Liquefactions of peat in supercritical water with a novel iron catalyst

被引:28
作者
Li, Hanning [1 ]
Hurley, Scott [1 ]
Xu, Chunbao [1 ]
机构
[1] Lakehead Univ, Dept Chem Engn, Thunder Bay, ON P7B 5E1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Peat; Direct liquefaction; Bio-crude; Supercritical water; Iron ore; BIOMASS GASIFICATION; WOODY BIOMASS; METALLIC IRON; BIO-OILS; TEMPERATURE; PYROLYSIS; LIMONITE; MODEL;
D O I
10.1016/j.fuel.2010.09.004
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Raw iron ore has been investigated for use as a catalyst in direct liquefaction of peat into bio-crude by supercritical water treatment. The liquefaction treatments were conducted at temperatures from 350 degrees C to 500 degrees C for a residence time from 10 min to 4 h. The supercritical water treatment of peat with the iron ore generally resulted in 19-40 wt% yield of heavy oil (HO) that has a higher heating value (HHV) of 30-37 MJ/kg. An increase in the operating temperature generally increased gas yield and decreased oil and char yields, while a maximum HO formation was observed at around 400 degrees C. At 400 degrees C for a residence time of 2 h, the addition of the raw iron ore in the operation produced HO at a very high yield of about 40 wt%, nearly doubling that of the treatment without catalyst. An increase of water-to-peat ratio led to enhanced formation of HO products, accompanied by a decrease in gas or char yield. The optimal reaction time appeared to be 2 h for the maximum HO production, and a longer residence time than 2 h generally led to a decrease in HO yield but an increase in gas yield. Compared with the raw iron ore, its H-2-reduced form and two synthesized iron-based catalysts (FeOOH and Fe2O3) all showed a lower activity for HO production. Some conventional biomass liquefaction catalysts (i.e., KOH, FeCl3 and FeSO4) showed negligible or even negative effects on the HO yield, while these catalysts were found very active for promoting the gas yields and hydrogen formation. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:412 / 420
页数:9
相关论文
共 29 条
[1]  
[Anonymous], 1971, 7560 US BUR MIN
[2]   Biomass gasification in supercritical water [J].
Antal, MJ ;
Allen, SG ;
Schulman, D ;
Xu, XD ;
Divilio, RJ .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2000, 39 (11) :4040-4053
[3]  
Antal MJ, 1992, ADV THERM BIOM CONV
[4]   The influence of temperature on the yields of compounds existing in bio-oils obtained from biomass samples via pyrolysis [J].
Demirbas, Ayhan .
FUEL PROCESSING TECHNOLOGY, 2007, 88 (06) :591-597
[5]   Crystallinity of lyophilised carrot cell wall components [J].
Georget, DMR ;
Cairns, P ;
Smith, AC ;
Waldron, KW .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 1999, 26 (05) :325-331
[6]   Steam gasification of apricot stones with olivine and dolomite as downstream catalysts [J].
Hu, G ;
Xu, SP ;
Li, SG ;
Xiao, CR ;
Liu, SQ .
FUEL PROCESSING TECHNOLOGY, 2006, 87 (05) :375-382
[7]   Determination of parameters in mechanical model for cellulose III fibre [J].
Ishikawa, A ;
Kuga, S ;
Okano, T .
POLYMER, 1998, 39 (10) :1875-1878
[8]   Highly active limonite catalysts for direct coal liquefaction [J].
Kaneko, T ;
Sugita, S ;
Tamura, M ;
Shimasaki, K ;
Makino, E ;
Silalahi, LH .
FUEL, 2002, 81 (11-12) :1541-1549
[9]   Effect of Rb and Cs carbonates for production of phenols from liquefaction of wood biomass [J].
Karagöz, S ;
Bhaskar, T ;
Muto, A ;
Sakata, Y .
FUEL, 2004, 83 (17-18) :2293-2299
[10]   Batch microreactor studies of lignin and lignin model compound depolymerization by bases in alcohol solvents [J].
Miller, JE ;
Evans, L ;
Littlewolf, A ;
Trudell, DE .
FUEL, 1999, 78 (11) :1363-1366