Critical comparison of ICP-OES, XRF and fluorine volatilization-FTIR spectrometry for the reliable determination of the silicon main constituent in ceramic materials

1995 ◽  
Vol 352 (3-4) ◽  
pp. 318-326 ◽  
Author(s):  
G. Kaiser ◽  
A. Meyer ◽  
M. Friess ◽  
R. Riedel ◽  
M. Harris ◽  
...  
2015 ◽  
Vol 30 (7) ◽  
pp. 1655-1662 ◽  
Author(s):  
Michael Krachler ◽  
Rafael Alvarez-Sarandes

High resolution ICP-OES allows for the reliable determination of plutonium in radioactive samples.


2013 ◽  
Vol 11 (9) ◽  
pp. 1548-1553
Author(s):  
Ekaterina Stoyanova ◽  
Irina Karadjova ◽  
Methody Karadjov ◽  
Neli Koseva

AbstractAbstract Cis-diamminedichloroplatinum(II) (cisplatin) was immobilized in a star-shaped polymer carrier. In order to define whether this polymer could be used as a drug delivery system for cisplatin, its characteristics, e.g. loading efficiency and release profile of cisplatin from the polymer in phosphate buffered saline (PBS), have to be assessed, and hence an appropriate analytical procedure for precise and reliable determination of Pt(II) must be established. Optimal instrumental parameters for Pt measurement by commonly used atomic spectrometric methods ETAAS and ICP-OES in various examined media were defined. Matrix interferences observed that were related to both techniques were evaluated, and analytical figures of merit were compared and critically discussed. Graphical abstract


2001 ◽  
Vol 120 (5) ◽  
pp. A599-A599
Author(s):  
C ARNOLD ◽  
A GOEL ◽  
J CARETHERS ◽  
L WASSERMAN ◽  
C COMPTON ◽  
...  

2013 ◽  
Vol 12 (7) ◽  
pp. 460-465
Author(s):  
Sameer Amereih ◽  
Zaher Barghouthi ◽  
Lamees Majjiad

A sensitive colorimetric determination of fluoride in drinking water has been developed using a polymeric zirconium complex of 5-(2-Carboxyphenylazo)-8-Hydroxyquinoline as fluoride reagents. The method allowed a reliable determination of fluoride in range of (0.0-1.5) mg L-1. The molar absorptivity of the complex formation is 7695 ± 27 L mol-1 cm-1 at 460 nm. The sensitivity, detection limit, quantitation limit, and percentage recovery for 1.0 mg L-1 fluoride for the proposed method were found to be 0.353 ± 0.013 μg mL-1, 0.1 mg L-1, 0.3 mg L-1, and 101.7 ± 4.1, respectively.


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