A new process for separating biofuel based on the salt + 1-butanol + water system

•A new process for separating biobutanol.•Biobutanol was recovered to the organic phase.•Most of water was attracted to the aqueous phase.•>97% salt-free biobutanol was obtained. Compared with bioethanol, biobutanol with higher energy density and lower vapor pressure is more suitable as a fuel fo...

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Veröffentlicht in:Fuel (Guildford) 2020-10, Vol.278, p.118402, Article 118402
Hauptverfasser: Fu, Chuhan, Li, Zhuoxi, Song, Wenli, Yi, Conghua, Xie, Shaoqu
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Sprache:eng
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Zusammenfassung:•A new process for separating biobutanol.•Biobutanol was recovered to the organic phase.•Most of water was attracted to the aqueous phase.•>97% salt-free biobutanol was obtained. Compared with bioethanol, biobutanol with higher energy density and lower vapor pressure is more suitable as a fuel for motor engines. However, the typical low acetone-butanol-ethanol (ABE) concentration hinders the competitiveness of biobutanol because of 1-butanol tolerance. In addition, the dehydration of 1-butanol involves the separation of 1-butanol + water heterogeneous azeotrope, which was usually achieved in a two-column distillation + decantation system. A new process based on the determination of the salt + 1-butanol + water system was proposed to separate biobutanol from a 1-butanol + water system. The salting out resulted in the formation of an organic solvent-rich phase and an aqueous phase. All the 1-butanol in the water-rich phase was recovered to the organic phase, and most of the water in the 1-butanol-rich phase was attracted to the aqueous phase by the salting-out effects of the electrolytes, namely potassium carbonate, dipotassium hydrogen phosphate, tripotassium phosphate, and potassium pyrophosphate. This effect produces a top phase containing greater than 97% salt-free 1-butanol. The salting-out effect, the solubility, and the solvation effect of an electrolyte play essential roles in the separation of 1-butanol.
ISSN:0016-2361
1873-7153
DOI:10.1016/j.fuel.2020.118402