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Title: Oxidation, reduction, and isomerization of allyl alcohol and 1-propanol over Cu[sub 2]O(100)

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100105a019· OSTI ID:6305907
;  [1]
  1. Virginia Polytechnic Inst. and State Univ., Blacksburg (United States)

The reactivity of allyl alcohol and 1-propanol has been studied with TDS and XPS on the polar, Cu[sup +]-terminated, Cu[sub 2]O(100) surface. Allyl alcohol reacts on the (100) surface to give selective and nonselective oxidation products (acrolein, CO, CO[sub 2], H[sub 2]O), an isomerization product (propionaldehyde), and a reduction product (propene). 1-Propanol also reacts on the (100) surface to give selective and nonselective oxidation products (acrolein, propionaldehyde, CO, CO[sub 2], H[sub 2]O) and a reduction product (propene). Both alcohols dissociatively adsorb to form alkoxides. The alkoxide species undergo hydride elimination on the carbon [alpha] to the oxygen to form the corresponding aldehydes. The acrolein and propionaldehyde formed from the alcohols are linked by a common surface enolate intermediate which explains the similarity in C[sub 3] products observed from the two alcohols. A low-temperature reaction to propene is attributed to pathways involving C-O bond scission from unsaturated surface oxygenates to give a surface allyl. Hydrogenation of the resulting allyl produces propene at low temperature. 28 refs., 6 figs., 2 tabs.

OSTI ID:
6305907
Journal Information:
Journal of Physical Chemistry; (United States), Vol. 97:3; ISSN 0022-3654
Country of Publication:
United States
Language:
English