite from solution at earth surface conditions. Summaries of these studies are given to exemplify the capabilities of synchrotron microanalytical techniques.


2017 ◽  
Vol 32 (10) ◽  
pp. 2041-2045 ◽  
Author(s):  
G. L. Scheffler ◽  
Y. Makonnen ◽  
D. Pozebon ◽  
D. Beauchemin

ETV-ICPOES is applied to the fast determination of trace and minor elements in a Mg alloy.


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