Citation: WANG Shao-Zeng, ZOU Hong-Hu, MENG Ming, LI Zhi-Jun, BAO Jun, LI Xin-Gang. The Performance of the NOx Storage Capacity and Sulfur Tolerance of the La0.7Sr0.3Co1-xFexO3 Catalyst[J]. Acta Physico-Chimica Sinica, ;2012, 28(06): 1474-1480. doi: 10.3866/PKU.WHXB201203311 shu

The Performance of the NOx Storage Capacity and Sulfur Tolerance of the La0.7Sr0.3Co1-xFexO3 Catalyst

  • Received Date: 16 January 2012
    Available Online: 31 March 2012

    Fund Project: 国家自然科学基金(20806056, U1162103) (20806056, U1162103) 国家高技术研究发展计划(863 计划) (2008AA06Z323) (863 计划) (2008AA06Z323) 天津市自然科学基金(11JCYBJC03700) (11JCYBJC03700) 教育部新世纪优秀人才支持计划(NCET-10-0615) (NCET-10-0615) 教育部留学归国人员科研启动基金(2011-1568)以及天津大学内燃机燃烧学国家重点实验室开放基金(K2012-05)资助项目 (2011-1568)以及天津大学内燃机燃烧学国家重点实验室开放基金(K2012-05)

  • In this paper, a series of La0.7Sr0.3Co1-xFexO3 (x=0, 0.2, 0.6, and 1.0) catalysts was synthesized by a sol-gel method with calcination at 700 °C in static air. The effect of the Fe doping on the structure, the performance of the NOx storage, sulfur tolerance and regeneration of the perovskite catalysts was investigated. Our results showed that the partial substitution of Co with Fe improved the depersion of the SrCO3 phase, and that the perovskite phase became the only species detected from the X-ray diffraction (XRD) patterns. The NOx storage capacity (NSC) of the catalysts dropped following an increase in the proportion of Fe doping. The deposition of sulfate on the surface and the partial structural damage of the La0.7Sr0.3CoO3 catalyst led to a dramatic reduction in the NSC and the NO oxidation capacity after the sulfation treatment: the NSC being reduced by 64.2%, and the conversion of NO-to-NO2 falling to 43.4% from 72.8%. The sulfur tolerance of the perovskite catalyst, however, was improved after doping with Fe at the B sites of the La0.7Sr0.3CoO3 catalyst. Of all of these catalysts, the perovskite with 60% of Fe doping (the Fe60 sample) gave the best performance for sulfur tolerane properties and regeneration ability. The NSC of the Fe60 sample was reduced by only 16.6%, and the NO-to-NO2 conversion reached the value almost similar to that of the fresh sample (i.e. 69.1%).
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