Characteristics of High Surface Area Molybdenum Nitride and Its Activity for the Catalytic Decomposition of Ammonia

被引:18
作者
Baek, Seo-Hyeon [1 ]
Yun, Kyunghee [1 ]
Kang, Dong-Chang [2 ]
An, Hyejin [3 ]
Park, Min Bum [3 ]
Shin, Chae-Ho [1 ]
Min, Hyung-Ki [4 ]
机构
[1] Chungbuk Natl Univ, Dept Chem Engn, Chungbuk 28644, South Korea
[2] Pohang Univ Sci & Technol, Dept Chem Engn, Pohang 37673, South Korea
[3] Incheon Natl Univ, Dept Energy & Chem Engn, Incheon 22012, South Korea
[4] Lotte Chem Res Inst, Daejeon 34110, South Korea
基金
新加坡国家研究基金会;
关键词
molybdenum nitride; ammonia decomposition; hydrogen production; nitridation; topotactic transition;
D O I
10.3390/catal11020192
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
High surface area (>170 m(2) g(-1)) molybdenum nitride was prepared by the temperature-programmed nitridation of alpha-MoO3 with pure ammonia. The process was optimized by adjusting the experimental variables: the reaction temperature, heating rate, and molar flow rate of ammonia. The physicochemical properties of the as-formed molybdenum nitride were characterized by X-ray diffraction, N-2 sorption, transmission electron microscopy, temperature-programmed oxidation/reduction, and X-ray photoelectron spectroscopy. Of the experimental variables, the nitridation temperature was found to be the most critical parameter determining the surface area of the molybdenum nitride. When the prepared molybdenum nitride was exposed to air, the specific surface area rapidly decreased because of the partial oxidation of molybdenum nitride to molybdenum oxynitride. However, the surface area recovered to 90% the initial value after H-2 treatment. The catalyst with the highest degree of nitridation showed the best catalytic activity, superior to that of unmodified alpha-MoO3, for the decomposition of ammonia because of its high surface area.
引用
收藏
页码:1 / 15
页数:15
相关论文
共 47 条
  • [1] Alternative catalytic materials: carbides, nitrides, phosphides and amorphous boron alloys
    Alexander, Anne-Marie
    Hargreaves, Justin S. J.
    [J]. CHEMICAL SOCIETY REVIEWS, 2010, 39 (11) : 4388 - 4401
  • [2] H2 Production via Ammonia Decomposition Using Non-Noble Metal Catalysts: A Review
    Bell, T. E.
    Torrente-Murciano, L.
    [J]. TOPICS IN CATALYSIS, 2016, 59 (15-16) : 1438 - 1457
  • [3] Molybdenum nitrides: a study of synthesis variables and catalytic performance in acetylene hydrogenation
    Cardenas-Lizana, Fernando
    Lamey, Daniel
    Kiwi-Minsker, Lioubov
    Keane, Mark A.
    [J]. JOURNAL OF MATERIALS SCIENCE, 2018, 53 (09) : 6707 - 6718
  • [4] β-Molybdenum nitride: synthesis mechanism and catalytic response in the gas phase hydrogenation of p-chloronitrobenzene
    Cardenas-Lizana, Fernando
    Gomez-Quero, Santiago
    Perret, Noemie
    Kiwi-Minsker, Lioubov
    Keane, Mark A.
    [J]. CATALYSIS SCIENCE & TECHNOLOGY, 2011, 1 (05) : 794 - 801
  • [5] Phase transformation of molybdenum trioxide to molybdenum dioxide: An in-situ transmission electron microscopy investigation
    Chen, Jian
    Wei, Qiang
    [J]. INTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, 2017, 14 (05) : 1020 - 1025
  • [6] The reaction route and active site of catalytic decomposition of hydrazine over molybdenum nitride catalyst
    Chen, XW
    Zhang, T
    Zheng, MY
    Wu, ZL
    Wu, WC
    Li, C
    [J]. JOURNAL OF CATALYSIS, 2004, 224 (02) : 473 - 478
  • [7] SYNTHESIS AND CHARACTERIZATION OF MOLYBDENUM NITRIDE HYDRODENITROGENATION CATALYSTS
    CHOI, JG
    BRENNER, JR
    COLLING, CW
    DEMCZYK, BG
    DUNNING, JL
    THOMPSON, LT
    [J]. CATALYSIS TODAY, 1992, 15 (02) : 201 - 222
  • [8] MOLYBDENUM NITRIDE CATALYSTS .1. INFLUENCE OF THE SYNTHESIS FACTORS ON STRUCTURAL-PROPERTIES
    CHOI, JG
    CURL, RL
    THOMPSON, LT
    [J]. JOURNAL OF CATALYSIS, 1994, 146 (01) : 218 - 227
  • [9] Clayton C.R, 1986, PASSIVITY MECH STAIN
  • [10] Topotactical Nitridation of α-MoO3 Fibers to γ-Mo2N Fibers and Its Field Emission Properties
    Dewangan, Khemchand
    Patil, Sandip S.
    Joag, Dilip S.
    More, Mahendra A.
    Gajbhiye, N. S.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2010, 114 (35) : 14710 - 14715