摘要
This study proposes a polygeneration hybrid thermochemical Carnot battery that integrates calcium-looping thermochemical storage with methane dry reforming in an electrically heated calciner, coupled to a supercritical CO2 Brayton cycle for power discharge. Operating the calciner in a methane atmosphere lowers the calcination temperature by ∼200 °C, mitigates sorbent deactivation, and enables in situ CO2 utilization for synthesis-gas coproduction. A steady-state system model combined with multi-objective optimization is developed to examine efficiency–cost trade-offs. The Pareto-optimal compromise achieves a levelized cost of electricity (LCOE) of 0.94 ¥ per kWh, with a simplified recuperated cycle delivering 22.6 MW net output at a round-trip efficiency of 20.5%. Accounting for synthesis gas coproduct and ∼90% CO2 capture increases the overall energy and exergy efficiencies to 88.0% and 85.0%, respectively. Sensitivity analyses identify favorable operating windows of 30–50% CaO conversion and 5–10 °C minimum temperature approach in recuperators. Economies of scale are evident: as capacity expands from 1 to 100 MW, the LCOE declines from 2.37 to 0.83 ¥ per kWh. These findings demonstrate that incorporating methane dry reforming into calcium looping enables long-duration storage with inherent CO2 capture and valuable syngas coproduction, offering attractive thermo-economic trade-offs for grid-scale applications.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 947-961 |
| 页数 | 15 |
| 期刊 | EES Batteries |
| 卷 | 2 |
| 期 | 3 |
| DOI | |
| 出版状态 | 已出版 - 1 6月 2026 |
| 已对外发布 | 是 |
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