The necessity to contain CO2 emissions has been leading to a growing interest in renewable and CO2 free energy sources. So far, co-gasification of coal and biomass is appealing for the production of a valuable energy or chemical vector as syngas. However, depending on the specific end-use, further treatments of the producer gas are required in order to reduce impurities including tars, dust and inorganic substances and/or to adjust the H2/CO/CO2 ratio. In this respect, sorption enhanced water gas shift reaction process with in situ CO2 capture by solid sorbents represents an intensified option for producing a H2-rich product stream. In addition to enhanced H2 production, due to a shift in the key equilibrium reactions of gasification, this process has, in fact, several advantages including: a) the production of a concentrated stream of CO2, suitable for storage (sequestration), as a consequence of the reversibility that generally characterizes these processes.; b) the exothermic carbonation reaction can supply most of the heat demand of the endothermic gasification reactions; c) particles sorbents, such as limestone, dolomite, olivine and high-iron solids, show some catalytic activity for tar reforming and cracking. The paper reports on the mutual influence in the reactor between coal/biomass steam-oxygen gasification and CO2 separation by means of a chemical sorbent. Experimental tests in a BFB (Bubbling Fluidized Bed) gasifier demonstrate that using a CaO-alumina mixed bed the H2/CO ratio can be strongly enhanced, provided that a good control of the temperature is assured because of the high thermal character of the carbonation. The use of CaO-alumina mixed bed offers the advantage of reducing the tar concentration and prevent the bed agglomeration typically observed when olive husk and quartzite sand are used.

In situ carbon dioxide capture during biomass fluidized bed gasification

G Ruoppolo;F Miccio;P Brachi;A Picarelli;R Chirone
2015

Abstract

The necessity to contain CO2 emissions has been leading to a growing interest in renewable and CO2 free energy sources. So far, co-gasification of coal and biomass is appealing for the production of a valuable energy or chemical vector as syngas. However, depending on the specific end-use, further treatments of the producer gas are required in order to reduce impurities including tars, dust and inorganic substances and/or to adjust the H2/CO/CO2 ratio. In this respect, sorption enhanced water gas shift reaction process with in situ CO2 capture by solid sorbents represents an intensified option for producing a H2-rich product stream. In addition to enhanced H2 production, due to a shift in the key equilibrium reactions of gasification, this process has, in fact, several advantages including: a) the production of a concentrated stream of CO2, suitable for storage (sequestration), as a consequence of the reversibility that generally characterizes these processes.; b) the exothermic carbonation reaction can supply most of the heat demand of the endothermic gasification reactions; c) particles sorbents, such as limestone, dolomite, olivine and high-iron solids, show some catalytic activity for tar reforming and cracking. The paper reports on the mutual influence in the reactor between coal/biomass steam-oxygen gasification and CO2 separation by means of a chemical sorbent. Experimental tests in a BFB (Bubbling Fluidized Bed) gasifier demonstrate that using a CaO-alumina mixed bed the H2/CO ratio can be strongly enhanced, provided that a good control of the temperature is assured because of the high thermal character of the carbonation. The use of CaO-alumina mixed bed offers the advantage of reducing the tar concentration and prevent the bed agglomeration typically observed when olive husk and quartzite sand are used.
2015
Istituto di Ricerche sulla Combustione - IRC - Sede Napoli
Istituto di Scienza, Tecnologia e Sostenibilità per lo Sviluppo dei Materiali Ceramici - ISSMC (ex ISTEC)
Istituto di Scienze e Tecnologie per l'Energia e la Mobilità Sostenibili - STEMS
gasification
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/294190
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