Reductive dehydration of butanone to butane over Pt/γ-Al 2O3 and HZSM-5

Samuel D. Blass, Corey Rosenthal, Aditya Bhan, Lanny D. Schmidt

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

We show that butanone can be reacted to form n-butane in an isothermal reactor containing a 1 wt.% Pt/γ-Al2O3 and an HZSM-5 catalyst (total mass of 12-400 mg, Si/Al = 11.5) below 160 C with up to 99% selectivity and 67% yield. The catalyst loading (12-400 mg) and temperature (100-250 C) were varied to obtain primary products whose selectivities decreased with conversion and secondary/tertiary products whose selectivities increased with conversion. As conversion increased, the selectivities of butanol and butene decreased, showing the formation of butane from butanone through a series reaction pathway: butanone → 2-butanol → butene → butane. Butane selectivity increased as the temperature was increased from 100 to 200 C when compared at similar conversions due to higher dehydration rates over the zeolite. Processing ketones at low temperatures over bifunctional catalysts may be an efficient means of obtaining high yields of stable paraffins from reactive oxygenates.

Original languageEnglish (US)
Pages (from-to)54-57
Number of pages4
JournalCatalysis Communications
Volume42
DOIs
StatePublished - 2013

Bibliographical note

Funding Information:
The authors acknowledge financial support from the National Science Foundation: Emerging Frontiers in Research and Innovation (EFRI) — Hydrocarbons from Biomass (Award number: 0937706 ). SB acknowledges the National Science Foundation for a graduate research fellowship.

Keywords

  • Bifunctional zeolite
  • Butanone
  • Dehydration
  • Hydrogenation
  • Reductive dehydration

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