scholarly journals Fluorometric Determination of Hydrogen Peroxide in Natural Water Samples by Flow Injection Analysis with a Reaction Column of Peroxidase Immobilized onto Chitosan Beads.

1999 ◽  
Vol 15 (11) ◽  
pp. 1077-1082 ◽  
Author(s):  
Tetsuyuki TANIAI ◽  
Akio SAKURAGAWA ◽  
Tadao OKUTANI
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.


1990 ◽  
Vol 47 (5) ◽  
pp. 888-893 ◽  
Author(s):  
William J. Cooper ◽  
Richard G. Zepp

Hydrogen peroxide decay studies have been conducted in suspensions of several well-characterized soils and in natural water samples. Kinetic and product studies indicated that the decay was biologically-mediated, and could be described by pseudo first-order rate expressions. At an initial H2O2 concentration of 0.5 μM, the hydrogen peroxide half-life varied from 1 to 8 h. The decay was inhibited by thermal and chemical sterilization of the soils. Peroxidase activity was inferred in several natural water samples, where the suspended particles catalyzed the oxidation of p-anisidine by hydrogen peroxide. The mass spectrum of the major reaction product indicated that it was the dimer, possibly benzoquinone-4-methoxyanil, a product that also was observed from the horseradish peroxidase-catalyzed oxidation of p-anisidine by hydrogen peroxide.


2020 ◽  
Vol 35 (8) ◽  
pp. 1632-1640
Author(s):  
Vikas Kumar Shukla ◽  
Sangita Dhara ◽  
N. L. Mishra

A total reflection X-ray fluorescence (TXRF) method in conjugation with dispersive liquid–liquid micro-extraction (DLLME) was developed for the determination of uranium present at ultra-trace levels in water samples.


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