scholarly journals Diaminodiphenylmethane Derivatives as a New Chromogenic Hydrogen Donor in Peroxidase-Catalyzed Oxidation Reaction with Hydrogen Peroxide.

1993 ◽  
Vol 41 (3) ◽  
pp. 620-623 ◽  
Author(s):  
Makoto MIZOGUCHI ◽  
Masanobu SHIGA ◽  
Kazumi SASAMOTO
2011 ◽  
Vol 46 (4) ◽  
pp. 345-354
Author(s):  
Zoheb Karim ◽  
Qayyum Husain ◽  
Rohana Adnan ◽  
Naseem Akhtar

The peroxidase/reverse micelle (RM) system effectively catalyzed the oxidation reaction in cyclohexane, while peroxidase from bitter gourd in aqueous buffer exhibited low catalytic activity. The oxidation of methyl parathion (MPT) has been optimized with effects of pH in the water pools, concentration of peroxidase and degree of surfactant hydration (Wo). The peroxidase/RM system showed a strong pH dependency. Its optimum catalytic activity was obtained when the peroxidase/RM was prepared in a buffer of pH 3.0. The effect of different redox mediators on the peroxidase-catalyzed oxidation of MPT was investigated. MPT was slowly oxidized by the peroxidase/RM system while the addition of phenol as a redox mediator strongly enhanced the catalytic performance of the peroxidase/RM system. Hydrogen peroxide strongly inhibited the activity of peroxidase; when the H2O2 was present at more than 0.80 mM, the MPT transformation was significantly reduced.


1988 ◽  
Vol 37 (5) ◽  
pp. 248-252
Author(s):  
Toshio DEGUCHI ◽  
Ryoichi TAKESHITA ◽  
Akira TANAKA ◽  
Isao SANEMASA

2015 ◽  
Vol 723 ◽  
pp. 601-604 ◽  
Author(s):  
Ran Li ◽  
Ge Wang ◽  
Yan Chun Liu ◽  
Xiao Bin Chen ◽  
Zhi Min Sun ◽  
...  

Benzyl alcohol was selectively oxidized to benzaldehyde with iron (III) complexed to tetra amido macrocyclic ligands (FeIII–TAML) as catalyst and 30% H2O2 as oxidant. The effect of reaction temperature, reaction time, solvent, amount of catalyst and oxidant on the reaction of catalyzed oxidation of benzyl alcohol were explored. The conversion and selectivity of this oxidation reaction were calculated from calibrated GC yields of benzyl alcohol and benzaldehyde. When oxidation reaction was conducted under the conditions: solvent NMMO: ethanol = 1: 1, n (H2O2): n (benzyl alcohol) = 2, n (catalyst): n (benzyl alcohol) = 1%, temperature 80 ̊C and reaction time 60 minutes, the conversion was 91.23% and the selectivity was 90.12%.


1986 ◽  
Vol 34 (12) ◽  
pp. 1667-1672 ◽  
Author(s):  
F Gallyas ◽  
J R Wolff

Physical developers can increase the visibility of end products of certain histochemical reactions, such as oxidative polymerization of diaminobenzidine and selective binding of complex silver iodide ions to Alzheimer's neurofibrillary changes. Unfortunately, this intensification by silver coating is generally superimposed on a nonspecific staining originating from the argyrophil III reaction, which also takes place when tissue sections are treated with physical developers. The present study reveals that the argyrophil III reaction can be suppressed when tissue sections are treated with certain metal ions and hydrogen peroxide before they are transferred to the physical developer. The selective intensification of Alzheimer's neurofibrillary changes requires a pre-treatment with lanthanum nitrate (10 mM/liter) and 3% hydrogen peroxide for 1 hr. The diaminobenzidine reaction can be selectively intensified when physical development is preceded by consecutive treatments with copper sulfate (10 mM/liter, pH 5, 10 min) and hydrogen peroxide (3%, pH 7, 10 min). In peroxidase histochemistry, this high-grade intensification may help to increase specificity and reduce the threshold of detectability in tracing neurons with horseradish peroxidase or in immunohistochemistry when the peroxidase-antiperoxidase method is used.


ChemInform ◽  
2013 ◽  
Vol 44 (29) ◽  
pp. no-no
Author(s):  
Xiaomei Yang ◽  
Si Tang ◽  
Tianliang Lu ◽  
Chen Chen ◽  
Lipeng Zhou ◽  
...  

1992 ◽  
Vol 27 (1) ◽  
pp. 57-68 ◽  
Author(s):  
D.W. Sundstrom ◽  
B.A. Weir ◽  
T. A. Barber ◽  
H. E. Klei

Abstract This project investigated the destruction of organic compounds and microorganisms in water by ultraviolet catalyzed oxidation using hydrogen peroxide as the oxidizing agent. The combination of UV light and hydrogen peroxide was effective in decomposing all of the organic compounds studied. The rates of destruction increased with increasing peroxide concentration and UV light intensity, and were highly dependent on chemical structure. The destruction of mixtures of organic compounds showed strong interactions between reacting components. The inactivation of E. coli and B. subtilis spores by UV light and/or hydrogen peroxide was studied in flat plate reactors. By using thin liquid films, the combination of UV light and peroxide greatly increased the rates of inactivation of both microorganisms. The results were correlated by a mixed second order kinetic model.


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