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Characterization of the adsorbed state of isoprene on alumina and copper-alumina catalysts by sup 13 C NMR and in situ diffuse reflectance infrared spectroscopy

Journal Article · · Journal of Physical Chemistry; (USA)
DOI:https://doi.org/10.1021/j100380a040· OSTI ID:6331228
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  1. Universite des Sciences et Techniques de Lille Flandres-Artois, Villeneuve d'Ascq (France)

In situ {sup 13}C NMR spectroscopy and diffuse reflectance infrared spectroscopy (DRIFTS) have been used to characterize the adsorbed states of isoprene on both {gamma}-Al{sub 2}O{sub 3} and Cu/{gamma}-Al{sub 2}O{sub 3} catalysts. Both techniques have been shown to be quite complementary and provide very fine information. Isoprene molecules are physisorbed only at room temperature on alumina. On reduced copper-alumina, isoprene is mainly physisorbed, but a few chemisorbed species are evidenced. Taking into account the {sup 13}C NMR line-width variations and the IR results, an adsorption model is proposed for Cu/{gamma}-Al{sub 2}O{sub 3}: reduced copper induces a selective orientation for the physisorbed isoprene molecules. The chemisorbed species detected by DRIFTS is attributed to a {pi}-complex of isoprene with Cu{sup +} sites on the reduced copper-alumina spinel surface. The physisorbed species is the precursor of this {pi}-complex, and this view agrees with the selectivity of isoprene hydrogenation on copper catalysts.

OSTI ID:
6331228
Journal Information:
Journal of Physical Chemistry; (USA), Journal Name: Journal of Physical Chemistry; (USA) Vol. 94:17; ISSN 0022-3654; ISSN JPCHA
Country of Publication:
United States
Language:
English