“…Moreover, HPA-n with high n are more active because the time of complete DAP conversion is decreased in their presence. This may be explained by the increase in the oxidation potential of the HPA-n molecule [22]. The initial HPA-n must possess rather high oxidation potential, so that DAP can be oxidized via reaction (2) and loose, at least, four electrons according to the stoichiometry of the reaction.…”
Section: Resultsmentioning
confidence: 99%
“…That was the reason why we studied some acidic HPA-n salts as well. For acidic salts of HTPMOsO4o (HPA-4), the replacement of one proton in a HPA-n molecule by a cation (Co 2+, Mg 2+, AP +, Mn 2+, Na +) decreases the selectivity by 10-15% due to a decrease of the oxidation potential of HPA-n [22]. The optimal [HPA-n]/[DAP] ratio ranges from 5 to 7, and the selectivity to DMQ and DTQ is 75-85% and 70-77%, respectively.…”
A new method is proposed for synthesis of 2,6-dialkyl-l,4-benzoquinones by oxidation of 2,6-dimethyl and 2,6-di-tert-butylphenols with oxygen in a twophase "water-organic" system in the presence ofP-Mo-V heteropoly acids.
“…Moreover, HPA-n with high n are more active because the time of complete DAP conversion is decreased in their presence. This may be explained by the increase in the oxidation potential of the HPA-n molecule [22]. The initial HPA-n must possess rather high oxidation potential, so that DAP can be oxidized via reaction (2) and loose, at least, four electrons according to the stoichiometry of the reaction.…”
Section: Resultsmentioning
confidence: 99%
“…That was the reason why we studied some acidic HPA-n salts as well. For acidic salts of HTPMOsO4o (HPA-4), the replacement of one proton in a HPA-n molecule by a cation (Co 2+, Mg 2+, AP +, Mn 2+, Na +) decreases the selectivity by 10-15% due to a decrease of the oxidation potential of HPA-n [22]. The optimal [HPA-n]/[DAP] ratio ranges from 5 to 7, and the selectivity to DMQ and DTQ is 75-85% and 70-77%, respectively.…”
A new method is proposed for synthesis of 2,6-dialkyl-l,4-benzoquinones by oxidation of 2,6-dimethyl and 2,6-di-tert-butylphenols with oxygen in a twophase "water-organic" system in the presence ofP-Mo-V heteropoly acids.
“…1), the conventional route using 2-methylnaphthalene and chromium oxide in sulphuric acid as the oxidant, co-produces a large amount of inorganic salts. Therefore, many efforts are aimed at developing a catalytic route, and several systems have been investigated which make use of either hydrogen peroxide [48] or O 2 [49] as the oxidant for either 2-methylnaphthalene or 2-methyl-1-naphthol. Matveev et al [49] first described the use of aqueous solutions of Keggin-type P/Mo/V polyoxometalates for the selective, stoichiometric oxidation of 2-methyl-1-naphthol, in a liquid bi-phasic system, at moderate reaction conditions (Vikasib technology).…”
Section: The Anaerobic Synthesis Of 2-methyl-14-naphthoquinone (Menamentioning
This short review documents some examples of the recent innovations in the field of catalytic selective oxidation aimed at improving process performance and process sustainability in general. Some strategies adopted in order to increase selectivity to the desired product are illustrated, including unconventional procedures for the oxidation reaction-the cyclic mode as compared to the cofeed mode-and special arrangements of the catalytic bed, as in the case of the oxidation of o-xylene to phthalic anhydride. The choice of which oxidant to use is also discussed, in relation to the process of oxidative desulphurization of gasoil.
“…In catalysis, it is their redox and acido-basic properties that are exploited for applications [6][7][8][9][10]. They are used for example as oxidation catalysts in liquid phase [11][12][13], with the possibility of catalyzing multi-electron redox reactions. The so-called heteropolyacids (HPAs) are used as strong inorganic acids in various catalytic processes [14,15], in solution or as solid acid catalysts [7].…”
Catalysts Pd/C were prepared in the presence of Mo oxoanions. The size of Mo precursor and the electrostatic interactions with the Pd precursor during the synthesis were found to be responsible for high Pd dispersions. These catalysts were very active for glyoxal oxidation into glyoxalic acid.
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