scholarly journals Analytical application of acidic victoria blue 4R mixture with KBrO3 for the kinetic determination of traces of antimony(III) by spectrophotometry

2012 ◽  
Vol 31 (1) ◽  
pp. 29
Author(s):  
Violeta Mitić ◽  
Snežana Nikolić-Mandić ◽  
Vesna Stankov-Jovanović

The present paper describes a simple, selective and sensitive kinetic method for the determination of trace amounts of Sb(III) in the presence of Sb(V) based on its inhibition effect on the redox reaction between bromate and Victoria blue 4R (V.B. 4-R) in hydrochloric acid media. The reaction was followed spectrophotometrically by measuring the decrease in the absorbance of V.B. 4-R at 596.3 nm. Optimum operating conditions regarding reagent concentrations were established. The optimized conditions yielded a theoretical detection limit of 1.30·10‒8 g cm–3 Sb(III) based on the 3S0 criterion. The method allows the determination of Sb(III) in the range of 5·10‒8 ‒ 1.1·10‒6 g cm–3. The effects of certain foreign ions the reaction rate were determined for an assessment of the selectivity of the method. The kinetic parameters of the reaction were reported, and the rate equations were suggested. The results were validated statistically and through recovery studies. The proposed method has been successfully applied to the determination of Sb(III) in various model and real samples.

2003 ◽  
Vol 68 (10) ◽  
pp. 765-769
Author(s):  
Sofija Rancic ◽  
Rangel Igov ◽  
Todor Pecev

A new reaction is suggested and a new kinetic method is elaborated for the As(HI) traces determination in solution, on the basis of their catalyzing effect on komplexon III (EDTA) oxidation by KMnO4 in a strong acid solution (H2SO4). Using a spectrophotometric technique, a sensitivity of 72 ng/cm3 As(IIl) was achieved. The relative error of method varies from 5.5 to 13.9 % for As(HT) concentration range from 83 to 140 ng/cm-1. Appropriate kinetic equations are formulated and the influence of some other ions, including the As(V), upon the reaction rate is tested.


2000 ◽  
Vol 65 (8) ◽  
pp. 595-601
Author(s):  
S.S. Mitic ◽  
J.I. Vucetic ◽  
S.M. Miletic ◽  
D.A. Kostic

A kinetic method is described for the determination of Se(IV) based on its inhibiting effect on the Fe(III) catalysis of the oxidation of C6H5COONa with hydrogen peroxide. The detection limit is 0.06 pg cmT The relative error ranges between 2.1 and 9.5 % for the concentration interval 0.26 to 2.6 ?g cm-3. Kinetic equations are proposed for the investigated process. The effects of certain foreign ions upon the reaction rate were determined in order to assess the selectivity of the method. The method was applied for the determination of Se(IV) in pharmaceutical samples.


2003 ◽  
Vol 68 (3) ◽  
pp. 219-226 ◽  
Author(s):  
Zora Grahovac ◽  
Snezana Mitic ◽  
Emilija Pecev

A new kinetic method is described for the determination of ultramicro amounts of Cu(II) based on its catalytic effect on the oxidation of trisodium-2-hydroxy 1-(4-sulphonato-1-naphthylazo)naphthalene-6,8-disulphonato (red artificial color PONCEAU 4R) by hydrogen peroxide in borate buffer (B.B). The detection limit given by Perez-Bendito is 0.8 ng/cm3, but the detection limit that we experimentaly determined is 3.8 ng/cm3. The relative error ranges between 7.77 and 2.09%for the concentration interval 3.8 to 50.1 ng/cm3. Kinetic equations are proposed for the investigated process. The effects of certain foreign ions upon the reaction rate were determined for an assessment of the selectivity of the method. The method was applied for the determination of Cu(II) ions in samples of alloy.


2003 ◽  
Vol 68 (2) ◽  
pp. 131-136 ◽  
Author(s):  
Aleksandar Igov ◽  
Ranko Simonovic ◽  
Rangel Igov

A new catalytic reaction is proposed and a kinetic method developed for the determination of ultramicro amounts of As(III) on the basis of its catalytic activity in the oxidation of ethylenediamine-N,N?-diacetic-N,N? dipropionic acid (EAP) by KMnO4 in the presence of hydrochloric acid. Under optimal conditions, the sensitivity of the method is 20 ng/cm3. The probable relative error is 7.6 ? 14.5 % for the concentration range 50 ? 200 ng/cm3 As(III). The effect of certain foreign ions upon the reaction rate were determined for the assessment of the selectivity of the method. The method has relatively good selectivity. Kinetic equations were proposed for the investigated process.


2002 ◽  
Vol 67 (10) ◽  
pp. 661-667 ◽  
Author(s):  
Snezana Mitic ◽  
Valentina Zivanovic

Akinetic method for the determination of phenol is proposed. The method is based on the inhibiting effect of phenol on the Mn(II) catalysis of the oxidation of malachite green with potassium periodate. The reaction rate was followed spectrophotometrically at 615 nm. Kinetic expression for the reaction in the presence and absence of phenol are postulated. The optimal experimental conditions for the determination of phenol were established and phenol was determined in concentrations from 30.0 to 188.0 ng/cm3 with a relative standard deviation of 5.5%. The lower detecton limit is 7.8 ng/cm3. The effects of certain foreign ions upon the reaction rate were determined for the assessment of the selectivity of the method. The method was applied for the determination of phenol in tap and river water.


2001 ◽  
Vol 66 (9) ◽  
pp. 631-636
Author(s):  
Rangel Igov ◽  
Violeta Mitic ◽  
Todor Pecev ◽  
Vesna Stankov-Jovanovic

A new reaction is suggested and a new method is elaborated for determination of micro amounts of Sn(II) based on its inhibiting effect on the oxidation of {4-bis[n-(dimethylamino) phenyl]methylene-2,5-cyclohexadiene-1-ilydene}dimethyl-ammonium chloride (crystal violet CV) by H2O2. The method sensibility is 0.4 ?g/cm3. The probable relative error is 2.8-12.8 % for Sn(II) in the concentration interval of 3 to 0.8 ?g/cm3. The kinetic equation for this process is given. The influence of some other ions on the reaction rate was tested. The method was applied to the determination of Sn(II) in a sample of microalloy.


1977 ◽  
Vol 23 (10) ◽  
pp. 1928-1930 ◽  
Author(s):  
L H Bernstein

Abstract A steady-state kinetic method has been revised for measuring lactate dehydrogenase isoenzyme activities, which relates the inhibition of heart-type isoenzyme activity to the overall isoenzyme composition of the enzyme subunits. The method depends on the pH-dependent formation of an inhibitory ternary complex by the heart-type isoenzyme with NAD+ and pyruvate (if the reaction is measured by NADH oxidation). A preincubation step in the previous method is eliminated. The isoenzymes are measured by measuring the reduction of pyruvate in two different concentrations, which favor either the total or fractional activity, depending on the concentrations of pyruvate and the percentage of heart-type subunits. The method has been adapted to a centrifugal analyzer, which has speeded automated isoenzyme determinations, with an accuracy comparable to that for electrophoretic methods.


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.


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