کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
61159 47567 2013 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
CO2 hydrogenation on Au/TiC, Cu/TiC, and Ni/TiC catalysts: Production of CO, methanol, and methane
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
CO2 hydrogenation on Au/TiC, Cu/TiC, and Ni/TiC catalysts: Production of CO, methanol, and methane
چکیده انگلیسی


• Au, Cu, and Ni particles deposited on TiC(0 0 1) display a very high activity for the hydrogenation of CO2.
• Titanium carbide enhances the reactivity of the supported metals by 1–2 orders of magnitude.
• A major product is CO produced by the reverse water–gas shift reaction through a HOCO intermediate.
• For Au/TiC and Cu/TiC, a substantial amount of methanol is produced and no methane is detected.
• Ni/TiC produces a mixture of CO, methanol, and methane.

Small Au, Cu, and Ni particles in contact with TiC(0 0 1) display a very high activity for the catalytic hydrogenation of CO2. The major product over these catalysts is CO which is produced by the reverse water–gas shift reaction (RWGS, CO2 + H2 → CO + H2O). In the cases of Au/TiC(0 0 1) and Cu/TiC(0 0 1), a substantial amount of methanol is also produced, but no methane is detected. Ni/TiC(0 0 1) produces a mixture of CO, methanol, and methane. The highest catalytic activity is found for small two-dimensional particles or clusters of the admetals in close contact with TiC(0 0 1). The catalytic activity of the supported metals can be orders of magnitude higher than those of Au(1 0 0), Cu(1 0 0), or Ni(1 0 0). Density functional calculations point to HOCO as a key intermediate for the generation of CO through the RWGS, with the production of methanol probably involving the hydrogenation of a HCOO intermediate or the CO generated by the RWGS.

Small Au, Cu and Ni particles in contact with TiC display a very high catalytic activity for the hydrogenation of CO2 being orders of magnitude more active than bulk Au, Cu or Ni.Figure optionsDownload high-quality image (175 K)Download as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Catalysis - Volume 307, November 2013, Pages 162–169
نویسندگان
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