4.8 Article

Enhancing the stability of copper chromite catalysts for the selective hydrogenation of furfural with ALD overcoating (II) - Comparison between TiO2 and Al2O3 overcoatings

Journal

JOURNAL OF CATALYSIS
Volume 326, Issue -, Pages 172-181

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2015.03.017

Keywords

Selective hydrogenation; 2-Furfuraldehyde; Furfuryl alcohol; Stability; Copper chromite; TPR; XAFS; ALD; In-situ experiment

Funding

  1. Institute for Atom-efficient Chemical Transformations (IACT), an Energy Frontier Research Center - U.S. Department of Energy, Office of Science and Office of Basic Energy Sciences
  2. U.S. Department of Energy, Office of Science, and Office of Basic Energy Sciences [DE-AC02-06CH11357]

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TiO2 atomic layer deposition (ALD) overcoatings were applied to copper chromite catalysts to increase the stability for 2-furfuraldehyde (furfural) hydrogenation. After overcoating, about 75% activity was preserved compared to neat copper chromite: much higher activity than an alumina-ALD-overcoated catalyst with a similar number of ALD cycles. The effects of ALD TiO2 on the active Cu nanoparticles were studied extensively using both in-situ TPR/isothermal-oxidation and in-situ furfural hydrogenation via Cu XAFS. The redox properties of Cu were modified only slightly by the TiO2 ALD overcoat. However, a subtle electronic interaction was observed between the TiO2 ALD layers and the Cu nanoparticles. With calcination at 500 degrees C, the interaction between the TiO2 overcoat and the underlying catalyst is strong enough to inhibit migration and site blocking by chromite, but is sufficiently weaker than the interaction between the Al2O3 overcoat and copper chromite that it does not strongly inhibit the catalytic activity of the copper nanoparticles. (C) 2015 Elsevier Inc. All rights reserved.

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