Nickel-catalysed pyrolysis/gasification of biomass components

被引:50
|
作者
Wu, Chunfei [1 ]
Wang, Zichun [2 ]
Dupont, Valerie [1 ]
Huang, Jun [2 ]
Williams, Paul T. [1 ]
机构
[1] Univ Leeds, Energy Res Inst, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Sydney, Lab Catalysis Engn, Sch Chem & Biomol Engn, Sydney, NSW 2006, Australia
基金
英国工程与自然科学研究理事会;
关键词
Biomass; Cellulose; Xylan; Lignin; Gasification; Hydrogen; HYDROGEN-PRODUCTION; STEAM GASIFICATION; MODEL-COMPOUND; PYROLYSIS; TAR; POLYPROPYLENE; TEMPERATURE; TOLUENE;
D O I
10.1016/j.jaap.2012.10.010
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Hydrogen and syngas production have been investigated from the pyrolysis/gasification of biomass components (cellulose, xylan and lignin) in the presence of Ni-based catalysts by using a two-stage fixed-bed reaction system. Biomass samples were pyrolysed at the first stage and the derived products were gasified at the second stage. The Ni-Mg-Al and Ni-Ca-Al catalysts, prepared by co-precipitation, were applied in the gasification process. The lignin sample pyrolysed with more difficulty (56.0 wt.% of residue fraction) compared with cellulose and xylan at 500 degrees C, and therefore resulted in the lowest gas yield (42.7 wt.%) for the pyrolysis/gasification of lignin. However, the highest H-2 concentration from the three types of feedstock (55.1 vol.%) was collected for the lignin sample in the presence of steam and catalyst. Carbon deposition was very low as indicated from the TPO and SEM analyses of the reacted Ni-Mg-Al catalyst. The investigation of reaction conditions showed that water injection rate (0.02 and 0.05 g min(-1)) had little influence on the gas production from the pyrolysis/gasification of lignin in the presence of the Ni-Ca-Al catalyst; however, the increase of gasification temperature from 700 to 900 degrees C resulted in a higher gas and hydrogen production due to the promotion of secondary reactions during the gasification process. Furthermore, coking was highest for the reacted Ni-Ca-Al catalyst at the gasification temperature of 800 degrees C (7.27 wt.%), when the temperature was increased from 700 to 900 degrees C. This work shows that the components of biomass have a significant influence on the catalytic gasification process related to hydrogen and syngas production. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 148
页数:6
相关论文
共 50 条
  • [21] Nickel-catalysed decarbonylative borylation of aroyl fluorides
    Wang, Zhenhua
    Wang, Xiu
    Nishihara, Yasushi
    CHEMICAL COMMUNICATIONS, 2018, 54 (99) : 13969 - 13972
  • [22] Nickel-catalysed hydrodimerization of unactivated terminal alkenes
    Li Cheng
    Jiandong Liu
    Yunrong Chen
    Hegui Gong
    Nature Synthesis, 2023, 2 : 364 - 372
  • [23] Nickel-catalysed carbonylative homologation of aryl iodides
    Jin-Bao Peng
    Fu-Peng Wu
    Xinxin Qi
    Jun Ying
    Xiao-Feng Wu
    Communications Chemistry, 1
  • [24] Recent developments in enantioselective nickel-catalysed cycloadditions
    Pellissier, Helene
    TETRAHEDRON, 2024, 153
  • [25] Nickel-catalysed novel β,γ-unsaturated nitrile synthesis
    Tang, Shan
    Liu, Chao
    Lei, Aiwen
    CHEMICAL COMMUNICATIONS, 2013, 49 (24) : 2442 - 2444
  • [26] Nickel-catalysed Suzuki-Miyaura coupling of amides
    Weires N.A.
    Baker E.L.
    Garg N.K.
    Nature Chemistry, 2016, 8 (1) : 75 - 79
  • [27] Competing nickel-catalysed dimerisation and degenerate isomerisation of propene
    Brown, JM
    Hughes, GD
    INORGANICA CHIMICA ACTA, 1996, 252 (1-2) : 229 - 237
  • [28] Unusual mechanism of paramagnetic nickel-catalysed α-alkylation of amides
    Du, Chao
    Zhou, Xiaoyu
    Li, Weikang
    Wen, Xiuling
    Ke, Zhuofeng
    Zhao, Cunyuan
    DALTON TRANSACTIONS, 2021, 50 (20) : 6923 - 6932
  • [29] NICKEL-CATALYSED REACTIONS OF ALLYL HALIDES AND RELATED COMPOUNDS
    CHIUSOLI, GP
    CASSAR, L
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1967, 6 (02) : 124 - +
  • [30] Nickel-catalysed electrochemical reductive deprotection of allyl ethers
    Olivero, S
    Dunach, E
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (24) : 2497 - 2498