- Title
- Enhancing allyl alcohol selectivity in the catalytic conversion of glycerol; influence of product distribution on the subsequent epoxidation step
- Creator
- Harvey, Luke; Sánchez, Gizelle; Kennedy, Eric M.; Stockenhuber, Michael
- Relation
- Asia-Pacific Journal of Chemical Engineering Vol. 10, Issue 4, p. 598-606
- Publisher Link
- http://dx.doi.org/10.1002/apj.1909
- Publisher
- John Wiley & Sons
- Resource Type
- journal article
- Date
- 2015
- Description
- Conversion of glycerol to allyl alcohol in a flow reactor and subsequent conversion to glycidol in a batch reactor are discussed in this paper. To increase reaction selectivity in the glycerol to allyl alcohol reaction, the catalyst was modified with alkali metal salts. The treatment of the catalyst (Fe/Al₂O₃) with potassium, caesium and rubidium salts enhanced the allyl alcohol yield when a 35 wt% glycerol solution was used as feed. Furthermore, the addition of organic reductants or hydrogen to the glycerol feed increased the allyl alcohol yield. Optimisation of allyl alcohol selectivity was achieved by a combination of alkali metal cation modifiers and the addition of reductants. The influence of acid, base and redox properties on selectivity is presented, focusing on the effect of these properties on product distribution. The effect of by-products from the conversion of glycerol to allyl alcohol on the epoxidation reaction was examined to identify the ideal reaction conditions for maximising the glycidol yield. Epoxidation of allyl alcohol by 30 wt% hydrogen peroxide was conducted in a batch reactor at 333K using titanium silicate-1 catalyst. Conversion of allyl alcohol was high for all conditions; however, hydrolysis of glycidol to glycerol reduces selectivity.
- Subject
- glycerol conversion; allyl alcohol; glycidol; iron oxide; acrolein; acid-base properties
- Identifier
- http://hdl.handle.net/1959.13/1339440
- Identifier
- uon:28256
- Identifier
- ISSN:1932-2135
- Language
- eng
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