In this work, a combined calcium looping and chemical looping combustion (CaL–CLC) technology is simulated at thermodynamic equilibrium conditions and the results in terms of efficiency, power production, and solids circulation rates are compared with the case of using CaL alone. In addition, a new solids looping configuration in the CaL–CLC process is proposed with the purpose of mitigating the loss of calcium oxide conversion after high cycle numbers. Simulations show an improved process efficiency of the CaL–CLC method compared with CaL alone (34.2 vs. 31.2 % higher heat value) and an increased power output (136 vs. 110 MWe additional power) due to the higher energy requirement to preheat the reactants. A sensitivity analysis of the process operating parameters highlights the particular importance of the temperature difference between reactors, which has a strong impact on the required mass of solids circulating in the loops. Finally, partial carbon dioxide capture scenarios are considered and indicate that lower capture levels are suitable to match regulation targets.
The Canadian regulations on carbon dioxide emissions from power plants aim to lower the emissions from coal‐fired units down to those of natural gas combined cycle (NGCC) units. Since coal is significantly more carbon intensive than natural gas, coal‐fired plants must operate at higher net efficiencies and implement carbon capture to meet the new regulations. Calcium looping (CaL) is a promising post‐combustion carbon capture (PCC) technology that, unlike other capture processes, generates additional power. By capturing carbon dioxide at elevated temperatures, the energy penalty that carbon capture technologies inherently impose on power plant efficiencies is significantly reduced. In this work, the CO2 capture performance of a calcium‐based sorbent is determined via thermogravimetric analysis under relatively high carbonation and low calcination temperatures. The results are used in an aspenONE™ simulation of a CaL process applied to a pressurized fluidized bed combustion (PFBC) system at thermodynamic equilibrium. The combustion of both natural gas and coal are considered for sorbent calcination in the CaL process. A sensitivity analysis on several process parameters, including sorbent feed rate and carbonator operating pressure, is undertaken. The energy penalty associated with the capture process ranges from 6.8–11.8 percentage points depending on fuel selection and operating conditions. The use of natural gas results in lower energy penalties and solids circulation rates, while operating the carbonator at 202 kPa(a) results in the lowest penalties and drops the solids circulations rates to below 1000 kg/s.
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