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Fe、Ce掺杂六铝酸盐催化剂制备及脱硝抗硫性能

Preparation of Fe and Ce doped hexaaluminate catalysts and their property of denitrification and sulfur tolerance
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摘要 用共沉淀法制备六铝酸盐催化剂LaMxAl12-xO19-δ(M=Fe、Ce、FeCe)。用XRD、H2-TPR以及NO转化率对催化剂进行表征和活性验证,分析不同离子取代Al3+对六铝酸盐结构和脱硝抗硫活性的影响。结果表明,Fe离子易于进入六铝酸盐晶格,形成完整的六铝酸盐结构,LaFeAl11O19-δ催化剂具有良好的低温脱硝活性。Ce离子不易进入六铝酸盐晶格,主要以CeO2的形式存在,LaCeAl11O19-δ催化剂有良好的高温脱硝活性。加入SO2后,两种催化剂都有不同程度的失活现象,其中,LaFeAl11O19-δ催化剂失活较为明显。LaFeCeAl10O19-δ催化剂中,Fe离子和Ce离子间会产生协同作用,提高了催化剂的脱硝抗硫活性。 Hexaaluminate catalysts LaMxAl2 -xO19 - δ ( M = Fe, Ce, FeCe) were prepared by co-precipitati- on method. The effects of various ions substitution on crystal structure and the properties of the catalysts were investigated by means of XRD, H2-TPR and activity evaluation for denitrification. The results showed that Fe ions were apt to enter crystal lattice of hexaaluminate to form complete hexaaluminate phase. LaFeAl11O19-δ catalyst possessed good low-temperature denitrifieation activity. Ce ions were difficult to enter crystal lattice of hexaaluminate, and existed mainly in the form of CeO2. LaCeAl11 Ol9-δ catalyst had good catalytic activity at high temperature. After the introduction of SO2 , the denitrification activity of both aforesaid hexaaluminate catalysts declined to some extent, and LaFeA111 O19-δ catalyst was poisoned by SO2 more seriously. The activity of denitrifieation and sulfur tolerance of LaFeCeAllo O19-δ catalyst were enhanced due to the synergistic effect between Fe and Ce ions.
出处 《工业催化》 CAS 2012年第9期65-70,共6页 Industrial Catalysis
基金 国家自然科学基金(21076025)资助项目
关键词 催化化学 脱硝 六铝酸盐 NO 抗硫 共沉淀法 catalytic chemistry denitrifieation hexaaluminate NO sulfur tolerance co-precipitation method
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  • 1刘延,周广栋,王君霞,李文兴,毕颖丽,甄开吉.CO_2/CH_4重整六铝酸盐催化剂制备与反应性能研究[J].燃料化学学报,2001,29(z1):102-104. 被引量:1
  • 2张占辉,王育华,都云昆.BaMgAl_(10)O_(17)∶Eu^(2+)荧光粉的化学共沉淀法合成及其发光性质[J].功能材料,2004,35(5):627-629. 被引量:20
  • 3.催化裂化.1998.7 Vol 16 98年美国炼制协会(NPRA)年会介绍[Z].,..
  • 4国家环保总局信息中心.中国环境状况公报[EB/OL].http:∥www.zhb.gov.cn/eic/649371571659472896/20050610/8632.shtml:2005-06-10.
  • 5US Department of Energy.ABB environmental system SNOXTM flue gas cleaning demonstration project[P].US:DOE/FE-0395,1999.
  • 6Kawamura K.On the Removal of NOx and SO2 in Exhaust Gas from the Sintering Mashine by Eletron Baem Irradiation[J].Radiat Phys Chem,1980,16:133-138.
  • 7Haslbeck J L,Wang C J,Neal L G,et al.Evaluation of the NOXSO Combined NOx/SO2 Flue Gas Treatment Process[P].US:DOE/FE/60148-T2,1984.
  • 8Ma W T,Haslbeck J L,Neal L G.Life-cycle Test of the NOXSO Process[P].US:DOE/DE-FC22-85PC81503,1990.
  • 9Tsuji K,Shiraishi I.Mitsui-BF dry desulphurization and denitrification process using avtivated coke[A].Proceedins of the 1991 SO2 Control Symposium[C].Washington DC:EPA Research and Development,1991.13.
  • 10Nakamura H,Katsuki Y.Simultaneous SOx NOx Removal Employing Absorbent Prepared from Fly Ash[A].Proceedings of 1991 SO2 Control Symposium[C].Washington DC:EPA Research and Development,1991,3(5B,6).

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