scholarly journals Determination of peracetic acid and hydrogen peroxide in the mixture

2002 ◽  
Vol 59 (3) ◽  
pp. 277-279 ◽  
Author(s):  
Milanka Bodiroga ◽  
Jasminka Ognjanovic

Iodometric and permanganometric titrations were used for determination of peracetic acid and hydrogen peroxide (H2O2) in the mixture. Two procedures were described and compared. Titrations could be done in only one vessel, in the same reaction mixture, when iodometric titration of peracetic acid was continued after the permanganometric titration of H2O2, (procedure A). Peracetic acid and H2O2, as oxidizing agents, reacted with potassium iodide in an acid medium, evolving iodine. This reaction was used for the quantitative iodometric determination of total peroxide in procedure B. H2O2 reacted with potassium permanganate in acid medium, but peracetic acid did not react under the same conditions. That made possible the selective permanganometric determination of H2O2 in the presence of peracetic acid. The procedure B was performed in two titration vessels (KV=3.4% for peracetic acid, 0.6% for H2O2). The procedure A for iodometric determination of peracetic acid in one titration vessel after permanganometric titration of H2O2 was recommended (KV=2,5% for peracetic acid, 0,45% for H2O2).

2019 ◽  
Vol 11 (14) ◽  
pp. 1930-1938 ◽  
Author(s):  
Junyang Xiao ◽  
Mengyun Wang ◽  
Zijun Pang ◽  
Lin Dai ◽  
Jinfeng Lu ◽  
...  

Recently, increasing attention has been paid towards using commercial peracetic acid (PAA) solution as an efficient disinfectant or a strong oxidant in water treatment.


2006 ◽  
Vol 4 (4) ◽  
pp. 708-722 ◽  
Author(s):  
Akram El-Didamony ◽  
Alaa Amin ◽  
Ahmed Ghoneim ◽  
Ayman Telebany

AbstractFour simple, accurate, sensitive and economical procedures (A–D) for the estimation of gentamicin sulphate and vancomycin hydrochloride, both in pure form and in pharmaceutical formulations have been developed. The methods are based on the oxidation of the studied drugs by a known excess of potassium permanganate in sulphuric acid medium and subsequent determination of unreacted oxidant by reacting it with amaranth dye (method A), acid orange II (method B), indigocarmine (method C) and methylene blue (method D), in the same acid medium at a suitable λmax=521, 485, 610 and 664 nm, respectively. The reacted oxidant corresponds to the drug content. Regression analysis of Beer-Lambert plots showed good correlations in the concentration ranges 4–8, 3–8, 4–9 and 5–9 µg ml−1 with gentamicin and 4–8, 1.5–4, 1.5–4 and 3.5–5.5 µg ml−1 with vancomycin for methods A, B, C, and D, respectively. The molar absorptivity, sandell sensitivity, detection and quantification limits were calculated. The stoichiometric ratios for the cited drugs were studied. The optimum reaction conditions and other analytical parameters were evaluated. The influence of the substance commonly employed as excipients with these drugs were studied. The proposed methods were applied to the determination of these drugs in pharmaceutical formulations. The results have demonstrated that the methods are equally accurate and reproducible as the official methods.


2007 ◽  
Vol 4 (2) ◽  
pp. 180-190
Author(s):  
Baghdad Science Journal

New microphotometer was constructed in our Laboratory Which deals with the determination of Molybdenum (VI) through its Catalysis effect on Hydrogen peroxide and potasum iodide Reaction in acid medium H2SO4 0.01 mM. Linearity of 97.3% for the range 5- 100 ppm. The repeatability of result was better than 0.8 % 0.5 ppm was obtanined as L.U. (The method applied for the determination of Molybdenum (VI) in medicinal Sample (centrum). The determination was compared well with the developed method the conventional method.


1965 ◽  
Vol 48 (4) ◽  
pp. 709-717
Author(s):  
Al Steyermark

Abstract Thirty collaborators participated in a study of the use of oxygen flask combustion for the microdeterminations of bromine, chlorine, and iodine in organic compounds. Generally, there was little difference in the precision of the various methods. Argentometric titration gave better results than did iodometric titration only in the case of bromine. The use of hydrazine sulfate gave better results in the case of iodine than when it was omitted; the same held true for hydrogen peroxide. It is recommended that the study be continued.


1999 ◽  
Vol 71 (10) ◽  
pp. 1935-1939 ◽  
Author(s):  
Bingquan Wang ◽  
Bin Li ◽  
Zhenxin Wang ◽  
Guobao Xu ◽  
Qun Wang ◽  
...  

2014 ◽  
Vol 6 (7) ◽  
pp. 2406-2409 ◽  
Author(s):  
Frank Sode

This paper describes a fast and easy method to analyze peracetic acid in mixtures with both acetic acid and hydrogen peroxide.


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