Core-shell structured iron nanoparticles for the generation of COx-free hydrogen via ammonia decomposition

被引:51
|
作者
Li, Yanxing [1 ,2 ]
Liu, Shunqiang [1 ]
Yao, Lianghong [1 ,2 ]
Ji, Weijie [1 ]
Au, Chak-Tong [2 ]
机构
[1] Nanjing Univ, Key Lab Mesoscop Chem, Minist Educ, Sch Chem & Chem Engn, Nanjing 210093, Peoples R China
[2] Hong Kong Baptist Univ, Dept Chem, Ctr Surface Anal & Res, Kowloon Tong, Hong Kong, Peoples R China
关键词
Core-shell structure; Iron nanoparticles; Silica; COx-free hydrogen; Ammonia decomposition; FUEL-CELL APPLICATIONS; CORE/SHELL NANOCRYSTALS; COLLOIDAL PARTICLES; PHOTONIC CRYSTALS; SILICA SPHERES; CARBON; CATALYSTS; FABRICATION; METHANE; SYNGAS;
D O I
10.1016/j.catcom.2009.11.003
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
The iron nanoparticles that are encapsulated by microporous and mesoporous silica shells were synthesized for the generation of COx-free hydrogen through the catalytic decomposition of ammonia. The encapsulated iron nanoparticles show excellent catalytic activity, giving 100% ammonia conversion in the 650-670 degrees C range. The core-shell structured catalysts are highly stable under the adopted reaction conditions owing to the stable silica shells that effectively prevent aggregation of iron nanoparticles. In contrast, the naked iron nanoparticles deactivated gradually at 670 degrees C and lost 18% ammonia conversion in a period of 63 h. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:368 / 372
页数:5
相关论文
共 50 条
  • [31] Highly effective ruthenium catalyst support on La2Zr2O7 for ammonia decomposition to COx-free hydrogen
    Wu, Qin
    Li, Dexing
    Yin, Zhili
    Wang, Peixian
    Wang, Ziqing
    Wei, Zhong
    FUEL, 2025, 379
  • [32] Synthesis of core-shell structured magnetic nanoparticles with a carbide shell
    Hou, Shushan
    Chi, Yue
    Zhao, Zhankui
    17TH IUMRS INTERNATIONAL CONFERENCE IN ASIA (IUMRS-ICA 2016), 2017, 182
  • [33] Carbon nanotubes-supported Ru catalyst for the generation of COx-free hydrogen from ammonia
    Yin, SF
    Xu, BQ
    Zhu, WX
    Ng, CF
    Zhou, XP
    Au, CT
    CATALYSIS TODAY, 2004, 93-5 : 27 - 38
  • [34] COx-free hydrogen production from ammonia decomposition over sepiolite-supported nickel catalysts
    Kurtoglu, Samira Fatma
    Sarp, Seda
    Akkaya, Ceren Yllmaz
    Yagci, Baris
    Motallebzadeh, Amir
    Soyer-Uzun, Sezen
    Uzun, Alper
    INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2018, 43 (21) : 9954 - 9968
  • [35] Cobalt catalysts for COx-free hydrogen production: Effect of catalyst type on ammonia decomposition in gliding discharge plasma reactor
    Ronduda, Hubert
    Mlotek, Michal
    Goral, Weronika
    Zybert, Magdalena
    Ostrowski, Andrzej
    Sobczak, Kamil
    Krawczyk, Krzysztof
    Rarog-Pilecka, Wioletta
    JOURNAL OF CO2 UTILIZATION, 2024, 82
  • [36] Co-Ni supported yttrium oxide material as a catalyst for ammonia decomposition to COx-free hydrogen
    Li, Honghai
    Guo, Lexin
    Qu, Jianing
    Fang, Xianxin
    Fu, Yaqian
    Duan, Jihai
    Wang, Weiwen
    Li, Chaojie
    INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2023, 48 (24) : 8985 - 8996
  • [37] Fe Nanocatalysts Supported on Dealuminated ZSM-5 for Efficient Decomposition of Ammonia to COx-Free Hydrogen
    Hu, Zhong-Pan
    Chen, Lei
    Weng, Chen-Chen
    Yuan, Zhong-Yong
    CHEMISTRYSELECT, 2018, 3 (16): : 4439 - 4447
  • [38] Catalytic decomposition of ammonia to COx-free hydrogen over Ni/ZSM-5 catalysts: A comparative study of the preparation methods
    Hu, Zhong-Pan
    Weng, Chen-Chen
    Chen, Chong
    Yuan, Zhong-Yong
    APPLIED CATALYSIS A-GENERAL, 2018, 562 : 49 - 57
  • [39] Methane decomposition under a corona discharge to generate COx-free hydrogen
    Aleknaviciute, I.
    Karayiannis, T. G.
    Collins, M. W.
    Xanthos, C.
    ENERGY, 2013, 59 : 432 - 439
  • [40] Ammonia decomposition reaction to produce COx-free hydrogen using carbon supported cobalt catalysts in microwave heated reactor system
    Seyfeli, Rukan Can
    Varisli, Dilek
    INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2020, 45 (60) : 34867 - 34878