BIOADSORB
Biomass-derived Microporous Carbon Adsorbents for CO2 Capture and Storage
| Coordinatore | QUEEN MARY UNIVERSITY OF LONDON
Organization address
address: 327 MILE END ROAD contact info |
| Nazionalità Coordinatore | United Kingdom [UK] |
| Totale costo | 299˙558 € |
| EC contributo | 299˙558 € |
| Programma | FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) |
| Code Call | FP7-PEOPLE-2013-IEF |
| Funding Scheme | MC-IEF |
| Anno di inizio | 2014 |
| Periodo (anno-mese-giorno) | 2014-09-01 - 2016-08-31 |
Partecipanti
| # | ||||
|---|---|---|---|---|
| 1 |
QUEEN MARY UNIVERSITY OF LONDON
Organization address
address: 327 MILE END ROAD contact info |
UK (LONDON) | coordinator | 299˙558.40 |
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Obiettivo del progetto (Objective)
'This Marie Curie proposal, BIOADSORB aims the development of new and low cost biomass-derived carbon adsorbents for CO2 capture using the following strategies:
(i) a new synthetic route based on hydrothermal carbonization (HTC) process and in situ salt templating for the efficient conversion of waste biomass into functional porous carbon materials (HTCs) for CO2 capture (ii) a theoretical approach based on molecular simulations and density functional theory to model and understand the HTC structure along with the adsorption and transport behavior of CO2 and other gases in those structures. (iii) An in-silico method to demonstrate the potential of HTCs for CO2 capture from real industrial streams in a cyclic separation process.
The proposed synthetic path will bring new horizons to the production of biomass-derived microporous carbon materials. The theoretical studies will demonstrate the potential of the as-synthesized materials for CO2 capture from industrial streams in a cyclic separation process. The theoretical studies will also advance the understanding of the mechanism of surface-gas interactions, gas adsorption and transport behaviour inside the complex pore matrix.'