Sorption-enhanced gasification of municipal solid waste for hydrogen production: a comparative techno-economic analysis using limestone, dolomite and doped limestone

Mónica P.S. Santos, Dawid P. Hanak

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Sorption-enhanced gasification has been shown as a viable low-carbon alternative to conventional gasification, as it enables simultaneous gasification with in-situ CO2 capture to enhance the production of H2. CaO-based sorbents have been a preferred choice due to their low cost and wide availability. This work assessed the technical and economic viability of sorption-enhanced gasification using natural limestone, doped limestone with seawater and dolomite. The techno-economic performance of the sorption-enhanced gasification using different sorbents was compared with that of conventional gasification. Regarding the thermodynamic performance, dolomite presented the worst performance (46.0% of H2 production efficiency), whereas doped limestone presented the highest H2 production efficiency (50.0%). The use of dolomite also resulted in the highest levelised cost of hydrogen (5.4 €/kg against 5.0 €/kg when limestone is used as sorbent), which translates into a CO2 avoided cost ranging between 114.9 €/tCO2 (natural limestone) and 130.4 €/tCO2 (dolomite). Although doped limestone has shown a CO2 avoided cost of 117.7 €/tCO2, this can be reduced if the production cost of doped limestone is lower than 42.6 €/t. The production costs of new sorbents for CO2 capture and H2 production need to be similar to that of natural limestone to become an attractive alternative to natural limestone.

Original languageEnglish
JournalBiomass Conversion and Biorefinery
DOIs
Publication statusPublished - 23 Jun 2022
Externally publishedYes

Bibliographical note

Funding Information:
This publication is based on research conducted within the “Clean heat, power and hydrogen from biomass and waste” project funded by UK Engineering and Physical Sciences Research Council (EPSRC reference: EP/R513027/1).

Publisher Copyright:
© 2022, The Author(s).

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