Continuous CO2 capture and reduction to CO by circulating transition-metal-free dual-function material in fluidized-bed reactors
Tomone Sasayama (National Institute of Advanced Industrial Science and Technology (AIST))
Yuya Ono (National Institute of Advanced Industrial Science and Technology (AIST))
Fumihiko Kosaka (National Institute of Advanced Industrial Science and Technology (AIST))
Yanyong Liu (National Institute of Advanced Industrial Science and Technology (AIST))
Shih Yuan Chen (National Institute of Advanced Industrial Science and Technology (AIST))
Takehisa Mochizuki (National Institute of Advanced Industrial Science and Technology (AIST))
Koichi Matsuoka (National Institute of Advanced Industrial Science and Technology (AIST))
A. Urakawa (TU Delft - ChemE/Catalysis Engineering)
Koji Kuramoto (National Institute of Advanced Industrial Science and Technology (AIST))
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Abstract
To mitigate global warming and achieve a sustainable society, innovative technologies for efficient CO2 utilization are required. Integrated CO2 capture and reduction (CCR) using dual-function materials (DFMs) is favorable owing to its potentially low energy consumption, capital investment, and processing costs. Although numerous studies have focused on catalytic science, continuous and steady-state CCR operations have not been sufficiently addressed from an engineering perspective. In this study, a circulating fluidized bed (CFB) system is investigated for continuous CCR to syngas (CO + H2). In the CFB system, transition-metal-free DFM (Na/Al2O3) particles are circulated between two bubbling fluidized-bed reactors. The DFM captures CO2 in one reactor (CO2 capture reactor) and reduces the captured CO2 to CO by the reaction with H2 in the other reactor (H2 reactor). The effluent gas concentrations from both reactors reach steady state and are maintained for over 8 h. For the product gas from the H2 reactor, the CO2 conversion and CO selectivity exceed 80 % and 99 %, respectively. However, the H2 conversion is <20 %, indicating a potential challenge for the CFB system for integrated CCR. Furthermore, this study confirms that the H2/CO ratio for syngas can be controlled by adjusting the experimental conditions (particularly, the H2 flow rate). Consequently, the CFB system can be modified to facilitate the interaction between H2 gas and the DFM particles.