Ullmann's Encyclopedia of Industrial Chemistry 2018
DOI: 10.1002/14356007.a22_173.pub3
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Propanols

Abstract: The article contains sections titled: 1. Introduction 2. Physical Properties 3. Chemical Properties 4. … Show more

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Cited by 19 publications
(17 citation statements)
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“…The produced acetone can be rehydrogenated to isopropanol with hydrogenation catalysts. For example, Raney nickel catalyst showed 99.9% conversion of acetone and 99.9% selectivity of isopropanol in the liquid phase . In addition to the conversion of isopropanol to acetone, dehydration of isopropanol also occurred, producing some of propene (0.2 mmol) and diisopropyl ether (1.8 mmol) in the reaction solution (Table S4).…”
Section: Results and Discussionmentioning
confidence: 91%
“…The produced acetone can be rehydrogenated to isopropanol with hydrogenation catalysts. For example, Raney nickel catalyst showed 99.9% conversion of acetone and 99.9% selectivity of isopropanol in the liquid phase . In addition to the conversion of isopropanol to acetone, dehydration of isopropanol also occurred, producing some of propene (0.2 mmol) and diisopropyl ether (1.8 mmol) in the reaction solution (Table S4).…”
Section: Results and Discussionmentioning
confidence: 91%
“…1-Propanol is manufactured at the industrial level from the reduction of propanal ( 21 ), itself produced from the hydroformylation of petro-based ethylene. It comes with a broad range of applications, including its use as a solvent . Zhu and coworkers demonstrated both the selective conversions of 1,2-PDO and 1,3-PDO into 1-propanol over a Cu–Ce–SBA catalyst .…”
Section: Upgrading Of Polyolsmentioning
confidence: 99%
“…The larger production scale of isopropanol is linked to its larger industrial significance [ 92 ]. Additionally, isopropanol can be obtained from biomass materials, making it more environmentally friendly than the linear isomer [ 59 , 193 ].…”
Section: Electrooxidation Of Alcoholsmentioning
confidence: 99%
“…Additionally, isopropanol can be obtained from biomass materials, making it more environmentally friendly than the linear isomer [ 59 , 193 ]. Both propanol isomers on an industrial scale are produced by hydrogenation—isopropanol is a result of the hydrogenation of acetone (reaction (36)), and propanol is obtained by the hydrogenation of propanal (reaction (37)) [ 92 ]: CH 3 C(O)CH 3 + H 2 → CH 3 CH(OH)CH 3 CH 3 CH 2 CHO + H 2 → CH 3 CH 2 CH 2 OH …”
Section: Electrooxidation Of Alcoholsmentioning
confidence: 99%