Kinetics and mechanism of epoxidation of acrylic acid with aqueous hydrogen peroxide catalyzed by sodium tungstate

1983 ◽  
Vol 23 (3-4) ◽  
pp. 207-212 ◽  
Author(s):  
Pratibha Khare ◽  
Girdhari Lal Agrawal
Keyword(s):  
Hydrogen Peroxide ◽  
Acrylic Acid ◽  
Sodium Tungstate ◽  
Kinetics And Mechanism ◽  
Aqueous Hydrogen Peroxide

Preparation of 4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl A Reinvestigation of Methods Using Hydrogen Peroxide in the Presence of Catalysts

1976 ◽  
Vol 31 (10) ◽  
pp. 1376-1378 ◽  
Author(s):  
G. Sosnovsky ◽  
M. Konieczny
Keyword(s):  
Hydrogen Peroxide ◽  
Phosphotungstic Acid ◽  
Sodium Tungstate ◽  
Spin Labeling ◽  
Quantitative Yield ◽  
Hydrogen Peroxide Solution ◽  
Aqueous Hydrogen Peroxide ◽  
Molar Excess

The preparation of the key intermediate for spin labeling, 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (2), was reinvestigated using sodium tungstate or phosphotungstic acid with or without either Trilon or Triton B. A two-fold and a 3.5-fold molar excess of a 30% aqueous hydrogen peroxide solution was used. The oxidation of 4-hydroxy-2,2,6,6-tetramethylpiperidine (1) with a two-fold molar excess of a 30% aqueous hydrogen peroxide solution in the presence of sodium tungstate alone, under vigorous stirring for two hours, is the superior method (A) for the preparation of 2 in virtually quantitative yield.

Kinetics of the oxidation of dimethyl sulfoxide with aqueous hydrogen peroxide catalyzed by sodium tungstate

1981 ◽  
Vol 59 (4) ◽  
pp. 718-722 ◽  
Author(s):  
Yoshiro Ogata ◽  
Kazushige Tanaka
Keyword(s):  
Hydrogen Peroxide ◽  
Dimethyl Sulfoxide ◽  
Sodium Tungstate ◽  
Catalytic Amount ◽  
Active Oxygen ◽  
Probable Mechanism ◽  
Polarographic Study ◽  
Aqueous Hydrogen Peroxide ◽  
First Order ◽  
Kinetics Of

The oxidation of dimethyl sulfoxide (DMSO) by hydrogen peroxide in the presence of a catalytic amount of sodium tungstate (Na2WO4) has been studied kinetically by means of iodometry of hydrogen peroxide. The reaction is first-order with respect to the substrate and the catalyst, but independent of the concentration of hydrogen peroxide which is present in excess of the catalyst. The polarographic study implies that in solutions two main kinds of peroxytungstic acids (H2WO5 and H2WO8) are formed which contain active oxygen in ratios (active oxygen):(Na2WO4) of 1:1 and 4:1, respectively. The effect of acidity on the oxidation rate and a probable mechanism involving a rate-determining attack of peroxytungstic acids are discussed.

scholarly journals Metal-Organic Frameworks in Oxidation Catalysis with Hydrogen Peroxide

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 283
Author(s):  
Oxana Kholdeeva ◽  
Nataliya Maksimchuk
Keyword(s):  
Hydrogen Peroxide ◽  
Liquid Phase ◽  
Selective Oxidation ◽  
Metal Organic Frameworks ◽  
Short Review ◽  
Catalytic Performance ◽  
Oxidation Catalysis ◽  
Catalyst Stability ◽  
Aqueous Hydrogen Peroxide ◽  
Metal Organic

In recent years, metal–organic frameworks (MOFs) have received increasing attention as selective oxidation catalysts and supports for their construction. In this short review paper, we survey recent findings concerning use of MOFs in heterogeneous liquid-phase selective oxidation catalysis with the green oxidant–aqueous hydrogen peroxide. MOFs having outstanding thermal and chemical stability, such as Cr(III)-based MIL-101, Ti(IV)-based MIL-125, Zr(IV)-based UiO-66(67), Zn(II)-based ZIF-8, and some others, will be in the main focus of this work. The effects of the metal nature and MOF structure on catalytic activity and oxidation selectivity are analyzed and the mechanisms of hydrogen peroxide activation are discussed. In some cases, we also make an attempt to analyze relationships between liquid-phase adsorption properties of MOFs and peculiarities of their catalytic performance. Attempts of using MOFs as supports for construction of single-site catalysts through their modification with heterometals will be also addressed in relation to the use of such catalysts for activation of H2O2. Special attention is given to the critical issues of catalyst stability and reusability. The scope and limitations of MOF catalysts in H2O2-based selective oxidation are discussed.

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