Low temperature selective catalytic reduction of nitric oxide with urea over activated carbon supported metal oxide catalysts

被引:21
作者
Liu, Kaijie [1 ]
Yu, Qingbo [1 ]
Wang, Baolan [1 ]
Qin, Qin [1 ]
Wei, Mengqi [1 ]
Fu, Qi [1 ]
机构
[1] Northeastern Univ, Sch Met, State Environm Protect Key Lab Ecoind, 11,Lane 3,Wenhua Rd, Shenyang 110819, Shenyang, Peoples R China
基金
中国国家自然科学基金;
关键词
Selective catalytic reduction; catalyst; oxygen-rich; low-temperature; metal oxide; DE-NOX-SCR; NH3; PERFORMANCE; PROMOTION; KINETICS; REMOVAL; IRON; GAS;
D O I
10.1080/09593330.2018.1511752
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Selective catalytic reduction of nitrogen oxides (SCR) with loaded urea is a method for removing NO under oxygen-rich and low-temperature conditions, which can solve the inhibitory effect of oxygen on the catalyst and the slip of ammonia. In present study, a series of activated carbon (wo-AC, co-AC, cs-AC and nu-AC) supported metal (Mn, Fe, Co, Cu and Zn) oxide catalysts with loading urea were prepared by ultrasonic assisted impregnation. The catalysts were used for NO removal at 50-120 degrees C and characterized by XRD, SEM, GFAAS, EDS, XPS, BET and FTIR techniques. The effects of activated carbon type, loaded active element, metal oxides loading, temperature fluctuation on catalytic activity and the catalytic stability were also studied in this paper. The results indicated that nutshell-based activated carbon was more suitable as a carrier than other activated carbons, and urea-10Mn/nu-AC catalyst yielded a higher NO conversion than other catalysts. Besides, for used activated carbons, the larger specific surface area, more micropores distribution and the larger number of hydroxyl group and cyano terminal group are beneficial to the catalytic process. Moreover, the downward trend of NO conversion with increasing temperature suggested the adsorption of reactant gases played a crucial role in the catalytic process of urea-SCR.
引用
收藏
页码:808 / 821
页数:14
相关论文
共 48 条
  • [1] Remarkable enhancement of the selective catalytic reduction of NO at low temperature by collaborative effect of ethanol and NH3 over silver supported catalyst
    Barreau, M.
    Tarot, M-L.
    Duprez, D.
    Courtois, X.
    Can, F.
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 2018, 220 : 19 - 30
  • [2] On a theory of the van der Waals adsorption of gases
    Brunauer, S
    Deming, LS
    Deming, WE
    Teller, E
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1940, 62 : 1723 - 1732
  • [3] Chemical and mechanistic aspects of the selective catalytic reduction of NOx by ammonia over oxide catalysts:: A review
    Busca, G
    Lietti, L
    Ramis, G
    Berti, F
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 18 (1-2) : 1 - 36
  • [4] Present status and perspectives in de-NOx SCR catalysis
    Forzatti, P
    [J]. APPLIED CATALYSIS A-GENERAL, 2001, 222 (1-2) : 221 - 236
  • [5] Vanadium supported on carbon-coated monoliths for the SCR of NO at low temperature:: effect of pore structure
    García-Bordejé, E
    Calvillo, L
    Lázaro, MJ
    Moliner, R
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 2004, 50 (04) : 235 - 242
  • [6] Comparative study of Pt-based catalysts on different supports in the low-temperature de-NOx-SCR with propene
    García-Cortés, JM
    Pérez-Ramírez, J
    Illán-Gómez, MJ
    Kapteijn, F
    Moulijn, JA
    de Lecea, CSM
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 2001, 30 (3-4) : 399 - 408
  • [7] Nitrogen-promoted active carbons as catalytic supports - 2. The influence of Mn promotion on the structure and catalytic properties in SCR
    Grzybek, T.
    Klinik, J.
    Motak, M.
    Papp, H.
    [J]. CATALYSIS TODAY, 2008, 137 (2-4) : 235 - 241
  • [8] SELECTIVE REDUCTION OF NO BY HYDROCARBONS AND OXYGENATED HYDROCARBONS OVER METAL-OXIDE CATALYSTS
    HAMADA, H
    [J]. CATALYSIS TODAY, 1994, 22 (01) : 21 - 40
  • [9] Held W., 1990, SAE Tech. Pap, P209, DOI DOI 10.4271/900496
  • [10] Low temperature SCR of NO with NH3 over carbon nanotubes supported vanadium oxides
    Huang, Bichun
    Huang, Rong
    Jin, Dongjie
    Ye, Daiqi
    [J]. CATALYSIS TODAY, 2007, 126 (3-4) : 279 - 283