Catalytic performance of monolithic Ir/SiO2 based catalysts for selective reduction of NO with CO

Motoi Sasaki, Atsushi Takahashi, Masaaki Haneda, Tadahiro Fujitani, Hideaki Hamada

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

Abstract

Ir/SiO2, Ir/WO3-SiO2 and Ba doped Ir/WO3-SiO2 powder catalysts have high activity for the SCR of NO with CO in the presence of O2 (CO-SCR). The activity of these three Ir/SiO2-based catalysts was studied in monolithic form for industrial applications. The catalytic activity was evaluated during heating and cooling cycles between 200° and 600°C. All monolithic catalysts showed low activity for NO reduction during the first heating cycle but high activity appeared from the next cycle. The active temperatures for the monolithic catalysts are different to those for the powder catalysts, probably because of the differences in heat and mass transfer. The activities for CO-SCR gradually decreased with the number of cycles. The activity and durability of the monolith catalysts were consistent with those of the powder catalysts. Ba doped Ir/WO3-SiO2 monolith catalyst was the best catalyst. Catalyst deactivation was caused by oxidation of iridium metal, which is the active species, because the activities of the aged catalysts were recovered by hydrogen reduction. The presence of SO2 in the reaction gas increased the activity of Ir/SiO2 catalyst, but had little effect on the activities of Ir/WO3-SiO2 and Ba doped Ir/WO3-SiO2 catalysts.

Original languageEnglish
Pages (from-to)94-101
Number of pages8
JournalJournal of The Japan Petroleum Institute
Volume50
Issue number2
DOIs
Publication statusPublished - 2007
Externally publishedYes

Keywords

  • Carbon monoxide
  • Iridium catalyst
  • Monolith
  • Nitric oxide
  • Selective reduction
  • Tungsten oxide support

ASJC Scopus subject areas

  • Fuel Technology
  • Energy Engineering and Power Technology

Fingerprint

Dive into the research topics of 'Catalytic performance of monolithic Ir/SiO2 based catalysts for selective reduction of NO with CO'. Together they form a unique fingerprint.

Cite this