2001
DOI: 10.1016/s0926-860x(01)00472-0
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Cyclohexane oxidation continues to be a challenge

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Cited by 640 publications
(392 citation statements)
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“…37,39 Because of the weaker reducibility of n-butanol than cyclohexane, [40][41][42][43] n-butanol modulates the resistance less than cyclohexane does.…”
Section: Resultsmentioning
confidence: 99%
“…37,39 Because of the weaker reducibility of n-butanol than cyclohexane, [40][41][42][43] n-butanol modulates the resistance less than cyclohexane does.…”
Section: Resultsmentioning
confidence: 99%
“…Results are shown in Table III. The oxidized products are cyclohexanol (CyOH) and cyclohexanone (CyONE), as in (1). In this work cyclohexyl hydroperoxide was not detected from the reaction.…”
Section: B Cyclohexane Oxidationmentioning
confidence: 59%
“…cyclohexanone (80% selectivity, ca. 4% conversion), at a considerably high temperature (150 ˚C) and pressure (15 bar) [1]. Catalytic oxidation of cyclohexane have been carried out using a variety of oxidants such as iodosylbenzene [2], alkyl hydroperoxides [3], m-chloroperbenzoic acid [4] and oxygen [5].…”
Section: Introductionmentioning
confidence: 99%
“…The direct oxidation of cyclohexane to AA would thus join a sustainable approach with better economics, deriving from the lower investment, because of both the smaller number of reactors required, and lower operating costs. 4,116 Despite the good yields to AA achieved by the various technologies developed, the one-step AA process has not yet been implemented at a commercial level because of the high corrosiveness of acetic acid -the solvent for the autoxidation reaction -and the high energy demand for solvent recycle and product workup.…”
Section: Reactions Still Requiring Further Inves-tigation the Synthementioning
confidence: 99%