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

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

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article

A carbonator model for CO2 capture based on results from pilot tests. Part II: Deactivation and reaction model

Martin Greco-Coppi, Jochen Ströhle, Bernd Epple
8 citations
Chemical Engineering Journal
Chemical Looping and Thermochemical Processes
1.48
article

A carbonator model for CO2 capture based on results from pilot tests. Part II: Deactivation and reaction model

Martin Greco-Coppi, Jochen Ströhle, Bernd Epple
article en
8 citations

Abstract

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.

Chemical Engineering JournalVol. 508
Department for Business, Energy and Industrial Strategy, UK Government, General Secretariat for Research and Technology, Horizon 2020
Openalex Percentile: Top 18%
Chemical Looping and Thermochemical Processes
1.48
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A carbonator model for CO2 capture based on results from pilot tests. Part II: Deactivation and reaction model — Martin Greco-Coppi, Jochen Ströhle, et al. · Chemical Engineering Journal (2024) | TGRS Research Map | TGRS