A Study on the Structure of the Stable Inverse Diffusion Flame from the Producer Gas of Woody Biomass: Effects of Concentration of Carbon Dioxide on Partial Combustion

被引:0
作者
Bai, Zhiren [1 ]
Nakatsuka, Noriaki [1 ]
Hayashi, Jun [1 ,2 ]
Akamatsu, Fumiteru [1 ]
机构
[1] Osaka Univ, Dept Mech Engn, 2-1 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Kyoto Univ, Grad Sch Energy Convers Sci, Sakyo Ku, Yoshidahonmachi, Kyoto, Kyoto 6068501, Japan
关键词
Tar reforming; Partial combustion; Inverse diffusion flame; PAHs; Soot; POLYCYCLIC AROMATIC-HYDROCARBONS; LASER-INDUCED INCANDESCENCE; SOOT; GASIFICATION;
D O I
10.3775/jie.98.176
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
An inverse diffusion flame is formed during the partial combustion of the reformed gas for tar reduction in the producer gas generated by the gasification of woody biomass. The polymerization and decomposition of tar occur simultaneously in the vicinity of this inverse diffusion flame. The combustion reaction of producer gas proceeds in the diluted phase. In order to decompose tar without it polymerizing into soot, it is necessary to understand the flame structure. Therefore. this study is aimed at understanding the flame structure of an inverse diffusion flame. In particular, in order to analyze the influence of the diluent. the effect of the concentration of carbon dioxide as an oxidizer on the flame structure and tar decomposition was investigated by observing the CH* chemiluminescence, the planar laser-induced fluorescence (LIF) of polycyclic aromatic hydrocarbons (PAHs), and the laser-induced incandescence (LII) of soot. The results showed that the peak intensities of CH*chemiluminescence, LIF signals from PAHs, and LII signals from soot are distributed in the stated order in a radial direction from the central axis. While PAHs are formed in the upstream of the flame and decrease gradually along the mainstream direction. the relative volume fraction of primary soot particles continued to increase along the mainstream direction. Further, a high carbon dioxide concentration resulted in a longer flame. At the same time, it led to a large volume fraction of soot downstream of the flame. As the concentration of carbon dioxide in the oxidizer increased, carbon yield decreased, suggesting an increase in soot formation.
引用
收藏
页码:176 / 185
页数:10
相关论文
共 30 条
[1]  
Aizawa T, 2004, T JAPAN SOC MECH E B, P194
[2]  
Bai Z, 2019, T JAPAN SOC MECH E B, P321
[3]   Laser induced fluorescence spectroscopy of aromatic species produced in atmospheric sooting flames using UV and visible excitation wavelengths [J].
Bejaoui, Salma ;
Mercier, Xavier ;
Desgroux, Pascale ;
Therssen, Eric .
COMBUSTION AND FLAME, 2014, 161 (10) :2479-2491
[4]  
Colket M.B., 1994, Proc. Combust. Inst, V25, P883, DOI DOI 10.1016/S0082-0784(06)80723-X
[5]   Reforming Technologies to Improve the Performance of Combustion Systems [J].
Hassan, Hashim ;
Khandelwal, Bhupendra .
AEROSPACE, 2014, 1 (02) :67-96
[6]   Soot formation characteristics in a lab-scale turbulent pulverized coal flame with simultaneous planar measurements of laser induced incandescence of soot and Mie scattering of pulverized coal [J].
Hayashi, Jun ;
Hashimoto, Nozomu ;
Nakatsuka, Noriaki ;
Tsuji, Hirofumi ;
Watanabe, Hiroaki ;
Makino, Hisao ;
Akamatsu, Fumiteru .
PROCEEDINGS OF THE COMBUSTION INSTITUTE, 2013, 34 :2435-2443
[7]   New concepts in biomass gasification [J].
Heidenreich, Steffen ;
Foscolo, Pier Ugo .
PROGRESS IN ENERGY AND COMBUSTION SCIENCE, 2015, 46 :72-95
[8]   The design, construction and operation of a 75 kW two-stage gasifier [J].
Henriksen, Ulrik ;
Ahrenfeldt, Jesper ;
Jensen, Torben Kvist ;
Gobel, Benny ;
Bentzen, Jens Dall ;
Hindsgaul, Claus ;
Sorensen, Lasse Holst .
ENERGY, 2006, 31 (10-11) :1542-1553
[9]   Tar reduction through partial combustion of fuel gas [J].
Houben, MP ;
de Lange, HC ;
van Steenhoven, AA .
FUEL, 2005, 84 (7-8) :817-824
[10]   Thermochemical Biomass Gasification: A Review of the Current Status of the Technology [J].
Kumar, Ajay ;
Jones, David D. ;
Hanna, Milford A. .
ENERGIES, 2009, 2 (03) :556-581