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Woody biomass and RPF gasification using reforming catalyst and calcium oxide.
- Source :
-
Chemosphere [Chemosphere] 2011 May; Vol. 83 (9), pp. 1273-8. Date of Electronic Publication: 2011 Apr 02. - Publication Year :
- 2011
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Abstract
- This study focused on steam gasification and reforming of waste biomass using a reforming catalyst. The purpose of the study was to evaluate the durability of a commercial Ni reforming catalyst and the effect of CaO on the reforming behavior, and to clarify detailed factors of catalytic performance, as well as the effect of operating parameters on the characteristics of produced gas composition. Moreover, catalyst regeneration was carried out and the behavior of catalytic activity based on gas composition was investigated. Using a fluidized bed gasifier and a fixed bed reformer, gasification and reforming of waste biomass were carried out. Commercial Ni-based catalyst and calcined limestone (CaO) were applied to the reforming reaction. Temperature of the gasifier and reformer was almost 1023K. Ratio of steam to carbon in the feedstock [molmol(-1)] and equivalence ratio (i.e., ratio of actual to theoretical amount of oxygen) [-] were set at about 2 and 0.3, respectively. The feed rate of the feedstock into the bench-scale gasifier was almost 15kgh(-1). The results of waste biomass gasification confirmed the improvement in H(2) composition by the CO(2) absorption reaction using the reforming catalyst and CaO. In addition, CaO proved to be especially effective in decreasing the tar concentration in the case of woody biomass gasification. Catalytic activity was maintained by means of catalyst regeneration processing by hydrogen reduction after air oxidation when woody biomass was used as feedstock.<br /> (Copyright © 2011 Elsevier Ltd. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1879-1298
- Volume :
- 83
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Chemosphere
- Publication Type :
- Academic Journal
- Accession number :
- 21459406
- Full Text :
- https://doi.org/10.1016/j.chemosphere.2011.03.010