Kinetic method for the determination of nanogram amounts of lead(II) using its catalytic effect on the reaction of manganese(II) with 5,10,15,20-tetrakis(4-sulphonatophenyl)porphine

The Analyst ◽  
1987 ◽  
Vol 112 (2) ◽  
pp. 141 ◽  
Author(s):  
Masaaki Tabata
2009 ◽  
Vol 74 (8-9) ◽  
pp. 977-984
Author(s):  
Sofija Rancic ◽  
Snezana Nikolic-Mandic

A new reaction was suggested and a new kinetic method was elaborated for determination of Bi(III) in solution, based on its catalytic effect on the oxidation of phenyl-fluorone (PF) by hydrogen peroxide in ammonia buffer. By application of spectrophotometric technique, a limit of quantification (LQ) of 128 ng cm-3 was reached, and the limit of detection (LD) of 37 ng cm-3 was obtained, where LQ was defined as the ratio signal: noise = 10:1 and LD was defined as signal 3:1 against the blank. The RSD value was found to be in the range 2.8-4.8 % for the investigated concentration range of Bi(III). The influence of some ions upon the reaction rate was tested. The method was confirmed by determining Bi(III) in a stomach ulcer drug ('Bicit HP', Hemofarm A.D.). The obtained results were compared to those obtained by AAS and good agreement of results was obtained.


Talanta ◽  
2008 ◽  
Vol 74 (5) ◽  
pp. 1556-1561 ◽  
Author(s):  
Ferenc T. Pastor ◽  
Gordana A. Milovanović ◽  
Marija Todorović

2018 ◽  
Vol 39 (4) ◽  
pp. 49
Author(s):  
Halil İbrahim Ulusoy ◽  
Ramazan Gürkan

A novel sensitive and relatively selective kinetic method is presented for the determination of V(V), based on its catalytic effect on the oxidation reaction of Ponceau Xylydine by potassium bromate in presence of 5-sulfosalicylic acid (SSA) as activator. The reaction was monitored spectrophotometrically by measuring the decrease in absorbance of Ponceau Xylydine at 640 nm between 0.5 to 7 min (the fixed time method) in H3PO4 medium at 25oC. The effect of various parameters such as concentrations of H3PO4, SSA, bromate and Ponceau Xylydine, temperature and ionic strength on the rate of net reaction were studied. The method is free from most interferences, especially from large amounts of V(IV). The decrease in absorbance is proportional to the concentration of V(V) over the entire concentration range tested (1–15 ng mL−1) with a detection limit of 0.46 ng mL–1 (according to statistical 3Sblank/k criterion) and a coefficient of variation (CV) of 1.8% (for ten replicate measurement at 95% confidence level).The proposed method suffers few interferences such as Cr(VI) and Hg(II) ions. The method was successfully applied to the determination of V(V) in tap water, drinking water, bottled mineralwater samples and a certified standard reference material such as SRM-1640 with satisfactory results. The vanadium contents of water samples were also determined by FAAS for a comparison.The recovery of spiked vanadium(V) was found to be quantitative and the reproducibility was satisfactory. It was observed that the results of the SRM 1640 were in good agreement with the certified value.


2005 ◽  
Vol 539 (1-2) ◽  
pp. 317-325 ◽  
Author(s):  
Gastón Adrián Crespo ◽  
Francisco Javier Andrade ◽  
Fernando Alberto Iñón ◽  
Mabel B. Tudino

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