2008
DOI: 10.1016/j.catcom.2008.09.005
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Kinetic study of oxidation of cyclohexanol using bimetallic iron–copper macrocyclic complex catalyst

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Cited by 11 publications
(4 citation statements)
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“…In the conventional two-step process, phenol is firstly hydrogenated to cyclohexanol, and cyclohexanol is subsequently dehydrogenated to yield cyclohexanone. [13][14][15][16] Therefore, the one-step process, the selective hydrogenation of phenol to cyclohexanone, has a large number of advantages. It simplifies the reaction steps, improves the efficiency of the hydrogen utilization, reduces waste disposal, 3,[17][18][19] and avoids the difficult separation of phenol-cyclohexanol and phenolcyclohexanone azeotropes.…”
Section: Introductionmentioning
confidence: 99%
“…In the conventional two-step process, phenol is firstly hydrogenated to cyclohexanol, and cyclohexanol is subsequently dehydrogenated to yield cyclohexanone. [13][14][15][16] Therefore, the one-step process, the selective hydrogenation of phenol to cyclohexanone, has a large number of advantages. It simplifies the reaction steps, improves the efficiency of the hydrogen utilization, reduces waste disposal, 3,[17][18][19] and avoids the difficult separation of phenol-cyclohexanol and phenolcyclohexanone azeotropes.…”
Section: Introductionmentioning
confidence: 99%
“…1d, the Pd presents a doublet corresponding to Pd 3d 5/2 and Pd 3d 3/2 . The Pd 3d 3/2 peak at 340.8 eV and the Pd 3d 5/2 peak at 335.6 eV are attributed to Pd 0 , while the peaks at 337.5 eV (Pd 3d 3/2 ) and 342.5 eV (Pd 3d 5/2 ) can be assigned to Pd +   2 .…”
Section: Resultsmentioning
confidence: 98%
“…Generally, phenol can be hydrogenation to cyclohexanone in a “one-step” or a “two-step” process. In two-step, phenol is hydrogenated to cyclohexanol firstly and cyclohexanol is dehydrogenated to yield cyclohexanone subsequently 2, 3 . The one-step process avoids the endothermic step of dehydrogenation and therefore is certainly preferable in terms of capital costs and energy savings.…”
Section: Introductionmentioning
confidence: 99%
“…Oxidation of alcohols to the corresponding ketones and aldehydes is a key reaction in organic synthesis [20][21][22], since the selective formation of carbonyl functional groups in hydrocarbons makes them useful intermediaries for pharmaceuticals and cosmetic products [23]. Cr-containing catalysts have found application on the oxidation of several organic substrates, including cyclohexene and cyclohexanol [24][25][26].…”
Section: Introductionmentioning
confidence: 99%