Use of Hydrogen Chemisorption and Ethylene Hydrogenation as Predictors for Aqueous Phase Reforming of Lactose over Ni@Pt and Co@Pt Bimetallic Overlayer Catalysts [electronic resource]

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Tác giả:

Ngôn ngữ: eng

Ký hiệu phân loại: 668.5 Perfumes and cosmetics

Thông tin xuất bản: Argonne, Ill. : Oak Ridge, Tenn. : Argonne National Laboratory ; Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy, 2016

Mô tả vật lý: Size: p. 8587-8596 : , digital, PDF file.

Bộ sưu tập: Metadata

ID: 263395

 Overlayer Pt on Ni (Ni@Pt) or Co (Co@Pt) were synthesized and tested for H<
 sub>
 2<
 /sub>
  generation from APR of lactose. H<
 sub>
 2<
 /sub>
  chemisorption descriptor showed that Ni@Pt and Co@Pt overlayer catalysts had reduced H<
 sub>
 2<
 /sub>
  adsorption strength compared to a Pt only catalyst, which agree with computational predictions. The overlayer catalysts also demonstrated lower activity for ethylene hydrogenation than the Pt only catalyst, which likely resulted from decreased H<
 sub>
 2<
 /sub>
  binding strength decreasing the surface coverage of H<
 sub>
 2<
 /sub>
 . XAS results showed that overlayer catalysts exhibited higher white line intensity than the Pt catalyst, which indicates a negative d-band shift for the Pt overlayer, further providing evidence for overlayer formation. Lactose APR studies showed that lactose can be used as feedstock to produce H<
 sub>
 2<
 /sub>
  and CO under desirable reaction conditions. The Pt active sites of Ni@Pt and Co@Pt overlayer catalysts showed significantly enhanced H<
 sub>
 2<
 /sub>
  production selectivity and activity when compared with that of a Pt only catalyst. The single deposition overlayer with the largest d-band shift showed the highest H<
 sub>
 2<
 /sub>
  activity. Here, the results suggest that overlayer formation using directed deposition technique could modify the behavior of the surface metal and ultimately modify the APR activity.
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