4.6 Article

CaO-Based Nanomaterials Promoted with CaZrO3 for High-Temperature Carbon Capture

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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
卷 61, 期 23, 页码 5514-5526

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AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.2c00121

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  1. Natural Sciences and Engineering Research Council of Canada (NSERC)

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Calcium looping is a promising method for reducing carbon emissions, and the development of sorbents with high CO2 uptake capacity and cyclic stability is crucial for its commercialization. In this study, CaO-based sorbents stabilized with CaZrO3 were synthesized using the solution combustion synthesis method. The use of different fuels (citric acid and beta-alanine) had an impact on the physical properties and carbon capture performance of the sorbents. The results showed that sorbents synthesized with citric acid had a higher surface area and CO2 uptake capacity compared to those synthesized with beta-alanine. The cyclic stability of the sorbents decreased under harsh calcination conditions, indicating the need for improvement in practical applications.
Calcium looping is a promising route for decarbonization of carbon-intensive fossil fuel-reliant industries. Development of sorbents with high CO2 uptake capacity and cyclic stability is of paramount importance for commercialization of the calcium looping process. In this work, novel CaO-based sorbents stabilized with CaZrO3 were produced using the solution combustion synthesis method. The effect of using different fuels (citric acid and beta-alanine) on the physical properties and the carbon capture performance of the sorbents was investigated. Citric acid-synthesized sorbents indicated a higher surface area (30.0 m(2)/g) compared to beta-alanine-derived sorbents (9.3 m(2)/g), resulting in a superior CO2 uptake capacity. Sorbents were calcined under mild (850 degrees C, under 100% N-2) and harsh (950 degrees C, under similar to 50% CO2 in N-2) calcination conditions in 20-cycle experiments. Under harsh calcination conditions, sorbents exhibited a decreased stability over cycles due to sintering and loss of surface area at high temperatures. The CA20-1x sorbent maintained 96 and 57% of its initial uptake capacity after 20 cycles under mild and harsh calcination conditions, respectively. Sorbents were further spheronized and tested for their uptake capacity and stability. Spheronized sorbents exhibited a reduced uptake capacity under similar testing conditions due to diffusion limitations and a broader uptake rate profile. A longer carbonation time was recommended for spheronized sorbents to improve the uptake capacity.

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