A carbonator model for CO2 capture based on results from pilot tests. Part II: Deactivation and reaction model
Carbonate looping (CaL) is a promising technology for CO₂ capture from carbon-intensive processes. The performance of CaL strongly depends on sorbent kinetics and carrying capacity. In this work, we present a novel particle sub-model to predict the carbonation behavior of CaO for CO₂ capture in a CaL process. The sub-model deals with sorbent deactivation and reaction kinetics. We follow an original approach to non-ideal calcination and introduce a new calculation methodology for sorbent aging that considers fluctuations in sorbent circulation and make-up rates. The sub-model presented in this article is used in conjunction with the reactor model of Part I [1] to predict the CO₂ capture efficiency of a CaL pilot plant. The results of the particle sub-model were validated with experimental data from thermogravimetric analysis (TGA) and pilot tests at the 300-kWth scale. Our study provides new insights for more accurately selecting assumptions and better modeling sorbent behavior in CaL systems.
Authors
- Martin Greco-Coppi (ORCID: https://orcid.org/0000-0002-0374-3673)
- Jochen Ströhle (ORCID: https://orcid.org/0000-0003-2092-326X)
- Bernd Epple (ORCID: https://orcid.org/0000-0003-0739-9598)
Publication Details
- Journal
- Chemical Engineering Journal
- Published
- 2024-12-30
- DOI
- https://doi.org/10.1016/j.cej.2024.159041
- Citations
- 8
- Primary Topic
- Chemical Looping and Thermochemical Processes
- Type
- article
- Field-Weighted Citation Impact
- 1.48
Funders
- Department for Business, Energy and Industrial Strategy, UK Government
- General Secretariat for Research and Technology
- Horizon 2020