Destruction of the Tar Present in Syngas by Combustion in Porous Media

被引:5
作者
Carvalho, T. [1 ]
Costa, M. [1 ]
Casaca, C. [1 ,2 ]
Catapan, R. C. [3 ]
Oliveira, A. A. M. [4 ]
机构
[1] Univ Lisbon, Inst Super Tecn, Dept Mech Engn, Inst Engn Mecan IDMEC, P-1049001 Lisbon, Portugal
[2] Inst Politecn Nacl, Inst Super Engn Lisboa, P-1549020 Lisbon, Portugal
[3] Univ Fed Santa Catarina, Ctr Mobil Engn, BR-89218000 Joinville, SC, Brazil
[4] Univ Fed Santa Catarina, Dept Mech Engn, BR-88040900 Florianopolis, SC, Brazil
关键词
LOW CALORIFIC VALUE; RICH GASEOUS FUELS; ENERGY-PRODUCTION; HEAT-TRANSFER; BIOMASS; CONVERSION; REDUCTION; BURNERS;
D O I
10.1021/ef501807p
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
The cleaning of syngas is one of the most important challenges in the development of technologies based on gasification of biomass. Tar is an undesired byproduct because, once condensed, it can cause fouling and plugging and damage the downstream equipment. Thermochemical methods for tar destruction, which include catalytic cracking and thermal cracking, are intrinsically attractive because they are energetically efficient and no movable parts are required nor byproducts are produced. The main difficulty with these methods is the tendency for tar to polymerize at high temperatures. An alternative to tar removal is the complete combustion of the syngas in a porous burner directly as it leaves the particle capture system. In this context, the main aim of this study is to evaluate the destruction of the tar present in the syngas from biomass gasification by combustion in porous media. A gas mixture was used to emulate the syngas, which included toluene as a tar surrogate. Initially, CHEMKIN was used to assess the potential of the proposed solution. The calculations revealed the complete destruction of the tar surrogate for a wide range of operating conditions and indicated that the most important reactions in the toluene conversion are C6H5CH3 + OH <-> C6H5CH2 + H2O, C6H5CH3 + OH <-> C6H4CH3 + H2O, and C6H5CH3 + O <-> OC6H4CH3 + H and that the formation of toluene can occur through C6H5CH2 + H <-> C6H5CH3. Subsequently, experimental tests were performed in a porous burner fired with pure methane and syngas for two equivalence ratios and three flow velocities. In these tests, the toluene concentration in the syngas varied from 50 to 200 g/Nm(3). In line with the CHEMKIN calculations, the results revealed that toluene was almost completely destroyed for all tested conditions and that the process did not affect the performance of the porous burner regarding the emissions of CO, hydrocarbons, and NOx.
引用
收藏
页码:1130 / 1136
页数:7
相关论文
共 40 条
  • [1] Experimental study of combustion of hydrogen-syngas/methane fuel mixtures in a porous burner
    Alavandi, S. K.
    Agrawal, A. K.
    [J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2008, 33 (04) : 1407 - 1415
  • [2] Alzueta MU, 2000, INT J CHEM KINET, V32, P498, DOI 10.1002/1097-4601(2000)32:8<498::AID-KIN8>3.0.CO
  • [3] 2-H
  • [4] HCCI experiments with toluene reference fuels modeled by a semidetailed chemical kinetic model
    Andrae, J. C. G.
    Brinck, T.
    Kalghatgi, G. T.
    [J]. COMBUSTION AND FLAME, 2008, 155 (04) : 696 - 712
  • [5] Tar reduction in biomass producer gas via mechanical, catalytic and thermal methods: A review
    Anis, Samsudin
    Zainal, Z. A.
    [J]. RENEWABLE & SUSTAINABLE ENERGY REVIEWS, 2011, 15 (05) : 2355 - 2377
  • [6] Heat recirculation and heat transfer in porous burners
    Barra, AJ
    Ellzey, JL
    [J]. COMBUSTION AND FLAME, 2004, 137 (1-2) : 230 - 241
  • [7] Basu P, 2010, BIOMASS GASIFICATION AND PYROLYSIS: PRACTICAL DESIGN AND THEORY, P1
  • [8] Beenackers AACM, 1997, BIOMASS GASIFICATION AND PYROLYSIS: STATE OF THE ART AND FUTURE PROSPECTS, P24
  • [9] Use of amino phase adsorbent for biomass tar sampling and separation
    Brage, C
    Yu, QZ
    Chen, GX
    Sjostrom, K
    [J]. FUEL, 1997, 76 (02) : 137 - 142
  • [10] Non-uniform velocity profile mechanism for flame stabilization in a porous radiant burner
    Catapan, R. C.
    Oliveira, A. A. M.
    Costa, M.
    [J]. EXPERIMENTAL THERMAL AND FLUID SCIENCE, 2011, 35 (01) : 172 - 179