1994
DOI: 10.1002/chin.199420084
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ChemInform Abstract: Hydrogenation of Phenol to Cyclohexanone on Membrane Catalysts.

Abstract: Hydrogenation of Phenol to Cyclohexanone on Membrane Catalysts. -Hydrogenation of phenol on membrane catalysts consisting of palladium melts allows the one-step preparation of cyclohexanone in high yield and selectivity. -(BASOV, N. L.; GRYAZNOV, V. M.; ERMILOVA, M. M.; Zh.

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“…• dehydrogenation: 1,2-cyclohexanediol [41], 2-butanol [42], ammonia [43], butane [44], cis-3-hexen-1-ol [45], cyclohexane [46], cyclohexene [47], cyclohexanol [48], ethane [49], ethylbenzene [50], heptane [51], hydriodic acid [52], hydrogen sulphide [53], isoamylene [54], isobutane [55], isopropanol [56], methylcyclohexane [57], n-hexane [58], octane [58], propane [59], b-ionol [60], water [61]; • dry reforming of methane [62]; • oxidative dehydrogenation: ethane [63], isobutene [64], methane [65], methanol [66]);…”
Section: Development Of Inorganic Mrsmentioning
confidence: 99%
“…• dehydrogenation: 1,2-cyclohexanediol [41], 2-butanol [42], ammonia [43], butane [44], cis-3-hexen-1-ol [45], cyclohexane [46], cyclohexene [47], cyclohexanol [48], ethane [49], ethylbenzene [50], heptane [51], hydriodic acid [52], hydrogen sulphide [53], isoamylene [54], isobutane [55], isopropanol [56], methylcyclohexane [57], n-hexane [58], octane [58], propane [59], b-ionol [60], water [61]; • dry reforming of methane [62]; • oxidative dehydrogenation: ethane [63], isobutene [64], methane [65], methanol [66]);…”
Section: Development Of Inorganic Mrsmentioning
confidence: 99%