chromatographic monitoring
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2020 ◽  
Vol 4 ◽  
pp. 58-61
Author(s):  
M.V. Sharashkina ◽  
◽  
N.N. Polskaya ◽  
A.Yu. Samoylenko ◽  
M.Yu. Golenkin ◽  
...  


2016 ◽  
Vol 26 (5) ◽  
pp. 455-456
Author(s):  
Yurii N. Zhitnev ◽  
Boris S. Lunin ◽  
Evgeniya A. Tveritinova ◽  
Valerii A. Kreisberg


2014 ◽  
Vol 39 (2) ◽  
pp. 240-245 ◽  
Author(s):  
T. Terabayashi ◽  
S. Endo ◽  
Y. Uemura ◽  
M. Morita ◽  
K. Fukuda ◽  
...  


Talanta ◽  
2011 ◽  
Vol 83 (4) ◽  
pp. 1134-1146 ◽  
Author(s):  
Sílvia Mas ◽  
Albert Carbó ◽  
Sílvia Lacorte ◽  
Anna de Juan ◽  
Romà Tauler


2009 ◽  
Vol 113 (1) ◽  
pp. 190-198 ◽  
Author(s):  
Alina M. Alb ◽  
Michael F. Drenski ◽  
Wayne F. Reed


2007 ◽  
Vol 5 (2) ◽  
pp. 455-465
Author(s):  
Giedrė Kesiũnaitė ◽  
Birutė Pranaitytė ◽  
Audrius Padarauskas ◽  
Arvydas Dikčius ◽  
Romas Ragauskas

AbstractIon-pair chromatographic technique was developed for the rapid and simple determination of the main contaminants (bromide, iodide, sulphite, thiosulphate, thiocyanate, iron(III)-EDTA chelate, free EDTA, hydroquinone and phenidone) in spent photographic solutions. Free EDTA was converted into stable Ni(II)-EDTA chelate prior to analysis. The optimal mobile phase conditions were established by varying the concentrations of tetrabutylammonium (TBA) phosphate and acetonitrile, pH and ionic strength. Separation of five inorganic anions, two metal chelates and two neutral compounds was accomplished in about 30 min using a mobile phase containing 7.5 mmol/L TBA-phosphate, 10 mmol/L NaCl (pH 6.5) and 20% (v/v) acetonitrile. The detection limits (UV detection at 210 nm) ranged from 0.4 µmol/L for phenidone to 8 µmol/L for sulphite with a linearity of 2–2.5 orders of magnitude. The method was applied to the rapid monitoring of spent photographic solutions before and after decomposition. The recovery tests established for two samples were within the range 95–103%.



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