Combination of autothermal reforming with water-gas-shift reaction - small-scale testing of different water-gas-shift catalysts

被引:17
|
作者
Pasel, J [1 ]
Cremer, P [1 ]
Wegner, B [1 ]
Peters, R [1 ]
Stolten, D [1 ]
机构
[1] Forschungszentrum Julich, Inst Mat & Proc Energy Syst IWV 3, D-52425 Julich, Germany
关键词
autothermal reforming; water-gas-shift reaction; hydrogen; fuel cell;
D O I
10.1016/j.jpowsour.2003.09.037
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 amount of carbon monoxide in the reformate of the autothermal reforming (ATR) of liquid hydrocarbons can be significantly reduced by means of the water-gas-shift (WGS) reaction. It is possible to directly feed the reformate from the ATR of liquid hydrocarbons to the WGS reactor without deactivation of the WGS catalyst. In a first step, the dry reformate from the ATR and a separately fed stream of steam were used to conduct the WGS reaction. Special emphasis was given to the chemical composition of the reformate which under convenient reaction conditions did not feature any detrimental higher aliphatic or aromatic hydrocarbons. Applying these premises, no catalyst deactivation could be observed. Strong differences concerning the catalytic activity between the three investigated commercial monolithic catalysts could be observed. The most active one showed a very promising catalytic behaviour. At a gas hourly space velocity (GHSV) of 12,250h(-1), CO conversion amounted to 85% at 280degreesC. This result reduces the CO concentration in the reformate from 6.1 to about 0.9 vol.%. In a second step, also the non-converted water from the ATR was fed to the reactor for the WGS reaction together with the additional components of the reformate. In this case, also the amount of total carbon dissolved in the water was analysed, which might - after adsorption - have a deleterious effect on the accessibility of the active sites of the WGS catalyst. No catalyst deactivation was observed within almost 90 h under ATR conditions generating only traces of carbon dissolved in the water. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:112 / 118
页数:7
相关论文
共 50 条
  • [41] Kinetic and equilibrium study on formic acid decomposition in relation to the water-gas-shift reaction
    Yasaka, Yoshiro
    Yoshida, Ken
    Wakai, Chihiro
    Matubayasi, Nobuyuki
    Nakahara, Masaru
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 2006, 110 (38): : 11082 - 11090
  • [42] Engineering nanointerfaces of Cu-based catalysts for balancing activity and stability of reverse water-gas-shift reaction
    Zhang, Ling
    Yu, Jiafeng
    Sun, Xingtao
    Sun, Jian
    [J]. JOURNAL OF CO2 UTILIZATION, 2023, 71
  • [43] New Catalytic System for Producing Pure Hydrogen -Water-gas-shift Reaction of Supported Copper Catalysts-
    Yahiro, H.
    Saiki, K.
    Yamamoto, T.
    Sagata, K.
    Asamoto, M.
    Yamaura, H.
    [J]. CLEAN TECHNOLOGY 2008: BIO ENERGY, RENEWABLES, GREEN BUILDING, SMART GRID, STORAGE, AND WATER, 2008, : 290 - 293
  • [44] Nanostructuring mixed Ce/La oxides for water-gas-shift catalysis
    Liang, Shuang
    Wang, Yanan
    Veser, Goetz
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2010, 239
  • [45] STUDY OF MECHANISM OF WATER-GAS-SHIFT REACTION ON AN IRON OXIDE CATALYST USING A GAS CHROMATOGRAPHIC TECHNIQUE
    NAKANISHI, J
    TAMARU, K
    [J]. TRANSACTIONS OF THE FARADAY SOCIETY, 1963, 59 (486): : 1470 - &
  • [46] Screening of Supported Ionic Liquid Phase (SILP) catalysts for the very low temperature water-gas-shift reaction
    Werner, Sebastian
    Szesni, Normen
    Bittermann, Agnes
    Schneider, Martin J.
    Haerter, Peter
    Haumann, Marco
    Wasserscheid, Peter
    [J]. APPLIED CATALYSIS A-GENERAL, 2010, 377 (1-2) : 70 - 75
  • [47] Promotion of the Water-Gas-Shift Reaction by Nickel Hydroxyl Species in Partially Reduced Nickel-Containing Phyllosilicate Catalysts
    Ashok, Jangam
    Li Ang, Ming
    Terence, Puar Zhi Liang
    Kawi, Sibudjing
    [J]. CHEMCATCHEM, 2016, 8 (07) : 1308 - 1318
  • [48] Nano-scale sulfur-tolerant lanthanide oxysulfide/oxysulfate catalysts for water-gas-shift reaction in a novel reactor configuration
    Tan, Shuai
    Paglieri, Stephen N.
    Li, Dongmei
    [J]. CATALYSIS COMMUNICATIONS, 2016, 73 : 16 - 21
  • [49] CO hydrogenation combined with water-gas-shift reaction for synthetic natural gas production: a thermodynamic and experimental study
    Meng F.
    Li X.
    Lv X.
    Li Z.
    [J]. International Journal of Coal Science & Technology, 2018, 5 (4) : 439 - 451
  • [50] A thermostable cu-mn based catalyst for high temperature water-gas-shift reaction
    Liu, QS
    He, RX
    Cu, XL
    Zhi, KD
    Ma, WP
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 230 : U1675 - U1675