Iron-substituted TNU-9, TNU-10, and IM-5 zeolites and their steam-activated analogs as catalysts for direct N2O decomposition

被引:34
作者
Lee, Jun Kyu [1 ,2 ]
Kim, Young Jin [1 ,2 ]
Lee, Heung-Ju [1 ,2 ]
Kim, Su Hyun [3 ]
Cho, Sung June [3 ]
Nam, In-Sik [1 ,2 ]
Hong, Suk Bong [1 ,2 ]
机构
[1] POSTECH, Sch Environm Sci & Engn, Pohang 790784, South Korea
[2] POSTECH, Dept Chem Engn, Pohang 790784, South Korea
[3] Chonnam Natl Univ, Dept Appl Chem Engn, Kwangju 500757, South Korea
基金
新加坡国家研究基金会;
关键词
Iron-substituted zeolites; Steaming; N2O decomposition activity; Framework structure; EX-FRAMEWORK FEZSM-5; FEMFI ZEOLITES; NITROUS-OXIDE; BENZENE HYDROXYLATION; SELECTIVE OXIDATION; FE/ZSM-5; CATALYSTS; NOX REDUCTION; FE; PHENOL; SITES;
D O I
10.1016/j.jcat.2011.08.012
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Isomorphously substituted Fe-TNU-9, Fe-TNU-10, and Fe-IM-5 zeolites containing both Fe and Al in framework positions have been hydrothermally synthesized and tested as catalysts for direct N2O decomposition, together with their steam-activated analogs. When compared with the catalytic results obtained from the corresponding forms of Fe-ZSM-5 with a similar Fe content, the specific activity per mole of iron is higher in the order Fe-TNU-10 < Fe-IM-5 < Fe-TNU-9 < Fe-ZSM-5. While all these catalysts have a promoting effect of NO on N2O decomposition, they exhibit different extents of increase in activity by NO addition, suggesting differences in the type of their extra-framework iron species. From the overall characterization results of our study, we can conclude that the thermal stability of Fe in framework positions differs notably according to the structure type of zeolites, which may have an intrinsic effect upon the nature and distribution of extra-framework iron species, and thus upon their N2O decomposition activity. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:23 / 33
页数:11
相关论文
共 53 条
  • [1] Theoretical interpretation of XAFS and XANES in Pt clusters
    Ankudinov, AL
    Rehr, JJ
    Low, JJ
    Bare, SR
    [J]. TOPICS IN CATALYSIS, 2002, 18 (1-2) : 3 - 7
  • [2] [Anonymous], 1997, KYOTO PROTOCOL UN FR
  • [3] Baerlocher Ch., Database of zeolite structures
  • [4] Structure of the polycrystalline zeolite catalyst IM-5 solved by enhanced charge flipping
    Baerlocher, Christian
    Gramm, Fabian
    Massueger, Lars
    McCusker, Lynne B.
    He, Zhanbing
    Hovmoeller, Sven
    Zou, Xiaodong
    [J]. SCIENCE, 2007, 315 (5815) : 1113 - 1116
  • [5] Structure and reactivity of framework and extraframework iron in Fe-silicalite as investigated by spectroscopic and physicochemical methods
    Bordiga, S
    Buzzoni, R
    Geobaldo, F
    Lamberti, C
    Giamello, E
    Zecchina, A
    Leofanti, G
    Petrini, G
    Tozzola, G
    Vlaic, G
    [J]. JOURNAL OF CATALYSIS, 1996, 158 (02) : 486 - 501
  • [6] Environmental catalysis: trends and outlook
    Centi, G
    Ciambelli, P
    Perathoner, S
    Russo, P
    [J]. CATALYSIS TODAY, 2002, 75 (1-4) : 3 - 15
  • [7] Activity and durability of Fe/ZSM-5 catalysts for lean burn NOx reduction in the presence of water vapor
    Chen, HY
    Sachtler, WMH
    [J]. CATALYSIS TODAY, 1998, 42 (1-2) : 73 - 83
  • [8] Reversible structural transformation of palladium catalyst supported on La-Al2O3 probed with X-ray absorption fine structure
    Cho, SJ
    Kang, SK
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (34) : 8124 - 8128
  • [9] Characterization of iridium catalyst for decomposition of hydrazine hydrate for hydrogen generation
    Cho, Sung June
    Lee, Jun
    Lee, Yun Sung
    Kim, Dong Pyo
    [J]. CATALYSIS LETTERS, 2006, 109 (3-4) : 181 - 187
  • [10] Introduction of Zn, Ga, and Fe into HZSM-5 cavities by sublimation: Identification of acid sites
    El-Malki, EM
    van Santen, RA
    Sachtler, WMH
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (22) : 4611 - 4622