Effect of N3- species on selective acetylene hydrogenation over Pd/SAC catalysts

Maocong Hu, Xianqin Wang

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Selective hydrogenation of acetylene to ethylene is very important for removing a trace amount of acetylene from ethylene. Tuning catalyst acidity is critical for hydrogenation reaction to prevent oligomerization. In this work, NaN3 was introduced to Pd catalyst serving as Lewis base sites. NaN3-Pd/SAC catalysts with different N3- loadings (0-15 wt.%) were prepared by impregnation method and analyzed with BET, temperature-programmed reduction (TPR), Fourier-transferred Infrared (FTIR) spectroscopy, CO pulse chemisorption, temperature-programmed desorption (TPD) of hydrogen and acetylene. The results showed NaN3 covered some Pd species and increased the reduction temperatures of catalysts. Also NaN3 addition decreased the catalyst surface areas due to blocking some pores on the support. N3- on the catalysts lowered hydrogen adsorption capacity but showed superior adsorption capability for acetylene, the selectivity and conversion of the acetylene hydrogenation was negatively affected by N3- species under the current operation conditions. The amount of the adsorbed hydrogen and the types of acetylene adsorption played important roles for the hydrogenation reaction. This work provides insights on how to prepare an effective catalyst for removing acetylene impurity from ethylene.

Original languageEnglish (US)
Pages (from-to)98-104
Number of pages7
JournalCatalysis Today
Volume263
DOIs
StatePublished - Apr 1 2016

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)

Keywords

  • Dual functional sites
  • Lewis base
  • NaN
  • Pd/SAC
  • Selective acetylene hydrogenation

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