Hydrogen production from glucose using Ru/Al2O3 catalyst in supercritical water

被引:99
作者
Byrd, Adam J.
Pant, K. K.
Gupta, Ram B. [1 ]
机构
[1] Auburn Univ, Dept Chem Engn, Auburn, AL 36849 USA
[2] Indian Inst Technol, Dept Chem Engn, New Delhi 110016, India
关键词
D O I
10.1021/ie070241g
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Glucose, as a model biomass compound, was catalytically reformed in supercritical water to produce hydrogen. The reforming experiments were conducted in a continuous tubular reactor with and without Ru/Al2O3 catalyst at short residence times. The addition of catalyst significantly enhanced the overall conversion and hydrogen yield, and reduced methane formation. The gaseous products contained mainly hydrogen, carbon dioxide, methane, and a small amount of carbon monoxide. The effects of experimental conditions such as temperature, reaction time, and concentration of glucose in the feed on formation of hydrogen product were investigated. Experimental hydrogen yields as high as 12 mol of H-2/mol of glucose were obtained, which is the stoichiometric limit. The gas yield was sensitive to temperature, residence time, and feed concentration. High yield of H-2 with low CO and CH4 yields were obtained at high reaction temperature and low glucose concentrations. Tar formation was observed at high glucose concentrations (> 5 wt %). The catalytic conversion of glucose with ruthenium catalyst in supercritical water is an effective method for hydrogen production directly at a high pressure, which can be extended to other biomass materials. A reaction mechanism for catalytic reforming in supercritical water is also discussed.
引用
收藏
页码:3574 / 3579
页数:6
相关论文
共 32 条
[21]   Key compounds of the hydropyrolysis of glucose in supercritical water in the presence of K2CO3 [J].
Sinag, A ;
Kruse, A ;
Schwarzkopf, V .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2003, 42 (15) :3516-3521
[22]   Kinetics of steam reforming of ethanol over a Ru/Al2O3 catalyst [J].
Vaidya, Prakash D. ;
Rodrigues, Alirio E. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2006, 45 (19) :6614-6618
[23]   Catalytic effects of NaOH and ZrO2 for partial oxidative gasification of n-hexadecane and lignin in supercritical water [J].
Watanabe, M ;
Inomata, H ;
Osada, M ;
Sato, T ;
Adschiri, T ;
Arai, K .
FUEL, 2003, 82 (05) :545-552
[24]   Catalytic hydrogen generation from biomass (glucose and cellulose) with ZrO2 in supercritical water [J].
Watanabe, M ;
Inomata, H ;
Arai, K .
BIOMASS & BIOENERGY, 2002, 22 (05) :405-410
[25]   A VISCOSITY EQUATION FOR GAS MIXTURES [J].
WILKE, CR .
JOURNAL OF CHEMICAL PHYSICS, 1950, 18 (04) :517-519
[26]   Subcritical and supercritical water gasification of cellulose, starch, glucose, and biomass waste [J].
Williams, PT ;
Onwudili, J .
ENERGY & FUELS, 2006, 20 (03) :1259-1265
[27]   Carbon-catalyzed gasification of organic feedstocks in supercritical water [J].
Xu, XD ;
Matsumura, Y ;
Stenberg, J ;
Antal, MJ .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1996, 35 (08) :2522-2530
[28]   Thermodynamic analysis of hydrogen production from biomass gasification in supercritical water [J].
Yan, QH ;
Guo, LJ ;
Lu, YJ .
ENERGY CONVERSION AND MANAGEMENT, 2006, 47 (11-12) :1515-1528
[29]   Partial oxidative and catalytic biomass gasification in supercritical water: A promising flow reactor system [J].
Yoshida, T ;
Oshima, Y .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2004, 43 (15) :4097-4104
[30]   Gasification of biomass model compounds and real biomass in supercritical water [J].
Yoshida, T ;
Oshima, Y ;
Matsumura, Y .
BIOMASS & BIOENERGY, 2004, 26 (01) :71-78