Conversion of hot coke oven gas into light fuel gas over Ni/Al2O3 catalyst

被引:33
|
作者
Li, Liuyun [1 ]
Morishita, Kayoko [1 ]
Takarada, Takayuki [1 ]
机构
[1] Gunma Univ, Dept Biol & Chem Engn, Gunma 3768515, Japan
关键词
coke oven gas; tarry material; hydropyrolysis; light fuel gas; Ni/Al2O3; catalyst;
D O I
10.1252/jcej.39.461
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Conversion of hot coke oven gas (COG, containing tarry material) into light fuel gas over a Ni/Al2O3 catalyst was studied. Laboratory scale tests were carried out in a two-stage fixed-bed reactor at ambient pressure. The nickel catalyst promoted the hydropyrolysis reaction of tarry materials. High yields of total product gas and methane were obtained at high hydrogen concentrations. If the hydrogen supply was adequate for hydropyrolysis of the tarry material, conversion of coal volatiles was high, at more than 95% on carbon balance, even with a gas residence time as short as 0.15 s in the catalyst bed. The product gas yield depended on catalytic temperature. At 923 K, the maximum conversion of coal volatiles into the light gas was achieved at 95.0% on carbon balance, with methane 86.7 vol% of the carbonaceous gas product. Although carbon deposits deactivated the catalyst after a long period of use, the catalyst could be regenerated by treatment with oxygen at 800 K, providing high activity in subsequent decomposition of tarry material. The influence of sulphide on the tarry material decomposition reaction was small even in a 2000 ppm H2S atmosphere.
引用
收藏
页码:461 / 468
页数:8
相关论文
共 50 条
  • [1] Conversion and reaction kinetics of coke oven gas over a commercial Fe−Mo/Al2O3 catalyst
    Yi-xin Qu
    He-ming Xu
    Jian-feng Zhao
    Zhi-yan Wang
    Ya-tao Wang
    [J]. Journal of Central South University, 2016, 23 : 293 - 302
  • [2] Conversion and reaction kinetics of coke oven gas over a commercial Fe-Mo/Al2O3 catalyst
    屈一新
    徐贺明
    赵见峰
    王志彦
    王亚涛
    [J]. Journal of Central South University, 2016, 23 (02) : 293 - 302
  • [3] Conversion and reaction kinetics of coke oven gas over a commercial Fe-Mo/Al2O3 catalyst
    Qu Yi-xin
    Xu He-ming
    Zhao Jian-feng
    Wang Zhi-yan
    Wang Ya-tao
    [J]. JOURNAL OF CENTRAL SOUTH UNIVERSITY, 2016, 23 (02) : 293 - 302
  • [4] Catalytic Conversion of Tar Components from Hot Coke Oven Gas over Ni/MgAl(O) Catalyst
    Yue Baohua
    Kong Linghua
    Wang Xueguang
    Lu Xionggang
    Ding Weizhong
    [J]. CHINESE JOURNAL OF CATALYSIS, 2010, 31 (02) : 218 - 224
  • [5] Catalytic Conversion of Tar Components in Hot Coke Oven Gas over Ni/MgO-Al2O3 Catalysts
    Ai Xin-Peng
    Yue Bao-Hua
    Wang Xue-Guang
    Yang Jun
    Lu Xiong-Gang
    Ding Wei-Zhong
    [J]. ACTA PHYSICO-CHIMICA SINICA, 2009, 25 (08) : 1517 - 1522
  • [6] CO2 reforming of coke oven gas over a Ni/γAl2O3 catalyst to produce syngas for methanol synthesis
    Bermudez, J. M.
    Fidalgo, B.
    Arenillas, A.
    Menendez, J. A.
    [J]. FUEL, 2012, 94 (01) : 197 - 203
  • [7] Catalytic Conversion of 1-Methylnaphthalene as Tar Model Compound from Hot Coke Oven Gas over Ni/MgO/Al2O3 Catalysts
    Yang Jun
    Wang Xue-Guang
    Li Lin
    Shen Kui
    Lu Xiong-Gang
    Ding Wei-Zhong
    [J]. CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE, 2010, 31 (09): : 1841 - 1847
  • [8] The water-gas shift reaction for hydrogen production from coke oven gas over Cu/ZnO/Al2O3 catalyst
    Wang, Chunling
    Liu, Cheng
    Fu, Wei
    Bao, Zhenghong
    Zhang, Jieyu
    Ding, Weizhong
    Chou, Kuochih
    Li, Qian
    [J]. CATALYSIS TODAY, 2016, 263 : 46 - 51
  • [9] Hydrocracking of Tar Components from Hot Cole Oven Gas over a Ni/Ce-ZrO2/γ-Al2O3 Catalyst at Atmospheric Pressure
    Yu Fei
    Yue Baohua
    Wang Xueguang
    Geng Shuhua
    Lu Xionggang
    Ding Weizhong
    [J]. CHINESE JOURNAL OF CATALYSIS, 2009, 30 (07) : 690 - 696
  • [10] Syngas from CO2 reforming of coke oven gas: Synergetic effect of activated carbon/Ni-γAl2O3 catalyst
    Bermudez, J. M.
    Arenillas, A.
    Menendez, J. A.
    [J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2011, 36 (21) : 13361 - 13368