Catalyst-loaded micro-encapsulated phase change material for thermal control of exothermic reaction
CO 2 methanation is a promising technology to enable the use of CO 2 as a resource. Thermal control of CO 2 methanation, which is a highly active exothermic reaction, is important to avoid thermal runaway and subsequent degradation of the catalyst. Using the heat storage capacity of a phase change m...
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Veröffentlicht in: | Scientific reports 2021-04, Vol.11 (1), p.7539-7539, Article 7539 |
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Sprache: | eng |
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Zusammenfassung: | CO
2
methanation is a promising technology to enable the use of CO
2
as a resource. Thermal control of CO
2
methanation, which is a highly active exothermic reaction, is important to avoid thermal runaway and subsequent degradation of the catalyst. Using the heat storage capacity of a phase change material (PCM) for thermal control of the reaction is a novel passive approach. In this study a novel structure was developed, wherein catalysts were directly loaded onto a micro-encapsulated PCM (MEPCM). The MEPCM was prepared in three steps consisting of a boehmite treatment, precipitation treatment, and heat oxidation treatment, and an impregnation process was adopted to prepare a Ni catalyst. The catalyst-loaded MEPCM did not show any breakage or deformation of the capsule or a decrease in the heat storage capacity after the impregnation treatment. MEPCM demonstrated a higher potential as an alternative catalyst support in CO
2
methanation than the commercially available α-Al
2
O
3
particle. In addition, the heat storage capacity of the catalyst-loaded MEPCM suppressed the temperature rise of the catalyst bed at a high heat absorption rate (2.5 MW m
−3
). In conclusion, the catalyst-loaded MEPCM is a high-speed, high-precision thermal control device because of its high-density energy storage and resolution of a spatial gap between the catalyst and cooling devices. This novel concept has the potential to overcome the technical challenges faced by efficiency enhancement of industrial chemical reactions. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-021-86117-1 |