On the relevant role of solids residence time on their CO2 capture performance in the Calcium Looping technology
The multicycle CO capture performance of CaO derived from natural limestone and dolomite has been investigated by means of thermogravimetry under realistic Calcium-Looping conditions, which necessarily involve high CO concentration and high temperatures in the calcination stage and fast transitions...
| Autores: | , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2016 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/149743 |
| Acceso en línea: | http://hdl.handle.net/10261/149743 |
| Access Level: | acceso abierto |
| Palabra clave: | dolomite CO2 capture thermogravimetry *Corresponding Calcium looping limestone |
| Sumario: | The multicycle CO capture performance of CaO derived from natural limestone and dolomite has been investigated by means of thermogravimetry under realistic Calcium-Looping conditions, which necessarily involve high CO concentration and high temperatures in the calcination stage and fast transitions between the carbonation and calcination stages. Natural dolomite allows reducing the calcination temperature as compared to limestone while high calcination efficiency is maintained. This could help reducing the energy penalty of the CaL process thus further enhancing the industrial competitiveness for the integration of this technology into fossil fuel power plants. Importantly, the CO capture capacity of the sorbents is critically affected by the solids residence time in the carbonation and calcination stages within the feasible range in practice. Thus, carbonation/calcination residence times play a critical role on the multicycle CO capture performance, which has been generally dismissed in previous studies. A main observation is the enhancement of carbonation in the solid-state diffusion controlled phase, which is against the commonly accepted conception that the only relevant phase in the carbonation stage is the fast reaction-controlled stage on the surface of the solids. Thus, the CO capture efficiency may be significantly enhanced by increasing the solids residence time in the carbonator. |
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